young adult survivors of childhood leukemia
please write.
Comments
-
You might try calling your local chapter of the Leukemia and Lymphoma Society of America (formerly Leukemia Society of America) concerning their psycho-social support groups. There may be one in your area designed for young adults. Also, contact the social work department of your treatment centers. Many hospitals offer patient support groups.
Good luck!0 -
WOW!!! I ALSO was around 3yrs when i was diagnosed with ALL. I received Chemo and radiation. Im now 29. and I'd LOVE to talk. Im in central NY. Email is elizabethmessick@hotmail.com ID LOVE TO HEAR FROM YOU!!0
-
Hi Kerrie:terato said:You might try calling your local chapter of the Leukemia and Lymphoma Society of America (formerly Leukemia Society of America) concerning their psycho-social support groups. There may be one in your area designed for young adults. Also, contact the social work department of your treatment centers. Many hospitals offer patient support groups.
Good luck!
I am a 32 year old survivor of Wilms and lung mets. I was 2 when first diagnosed. I have looked long and hard for a survivor support group. I have had no luck in my area. I have been told only about groups for those currently in treatment or shortly thereafter. Since I had it so long ago and my issues are so different, that doesn't interest me at all.
The best thing I've found is an online group of long-term survivors. It's a VERY active list. And I think that Elizabeth might be interested as well. Follow this link to find out more:
http://listserv.acor.org/archives/lt-survivors.html
Not only are there survivors of many types of cancers, but also physicians and other types of specialists knowledgeable about late effects. I mean no disrespect to this list, but I can't keep this resource to myself.
Also, as I told Elizabeth on another post, if you don't have this book, GET IT:
"Childhood Cancer Survivors-A Practical Guide to your Future" by Nancy Keene, Wendy Hobbie, and Kathy Ruccione.
Best wishes,
Fran0 -
It's nice to find someone else that had all when they were little. It's hard to find people who had it so young. Do you remember alot about it? I use to live in ny too. I lived outside of Rochester. I had two years of chemo and radiation. I'd love to talk. my email is wolffy22@aol.comelizabethe said:WOW!!! I ALSO was around 3yrs when i was diagnosed with ALL. I received Chemo and radiation. Im now 29. and I'd LOVE to talk. Im in central NY. Email is elizabethmessick@hotmail.com ID LOVE TO HEAR FROM YOU!!
Kerrie0 -
Hi!!! I am 24 years old and had All when I was 3 and a half. I too have been wondering if there was someone who may have had my shared experiances. I have not found any adult support groups yet. It's been a long time sence my bout with cancer however after effects are lingering. (long and short term memorie problems, graphs, and map reading skills, and math is just about impossiable for me) However, I do have an Associates degree and am now working towards a Bachelors. intrested in hearing from you, Rose0
-
Hi Kerrie, I am 22 as well. I fell out of remission a month ago and am now dealing with non hodgkins lymphoma again after being in remission for 7 years. I was first diagnosed when I was 14. I have never known anyone my age who has gone through this. I am glad to know that you are doing ok. My treatment is going well and the doctors are very optimistic so far. It just really sucks and its really unfair. Nobody should have to go through this once, nevermind twice. My friends and family are being really great about it though. Write back and tell me more about you. (:0
-
Hi Kerrie, I am 22 as well. I fell out of remission a month ago and am now dealing with non hodgkins lymphoma again after being in remission for 7 years. I was first diagnosed when I was 14. I have never known anyone my age who has gone through this. I am glad to know that you are doing ok. My treatment is going well and the doctors are very optimistic so far. It just really sucks and its really unfair. Nobody should have to go through this once, nevermind twice. My friends and family are being really great about it though. Write back and tell me more about you. (:0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.9K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 398 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 671 Leukemia
- 794 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 238 Multiple Myeloma
- 7.1K Ovarian Cancer
- 63 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 540 Sarcoma
- 734 Skin Cancer
- 654 Stomach Cancer
- 192 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards