Be the Match.com
Feb. 17th, 2010 06:25 amThis morning, I completed the process to become a registered donor at the National Bone Marrow Donor's Be the Match registry. In five or six weeks, after they've typed the cheek swabs I sent in, I'll be part of the database that doctors search on behalf of 6,000 patients a day. Patients with leukemia, sickle cell anemia, what-have-you where the donation of healthy bone marrow cells and other blood-products are really the best hope for a cure. I found it crushing to read that presently only about 30% of patients are finding close enough genetic matches in the database.
I hope you'll consider joining, too!
Right now, there are enough funds to cover the costly testing process, so you can sign up and join the registry for free. (They'll send you information and a set of cotton-tipped swabs to play CSI with and send back.) The registry is for anyone, barring certain health concerns, from the age of 18-60 that is willing to donate blood product and/or marrow if your genetic match is in need. (The donation process also looked way simpler than the scary words "bone marrow" would imply.) Sign up once and they'll keep your information in the database until you turn 61 years old. If they ever need you for a specific patient, they'll call.
It feels powerful, throwing myself into the void. I have an unreasonably strong medical phobia, but I still hope that somewhere, sometime, my perfectly unique blend of Swedish/Scottish/Irish/English genes will offer what others could not. It is my Valentine to the rest of the embodied world--a hand outstretched if ever it should be needed.
I hope you'll consider joining, too!
Right now, there are enough funds to cover the costly testing process, so you can sign up and join the registry for free. (They'll send you information and a set of cotton-tipped swabs to play CSI with and send back.) The registry is for anyone, barring certain health concerns, from the age of 18-60 that is willing to donate blood product and/or marrow if your genetic match is in need. (The donation process also looked way simpler than the scary words "bone marrow" would imply.) Sign up once and they'll keep your information in the database until you turn 61 years old. If they ever need you for a specific patient, they'll call.
It feels powerful, throwing myself into the void. I have an unreasonably strong medical phobia, but I still hope that somewhere, sometime, my perfectly unique blend of Swedish/Scottish/Irish/English genes will offer what others could not. It is my Valentine to the rest of the embodied world--a hand outstretched if ever it should be needed.