Hello,
You are right this type of cancer is rare and aggressive. And quite scary.
There is a support group for this type of cancer that is quite helpful, and provides information. There are members who have the same case or one of ther loved ones, and they have all quite helpful.
Just email to the group below.
UterineMMMT@yahoogroups.com
I guess important is the diet that we follow. I am trying to do the same for my mom. Her recurrance was local, so she is currently undergoing radiation. We all hope for the best.
God Bless
On 3/19/2007 Little Sis v wrote:
My sister who is 49 years old, has just been diagnosed with MMMT. I am trying to gather information from others who has been through this or know of someone that has. As all know, when you first hear of this your mind reels and you panic trying to get as much knowledge as possible.
My sister had a hysterectomy and biopsy of the lymph nodes in the pelvic area. Unfortunately, the tumor has spread into the cervix and attached to the bladder. The lymph nodes also have mets. The dr has suggested chemo first followed by radiation if needed. She has other health problems that complicate radiation therapy.
I know no one can tell me what to expect as every case is different. However, I would like to know how other cases have went and turned out. Good or bad. Having someone else to talk to that has been there will help tremendously. Thanks