Inching Away

This is ALS…

Trapped in Silence, Trapped in Sight: The Unimaginable Struggle of ALS.

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https://youtu.be/dgxNblRWVFg?si=aBRmGpL6ojf8u5D8

Tow Trailer Hitch Receiver Installation - 2013 Toyota Camry Installing, Tow Trailer Hitch Receiver for my wife’s 2013 Toyota Camry.Struggle with me, mounting a trailer hitch, making a 1–2-hour job into a 2-day journey...

TikTok · Good Morning America 44K likes, 891 comments. ““Euphoria” actor Eric Dane revealed to People that he has been diagnosed with ALS, also known as Lou Gehrig’s disease: “I am grateful to have my loving family by my side as we navigate this next chapter.””

https://youtu.be/oKonLJTujJE

UNBOXING, HARBOR FREIGHT – CHICAGO, 10 IN MITER SAW Having a look at my first miter saw, Harbor Freight – Chicago, 10 in. I am excited to start using it for my home DIY projects and demonstrating how I get aro...

https://youtu.be/ICV6EGBjYPo

ALS My Life Project My life project living with ALS; While Creating / Building, Sharing and Blogging about all my Home DIY projects "and breaks in between".Join Me On: https://w...

She has a terminal illness. Why can't she get the health coverage she needs? She doesn't want to spend time fighting with her health insurer. After all, she's terminally ill. However, she said she continually battles delays and denials for care and treatment.

Join us Tuesday, March 25, at 8 p.m. ET for the livestream debut of ALS Matters—a new series of conversations led by the ALS community, for the ALS community. Hosted by Cory Mosley, who is living with a genetic form of ALS, this powerful first episode dives into how ALS has impacted Cory, his cousins, and the game-changing role of new ALS treatments. Why tune in? Because these conversations matter. Because ALS Matters. Don’t miss it—join us for part one of the first conversation tomorrow night!

Oklahoma family shares ALS journey as HB 1278 advances forward As Oklahoma lawmakers consider House Bill 1278, which aims to fund research and care for those battling Amyotrophic Lateral Sclerosis (ALS), Michael Wilson and his family share firsthand their experiences with this disorder.