The beginning and middle of the day as well.
#EndALS

The beginning and middle of the day as well.
#EndALS
Listen to the full interview with Mindy Henderson of the Muscular Dystrophy Association:
audioboom.com/posts/833722...
And read this beautiful remembrance by Mindy:
mdaquest.org/remembering-...
She could always find a way to bring humor into whatever situation she was facing. I didn't know her, but I knew her. RIP #BrookeElby #EndALS
The Senate passed ACT for ALS! As we await the President's signature, we honor those who advocated, testified, and told their stories but didn't live to see this day. Their courage is written into this law. We carry their names with us. Rest in power. #ACTforALS #EndALS
When He told us to love others, this is what He meant.
Here’s a glimpse of how to live with #ALS in New York City.
Donate: iamals.donordrive.com/participant/...
Take action: www.iamals.org/progress
#EndALS #ALSAwareness #MND @iamals.bsky.social
Inspired by HBO’s How To with John Wilson
@hbomax.bsky.social @hbo.bsky.social
The I AM ALS community secured historic research funding, held record-breaking meetings with lawmakers, and drove massive legislative action. We're closer than ever to a cure. Next week is Week of Impact. Be part of it: bit.ly/weekofimpact
The House wants to leave DC early. We want them to pass #ACTforALS before they go.
We already hit 1,600 signatures in 48 hours — now let's DOUBLE it. Petition closes on Sunday! Please share.
We're over 1,100 signatures strong and counting. ACT for ALS expires September 30 — Congress needs to act now to reauthorize it. Add your name and keep the pressure on: www.iamals.org/a4apetition/ #ActForALS #EndALS
Lifelong Dodger h8tr, but I always root for Sheehan 🎗️
#EndALS