Meet Ford (10031) – Open ID Donor.

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  • Eyes: Brown
  • Hair: Brown
  • Height: 6'00"
  • Weight (lbs): 160
  • Blood: B Rh-
  • CMV: -
  • Ethnicity: Australian, Caucasian, German, Italian, Native American
  • Jewish Ancestry: No
  • Education/Occupation: B.A. Criminology / Police Officer
  • Live Birth / Pregnancy Confirmed: Yes
  • Extended Testing: Yes
  • Genetically tested for: View

Ford is 6 feet tall with a lean and muscular build. He does regular cardio and weightlifting and maintains a healthy vegan diet to stay in peak physical shape. He has brown eyes and brown hair, although he keeps his head shaved. Ford is clean shaven and almost always smiling to show off straight white teeth and dimples on either side. Ford has an infectious laugh and his presence always puts us in a good mood.

Ford has a very jovial personality and loves to laugh. He is usually outgoing and chatty when he comes in which makes it hard for us to picture him as a tough cop, but he assures us that he turns on his cop personality for work. Ford likes to keep busy with a wide range of hobbies and is always looking to learn something new. His time in the military and current career as a police officer show just how hard working he is. Ford is a very intelligent and unique donor with a great personality.

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