Little Jasmina Anema's mom will have a very happy Mother's Day on Sunday. You see, 6-year-old, Jasmina, from New York, is fighting a rare and very deadly form of leukemia.
The good news is that widespread public appeal for African Americans to register as bone marrow donors worked. Thousands were tested, and the results have turned up not one but two likely bone marrow-matched donors who may give Jasmina what she needs to knock out the disease once and for all.
"I am just thrilled," Theodora Anema, Jasmina's mother, said Tuesday. "I've never lost hope. I always expected a miracle, and this is like finding a miracle."Source: Two bone marrow matches found
Jasmina, who has been hospitalized since January with a rare and especially deadly form of leukemia, [underwent] another bone marrow test [Wednesday].
If her cancer cells are once again undetectable and either of the donors pass a medical screening, prepping for her transplant will likely begin in a few weeks.
"I'm still a bit nervous, but it's never looked this good," Theodora Anema said.
Sadly, blacks are much less likely to find a life-saving bone marrow donor than a white person. Why? Not enough black people or people with black ancestry join the bone marrow registry.
For Caucasians in need of a bone marrow transplant, 88 percent find a suitable donor. For African Americans, that number tumbles to 60 percent.Source: Shakesville: African Americans are dying for bone marrow donors - a call to action
While any person of any race can be a suitable person for anyone in need, the simple fact is this: ethnicity matters when it comes to bone marrow. A Caucasian person has a much better chance of getting a match from another Caucasian. An Asian person has a much better chance of being matched with another Asian. An African American has a better chance of being matched with another of African descent.
According to the National Marrow Donor Program, there are just 11 million people on the bone marrow donor registry. And that's not in the U.S.; that's in the world. In the U.S., there are 5 million white people on the registry. There are 500,000 blacks. There lies the difference between the 88 percent and 60 percent figures.
This is a call to the black community. The National Marrow Donor Program needs you. And those of African descent need you even more. They are literally dying for a better representation of blacks on the bone marrow registry.
Check out the National Marrow Donor program for more information.
Cervical Cancer Awareness Quiz
Awareness of Cervical Cancer is very important for Black women's health. Compared to white women, Black woman are more likely to die of the disease at what rate?
- Twice the rate
- Three times the rate
- Five times the rate
What is cervical cancer?
- A disease of the abdomen
- A disease of the reproductive tract
- A disease of the intestines
Is cervical cancer easy to prevent and treat?
- Yes
- No
- It depends
When should a women begin getting screened for cervical cancer?
- By age 21
- By age 31
- By age 40
How many cervical cancer screening options are there for a woman aged 30-40?
- 4
- 2
- 10
At what age can a woman stop getting her yearly screenings for cervical cancer, and be sure she will remain healthy?
- 45
- 55
- 65
What do the best medical professionals recommend to maintain your feminine health, regardless of your age?
- Only getting cervical cancer screenings
- Annual gynecologic examinations, including pelvic exams
- Waiting until you have symptoms
Are there conditions that require more frequent tests for cervical cancer?
- Yes
- No
- I'm not sure
What is the name of the cervical cancer vaccine?
- HibTITER
- Gardasil
- Menomune
During what age range should a woman consider getting vaccinated with Gardasil?
- Ages 5-10
- Ages 32-44
- Ages 9-26


Comments: (4)
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By: C. on 5/08/2009 11:04PM
Please register, it only takes a couple of minutes.You fill out the application online. The information is mailed to you, you swab your mouth with what they send and you mail it back in a postage paid envelope. It could save a life, a life in your family, or even your own.
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By: Sheryl on 5/10/2009 6:41PM
How do I find out where/when/how to register or be tested? I think this is something I would like to be involved in.
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By: Rosalie on 5/11/2009 1:38PM
I wish this little girl well.
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By: William K. Wolfrum on 5/14/2009 6:20PM
I'm very very happy to hear about Jasmine and wish her well in her transplant. I understand the excitement her family is feeling. A transplant is her chance to beat this leukemia.
I am the author of the above passage you quoted from Shakesville. One thing I'd like to dd is that there is often a charge for getting on the marrow list (the cost goes for tissue typing). While I can't say I like that, that debate is for another day.
But my point is that African-Americans (and I believe Latinos, as well) have the fees waived and there will be no charge to join the list. They need the diversity of donors. Also, there are often bone marrow drives that will have sponsors to help either defray any fees, or have them waived entirely.
If anyone would want to contact me about this, please feel free at wkwolfrum(at)gmail(dot)com
Bill
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