Meet Bodhi (12046) – Open ID Donor – New Donor!.

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Bodhi looks like the quintessential ‘boy next door,’ and is one of the most all-around attractive donors in our program. He has a slender but athletic build, strong shoulders, and a rugged square jawline. His Italian heritage comes through in his perfect, medium olive tone skin, thick, dark brown hair, and big, soulful, dark brown eyes.

Bodhi has always had a natural ability to do well in math and science, and is currently pursuing a degree in Mechanical Engineering. When he’s not busy studying, he is an absolute outdoors fanatic, spending as much time as he can hiking, backpacking, bike riding, and generally enjoying the Pacific Northwest. He is also a gifted guitar player and has a very mature and well-educated taste in music. Socially, Bodhi is a natural extrovert and a great communicator. Our personal favorite thing about him is his constant upbeat, cheery, and positive attitude- his energy is truly infectious, and we are so happy he is in our donor program!

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