Association for Frontotemporal Degeneration
AFTD strives to improve the quality of life of people affected by FTD. We fund competitive grant programs including FTD Biomarkers, TreatFTD (clinical trials), Diagnostics Accelerator (in partnership with ADDF and Gates Ventures) and provide education and support to families living with FTD disorders. The FTD Disorders Registry was founded by AFTD and The Bluefield Project. The Registry is open to persons diagnosed with an FTD disorder, their caregivers, family members and friends in the US and Canada. Registry data will be used to support research studies and clinical trials.
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