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Patty Morris-Hildebrand (ibpatti32)


March 12, 2007


Click here.


Granite CIty, Illinois


August 29, 1955


Chronic Myelogenious Leukemia


10-12-94


Lumpectomy


No, but it is now needed


Cancer Survivor


The inability to work and provide for my family as I NEVER remarried since div. in 1986. And, being in this ALONE, for I do NOT LIKE to burden my children


To live each day like it is hte gift that it truly is


just support


Low grade fevers, fatigue, extreme headaches, anemia, bone pain


stem cell harvest,central line insertion,(1995) multiple bone marrow biopsies,(every 12 months, then 6 months, vertioblasty (2005) unable to breathe, stand up straight or walk.Sep. 2007 after raising my GLEEVEC dosage to 800 mg per day I am happy to say that I am now back in REMISSION Yeh


No radiation


Interferon from onset- continued hospital admissions,recurrent infections, suppressed immune system
Gleevec May 2002 to present, minimal side effects, mostly nausea, malaise


No match found. All my children tested immediately after diagnosis. They are all in the Natl Bone Marrow Registry and all say they hope they are a match for someone at some point so that they can help them unlike their MOM never having a match to date.


NONE, though only income is disability.

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ibpatti32's Cancer Blog

November 21, 2007

I hope that you are doing better on GLEEVECViews: 118

http:///2007/11/21/

Hi Bob,
I have been on GLEEVEC SINCE 2002, AS I WAS DX WITH CML IN 1994 SO WHEN THE FDAA PASSED GLEEVEC is was such a BLESSING. I had the same problem with my hgm and hct dropped so drastically that they had to DC the GLEEVEC for 2 months, but if you get the chance to read my blog I just learned that I am back in REMISSION after being out for 1 1/2 years. What a BLESSING I feel. I no longer have the support that I had when I was dx, as I lost both of my parents and since they were the youngest of their siblings all of my other family has already passed. My children are now 21, 23 and 27 which I am extremely thankful for. That was probably my biggest fear for I have been div. for 20 years and once dx. I was fearful if something would happen then what would happen to my children. IT CAN BE VERY LONELY BY MYSELF, I DON’T GO ON AND ON ABOUT MY ACHES AND PAINS TO MY CHILDREN AS THEIR ARE ALL PURSUING THEIR YOUNG ADULT LIVES IN COLLEGE. Just how do you even consider meeting someone once diagnosed with CML?????


Ibpatti32's Stats

Posts: 11
Photos: 3
Events: 0
My Supporters: 11
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Comments: 21
Views: 1418




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