Cancers, HIV, Cerebral Palsy, Heart Disease, Liver Disease, and More
Cord blood is an FDA-approved treatment for 80+ diseases including numerous types of malignancies, anemias, inherited metabolic disorders and deficiencies of the immune system.
Blood Disorders & Anemia
- Aplastic Anemia
- Congenital Dyserythropoietic Anemia
- Fanconi Anemia
- Sickle Cell Disease
- Beta Thalassemia Major (Cooley’s Anemia)
- Blackfan-Diamond Anemia
- Pure Red Cell Aplasia
- Myeloproliferative Disorders
- Acute Myelofibrosis
- Agnogenic Myeloid Metaplasia (Myelofibrosis)
- Polycythemia Vera
- Essential Thrombocythemia
Lymphomas & Leukemias
- Hodgkin’s Lymphoma
- Neuroblastoma
- Medulloblastoma
- Retinoblastoma
- Acute Lymphoblastic Leukemia
- Acute Myelogenous Leukemia (AML)
- Chronic Lymphocytic Leukemia (CLL)
- Juvenile Chronic Myelogenous Leukemia (JCML)
- Juvenile Myelomonocytic Leukemia (JMML)
- Refractory Anemia (RA)
- Refractory Anemia with Ringed Sideroblasts (RARS)
- Refractory Anemia with Excess Blasts (RAEB)
- Refractory Anemia with Excess Blasts in Transformation (RAEB-T)
- Chronic Myelomonocytic Leukemia (CMML)
Immune Disorders
- Epstein–Barr Virus Susceptibility
- SCID with Adenosine Deaminase Deficiency (ADA-SCID)
- SCID which is X-linked
- SCID with absence of T & B Cells
- SCID with absence of T Cells, Normal B Cells Omenn Syndrome
- Kostmann Syndrome
- Ataxia–Telangiectasia
- Bare Lymphocyte Syndrome
- Common Variable Immunodeficiency
- DiGeorge Syndrome
- Leukocyte Adhesion Deficiency
- Lymphoproliferative Disorders (LPD)
- Wiskott–Aldrich Syndrome
Neurological & Other Disorders
- Cartilage–Hair Hypoplasia
- Günther Disease (Congenital Erythropoietic Porphyria)
- Hermansky–Pudlak Syndrome
- Pearson’s Syndrome
- Shwachman–Diamond Syndrome
- Systemic Mastocytosis
- Adrenoleukodystrophy (ALD) / Adrenomyeloneuropathy (AMN)
- Krabbe Disease (Globoid Cell Leukodystrophy)
- Metachromatic Leukodystrophy
- Pelizaeus–Merzbacher Disease
- Gaucher Disease
- Niemann–Pick Disease
- Sandhoff Disease
- Wolman Disease
- Lesch–Nyhan Syndrome
Metabolic & Genetic Disorders
- Chediak–Higashi Syndrome
- Neutrophil Actin Deficiency
- Reticular Dysgenesis
- Mucopolysaccharidoses (MPS)
- Hurler’s Syndrome (MPS–IH)
- Scheie Syndrome (MPS–IS)
- Hunter’s Syndrome (MPS–II)
- Sanfilippo Syndrome (MPS–III)
- Morquio Syndrome (MPS–IV)
- Maroteaux–Lamy Syndrome (MPS–VI)
- Sly Syndrome, Beta–Glucuronidase Deficiency (MPS–VII)
- Mucolipidosis II (I–cell Disease)
What happens if I don't bank cord blood?
You would have to find a donor's cord blood, tissue, or placenta stem cells.
You may experience difficulties finding a donor match, especially if you're a person of color.
Using a donor’s stem cells (vs. your own) enhances the probability of potentially fatal rejection.
It can be difficult to find a public donor match
Saving your own stem cells gives you access whenever you may need them.
Stem cells can be useful for your whole family
Some diseases can be treated using the baby's own cord blood (allogenic use) since they are 100% match! Biological family members can benefit as well.
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