As promised we are closing our #NealsMtg 2025 report out with this post. We will tempt you to a click by sharing one item from our final 3 updates.
To see the full lists (they are interesting!) click through to https://www.endthelegacy.org/neals-report-2025
#EndtheLegacy #AtRisk #ftd

As promised , linked is our written report for the Genetic ALS and FTD community from NEALS 2024. We will be providing 4 sections with the first debuting today. To read the analysis along with the list visit: https://www.endthelegacy.org/neals-report-2025 #endthelegacy #c9orf72 #sod1 #nealsmtg

We are still buzzing from the amazing experience of the 2025 NEALS annual conference. Cheers to that organization and all it's members and staff for a great event and so much excellent work to report on for the year. #Nealsmtg #EndtheLegacy

Great meeting. Lots of work to do.
#BetterTogether #EndALS #NEALS2025 #NEALSMtg

FTD Disorders Registry Director Carrie Milliard and @theaftd.bsky.social's Amanda Gleixner joined the NEALS Consortium Annual Meeting, raising awareness of FTD and connecting with the ALS community to advance research, collaboration, and hope.

#NEALS #NEALS2025 #NEALSMtg

Connect with us at #NealsMtg ! We are thrilled to be joining the NEALS meeting once again in person this coming week. For anyone impacted by ALS virtual registration is free. Cheers to NEALS for such an open policy. See more at https://meeting.neals.org/ . #EndtheLegacy #NEALS

#nealsmtg just some genetic carriers and Ally’s !