To view current Seattle Sperm Bank Donor Availabilities please visit the following link of SSB Donors on CanAm Cryoservices website
Meet Reilly (8780) – Open ID Donor
Back to Donor Search- Eyes: Blue
- Hair: Brown
- Height: 6'00"
- Weight (lbs): 172
- Blood: A Rh-
- CMV: -
- Ethnicity: Caucasian, French, German, Irish
- Jewish Ancestry: No
- Education/Occupation: BS biochemistry/ Medical School / Doctor
- Live Birth / Pregnancy Confirmed: Yes
Test Results
- Extended Testing: No
- Carrier For:
- No disease causing mutations detected
- Results for Karyotyping / Spinal Muscular Atrophy:
- Spinal Muscular Atrophy: Copy number 2
- Results with No Disease Causing Mutations: View full list
- Karyotyping
- Cystic Fibrosis
- Adenosine Deaminase Deficiency
- ABCC8-related Hyperinsulinism
- Alpha-1 Antitrypsin Deficiency
- Andermann Syndrome
- Argininosuccinic Aciduria
- ARSACS
- Aspartylglycosaminuria
- Ataxia-telangiectasia
- Autosomal Recessive Polycystic Kidney Disease
- Bardet-Biedl Syndrome, BBS1-related
- Bardet-Biedl Syndrome, BBS10-related
- Beta-Thalassemia
- Bloom Syndrome
- Canavan Disease
- Cartilage-hair Hypoplasia
- Citrullinemia Type 1
- CLN3-related Neuronal Ceroid Lipofuscinosis
- CLN5-related Neuronal Ceroid Lipofuscinosis
- CLN8-related Neuronal Ceroid Lipofuscinosis
- Cobalamin C Disease
- Congenital Disorder Of Glycosylation Type Ia
- Congenital Finnish Nephrosis
- Cystinosis
- D-bifunctional Protein Deficiency
- Dihydrolipoamide Dehydrogenase Deficiency
- Dihydropyrimidine Dehydrogenase Deficiency
- Ethylmalonic Encephalopathy
- Familial Dysautonomia
- Familial Mediterranean Fever
- Fanconi Anemia Type C
- Galactosemia
- Gaucher Disease
- Glutaric Acidemia Type 1
- Glutathione Synthetase Deficiency
- Glycine Encephalopathy
- Glycogen Storage Disease Type Ia
- Glycogen Storage Disease Type Ib
- Glycogen Storage Disease Type II
- Glycogen Storage Disease Type III
- GRACILE Syndrome
- Hb Beta Chain-related Hemoglobinopathy (including Beta Thalassemia And Sickle Cell Disease)
- Hereditary Fructose Intolerance
- HMG-CoA Lyase Deficiency
- Holocarboxylase Synthetase Deficiency
- Homocystinuria Caused By Cystathionine Beta-synthase Deficiency
- Hurler Syndrome
- Hyperoxaluria Type 1
- Hyperoxaluria Type 2
- Joubert Syndrome 2
- Junctional Epidermolysis Bullosa, LAMA3-related
- Junctional Epidermolysis Bullosa, LAMB3-related
- Junctional Epidermolysis Bullosa, LAMC2-related
- Krabbe Disease
- Long Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
- Leigh Syndrome
- Maple Syrup Urine Disease Type 1A
- Maple Syrup Urine Disease Type 1B
- Maple Syrup Urine Disease Type 3
- Medium Chain Acyl-CoA Dehydrogenase Deficiency
- Metachromatic Leukodystrophy
- Methylmalonic Acidemia MMAA-related
- Methylmalonic Acidemia MMAB-related
- Methylmalonic Acidemia MUT-related
- Methylmalonic Aciduria And Homocystinuria Type CbIC
- Mucolipidosis IV
- Mucopolysaccharidosis Type I
- NEB-related Nemaline Myopathy
- Niemann-Pick Disease Type A
- Niemann-Pick Disease Type B
- Niemann-Pick Disease Type C
- Nijmegen Breakage Syndrome
- Non-Ketonic Hyperglycinemia, GLDC-Related
- PEX1-related Zellweger Syndrome Spectrum
- Phenylalanine Hydroxylase Deficiency
- PPT1-related Neuronal Ceroid Lipofuscinosis
- Primary Hyperoxaluria Type 1
- Primary Hyperoxaluria Type 2
- Propionic Acidemia, PCCA-Related
- Propionic Acidemia, PCCB-Related
- Rhizomelic Chondrodysplasia Punctata Type 1
- Salla Disease
- Sandhoff Disease
- Sickle Cell Disease
- Sjogren-Larsson Syndrome
- Smith-Lemli-Opitz Syndrome
- Sulfate Transporter-related Osteochondrodysplasia (SLC26A2)
- Tay-Sachs Disease (Counsyl)
- TPP1-related Neuronal Ceroid Lipofuscinosis
- Tyrosinemia Type I
- Usher Syndrome Type 1F
- Usher Syndrome Type 3
- Walker-Warburg Syndrome
- Wilson Disease
- Nephrotic Syndrome (NPHS1-Related)
- Nephrotic Syndrome (NPHS2-Related)
Donor Description
Reilly is quite attractive with brown hair and dark blue eyes. He has a medium complexion and his skin tans easily. Reilly is a competitive swimmer and avid cyclist so he is in great physical condition to perform in these athletic sports. He has a beautiful smile that he flashes quite often and it certainly grabs our attention! Reilly is typically dressed comfortably in stylish tees or button up shirts and slacks or jeans.
Reilly is laid back, polite, and kind. He has an upbeat personality that is sure to make you smile when you interact with him. He is intelligent, bright, and witty. He is currently in medical school and balances his study time with outdoor activities and hanging out with friends. Reilly is a very independent person with a desire to help others. When we asked Reilly why he wanted to be a donor he said, “I have been a blood donor for many years because I value the opportunity to give something to somebody else in a way that does not hurt me, or take anything away from my life, other than a little time. When I heard about the opportunity to become a donor in a way that could help a couple or individual fulfill their dream of having a child, it seemed like the logical next step beyond being a blood donor…”