Meet Walker (8676) – Open ID Donor.Back to Donor Search
- Eyes: Blue
- Hair: Black
- Height: 6'02"
- Weight (lbs): 172
- Blood: A Rh+
- CMV: -
- Ethnicity: Caucasian, Irish
- Jewish Ancestry: No
- Education/Occupation: M.A. Philosophy / University Admin
- Live Birth / Pregnancy Confirmed: Yes
- Extended Testing: Yes
Walker is a handsome man! He stands at 6 feet 2 inches tall with thick dark black hair and dark blue eyes. He has a beautiful creamy white complexion and a chiseled jaw line. He has a medium muscular build and is an active cyclist. Walker is usually dressed in trendy business casual with slacks and button up shirts.
Walker is funny and witty with a somewhat cynical sense of humor. He is incredibly genuine and enjoys helping others. He adores his family and speaks very lovingly of his wife and young daughter. When we asked Walker why he wants to be a donor he said, “When my wife and I had our daughter we met lots of other new parents and it became evident that regardless how easy it was for us for many people it's a struggle to get pregnant. Some of the folks we met, it was incredibly gut wrenching to hear what they went through, if it's possible that I can be of help, I'm happy to do that. “
Over the years, we have expanded our genetic testing of donors as genetic knowledge and technology have advanced. As a result, not all donors have been tested for the same conditions or with the same methods. All donors have undergone genetic testing for Cystic Fibrosis, Spinal Muscular Atrophy and Karyotyping. However, many donors have had more extensive testing performed.
This donor has been evaluated for carrier status of the listed conditions. A negative result reduces, but does not eliminate, the likelihood of the donor being a carrier. If you are a known carrier of a genetic condition please contact us, and we will provide a copy of the donor's test reports to your physician and/or genetic counselor.
|Karyotyping||Normal Male Karyoptype, 46XY|
|limb-girdle muscular dystrophy type 2E||Non-Carrier|
|spinal muscular atrophy||No disease-causing mutations detected (2 copies or more)|