Meet Aaron (10023) – Open ID Donor.

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Aaron is tall and exercises regularly by staying active with activities such as running lifting, hiking, etc. He is tan with a medium skin tone and smooth complexion. Aaron keeps his face clean shaven to display the freckles that run across his nose and cheeks.  He has thick, wavy brown hair and matching brown eyes that twinkle when Aaron shows his shy smile. These features make Aaron a very good looking donor.


Aaron is very intelligent and hardworking with great ambitions. He is truly a man of many talents and is extremely handy and also play guitar. These talents come with a great personality that is both fun and outgoing. We love how patriotic Aaron is and how proud he is of the time he served the U.S. Army. When asked why he became a donor, Aaron responded “… Before making sure our family is complete, we decided it was now or never to help others start theirs by becoming a donor.” Aaron is hardworking, caring and thoughtful and would make a great 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