Physical

Height:
5'9"
(175 cm)
Weight:
177 lb
(80 kg)
Eye Color:
Green
Hair:
Brown/
Straight
Skin Tone:
Light
Ancestry:
Caucasian
Blood Type:
B+
Ethnic Background:
German-Irish/German-Irish
Education:
BS/Criminal Justice
Occupation:
Advocate Coordinator
Interests:
Football, Lacrosse, Soccer, 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 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 63
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 65
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Disease
Age Diagnosed
Treatment For Condition
High blood pressure
55
Medication
High cholesterol
55
Medication
Question Response
Current age or age at death 33
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
Healthy
Question Response
Current age or age at death 74
Living / DeadDead
Cause of death and any treatment prior to deathHeart Attack
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Other
 
Had had heart and lung issues due to chemical weapons exposure during World War II.
Question Response
Current age or age at death 85
Living / DeadDead
Cause of death and any treatment prior to deathHeart Attack and Stroke
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 65
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
Question Response
Current age or age at death 50
Living / DeadDead
Cause of death and any treatment prior to deathCancer
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 90
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 67
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
Healthy

Religion:

Faith Christian
Denomination Non-denominational

Updates to Profile

Update AvailableN/A
Updates - PersonalN/A
Updates - MedicalN/A
Updates - Family Medical HistoryUPDATE September 2025: A client reported a twin pregnancy (non-identical male/female) conceived with the help of donor 7008 in which both twins were identified via chromosome microarray analysis (CMA) to have missing chromosome material in one part of chromosome 16 (16p12.2 deletion). The donor was identified to carry this deletion, and therefore each of his offspring has a 50% chance to also carry this deletion. The risk, however, that a child would have any clinical symptoms (see below) is less than 50% as not all individuals who carry this deletion show signs or experience symptoms. People with a 16p12.2 deletion can show and experience a wide range of clinical signs and symptoms that include developmental delay, intellectual disability, psychiatric and/or behavioral issues, autism, growth impairment, heart defects, musculoskeletal findings, low muscle tone, and seizures. Less frequent findings can include hearing loss, dental abnormalities, renal issues, genital anomalies in males, and cleft palate and/or cleft lip. Not all individuals identified to have this deletion show signs or experience symptoms. This is called reduced penetrance. Furthermore, individuals with this deletion can experience a wide range of severity of symptoms. This is known as variable expressivity. Per research on this deletion, individuals without an additional extra or missing piece of DNA elsewhere in their genetic material were typically found to be unaffected or to have milder symptoms such as learning disability, depression, or seizures. It has been suggested that having this deletion predisposes a person to neurological and psychiatric conditions rather than is a single cause of them. It should also be noted that there is a significant bias of reported cases in that those who show signs or experience symptoms are more likely to undergo genetic testing than those who are not experiencing medical issues. As such, the frequency of this deletion in the general population, which would represent a larger number of unaffected individuals, is unknown. In addition, studies consistently report on a larger deletion (520kb) rather than the smaller deletion (474kb) identified in this donor and twin pregnancy. As such, the signs and symptoms of those who carry the 474kb deletion may be less severe.As the donor was identified to carry this deletion, each of his offspring have a 50% chance to also carry this deletion however, the risk a child would be affected is less than 50% because of reduced penetrance for the deletion. As such, it is not possible to reliably predict if and what signs and symptoms a child will have based on the laboratory finding of a 16p12.2 deletion. This donor has over 20 births. No other medical updates have been reported for this donor or any children conceived by this donor.UPDATE September 2025: Client reports baby born with donor's known deletion. Died at 6 hours of birth due to probable sepsis due to pneumonia due to intraamniotic infection. Death was NOT connected to the presence of this deletion, which is considered an incidental finding. Physical findings in autopsy were within normal limits.UPDATE December 2025: Fairfax has been notified that an 11 month old girl carries the donor's known 16p12.2 deletion. Testing was proactive; she has no signs or symptoms and is reportedly healthy.