DIANN SHADDOX FOUNDATION
#Essentialtremor #diannshaddoxfoundation.org finding treatments cure bringing awareness follow #teamdsf uniting the ET community worldwide #endet MISSION To advance knowledge and recognition of Essential Tremor to the world and find new treatments and a cure Purpose DSF's purpose and commitment is to expand understanding of Essential Tremor throughout the world along with critical information, medical research, and ease the suffering for everyone with ET. Impact The Diann Shaddox Foundation for Essential Tremors resolution is to support medical breakthroughs that will improve the lives of those affected by ET. Support work of the worldwide scientific community to benefit everyone with ET and their families. VISION: End Essential Tremor in our Lifetime & Unite the ET community.
ICO
471008505
3000
X (Twitter)
149
Address
Aiken
About DSF Resources Essential Tremor Ways to GIVE ET Treatment ET Videos contact Team DSF Newsletters FAQ collaboration Our Foundation Our Partners Join Our Team FoundationLeadership Diann Shaddox Executive Director Participate ET Talks Be countedfor ET ET Champions Millions of Faces ET A Night to Shine for ET Gala Patient Council 2025 ET Conference Our Mission Statement Our Vision Our History Join Team DSF Why Give to Diann Shaddox Foundation PURPOSE COMMITMENT . .
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The Diann Shaddox Foundation would like to express its gratitude to FHC for participating and sponsoring the 2025 National Essential Tremor Conference. “FHC is a world leader in neuroscience and neuroscience and neurosurgery research and treatment. ” To learn more, go to https://www.
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Brain Disorders Category
Organisations with similar rank to DIANN SHADDOX FOUNDATION in category Brain Disorders
54. BRAIN INJURY ASSOCIATION OF
Creating a better future through brain injury prevention, education, advocacy, and support.
A strong and powerful voice for the millions of people with disabling brain disorders.
57. ADNP KIDS RESEARCH FOUNDATION
The mission of The ADNP Kids Research Foundation is to enhance the lives of people affected by ADNP Syndrome by providing family support, raising awareness, and supporting research and education.
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Aiken
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