For Newborns

Sibling Connection

ViaCord's Newborn Stem Cell Donor Program
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COLLECTION TYPE:

Cord Blood Banking

Talk to a dedicated specialist

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What is The Sibling Connection Program?

ViaCord’s Sibling Connection Program provides our high-quality cord blood collection, processing, and lifetime cord blood storage (78 years) at no cost to expecting parents who have a child with an established diagnosis that is currently treatable with a sibling cord blood transplant and meet the criteria and enrollment requirements of the program.

  • Sibling Cord Blood Transplants
  • Nearly 80 eligible diagnoses
  • Free cord blood collection, processing, and lifetime storage 
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HERE FOR YOU

Nearly 10,000 families have joined our Sibling Connection Program

Download Our Brochure

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Who's Eligible?

See if The Sibling Connection Program is right for your family

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Full Sibling

The baby whose cord blood will be stored must be a full sibling (same biological parents) of the child in need. 

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Currently Treatable

The child in need must have a condition that is currently treatable with sibling cord blood in transplant. See Eligible Diagnoses below.

Eligible Diagnoses

    Cancers

    Acute lymphoblastic leukemia (ALL)
    Acute myeloid leukemia (AML)
    Biphenotypic Leukemia
    Burkitt's lymphoma 
    Chronic myeloid leukemia (CML)
    Chronic myelomonocytic leukemia (CMML)
    Hodgkin's lymphoma
    Juvenile myelomonocytic leukemia (JMML)
    Lymphomatoid granulomatosis
    Mixed Lineage Leukemia
    Myelodysplastic syndrome (MDS)
    Myelofibrosis
    Non-Burkitt’s lymphoma
    Non-Hodgkin's lymphoma

     

    Download Medical Referral Form 

      Bone Marrow Failure Syndromes

      Amegakaryocytic thrombocytopenia
      Autoimmune neutropenia (severe)
      Congenital dyserythropoietic anemia
      Congenital sideroblastic anemia
      Cyclic Neutropenia
      Diamond-Blackfan anemia
      Dyskeratosis congenita
      Evan's syndrome
      Fanconi anemia
      Glanzmann's disease
      Kostmann's syndrome (severe congenital neutropenia)
      Pure Red Cell Aplasia
      Severe aplastic anemia
      Shwachman syndrome
      Thrombocytopenia with absent radius (TAR syndrome)


      Download the Medical Referral Form

        Metabolic Disorders

        Adrenoleukodystrophy
        Alpha mannosidosis
        Fucosidosis
        Gaucher's disease (infantile)
        Gunther disease (congenital erythropoitic porphyria)
        Hermansky-Pudlak syndrome
        Hunter syndrome 
        Hurler syndrome
        Hurler-Scheie syndrome
        Krabbe disease (globoid cell leukodystrophy)
        Lesch-Nyhan disease
        Maroteaux-Lamy syndrome
        Metachromatic leukodystrophy
        Mucolipidosis Type II, III
        Niemann Pick Syndrome, type A and B
        Sandhoff Syndrome
        Sanfilippo syndrome
        Sly syndrome
        Tay-Sachs Disease
        Wolman Syndrome


        Download Medical Referral Form

          Immunodeficiencies

          Adenosine deaminase deficiency
          Ataxia telangiectasia
          Chronic granulomatous disease
          Complete IFN-γ Receptor 2 Deficiency
          DiGeorge syndrome
          IKK gamma deficiency
          Immune dysregulation polyendocrineopathy
          Leukocyte adhesion deficiency
          LRBA deficiency
          Myelokathexis X-linked immunodeficiency
          Omenn's syndrome
          Reticular dysplasia
          Severe combined immunodeficiency (SCID)
          Thymic dysplasia
          Wiskott-Aldrich syndrome
          X-linked agammaglobulinemia
          X-linked lymphoproliferative disease
          X-linked Mucolipidosis, Type II


          Download the Medical Referral Form

            Other

            Epidermolysis bullosa
            Hemophagocytic lymphohistiocytosis 
            Juvenile Dermatomyositis 
            Langerhans cell histiocytosis 
            Osteopetrosis

             

            Download Medical Referral Form

              HOW IT WORKS

              Interested in Sibling Connection?

              Here are next steps and what to expect . . . 

              • Talk your child's physician about The Sibling Connection Program
              • If it's determined as an option, call our Sibling Connection Specialists 866-861-8435
              • You and your doctor will complete our required enrollment forms (see below)
              • Once approved, we'll send a ViaCord Collection Kit to your house and a letter to your delivering doctor
              • Bring your kit to the hospital on the day of delivery and give it to the medical staff
              • Remind your doctor that the cord blood being collected may be used by a sibling. Thoroughly cleaning the cord and collecting as much cord blood as possible are important. 
              Sibling Connection

              REQUIRED

              Enrollment Forms

              Parent and Doctor forms must be completed and returned to ViaCord prior to enrollment. Send completed forms to siblingconnection@viacord.com or fax 1-781-240-8427. 

                SIBLING CONNECTION

                Required Enrollment Forms For Parents

                Parent(s) must complete all three forms for enrollment. The Health History Questionnaire is required should you need to use your newborn's stem cells.

                SIBLING CONNECTION

                Required Medical Referral Forms

                Medical Referral Forms must be completed by the doctor caring for the sibling with the qualifying condition (the newborn must be a full sibling).  Find the appropriate form below or from the Eligible Diagnoses list.

                Questions?

                Talk to a Sibling Connection Program Specialist 
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