Meet BFA0215 (BFA0215)
New Donor
BFA0215 stands at 1.78m tall, with dark brown hair, brown eyes and a small bone structure. He has
a friendly, open nature that makes him a real joy to be around. He is always happy to engage with
us, share stories from his day-to-day life and talks openly about his hopes and ambitions for the
future.
We affectionately call him our “Action Man”, as he is rarely sitting still and is always getting involved
in something active. He is extremely athletic, with rock climbing being his favourite sport—
something he enjoys regularly. However, his interests extend far beyond sport. He loves learning
new languages and has a genuine interest in Geography and History, reflecting his curious and
adventurous nature.
One of the qualities we particularly admire in him is his relaxed approach to life. He takes things in
his stride and is not easily fazed. At the same time, he is strong-willed, determined and possesses
an impressive inner strength. He is also very much in touch with his emotions and has a wonderful
balance of physical and mental resilience with genuine warmth, compassion and sensitivity.
He speaks fondly of the love and compassion he has learned from his mum and her family, as well
as the positive examples they have given him throughout his life. These influences are clearly
reflected in the person he has become and in the way he treats others.
His ambitions are equally inspiring. He hopes to travel more, live a wholesome and meaningful life,
and help people wherever he can. He is passionate about life and curious about the world, while
remaining calm, grounded and compassionate.
He is a beautiful mix of happiness, calmness, compassion and strength. His open and relaxed
personality makes him wonderful company, and we always look forward to his visits. He is genuinely
a pleasure to spend time with, and we love hearing about his latest adventures, interests and plans
for the future.
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Meet BFA0215 (BFA0215)
New Donor
BFA0215 stands at 1.78m tall, with dark brown hair, brown eyes and a small bone structure. He has
a friendly, open nature that makes him a real joy to be around. He is always happy to engage with
us, share stories from his day-to-day life and talks openly about his hopes and ambitions for the
future.
We affectionately call him our “Action Man”, as he is rarely sitting still and is always getting involved
in something active. He is extremely athletic, with rock climbing being his favourite sport—
something he enjoys regularly. However, his interests extend far beyond sport. He loves learning
new languages and has a genuine interest in Geography and History, reflecting his curious and
adventurous nature.
One of the qualities we particularly admire in him is his relaxed approach to life. He takes things in
his stride and is not easily fazed. At the same time, he is strong-willed, determined and possesses
an impressive inner strength. He is also very much in touch with his emotions and has a wonderful
balance of physical and mental resilience with genuine warmth, compassion and sensitivity.
He speaks fondly of the love and compassion he has learned from his mum and her family, as well
as the positive examples they have given him throughout his life. These influences are clearly
reflected in the person he has become and in the way he treats others.
His ambitions are equally inspiring. He hopes to travel more, live a wholesome and meaningful life,
and help people wherever he can. He is passionate about life and curious about the world, while
remaining calm, grounded and compassionate.
He is a beautiful mix of happiness, calmness, compassion and strength. His open and relaxed
personality makes him wonderful company, and we always look forward to his visits. He is genuinely
a pleasure to spend time with, and we love hearing about his latest adventures, interests and plans
for the future.
Brown
Dark Brown
178
78
O Rh-
+
Caucasian, Italian, Portuguese
No
BA Anthropology and History / Children's Playcare Worker (Part time)
No
Fulgent Comprehensive Carrier Screen (176 conditions)
-
- Spinal Muscular Atrophy : No disease causing mutations detected
-
- Cystic Fibrosis
- Adenosine Deaminase Deficiency
- ABCC8-related Hyperinsulinism
- Andermann Syndrome
- Argininosuccinic Aciduria
- ARSACS
- Aspartylglycosaminuria
- Ataxia With Vitamin E Deficiency
- Ataxia-telangiectasia
- Autosomal Recessive Polycystic Kidney Disease
- Bardet-Biedl Syndrome, BBS1-related
- Bardet-Biedl Syndrome, BBS10-related
- Biotinidase Deficiency
- Bloom Syndrome
- Canavan Disease
- Carnitine Palmitoyltransferase IA Deficiency
- Carnitine Palmitoyltransferase II Deficiency
- Cartilage-hair Hypoplasia
- Citrullinemia Type 1
- CLN3-related Neuronal Ceroid Lipofuscinosis
- CLN8-related Neuronal Ceroid Lipofuscinosis
- Cohen Syndrome
- 21-hydroxylase Deficient Congenital Adrenal Hyperplasia
- Congenital Disorder Of Glycosylation Type Ia
- Congenital Disorder Of Glycosylation Type Ib
- Costeff Optic Atrophy Syndrome
- Cystinosis
- D-bifunctional Protein Deficiency
- Dihydrolipoamide Dehydrogenase Deficiency
- Familial Mediterranean Fever
- Fanconi Anemia Type C
- Fragile X Syndrome
- Galactosemia
- Gaucher Disease
- GJB2-related DFNB1 Nonsyndromic Hearing Loss And Deafness
- Glutaric Acidemia Type 1
- 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
- Hexosaminidase A Deficiency (including Tay-Sachs Disease)
- Homocystinuria Caused By Cystathionine Beta-synthase Deficiency
- Hypophosphatasia, Autosomal Recessive
- Inclusion Body Myopathy 2
- Isovaleric Acidemia
- Joubert Syndrome 2
- Junctional Epidermolysis Bullosa, LAMA3-related
- Junctional Epidermolysis Bullosa, LAMB3-related
- Junctional Epidermolysis Bullosa, LAMC2-related
- Krabbe Disease
- Limb-girdle Muscular Dystrophy Type 2D
- Limb-girdle Muscular Dystrophy Type 2E
- Long Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
- Maple Syrup Urine Disease Type 1A
- Maple Syrup Urine Disease Type 1B
- Medium Chain Acyl-CoA Dehydrogenase Deficiency
- Megalencephalic Leukoencephalopathy With Subcortical Cysts
- Metachromatic Leukodystrophy
- Methylmalonic Acidemia MMAA-related
- Methylmalonic Acidemia MMAB-related
- Methylmalonic Acidemia MUT-related
- Mucolipidosis IV
- Mucopolysaccharidosis Type I
- Muscle-eye-brain Disease
- NEB-related Nemaline Myopathy
- Niemann-Pick Disease, SMPD1-associated
- Nijmegen Breakage Syndrome
- Pendred Syndrome
- PEX1-related Zellweger Syndrome Spectrum
- Phenylalanine Hydroxylase Deficiency
- Polyglandular Autoimmune Syndrome Type 1
- PPT1-related Neuronal Ceroid Lipofuscinosis
- Primary Carnitine Deficiency
- Primary Hyperoxaluria Type 1
- Primary Hyperoxaluria Type 2
- Propionic Acidemia, PCCA-Related
- Propionic Acidemia, PCCB-Related
- PROP1-related Combined Pituitary Hormone Deficiency
- Pycnodysostosis
- Rhizomelic Chondrodysplasia Punctata Type 1
- Salla Disease
- Sandhoff Disease
- Segawa Syndrome
- Short Chain Acyl-CoA Dehydrogenase Deficiency
- Sjogren-Larsson Syndrome
- Smith-Lemli-Opitz Syndrome
- Sulfate Transporter-related Osteochondrodysplasia
- Tyrosinemia Type I
- Usher Syndrome Type 1F
- Usher Syndrome Type 3
- Very Long Chain Acyl-CoA Dehydrogenase Deficiency
- Walker-Warburg Syndrome
- Wilson Disease
- Maple Syrup Urine Disease Type II
- 6-pyruvoyl-tetrahydropterin Synthase Deficiency
- 11-beta-hydroxylase-deficient Congenital Adrenal Hyperplasia
- Alstrom Syndrome
- AMT-related Glycine Encephalopathy
- Argininemia
- ATP7A-related Disorders
- Autosomal Recessive Osteopetrosis Type 1
- Bardet-Biedl Syndrome, BBS12-related
- Bardet-Biedl Syndrome, BBS2-related
- Calpainopathy
- Carbamoylphosphate Synthetase I Deficiency
- Cerebrotendinous Xanthomatosis
- CLN6-related Neuronal Ceroid Lipofuscinosis
- COL4A3-related Alport Syndrome
- COL4A4-related Alport Syndrome
- Congenital Disorder Of Glycosylation Type Ic
- Delta-sarcoglycanopathy
- Dysferlinopathy
- Dystrophinopathy (including Duchenne/Becker Muscular Dystrophy)
- ERCC6-related Disorders
- ERCC8-related Disorders
- EVC-related Ellis-van Creveld Syndrome
- EVC2-related Ellis-van Creveld Syndrome
- Fabry Disease
- Fanconi Anemia Complementation Group A
- FKRP-related Disorders
- Galactokinase Deficiency
- Gamma-sarcoglycanopathy
- GLB1-related Disorders
- GLDC-related Glycine Encephalopathy
- Hydrolethalus Syndrome
- KCNJ11-related Familial Hyperinsulinism
- LAMA2-related Muscular Dystrophy
- Leigh Syndrome, French-Canadian Type
- Lipoid Congenital Adrenal Hyperplasia
- Lysosomal Acid Lipase Deficiency
- MKS1-related Disorders
- Mucolipidosis III Gamma
- Mucopolysaccharidosis Type II
- Mucopolysaccharidosis Type IIIA
- Mucopolysaccharidosis Type IIIB
- Mucopolysaccharidosis Type IIIC
- Niemann-Pick Disease Type C2
- Ornithine Transcarbamylase Deficiency
- Peroxisome Biogenesis Disorder Type 3
- Peroxisome Biogenesis Disorder Type 4
- Peroxisome Biogenesis Disorder Type 5
- Peroxisome Biogenesis Disorder Type 6
- Primary Hyperoxaluria Type 3
- Pyruvate Carboxylase Deficiency
- RTEL1-related Disorders
- Spastic Paraplegia Type 15
- Spondylothoracic Dysostosis
- TGM1-related Autosomal Recessive Congenital Ichthyosis
- Tyrosinemia Type II
- USH1C-related Disorders
- USH2A-related Disorders
- X-linked Adrenoleukodystrophy
- X-linked Congenital Adrenal Hypoplasia
- X-linked Juvenile Retinoschisis
- X-linked Severe Combined Immunodeficiency
- Xeroderma Pigmentosum Group A
- Xeroderma Pigmentosum Group C
- Niemann-Pick Disease, Type C (NPC1-Related)
- Nephrotic Syndrome (NPHS1-Related) / Congenital Finnish Nephrosis
- Nephrotic Syndrome (NPHS2-Related) / Steroid-Resistant Nephrotic Syndr
- Familial Dysautonomia (ELP1)
- GJB6-CRYL1 Related Nonsyndromic Hearing Loss UK
- GJB6-CRYL1 Related Nonsyndromic Hearing Loss
- Alpha-Mannosidosis
- Methylmalonic Aciduria And Homocystinuria, CblC
- Usher Syndrome, Type 1B
- Neuronal Ceroid Lipofuscinosis, TPP1-related