AFTD Revamps Website
AFTD has redesigned and updated our website. Through this effort, we seek to deliver more streamlined information, to better help members of our community to find resources that can help, and to foster new ways to connect and be part of our mission.
Designed to be easier to navigate for both care partners and persons diagnosed with FTD, the website offers new information and resources for different stages of the FTD journey:
- What Is FTD – Learn more about FTD, its various subtypes, and genetic information.
- Living with FTD – Access practical information about coordinating FTD care, managing symptoms, and legal and financial planning, along with various ways for persons diagnosed and care partners to find support and access important resources to help them on their journey.
- Get Involved – Discover ways to join our community, whether on a local or national level, by hosting a grassroots event, volunteering for AFTD, or advocating on behalf of persons diagnosed and their care partners. This section also shows how you can support AFTD’s mission by making a tax-deductible gift.
- Research & Clinical Trials – Find out about ongoing studies and clinical trials that can allow you to participate in furthering FTD research.
The new website reflects the results of in-person focus groups and surveys that drew input from hundreds in our community. It is part of a larger branding update that sees AFTD updating its logo, tagline, and the look of many of our resources over the course of 2018.
How does it look? We welcome your feedback! Send any comments or questions to AFTD’s Communications Manager, Matt Ozga, at email@example.com.
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