Meet Ethan (10017) – Open ID Donor.

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Ethan is a good-looking young man. He has long, thick wavy brown hair that create a stunning contrast with his bright blue eyes. Ethan usually has a beard, but will occasionally come in clean shaven and looks handsome either way. He is 5’10” with a medium build and well defined muscles. Ethan is extremely healthy and active, maintaining a vegan diet and engaging in high intensity workouts on an almost daily basis.


Ethan has an amazing personality! He is genuine, passionate and enthusiastic about life and all it has to offer. At the same time, Ethan is incredibly laid back and go-with-the-flow. He believes that everything happens for a reason and makes the most of every experience he has. Ethan loves to travel, meet new people and discover new cultures. He is excited to be part of the program and is looking forward to helping families and possibly meeting future offspring. We truly cannot say enough good things about Ethan.

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