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:
5'11"
(180 cm)
Weight:
195 lb
(88 kg)
Eye Color:
Hazel
Hair:
Brown/
Straight
Skin Tone:
Light
Ancestry:
Caucasian
Blood Type:
O+
Ethnic Background:
Polish/English-Irish
Education:
BBA/Accounting
Occupation:
Financial Accountant
Interests:
Minature Painting, Reading, Stock Trading, Video games

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 AntibodyNegative
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 62
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 63
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 34
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 32
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 29
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 77
Living / DeadDead
Cause of death and any treatment prior to deathHeart Failure
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Other
 
No other diagnosed health problems at time of death
Question Response
Current age or age at death 85
Living / DeadDead
Cause of death and any treatment prior to deathHeart Failure
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Other
 
No other diagnosed health problems at time of death
Question Response
Current age or age at death 73
Living / DeadDead
Cause of death and any treatment prior to deathLung Cancer (smoker)
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Other
 
No other 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
Healthy
Question Response
Current age or age at death 75
Living / DeadDead
Cause of death and any treatment prior to deathStroke
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Other
 
No other diagnosed health problems at time of death
Question Response
Current age or age at death 80
Living / DeadDead
Cause of death and any treatment prior to deathHeart Attack
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 60
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 67
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy

Religion:

Faith None
Denomination N/A

Updates to Profile

Update AvailableYes
Updates - PersonalNo change to profile: September 2025.
Updates - MedicalNo change to profile: September 2025.
Updates - Family Medical HistoryJune 2025 Update: An embryo reportedly conceived with donor 7042 was identified to have a duplication during a routine chromosome microarray analysis. Despite our efforts, confirmation of the client's use of donor 7042 was not provided by the reporting clinic. The size of the duplication is 303 kbp and the genes involved are PPP1R3A and FOXP2. The laboratory classified this finding as a variant of uncertain significance. When a variant of uncertain significance is identified, it is unclear whether that variant is associated with a specific health condition. In many cases, the variant is so rare in the general population that it has not been described in the literature or variant databases, thus there is little published information to review. Identification of a variant of uncertain significance does not establish or rule out the diagnosis of a disorder and no medical management recommendations are made based solely on the finding of a variant of uncertain significance. As the finding in the proband is a variant of unknown significance AND maternal results were never provided to Fairfax, testing of the donor for this duplication was not pursued. Therefore, it is unknown if this duplication was inherited from the egg source, inherited from the sperm source, or new to this embryo nor is the potential impact of this finding known. Obviously, as testing was conducted on an embryo, no clinical signs or symptoms initiated this testing. No change to profile: September 2025.