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What cancer patients, their families, and caregivers need to know about COVID-19.

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jimi_c_1976
Posts: 3
Joined: Mar 2004
Mar 29, 2004 - 12:43 pm

Hi everyone. This is my first time talking on line. Would like to here from anyone, who is going through treatments, and survivors. Im 28, almost 3 years post transplant. Cml survivor. I also posted on Niky's subject, but its about a month late. I tried the chat room. Cant keep up with everyone.
Maria001
Posts: 3
 Joined: Mar 2004
Mar 29, 2004 - 1:08 pm

Hello :) I'm so happy tht you are here and I hope tht you continue to post. I am just a caregiver. my sister was recently diagnosed w/CML. She's 26..could u tell me abt ur experience? Have ur already gotten ur BMT? I'm so glad ur here >:D

dflannigan
Posts: 5
 Joined: Apr 2004
Apr 12, 2004 - 1:28 pm

I'm 36 and 14+ years post for CML. I had my bone marrow transplant at Wilford Hall Medical Center in Texas. I'm doing well these days. davidflannigan@hotmail.com
kevinleeconrad's picture
kevinleeconrad
Posts: 1
 Joined: May 2004
May 07, 2004 - 4:23 am

Hi, I wanted to respond to your message and say that I'm interested in contacting fellow survivors. I had a transplant in 89 and am doing great. I want to talk about the perspective that one gains after an experience such as this. I have no health problems, but feel that the experience changed my life dramatically. I am curious to see how you view life. What path you have taken post transplant, etc. Kevin
cadmaine
Posts: 2
 Joined: May 2004
Jul 31, 2004 - 9:37 pm

Hi, I am 51 and 4 years post transplant for CML. I had my BMT at the Fred Hutchinson Cancer Reserach Center in Seattle. I am holding my own but was wondering how long after transplant you start to feel better. cdavis4@verizon.net
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