Meet Sheldon (12035) – Open ID Donor.

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Sheldon has sharp good looks, and an even sharper wit! He has a fair complexion with dark brown hair, thick dark eyebrows, and piercing blue/green eyes. He has nice, high cheek bones, a handsome jawline, a small nose, and a quirky smile. He has a small to medium build with lean muscles, and stays in great shape without being overly athletic.

Sheldon has a very smart look about him, which is fitting considering he is a highly intelligent person. He was a Software Engineer for many years, before deciding to quite a lucrative job and chase his dream of “saving the world” by pursuing a PhD in Public Policy. His work ethic, passion, and commitment to improving the lives of others are unmatched. He’s also incredibly well-rounded, coming from a family of accomplished outdoorsmen (backpacking, rafting, skiing, etc), he is a very active person, and he is very well-traveled. Sheldon is outgoing, thoughtful, and truly unique. He would be an outstanding donor for any family!

Genetic Testing

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
ABCC8-related hyperinsulinism Non-Carrier
alpha thalassemia Non-Carrier
ARSACS Non-Carrier
Bloom syndrome Non-Carrier
Canavan disease Non-Carrier
cystic fibrosis Non-Carrier
familial dysautonomia Non-Carrier
Fanconi anemia type C Non-Carrier
Gaucher disease Non-Carrier
glycogen storage disease type Ia Non-Carrier
Hb beta chain-related hemoglobinopathy (including beta thalassemia and sickle cell disease) No disease-causing mutations detected; normal complete blood count and hemoglobin analysis
hexosaminidase A deficiency (including Tay-Sachs disease) Non-Carrier
Joubert syndrome 2 Non-Carrier
lipoamide dehydrogenase deficiency Non-Carrier
maple syrup urine disease type 1B Non-Carrier
mucolipidosis IV Non-Carrier
NEB-related nemaline myopathy Non-Carrier
Niemann-Pick disease, SMPD1-associated Non-Carrier
spinal muscular atrophy No disease-causing mutations detected (2 copies or more)
Usher syndrome type 1F Non-Carrier
Usher syndrome type 3 Non-Carrier
Walker-Warburg syndrome Non-Carrier