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EHA Support and Care Survey

The Euro Huntington Association (EHA) have launched a survey to map how people living with Huntington's disease and family members experience access to support and care all over Europe.  The EHA will present a report on the survey results which can then be used as a tool to advocate for the needs of families impacted by Huntington's disease throughout Europe. 

Please consider taking this survey if you are living with HD or are a family member:



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