Meet Casey (12045) – Open ID Donor.

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Casey Staff Impression

Casey is tall and lean, with a strong core and built up shoulders, arms, and leg muscles from competing in triathlons. His face is caring and bright, with handsome, green/brown eyes, an energetic smile, rosy cheeks, and a strong brow line. He has a fair skin tone, dark brown hair, and a bunch of fun freckles on his face and arms.

Casey is beyond charming. His intellect, wit, and amazing interpersonal skills make him one of the staff’s absolute favorites to chat with. His personal accomplishments make him an undeniably great donor. He is a resident physician, currently specializing in Anesthesiology and Pain Medicine. Prior to his residency, he earned his MPH (Masters of Public Health), and, fueled by his passion for providing Global Health services, traveled to and lived in Africa for two years. In general, Casey is extremely well-traveled, and has an inspired world view from being a part of so many different cultures. He is also very musically inclined, coming from a family of singers, musicians, and performers- he has sung professionally for some time, as well as playing piano, sax, and jazz bass. There is much more we could say about Casey- suffice it to say, he would be an amazing choice 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