Physical
Medical
Family Medical History
Religion
Updates to ProfilePhysical
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Height:
5'11"
(180 cm) |
Weight:
154 lb
(69 kg) |
Eye Color:
Brown
|
Hair:
Brown/
Wavy |
Skin Tone:
Light
|
Ancestry:
Multi
|
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Blood Type:
AB+
|
Ethnic Background:
French-Italian-Swedish/Korean
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Education:
Pursuing BS/Computer Science
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Occupation:
Software Engineer
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Interests:
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Baseball, Guitar, Hiking, Keyboard, Singing, Software Engineering, Writing
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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: | Yes - Amoxicillin/Levofloxacin: Hives |
| CMV IgG Antibody | Positive |
| CMV IgM Antibody | Negative |
| Note any comments regarding above items: | N/A |
Family Medical HistorySee list of questions asked here
Your Mother
| Question | Response |
| Current age or age at death | 51 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Healthy
Your Father
| Question | Response |
| Current age or age at death | 52 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Disease
Age Diagnosed
Treatment For Condition
High blood pressure
37
Diet change, exercise
Sisters
Your Sister 1
| Question | Response |
| Current age or age at death | 15 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Healthy
Your Sister 2
| Question | Response |
| Current age or age at death | 13 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Healthy
Your Mother's Father
| Question | Response |
| Current age or age at death | 77 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Disease
Age Diagnosed
Treatment For Condition
High cholesterol
55
Diet and exercise
Your Mother's Mother
| Question | Response |
| Current age or age at death | 71 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Healthy
Your Mother's Sisters 1
| Question | Response |
| Current age or age at death | 44 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Systemic lupus
22
Medication
Your Mother's Brothers 1
| Question | Response |
| Current age or age at death | 46 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Disease
Age Diagnosed
Treatment For Condition
High blood pressure
31
Diet, exercise
Your Father's Father
| Question | Response |
| Current age or age at death | 74 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Healthy
Your Father's Mother
| Question | Response |
| Current age or age at death | 68 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Healthy
Your Father's Brothers 1
| Question | Response |
| Current age or age at death | 55 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Healthy
Your Father's Brothers 2
| Question | Response |
| Current age or age at death | 54 |
| Living / Dead | Living |
| Cause of death and any treatment prior to death | N/A |
Health Problems
Healthy
Religion:
| Faith | Other |
| Denomination | I was raised Christian, but I currently find it difficult to identify with a single line of faith. I think many religions follow tenets that I agree with regarding tolerance, compassion, and charity, but I don't agree with a lot of the bigotry and proselytizing that can be tied in. There's also something about matter-of-factly identifying the unidentifiable that doesn't quite sit well with me. |
Updates to Profile
| Update Available | Yes |
| Updates - Personal | Updated received December 2024: Donor has completed two post-baccalaureate degrees in Computer Science. |
| Updates - Medical | Update recieved September 2025: Donor's height was corrected from 5'10" to 5'11" based on a measurement performed by lab staff. UPDATE Dec 2025: The donor was identified to have an Xp22.31 duplication. His specific breakpoints are Xp22.31(6440776_8135644)x2. He reports no health problems, and this finding was only discovered after genetic testing was done on two embryos created using his sperm. Based on what is known, we believe that female children conceived with this donor would inherit this extra piece of DNA, while male children would not. The laboratory that performed the testing classified this finding as benign, meaning it is not expected to cause health problems. Duplications of this region of the X-chromosome have been reported in both healthy people and in those with serious medical issues. This range is likely related to the size of the duplication, though other factors cannot be ruled out. At the current time, we cannot be certain whether a child conceived by this donor might be affected and what symptoms they would have. When health issues are present, they may include developmental delays, learning difficulties, autism, low muscle tone, seizures, clubfoot, a smaller-than-average head size, heart differences, extra fingers or toes, or feeding difficulties. Not everyone with health issues will have the same features. At this point, twelve births have been reported from this donor. To date, no children have reported medical issues. Most affected children reported in the literature have medical issues present at birth or early childhood.UPDATE Jan 2026: In light of the recent finding of a duplication of Xp genetic material in the donor, Fairfax contacted the donor to review his personal and family history. The donor denies any personal or family history of the following conditions that can be assocaited with a duplication of this region: developmental delays, learning difficulties, autism, low muscle tone, seizures, clubfoot, a smaller-than-average head size, heart differences, extra fingers or toes, or feeding difficulties. |
| Updates - Family Medical History | UPDATE Nov 2025: Fairfax was notified that two XX embryos were identified to have a Xp22.31 duplication. Records have been requested to investigate this report and to assess next steps. Additional information will be provided as it becomes available. UPDATE Dec 2025: The donor was confirmed to have a duplication of Xp22.31. Please review the information under Updates -Medical for additional information regarding the potential impact and risks of occurrence associated with this finding. UPDATE March 2026: A client notified Fairfax that her 3 month old daughter is experiencing cluster seizures. They started ~8 weeks of age. Per the client's neurologist, "they’re not sure if it is something due to her immature neurological system that still needs to develop or if this is something that will be with her long-term. Time will tell at this point." Per the client, her daughter carries the Xp duplication previously identified in the donor, however no additional genetic testing is currently planned. UPDATE April 2026: Additional details to the update from March of this year - The client reports that the seizures typically lasts 1 second and occur 3-4 times aday (in clusters). They typically happen 1-2x a week. Per the client, her daughter had an EEG (50 minutes and 24 hours) that showed rare focal epileptiform discharges in the left parieto-temporal region during wakefulness and drowsiness.The child is followed by a pediatric neurologist and is currently treated with Keppra 2mL, taken two times per day. Per the client, her daughter is otherwise healthy. The cause of this child’s seizure disorder has not been determined. Epilepsy can be caused by several factors including head trauma, infection, and brain malformations. About 30-40 percent of epilepsy is caused by a genetic predisposition, including an inherited genetic condition, a sporadic genetic variant that was not inherited, or chromosomal deletions or duplications. Without specific information, it is difficult to determine if there is any increased risk for othersconceived with the help of this donor to be affected. Multiple births have been reported with the use of this donor; no other children have been reported with simliar issues. UPDATE June 2026: Fairfax has been notified that a client's child was born with type-c esophageal atresia and is in the NICU. No additional information is available at this time. This medical update is currently being investigated; however, this donor's status has previously been changed to Restricted and will remain so. UPDATE June 2026: Regarding the child with type-c esophageal atresia mentioned above, the child’s mother reports that she has no associated medical issue, that PGT-A testing was within normal limits, and that no further genetic testing was pursued. Causes of esophageal atresia are not fully understood. While the exact cause remains unknown, evidence points to a combination of genetic, environmental, and developmental factors. Some children are born with EA (and Tracheoesophageal fistula, TEF) as part of a larger syndrome or associated anomalies of the heart, urinary or digestive tract, while others have isolated EA/TEF without these additional problems. With the history provided at the time of this report, there is no current evidence for syndromic EA/TEF. There is no indication that this child's esophageal atresia is linked solely, if at all, to the donor; however, risk for recurrence in other donor conceived children remains unknown. |