This donor is a healthy carrier for a genetic disease.
Please see his Genetic Testing Summary and Acknowledgment of Genetic Risk for details

Physical

Height:
6'3"
(190 cm)
Weight:
213 lb
(96 kg)
Eye Color:
Blue
Hair:
Blond/
Straight
Skin Tone:
Medium Light
Ancestry:
Caucasian
Blood Type:
O+
Ethnic Background:
Finnish-Swedish/Canadian-Scottish
Education:
BS/Kinesiology
Occupation:
Fitness Studio Manager
Interests:
Basketball, Football, Hiking, Reading, Strength Training, Travel

Medical

Question Response
Have you or any of your family members been diagnosed with alcoholism or drug addiction?
If yes, relation and age affected:
No
Any dietary restrictions?
If yes, explain:
No
Do you wear glasses or contact lenses?
Are you near or far-sighted?
No
Allergies (medicines, food, pollens)?
If yes, please list substance and reaction caused:
No
CMV IgG AntibodyPositive
CMV IgM AntibodyNegative
Note any comments regarding above items:N/A

Family Medical History
See list of questions asked here

Question Response
Current age or age at death 58
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Disease
Age Diagnosed
Treatment For Condition
High blood pressure
50
Medication
Question Response
Current age or age at death 57
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 26
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Anxiety
20
Took medication intermittently in college but as of age 23, only uses therapy as treatment.
Question Response
Current age or age at death 38
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 50
Living / DeadDead
Cause of death and any treatment prior to deathWork accident
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Other
 
No diagnosed health problems at time of death
Question Response
Current age or age at death 77
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Rheumatoid Arthritis
50
Medication
Question Response
Current age or age at death 50
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Other
 
Fibromyalgia at age 40, uses medication for treatment
Question Response
Current age or age at death 89
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 85
Living / DeadDead
Cause of death and any treatment prior to deathDementia
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Dementia or degenerative disorders
80
Assisted living facility
Question Response
Current age or age at death 55
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 60
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Diabetes mellitus not requiring insulin therapy
55
Ozempic

Religion:

Faith None
Denomination N/A

Updates to Profile

Update AvailableN/A
Updates - PersonalN/A
Updates - MedicalN/A
Updates - Family Medical HistoryFebruary 2026 UPDATE: Pregnancy with possible AKT2-related condition. Donor placed in Investigation while additional information is obtained. APRIL 2026 UPDATE: As noted above, Fairfax was notified by a clinical genetic counselor that a client’s pregnancy was identified to have nephromegaly, possible macroglossia, and be above the 95% percentile for fetal weight, head diameter, and waist circumference. Whole genome sequencing was conducted on the client and her pregnancy; no reportable variants were identified related or possibly related to the pregnancy’s phenotype (the set of observable characteristics and physical traits). Other findings included a variant of uncertain significance (c.508C>T (p.Arg170Trp) in the AKT2 gene that was not maternally inherited. Given the questionable association between the identified variant and the clinical presentation ofthe pregnancy, and the fact that the variant is classified as a variant of uncertain significance, genetic testing on the donor was not conducted. Despite attempts by Fairfax, no additional information regarding this case was made available.As the donor was not tested, the chance for a child conceived by this donor to have this variant is unknown. In addition, no information is available to determine the potential impact of this variant of uncertain significance. In many cases, these variants are very rare and have not been studied enough to determine their impact. The presence of a VUS does not confirm or rule out a medical diagnosis. At this time, no clear link has been established between this VUS and the findings in this pregnancy. At present, three other births have been reported from this donor with no significant medical updates.