Frontotemporal degeneration, or FTTD, is a complex brain disorder where each step forward in research brings us closer to answers.

Because FTD is rare, researchers often face the challenge of finding enough participants for studies and clinical trials.

That's where the FD Disorders Registry comes in.

The registry makes it easier for FTD families to help move science forward.

Anyone can join to stay connected to the latest FTD research opportunities.

For those who are eligible, the optional registry research study offers a way to share lived experience with FTD.

This helps researchers better understand the community and whether there are enough potential participants for future studies.

Your privacy is protected.

Information is shared only in a de-identified way and personal details are never shared.

Every person who joins helps build a stronger research-ready community.

Because FTT is rare, every participant matters.

Numbers have power and together we can end FTD. Visit FTD Reg rare, every participant matters. Numbers have power, and together we can end FTD.

Visit FTD Registry.org today.

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