Meet Bryden.

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  • Eyes: Blue
  • Hair: Light Brown
  • Height: 6'00"
  • Weight (lbs): 160
  • Blood: O Rh+
  • CMV: -
  • Ethnicity: Caucasian, English, German, Irish, Polish, Scottish
  • Jewish Ancestry: No
  • Education/Occupation: B.A. Economics / Nonprofit Manager
  • Live Birth / Pregnancy Confirmed: No
  • Extended Testing: Yes

Bryden has chocolately brown hair, bright blue eyes, and fair skin, with slightly rosy cheeks and a great, big smile that lights up a room. He has a medium build, is in good shape, and is very well kept.

Bryden is particularly thoughtful and articulate, with a witty, dry sense of humor and great communication skills. Our favorite thing about Bryden is his compassion for helping others- Although majoring in Economics, he is extremely passionate about his career in the non-profit sector, currently managing a center for at-risk teens in the area to help them pursue and attain higher education. Bryden is also very well-traveled, and enjoys exercising outside, reading, playing drums, and camping. If you are looking for someone who is particularly intelligent and compassionate, Bryden would be a great choice for you!

 

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