FTD Research Roundup: What’s New This Fall - FTD Disorders Registry The Fall Research Roundup highlights new studies now enrolling people living with FTD, care partners, and biological family members.

New FTD studies are now recruiting.

See this season’s Fall Research Roundup to learn how you can help move FTD science forward: ftdregistry.org/press/ftd-re...

#endFTD #Research #NumbersHavePower

Registry Data Presented at the NEALS Consortium - FTD Disorders Registry Registry data is helping to bridge the gap between the FTD and ALS research communities and to accelerate recruitment for future clinical trials.

Data were shared at the NEALS Consortium Annual Meeting by Registry Director Carrie Milliard, showing how the Registry helps bridge FTD and ALS research and speed up clinical trial recruitment.

ftdregistry.org/press/regist...

#FTD #ALS #C9orf72 #ClinicalResearch #NumbersHavePower

This Passover, we extend warm wishes to all who celebrate. As we reflect on the themes of renewal and hope, we're reminded of the power of research to bring us closer to answers for FTD. Thank you to all who participate in the FTD Disorders Registry! #NumbersHavePower #EndFTD

I'm already off but watch this - we are not alone in deserting Twitter and Facebook - there's a whole movement! Are you joining the #GreatMetaWalkoff #GreatTwitterWalkoff - take a look at how many there are! #resistance #numbershavepower