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Are Sarcoma Centers the Right Place to Go?

By Mary Schnack July 17, 2009 - 1:05pm
 
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I had my last surgery on March 24 (my fifth surgery to remove endometrial sarcoma) and part of the small intestine had to be taken out due to the cancer spreading there and mangling part of it. About 10 days before the surgery I had horrible pains, so when they found that during the surgery, it made those pains make sense.

Well, I had those pains again two weeks ago and I also vomited blood that night. So I've been going through a series of GI tests to see if there's an internal bleed. My blood count went way down and I'm seriously anemic (although I feel OK in that area). But all the GI tests showed nothing.

I was told to do a tighter job trying to control the diarrhea (still! Three months later) and acid reflux. Be more diligent on taking the medication and take HIGH doses of iron.

Then I saw my medical oncologist yesterday (as opposed to my gynecological oncologist/surgeon at Stanford). He wants a CT scan now to make sure because every other time I have had pain in the pelvic area--its been cancer. So he doesn't just want to assume this time that it was a one-night blockage. I'll have the scan sometime next week.

I am on Femara now. He said if that doesn't work (i get a reocurrence) we'll move to the Faslodex injections and then if they don't work, he'll get me into clinical trials. It was refreshing getting a big picture plan rather than, "We hope it won't come back so we won't talk about it."

I asked him about going to a Sarcoma Center for a second opinion from Dr. Berek at Stanford as the women on my Yahoo support group for endometrial sarcoma suggested. He said the same thing he's said before--that all roads lead to Dr. Berek as one of the top specialists in this area in the country. (Although he would never ever discourage getting a second opinion).

Then he said--Plus, I would not go to a sarcoma center for the second opinion. The key is to find the doctors who see patients with ESS regularly. He said sarcoma centers generally see soft tissue sarcomas and our sarcoma is so different that a Sarcoma Center is not an automatic referral for us. He said to look for doctors with experience with this cancer.

 
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We value and respect the experiences of all of our HERWriters, but everyone is different. Many of our writers are speaking from personal experience, and what's worked for them may not work for you. Their articles are not a substitute for medical advice although we hope you can gain knowledge from their insight.

Mary Schnack View Profile

My story on EmpowHer is about my uterine cancer but there is so much more important about me! I am the mother of an ...

http://www.MarySchnack.com

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