Reviewed By:  Dr. Surangama Lehri

Table of Contents

• What is Lyme Disease and What’s Causing the Rise? 
• 2025’s New & Surprising Lyme Symptoms to Watch For 
• Lyme’s New Hotspots: Where Are You Most at Risk Now? 
• Next-Gen Diagnostics: Smarter Testing Is Here 
• Emerging Lyme Disease Treatments You Should Know 
• Prevention 2.0: How to Stay Safe in a Lyme-Heavy World 
• Overcome Lyme Disease At The Top US Lyme Clinic – LifeWorks
• What to Do If You Think You’ve Been Exposed 
• Can We Finally Get Ahead of Lyme Disease? 
• Lyme Disease Case Maps | Lyme Disease | CDC
• Dr Alok Patel lyme Disease – Search

Author Sarika Jassal 

Ticks, mosquitoes and fleas, oh my!

Cases of Lyme disease are on the rise, and it’s been reported that blacklegged ticks are carrying some other nasty vector-borne diseases that they can transmit to humans via their bloodsucking bites. According to the World Health Organization, vectors such as ticks, mosquitoes and fleas, account for more than 17% of all infectious diseases, causing more than 700,000 deaths annually.

Mosquitoes, the number one culprit worldwide, are known to spread such classic hits as malaria, dengue fever, West Nile virus disease The Vitals team is here with the answers about how vector-borne diseases spread, and what some researchers are doing to better understand why cases are on the rise.

Lyme Disease Cases Are Surging. Who Is Most At Risk? | Cascade PBS

Dr. Alok Patel chats with Dr. Christina Nelson, Medical Officer at the CDC’s Division of Vector-Borne Diseases (DVBD) to get the current “big picture” on Lyme disease, how it is transmitted and what you can do to stay safe while enjoying nature.

Also, Eloise Skinner, a researcher in the Mordecai Lab at Stanford University explains how her team is using machine learning to better understand how our human footprint can be a predictor for the transmission and prevention of VBDs. Don’t worry, we will also have a little health lesson on what to do if you get bit by a tick and where to turn if you get infected.

Lyme disease is on the rise again, and this time with more urgency than ever.  According to CDC (Centre for Disease Control and Prevention), emergency room visits for tick bites have reached their highest level in five years, with hundreds of Emergency Rooms visits reported weekly in peak regions. 

But it’s not just the numbers that are changing; the disease is also evolving, showing up in new places, with unfamiliar symptoms, and requiring faster, smarter treatments. 

If you think Lyme is only a concern in wooded areas of the Northeast United States, it’s time that you rethink. Cases are now being reported in the Midwest, the Pacific Northwest, and even parts of Canada that were previously unaffected. It’s affecting more areas than ever, including urban parks and states previously considered low-risk areas than ever, including urban parks, and states that were previously considered low-risk.  

So, what’s behind this alarming rise, and what can you do to protect yourself and your family? Let’s find out! Search Results for Lyme Disease | Cancer Quick Facts

  

What is Lyme Disease and What’s Causing the Rise? 

Lyme disease is a bacterial infection caused by Borrelia burgdorferi.  

It is transmitted to humans through an infected tick (primarily deer tick or black-legged tick) bite. However, the common ticks (wood tick or dog tick) do not carry the infection.  

The ticks carrying bacterial infection are mostly found in grassy, bushy, or wooded areas of the United States. But Lyme disease is most prevalent in the upper Midwest, northeastern and mid-Atlantic states. It’s also common in Europe, South Central and Southeastern Canada, and some parts of Asia. 

Characterized by early symptoms like bull’s eye rash, fatigue and fever, it progresses to affect joints, heart, brain and nervous system. 

Some most common causes for rise in the disease include: 

1. Longer Tick Seasons 

As our climate continues to warm, ticks stay active for up to 10 months of the year in many regions. Climate change has reduced the duration and intensity of cold seasons, resulting in higher tick survival rates. Mild winters and wet springs give them a perfect environment to breed and thrive.  

2. Urban Expansion 

Ticks are increasingly found in suburban backyards, city parks, dog trails, and even greenbelts in the city neighborhoods, not just deep forests.  

As cities expand into natural tick habitats, and as deer and small mammals (tick hosts) adapt to urban environments, ticks proliferate in areas where people live and recreate.   

3. More Outdoor Time 

People love spending more time outdoors, hiking, gardening, camping, especially post pandemic. While this return to nature is refreshing, it also increases the chances of tick bites; especially if people are unaware and inconsistent with tick prevention (proper clothing, tick checks, repellents).   

2025’s New & Surprising Lyme Symptoms to Watch

The most common early symptom of Lyme disease is “bull’s eye rash (erythema migrans).” But it’s no longer the reliable sign it used to be. 

As per CDC, only about 70-80% of people infected ever see this rash.  

This means a significant proportion of infected have never seen the hallmark rash, making early detection even more difficult.  

Here’s a list of some new or commonly missed symptoms of Lyme disease to watch for in 2025: 

1. Extreme Fatigue: The kind that doesn’t go away with rest 

2. Recurring Migraines: Persistent and painful headaches 

3. Brain Fog: Trouble focusing, forgetfulness or feeling off 

4. Memory Lapses: Forgetting names, appointments, or conversations 

5. Heart Symptoms: Irregular heartbeat, chest discomfort or dizziness 

These symptoms often mimic other conditions, which is why early diagnosis becomes tricky. Many people go weeks or even months before realizing they’re infected.  

Also Read: Flu Symptoms 2025  

Lyme’s New Hotspots: Where Are You Most at Risk Now? 

Lyme disease is on the move, spreading beyond its usual areas. It’s no longer limited to a few high-risk areas in the US Northeast and Upper Midwest, though these places are also seeing large numbers. 2025 has seen a noticeable shift in the Lyme map.  

New or Underrecognized Hotspots and Rising Risk Areas for Lyme Disease Include: 

• Northern California 

• British Columbia, Canada 

• The Great Lakes region (Michigan, Wisconsin, Minnesota) 

And ticks are no longer just in forests and trails.

They are adapting and more bites are now reported from: 

• Urban parks 

• Dog parks 

• School playgrounds 

• Community gardens 

Researchers believe changes in vegetation, local animal populations (like deer and mice), and urban landscaping have made these areas prime tick habitats. So, if you live or spend time in these areas, stay alert, ticks may be closer than you think. 

Next-Gen Diagnostics: Smarter Testing Is Here 

For years, Lyme disease testing has been unreliable. The traditional 2-step test (ELISA followed by Western blot) often misses early infections or gives false negatives.  

But 2025 is changing that. Cutting-edge innovations powered by AI are bringing in hope for faster, more accurate diagnosis, especially in the critical early stages.  

Let’s see what’s new in Lyme testing: 

• AI Powered Blood Tests 

New blood tests are developed by researchers that use AI to analyze unique immune responses to Lyme bacteria. These tests look for multiple protein markers simultaneously and boost accuracy to over 90%. It works even in early infection.  

• Faster Results:  

Next-gen tests can deliver results in under 30 minutes. This enables quicker diagnosis and timely treatment to prevent long-term complications. 

• Smarter Differentiation: 

AI enhanced tests detect immune patterns unique to each patient, thereby reducing false negatives and helping tailor more effective treatments.  

• On the Horizon: 

Several of these innovative diagnostics have already received FDA approval, and early studies are showing promising results. Commercial availability is expected soon, marking a new era in Lyme disease care.  

Emerging Lyme Disease Treatments You Should Know 

For years, Lyme treatment meant long courses of antibiotics. While they are helpful for many, these treatments often fall short, particularly for those with late-stage or chronic symptoms.  

Thankfully, things are changing fast, bringing in innovative therapies and a shift toward personalized care. What’s new? Check below: 

1. Targeted Drug Therapies: 

Scientists are developing new medications that specifically target the Lyme bacteria. An exciting approach is to block a key enzyme (called BbLDH), which is required by Lyme Bacteria to survive. 

These next-gen drugs attack the infection more precisely without harming your body’s healthy cells and microbiome.  

2. Herbal & Integrative Options: 

Natural remedies like Japanese knotweed and cryptolepis are showing real promise in lab studies for their strong antibacterial activity against Lyme. These are now being explored in both clinical research and as complementary options alongside standard care.  

3. Personalized Medicine: 

Doctors are beginning to map each patient’s microbiome to understand how their gut and immune system react to infection. This helps customize treatment, especially for people dealing with chronic or persistent Lyme symptoms. 

Prevention 2.0: How to Stay Safe in a Lyme-Heavy World 

With Lyme disease cases surging, prevention is more crucial than ever. And today’s strategies go far beyond just bug sprays. Here’s how you can protect yourself and your loved ones effectively: 

1. Smart Clothing: 

• Wear light-colored clothes to spot ticks easily. 

• Tuck your pants into your socks when hiking or gardening. 

• Consider permethrin-treated clothing as it repels and even kills ticks on contact. 

2. Repellents That Work: 

• Look for repellents that contain 20-30% DEET, picaridin, or oil of lemon eucalyptus. 

• Apply to exposed skin and reapply as required, especially after sweating or swimming. 

3. Vaccines on the Way: 

Valneva and Pfizer are testing a new Lyme disease vaccine called VLA15. It’s in the final stage of trials with 6,000 people in North America and Europe. The main three shots are done, and results are expected by the end of 2025.  

If it works well, the vaccine could be approved in 2026. VLA15 targets six types of Lyme bacteria and may help protect millions from getting sick. 

4. Community Level Prevention 

Neighborhoods are adopting smart strategies like: 

• Planting tick-repelling plants 

• Using tick tubes in yards targeting rodent hosts 

• Keeping pet tick control up to date 

• Public spaces like schools and parks are starting to add tick awareness signs and prevention zones. 

What to Do If You Think You’ve Been Exposed 

Tick bites are tiny and can be easily missed. Even if you never saw a tick, you could still be at risk.  

Watch for these symptoms: 

• Fever or chills 

• Body aches 

• Fatigue 

• Stiff neck 

• Unexplained rash (even if not a bull’s-eye) 

What to ask your doctor? 

• Request a modern Lyme test (not just ELISA/Western blot). Newer diagnostics are more accurate than traditional tests. 

• Consider a Lyme-literate or integrative practitioner if symptoms persist. 

• Keep a symptom diary; it helps your provider see patterns and track progress. 

Act Early: DO NOT wait for a rash to appear. If you feel off after spending time outdoors, reach out to your doctor promptly. Early treatment is the best way to prevent lasting complications. 

What to do if you find an attached tick?  Remove it as soon as possible with fine-tipped tweezers, pulling straight out without twisting. Clean the bite area and your hands with soap and water or alcohol.  Save the tick in a sealed bag (for possible identification) and note the date/location of the bite. Ask your provider if sending the tick for testing is recommended in your area.

Can We Finally Get Ahead of Lyme Disease? 

Yes, we have reasons to hope. With better testing, more personalized treatments, and rising public awareness, we’re finally starting to get ahead of Lyme disease.  

Schools, hospitals, and community centers across the country are launching tick safety campaigns, helping people stay informed and protected. Meanwhile, biotech companies are investing in research like never before to find better cures. 

We suggest people listen to their bodies and speak up when something feels wrong, thereby leading to earlier diagnosis and better outcomes. 2025 may mark a record-breaking year for Lyme disease cases, but it might also be the turning point toward clearer, faster, and more personalized Lyme care. 

Disclaimer: This article is for informational purposes only and is not intended to diagnose, treat, cure, or prevent any disease. Statements about emerging treatments, vaccines, or herbal remedies are based on current research and are subject to change as new evidence becomes available.

References: 

1. U.S. Environmental Protection Agency. Climate Change Indicators: Lyme Disease. EPA, 1 July 2016 (last updated Dec. 2024), www.epa.gov/climate-indicators/climate-change-indicators-lyme-disease. 

2. Association of Health Care Journalists. “Lyme Disease Is Changing in a Warming World and So Should the News.” Association of Health Care Journalists, 16 July 2025, https://healthjournalism.org/blog/2025/07/lyme-disease-is-changing-in-a-warming-world-and-so-should-the-news/.  

3. Centers for Disease Control and Prevention. “Signs and Symptoms of Untreated Lyme Disease.” Centers for Disease Control and Prevention, 15 May 2024, www.cdc.gov/lyme/signs‑symptoms/index.html.  

4. American Society for Microbiology. “Scientists Uncover Lyme Disease’s Hidden Achilles’ Heel – And How to Exploit It.” SciTechDaily, 20 Mar. 2025, scitechdaily.com/scientists-uncover-lyme-diseases-hidden-achilles-heel-and-how-to-exploit-it/. 

5. Dykstra, Mischa. “Ethnobotanical Medicine Is Effective Against the Bacterium Causing Lyme Disease.” Frontiers, 21 Feb. 2020, frontiersin.org/news/2020/02/21/ethnobotanical-medicine-is-effective-against-the-bacterium-causing-lyme-disease. 

6. Pfizer Inc. and Valneva SE. “Pfizer and Valneva Complete Recruitment for Phase 3 VALOR Trial for Lyme Disease Vaccine Candidate, VLA15.” Pfizer News Release, 4 Dec. 2023, www.pfizer.com/news/press-release/press-release-detail/phase-3-valor-lyme-disease-trial-valneva-and-pfizer. 

Thank you for this. Do you have a source for this one and seven people?

I want to share it, but I have people who always ask for sources.

Robin V Schwoyer

Roxanne Berardi Perkins what are your thoughts on this paragraph. What test do you think they used? I mean, I know it says that they went through 89 studies so I guess they’re just working on whatever analytic was used, but they’re saying if it was Western blot it’d be better. 

Can you imagine if the new iGenex was approved and used freely what the numbers might be?—-

“The study also said that research using an analytic technique called western blotting was more reliable and that its use “could significantly improve the accuracy” of future studies.”

Roxanne Berardi Perkins

Robin V Schwoyer

https://www.nbcnews.com/…/14-percent-world-population…

14 percent of the world population may have had Lyme disease, research finds

Giant Study Reveals Over 14% of The World Has Probably Had Lyme Disease : ScienceAlert
These statements always need to be backed up with facts! 

Roxanne Berardi Perkins

Joyce Youngman 95% of the population has EBV antibodies.

This study, which showed that looked for antibodies against Borrelia, not EBV. 

Roxanne Berardi Perkins

I have antibodies to both plus low CD57 + NK cells(complete) raised Hematocrit & DNA SNP for CVID, JAK2 V617F, & several oncogenes including diagnosis of conditions like FH deficient Leiomyoma, SDHC, calcified Adrenal glands RET related Hypercalcemia Primary-Hyperparathyroidism(MEN2a) Hirschsprung variant, liver cyst but Drs don’t want to know & tell me my blood tests are fine.

Roxanne Berardi Perkins

Joyce Youngman 95% of the population has EBV antibodies.

This study, which showed that 14% of the world population has Lyme, looked for antibodies against Borrelia, not EBV. 

Jason Valentine  If testing is inaccurate what test is used to determine that testing is inaccurate ??? If testing is inaccurate how is it determined then how many people have it ???? Lyme in itself doesn’t cause symptoms . The immune response to it is what causes symptoms . Lyme can go dormant for a short period not years but continues replicating in the body and can be asymptomatic then become symptomatic with an immune response that causes symptoms .

Dawn Keller

Jason Valentine Testing is generally inaccurate. I was tested several times and it either came out negative or inconclusive. It was when I had the Igenex test and found a Lyme Disease specialist with many misdiagnoses that I was finally found to be positive for it.

Jason Valentine

Dawn Keller oh I know it’s inaccurate . Just can’t quantify it with a number if we don’t have a means to weigh it against . So I don’t like data like that in posts or that people just believe what they read because they read it . Sorry I’m an engineer and I advocate that we give accurate info for our cause so people can’t dismiss us as a group that believes anything or doesn’t know what we are talking about etc . But I’m well versed sadly as to testing being inaccurate . Unless it’s a recent infection and positive IGM test . Not to be confused with a false negative . A positive IGM is all we got that’s accurate .

Dawn Keller Jason Valentine Yes I definitely understand this. I kinda take statistics with a grain of salt. When I was diagnosed and halfway through treatment, I knew of around 70 people or so in my area who had been diagnosed with Late stage/Chronic Lyme. Yet the CDC there was NO LYME in that area.

Jason Valentine

Dawn Keller this medical injustice needs to stop . If there are birds for example especially ones that migrate then how can’t they say oh no lyme in that area . Plus it has slowly spread from lyme ct all over the world .there’s data and maps and graphs all over . Like what small animals can’t slowly spread it ? Nonsense .

Dawn Keller Even MORE ridiculous is it was in Chattanooga, Tennessee where I lived and at the time (20+ years ago), Georgia was one of the leading states for Lyme Disease. Yet WE had none?! Plus Chattanooga is pretty much right on the border anyway. I guess THOSE ticks knew not to cross the state line, right?!,🙄🙄

Patty Frymire  I’ve had chronic Lyme for 30+ years,now I have Alpha Gal for last few years. I HATE TICKS!!!

Mindy Waddell RitchLab borne disease 🦠 bagan in bio lab in Lyme Connecticut

April Reddington Mindy Waddell Ritch Ritch actually, Plum Island. The first cases were found in children in Lyme, CT

Roxanne Berardi Perkins April Reddington

actually, the first known case was found in Otzi
5300-year-old “Iceman” is first recorded case of Lyme disease

Maureen Wilder  What do you expect from engineered viruses? Looking at you, covid, too.

Marcy ShulmanI tested negative after a bite over 20 years ago. 1.5 years ago my herbalist suggested that I be tested though I had no bite. I had unusual back pain and exhaustion. The test was positive. An herbal specialist suggested that it had been dormant but was reactivated by spike proteins from others who had the v-c was well as the chemtrails.

Samantha Jenner

I actually think Lyme tests are less accurate than that. I was tested last year 2x and nothing came up. I’m now working with a groups of functional physicians and have learned that there are 18 different strains of Lyme diseases. So in order to properly diagnose your lines and if you have multiple kinds, which I have four different strains of limes, disease, and my doctors and I know for sure that I have had at least two of those for about 20 years and I have never been diagnosed properly with any of my medical issues. Not only my four types of lymes disease, but also Hashimoto’s since I was in middle school and just diagnosed a year and a half ago at the age of 41, Epstein-Barr virus, which comes from mono, which I never had mono, but my brother did 25 years ago so I’ve had that sitting in my body this whole time too.

The saddest part about what’s going on in this country and the world for women’s health is that we have never been studied ever. That’s why a man can go in and get tested and get a result and get treated when women with the same things get ignored. Because 99.9% of all medical professionals out there never learned how to treat and take care of women because researchers and scientists never studied us.

Sara Sanchez CollinsI’ve suffered most of my life, I’m 58 have been dealing with health issues since being bit the 1st time at 4. Doctors have missed & misdiagnosed me my whole damn life. I’m beyond fed up about this. 😭🤬😤

Flora Christian

Jason ValentineWhat’s the story with a weak positive IgG for Lyme low CD57+NK cells(complete) EBV IgG 3046 raised Hematocrit & DNA snp’s for several oncogenes including JAK2 V617F, MEN2a, HLRCC, SDHC & diagnosis for both Leiomyoma, & Hypercalcemia Primary-Hyperparathyroidism calcified adrenal gland & a liver cyst.

Flora Christian

Jason Valentine The Lyme & EBV & Hematocrit are mainstream testing the others are WGS DNA results I would recommend this type of test to anyone struggling with long term chronic conditions.

Hana Lynn  EVERYONE GET YOUR TEST PRINTED. DEMAND IT.

MORE THAN LIKELY YOU HAVE PRESENT BANDS!!!!!!

JUST NOT “enough” to qualify as valid for treatment in this HELL of a country!!!!!
I was told I am negative. I have 4 bands. That is not negative. once you learn what bands you have, you can specifically treat them and always dm me for help if needed

Robin V Schwoyer  
Because of working with the center for Lima action, I become fascinated by the statistics that everyone chooses to do. It also has to do with my training over 30 years ago at Drexel University where have degrees in finance and marketing. Basically what we were taught is numbers never lie but we can make them say anything that you want especially if you pay us enough lol
With that said, I was trying to figure out numbers that I saw back in March that changed the 476,000 persons a year to 620,000 and that was based on a change from those 30,000 to 60,000 people reported from Health departments. But I found this and trying to find the numbers—–

Lyme Disease Surveillance and Data | Lyme Disease | CDC
So this states that the most recent information shows that we have 89,000 cases being reported to through surveillance of Health departments. However, they’re still maintaining the 476,000 people from the compilation of insurance claims.

But there’s no way numbers actually lineup because if we have more people being reported than we probably have more claims for insurance. But again the 476,000 persons a year is an estimate that the CDC admits is underestimating. Now I’m saying all this because I’m fascinated with persister cells.

In other words, even if you’re treating cases of Lyme disease, there are the bacteria that know to change form. And I’ve been looking for statistics to show any research on how many cells we think get away. Especially when they know they are under pressure from doxycycline. Antibiotic pressure will definitely cause transformation of these cells.

Now when the sales transfer into her sister sis or biofilms that is not considered a replicating cell. However, it is capable of holding a pathogen. And when pressure is relieved it is capable of going back to its active form. This can explain why some people have dormant Lyme disease.

Or can explain why we think we treated something actively and because our testing is pathetic and ineffective you can show no act of Lyme and yet it is in the system. So what doing research for that and playing with the post that you just did if we have $89,000 people a year officially reported and the CDC says that there might be 14% of people who wind up with persistent lyme then that would mean that almost 13,000 people a year would wind up with something that is potentially a chronic lyme.

If we use the 476,000 number then that figure would be approximately 67000 people a year continuing with lyme related diseases. And of course this does not take into account any of the other tick-borne illnesses, which I think everybody should be standardly tested for given the endemic across the country.

Long story short, I think we do need to be definitely talking about the 89,000 people Up to over 600,000 people a year because this is information that needs to be in front of the doctors when they’re questioning why we want treatments or we want better testing. Lyme Disease Surveillance and Data | Lyme Disease | CDC

Linda Crowley 
+Long before Lyme became widely heard of, I remember pointing out the tick bite on my leg and commenting to my husband, “It looks like a bull’s eye!” We were overseas at the time. For years afterwards, I had health issues. “It sounds like Lyme”, more than one doctor said in later years, but all tests came back negative. I finally was in the hospital with a horrible reaction to another tick bite, and the specialist said, “Of course it never showed up. Our Lyme tests only catch the American variety, not the European variety.” The long dose of antibiotics helped, but I know the damage had already been done. I’m just not sure what issues are related, and what else needs to be watched for.

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Reds rallying around Fraley amid ‘most challenging season of my life’

‘It’s changed me for the better’: Cincinnati Reds’ Jake Fraley on daughter’s road to healing

Gordon Wittenmyer

Cincinnati Enquirer

But the Cincinnati Reds outfielder already is having his best season in two years, “When you go through something like that, it really puts into much more perspective just how little this job and all the (worldly) things that encompass life, and how minuscule they all are,” Fraley said. 

CINCINNATI (WXIX/Gray News) – A professional baseball player and his wife are sharing their young daughter’s story as she battles cancer.

In the middle of the 2023 MLB playoff race, Cincinnati Reds outfielder Jake Fraley and his wife Angelica could tell something was wrong with their 5-year-old daughter Avery.

“It all started with a limp and back pain,” Angelica Fraley said. “She stopped walking.”

After numerous visits to the doctor and the emergency room, doctors diagnosed Avery with acute lymphoblastic leukemia, a type of cancer of the blood and bone marrow.

“It was very difficult,” Jake Fraley said. “It’s something you can’t imagine.”

The Fraleys faced Avery’s cancer fight with one driving message and one word: purpose.

They shared that message on social media when they announced her diagnosis, one that put her battle and their faith in perspective.

The couple says they know their purpose as they help Avery fight for her young life.

Cincinnati Reds Player Trusts God Amid Daughter’s Cancer Battle

A glance at Fraley during spring training showed what he meant, with his wife and small kids enjoying the Arizona sunshine while he worked – 6-year-old daughter Avery, in particular, bouncing around camp near the ballfields.

“She’s got all her hair back, all her energy back; she’s back to our normal baby girl,” Fraley said. It’s been a long road for the family, but after more than a year of treatments for acute lymphocytic leukemia, Avery remains in remission.  

And if the Reds’ baseball plans this season play out into a postseason run, she might be finishing scheduled treatments right about the time her dad’s done playing this year.

“It’s tremendous. It’s a blessing,” Fraley said.

In one big way, he said, the recent offseason was no different than the one before, the one the family began the road from terrifying diagnosis to faith and focus on healing.

“I’m still resting in the Lord. I’m surrendering to Him,” Fraley said.

But Avery’s restored health over the past several months has admittedly breathed new life into Fraley, renewed peace and perspective. And he’s felt the difference professionally, too, this year.

Coping With a Child’s Cancer Diagnosis: MLB Player’s Wife, Angelica Fraley, Celebrates Daughter Being In Remission After Acute Lymphoblastic Leukemia Diagnosis: ‘The Best Birthday Present I Could Have Ever Asked For’ – NewsBreak

Jake Fraley Stats, Height, Weight, Position, Rookie Status & More | Baseball-Reference.com 

“Last year I was one foot in, and one foot out. It was just the nature of what we were going through,” said Fraley, who at one point last year took a six-day personal leave for Avery’s care. “When you go through something like that it definitely changes something inside you. 

“But going into this season,” he said, “obviously it’s different in the aspect of I’m not having to wake up at 6 o’clock in the morning and then going to watch my daughter get chemo and then shooting over to the field for a 6 o’clock game. That obviously has changed. So you feel like you have a little bit more energy.”

Not that anyone from the outside would have suspected that something so profound was going on in his personal life off the field.

“Incredible,” said Collin Cowgill, the Reds first base and outfield coach. “I mean, the toughness that the guy shows day in and day out in general is exemplary. With all the stuff with Avery last year, if you didn’t know him, you wouldn’t know what was going on.”

Through it all, he still managed to hit a career-high .277 in 116 games with 20 stolen bases last year. “He’s as tough of a human being as I’ve ever met,” Cowgill said. “This year, it’s not a noticeable difference, but I can tell the way he’s talking about his family life and in general just how much at peace he is there. And just a little bit more able to focus on baseball.”  

Said Fraley: “It’s just changed me. It’s changed me for the better.”

Fraley and his family leaned hard into their faith during the year that turned their lives upside down, and Fraley calls that the key, for getting through it and for that change, even when it comes to baseball.

“As a man and a disciple of Christ, that’s everything, because we get so sucked up into this game, because it’s so difficult, and it’s so hard to be the best player in the world and to stay atop of those for as long as you can,” he said, “that (it’s) getting to that place of understanding that we’re going to spend more of our life not playing this game than playing, right?

“The betterment of the change for me going through all of that was really just understanding how grateful I am for all the little things. And it’s really kind of taken me to a new place that I’ve never been to before.” 

Better at that even? On the field?

“I don’t want to lean on the side of a better player because there’s so much of this game that’s out of our control,” Fraley said. “I think it has made me a better husband. it has made me a better father. It has made me a better teammate. And I’m not 22, 23 years old anymore; I’m getting ready to turn 30 years old, and after this year I’m going to have just short of six years of service time. People look at me as a veteran, which is weird to say.

“It’s changed me in the aspect of just being able to recognize things for what they truly are.” Whether the transformed outlook and peace of mind helps take Fraley to an All-Star selection, it’s the better place he’s discovered over the past year and a half that he says is what matters. 

“When you live a life that’s not centered around Christ it’s a difficult way to live,” he said, “and especially when you’re playing a game that’s so difficult to play, and it’s dictated on the pressure, and everybody’s watching you, and you’ve got to do well, and you’ve got to do this, and you’ve got to do that.

“I think that it just takes you to a space where, like King Solomon wrote in Ecclesiastes, where he says that everything is meaningless,” Fraley said. “Everything has meaning, but it’s where our focus is. And it’s brought me to a deeper focus that Christ is everything, and everything else is like a passing in the wind.”

Jake Fraley, outfielder for the Cincinnati Reds, found peace and strength during one of the most challenging seasons of his life — his young daughter Avery’s battle with leukemia.

 Avery’s Diagnosis and Journey

• Avery, Fraley’s daughter, was diagnosed with acute lymphocytic leukemia after weeks of debilitating back pain that was initially misdiagnosed.
• The diagnosis came swiftly after a blood test, turning the family’s world upside down in just 15 minutes.
• After more than a year of treatments, Avery is now in remission, with her energy and hair restored — “back to our normal baby girl,” Fraley said.

 Faith and Perspective

• Fraley leaned heavily on his Christian faith, saying that “walking with Jesus” gave him peace, joy, and happiness even in the darkest moments.
• He described the experience as transformative: “It’s changed me for the better,” he said, noting how it shifted his perspective on life and baseball.
• The family shared on social media: “Our purpose as a family is to glorify God in every season… We see the hand of God at work every single day”.

 Support from the Reds

• The Reds organization played a crucial role in supporting Fraley, constantly checking in and offering comfort throughout the ordeal.
• Fraley took a six-day personal leave last season to care for Avery, and he admitted that he was “one foot in, one foot out” professionally during that time.

 A New Season, A Renewed Spirit

• With Avery’s health improving, Fraley entered the new season with renewed energy and focus.
• He reflected on the contrast: “I’m not having to wake up at 6 a.m. to watch my daughter get chemo and then shoot over to the field for a 6 p.m. game”.

Jake Fraley’s story is one of resilience, faith, and the power of community — both on and off the field. Avery has recently gone into remission from acute lymphoblastic leukemia, a rare blood cancer, and is no longer showing signs of cancer in her bone marrow.

However, she will continue to undergo frontline chemotherapy as part of her treatment plan. Avery Fraley is not cancer-free. 

Recent tests have detected no more cancer in her bone marrow, but she is still undergoing treatment, including chemotherapy, and has not yet reached the two-year mark for remission.

“It’s hard – things you can’t imagine” – Jake Fraley faces his greatest pain: his 5-year-old daughter has cancer 1sports.yahoo.com 2www.cincinnati.com 3thechristiantribune.com

Reds rallying around Fraley amid ‘most challenging season of my life’

13 Healthy Summer Habits to Strengthen Your Body and Mind

This spring—2025—is 26 years since I was diagnosed with pancreatic cancer.

Marisa Harris Pancreatic Cancer Survivor – Search

Given a poor prognosis after being diagnosed with stage IV pancreatic cancer

Found a doctor who combined chemotherapy and complementary treatments

Focused on positivity, and people who defied the odds

YOU HAVE CANCER …

These three words are probably the most frightening statement you or someone you love may ever hear. In 1998, I was diagnosed with Stage Four pancreatic cancer. Doctors at America’s leading hospitals told me that my disease was incurable.

They had no treatment to offer me, not even chemotherapy.

I had at most nine months to live.

However, I refused to accept their death sentence, and I embarked on a search for help. I was ultimately blessed to find a brilliant and imaginative oncologist who said, “There is so much you can do. Miracles happen every day. They are your birthright.”

Inspired by his encouragement, I undertook a scientifically based, nonmedical course of treatment that included supplements, healthful nutrition, exercise, singing bowls, but also, acupuncture, prayer, and meditation. I began attending a support group of cancer patients and survivors conducted by my new doctor. After nine months, he invited me to create and lead a support group for his patients.

I left my position as a corporate executive and dedicated myself to staying alive and helping other cancer patients to not only stay alive, but to live a life that was happier than ever before. ​After five months, I received objective, medical proof that my condition had dramatically improved. My tumor markers were significantly lower.

I began chemotherapy and also continued following my complementary practices. The combination proved to be a powerful integrated treatment. ​More than 25 years have passed since I was told, “Nothing can be done.” As I continue to be cancer-free and healthy, my life’s purpose is to eradicate that message for cancer patient. 

Now a long-term survivor helping others

I am celebrating twenty-six years of being alive after a stage four pancreatic cancer diagnosis. I have made it my life’s work to stay on the cutting edge of research and practice on what contributes to the health and well-being of people diagnosed with cancer. As a certified cancer coach practicing for over twenty years, I support cancer patients, their caregivers, and their supporters. My intention is to help my clients hone in on exactly what they need to heal and to thrive at every stage of the journey. Home | marisaharris

I had a long history of gastrointestinal problems, so any time I had stomach aches and back aches, I figured it was just my sensitive GI tract. Also I felt that my priorities were work, family, and training for a marathon. Because of my history, I didn’t pay attention to the symptoms.

But after a horseback riding accident I noticed a hard swelling in my groin. I went to my internist, who said it was an enlarged lymph node caused by my accident. However, when my gynecologist saw the swelling during a routine examination, she thought this needed immediate attention, and sent me to a surgeon. He suspected it was cancer, and immediately scheduled me for surgery.

After some tests, the oncologist sat down with my husband and me and said I had stage IV pancreatic cancer. I didn’t know where my pancreas was but I soon found out what stage IV meant. My husband asked what this meant in terms of my life span and the oncologist said I had six months, maybe nine if I was lucky.

I said “There must be something that can be done—chemotherapy, surgery.” But the doctor said I was medically incurable and medically untreatable. I was shocked. I felt like an outcast in my own world, like a sheet of glass came down in front of me, and I was exiled from everything I knew.

Changing How I Thought

Had that doctor said “Let’s try chemotherapy” I would have done it and looked no further. But I was told nothing could be done. Being told nothing can be done was life-changing for me.

I took a leave from my job and started researching. But the negativity increased when I went to a bookstore and looked up pancreatic cancer. Remember, the statistics were worse 20 years ago than they are today. I slammed the book shut and decided I was never going to read anything negative about pancreatic cancer or stage IV cancers of any type.

I had spent most of my lifetime asking the question “Why do some people manage or navigate more successfully through the worst circumstances—what do they bring to those situations?” I decided to put into practice those characteristics, to do what I could to live happier and if possible longer. In the first shock of the prognosis, I asked “How can I have the best death?” Soon after, I turned my attention to those people who live longer than the odds or even survive. The hundreds of articles and research studies became the basis of my healing program.

With years of experience of hiring at all levels in a corporation, I never would have hired someone who believed that we would fail. So the first step for me was to find a brilliant, impeccably trained oncologist who believed in the possibility that I could get well again. Also, I realized that positivity was key for both the quality and quantity of my life, so I decided to be the CEO of my own healing program.

I needed a team of experts, headed up by that oncologist, but one who understood that many factors contribute to getting well and staying well. I went from doctor to doctor asking the question, “Who do you know that would work with me to get better?” I asked and asked, until I got an answer.

Finding the Right Oncologist

Finally, I was referred to Dr. Mitchell Gaynor*, who practiced integrative oncology. He also believed that medicine alone was not sufficient, and that patients needed to include changes on the physical, mental, emotional, and spiritual realms. When I met with him, Dr. Gaynor said there was so much I could do. He also said whether or not I chose him for my treatment I should come to his support group.

I was astounded that he ran his own support group, which included chanting and Tibetan bowls. I was reluctant to go to the first meeting because I was scared to be around people who would be talking about pain and dying. At his group I met people who were exercising, even running, while in stage IV.

Meeting Dr. Gaynor’s patients, who were so filled with life, led me to choose him as my oncologist. The quality of their experience was a very important factor in my decision. Because of an extensive family history of cancer—my mother, father, sisters, uncles, and both grandmothers had died of cancer—Dr. Gaynor suggested genetic testing.

In fact, he was the first doctor to suggest this to me. He sent me for a biopsy, and I found out that I carried the BRCA2 gene. I didn’t start chemotherapy right away—the other oncologists I had seen were adamant that chemotherapy would at most give me a couple of extra months, and leave me sick as a dog! I told him that I wanted to try his non-medical interventions first. He agreed, realizing that I was not going to be persuaded at this time.

Dr. Gaynor changed my diet, put me on supplements and some prescription medications, recommended a trainer to teach me exercises to complement my running, recommended a cancer therapist to deal with fears around my diagnosis and unresolved trauma from the past. My tumor markers dropped, and I was physically, mentally, and emotionally feeling better, but the CT scans showed no improvement.

He persuaded me to do chemotherapy, saying that he felt that without it the cancer would spread to my brain. In truth, he scared me into doing it. He put me on a regimen of carboplatin, Taxol, and Taxotere. I had chemotherapy for seven months. He prescribed supplements and drugs to bolster my immune system, to alleviate some of the side effects and to destroy cancer cells.

Once I made the decision to undergo chemo, I decided I was going to have fun in the chemo room and was going to celebrate being there. Instead of seeing the chemo as toxic – I saw it as a gift from dedicated scientists. I made wonderful friends among patients and nurses. I lost my hair, which was tough, because I believed it was my best physical feature.

This unusual oncologist shared with me that sometimes we have to lose what we think is most important to us to realize who we truly are. Wigs made me itch, so I wore the cutest hats that hid nothing, realized I wouldn’t have another bad hair day, and, in some odd way felt more beautiful than I ever had before.

I continued eating foods that are good for the body, and taking supplements that strengthened my immune system. I underwent acupuncture to minimize or eradicate the side effects such as nausea and neuropathy. It took a while for the treatments to show results but I was feeling positive. I was also loving my life—going to the rehearsals of the Philharmonic—up-leveling my relationships with my family, colleagues, and even strangers!

After treatment ended I had regular follow-ups.

I had CT scans every eight weeks for 10 years, Dr. Gaynor realized I was getting a lot of radiation, so we switched to MRIs. I also had blood work every three months for tumor markers. Years later, because of continuing concerns about other cancers, I had genetic testing for a second time.

This time the test was done at a bigger lab, and I found out that I carried the BRCA1 mutation. Now I see my oncologist every six months for various scans and I have blood work every four months. I have a team of doctors at NYU Langone Health that works together proactively.

The Power Within

Once I started changing my diet and doing the other things Dr. Gaynor recommended, I felt empowered and confident. I was focusing on my quality of life, not just the quantity of life. I was not willing to hear negativity from anyone. I took charge of my life.

I immersed myself in getting well. I focused on making up a great life by the years, the months, the weeks, the days. I decided that if I recovered I would never have another unhappy day. Later I realized that in some ways the hardest work in the world is to think and act in a way that is congruent with what we would really love to think, feel and do.

It is so normal to react negatively to challenges. But I got better and better at deciding I could create a great life. I deepened my spiritual connections with my husband and my religion. And I continued to focus on positivity. This process of thinking, feeling, and acting in a way that supports what we most want is a lifelong commitment.

.

A Positive Life

The minute I started feeling more hopeful I started sharing my experience with anyone facing a life-ending diagnosis. I have become a certified master integrative coach, a cancer coach, and certified in mind-body medicine, and a resilience practitioner. These steps and more were to help guide and serve people going through what may seem like hopeless odds. I have found that serving others is one of the most uplifting things we can do.

It is important to educate the medical community to use everyday terms so we can understand. And we must ask questions when we don’t understand. Even more important, we can remind the medical community of the essential power of our minds to impact the qualitative experience and the quantitative experience.

I advise patients to choose doctors and healing professionals that have a positive attitude, that see patients as partners in the process of healing, and that share information with each other so that they can best serve the whole person.

The most important advice is don’t try to do this alone. Know that healing from cancer requires you to really heal every part of your life. Be part of a support group—real or online—get a coach, and ask for help and give help while navigating through treatment and after.

*Dr. Gaynor passed away in 2015.

Marisa tells her story in “Reimagining the Possible: A 20-year Survivor of Pancreatic Cancer,” part of the Survivor Video series.

Marisa Harris is a Coach and 20+ Year Survivor of Stage 4 Pancreatic Cancer Who Helps People with Cancer Reimagine the Possible—A Complete Recovery | LinkedIn

Marisa Harris – Have You or Someone You Know Received a Life-Threatening Diagnosis?

Pancreatic Cancer Survivors Marisa Harris & Wendy Hammers – Hirshberg Foundation for Pancreatic Cancer Research

Breaking Up With Cancer – Hirshberg Foundation for Pancreatic Cancer Research

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Marisa Harris: 27 Year Pancreatic Cancer Survivor!!

Marisa Harris Pancreatic Cancer Survivor – Search

My Cancer Journey | Marisa Harris

Our time together began two decades ago when our biggest challenges were small.

Meet sister Aidan Morris, Shenell Malloy with Brenna Johnson

But, in 2019, we experienced something new together: CANCER.

Shenell, Aidan & Brenna Cancer Story – Search Videos

This is the story of three friends and sisters.

Shenell and Aidan, friends and mothers in their thirties, were diagnosed weeks apart with aggressive cancers. First Shenell with stage 4 glioblastoma brain cancer, and then Aidan with stage 3 triple negative breast cancer and melanoma. Both were considered the picture of health: young, active, and focused on diet and exercise. They were thrust into dealing with devastating diagnosis, but they had each other and they had hope.

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When Shenell started her cancer journey, she made the choice to turn her death sentence into a life sentence. She looked for guidance and answers, but for her diagnosis, there were few. Piecing together what she could find on her own, she realized that long-term survivors defying the odds took a whole-person approach to their cancer treatment and healing.

So alongside grueling brain surgery, chemo, and radiation treatments for an incurable disease, Shenell embraced this new beginning with a full body, mind, and spirit approach to give herself the best chance of surviving longer with terminal cancer.

It was the beginning of her passion to align the latest medical advances and cancer-specific centers of excellence with whole-person healing. ‍As Shenell was in treatment, Aidan received a shocking diagnosis of triple negative breast cancer that had already spread quickly, between elective mammograms.

She was facing one of the harshest regimens available: years of chemotherapy, radiation and surgeries. Only weeks ahead of Aidan, Shenell had already experienced a lifetime of perspective.

She knew the necessary pain of treatment and the unfair emotional strain on all aspects of life. Shenell knew exactly what would support Aidan in the days to come, so she put together a guide of how to “do cancer” and made a care package with items she wished she had during the beginning of her treatment. She could walk with Aidan in a way no one else could.
‍
After eventually reaching stability, we knew we could turn what we had learned into a resource for those impacted by cancer. We knew exactly how it felt to be lost and intimidated when a cancer diagnosis hits. All we wanted in that moment was to find a person like us, who had our cancers.

We wanted to know everything that person was doing—from medicines they took and the hospitals they were treated at, to the products they loved and the alternative therapies they tried. We wanted to know if they experienced the same thoughts and emotions. Together as patients, caregivers, and sisters, we created a positive, empowering place where anyone impacted by cancer can get actionable information and guidance from survivors.

Aidan Morris 6 Year Survivor | Cancer Quick Facts Recognizing the need for guidance during such challenging times, they decided to share their knowledge, experiences, and resources with others facing similar struggles.

 Their shared mission: to provide guidance, comfort, and hope to the 1 in 3 individuals impacted by cancer, offering insights inspired by their own challenging yet enlightening journeys. Their mission is to provide a beacon of hope and guidance for

those lost and overwhelmed by the challenges of cancer. 

Together we are Stronger and Together we can Do Cancer!  

To learn more about our story and Do Cancer,

click on this link. Do Cancer – Resources, Inspiration & Hope  #cancercommunity #docancer #lifeaftercancer

Do Cancer does three things:

Makes proven treatments & survivor tips accessible to anyone
Provides free concierge care to those in and out of treatment
Sends clean, survivor-curated Healing Kits

Stunned to her core when she was diagnosed with the aggressive form of brain cancer, Shenell committed herself to doing whatever it took to defeat her cancer.

Meet Shenell Malloy | Co-Founder, Do Cancer – SHOUTOUT SOCAL

In early 2019, my world flipped upside down and my life changed forever.

One moment I am a healthy, active, 36-year-old mom of two beautiful children living a normal life. Next, I’m staring at an image of a mass in my brain, being told I needed brain surgery because I may have the deadliest form of all cancers, glioblastoma.

At that moment, time stopped and my breath was ripped away from me. I was in absolute shock, so many questions racing through my mind. While I was still recovering from brain surgery, my oncologist recommended I immediately begin 42 days of combined radiation and chemotherapy.

Those 42 days were the hardest and darkest days of my life, and I am so thankful for the love and support I received from my family, friends, integrative healers, and doctors. I was determined to fight and do whatever it took to heal. Not only was this a physical fight, but I knew I had to begin a mental, emotional, and spiritual healing journey.

I began listening to my body, using food as medicine by eating organic foods and eliminating refined sugar and grains. I did weekly hypnotherapy, acupuncture, reiki, cranial sacral massages, daily meditation, walks on the beach, and Epsom salt baths. Basically, anything and everything I could do to help my mind, body, and spirit heal.

I could not have made it through conventional cancer treatment without doing every one of these practices. I made the choice to fight, the choice to live, to be positive, and trust that my body has the power to heal.

I worked through stored trauma and negative emotions and let go of anything that felt heavy or stressful. Feeding my cells with positive, loving thoughts and visualizing a time when I would grow old and one day hold my grandchild.

A moment that I would fight to live for.

Every day I told myself these healing affirmations: I am healthy, I am strong, I am HEALED, because that was the truth I wanted my mind, body, and soul to hear so that it could one day become my reality. I believe everything happens for a reason and there are valuable lessons and growth when we are faced with hardship and pain. I know I am alive today to help others going through this horrible health crisis and to help give others the hope that better days are ahead.

I hope to share my journey and lessons learned through Do Cancer, a nonprofit I helped create to provide a place of hope, support, and positivity for those who hear the dreadful words, “you have cancer.” A resource to help those in need of finding hope, inspiration, and the strength to never stop believing in miracles, because I am one. I know together we can do this, we can do anything, we can Do Cancer!

A 4-Year Glioblastoma Survivor: Hope Is a Great Medicine – Conquer: the journey!!!

Until there is a cure for cancer, long-term survivors are the key to finding answers.

In Remembrance of our Founder, Shenell Malloy  

Hope is the greatest medicine of all.

 There are few people who are brave enough to make change happen.

They refuse to accept what is.

They volunteer to get involved in difficult situations. They serve others in ways that grow to impact many more. When you’re in the presence of one of these special people, you simply know. Our Founder Shenell Malloy was an inspiration in action. Shenell passed away from Glioblastoma in May 2024. She lived five years longer than expected, and she described those five years as deeper and more meaningful than the 36 years before. 

 She spent her final time living fully and vibrantly, doing what she loved most: being with her family and helping others battling cancer. She considered herself lucky. She never wanted to be seen as a victim because she truly understood what it meant to be alive—to get to live. During the early days of her cancer journey she was fixated on the gaps and injustices in cancer care. 

She vowed to push change for others if she survived against the odds, and she spent her last years on earth doing just that. 

She channeled her own pain into action, and what she learned into a new standard of cancer care to share with others.

She simply wanted to help others live longer and have better outcomes. 

She woke up every day with great purpose and clarity. 

Today, we have grown the organization to impact thousands of lives by offering free premium cancer care, survivor guidance, and transparent medical information to anyone who wants it, Shenell was a special change-maker. She saw a need, together we created and built a solution, and watched it fly. While Shenell’s loss leaves an incredible void in our lives, we live out her determination and compassion every day with Do Cancer patients. We will continue her legacy and spirit of service to others. 

Whether you are a patient, survivor, caregiver, or loved one touched by cancer, your story can have an enormous impact. You can provide hope and inspiration to someone recently diagnosed with cancer or a patient undergoing therapy.

This is the story of three friends and sisters.

About – Our Story – Do Cancer

Our time together began two decades ago when our biggest challenges were small. But, in 2019, we experienced something new together: CANCER.

SUMMARY

   Aidan with stage 3 triple negative breast cancer and melanoma.

 Despite being healthy, active, and devoted to health routines, they found themselves grappling with aggressive cancers. United in their fight, they embarked on their cancer journeys together determined to HEAL.

  Shenell chose to turn her terminal prognosis into a lifelong commitment to living.

  Alongside conventional treatments, she pursued a complementary holistic approach to healing, integrating mind, body, and spirit.

  Meanwhile, Aidan, thrust into an intense treatment regimen, leaned on Shenell’s invaluable insights gained from her own experience.

Recognizing the need for guidance during such challenging times, they decided to share their knowledge, experiences, and resources with others facing similar struggles.

 Brenna, a caregiver to loved ones battling cancer, also joined their mission, offering support and wisdom to fellow caregivers. Their collective experiences led them to create a resource hub for those navigating cancer’s complexities. 

4 years of life after a terminal diagnosis. | Brenna Johnson on LinkedIn: #cancer

Brenna Johnson على LinkedIn: I Got a Prenuvo Full Body Scan – here’s my experience

 Their shared mission: to provide guidance, comfort, and hope to the 1 in 3 individuals impacted by cancer, offering insights inspired by their own challenging yet enlightening journeys. Brenna Johnson on LinkedIn: #cancer #prevention

Aidan, now stable after years of treatment, aims to be the support she wished she’d found when first confronted with their diagnoses. The mission is to provide a beacon of hope and guidance for those lost and overwhelmed by the challenges of cancer. 

Meeting people where they are, is a powerful rule to live by. | Do Cancer

 #breastcancercare #cancerrecovery #cancersupport

Together we are Stronger and Together we can Do Cancer!

Surviving Cancer: Inspiring Stories of Hope and Recovery 2025

Shenell, Aidan & Brenna Cancer Story – Search Videos

 With love, commitment, and gratitude,

Do Cancer – Gratitude Report 2024

All Our Love,

Aidan & Brenna

Woman died for 11 minutes claims to have seen both heaven and hell – Search Videos

Story by Hiyah Zaidi – Search

The idea of heaven and hell has been around for thousands of years. However, since there is a requirement to be dead to get into these places, it’s been hard to document. But in 2019, one woman claims that she undertook an extraordinary journey to both heaven and hell after she was pronounced clinically dead for 11 minutes. So, what did she see? (Picture: The 700 Club/Youtube)

What happened?

Charlotte Holmes was 68 years old – Search when she was medically dead for 11 minutes after she took ill during a routine heart check. When she was visiting her cardiologist, her blood pressure suddenly began to spike to 234 over 134 so she was told to stay in hospital, as it needed to come down or she would have stroke or heart attack .

She was put on an IV drip to help bring her blood pressure down. But, suddenly, she coded, and required emergency intervention. During this time, Charlotte said she was above her body, in a sort of out of body experience, and the doctors were doing chest compressions. But then something happened – and she says she knew she was in heaven 

Speaking to The 700 Club, Charlotte, from Kansas, US, said: ‘I could see them, all the nurses around, I could smell the most beautiful flowers I’ve ever smelled and then I heard music. When I opened my eyes I knew where I was. I knew I was in heaven.’ She added: ‘I was above my body. I could see Danny standing in the corner. 

He had backed up. I could see them, all the nurses around then I opened my eyes. I looked around at the beauty. I could see the trees, I could see the grass and everything was swaying with the music because everything in heaven worships God. I can’t convey to you what heaven looked like because it’s so above what we can even imagine, a million times’.

She said that she was led into heaven by angels, adding there was no fear, and recognised family members who had died including her parents and sister, as well as ‘saints of old’. She said: ‘There’s no fear. It’s like pure joy when the angels take over there’s no fear when you’re going home. It’s pure joy. They didn’t look old, they didn’t look sick. None of them wore glasses, they looked like they were in their 30s but yet it says in the scriptures we will be known as we were known. I knew them, there in their new bodies. They looked wonderful’.

Charlotte added: ‘Standing behind mom and dad was a light so bright I couldn’t look upon it. It was so bright but I knew it was my heavenly father.’ And then she saw a toddler. She said: ‘I couldn’t understand and I can remember thinking “who is this?” and I heard my heavenly father say to me, it’s your child. I lost that child. I was five and a half months pregnant. I can remember them holding the baby up and saying Charlotte, it’s a boy, then he was gone.’ She says she asked God how this was possible. She said: ‘He says they continue to grow in heaven but there’s no time, it’s eternity. So 48 years and here my child, our child, is a toddler’.

Charlotte Experiences the Glory of Heaven – with Charlotte Holmes (Ep 41 Everyday Miracles Podcast)

I believe when you die you live within your conscious – Search Videos

11 Minutes in Heaven: Woman Dies and Comes Back to Tell Her Story

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“I’m a hospice nurse – here’s why you shouldn’t fear death”

I Was Homeless And Hated God, Until This Happened…

But it wasn’t only heaven she saw. Charlotte said she also saw something that she will never forget. ‘God took me to hell,’ she added. ‘I looked down and the smell and then rotten flesh, that’s what it smelled like and screams. After seeing the beauty of heaven the contrast to seeing hell is almost unbearable.’

Charlotte explained that she was shown this to warn people what could happen if they don’t change their ways. Then, she felt herself being drawn into her own body. And after remaining in hospital for two weeks following the incident, she made a full recovery and has been sharing her story ever since.

XXXX

First of all, anything reported on the 700 Club is simply not credible, right out of the starting gate. Secondly, it’s a well-known fact that as the brain loses oxygen, it has these sensory episodes she’s describing here. And thirdly, a lot of these images are ordinary, and they date back to mythologies from thousands of years ago, which in geological time was about 30 minutes ago.

Far more credible than CNN and MSNBC.

While everything reported on BSNBC and the Communist News Network is credible. We know how it works.

I didn’t believe this story for one second. I have died 2 times on the operating table, and I didn’t see anything. I vaguely remember waking up in ICU and the ICU nursing staff being happy that I was able to be resuscitated after dying. According to the doctor, after the second operation, I almost didn’t make it, the doctor calls me his miracle patient.

So, just because you didn’t doesn’t mean it’s not possible for someone else.

I’m happy that you survived. I believe the experience is different for different people.

I don’t believe it either but the problem is not us. The millions of people in this country that believe it, are the problem. If they are that stupid what else do they believe?

Why are those people who believe a problem? It has absolutely no impact on you or your life so… ?

“‘Standing behind mom and dad was a light so bright I couldn’t look upon it. It was so bright but I knew it was my heavenly father.” Thank you for explaining that light. I know what you’re talking about.

My dad said one day he saw mom in the corner and my sister ask and what did she say. he said nothing she just stood there, a few weeks later the same, and my sister again what did she say he said nothing she waved her hands to come to her , a few days later my dad passed,

The images that this woman saw is what is in her mind. Just like everyone when it’s your time, you will see your version of make believe that is shoved down your throat from the day you are born. There is no heaven or hell, just an ending of what you once were.

Maybe it depends on your relationship with Jesus Christ. I’d rather die believing and be proven wrong than die denying the truth and face the consequences.

Why are there only two options? Why must you face consequences because you did not know what lies after this life and questioned what people told you?

Maybe. But why would your brain focus on a fairy tale? And why would so many people report the same vision? Wouldn’t most dying people think about their families, the lives the leave behind?

what if you dont believe and was a good person, I never stole in my life and never hurt anybody on purpose? I know people that are believers and stole from their co workers or from their parents.

Because believing in Jesus Christ is what will save you. If you don’t believe, there is consequence to that. It is ok to question, but you must question with honesty, put your pride aside, ask Him to reveal Himself to you and He will. Most unbelievers do not question with honesty, they hold onto their unbelief because it suits their lifestyle and do not really explore what the Church proposes for eternal life.

I say this all the time! I’d rather be proven wrong. I died and went up to heaven and saw the same bright light and my father met me (he passed away in 84 and he was a fine Christian man) telling me I had to come back because it wasn’t my time. If having faith in Jesus Christ allows me to die with such a peace like I had at that moment, then it is well worth it.

I believe in Christ and the Ten Commandments! Thank you for your story. I believe that this vision came to you in your dark time. Prophets like Isaiah had visions brought to him most likely in a sleep-like state and he spoke of some scary things in the Book of Isaiah about the end times. Take heed to his words.

  I’ ll believe our late Pope came out and said Hell was fake.  all made up.  Pope Francis said the souls of sinners simply vanished after death and were not subject to an eternity of punishment.  Before the King James Version.  It was the valley of Hinnom / Gehenna.   The valley’s name has been corrupted over time, leading to the modern term “Gehenna” used in Christian theology to denote the place of eternal punishment. – Source Bible Gateway

None of the descriptions are scripture, so I’m going to say it may not be a lie, lack of oxygen to the brain can do some crazy things, but it wasn’t actually hell or heaven. Fact is scripture tells us no one goes to heaven, heaven comes to us and we all sleep in the heart of the earth until then, so no she didn’t see heaven or hell.  Sheol(paradise and torment) are on earth right now. not up and down but across a great chasm.    If she’s going to push Christianity (which i think everyone should)    Actually read the bible first. don’t promote lies like 99% of churches do

If one goes to Heaven or Hell after death, then what is the purpose of resurrection and judgement which is assigned to every human being after death. Moreover, the Bible states that one “sleeps” in the earth until the resurrection and that the “Dead know not anything” after death. I seriously doubt these incidents as being what they claim.

No fear, no shame, no guilt, throw out those 10 commandments because YHWH has never forgiven anyone EVER, he’s the accuser. He’ll keep you reincarnating in this trap and you don’t want to do that again. Take up JCs cross and figure out EVERYTHING in this universe is actually about JC, EVERYTHING. Take up his great commandment (love him and yourself and your neighbor) and throw out the guilt and resolve not to sin.

What Heaven Is Really Like According To Witnesses | Watch

Is Heaven real? Those who are convinced it is often point to accounts of people who say they’ve actually been there. For many, these stories are comforting, but they’ve also generated their fair share of skepticism. This is what Heaven is really like, according to people who’ve been there. 

Neal Walker

I worked with a former fireman who went out on calls involving death etc….. He said one woman passed out, no heartbeat. paramedics shocked her and she sat straight up and talked to the firemen as if nothing happened. She passed out again and they shocked her once more. Said she sat up and said, “I did it again, didn’t I?” She fell back and they couldn’t get her to come back again. It was her time.

G. M. K

I didn’t know about dying but getting knocked out for heart surgery was like losing time. When the anesthesia kicked in, I was out for hours. When I woke up, it was like I never fell asleep. No memories, no dreams, nothing but waking up and not even realizing I fell asleep.

user-8im2ir3587

Oxygen-starved brains hallucinate. It’s a simple fact. People see the gods they were brainwashed from infancy to believe in. There are ancient records of Greeks having NDEs (near death experiences). Guess who they reported seeing? 

Zeus and Apollo. It’s why Hindus see Vishnu during NDEs. It’s why Christians see Jesus. It’s why Muslims see Mohammad. If our civilization is going to survive, people are going to have to eventually grow up from this childish religious nonsense.

Kathy 16

I would think if one ever got what they believed to be a glimpse of Hell, they would be doing everything they could to not return. That’s why I did not believe Meagan Fox when she claimed to have seen Hell. I want to see Heaven only, God and Jesus. Father Thank you , thank you thank you for your son

Stgeorgeman

She better change her ways since “they” couldn’t decide which place wanted her.  Sounds like they gave her a 2nd chance to decide for herself where she will end up.

Debating Cancer: The Paradox in Cancer Research (Hardcover).

Faust Fearless

Heaven and hell? Just happens the pictures are from the 700 club? Why not Vishnu? Thor? Zeus? Funny how what she saw is exactly aligned with her religious view.

odr-an-eol

The Holy Spirit will give you everything you need as you rise up you’ll get more and more information. I’ve been given visions of things like the creep who tried running over me with his truck and the boss who humiliated me wrongly in front of 20 others, I was shown a VISION of the truck 40 years after the fact, and the bad boss and that was 2 dreams and I was able to TAKE BACK my power from him. Plus much much more.

Truth NJustice

What a game…. she played seven minutes in Heaven and four minutes in Hell….  I’ve only played the former….but who knows the latter could be fun…. Billy Joel – Only The Good Die Young (from Old Grey Whistle Test) Bing Videos.  Billy Joel said I’d rather laugh with the sinners than cry with the saints…..  not me though…. I laugh and cry with both.

• Come out, Virginia, don’t let me wait
  You Catholic girls start much too late
  Aw, but sooner or later it comes down to fate
  I might as well will be the oneWell, they showed you a statue, told you to pray
  They built you a temple and locked you away
  Aw, but they never told you the price that you pay
  For things that you might have doneWell, only the good die young
  That’s what I said
  Only the good die young
  Only the good die youngYou mighta heard I run with a dangerous crowd
  We ain’t too pretty, we ain’t too proud
  We might be laughing a bit too loud
  Aw, but that never hurt no oneSo come on, Virginia, show me a sign
  Send up a signal, I’ll throw you the line
  The stained-glass curtain you’re hiding behind
  Never let’s in the sunDarlin’, only the good die young
  Whoa-whoa-whoa-whoa
  I tell ya only the good die young
  Only the good die youngYou got a nice white dress and a party on your confirmation
  You got a brand new soul
  Mmm, and a cross of gold
  But, Virginia, they didn’t give you quite enough information
  You didn’t count on me
  When you were counting on your rosary
  Oh-whoa-whoaAnd they say there’s a heaven for those who will wait
  Some say it’s better, but I say it ain’t
  I’d rather laugh with the sinners than cry with the saints
  The sinners are much more funYou know that only the good die young, oh, baby
  I tell ya only the good die young
  Only the good die youngSaid your mother told you all that I could give you was a reputation
  Aw, she never cared for me
  But did she ever say a prayer for me?
  Oh-whoa-whoaCome out, come out, come out, Virginia, don’t let me wait
  You Catholic girls start much too late
  Sooner or later it comes down to fate
  I might as well will be the oneYou know that only the good die young
  Tell you, baby
  You know that only the good die young
  Only the good die young
  Only the good
  Only the good die youngOoh-ooh, ooh-hoo
  Ooh-ooh-hoo-hoo
  Ooh-ooh, ooh-hoo
  Ooh-ooh-hoo-hoo
  Ooh-ooh, ooh-hoo
  Ooh-ooh-hoo-hoo
  Only the good die young
  Only the good die youngWriter/s: Billy Joel
  Publisher: Capitol CMG Publishing, Universal Music Publishing Group
  Lyrics licensed and provided by LyricFind

odr-an-eol

Jack Spallino

 But satan will only go after the righteous, not the demonic like most of these ghouls sitting around earth now.

user-8im2ir3587

She didn’t “die” for 11 minutes. She was near death. Dead people come back to life only in fairy tales.

They brought her back before she could tour purgatory.

odr-an-eol

Here’s what JC sees about our fake law; the guy on the top of the mountain has to hunt for game to survive because nothing grows up there except pine trees, while the guy on the bottom can just pick food off trees so of course he calls the guy on the top of the hill a murderer. That’s our SICK law.

Leroy Kelly

Blessed is those who hunger and thirst for righteousness for they will be filled.

Kristin Guardado

 “It is appointed to men to die “once”, after this the judgement”. If you actually died you would be seeing nothing but the Great White Throne and would be standing there awaiting your fate.

lindahl1890

Then she doesn’t believe in the Bible, but it is crystal clear that NO ONE will see Heaven or Hell until it is the end of their life. Not dead for 11 minutes.  She was hallucinating. As the body releases chemicals at death.

She Was Given 21 Months to Live, but These Foods Helped Her Fight Cancer and Win

TALIA WISE

Her story is remarkable not just for surviving such an aggressive cancer, but for how she transformed her lifestyle and mindset to support healing. 

Kathy Mydlach Bero was first diagnosed with Stage 4 Inflammatory Breast Cancer in November 2005, at the age of 41. Her prognosis at the time was grim—just a 21-month survival expectation—but she chose to pursue an integrative healing approach that ultimately led to her full recovery.

Want to read more about how she did it?

1www.connect 2www.chrisbeatcancer.com 3www.wisn.com 4hope.com

A Wisconsin women’s health journey is garnering national attention after she beat cancer by simply eating organic fruits and vegetables. 

Kathy Mydlach-Bero’s world was turned upside down in 2005 when she was diagnosed with two rare and late-stage cancers.

The first was inflammatory breast cancer. She was given 21 months to live. 

“Eleven months after my first diagnosis, I was diagnosed with a high-grade tumor in my head and neck,” Bero told WISN-TV.

The then 41-year-old and mother of two immediately turned to surgery, chemotherapy, and radiation to fight the diseases. 

But cancer and chemotherapy were taking a toll. 

“My kidneys were failing; my liver was failing,” Bero said. “My lungs were damaged. My heart was damaged. I told my oncologist that I’m done with that protocol because one way or another, I’m going to die. And I don’t want to go that way.”

At that point, Bero decided to kick chemotherapy and take a more holistic approach suggested to her by a friend. 

“My friend kept saying you have to learn about anti-angiogenic foods,” Bero said.

Anti-angiogenic foods stop the growth of cancerous blood vessels by basically halting the spread of the disease. 

Some of this food includes organic vegetables such as purple potatoes, carrots, and leeks.

Bero said eating these foods is good medicine for your health. 

 https://www.facebook.com/KathyMydlachBero/photos/  Facebook 

“Leeks are at the top of the cancer-fighting list,” Bero said.

She adds that garlic is especially potent against cancerous cells.

“When a recipe calls for two cloves, I’m probably going to put in six because garlic is a really strong cancer fighter,” she adds.

It’s advice she is giving to her clients as an author, speaker, and a certified integrative health and cancer coach.

“She’s teaching me food is the best form of medicine,” one of her clients, Phil Baugh, said.

Baugh is a 43-year-old father of three, who is fighting brain cancer.

“It’s stopped growing now, so it’s wonderful,” Baugh said. “And a huge part of that is food.”

Successes like these have caught the attention of Harvard University researchers and they are now studying her case along with the cases of other cancer survivors.

“Our investigators are studying people who have had highly unusual/exceptional responses to cancer treatments,” Ekaterina Pesheva, director of science communications and media relations at the Harvard Medical School, tells CBN News.

“They’re looking at our genetics and the genetics of the tumor,” Bero said. “What the outliers did; their attitude, environment, faith, social support. What they’re trying to do is create a database of all these different things and look for the commonalities between these people.”

EDITOR’S NOTE: An earlier version of this story inaccurately stated that Harvard is studying Bero’s diet. Harvard tells CBN News they are not specifically studying the diets of participants. Instead they state: “Our researchers are collecting a wealth of data from registered and approved participants, including medical history, genetic profiles, physical activity, lifestyle and nutrition, among a constellation of other variables.”

SOURCE She Was Given 21 Months to Live, but These Foods Helped Her Fight Cancer and Win | CBN News

E.A.T.: An unconventional decade in the life of a cancer patient.: Kathy Mydlach-Bero: Amazon.com: Books

Kathy’s Story of Healing from Stage 4 Inflammatory Breast Cancer and High Grade Head & Neck Cancer

E.A.T. An Unconventional Decade In The Life Of A Cancer Patient by Kathy Mydlach Bero | BookLife

Using food as medicine: Woman’s battle against cancer being studied by researchers

How Kathy Mydlach Bero Survived Stage 4 Breast Cancer and Head & Neck Cancer

Kathy Mydlach Bero, Integrative Health and Cancer Coach – Nancy’s List

The Making of An Integrative Physician – Beat Cancer : Beat Cancer

Amazon.com: Kathy Mydlach Bero: books, biography, latest update

Cancer Survivor, Kathy Bero – Templeton Wellness Foundation. 

Survivor Stories Archives – Page 3 of 9 – Chris Beat Cancer

Add Sunshine To Your Day with Vitamin D — Kathy Bero

Kathy Mydlach-Bero’s cancer-fighting foods

https://www.facebook.com/KathyMydlachBero

https://www.instagram.com/kathybero

Blog — Kathy Bero

Learn more about this world-wide wellness phenomenon:

Shinrin-Yoku known as Forest Bathing — Kathy Bero

Shinrin-yoku or forest medicine has become an interdisciplinary science recognized by the National Institutes of Health (NIH) under the categories of alternative medicine, environmental medicine and preventive medicine, for its human health benefits.

Scientists discover that memories are not just saved in the brain

What happens when you lock your pulse to the grid… but unleash chaos on the rhythm?

 Discover the Rhythm Paradox now and find out!

Medically Reviewed | Last reviewed by an MD Anderson Cancer Center medical professional reviewed on January 24, 2022  

Leiomyosarcoma Cancer: My Story

Soft tissue sarcoma begins in the soft – or connective – tissues of the body, such as muscle, fat and blood vessels. There are dozens of  types of soft tissue sarcoma.  One of the more common subtypes of sarcoma in adults is leiomyosarcoma. But with an estimated incidence of 1 in 100,000 people per year, it’s still quite rare compared to lung or colorectal cancer. 

Leiomyosarcoma is believed to originate in the body’s smooth muscles, including the uterus, the intestines, stomach, bladder and blood vessels. Since smooth muscle is present throughout the body, leiomyosarcoma  can occur anywhere in the body.

To learn more about this form of soft tissue sarcoma, we spoke with Patrick Lin, M.D., an orthopaedic surgeon who treats leiomyosarcoma patients in MD Anderson’s Sarcoma and Orthopaedic Center, the nation’s largest program for bone and soft tissue sarcomas.

What is leiomyosarcoma?

Leiomyosarcoma is a rare type of cancer that falls into the category of sarcomas, which generally arise from connective tissue. Leiomyosarcoma generally forms in the smooth muscles of the body.

What are the symptoms of leiomyosarcoma?

The symptoms depend on where the tumor occurs, which can be almost anywhere. Leiomyosarcoma often presents as a firm, painless lump in the soft tissues of the body. It sometimes causes cramping or pain when it arises in an internal organ, such as the uterus or in the digestive tract. Symptoms rarely involve the bones, except in late stages of the disease.

How is leiomyosarcoma diagnosed?

The gold standard for diagnosis is tissue biopsy of the primary tumor. This can be accomplished by needle biopsy. This is when a needle is used to obtain a sample of cells from the tumor for laboratory testing.

What is the prognosis for someone diagnosed with leiomyosarcoma?

The prognosis for leiomyosarcoma varies greatly

A Metabolic Approach to Fighting Cancer With Dr. Thomas Seyfried

Cancer’s Metabolic Fuel: Glucose, Glutamine and Cellular Energy Dynamics

Leiomyosarcoma: 7 facts about this rare soft tissue cancer.

BY Lisa Garcia  

Leiomyosarcoma is a rare and aggressive form of soft tissue sarcoma that originates in the smooth muscles of the body. Here are seven key facts about this cancer:

1. Rarity: Leiomyosarcoma is estimated to occur in about 1 in 100,000 people per year, making it quite rare compared to other cancers like lung or colorectal cancer. 1
2. Location: It can occur almost anywhere in the body, but the most common location is the uterus, which is composed largely of smooth muscle. 1
3. Symptoms: Symptoms depend on where the tumor occurs, which can be almost anywhere. It often presents as a firm, painless lump in the soft tissues of the body, but it can cause cramping or pain when it arises in an internal organ. 1
4. Diagnosis: The gold standard for diagnosis is tissue biopsy of the primary tumor, which can be accomplished by needle biopsy. 1
5. Prognosis: The prognosis varies greatly depending on the stage of disease, size, and metastatic spread. Early detection and treatment are key to a better outcome. 1
6. Treatment: Treatments include surgery, chemotherapy, radiation therapy, and targeted therapy. Surgery is the main treatment for leiomyosarcoma. 1
7. Subtypes: Leiomyosarcoma can be classified into three subtypes: somatic soft tissue LMS, uterine leiomyosarcoma, and cutaneous or subcutaneous LMS. 1

These facts provide a comprehensive overview of leiomyosarcoma, its characteristics, and the importance of early detection and treatment for improving outcomes.

I am a “THRIVER”, not a survivor. We don’t survive this cancer. But we can thrive!

At this moment, I am thriving! help #endcancer – Search Results | Facebook

“I have been fighting stage 4 Uterine #Leiomyosarcoma (uLMS) for over 4 years.

Marge Brauer: Leiomyosarcoma – Search Videos

LMS is a rare incurable type of cancer which affects less than 2 out of 150,000 people. But there are treatments and hope! Read the story of our friend Marge who is THRIVING while facing the challenges of this rare disease!  

At 68 years young Marge Brauer is a retired teacher and business owner “enjoying life”. Spending time at home in Indiana or vacationing at her “happy place” in Florida, you may find her riding her bike, playing shuffleboard, or socializing at a community gathering. But keeping up this lifestyle isn’t as simple as it may look to the unknowing observer. Because for the last 5 years Marge Brauer has been living with leiomyosarcoma, a rare and aggressive form of cancer.

Marge describes that due to both her cancer and treatments, there are many days she wakes up fatigued or depressed, not wanting to leave the house, or even get out of bed. But over the past 5 years, Marge has pushed herself to get past the fatigue or depression by being active. As she has done this, she has been much happier falling asleep at night due to the “good exhaustion” her active life provides instead of being controlled by fatigue and depression brought on by the disease.

While Marge is reaping both physical and mental benefits of pushing herself, she also expresses the frustration that comes along with her efforts, “My husband and daughter in law are very supportive and see me when I am struggling.

Other friends, family, and neighbors see me out and say things like ‘You look great, you’re doing great, or you are so strong’. I know they mean well, but I just want to scream. I don’t feel like I’m looking great or doing great, and I definitely don’t feel strong … While I might be out now, I may barely have any energy in an hour. It’s important for me to stay positive and make the best of my life, but then because I appear positive, everyone thinks I’m fine. Meanwhile I struggle on a day to day basis”.

In order to help her cope with emotions brought on by those well-meaning, but misplaced comments, Marge has found comfort in support groups of fellow patients who have a shared life experience. “My advice to any cancer patient is to find a local support group where you’ll find other people who know exactly what you are going through. This will help you to not feel alone. They’ll understand your frustrations. Plus, you can learn so much more about your disease and treatment options”. For people like Marge who live with a rare cancer or in a small community, there may not be local support groups available. In those cases, Marge advocates for “online support groups” where people from around the world share, comfort, and educate each other.

As a former teacher, Marge’s quest for knowledge has never stopped. Through the support groups and her online research, she has educated herself on her diagnosis, treatment options, and provider options. She encourages her fellow survivors to do the same. “The more information you have the better you can advocate for your health”.

Research indicates that Former Teachers Have an Increase Cancer Rates due to various environmental and lifestyle factors. A study found that teachers share several factors that increase their cancer risk compared to non-teachers.

The California Teachers Study specifically highlighted higher rates of breast cancer among female teachers, attributing these disparities to various factors.

Former teacher’s stress causes her cancer – Search

Additionally, a study examined the relationship between cancer incidence and the electrical environment in schools, suggesting that factors like high-frequency voltage transients may contribute to increased cancer rates among teachers.

These findings suggest a potential link between teaching and increased cancer risk, warranting further investigation. Marge describes the power she feels having gained this knowledge.

She recalls a visit in September 2023, “I always review my labs, scans, test results. I think everyone should. You need to understand so you can talk to your doctor and advocate for yourself. You must have a doctor who you know will listen. Dr. Kassar always takes the time when I need it. On this visit in September 2023, I reviewed a radiologist report and was concerned with the radiologist’s conclusions. I pointed this out to Dr. Kassar. He took the time to listen, review the report, evaluate it further, and we changed the course of action”. This change of course may have stopped Marge’s health from taking an unnecessary change for the worse.

With a smile Marge relayed “I am a “THRIVER”, not a survivor. We don’t survive this cancer. But we can thrive! At this moment, I am thriving!” “In fact”, Marge reports, “This week’s scans showed stability!”

She is grateful for advancements in medicine, the efforts & knowledge of her doctors, the support of family, and having a treatment team close to home. But as Marge’s story illustrates, having the determination to push yourself, the knowledge to advocate for yourself, and the emotional support of fellow “thrivers” are the key components to “enjoying life”. 

Like most uLMS patients, it hides under the guise of uterine fibroids. I have undergone multiple chemo and radiation treatments that may not cure but hold this cancer at bay. Currently, I’m stable and grateful for that. I get through each and every day by finding something that puts a smile on my face – no matter how small it may be.  

Marge Brauer Facebook

I have undergone multiple chemo and radiation treatments that may not cure but hold this cancer at bay. Currently, I’m stable and grateful for that. I get through each and every day by finding something that puts a smile on my face – no matter how small it may be.

Participating in Count Me In’s LMS Project gives me hope. Hope that it will help, maybe not me, but future individuals that are fighting this very rare cancer. Hope that this research will better help understand LMS and working treatments are found.” – Marge Brauer | Join the movement that can impact the future understanding of cancer at  LMSProject.org – JoinCountMeIn.org #SarcomaAwarenessMonth#JoinCountMeIn

We offer support to patients, survivors and caregivers. Leiomyosarcoma is a subset type of Sarcoma, a rare cancer. Please share your experiences and journey with others and ask questions. We learn from each other and believe that knowledge is power. We have many members that may be going through a recent surgery or treatments, we are here for you and send everyone positive thoughts and healing energy. 

Please note we are not medical professionals although we do share our medical experiences including links to online sites and info. It is key to ask your medical team any medical questions regarding your health or any type of treatments or suggestions that you read about in any online groups.We do not allow graphic photos of medical procedures or of the human body related to this disease. 

Please post in a respectful courteous manner. All posts that are of a violent tone or argumentative will be removed. We do not sell products for profit and do not allow individual fundraising. We do not support any political party or religious groups. Lori Baylis McCourt is the Founder of our group and a caregiver for her husband who is a LMS survivor. 

Lori is also an Admin along with Marge Hodgetts Brauer, Cheryl Watson Davis, Jennifer Jones & Karen Navitsky Brake. Marge & Cheryl are both ulms survivor’s. This is a closed group on Facebook and all new members will need to be approved. We ask you to answer a few questions as a vetting process & agree to our rules. 

What you post can be seen by other members but will not show up on your FB page. Please do not share other members’ posts without their permission. If you have any questions or concerns please feel free to contact Lori, Marge or Cheryl through messenger. Together we are Stronger! 

LeioMyoSarcoma (LMS) support group | Facebook

 Survival Stories – Northwest Cancer Centers

Breelyn Wilky MD | Medical Oncology | UCHealth – Search Videos

Brauer has a long journey ahead of her, but she is strong, and she is fighting every day. Always remember to stop and smell the roses when times get rough. 

Nancy McGuire: Thriving with Leiomyosarcoma Thanks to Research | AACR Cancer Progress Report 2016

Thriving with and healing from incurable uterine leiomyosarcoma cancer

Salmon is encouraged as part of the MIND diet, a plant-focused eating plan designed to support brain health.exclusive-design – stock.adobe.com

I’m a neurosurgeon and my tasty 3-ingredient dinner to prevent Alzheimer’s: ‘I never get tired of it’

By Tracy Swartz

Dr. Jonathan J. Rasouli, a board-certified spinal neurosurgeon in New York, is spilling the details of his go-to meal rich in brain-beneficial omega-3 fatty acids and phytonutrients and low in carbs, sugar and fat.

“It tastes great, and I never get tired of it,” Rasouli, director of complex and adult spinal deformity surgery in the Department of Neurological Surgery at Staten Island University Hospital, recently told Parade. “It is super easy to make and doesn’t require too many ingredients.”

The MIND diet — which emphasizes leafy green vegetables, berries, beans, nuts, whole grains, fish and olive oil — was developed specifically for brain health. The eating plan is a blend of the plant-friendly Mediterranean diet and the DASH diet, which focuses on easing high blood pressure.

Salmon is encouraged as part of the MIND diet because it boasts omega-3 fatty acids, which are believed to preserve the integrity of cell membranes in the brain, facilitate communication between neurons, enhance blood flow to the brain, support the creation of new brain cells and lower inflammation.

Nearly 7 million Americans have been diagnosed with dementia, which is characterized by a decline in memory, thinking and learning.  piksel stock – stock.adobe.com

That’s why Rasouli often prepares grilled salmon seasoned with turmeric and  steamed broccoli on the side.

Turmeric’s main active ingredient is curcumin, which has shown potential in reducing inflammation, improving memory and slowing the development of amyloid plaques, a hallmark of Alzheimer’s disease.

Alzheimer’s is the most common form of dementia — it’s characterized by a decline in memory, thinking and learning. Nearly 7 million Americans have been diagnosed with dementia but researchers say millions more likely have dementia symptoms but no formal diagnosis.

For its part, broccoli contains glucosinolates, which transform into isothiocyanates when chewed. Isothiocyanates have been shown to reduce oxidative stress and inflammation. Broccoli also contains vitamins C, K and A as well as potassium, calcium and iron.

Rasouli warns against consuming sugary foods that can contribute to insulin resistance, a risk factor for dementia. Photographee.eu – stock.adobe.com

But Rasouli warns against adding too much salt to the salmon and subbing in a carb-heavy side for the broccoli. Excess salt and refined carbs can potentially contribute to brain inflammation.

“Any dinner that is low in processed ingredients, sugars and unhealthy fats would be a good dinner not only for Alzheimer’s prevention but also your general health,” Rasouli told Parade. “I like to stay away from red meats, processed meats like sausage and anything high in sugar. These have been shown to contribute to insulin resistance, which is a risk factor for dementia.”

For breakfast, Rasouli favors the “powerhouse” meal of grass-fed steak, pasture-raised eggs and leafy greens or avocado, which contain healthy fats.

Grass-fed steak boasts high-quality protein, iron and vitamin B12, Rasouli said, which support energy, focus and cognitive function.

“Additionally, grass-fed beef contains higher levels of omega-3 fatty acids and antioxidants like vitamin E compared to conventional beef, which can further benefit brain health,” Rasouli told The Post. “Pasture-raised eggs are rich in choline, an essential nutrient for memory and brain function, and they also offer a higher concentration of omega-3s compared to standard eggs.”

Another brain-healthy breakfast is avocado toast with whole-grain bread and a poached egg. For lunch, Rasouli is a fan of grilled chicken or salmon salad with leafy greens, olive oil and nuts, thanks to the antioxidants, omega-3s and healthy fats.

A second choice is a quinoa bowl with roasted vegetables, chickpeas and tahini dressing. “Quinoa is a complete protein and provides slow-releasing carbohydrates,” Rasouli explained. “Chickpeas add fiber and protein, while tahini offers brain-boosting fats.”

BREAKING NEWS:  The FDA Just Banned Alzheimer’s Medications! [Discover How to Naturally Restore Memory Just By Doing This at Home]

Updated: March 4, 2025

This morning, a shocking FDA decision rocked the medical community: all medications for treating Alzheimer’s were suddenly pulled from the market.

Why?

Serious side effects and questionable efficacy.

But what the pharmaceutical industry doesn’t want you to know could completely change the way we treat memory loss. Until now, the standard approach to combating Alzheimer’s has been through medications that, at best, merely delay the symptoms.

Dr. Michael Carter, a renowned neuroscientist, has argued for years that not only are these treatments ineffective, they can also be dangerous. That’s because the root of the Alzheimer’s problem is not something that can simply be medicated.

According to his research, a toxic protein directly linked to the modern diet is the true culprit. That’s right, you probably ate something today that is silently destroying your neural synapses, causing memory lapses, and triggering Alzheimer’s.

This discovery calls into question decades of medical guidance and points to a pharmaceutical industry conspiracy to keep this information from the public.  Despite all this sounding frightening, there is still hope…

During research in Okinawa, Japan—a place known for its high life expectancy and low incidence of Alzheimer’s—Dr. Carter discovered a simple practice that locals have been using to naturally prevent and reverse the effects of memory loss.

This technique, which can be done at home in less than one minute, is based on natural ingredients that combat the toxic protein responsible for brain deterioration.

“I thought my memory loss was just part of aging,” says Maria G., a follower of Dr. Carter’s recommendations. “But after applying the method he suggested, my mental clarity returned, and after just 16 days I threw my medications in the trash.”

If you or a loved one is suffering from memory loss, Alzheimer’s, or any other type of neurodegenerative disease… Dr. Carter’s video where he explains step-by-step how you can restore your brain’s health at home… In an exclusive interview, an expert in brain health Reveals: “Evil Protein” is Literally KILLING the memory of 200 Million Americans! (Learn How to solve it below!)

Dr Sanjay Gupta’s Calming Creamy Turmeric Tea Recipe |Calming Creamy Turmeric Tea

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Neurosurgeon reveals 3-ingredient dinner to prevent Alzheimer’s

Calming Creamy Turmeric Tea

Dr. Sanjay Gupta drinks a calming cup of Creamy Turmeric Tea every night to help calm his nerves, but the benefits of this colorful drink don’t end there: A recent study suggests that curcumin, a brain-boosting chemical in turmeric, could help slow the progression of Alzheimer’s by helping hippocampal brain cells grow.

Prep Time: 5 minutes 

Cook Time: 5 minutes 

Total Time: 10 minutes 

Course: Beverages

Cuisine: Healthy Spa Cuisine

Keyword: Ayurvedic, Ginger, Honey, Tea, Turmeric

Servings: 1 Serving

Calories: 162kcal

Courtesy Of: Dr Sanjay Gupta, MD – Search Videos is an Indian American neurosurgeon and an assistant professor of neurosurgery at Emory University School of Medicine and associate chief of the neurosurgery service at Grady Memorial Hospital in Atlanta, Ga.

Ingredients

• ▢1 cup almond milk (or coconut milk)
• ▢½ teaspoon turmeric
• ▢½ teaspoon fresh ginger juice Ginger People Juice. – Search Images
• ▢½ teaspoon cinnamon
• ▢1 teaspoon honey
• ▢1 dash cayenne pepper

** 1/2 teaspoon of regular honey and 1/2 teaspoon of Mike’s Hot Honey (that really peppery sweet honey)

Instructions

• Heat the almond milk in a microwave, or, on the stove top
• Stir in all spices, and blend.
• Drizzle honey on top of spiced milk.
• Expect sediment from the cinnamon to occur — just stir now and then while enjoying.

Spa Index Kitchen Notes

If you do not have fresh ginger juice (available bottled from The Ginger People, or, reserved from crushed fresh ginger), substitute a piece of sliced ginger, or, 1/4 teaspoon of ginger powder. Do not use candied or crystallized ginger, which is mostly sugar.

“Creamy Mug of Warming Deliciousness” is more accurate. It just plain feels good to drink this slightly sweet, slightly spicy blend of heated almond (or coconut) milk, turmeric, ginger, cayenne and honey. Turmeric tea will perk you up in the morning, calm you down at night and soothe sniffles and sore throats. It’s also a really pleasant way to end a meal.” — Mark’s Daily Apple

Nutrition

Serving: 1 Serving | Calories: 162 kcal (8%) | Carbohydrates: 23 g (8%) | Protein: 8 g (16%) | Fat: 4.5 g (7%) | Sodium: 125 mg (5%) | Fiber: 2 g (8%) | Sugar: 0.6 g (1%)

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An estimated 38% of adults will be diagnosed with cancer in their lifetimes, according to the National Cancer Institute, making cancer a top medical priority. The National Center for Health Statistics reports that cancer is the most-researched disease in the United States.

According to the most recent data, the NIH dedicated over an estimated $7.1 billion to cancer research in 2023. This research has led to various new treatments that offer hope for those diagnosed with the disease. In April 2025, researchers at Memorial Sloan Kettering reported that certain colorectal cancer patients may be able to make a full recovery via immunotherapy rather than surgery, chemotherapy, or radiation. 

With that said, although cancer mortality rates have consistently decreased throughout the 21st century, about one-third of patients will not survive five years after their diagnosis. This threat is still a long way from being eradicated.

More than 1.7 million people in America are diagnosed with cancer each year, and 1 in 4 deaths in the country is due to cancer. Recent research has also found worrying shifts in demographics among cancer patients. Data published in the Annals of Internal Medicine in June 2025 shows that compared to older generations, appendix cancers occur four times as often among millennials and three times as often among members of Gen X. 

You see a lot of Baby Boomers and not too much Gen Z on this map.

But as the years go by, this map should get a lot of more light blue popping up. Gen X looks poised to overtake southern California soon, but, for now, the Boomers still reign supreme in most of the United States. Of all the states in the Union, it looks like Alaska might be the most diverse in terms of generational cohorts. All ages are welcome in the Last Frontier!

Additionally, colorectal cancer is on the rise among people as young as 20 for reasons still largely unknown to medical researchers. A May 2025 report from the National Cancer Institute notes that some theories place the blame on obesity, high alcohol consumption, or the presence of microplastics in the human body. 

On the other end of the spectrum, new research has revealed lowered risks of cancer in elderly individuals. While cancer remains common in those between 65 and 70 years old, a December 2024 study from Memorial Sloan Kettering Cancer Center shows that rates decline among people between 80 and 85 years old. That doesn’t mean the risk disappears entirely, though. For example, in May 2025, former president Joe Biden was diagnosed with prostate cancer at the age of 82.

Suffice it to say, it’s difficult to generalize trends of how cancer spreads across different populations. The term “cancer” in fact refers to a collection of more than 100 related diseases, each of which involves a breakdown in normal body processes due to cells dividing uncontrollably and spreading into surrounding areas. Every one of these individual diseases has different potential causes, and scientists are still hard at work identifying links between possible carcinogens and actual disease rates. 

Still, we can see a clear variation between groups of people on a geographic level, particularly when comparing cancer rates across all 50 U.S. states. What factors might cause some states to have more people diagnosed with cancer each year than others? The question is still being investigated, but hospitals and other research centers in every state are working to find answers.

To examine this geographic cancer rates distribution, Stacker used data from the Centers for Disease Control and Prevention, which carefully tracked the rates at which cancer affects the U.S. population. We ranked 49 states and the District of Columbia by their incidence rates of cancer in 2019, the most recent data available. (Data from 2019 was not available for Nevada.)

 The incidence rate refers to the number of people out of 100,000 who are diagnosed with cancer in a given year and is age-adjusted to the 2000 U.S. standard population. We’ve also included incidence rates for the three most prevalent types of cancer in the U.S.: lung and bronchus cancer, prostate cancer, and breast cancer, which is the most common. Incidence rates for breast cancer and prostate cancer are only available for women and men, respectively, even though both of these conditions may impact all genders.

꧁swëët-pøïsøn꧂

Read on to find out how your state fares.

 The state with the lowest cancer rate in the US, according to the CDC—plus, see how your state compares

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Researchers embark on quest to find cause of cancer crisis plaguing US region: ‘It’s scary’

Iowa cancer rates are the second-highest in the nation and rising, and some think it could have to do with common agricultural chemicals.  

What’s happening?

“People in rural communities are getting sick. Cancer is just everywhere,” Kerri Johannsen, senior director of policy at the Iowa Environmental Council, told the Guardian, which reported on this health crisis. “Every person I talk to knows somebody that has [recently] had a cancer diagnosis. It’s just a constant drumbeat. It’s scary.”

The Guardian added that Iowa is just one of two states where cancer rates are increasing, but the cause has been unclear. However, many residents are blaming herbicides, pesticides, and other chemicals used on farms. Then there is the state’s problem with hazardous nitrates — often coming from agricultural fertilizers and manure from large-scale livestock operations — that wash off farm fields and enter the water supply. 

Now, a new study will look into these theories as well as cancer links to per- and polyfluoroalkyl substances and high radon levels, the Guardian reported.

“We really want to find out why these cancers are increasing,” Elise Pohl, a former community health consultant for the Iowa Department of Health who will be the study’s lead researcher, told the Guardian. “We’re homing in on the agriculture side of things.” 

Why is this study important?

Agriculture is integral to Iowa’s economy, contributing $159.5 billion to the state each year, according to the Iowa Farm Bureau. And around one in five Iowa residents are employed in agriculture or by agriculture-related businesses, the organization added.

 Related video: Why is there a rise in cancer among young people?

Meanwhile, a number of studies have found links between common agricultural chemicals and cancer. For instance, one recent investigation by Stanford University found that more than 20 types of pesticides may significantly increase the risk of prostate cancer. 

These pesticides also endanger wildlife. One conservation group states that malathion endangers more than 1,500 species and recently brought a lawsuit against the U.S. Fish and Wildlife Service for its alleged failure to rein in use of the substance. 

This problem is global in scope — one study estimated that 3.85 million tons of pesticides were used on crops worldwide in 2020.

What’s being done about potentially dangerous agricultural chemicals?

Farm Bureau Financial Services recommends that farmers wear personal protective equipment such as gloves, safety glasses and shoes, earplugs or muffs, hard hats, respirators, coveralls, vests, and full body suits when handling potentially dangerous chemicals.

However, some farmers are implementing more planet-friendly practices that reduce their need for conventional pesticides, herbicides, and fertilizers in the first place. Organic agriculture involves growing and processing food without using synthetic fertilizers or pesticides, and a number of studies have shown promise for organic fertilizers. 

For instance, one study found that using microbial biofertilizers and algae-based biostimulants instead of synthetic fertilizers on tomato crops improved both yield and quality.

Soil treated with organic fertilizers stores more carbon, study finds:

A recent study from Kansas State University has shown that soil treated with organic fertilizers stores more carbon than soil treated with chemical fertilizers or left unfertilized. The research, published in the Soil Science Society of America Journal, utilized advanced imaging techniques such as ultrabright synchrotron light to observe the carbon interactions within the soil.

The study focused on a cornfield in Kansas that had been farmed without tilling and using only manure and compost fertilizers for 22 years. The findings suggest that organic enhancements improve soil health, microbial diversity, and carbon sequestration, contributing to sustainable and regenerative agriculture practices.

by Rowan Hollinger

With carbon dioxide levels in the atmosphere increasing in recent decades, there is a growing urgency to find strategies for capturing and holding carbon. Researchers from Kansas State University (K-State) are exploring how different farming practices can affect the amount of carbon that gets stored in soil.

Using the Canadian Light Source (CLS) at the University of Saskatchewan (USask) and the Advanced Light Source in Berkeley, California, they analyzed soil from a cornfield in Kansas that had been farmed with no tilling for the past 22 years.

Signs of the Times

Soil treated with organic fertilizers stores more carbon, study finds …
Researchers from Kansas State University (K-State) are exploring how different farming practices can affect the amount of carbon that gets stored in soil. Using the Canadian Light …
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Soil treated with organic fertilizers stores more carbon; study finds …
Researchers from Kansas State University (K-State) are exploring how different farming practices can affect the amount of carbon that gets stored in soil. Using the Canadian Light …
https://www.sott.net › Search

During that time, the farm used a variety of different soil nitrogen management practices, including no fertilizer, chemical fertilizer, and manure/compost fertilizer.

The results are published in the Soil Science Society of America Journal.

“We were trying to understand what the mechanisms are behind increasing soil carbon storage using certain management practices,” says Dr. Ganga Hettiarachchi, professor of soil and environmental chemistry at Kansas State University. “We were looking at not just soil carbon, but other soil minerals that are going to help store carbon.”

As has been shown in other studies, the K-state researchers found that the soil enhanced (treated) with manure or compost fertilizer stores more carbon than soil that received either chemical fertilizer or no fertilizer. More exciting though, says Hettiarachchi, the ultrabright synchrotron light enabled them to see how the carbon gets stored: they found that it was preserved in pores and some carbon had attached itself to minerals in the soil.

The team also found that the soil treated with manure or compost contained more microbial carbon, an indication that these enhancements support more microorganisms and their activities in the soil. In addition, they identified special minerals in the soil, evidence Hettiarachchi says, that the treatments contribute to active chemical and biological processes.

“To my knowledge, this is the first direct evidence of mechanisms through which organic enhancements improve soil health, microbial diversity, and carbon sequestration.”

Because synchrotron imaging is non-destructive, the K-state researchers were able to observe what was going on in soil aggregate (clumps) without having to break up the soil; essentially, they were looking at the carbon chemistry in its natural state.

“Collectively, studies like this are going to help us to move forward to more sustainable, more regenerative agriculture practices that will protect our soils and environment as well as help feed growing populations, says Hettiarachchi. “As well, understanding the role of the different minerals, chemicals, and microbes involved will help improve models for predicting how different farming practices affect soil carbon storage.”

More information: Pavithra S. Pitumpe Arachchige et al, Direct evidence on the impact of organic amendments on carbon stabilization in soil microaggregates, Soil Science Society of America Journal (2024). DOI: 10.1002/saj2.20701

Journal information: Soil Science Society of America Journal 

Soil treated with organic fertilizers stores more carbon, study finds

High nitrogen input promotes the redistribution of new organic carbon to deeper soil layers

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You’re More Likely To Die From Cancer If You Live In These 10 States.

Cancer, a disease that doesn’t play favorites, has become one of the top killers in the U.S., with over two million new cases reported just in 2024. While factors like genetic inheritance, lifestyle, and smoking are well-known, your zip code also plays a crucial role in your survival odds. According to the National Cancer Institute, cancer rates vary wildly across the country, and some states have significantly higher mortality rates.

Take Kentucky, for instance, leading the pack with the highest cancer mortality rate in the U.S. The high prevalence of smoking and obesity are key culprits, along with a lack of routine screenings. The healthcare infrastructure faces challenges, especially in rural areas where access to care is limited. Plus, exposure to carcinogens from the mining industry worsens the situation, boosting lung cancer rates.

In Iowa, lung, breast, skin, and prostate cancers are common. Exposure to chemicals and agricultural pesticides due to the state’s farming industry is a major factor. Obesity and alcohol consumption also contribute to the high incidence of breast cancer. Despite these challenges, education and prevention efforts are underway to cut down cancer death risks.

In Louisiana, cancer incidence is 40% higher than the national average. The “Cancer Alley,” a region with a high concentration of petrochemical plants, is linked to higher rates of lung and breast cancer. Inequalities especially affect Black and low-income residents, who face higher cancer risks and mortality due to proximity to industrial pollutants.

West Virginia faces high cancer risks due to smoking, poor diet, and lack of screenings. The state has one of the highest tobacco consumption rates, contributing to lung cancer. The lack of access to quality healthcare in rural areas is a persistent issue, delaying diagnosis and treatment.

Arkansas also faces high cancer mortality rates, with lung, breast, prostate, and colorectal cancers on the rise. Smoking and obesity are significant risk factors. The lack of access to healthcare in rural areas hinders early detection and treatment, affecting survival rates.

Nebraska has higher mortality rates for certain cancers, like esophagus, blood, and kidney. Pediatric cancer rates are also concerning, with one of the highest incidences outside the Northeast. Exposure to chemicals in agricultural production and lack of exercise are identified risk factors.

In New Jersey, cancer is the second leading cause of death, with high rates of lung, breast, prostate, and colorectal cancers. Historical inequalities and exposure to tobacco smoke and air pollution are contributing factors. The lack of early detection and inaccessibility to effective treatments especially affect the state’s Black population.

Maine faces high cancer mortality rates, especially for lung and bronchus. Smoking and the lack of cancer treatment centers are key factors. The lack of access to treatment in rural areas means some patients must travel long distances for care, affecting their survival.

In New York, certain urban areas experience a spike in cancer diagnoses, with rates higher than the national average. Pollution and the state’s industrial roots are linked to carcinogens in the air, soil, and water. The lack of access to vital cancer care in rural areas delays diagnosis and treatment.

Mississippi has the highest breast cancer mortality rate in the country. The lack of screenings and widespread poverty are contributing factors. Most of the population lives in rural areas, making access to healthcare difficult. The lack of awareness and inaccessibility to effective treatments are persistent challenges.

Map shows states with best—and worst—health care

GOTTA KNOW THE FACTS

Lots of cancer deaths in Arkansas, Mississippi and Kentucky. I was a traveling nurse for 25 years before retiring and I saw the most
Why is everything red or blue? It has more to do with the tobacco use not red and blue

In many states where Marijuana was legal there was almost a 20% less risk of cancer because of reduced use of tobacco among the population so health does have to do with politics

We are talking about the able bodied Americans that CHOOSE not to work… Or are we talking about the people that cut lines for handouts?

You have to take into account also, the political climate of the area too. In Red states, education is considered a big no-no, as they are anti-education. They also don’t believe in science, so often wouldn’t really view a cancer diagnosis as real either.

Fortunately, everyone in cities like New York and LA are perfectly healthy, because they love science! No problems in those areas!

Also Red states welcome polluting industries with open arms!

I’m sure it’s difficult to keep up but we’re talking about statistics for states here, and if you actually READ the article its pretty clear that the states with the most cancer are red states.

Statistics are easily manipulated by whatever point the author wants to portray. It has always been that way. Ask any statistician or teacher of statistics.

This statement in no way refutes the data. Red states have higher mortality from preventable diseases for numerous reasons. Boohooing that changes nothing.

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Real education in Red states is a BIG yes!! It’s the DOGE that discovered Blue State waste and fraud That’s a BIG No No!!!
That’s a common belief that is false, just ask any statistician or teacher of statistics, they know I speak the truth.

So the lessons are clear: Keep your weight down. Exercise. Avoid toxic air, water, and food. Don’t smoke. And get regular healthcare by a qualified physician. I would add GET ALL YOUR VACCINATIONS PER YOUR PHYSICIAN.

I would agree, with smoking and obesity by far the leading risks

Stay out of Blue states and you’ll be fine…

Did you also not read nor take into account that most of these areas lack the medical resources needed for a proper diagnosis there are others who do not follow up nor seek preventive healthcare, and then lastly there are those who have cancer already but have to travel well outside their area for treatment. So the lesson is, we need to invest in accessible, affordable healthcare for all. Chemicals, pesticides, pollution and other contributing polluting factors need to be addressed. Just because one lives in a less than popular area doesn’t mean they deserve to be treated inhumanely.

Oh, and don’t live in a rural area in a Red State – they don’t have good medical care facilities anywhere close to you.

A study published in the American Journal of Medicine found that unvaccinated people were 72% more likely to be involved in a severe traffic accident than those who were vaccinated. This study implies that folks who are unwilling to follow common-sense public health safety guidelines are also unwilling to follow simple stuff like traffic laws.

Blue states just manipulate the data…get real.

A vaccine for cancers, diabetes, smallpox, tuberculosis, immune diseases, and numerous other diseases needs to be developed from the CCR5 delta 32 gene inherited by fewer than 1% of the European population who survived “the Plague” of 1347 to 1358.

Lot of cancer deaths in California as well, I know, I worked as an RN for 20 years in the state before retiring. Depends on which part of the state you live in. California has very RED northern agricultural, religious, poorly educated pockets. California does not have the death rates from cancer the red states have.

Has nothing to do with the income disparity within the state that affects people’s health and well-being.
Rates of cancer (or any other health issues) when one has a 40 million population becomes artificially lower because of the enormous population when compared with populations that are significantly lower, basic arithmetic.

Misleading comment there, and totally out of context. If you correlate the entire population of California to those cancer deaths, you would see we’re one of the lower states with cancer deaths. The highest states are ALWAYS the Red states! FACT.

We have one of the lowest cancer rates in the country FOR OUR POPULATION!

States with the highest cancer rates – Search Images Context matters!

No, basic arithmetic states you DO take population into consideration for this particular equation. For example, if we had 100 people and 50 of those had cancer, you could rightfully say we have a very HIGH cancer rate, however, if we had 50 people with cancer and 20,000 people you could say we have a low cancer rate. The population is critical when discussing percentages in this context.

Again, I would state that its important to use entire populations of states when comparing cancer deaths. We don’t want to be comparing apples to oranges do we? So if a state has a MUCH lower population rate we have to take that into consideration while looking at their cancer rates to come up with a correct PERCENTAGE. This is why her statement regarding California is off.

The rates per 100,000 are being diluted because of the 39+ million population. I would be more interested in the rates per 100 or 1,000, even 10,000 would be an improvement when comparing such a large population with states that are magnitudes smaller in population than California.

That is a loaded political statement, not any kind of scientific statistical statement.

For example Texas is regarded as a RED state. Here are the stats on party affiliation:
Party Registration Statistics
Total Registered Voters: 17,323,617
Democrats: 8,054,976 (46.50%)
Republicans: 6,574,201 (37.95%)
Third Party/Other: 0 (0.00%)
Unaffiliated: 2,694,440 (15.55%)

As one can see Democrats outnumber Republicans as far as registered voters in the state yet at the state level more people vote Republican, but in the large metropolitan areas more people vote Democrat. So, the whole RED state BLUE state belief isn’t true, its’ always a mixture.

Or, it raises issues that should cause suspicion, such as WHY do republicans seem to fare so well despite being outnumbered?

So it sounds as though UR suspicious of the republicans in Texas the same way I’m suspicious of the democrats in California.

These are all red states except for NY and NJ….yet tax dollars from the blue states pay for much of the treatments….although now that Medicaid is being stripped from all of us….it will be the cancer states that will feel it most.

 Well, the cost of healthcare is out of reach for a lot of Americans

Nothing is understood there

i live on the eastern ohio border of the west Virginia panhandle and Pennsylvania 35 minutes from pittsburgh, we have many cardinal plants, plus shipping Port smoke stacks everywhere, and the people around here all die of cancer and we didn’t even make the list

And the East Palestine derailment and fire will ensure the rates climb there.

But there are facilities close that can diagnose and treat…. which a lot of the listed states do not have.

Gonna get a lot worse with the cuts to Medicaid and subsequent closure of rural medical care facilities.

yeah because cancer just started affecting people Jan 20th 2025

Never mind this nonsense, just keep enjoying your low taxes along with low life expectancy.

Nothing funny about cancer.

I read and researched after reading that since 2022 lung cancer in non smoking people has risen quite dramatically. Things that make you go hmmmm.

You are most likely to be murdered if you live in Mississippi, Alabama, Louisiana, New Mexico, or Missouri.

Most metro areas and their counties are Democrat Blue, throughout the entire nation, except maybe Wyoming the only blue is Teton county.

Thank GOD for the fantastic duo MAGA AND MAHA!!

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