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Additional Patient Information |
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An organization that is researching the development and function of the cerebral cortex and genes involved, as well as, educating on genetics and DNA.
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The Fetal Hope Foundation's mission is to provide support, provide information, fund research, increase awareness and be an outlet for leading medical information pertaining to fetal distresses and syndromes.
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Local to Boston, this organization is run by volunteers, to help meet the needs of parents of children who were born with cleft lip and/or palate by offering resource material on specific areas of concern.
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The FFC is a non-profit, volunteer-led organization supporting and offering educational resources to families and children with craniofacial conditions.
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Established in 1983, this non-profit, all-volunteer organization's mission is to offer information, advocacy and networking to people and families with Down syndrome.
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Established in 1990 by a family dealing with a newborn diagnosed with Esophageal Artesia, Tef Vater is dedicated to offering support and insight on this fetal anomaly.
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This non-profit organization is run by families and friends of affected children to support families of children with Gastroschisis.
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The TTTS foundation provides immediate information about Twin to Twin Transfusion Syndrome including education, insight and support.
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Founded in 1983, this international organization is "network of caring and sharing for mutiple birth families." This site offers comprehensive information and reading material to provide insight for families expecting triplets or more.
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A nationwide, non-proft organization that is dedicated to serving those influenced by the loss of a baby through early pregnancy loss, stillbirth or during the first few months of life.
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A nationwide, non-profit organization that is dedicated to assisting families toward a positive resolution of grief following the death of a child of any age and to provide information to help others be supportive
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An international network of parents that offers educational materials and support systems to aid in the loss of one or more children during a multiple pregnancy.
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A non-profit organization that is dedicated to providing grief support and education following the loss of a baby, including miscarriage, ectopic pregnancy, stillbirth and infant death.
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Founded in 1995, by a parent with a child born with Congenital Diaphragmatic Hernia, this soley volunteer, non-profit organization offers support to those effected by a child born with CDH.
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