Meet Neil (10043) – Open ID Donor.

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  • Eyes: Blue/Green
  • Hair: Dark Brown
  • Height: 5'11"
  • Weight (lbs): 167
  • Blood: O Rh+
  • CMV: -
  • Ethnicity: Caucasian, Danish, French, German
  • Jewish Ancestry: No
  • Education/Occupation: B.A. Journalism and Film / Student
  • Live Birth / Pregnancy Confirmed: Yes
  • Extended Testing: Yes
  • Genetically tested for: View

Neil is a unique donor with passion and drive. He has a well-balanced mixture of creativity and intelligence. Neil is always questioning why things are done the way they are, and has an open mind so he can form his own thoughts and opinions. He is active in film and journalism with an interest in documentaries and hopes of directing a major television production. Neil is creative, thoughtful, outgoing and caring making him a wonderful donor with a sense of self that we rarely see in donors his age.

 

Neil is six feet tall with thick, wavy hair that we all envy. His brown hair and thick eyelashes really work to make his blue/green eyes pop. Neil has an adventurous personality and loves to go hiking and enjoy the outdoors. He also runs and swims on occasion, but most of his exercise comes from hiking and other outdoor activities. Neil has the laid-back attitude and look to match that attract people wherever he goes.

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