Soft Tissue Sarcoma

A very dear friend of mine also had a malignant nerve sheath tumor. She also has neurofibromatosis. The cancer has now metastisized to her lung and spine. She will begin her first round of chemotherapy Monday. How are you? I know my friend is wanting to correspond with someone who may be experiencing similar issues. I wish there was something I could do.

ilbeatit said:

Hi, Thanks for the note. I'm sorry to hear about your friend. I know she can beat it!! My particular tumor was not Neuro like your friends', however it is the same form of sarcoma.
Coincidentally, I to am beginning chemotherapy Monday, actually, in a few hours. I just completed radiaition, and it looks like I am more fortunate than your friend, as it appears to have not spread.
Please wish your friend good luck. Also, tell her to feel free to reply to me. I'll be in the hospital until Friday, but I should be be able to visit this site after.
Thanks

I hope you are feeling well following your chemo today. I'll keep you in my prayers. I've encouraged my friend to register with this site so hopefully she can benefit from your shared experiences. Having someone to talk to who understands what you may be going through can sometimes make a huge difference.

Please let me know how you are.

Cheryl

jcthomas said:

Hi. I was diagnosed with a soft tissue sarcoma in the hamstring muscle of my right leg in 1995
(I was 28). The tumor was a high grade tumor but the cancer had not spread. I live in Maryland so
I got opinions at Johns Hopkins and Univ. MD Medical Center. Went with the U. of MD
treatment regime because they had a "team" of doctors with a treatment plan. The treatment
plan consisted of high dose chemo/stem cell transplant, surgery, internal local radiation,
external radiation, and three follow-up courses of chemo. The treatment was long and drawn
out, and there were complications, but I feel it was worth it. Can you tell me a little more about
your tumor/cancer? How did you find out you had the tumor? I hope you find yourself well
during your chemotherapy treatment. If you need anyone to talk to or vent to while going
through the chemo I am all ears. Good luck. John

John,
What do we sarcoma people worry about after things are over. I find mysef paranoid with ervery ache and pain. I am three weeks into my radiation feel great but am in constant worry. Any thoughts with how you coped through your situation.

rjb1437 said:

John,
What do we sarcoma people worry about after things are over. I find mysef paranoid with ervery ache and pain. I am three weeks into my radiation feel great but am in constant worry. Any thoughts with how you coped through your situation.

This may sound strange but I found that after my treatment ended I was more worried than I had
been during the treatment. I think it had to do with severing the ties with the people treating me.
The worry never ends. It can be controlled and may diminish in time but the thoughts of the past
never disappear. Fighting cancer is not like barely avoiding a possibly fatal car crash which
occurs in a split second. Fighting cancer takes time and getting on with life afterwards takes
time. I worry about every lump I find. I have even had a lypoma removed from the same leg a
year ago though my doctor said it was not necessary. Stay positive, believe in life, and carry
on. It is human nature to try and survive. I found that enjoying the smaller things in life has
helped me greatly I always feel there are not enough hours in the day to think or talk about this
subject. I hope anyone reading this who is fighting cancer may one day find themself well.

ilbeatit said:

Hi, this is in reply to all those that that took time to inform, discuss, etc., my original message.
Thanks, the info has been helpful. I just finished my first six day hospital stay for Chemo, and survived the vomitting, nausea
etc. I have three cycles left, all requiring the 6 day stay. Like my web page says, take every day as your last, and appreciated thoses around you
that care so much. Talk to you soon!

Keep going... It only gets better.. I'm into my third week of radiation and I'm starting to "tan" or should I say "burn" Just went to a meeting to participate in the "Relay for Life" organized in my town for the last five years.. this year it seems a little more important to me. I'll be there taking my lap as a survivor..God willing.. and raising money to cure this foolishness.

I am 27 yrs old, recently had a neurofibroma removed from paraspinal area(T-10, T-11) it is sarcoma-a very rare sarcoma.Malignant Nerve Sheath Tumor, High Grade is what the pathology report says. I have been looking everywhere for anyone who has a case like mine!!! I start chemo in 2 weeks & then radiation! Please let me know if there is any info you may have!!! My Dr. has mentioned MAID to me regarding the chemo--what is it? He is also consulting with MD Anderson Cancer Center. Is there anyone who knows anything about this stupid rare cancer?

rjb1437 said:

I was diagnosed with a Synovial Sarcoma equally as rare. I just turned 40. I met with a radiation oncologist today, had tumor taked out 3 weeks ago. I did 4 rounds of chemo, Ifosfimide, dioxirubin. First two rounds weren't too bad last two nailed me. I lost twenty pounds and ended up in the hospital for three days after round four. The chemo is nasty but you can get through it, it is essential to kill any cells that mey have got away. I am looking for a complete recovery from this, stay positive and get good info. Dana Farber is Boston specializes in sarcomas they have been great. Also check out www.sarcoma.net. Dr. George Demetri runs the sight and is considered the best in sarcoma oncology.

Good Luck

I AM 48 YEAR OLD MOTHER,,OF 3 BOYS,,,,I HAVE BEEN DIAGNOSED WITH MYXOINFLAMMATORY SARCOMA,,,,IT AFFECTS THE EXTREMENTIES,,,I HAVE IT ON MY LEFT THUMB,,,,DRS AT THE UNIVERSTIY OF MICHIGAN,,SAYS ITS SOOO RARE,,,,ONLY 44 DOCUMENTED CASES IN THE WORLD SINCE 1949,,,,,,,,,,,,WHEW,,,,AND I AM NUMBER 45,,,THEY NEVER SAW THIS BEFORE AND SAID THEY PROBABLY NEVER WOULD AGAIN,,,,CHANCE OF ME WINNING THE LOTTERY IS MUCH BETTER,,,SO THE DRS AND ME HAVE DECIDED TO GO AHEAD AND AMPUTATE MY THUMB,,,,SO REOCCUANCE DON'T HAPPEN,,,,I HAD SURGURY ON IT A MONTH AGO,TO TAKE OUT THE TUMOR,,,BUT IT IS GROWING BACK,,IF THEY LEAVE JUST ONE CELL THERE,,,,,IT GROWS BACK,,,,,,,,,,,,,,,SOOOOOOO PLEASE GIVE ME SUPPORT,,,,,,,,,,,,,,,,,AND PRAYERS,,,,
EMAIL,,IS CONNER007@AOL.COM

unknown said:

This comment has been removed by the Moderator

bwolf was just dx with 13 in loww grade tuma wil be getting surgery and rad . i also like to run and workout but was told not too what did they tell you .any damage what was your recovery like

Chriztina said:

I am 27 yrs old, recently had a neurofibroma removed from paraspinal area(T-10, T-11) it is sarcoma-a very rare sarcoma.Malignant Nerve Sheath Tumor, High Grade is what the pathology report says. I have been looking everywhere for anyone who has a case like mine!!! I start chemo in 2 weeks & then radiation! Please let me know if there is any info you may have!!! My Dr. has mentioned MAID to me regarding the chemo--what is it? He is also consulting with MD Anderson Cancer Center. Is there anyone who knows anything about this stupid rare cancer?

okay this is a year late, so I hope and pray that you are doing well. I was diagnoised with Malignant Perphial Nerve Sheath Tumor back in 1992, when I was 18. Mine was in my right chest. I had 3 surgeries, the last one being in 1998. I have had the two upper lobes on my right lung and four ribs removed and way back in 1992-1993 went through chemotherapy. I went to MD Anderson Cancer Center for the majority of my treatment and my oncologist at the time hadn't seen this type of soft tissue sarcoma before. My last surgery was here in Oregon though and went well. My doctors debated at the time whether or not I should have radiation as this was my second recurrance and decided that it wouldn't do any good. The surgeon got it all though and I feel very lucky about that.