Endometrial Cancer Survivor

Moira
M.
Canada

My name is Moira and I had quite a journey with endometrial cancer. I noticed bleeding (non-mensural bleeding), so I saw my family doctor and outlined my fears that it could be endometrial cancer. My mother and my brother had died (at age 48 years of colon cancer); and I found in my research on the internet that the defective gene that causes colon cancer also causes other cancers including endometrial uterine cancer. My family doctor said that it might indeed be endometrial cancer (among other conditions). I was sent for a Trans-Vaginal ultrasound and then I was referred to a specialist at a hospital.

I met with this specialist, and informed him of my fears and also of my family history of colon cancer (and the link to the gene which can cause both cancers ). This specialist performed a uterine biopsy....horror of horror...without any pain-killer or any type of substance to deaden the pain. After 15 minutes of him snipping my uterus , he finally got a sample my uterine lining for the biopsy. I was shaken, to say the least. Afterwards, I thought , why is it that the other specialist who performs my colonoscopy, provides a needle in a vien on my hand to deaden any pain of the colonoscopy; and yet this Specialist gave me nothing; thus subjecting me to such agonizing pain. Next, I was given another appointment to see this Specialist again to be told the results of the biopsy. He merrily informed me that I did not have cancer, and that I should be happy and go and live my life. I was stunned and shocked. In the depth of my being, I knew that I was very ill...I told him this and asked him about the continuous bleeding and my extreme fatigue.

He just said that it was just the body clearing itself of an extra thick uterine lining. I argued again that perhaps the same biopsy that he took from my uterus may not have been cancerous, but perhaps other parts of the uterus were indeed cancerous. Again, he disagreed with me. To cut a long medical horror story short, I had lariscopic radical hysterectomy surgery, as I insisted. Still no mention of cancer. I thought that my gut feeling must have been wrong and that Specialist was correct in that I did not have cancer. Six weeks after the surgery, I received a letter saying that I had to report to the hospital for a radiation review. The biopsy of my surgically removed organs revealed that I had had Stage One -C , Type 1 Endometrial uterine cancer. I knew it!!! That Specialist had been deadly wrong.

I researched the internet, met with the cancer specialists, and I decided not to take Radiation. Three and a half years later, I am still free from cancer, I feel great and most of all I am so glad that I listened to my gut feeling and insisted on surgery. Listening to my body saved my life. I think that all women over 40 or 45 years of age should routinely have a transvaginal ultrasound, and should listen to their bodies, regardless of what doctors and Specialists tell them. I had a terrifying journey with cancer, but I am glad that although I felt physically ill and rather weak, I was emotionally strong enough to disagree with the Specialist , stand my ground and insist on life-saving surgery. I hope that in sharing this experience, it will help other women to save their lives by being strong and vigilant; to listen to their bodies, to have a questioning mind, and not to be intimidated by physicians and doctors.

I agree

Comments

Thank you for sharing your story. I too have been feeling very fatigue and have been diagnosed as being anemic. I had a Trans Vaginal Ultra Sound done and they discovered 2 Fibroids as well as benign tumors on my left ovary and on my Cervix. I had a Endometrial biopsy done and have been told it was not cancerous. I am 46 yrs old and am still bleeding very heavy with each mentrual cycle. The Dr. wants to put me on Hormone Replacement Therapy for the bleeding but i do not trust it. I do not think i will go this route and will look for another opinion.

God Bless and I will follow your lead and be vigilant in finding out what is wrong with my health.

Why do the Drs make you feel stupid. I went in, had the normal exams.. I went in because I felt I may have a problem.. He said everything seems normal even though I have a lump where my lymph nodes are located. He said he wouldn't remove it,it is just a lipoma. (fatty tumor) The locations seems odd to me... I have all the symptoms of gyn cancer except weight loss... Yet now I was told I am fine and other then getting tests back I am left with NO answer.. Am I just getting old? Should I go to a different Dr....
They leave you wondering if you are losing your mind. My sister told me about Fran.. I have been reading horrifying stories of people just like me... What do I do next...

Hi Michelle,
I hope that all is well with you. What should you do..? Here is my advice..Ask the doctors for copies of all your medical results.. all of them. Insist on it. Ask your doctor how he/she KNOWS that you do not have cancer. Ask why the doctor is not recommending the removal of that lymph node. Is this doctor a specialist? A cancer specialist? Perhaps consider going to a cancer centre and having your condition checked out there (and of course, take all of your copies of all your medical tests with you). So, first thing you must do is to request all of your medical reports/results of all testing, and then take it from there. Some doctors are incompetent, some are indifferent, some are burnt out, some hate their occupations, etc...the list goes on and on. Remember, you are your first priority! Don't be intimidated by them. God bless, and all the best to you, Michelle.

Hi Michelle,
I hope that all is well with you. What should you do..? Here is my advice..Ask the doctors for copies of all your medical results.. all of them. Insist on it. Ask your doctor how he/she KNOWS that you do not have cancer. Ask why the doctor is not recommending the removal of that lymph node. Is this doctor a specialist? A cancer specialist? Perhaps consider going to a cancer centre and having your condition checked out there (and of course, take all of your copies of all your medical tests with you). So, first thing you must do is to request all of your medical reports/results of all testing, and then take it from there. Some doctors are incompetent, some are indifferent, some are burnt out, some hate their occupations, etc...the list goes on and on. Remember, you are your first priority! Don't be intimidated by them. God bless, and all the best to you, Michelle

I have UPSC, which is Uterine Papillary Serous Carcinoma. I have stage 1A, but grade 3 which is the fastest spreading cancer. UPSC is the worst kind of uterine cancer. I had vaginal radiation 3 times, & Monday is my 3rd & last chemo (thank goodness)! I had a total hysterectomy, then 4 weeks later my doctor told me the bad news. I urge anyone who has this to have radiation & chemo because though they did not see more cancer they said it could be microscopic, which it was when I got a CA125 blood test & my count was 73 (should be 39 or less). The cancer can also spread to other parts of the body or new cancers can start from chemo, or just start on their own. I knew chemo kills cancer, but did not know that it also starts new cancers. I was in lots of pain after my first chemo so they changed the dose on my second & I feel much better, mainly just neuropathy. My doctor also misdiagnosed me, & it was not until I saw a Gyn/Oncologist & went through 3 hours of testing that I was diagnosed on March 1, 2012 with the cancer. Spread the word that a vaginal discharge is not normal after menopause. I had a clear or bloody discharge that got worse each day for 2 months until I was diagnosed. I hope this helps others because I have learned a lot the hard way & have learned online through others with the exact same thing through the American Cancer Society & cancer survivors.