Hello and welcome, we are glad you found us. Please feel free to join in the conversations. Here is a link to our cancer dx page for your type of cancer. Take a look at it to get you started on some information. You will notice at the bottom of that page 4 of our active users who have had that journey already, you may wish to contact them for their experience and wisdom. Also, I encourage you to go to the questions page now by clicking on the questions tab at the top of the page and post what is the most pressing issue you have right now. This will introduce you to the community and get you started on the help you need right now.
https://www.whatnext.com/conditions/cancer/endometrial-uterine-cancerThere are also subtypes listed on this page to narrow down the type of cancer to match your dx.
Also, if you can take a few minutes and fill in some details of your journey so far, it will help others as they try to answer questions for you, it also helps others as they search through the data base to find someone like themselves. Confirming your email will allow you to receive updates and notices from the site when someone answers your questions or writes on your wall.
Thanks for being with us and let me know if I can help you find any information on the site. After you have an opportunity to look the site over and see what great things there are here, we encourage you to invite your friends, family or anyone you know that may be helped by the connections on WhatNext to join the site also. Just click this link to invite them to join.
http://www.whatnext.com/recruit-a-friendFollow Us on Twitter Click Here =>
http://bit.ly/XExkce Find Us on Facebook Click Here =>
http://on.fb.me/zjBAPl Our Pinterest Page with Resources=>
http://bit.ly/12qVtEs Our Help Page with instructions for the site->
http://bit.ly/1aR5165 GregP 3X Survivor
Team WhatNext Community Mgr
Dear Mmsto70
Hi I go to Siteman Cancer center. Is this where you're going for treatment?0July 2014
Hello and welcome, we are glad you found us. Please feel free to join in the conversations. Here is a link to our cancer dx page for your type of cancer. Take a look at it to get you started on some information. You will notice at the bottom of that page 4 of our active users who have had that journey already, you may wish to contact them for their experience and wisdom. Also, I encourage you to go to the questions page now by clicking on the questions tab at the top of the page and post what is the most pressing issue you have right now. This will introduce you to the community and get you started on the help you need right now.
Mmsto, I was diagnosed last year withuLMS after a hysterectomy. I had adjuvant chemotherapy: six rounds of gem/ tax. So far I'm NED. The chemo was brutal, mostly the Taxotere. I am suffering what may be permanent effects: neuropathy in feet and hand, ongoing nausea and vomiting, extreme joint pain, dizziness and falls. Also drastic change in bowel movements. But i am alive. Stay hydrated. Drink little sips. Use antinausea meds. If you swell or have other changes, immediately tell your onc nurse. You can do this. Leiomyosarcoma is rare, so you need to see a sarcoma specialist. We are out here if you need us. God bless you.0June 2014
Welcome to the WhatNext family. I am an oncology nurse and I am always available to answer any questions you may have. There are many here with similar circumstances willing to share their experiences with you. Best of luck to you, Carm RN.0June 2014
