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There are currently no cures for #ALS, but there are a few treatments and medications that can combat its symptoms. Every person living with ALS progresses differently. Learn more about ALS and the services we offer through our ALS clinic: bit.ly/39GcNoK

Laine Day 27 #alsawarenessmonth

When you remember that you’re spending Sunday at Globe Life Field cheering on the Texas Rangers and raising #alsawareness #ALS #lougehrigday #letsgorangers #endalswithmda #mdapartner #heralsstory #sunnystrong

When your #AuntSunny hosts the #FightALSFilmFest but you know she only ever calls to talk to you #heralsstory #sunnystrong #ALSAwarenessMonth #alstdi ALS TDI Her ALS Story

This week I went back to full-time work for the first time since I had my son almost 14(!) years ago, and I could not be more proud to share this new email signature …

This week I hit 600 miles of my own (700 total) on this beauty since March 2024 💨💨 Catch me if you can! #ALSAwarenessMonth #sunnystrong #heralsstory #babewithamobilityaid #hicoilikeo

Day 28 #alsawarenessmonth #snapeawarenessmonth

🗣️ “Thanks to Bridging Voice, I’m ready to fight back.” Like many people diagnosed with ALS, one of Chris’s biggest fears is losing the ability to speak to his loved ones. But thanks to a webinar co-hosted with @IAMALS last month, Chris found Bridging Voice and took action.

9 years ago, a year into my diagnosis, I chased this guy around the Colonial Country Club and finally got to introduce myself and thank him for participating in the #icebucketchallenge Pat Green ColonialCountryClub #ALSAwarenessMonth #patgreen

Day 29 #alsawarenessmonth

Mahna Mahna Do doo be-do-do #ALSAwarenessMonth #itsgonnabejune Her ALS Story

EVERY ALS MND scientific conference needs to allow for those with ALS MND who want to attend to be there in person or virtually. It is simply wrong to exclude them.