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From now through 12/3, your gift will be matched dollar for dollar, up to $25,000, thanks to AFTD's Board Alumni network!

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AFTD is a 501(c)3 tax-exempt organization (EIN: 41-2073220), and your donation is tax-deductible within the guidelines of U.S. law. To claim a donation as a deduction on your U.S. taxes, please keep your e-mail donation receipt as your official record, which will be sent to you upon successful completion of your donation.

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Empowered Together on Giving Tuesday

Please consider making a tax-deductible gift today to advance our work on behalf of all facing this disease.

Together, we can support all on this journey.
Together, we are empowered to #endFTD.

Hear from our community on why you should support AFTD's mission.

Featured in video: AFTD Ambassador Scott Oxarart; Volunteer Kiley Kocian; AFTD Board Member Dr. Joseph Marquez; Support Group Volunteers Megan Badaglia and Amy Weeks

Advance Research

A donation of $500 can support cutting-edge research initiatives for earlier diagnosis and the development of treatments.
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Support People & Families

A donation of $250 can enable AFTD's HelpLine staff to share vital resources with people and families facing a diagnosis.
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Educate Professionals

A donation of $100 can help distribute materials to healthcare professionals, for better diagnosis and best FTD care practices.
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(L to R): Donald, Nancy, and Michele Howerter at AFTD's 2024 Education Conference

“AFTD helps connect people to others and now I want to do what I can to help raise awareness in the community...AFTD is making more doctors aware of FTD - that's where my hope is. In order to find a cure, we have to have awareness."
- Michele Howerter, care partner to her mom, Nancy, who is living with PPA

Michael Walkowski (left) and Peter

I'm prepared to take this head-on and be there with Peter to go through whatever he's going through. I dove into research like there was no tomorrow and AFTD's website and HelpLine have been very helpful in making sense of everything.
- Michael Walkowski, care partner to his partner, Peter, who is living with PPA

George De Gruccio

"I'm proud to say I've used the webinars, checklists, and one-pagers to help us know how to help Dad. I believe the work AFTD is doing is pivotal. If we didn't have this information, I wouldn't be able to advocate for myself and my dad."
- Jennifer De Gruccio, caregiver to her dad, George, who is living with PPA and Parkinson's disease

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