Meet Patrick (10032) – Open ID Donor – New Donor!.

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  • Eyes: Blue
  • Hair: Blonde
  • Height: 5'11"
  • Weight (lbs): 180
  • Blood: O Rh+
  • CMV: -
  • Ethnicity: Caucasian, English, German, Swedish
  • Jewish Ancestry: No
  • Education/Occupation: B.S. Health Policy / Student, event coordinator
  • Live Birth / Pregnancy Confirmed: No
  • Extended Testing: Yes

Patrick has a muscular build, a result of his very active lifestyle comprised of regular cardio and lifting weights. He has beautiful, blue eyes and thick, wavy blond hair to complement his medium skin tone that darkens with time in the sun. Patrick keeps his face clean shaven and his hair short, showing off the few freckles he has. All these features make Patrick an extremely good looking young man.

 

Patrick is very intelligent and dedicated, maintain a job while working through college. He is also incredibly kind and health conscious, wanting to help others especially in living healthy lives and improving the quality of their lives. Patrick is very athletic, playing a variety of sports with rugby as his favorite; he had scholarship offers until injury ended his competitive rugby career. He has a great sense of humor and it is easy to make him smile. Patrick is a truly incredible person, an amazing donor and we feel lucky to have him in the 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