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Top: Health: Support_Groups: Conditions_and_Diseases: Genetic_Disorders:
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» Alliance of Genetic Support Groups - National coalition of consumers, professionals, and genetic support groups to voice the common concerns of children, adults, and families living with, and at risk for, genetic conditions.
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» Chromosome 22 Central - Support group for families who have children with any chromosome 22 disorder, including trisomies, cat eye syndrome, translocations, deletions 22q11, 22q13, VCFS, Digeorge syndrome, rings and malformations.
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» Cornelia de Lange Syndrome (CdLS) Foundation Outreach - Family support organization which exists to ensure the early and accurate diagnosis of CdLS, promote research into the causes and manifestations of the syndrome, and help people with a diagnosis of CdLS, and others with similar characteristics, make informed decisions throughout their lifetime.
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» GendersInX.org - Support and encouragement for people with congenital gender variations.
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» Ideas - A support group for families and professionals interested in the chromosomal condition known as isodicentric 15 (formerly inverted duplication 15).
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» The Rainbow - A forum for people who have chromosome abnormalites to show support, give advice and comfort.
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» S.O.F.T. - A United Kingdom support organisation for parents of infants with Trisomy 13 and 18 and other related disorders.
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» S.O.F.T. - Support Organization in the United States for Trisomy 18, 13, and other related disorders. Provides literature, conferences, newsletter, chapter information, and international contacts.
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» Thomas Scott Davidson - This is a memorial website for Thomas Scott Davidson who died from Anencephaly.
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» Trisomy 18 Angel - This site was made in memory of our daughter Abigail Renee, to help other families who have been given a diagnosis of Trisomy 18.
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» Trisomy 18 Moms - Lists Trisomy 18, Edwards syndrome memorial site, help making a website, and share a story.
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» Trisomy 18 Support Online Community - Participate in this support group for those pregnant with, parenting, or grieving the loss of child with Trisomy 18. Includes resources for all stages of the journey.
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» Who is EPI ? - The mission of the European Porphyria Initiative (EPI) is to present an up to date approach to the understanding of porphyria.
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» Yahoo Support Group for CMT-HMSN-HNPP - A very active support group that prides itself on helping its members through the good - bad days and posting the latest CMT/HMSN/HNPP research information available on the web.
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