Working for the Cure

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My personal experience and motivation for this website is help with the toughest parts of dealing with the most challenging parts of those experience.  It was December 21st,  2005 when my father began to become gravely ill. After being pronounced cancer free 3 times in the previous 12 years then passing away April 3rd 2006;  it was December 21st, 2011 when   I began to blog  about  http://www.solitarius.org/?s=cancer+survivors
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If you read this blog post top to bottom and research the in – between you will began to understand cancer in a whole new light……  Weak mind and spirit means weak body. From the start my Mission was to Slay The Dragon 🙁
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Sarcoma is probably one of the worse cancers a patient can garner and when that’s combine with the fact these types are usually amongst the rarest of cancer types —             with little known about them. . . . it can become emotionally taxing.

Leiomyosarcoma and with treatments being given it can be gut wretching difficult and unresponsive with the roller coaster ride taken from the time, hope and disappointment. Although when you consider the story  From Incurable To Incredible  and this great read from Tami Boehmer mention Yvonne Cooper of Cincinnati overcoming this very incurable through the Bill Peeples Protocol and Dr Elyse Lower at UC Barrett Cancer Center or the right doctor elsewhere that can be found in forums. http://www.solitarius.org/2013/04/22/surviving-cancer/

 William Peeples began his research into this subject late 1996, when his wife, Vera,        was diagnosed with endometrial stromal sarcoma, stage IVa upon presentation. In early December, 1996,  she was also scheduled for a total abdominal hysterectomy including removal of the ovaries and fallopian tubes, an omentectomy and pelvic sidewall reduction.

After completion of surgical staging, the surgeon closed the incision and stated that her cancer was inoperable. He further stated that chemotherapy and radiation would be ineffective. Vera was sent home with Bill to get her affairs in order.

Somehow, the Peeples family got through what they thought might be their last Christmas together. Bill had already lost several close family members to cancer and was now faced with the potential loss of his beloved wife.

In January 1997, Bill and his wife went to M.D. Anderson Cancer Center in Houston for a second opinion. After three days of examinations they were again told that she had a rare and aggressive tumor that was not responsive to chemotherapy or radiation. Essentially, she still had no options. Bill and Vera went home.

Bill then began his all-out search for something that might help his wife. In his profession as a firefighter, he works the standard shifts, 24 hours on, 48 hours off. This schedule gave him the time he needed to pursue his research and fortunately the internet was in full swing.

Centering his research on the internet, he soon discovered angiogenesis and the potential it has for shrinking tumors. He immediately began giving Vera high doses of low potency angiogenesis inhibitors that could be purchased over the counter.

Also during this time, Vera began taking Megace, a prescription drug, in an attempt to slow down the tumor which was estrogen receptive. Megace is a synthetic derivation of progesterone which helps to lower estrogen.

On March 28, 1997, Bill and Vera went back to the oncology unit at the University of Miami’s Sylvester Cancer Treatment Center for a new CAT scan. At that time, the doctors found only scar tissue. Vera remains alive and healthy today.

Bill Peeples however, didn’t stop once his wife was safe. He continued his research over the next two years, and gradually formed the full picture of this combination cancer protocol.

Although Bill Peeples protocol may have helped Yvonne Cooper of Cincinnati and         Bill’s wife Vera it may not be for everyone.

For Jeannie Ross It was November of 2008 when she was diagnosed with Uterine Leiomyosarcoma. Her lab report said it was Stage II/III with a mitotic count of 100   in a 10X magnification field.

The sky high mitotic count definitely downgraded my prognosis. Typically      a mitotic count of 1-2 is low and 9-10 is high. My score of 100 indicated that the cancer had been multiplying rapidly. I was told I’d have a 50% chance to live 2 years, and a 27% chance to live 5 years. That’s when I immediately embarked on a total change of lifestyle, one that would nourish my physical body    and create a pervasive sense of relaxation and well-being.

If I was going to ask my immune system  to prevent this cancer from returning, I had to do my part by adopting the best practices to optimize my own body’s healing ability.

In 2008, when I was also diagnosed with uterine leiomyosarcoma. I was told that I had a 50% chance of living two years, and a 20% chance of living  five years. That’s enough to scare anybody! Well, it has been almost six years now, and I am completely healthy with absolutely no recurrence of the disease.
My doctor says, “Remarkable! You’re remarkable! You give me hope. Keep doing what you are doing.” Part of my healing protocol has been to do guided imagery and meditation every single day. I knew from the start that my mind was the battlefront, because every part of our being, including our cells, sympathizes or responds to the positive and negative states of our minds. For this reason, when we are diagnosed with cancer, we must find a way to alleviate mental and emotional stress in order to allow our mind to be free to instruct the body to heal itself.

Stress produces hormones that can sabotage your entire healing program by interfering with the function of your natural killer cells, the ones that identify cancer cells and mark them for destruction. Your body chemistry reacts dramatically to your thoughts and your emotions. You may experience trouble sleeping, feel sick to your stomach, have difficulty thinking clearly, and suffer debilitating fatigue. Many health problems, especially cancer, do not permanently clear up unless the mental aspect is also addressed. The mind-body connection is powerful, and just as surely as your mind can make your body sick, it can make your body well. 

My number one goal each day is to stay peaceful and calm inside, like it feels when you’ve just had a massage, or upon awakening from a deep and peaceful sleep. Guided imagery, affirmations and meditation help me to do this, along with walks in nature, acupuncture and deep breathing. My second job is to focus on the physiological and biochemical needs of my body – my nutrition, my supplements, my juicing, my exercise… and so much more. Since my diagnosis my body demands that I put my physical and emotional health first, and I don’t feel guilty about doing it. You will need to decide that your health is more important than anything else and that your full-time job is taking care of you. At first,    this is all I want you to do.

Your mind can aid in making your body well, but you will need to be actively involved in the process. I recommend that you take time off from your job for at least one year after surgery. I waited two years before resuming part-time work. Right now your full-time job is to make yourself well.   Weak mind and spirit means weak body.

You will begin a rigorous program of mind-body training, detoxification, and exercise. Time will be needed to shop for organic foods, juice vegetables, and prepare nutritious raw, vegan meals. My husband and my mother both remind me that my job is to focus on wellness, and everything else must be subservient to that goal.

Your body listens and responds to your subconscious thoughts, so it is not enough just to verbalize that you are going to become well – you must believe it in your core, in your spirit, in your energy body, in your subconscious mind.

Right now, your mind is the battlefront. Focus on everything that is uplifting.

Realize that when you entertain negative thoughts, your are effectively using negative guided imagery on yourself!
Learn to listen to your heart – when your spirit is in balance, you will feel love, joy, peace, perseverance, gentleness, goodness, humility and self-control. When your spirit is out of balance and in distress, you will experience anger, resentment, hatred, bitterness, excessive worry, and the ultimate spiritual stronghold of cancer – fear.
I began this blog because when I was diagnosed there was NOTHING positive to read about survivors of Uterine Leiomyosarcoma. In fact, my doctor told me NOT to look it up on the internet! Since that time my blog has been reaching women all over the world, in nearly every country you can think of. I’ve also started a Facebook page where women and caregivers can comment and ask questions as well.
I realize that if you are newly diagnosed, or if you are a caregiver of a newly diagnosed patient, that sifting though all of these blog pages can be a bit overwhelming. For that reason I have decided to write a book so that you can have the information at home in your own hands to refer to again and again. I hope to have my book available in the coming months.
Remember that your body is designed to prevent cancer from multiplying. At one point, something got out of balance and your immune system failed to work properly. I know that stress played a huge role in my own cancer.  I also know that my body can change. It can be made well, nourished and strong, able to prevent the cancer from returning.
It has been five years since my diagnosis, and I have not had any recurrence of the disease. My body is preventing the cancer from returning. When I saw my doctor he said, ” Remarkable! Remarkable! Keep doing what you are doing!” I most certainly will.
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The term soft-tissue sarcomas (STS) embraces more than 50 different sub-types that are often associated with poor prognosis. Only a very limited number of agents are active against STS. Doxorubicin and ifosfamide are widely accepted as the most effective compounds. However, their low response rates and poor impact on the overall survival of the patients illustrate the need for new treatment options. Among them, leiomyosarcomas are one of the most frequently occurring subtypes. In spite of the relatively high incidence of leiomyosarcomas, the overall effectiveness of the currently available systemic treatments is still poor.
 The heterogeneity of its biological origin, clinical behavior and responsiveness to chemotherapy, together with the scarcity of successful clinical trials, makes the treatment of leiomyosarcoma especially challenging. In addition, the evidence-based treatment for leiomyosarcoma comes from trials in which, in the majority of cases, no distinctions have been made among the different STS sub-types. As a result, every therapeutic decision should be made on an individual basis in collaboration with the patient. The results of new specific histology-designed clinical trials should aid decision making in this complex field. http://pubmedcentralcanada.ca/pmcc/articles/PMC4204552/
Contact Dr. Kent, Dr. Gitelis, & Dr. Abrams at Rush University Medical Center.  I was in a lot of pain for over 2 years, & finally found out in September of ’08 that I had a 12cm lms + osteo tumor in my pelvis & possible metastisis in my lungs.  I had 14 rounds of chemo + concurrent radiation & ressection of the tumor.  The chemo I did was Taxotere + Gemcitabine + Avastin and then later w/ the radiation I did Ifosfamide & Doxorubicin + more rounds of just the Ifos & Doxy post surgery.  I’m alive and doing well, and back to all the outdoor activities I used to enjoy.  The staff at Rush is amazing.   https://cancercompass.com/message-board/message/all,10634,2.htm
Hi! Thanks for the reply. Do you know if the woman who plays bingo has the lms that started in her uterus? I had had fibroid tumors a few years back, and the cancer started at that sight.  There seems to be a connection being discovered that a small percentage of women with fibroids will develop this.  Do you know what kind of treatment she got that’s kept her alive for 6-7 years?  I’ve taken a break from the chemo for a couple of months and my oncologist has me taking Femara, an estrogen inhibitor, and this coming week I’m starting on Avastin. I guess they’re having good results with this, and I also have a lot of fluid build-up in my abdomen that this is supposed to help with also.  In addition, I’ve been taking complementary things to help.  These are all natural, well-proven things, but the FDA doesn’t want us to know about them!  I take Paw Paw Cell-Reg, Maitake Gold Compound, Liquid Zeolite, and I’m going to start taking another mushroom extract, Coriolus Versicolor. These are all things that have been used for a long time in other countries and are gaining in this country as people find out about them. In 4 months of chemo I’ve been able to get rid of tumors in my lung, breast, liver, and abdomen.  All I have left is a little bit in my uterus and in my spine.  I’m determined to beat this, in spite of “statistics”!  Statistics are based only on use of chemo!  I hope this helps, and I’ll be looking forward to hearing more about the survivor you know!  I’ll pray for your mom, too.  Karen 🙂
For Karen and others, there is a very powerful nutritional supplement named Biobran which is considered at the moment one of the best choice for cancer patients. It’s made from breaking down rice bran with enzymes from the Shitake mushroom, and it has been shown that Biobran MGN-3 can stimulate sluggish NK cell activity by as much as 300% or more. Read also about Pau d’Arco tea, Reishi, Cordiolus, Curcumin and Cordiceps. These mushrooms have powerful anticancer properties. Best wishes for all of you. https://cancercompass.com/message-board/message/all,10634,0.htm

Background: a sarcoma is a type of cancer that develops from certain tissues such as bone or muscle. Bone and soft tissue sarcomas are the main kinds. Soft tissue can develop from tissues like muscle, nerves, fat, and blood vessels. They can be found in any area of the body, but most develop in the arms or legs. Sarcomas are not common tumors, most are the type of tumors called carcinomas. Not all sarcomas are cancerous; the term sarcoma means the tumor is malignant. There are more than fifty different types of sarcoma, including but not limited to; adult fibrosarcoma, clear cell sarcoma, epithelioid sarcoma, kaposi sarcoma, leiomyosarcoma, malignant mesenchymoma, rhabdomyosarcoma, and undifferentiated pleomorphic sarcoma.
(source: https://www.cancer.org/cancer/soft-tissue-sarcoma/about/soft-tissue-sarcoma.html)

Synovial sarcoma: it is one of the rarer forms, and can occur at any age but is more common among teenagers and young adults. Despite the name it is not related to the synovial tissues that are part of the joints. It is unknown whether this mutation occurs randomly or following a specific chain of events. The primary treatment for synovial sarcoma is surgery to remove the entire tumor with clear margins whenever possible.

This happens when healthy tissue surrounding the tumor is removed along with the tumor, making it more likely that all cancer cells have been removed from the area. Depending on the location and size of the mass,  it may be difficult for a surgeon to   remove adequate margins while preserving function.  Radiotherapy or chemotherapy     may also be recommended, especially in the advanced or metastatic stages. This is on          a case by case basis, and is decided by the oncologist and the patient. The Prognosis is influenced by the quality of surgery that the patients receive and characteristics of the     disease among other things.
(source: http://sarcomahelp.org/synovial-sarcoma.html)             http://www.wndu.com/content/news/LV305-vaccine-helps-patients-with-synovial-sarcoma-463981073.html

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Leiomyosarcoma patients should turn to food to help recover.

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