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FormEXTENDED TO NOVEMBER 15, 2018990OMB No. 15450047Return of Organization Exempt From Income Tax2017Under section 501(c), 527, or 4947(a)(1) of the Internal Revenue Code (except private foundations)
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Start by visiting the website of the Huntington's Disease Society of (replace with the specific country/region)
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Anyone who has Huntington's disease (HD) or has a family member or loved one with HD may need the support and resources provided by the Huntingdon's Disease Society of (replace with the specific country/region). The society helps individuals and families affected by HD to navigate the challenges associated with the disease, offers support, education, and resources, and raises awareness about HD in the community. They also provide valuable information to healthcare professionals and researchers who are working towards understanding and finding a cure for HD.
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What is Huntington's Disease Society of?
Huntington's Disease Society of America (HDSA) is a non-profit organization dedicated to improving the lives of people affected by Huntington's disease through education, advocacy, and research.
Who is required to file Huntington's Disease Society of?
Typically, members of HDSA and those involved in research or fundraising activities related to Huntington's disease may be required to file specific reports or documents with the society.
How to fill out Huntington's Disease Society of?
To fill out forms or reports for HDSA, one should carefully read the guidelines provided by the society, ensure all required information is accurately completed, and submit the materials by the specified deadlines.
What is the purpose of Huntington's Disease Society of?
The purpose of the Huntington's Disease Society of America is to provide support for individuals and families affected by Huntington's disease, promote research advancements, and raise public awareness about the condition.
What information must be reported on Huntington's Disease Society of?
Information that may need to be reported includes contact details, participant demographics, fundraising activities, and any relevant health data related to Huntington's disease.
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