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 offers our high-quality cord blood collection, processing, and lifetime storage (up to 78 years) at no cost to expecting parents. This program is available to families who have a child with an established diagnosis that is currently treatable with a sibling cord blood transplant and who meets the program’s eligibility and enrollment requirements.

  • 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

        Blood Disorders

        E-β+ thalassemia
        E-βo thalassemia
        Sickle βo Thalassemia
        Sickle-cell anemia (hemoglobin SS)
        β-thalassemia intermedia
        β-thalassemia major (Cooley's anemia)
        Other Transfusion Dependent Sickle cell or Thalassemia

        Download 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 to 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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