COLUMBUS, Ga., Dec. 15 /PRNewswire/ -- Hundreds of Aflac agents and employees will be queuing up in the next few days to have their cheeks swabbed as part of a new company initiative to boost the rolls of the National Marrow Donor Program. Aflac's Bone Marrow program kicks off at the company's annual national sales conference on December 12 in Atlanta.
The bone marrow registration effort was inspired by Steve Karas, an Aflac regional sales coordinator in Boston, whose stem cell donation recently helped save the life of Matthew Welling, a young Aflac claimant in New York. Matthew's parents had been told that without a transplant, he stood little chance of living beyond childhood. Matthew's doctors searched the National Bone Marrow registry for a donor and found Steve Karas.
"Through Steve's story we learned more about the pressing need for bone marrow registrants and wanted to do something as an organization to help," said Paul Amos, president and chief operating officer of the Georgia-based insurance company.
Indeed, the need is great. Individuals with life-threatening diseases
such as leukemia and lymphoma must find a donor whose tissue type matches
their own. Ideal candidates for a match are usually from the same ethnic
background and race. The National Marrow Donor Program has about 11 million
registrants today, but 61 percent of patients who need a bone marrow
transplant do not receive one. And that's just among Caucasians. Among other
racial groups, the match rate is far lower. For instance, about 83 percent of
African Americans in need of a transplant do not receive one because African
Americans are severely underrepresented on the donor registry. Individuals
from racially or ethnicall
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