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Families will require a wide range of supports and services while living  with HD. it is important to be aware that health and social care professionals may not be familiar with the condition as your family may be their first encounter with HD. HDAI can get in touch with service providers on your behalf so that together with you we can provide an improved  understanding  of the complexities of Huntington’s disease. HDAI also works directly with health educators to inform future health care professionals. Family members have the best insight into all aspects of HD therefore we rely on the participation of people impacted to help in spreading awareness.