Meet Baxter (10016) – Open ID Donor.

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As a collegiate cross country and track runner, Baxter has a runner’s body; he is thin with long, lean muscles. He has a medium skin tone that is usually very tan due to his time spent running in the sun. Baxter has large, green/ brown eyes and straight brown hair.  He has a clean, clear complexion which shows the few freckles he has (which seem to become more prominent with time in the sun). With his broad smile and athletic build, Baxter is a very attractive young man.


Baxter always comes in smiling ear to ear and his jovial attitude is contagious. Baxter is naturally happy with a laid-back demeanor with his friends and family but at the same time is driven and goal oriented. He is very analytical but definitely has a sweet side and always does his best to improve himself and those around him. His goal in life is “to be remembered as somebody who had an impression on others and who made everything around him better.” We love this attitude and believe it is one of the many characteristics that make Baxter a magnificent donor.

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.

Since this donor is a carrier for 1 or more conditions, we require that you fill out the Informed Consent document found HERE
This consent form needs to be completed and sent to us, prior to shipment.

Karyotyping  Normal Male Karyoptype, 46XY
ABCC8-related hyperinsulinism Non-Carrier
alpha thalassemia 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