For Healthcare Providers

Cord blood banking is a safe and completely non-invasive way for your patients to gain access to the disease-fighting potential offered by stem cells. Already proven to treat a variety of chronic and acute diseases, cord blood banking currently represents among the best ways to harvest the hematopoietic stem cells that can multiply and separate into red blood cells, white blood cells and platelets.

“….stem cells in cord blood should be normal and free of malignancy, giving them a potential advantage over autologous cells collected during hematologic remission from a patient with malignancy.” Wiley JM, Kuller JA, Obstetrics and Gynecology, Vol 89, No2

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Why Your Patients Should Save Cord Blood

We at BabyCord are aware of the tremendous potential offered by cord blood banking, especially for families with a history of cancer and genetic diseases. As advances in stem cell research continue, science and medicine have seen ever-growing uses for stem cells and stem cell therapy. As the research moves forward, potential of infinite proportions for the health benefits of stem cells and cord blood banking will become increasingly evident.

Unlike traditional bone marrow collection, which usually requires general anesthesia and recovery, the process of collecting cord blood is non-invasive, painless and generally takes just three to five minutes to complete. BabyCord will supply you with a cord blood collection kit prior to your baby’s delivery date. You simply bring the kit to the hospital for the physician, nurse or midwife to collect the cord blood after you deliver.

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if you think it's just you're looking for. Please contact us!

Diseases Treated with Cord Blood Stem Cells

The efficacy of treating disease with cord blood stem cells is real. Beyond their potential to grow and rejuvenate specific cells or tissues, which can ultimately be used to treat a host of diseases, cord blood stem cells are currently being used to treat more than 80 acute and chronic diseases today.

Aplastic Anemia (Severe)

  • Fanconi Anemia
  • Paroxysmal Nocturnal Hemoglobinuria (PNH)
  • Acute Leukemias

Acute Lymphoblastic Leukemia (ALL)

  • Acute Myelogenous Leukemia (AML)
  • Acute Biphenotypic Leukemia
  • Acute Undifferentiated Leukemia

Lymphoproliferative Disorders

  • Non-Hodgkin’s Lymphoma
  • Hodgkin’s Disease
  • Prolymphocytic Leukemia

Inherited Erythrocyte Abnormalities

  • Beta Thalassemia Major
  • Pure Red Cell Aplasia
  • Sickle Cell Disease

Inherited Erythrocyte Abnormalities

  • Familial Erythrophagocytic Lymphohistiocytosis
  • Histiocytosis-X
  • Hemophagocytosis

Plasma Cell Disorders

  • Multiple Myeloma
  • Plasma Cell Leukemia
  • Waldenstrom’s Macroglobulinemia

Chronic Leukemias

  • Chronic Myelogenous Leukemia (CML)
  • Chronic Lymphocytic Leukemia (CLL)
  • Juvenile Chronic Myelogenous Leukemia (JCML)
  • Juvenile Myelomonocytic Leukemia (JMML)

Myeloproliferative Disorders

  • Acute Myelofibrosis
  • Agnogenic Myeloid Metaplasia (myelofibrosis)
  • Polycythemia Vera
  • Essential Thrombocythemia

Other Inherited Disorders

  • Lesch-Nyhan Syndrome
  • Cartilage-Hair Hypoplasia
  • Glanzmann Thrombasthenia
  • Osteopetrosis

Other Malignancies

  • Breast Cancer
  • Ewing Sarcoma
  • Neuroblastoma
  • Renal Cell Carcinoma

Inherited Platelet Abnormalities

Amegakaryocytosis / Congenital Thrombocytopenia

Congenital Immune System Disorders

  • Ataxia-Telangiectasia
  • Kostmann Syndrome
  • Leukocyte Adhesion Deficiency
  • DiGeorge Syndrome
  • Bare Lymphocyte Syndrome
  • Omenn’s Syndrome
  • Severe Combined Immunodeficiency (SCID)
  • SCID with Adenosine Deaminase Deficiency
  • Absence of T & B Cells SCID
  • Absence of T Cells, Normal B Cell SCID
  • Common Variable Immunodeficiency
  • Wiskott-Aldrich Syndrome
  • X-Linked Lymphoproliferative Disorder

Liposomal Storage Diseases

  • Mucopolysaccharidoses (MPS)
  • Hurler 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)
  • Adrenoleukodystrophy
  • Mucolipidosis II (I-cell Disease)
  • Krabbe Disease
  • Gaucher’s Disease
  • Niemann-Pick Disease

Liposomal Storage Diseases

  • Refractory Anemia (RA) Refractory Anemia with Ringed Sideroblasts (RARS)
  • Anemia with Ringed Sideroblasts (RARS)

Myelodysplastic Syndromes

  • 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)