CSN Login
Members Online: 2

You are here

Great news!

CSN is getting an upgrade. All of your posts will still be here, but the website will have a new look, new features and be mobile-friendly. To prepare for the changes, the site will be down briefly at the end November. We’ll continue to provide updates as we get closer.    

NEW DX Myeloproliferative Disorder

Posts: 1
Joined: Jan 2008

Dad (76 yo) just diagnosed today, with 11% blasts. Doc says no treatment? Could use some help finding treatment options, if any. Thanks.

curlee8661's picture
Posts: 57
Joined: May 2007

Hi Ron's daughter,
I'm sorry to see that your post isn't getting any replies. I'm usually on the ovarian cancer board (since I was diagnosed with that 9 months ago) where I'm used to posts being answered the same day, usually by several people. My Mom was diagnosed with early signs of Leukemia last week, and I figured this would be a great place to find answers and support, but this board is surprisingly quiet.

Anyway, my Mom lives in Europe, so it's difficult for me to get a clear picture on her diagnosis. She said it's too early for them to know exactly what type of leukemia it is, so I'm trying to prepare for the worst case scenario. From what I've read, the outlook can be very different depending on which type it is, varying from having just a couple of months left if it's the acute form, to as much as 7 years on the average if it's the chronic. It's hard to know what to do or even say to her without knowing exactly what's going on. The only specifics I could get from her is that her current white cell count is 25,000 and that there are a lot of immature white cells in her blood. My mom said that there's no treatment for her illness, just as in your Dad's situation. She's 80, so I wonder if age has something to do with that. Assuming that it's the slowly progressing form of this disease, I guess it doesn't make much sense to put someone at that age through chemo, and/or other treatments which can be very difficult, just to gain a little time.

I don't know how much online research you've done, but the websites I've found most helpful so far are:




If you would like to keep in touch and compare notes regarding our parents, that would be great.

Take care,

Anonymous user (not verified)

This comment has been removed by the Moderator

Subscribe to Comments for "NEW DX Myeloproliferative Disorder"