Kelly Rowland, Rihanna and NY Knick, Chris Wilcox Assist In Bone-Marrow Drive

March 6th, 2009


Kelly Rowland & friends offer support….. Celebrities have stepped up to help a 6-year-old New York City girl who is suffering from a rare and particularly deadly form of leukemia.

Doctors fear Little Jasmina Anema could die unless she receives a bone-marrow transplant soon. Singers Kelly Rowland and Rihanna, and New York Knick Chris Wilcox among many who are spreading the word about a bone marrow drive to be held Saturday in hopes of finding a match for Jasmina.

Former Destiny’s Child singer, Kelly Rowland  joined Jasmina and her best friend, Isabelle, at NYU Medical Center Wednesday to help her young fan celebrate her sixth birthday told Access Hollywood, “The message I would like for everybody out there to know is that this Saturday is a [bone marrow] drive and it’s an outpatient surgery – it’s not an invasive procedure …  Just think about if it were you, if it were your family member, someone that you’re extremely close to and look at her face. This life.”

Rihanna told People, “when I saw the video of Jasmina it broke my heart.
It is so unfair that for a black patient it’s so much harder to find a bone marrow match.
The singer who helped out another child with leukemia last year added:

“Leukemia is the most common disease children in the U.S. die of and we need to change that. I urge everyone to sign up as a bone marrow donor with DKMS. If we have more donors, we can save more children like Jasmina.”

Chris Wilcox visited Jasmina in the hospital and was touched by this adorable, vibrant little girl who is unknowingly fighting for her life.

“I have a sister who suffers from Lupus so unfortunately she is in and out of the hospital and has undergone chemo therapy,” said Wilcox. “I just can’t bear to see a 5-year-old who literally could die if we don’t find her a match soon – and it’s not an organ that she needs, it is blood cells!  It could be any one of us that could save her life.”

Dr. William  L.  Carroll, M.D, Jasmina’s doctor at NYU Medical Center, explained that “the problem is  that finding a perfect bone marrow donor is difficult because Jasmina  has no full siblings.  To make matters worse, says Dr. Carroll, “African-Americans are under-represented in the donor base thus finding the perfect match even harder.”

Jasmina, along with her best friend Isabelle Huurman first caught the attention Wilcox when he saw a heartbreaking video where Isabelle is asking to help find the “ONE for Jasmina” – the perfect donor match.

View the video at www.oneforjasmina.org

A bone marrow drive is set for Saturday at PS 41 in the Village where Jasmina goes to school. Those who want to help can also order a do-it-yourself bone marrow test kit from www.oneforjasmina.com.

 

 

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Comments

Sarah Said on

I recently came across your blog and have been reading along. I thought I would leave my first comment. I don’t know what to say except that I have enjoyed reading. Nice blog. I will keep visiting this blog very often.

Sarah

http://www.lyricsdigs.com



eric charo Said on

i think that it is cool about what u are doing and just wanna tell you to keep it up.



cindy Said on

i just want to say what you are doing for this little girl is wonderful i too have a son with lekuemia and its a hard experience but when you have so much support and love it really help keep doing what your doing godbless u all



DEJA Said on

I think what u r doing is very commendable, i recently found out that I, as well as my 17 yr old daughter, both have Lupus and it’s good to see those inyour field speaking out as well as getting involved personally. I’ll keep this little Beautiful angel and her family in my prayers….. God Bless You as well





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