Donor Number 982

General Information

Donor Code:
982
Ethnic Origin:
American Indian, Dutch, English, German, Irish, Scottish
Blood Type:
AB Negative
Hair Color:
Brown
Type of Hair:
Straight
Thickness of Hair:
Average
Age at Time of Retrieval:
25-26
Eye Color:
Blue
Complexion Relative to Race:
Fair
Bone Structure:
Small
Height:
5'7"
Weight:
130
Handedness:
Ambidextrous

Spending time in the gym and working with collaborative teams on artistic projects (photography, illustrating, modeling, styling models). Also enjoys hiking, rock climbing, and running.

Education Status: Vocational Student

Area of Study: Art Education, Athletic Training, Dietetics, Nutrition and Food Sciences, Exercise and Movement Science, Marketing, Nutrition and Food Sciences, Physical Education

Vision: Excellent, does not wear lenses

Hearing: Excellent

Dentition: Good, orthodontia required

Allergies: None known

Hospitalization: 1990s, 1990s

Alcohol Usage: Does not drink alcohol

Tobacco Usage: Does not smoke

Drug Usage: Tests NEGATIVE for Drugs of Abuse.

Paternal Grandfather: Died in his 70's, Melanoma in his 70's (due to sun exposure) which led to lesions on his brain

Paternal Grandmother: Alive and in her 70's, Healthy

Maternal Grandfather: Died in his 60's, Heart attack in his 60's (smoker)

Maternal Grandmother: Alive and in her 70's, Skin cancer in her 70's (due to sun exposure), Osteoarthritis in her 50's treated with Tylenol

Father: Alive and in his 50's, Osteoarthritis in his 40's that does not need treatment

Mother: Alive and in her 40's, Type II diabetes in her 40's (lifestyle related), Childhood asthma due to second hand smoke, Osteoarthritis in her 40's treated with Tylenol

Siblings: At least one sibling, all in good health.

Genetic Screening Performed: Yes

This donor has been screened for 107 genetic diseases (via targeted mutation analysis) and has been found to test positive for the following:

Alpha-1 Antitrypsin Deficiency

MTHFR Deficiency

Glycogen Storage Disease Type V

All people carry mutations for genetic disorders. Genetic testing can identify some of those mutations. We perform testing for a large number of conditions that are inherited in a recessive manner to help detect some of the mutations in our donors. Since all people carry mutations, donors are not excluded from our program when these mutations are identified. The donors' offspring are not at risk to develop the condition unless the other biological parent also carrier a mutation for the same inherited disorder. We encourage you to use the results of the donor's testing and consider your own genetic testing to help identify a donor suitable for your needs.

ORIGINAL FAMILY HEALTH HISTORY:

The donor's personal and family health history was originally reported on 8/22/2014

UPDATED HEALTH HISTORY:

No new information reported at this time.

Donor Communication (Type): Open

Limited Available? No

Past Pregnancy: Yes

Face: Oval in shape with average forehead set and slight freckles across the bridge of the nose and cheeks

Lips: Medium fullness to upper and lower lips

Nose: Straight shape, average in length, with a straight tip

Ears: Medium in size, tucked back, attached lobes

Eyes: Round in shape, large size, average set, with long lashes

Eyebrows: Medium fullness, curved

Summary: Her energy is the first thing you notice! She is very fast paced and full of life. Lives a very healthy lifestyle and is proud of the fact that she eats healthy and works out on a regular basis.

 

Childhood Photos

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