Roll Call For UPSC only

Pat51 said:

Pat from Berlin, WI

I have UPSC.  I was 59.6 years when diagnosed.  I was diagnosed in Feb. 2011 with UPSC Stage 1B (I think I may be a Stage 1A on the newer charts)  I had a radical hysterectomy, 6 carboplatin,taxotere chemos and then 3 brachytherapy internal radiation treatments.  My CA125 in July 2014 was 15.2. (CA125 was 27 at the time I was diagnosed.)  I had surgery at Theda Clark Medical Center, Neenah, WI , chemo at Martha Seikman Cancer Center, Appleton, WI and radiation at the University of Wisconsin Clinics, Madison, WI.  I finished treatment in September, 2011.   I have been NED for almost 3 years.

Feeling very blessed at this time.

Pat

I was 59 1/2 years old when diagnosed in February of 2011.  I clinically was diagnosed with UPSC Stage 1A (a large polyp of 5 centimeters).  I had a hysterectomy, 6 carboplatin/taxol chemo treatments from April to August of 2011 and then 3 brachytherapy internal radiation treatments after my chemo ended the end of Sept/Oct of 2011.

My CA 125 in May 2014 was 7.  I have had numerous CT scans and they all show with no evidence of disease.  I have been NED for almost 3 1/2 years.

I am very grateful and thankful to continue to be with No evidence of disease and I feel thankful for each and every day.

Cheerful

a/k/a Jane

NoTimeForCancer said:

Indianapolis, IN.  DX on

Indianapolis, IN.  DX on April 5, 2012 at the age of 49 after irregular bleeding and atypical cells after PAP.  D&C said I had Type I (garden variety type) and Type II (UPSC) Stage 1A.  Surgery was the DaVinci complete hysterectomy where they took a ton of lymph nodes.  All lymph nodes were negative for cancer but since UPSC was found it was determined I need the full-Monty of 3 chemo (Taxol/Carbo), 25 external / 3 internal IMRT radiation, 3 chemo (Taxol/Carbo). 

Developed lymphodemia and have a lovely collection of compression garments, as I suspect many of the ladies out here have as well.

NED since the treatment ended December 19, 2012 (Specific dates in 2012 are burned in my memory!)  I feel so lucky to have caught this devil early and to have found all you beautiful warriors, and all the sisters of all the other "below the belt" cancers at all.

Diane, Houston, Texas, 58 years at diagnosis. UPSC stage 1a discovered June 2011, and treated with 6 rounds of Taxol/Carboplatin. No radiation. Chemo finished in November, 2011, so will be 3 years post treatment at that time. CA125 goes between 7 and 8, and was 4 after surgery. CA125 not taken before surgery because cancer wasn't suspected, Pelvic wash clear but lymph nodes weren't tested. 

NED so far, and grateful for each day!

joannewtta said:

Roll Call for UPSC only

I joined the UPSC club in June of 2013. I was 67 years only when dx.(average age for UPSC). My surgery was July 10 and it involved full hysterctomy. I was a stage 3 grade IIIC I believe.  One pelvic lymph node was malignant, the pelvic washings showed malignant cells etc. etc. Started Chemo in August which was the taxol and carbo. Had 18 treatments(mine was one week with both drugs, two weeks with just taxol and then one week off with a Newlasta shot at end of each series. I also had two blood tranfusions. Completed chemo in Jan and had 4 braciatherapy(sp) in Feb. 2014. I had CT scan in April and checkups in April and July. NED and CA125 is down to 7. I feel good  but understand how scary this is. I only just found this blog about a month ago and just wish I had found it sooner.

My husband was diagnosed in May 2013 with Renal Cell Carcinoma and had his right kidney removed two weeks before my surgery. He has small tumor on his other kidney but we are just watching it and has had no change in shape or size in 14 months. No chemo or radiation for him. I say I got the full-meal deal and he just lost a kidney. Needless to say this has been a year in our lives we don't want to relive.

It is really good to read this site and see the great women posting here. I read somewhere that you don't know how strong you are until you have to be strong. So true.

My post chemo and radiation issues are neuropathy in my feet(really bad) I am seeing a neurologist in Sept and hope there is some relief. Bladder will probably never be the same!!! If anyone has any good ideas about the neuropathy I would appreciate hints. Sitting around in 80 degree weather with a blanket on them looks rediculous but gives relief.

my oncologist believes in trying accupuncture.  I have neuropathy and am working on accupuncture for that and my immune system.  From   your description your neuropathy might be a little more intense than mine.  My oncologist has shared that she has seen good results.  She does recommend an accupuncturist that deals with cancer patients, hopefully on a cancer hospital integrated team.  Mine is and I love him.   She also believes in the B vitamins.  Deficient B-6 or too high B-6 can cause neuropathy.  So she would periodically check my B-6 levels.  My naturopath has taken over that monitoring.

hope this helps

I was diagnosed with stage IVb in May of 2010 at the age of 61.  I was NED  for 4 years, and I don't know where I stand right now.  I had pain in the left side of my abdomen this past May, had a CT scan, then a PET/CT.  Nothing was found in the left side, other than diverticulosis which was scattered, but a 1 x 1.4 cm. mass was found in the right side in the paracolic gutter.  However, my CA-125 was only 6.3.  My gyn/onc has ordered another CA-125 and a CT scan for Sept. to see if it's grown.  If it has, it'll be removed.  If it hasn't, it won't.  I was told there was a chance it could be a fluid collection due to lymph node removal.  My gyn/onc wasn't at all sure what it was because of the low CA-125.  At my worst, before my surgery, even with stage IVb, my CA-125 was only 94.  I'd actually thought I had celiac disease since my mother was diagnosed at 84 with that, but all my tests had come out as normal.  I had diarrhea almost every day before work, but one doctor had said I'd had irritable bowel.  In high school, I probably did have that, as I often got diarrhea before tests.  I had a small amount of vatinal bleeding about 2 mos. before my diagnosis, which I'd blamed on being put on an estrogen cream because of the pessary I had.  Instead, it was because of a large uterine polyp.

My treatment was total hysterectomy, bilateral salpingo-oophorectomy, omentectectomy, iliectomy (had a small spread into the small intestine) along with removal of my gallbladder for gallstones I never knew I had plus an incidental appendectomy. These were done at St. Peter's Hospital in Albany, NY.   I had 6 rounds of carboplatin and taxo where l worked, at Glens Falls Hospital, and no other treatments.  I've had follow ups every 3 months for awhile, then 6 months, and I was supposed to be down to once a year at my gyn/onc at St. Peter's when I developed this new mass.  My PA at my family doctor ordered the scan for my pain.  I continue to follow up with the oncologist in Glens Falls Hospital every 6 mos., as I was diagnosed with hemochromatosis at 3 months out from surgery, and I have to be checked for that.  I also had surgery in August, 2012 for an incisional hernia with a mesh implant.  I don't know what will become of that if I have to have surgery for this new mass. 

Pat from valencia California, diadnosed fall 2010.  6 carbo-tax tx f/b 3 brachytherapy  NED 3 years But I have neuropathy in hands and feet. Tried various products nothimg has worked so far, can't even write a letter. Other than neuropathy, feel good. Hair will grow back, mine came back better than before except I never got my eyebrows back.  Roberta when I found this site, you were one  of 4 women who posted regularly and gave me great support. You are the only survivor and the reason why I occasionally log on is to check on you. You hang in there!!  my prayers are with every woman battling this disease.  

lkchapman said:

UPSC

Laura. Diagnosed in 2009 at age 46 with stage IIIC2 UPSC. Treated at MD Anderson with up front extended field pelvic XRT and cisplatinum, 3 HDR treatments, then 6 rounds of carbo/taxol combo. NED since.

So glad you are doing this roll call as I am recently diagnosed with UPSC and also thought that this diagnosis does not seem as unusual as research/internet information indicates. I just had complete minimally invasive hysterctomy on 8/13/14 and feel that I am recuperating well, I am 61 years old and live in Brooklyn, NY. I plan to recieve follow-up at NYU and expect to know more about stage/grade and treatment protocol within a week or so. I am very eager to learn from all of you and eventually share what I learn as my journey continues. I deeply appreciate the generous, supportive and knowledgeable women on this discussion board,

Ellen

Diagnosed at age 56 August 2010.  Treated MD Anderson. Robotic assisted surgery. Positive lymph vascular space. Staged 1a/1b Concurrent pelvic radiation x 5 wks with weekly Taxol X 5 doses.  3 Brady treatments and 5 21 day Taxol treatments changed to Taxotere due to neuropathy treatment. Lymphedema right leg 4 months post op.  Just completed CTs show still NED. 

I was dx in march,2014, stage 3 UPSC,   total hysto. on  May 2 ,2014.  mri in June  showed no mets to nodes or omentum.Feeling healthy but depressed.  scans will be repeated Aug 28 to determine course of treatment,  Questioning the benefit of Chemo/Radiation as opposed to using surgery only,if and when necessary.

Any advice or information will be greatly appreciated.Thanks.  Newby.