Donor Profile : Donor 3088

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Advisory

This is an xyLimited Donor.

Although we place limits on how many worldwide family units* can be conceived using a particular donor, our xyLimited Donors offer an even greater peace of mind by limiting the number of worldwide family units to 15. Clients must purchase at least 3 vials.

For more information, please contact us.
*Family units are determined by the number of births reported by clients.

Retired Donor

This donor is no longer active in the program. The number of vials available represents the remainder of the donor's inventory.

Donor ID: 3088

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Genetic Testing Performed: Please review the list of genetic tests performed before choosing a donor because donors have different levels of testing. Genetics is very complicated and testing can only reduce but not eliminate the risk of a donor being a carrier of a particular condition.

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Donor's "Name": Camden

Year of Birth: 1990

Marital Status: Single

Number of Children: 0

Occupation:
(last reported)
Marketing Specialist

Education: Associate in General Technology

Blood Type: A +

Nationality:
(self reported)
Maternal: Creole/Cajun
Italian
Indigenous American
Paternal: Creole/Cajun
Italian
English

Race:

CMV Status: NEG
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Last Medical History Update: 07/16/2015

  • Reported Pregnancy/Birth
  • xyIdentity Disclosure
  • Available Inventory
  • Retired

ADDITIONAL DONOR DETAILS

  • Height:
    5'10" (177.8 cm)
    Weight:
    171 lbs (77 kg)
    Eye Color:
    Brown, Dark
    Hair Color:
    Brown, Dark
    Hair Texture:
    Thick
    Hair Loss:
    None
    Hair Type:
    Curly
    Body Build:
    Medium
    Freckles:
    Few
    Skin Tone:
    Olive
  • ADVISORY

    This donor is a carrier of one or more genetic conditions.

    Below is a list of all conditions for which donor 3088 was tested, including the condition(s) of which he is a carrier. To purchase vials from this donor, the intended parent must sign an acknowledgment form. For more information, please contact us.

    Over the years, Xytex has expanded genetic testing of donors as genetic knowledge and technology have advanced. As a result, not all donors have been tested for the same conditions or with the same methods. For more information about genetic testing view our Genetics FAQs.

    This donor has been evaluated for carrier status of the listed conditions. A negative result reduces, but does not eliminate, the likelihood of the donor being a carrier. If you are a known carrier of a genetic condition please contact us, and we will provide a copy of the donor's test reports to your physician and/or genetic counselor.

    This donor was tested for 110 conditions.

    Phenylalanine Hydroxylase Deficiency also known as Phenylketonuria (PAH)
    Carrier
    3-Methylglutaconic Aciduria Type III also known as Costeff Optic Atrophy (OPA3)
    No disease-causing mutations detected
    Achromatopsia (CNGB3)
    No disease-causing mutations detected
    Alkaptonuria (HGD)
    No disease-causing mutations detected
    Alpha-1 Antitrypsin Deficiency (SERPINA1)
    No disease-causing mutations detected
    Alpha-Mannosidosis (MAN2B1)
    No disease-causing mutations detected
    Alpha-Thalassemia
    Normal complete blood count and hemoglobin analysis; does not exclude silent carrier status or alpha thalassemia minor
    Andermann Syndrome (SLC12A6)
    No disease-causing mutations detected
    Aspartylglucosaminuria (AGA)
    No disease-causing mutations detected
    Ataxia With Vitamin E Deficiency (TTPA)
    No disease-causing mutations detected
    Ataxia-Telangiectasia (ATM)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS1-Related (BBS1)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS10-Related (BBS10)
    No disease-causing mutations detected
    Beta-Thalassemia, Sickle Cell Disease, and Beta-Globin Disorders (HBB)
    No disease-causing mutations detected; normal red blood cell indices and hemoglobin analysis
    Biotinidase Deficiency (BTD)
    No disease-causing mutations detected
    Bloom Syndrome (BLM)
    No disease-causing mutations detected
    Canavan Disease (ASPA)
    No disease-causing mutations detected
    Carnitine Palmitoyltransferase IA Deficiency (CPT1A)
    No disease-causing mutations detected
    Carnitine Palmitoyltransferase II Deficiency (CPT2)
    No disease-causing mutations detected
    Cartilage-Hair Hypoplasia (RMRP)
    No disease-causing mutations detected
    Choroidemia, X-Linked (CHM)
    No disease-causing mutations detected
    Chromosomal Analysis
    Normal male karyotype
    Citrullinemia Type 1 (ASS1)
    No disease-causing mutations detected
    Cohen Syndrome (VPS13B)
    No disease-causing mutations detected
    Combined Pituitary Hormone Deficiency 2 (PROP1)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1a, PMM2-Related (PMM2)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1b (MPI)
    No disease-causing mutations detected
    Congenital Finnish Nephrosis
    See results for Nephrotic Syndrome, NPHS1-Related (NPHS1)
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing mutations detected
    Cystinosis (CTNS)
    No disease-causing mutations detected
    D-Bifunctional Protein Deficiency (HSD17B4)
    No disease-causing mutations detected
    Factor XI Deficiency (F11)
    No disease-causing mutations detected
    Familial Dysautonomia (IKBKAP)
    No disease-causing mutations detected
    Familial Hyperinsulinism and Other ABCC8-Related Disorders (ABCC8)
    No disease-causing mutations detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing mutations detected
    Fanconi Anemia Type C (FANCC)
    No disease-causing mutations detected
    Galactosemia, GALT-Related (GALT)
    No disease-causing mutations detected
    Gaucher Disease (GBA)
    No disease-causing mutations detected
    GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2)
    No disease-causing mutations detected
    Glutaric Acidemia Type 1 (GCDH)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ia (G6PC)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ib (SLC37A4)
    No disease-causing mutations detected
    Glycogen Storage Disease Type III (AGL)
    No disease-causing mutations detected
    Glycogen Storage Disease Type V (PYGM)
    No disease-causing mutations detected
    GRACILE Syndrome (BCS1L)
    No disease-causing mutations detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing mutations detected
    Hereditary Thymine-Uraciluria also known as Dihydropyrimidine Dehydrogenase Deficiency (DPYD)
    No disease-causing mutations detected
    Homocystinuria (CBS)
    No disease-causing mutations detected
    Hurler Syndrome
    See results for Mucopolysaccharidosis Type I (IDUA)
    Hyperoxaluria Type 1
    See results for Primary Hyperoxaluria Type 1 (AGXT)
    Hyperoxaluria Type 2
    See results for Primary Hyperoxaluria Type 2 (GRHPR)
    Hypophosphatasia, Autosomal Recessive (ALPL)
    No disease-causing mutations detected
    Inclusion Body Myopathy 2 (GNE)
    No disease-causing mutations detected
    Isovaleric Acidemia (IVD)
    No disease-causing mutations detected
    Joubert Syndrome 2 (TMEM216)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMA3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMB3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMC2)
    No disease-causing mutations detected
    Juvenile Retinoschisis, X-Linked (RS1)
    No disease-causing mutations detected
    Krabbe Disease (GALC)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2D also known as Alpha-Sarcoglycanopathy (SGCA)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2E also known as Beta-Sarcoglycanopathy (SGCB)
    No disease-causing mutations detected
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 1B (BCKDHB)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing mutations detected
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing mutations detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts Type 1 (MLC1)
    No disease-causing mutations detected
    Metachromatic Leukodystrophy (ARSA)
    No disease-causing mutations detected
    Mucolipidosis Type IV (MCOLN1)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type I also known as Hurler Syndrome (IDUA)
    No disease-causing mutations detected
    Muscle-Eye-Brain Disease (POMGNT1)
    No disease-causing mutations detected
    Nemaline Myopathy 2 (NEB)
    No disease-causing mutations detected
    Nephrotic Syndrome, NPHS1-Related also known as Congenital Finnish Nephrosis (NPHS1)
    No disease-causing mutations detected
    Nephrotic Syndrome, NPHS2-Related also known as Steroid-Resistant Nephrotic Syndrome (NPHS2)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN3-Related (CLN3)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN5-Related (CLN5)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN8-Related also known as Northern Epilepsy (CLN8)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN8-Related also known as Northern Epilepsy (CLN8)
    See results for Neuronal Ceroid-Lipofuscinosis, CLN8-Related (CLN8)
    Neuronal Ceroid-Lipofuscinosis, PPT1-Related (PPT1)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, TPP1-Related (TPP1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type C, NPC1-Related (NPC1)
    No disease-causing mutations detected
    Nijmegen Breakage Syndrome (NBN)
    No disease-causing mutations detected
    Osteochondrodysplasias, Sulfate Transporter-Related (SLC26A2)
    No disease-causing mutations detected
    Pendred Syndrome (SLC26A4)
    No disease-causing mutations detected
    Polycystic Kidney Disease, Autosomal Recessive (PKHD1)
    No disease-causing mutations detected
    Polyglandular Autoimmune Syndrome Type 1 (AIRE)
    No disease-causing mutations detected
    Pompe Disease also known as Glycogen Storage Disease Type II (GAA)
    No disease-causing mutations detected
    Primary Carnitine Deficiency (SLC22A5)
    No disease-causing mutations detected
    Primary Hyperoxaluria Type 1 (AGXT)
    No disease-causing mutations detected
    Primary Hyperoxaluria Type 2 (GRHPR)
    No disease-causing mutations detected
    Pseudocholinesterase Deficiency (BCHE)
    No disease-causing mutations detected
    Pycnodysostosis (CTSK)
    No disease-causing mutations detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing mutations detected
    Salla Disease (SLC17A5)
    No disease-causing mutations detected
    Segawa Syndrome (TH)
    No disease-causing mutations detected
    Short Chain Acyl-CoA Dehydrogenase Deficiency (ACADS)
    No disease-causing mutations detected
    Sjogren-Larsson Syndrome (ALDH3A2)
    No disease-causing mutations detected
    Smith-Lemli-Opitz Syndrome (DHCR7)
    No disease-causing mutations detected
    Spastic Ataxia of Charlevoix-Saguenay, Autosomal Recessive (SACS)
    No disease-causing mutations detected
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Steroid-Resistant Nephrotic Syndrome
    See results for Nephrotic Syndrome, NPHS2-Related (NPHS2)
    Tay-Sachs Disease also known as Hexosaminidase A Deficiency (HEXA)
    No disease-causing mutations detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing mutations detected
    Usher Syndrome Type IF (PCDH15)
    No disease-causing mutations detected
    Usher Syndrome Type IIIA (CLRN1)
    No disease-causing mutations detected
    Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
    No disease-causing mutations detected
    Wilson Disease (ATP7B)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX1-Related (PEX1)
    No disease-causing mutations detected
  • Medication Allergy:
    No
    Food Allergy:
    No
    Pet Allergy:
    No
    Hay Fever Allergy:
    No
    Insect Allergy:
    No
    Vaccine Allergy:
    No
    Healthy Teeth:
    Yes
    Braces:
    No
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    Yes
    Chicken Pox Age:
    13
    Vertigo:
    No
    Eyesight Correction:
    Yes
    Near or Far Sighted:
    Farsighted
    Skin Infection:
    No
    Gallstones:
    No
    Removed Gall Bladder:
    No
    Hernia:
    No
    Mumps:
    No
    Measles:
    No
    Measles Age:
    German Measles:
    No
    German Measles Age:
    Sinus Infection:
    No
    Stomach Ulcers:
    No
  • Skills, Hobbies and Interests:
    Adventurous, Avid Learner, Enjoy Going Out, Love Going to New Places, Technical IT Specialist

  • In School:
    Yes
    In School Major:
    Business in Marketing
    Post Graduate:
    No
    Training Type:
    Computers, Specialized training in Basic & Defense Tactics
    Degrees Earned:
    Associate in General Technology
  • The following medical conditions apply to the donor and his BLOOD RELATIVES ONLY (grandparents, parents, aunts, uncles, cousins, brothers, sisters, nieces, nephews and children of the donor).

    If a donor answers "yes" to any high-risk question on his Medical History Questionnaire, the donor is ineligible.

    Autoimmune Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    CREST Syndrome X
    Lupus X
    Scleroderma X
    Sjorgen's Syndrome X
    Blood Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Anemia X
    Fanconi Anemia X
    Hemophilia X
    Immunodeficiency X
    Leukemia X
    Sickle Cell X
    Thalassemia X
    VonWillebrand's disease X
    Cancer Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Cancer (Breast) X Grandmother X 76
    Cancer (Lung) X
    Cancer (Other) X
    Cancer (Skin) X
    Lymphoma X
    Melanoma X
    Tumor X
    Cardio Vascular Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Congenital Heart Disease X
    Heart Attack X Grandfather X 73
    Heart Disease X
    High Blood Pressure X
    High Cholesterol/Triglycerides X
    Stroke X
    Congenital Malformations Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Deviated Septum X
    Malformations (Cleft Lip) X
    Malformations (Cleft Palate) X
    Malformations (Club Foot) X
    Malformations (Hypospadias) X
    Malformations (Other) X
    Malformations (Polydactyly) X
    Undescended Testicles X
    Gastro-Intestinal Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Gallstones X
    GI (Crohns) X
    GI (Diverticulitis) X
    GI (Other) X
    GI (Pyloric Stenosis) X
    GI (Ulcerative Colitis) X
    GI (Ulcers) X
    Hemochromatosis X
    Hepatitis X
    Kidney Disease Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Adrenal Hyperplasia X
    Born with 1 kidney X
    Kidney (Other) X
    Kidney disease of urinary tract disorder X
    Kidney Disorder X
    Polycystic Kidney Disease X
    Progressive Kidney Disease X
    Mental Health Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Mental (Depression) X
    Mental (Manic Depressive) X
    Mental (Schizophrenia) X
    Mental Retardation X
    Obsessive-compulsive disorder X
    Metabolic/Endrocrine Dis. Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Diabetes (Insulin Dependent) X
    Diabetes (Non-Insulin Dependent) X
    Galactosemia X
    Gaucher's disease X
    Goiter X
    Hypoglycemia X
    Maple Syrup disease X
    PKU or Inherited Metabolic Disorder X
    Tay Sachs X
    Thyroid Disorder X
    Muscular/Bones/Joint Disease Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Acondroplasia (Dwarfism) X
    Arthritis (Other) X
    Congenital Hip Disease X
    Gout X
    Loss of Muscle Coordination X
    Marfan's Disease X
    Muscular Dystrophy X
    Osteoarthritis X
    Osteoporosis X
    Rheumatoid Arthritis X
    Scoliosis X
    Spinal Muscular Atrophy X
    Neurological Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    ADD or ADHD X
    Autism/ Aspergers X
    Canavan's disease X
    Cerebral Palsy X
    Disorders of the spinal cord X
    Dyslexia X
    Familial dysautonomia X
    Lesch-Nyhan Syndrome X
    Migraines X
    Mucolipidosis type IV X
    Neurologic (Alzheimer's) X
    Neurologic (Creutzfeld-Jacob Disease) X
    Neurologic (Epilepsy) X
    Neurologic (Guillain Barre) X
    Neurologic (Huntington's) X
    Neurologic (JC Virus) X
    Neurologic (Lou Gehrig's Disease) X
    Neurologic (Multiple Sclerosis) X
    Neurologic (Neural Tube Defect) X
    Neurologic (Neurofibrimatosis) X
    Neurologic (Parkinson's Disease) X
    Neurologic (Subacute Sclerosing Panencephalitis) X
    Nieman-Pick X
    Spongioform encephalopathy/prion disease X
    Tourette Syndrome X
    Other Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Alcoholism X
    Bloom syndrome X
    Cystic Fibrosis X
    Down Syndrome X
    Drug Abuse X
    Fragile X X
    Klinefelter X
    Noonan or Turner Syndrome X
    Other - Early Death X
    Other - Inherited Genetic Condition X
    Other Disease/Condition X
    Premature Organ Degeneration X
    Radiation Exposure X
    SIDS X
    Toxic Chemical Exposure X
    Turner's Syndrome X
    West Nile (suspected or confirmed by lab testing) X
    Respiratory Disease Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Allergies (Drug) X
    Allergies (Food) X
    Allergies (Hay Fever) X
    Allergies (Insect) X
    Allergies (Other) X
    Allergies (Pet) X
    Asthma X
    Emphysema X
    SARS X
    Tuberculosis X
    Sight/Sound/Smell Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Cataracts X
    Deafness X
    Deafness (before age 50) X
    Ear deformity X
    Eyesight (Blindness) X
    Eyesight (Color Blindness) X
    Eyesight (Glaucoma) X
    Eyesight (Other) X
    Eyesight (Retinoblastoma) X
    Macular degeneration X
    Skin Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Albinism X
    Eczema X
    Pigmentation disorders (including Vitiligo) X
    Psoriasis X
    Skin Disease X
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Father
    Hair Color: Brown, Dark Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 1965 Cause of Death: Hair Loss:
    Height: 6'00" (182.88 cm) Age at Death: Body Hair: Curly
    Weight: 215 lbs. (97 kg) Occupation: Retired Military/Nuclear Security Eye Color: Brown, Dark
    Half Siblings: No Education: College (Some) Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Features include strong jawline and broad shoulders. He sells cars, fishes, goes on camping trips, and travels. Enjoys doing projects. Lived everywhere from Germany to Washington and has lifetime experiences that are hard to match.
    FAMILY MEMBER: Mother
    Hair Color: Brown, Dark Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1959 Cause of Death: Hair Loss:
    Height: 5'04" (162.56 cm) Age at Death: Body Hair: Wavy
    Weight: 155 lbs. (70 kg) Occupation: Casino Worker Eye Color: Brown, Dark
    Half Siblings: No Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She has distinguishing eyebrows and slightly red tinted hair. She’s Native American and was raised in Seattle while working in a casino environment. She’s very big on family, has ability to cook, and makes numerous artistic projects.
    FAMILY MEMBER: Sister
    Hair Color: Brown, Light Eyesight:
    Freckles: Numerous Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1983 Cause of Death: Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: Body Hair: Wavy
    Weight: 135 lbs. (61 kg) Occupation: Accountant Eye Color: Brown, Light
    Half Siblings: Yes Education: College Body Build: Small
    Half Siblings Parent: Mother Eyesight Correction: Near or Far Sighted:
    Comments: She has various freckles, and a distinguishing smile and eyes. She’s a great full time mom who mainly focuses on her son along with eating all-natural. She’s also a financial planner who goes to shows.
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Brown, Light Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Deceased Skin Tone: Olive Dominant Hand:
    Year of Birth: 1935 Cause of Death: Heart Attack Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: 73 Body Hair: Wavy
    Weight: 175 lbs. (79 kg) Occupation: USPS Worker Eye Color: Brown, Light
    Half Siblings: Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He had a Roman nose. Enjoyed football, sports, family, and going out. He is 100 % full Italian born and raised.
    Health Condition: Heart Attack at age 73
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Light Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Deceased Skin Tone: Fair Dominant Hand:
    Year of Birth: 1937 Cause of Death: Cancer Came Back Hair Loss:
    Height: 5'04" (162.56 cm) Age at Death: 76 Body Hair: Straight
    Weight: 145 lbs. (65 kg) Occupation: Homemaker/Caretaker Eye Color: Blue/Green
    Half Siblings: Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She had dimples. Enjoyed playing board games, cooking, crossword puzzles, and caring for people. She was a warm hearted woman until the end of her days and kept being very positive.
    Health Condition: Cancer (Breast) at age 76
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1962 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1955 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1960 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1962 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1957 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Grandfather
    Hair Color: Brown, Dark Eyesight:
    Freckles: Numerous Hair Texture:
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 1935 Cause of Death: Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Wavy
    Weight: 185 lbs. (83 kg) Occupation: Retired Military Eye Color: Brown, Light
    Half Siblings: Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He has a mustache. Enjoys taking care of others, reading, poetry, and traveling. He raised my sister and I’m named after him in his honor.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Light Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1940 Cause of Death: Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: Body Hair: Straight
    Weight: 155 lbs. (70 kg) Occupation: Crafts Eye Color: Brown, Light
    Half Siblings: Education: College (Some) Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She has freckles. Enjoys arts/crafts, cooking, getting family together, joking and loved Native American traditions. She was almost full Native American descent that can register.

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