
Do you remember the athlete Kareem Abdul- Jabbar? It appears that Mr.Abdul-Jabbar has been diagnosed with a rare cancer "chronic myeloid leukemia." Rare in deed. When I heard of his diagnosis a shudder went through my body. I have only heard of two other people with this disease, although I am sure that there are many more. One of the people was a patient I cared for and the other was my sister.
A Rare cancer indeed, you could imagine back in 2002 when my sister was diagnosed that we were all shocked and in disbelief. This cancer when detected generally is found in the male population and males in their 60's to 70's. My sister for obvious reason did not seem to fit this group. This disease in the simplest of terms is a disease that effects the bone marrow where blood cells are made. Her diagnosis was detected from a simple blood test. This test discovered she had what they called Myelodasplastic Syndrome. The first and only chance my sister had for survival at that time was to undergo chemotherapy and then a bone marrow transplant. Her first obstacle was trying to find a bone marrow match. Needless to say that every member in my family wanted to be a donor. It was my sister Kathleen who ended up being a perfect match. How extremely fortunate for my sister Eileen, as finding an exact match can be very difficult and time consuming...something that she didn't have. My sister Eileen underwent the transplant and spent 8 weeks in an isolation room as they had to wipe out her immune system and then hope that the bone marrow would take.
It was December 2002 Eileen was given the go ahead to be released from hospital. She was in great spirits. She celebrated a wonderful Christmas with her family and was surround by so much love.
This was taken in the later part of January 2003....She makes bald beautiful!
This was taken in the later part of January 2003....She makes bald beautiful!January 2003, she took a turn for the worst Her platelet counts were falling at alarming rates. She required platelet transfusions every other day. We all took turns taking her to those appointments. She endured so much. She tried all kinds of treatments. But it wasn't to be. My dear sister lost her battle to MDS on March 4th 2003 just, 7 months after being diagnosed and a month shy of her 50th birthday.
So the other day when the news broke about Kareem, it was my husband who drew the comparison of Kareem and my sister to my attention. There are many forms of MDS which they seem to rate at low and high risk. My sister fell into the high risk category.
Since my sisters passing, my family has entered a family team in a walk called "Light the Night" walk for Lymphoma and Leukemia. This walk took place just last month. Our team ended up in the top 10 fundraising groups and my brother was in the top 5 fundraisers. My dear sister may be gone but never forgotten. The Light the Night for Lymphoma and Leukemia is not only a walk to raise money for research but a walk to draw "light" to this devastating disease. Now with Mr. Jabbar's diagnosis, maybe this might draw more attention to this rare disease and provide education and encourage more research into this disease.
I wish Kareem all the best in his journey for good health and hope he continues to have strength and courage to keep this disease at bay and to keep it in the public forefront.








































