Revision of Huntington's Disease Society of America


← Back to history

AB · · mediawikibotAB-V1

Rendered

The Huntington's Disease Society of America is a US non-profit organization dedicated to improving the lives of those affected by Huntington's disease, an incurable, genetically transmitted degenerative disease of the nervous system that affects movement, thinking, and some aspects of personality.The Huntington's Disease Society of America is the largest 501(c)(3) non-profit volunteer organization dedicated to improving the lives of everyone affected by Huntington's Disease. Founded in 1968 by Marjorie Guthrie, wife of folk legend Woody Guthrie who died of HD, the Society works to provide the family services, education, advocacy and research for the more than 30,000 people diagnosed with HD in the United States.HDSA supports and participates in the HD Drug Research Pipeline, which develops potential therapies to treat and eventually cure HD; and HDSA also supports 50 HDSA Centers of Excellence at major medical facilities throughout the U.S., where people with HD and their families receive comprehensive medical, psychological and social services, in addition to physical and occupational therapy and genetic testing and counseling. from Wikipedia

VIAF: 124469031

non-profit organization in the USA

Wikitext diff vs parent

{{DISPLAYTITLE:Huntington's Disease Society of America}}
The Huntington's Disease Society of America is a US non-profit organization dedicated to improving the lives of those affected by Huntington's disease, an incurable, genetically transmitted degenerative disease of the nervous system that affects movement, thinking, and some aspects of personality.The Huntington's Disease Society of America is the largest 501(c)(3) non-profit volunteer organization dedicated to improving the lives of everyone affected by Huntington's Disease. Founded in 1968 by Marjorie Guthrie, wife of folk legend Woody Guthrie who died of HD, the Society works to provide the family services, education, advocacy and research for the more than 30,000 people diagnosed with HD in the United States.HDSA supports and participates in the HD Drug Research Pipeline, which develops potential therapies to treat and eventually cure HD; and HDSA also supports 50 HDSA Centers of Excellence at major medical facilities throughout the U.S., where people with HD and their families receive comprehensive medical, psychological and social services, in addition to physical and occupational therapy and genetic testing and counseling.<small> from [https://en.wikipedia.org/wiki/Huntington%27s_Disease_Society_of_America Wikipedia]</small>
{{SF|
{{Twt|hdsa}}
{{Wb|http://www.hdsa.org|hdsa.org}}
{{Ins|hdsanational}}
{{Fb|HDSofA}}
}}
{{IDF|
{{Isni|000000045906464X}}
}}
{{VIAF|124469031}}

{{VHID|47333611356}}{{#subtitle: <big>non-profit organization in the USA</big>}}