By: Steven Westermann

Steven Westermann — Mon, 23 Jun 2025 16:44:14 +0000

I received a diagnosis of bulbar ALS in May 2024. Residing in Texas, I am 68 years old. To manage my emotional outbursts of laughter and tears, I take Nudexta medication. The progression of weakness, slurred speech, and muscle loss has been rapid. Since December 26, when I fell and fractured my hip, mobility has been a challenge. Although I initially made some small improvements, it felt as though my life was on a countdown, given that there was no known cure aside from the prescription of riluzole medications, vitamins, and therapies. As the disease advanced, my symptoms became more severe. With the support of my neurologist, we opted to explore alternative treatments and began the ALS/MND therapy, which transformed my situation. Within five months, I observed increased strength in my limbs, clearer speech, and I have been able to stop using feeding tubes. I am beginning to relearn how to walk and I am now enjoying better sleep.

By: Meghan

Meghan — Tue, 27 May 2025 19:45:09 +0000

My Dad was diagnosed with MND ALS (amyotrophic lateral sclerosis) when he was 57 years old.

By: Rosalynn C

Rosalynn C — Tue, 27 May 2025 12:47:15 +0000

It’s crucial to spread knowledge about Lou Gehrig’s Disease and the challenges faced by those affected.

By: Annette

Annette — Tue, 27 May 2025 11:20:18 +0000

Thank you for bringing attention to ALS Awareness Month.

By: Geoff Roy

Geoff Roy — Tue, 27 May 2025 07:26:18 +0000

Great reminder

Comments on: ALS Awareness Month: Understanding Lou Gehrig’s Disease

By: Steven Westermann

By: Meghan

By: Rosalynn C

By: Annette

By: Geoff Roy