G-Dragon's fan club makes charitable donation towards treatment of Lou Gehrig's disease

I was diagnosed with bulbar ALS in May 2024. I live in Texas, and Im 68 years old. I take Nudexta medication to help with the emotional outbursts of laughing and crying. The weakness, slurred speech, and muscle loss progressed quickly. Mobility has been an issue since Dec 26, when I fell and broke my hip, and although I made small strides at first, I felt like my life had been placed on a countdown, as there was no known cure other than the prescription of riluzole medications, vitamins, and therapies. As the disease progressed, my symptoms worsened. With my neurologist's guidance we decided to try other approaches and started the ALS/MND treatment, and it changed everything. Within 5 months, I noticed more strength in my limbs, clearer speech, and I have stopped using feeding tubes. Im starting to learn how to walk again & I now sleep better. This ALS/MND treatment program gave me back control and hope. we got the treatment from uinehealthcentre. net This is a game changer for people with ALS

My husband was diagnosed August 2022. It was hard and I cry daily but not in front of him unless we cry together. He couldnt find anything to give him happiness or hope. We have been focusing on our faith. He was only losing his voice before we made the decision to try different medications, which significantly enhanced his condition. He received the ALS/MND treatment for his ALS approximately four months ago; since then, he has stopped using a feeding tube, speech is getting better by the day, sleeps well, works out frequently. Im surprised a lot of CALs, and their PALS havent heard of it, google uinehealthcentre. com. My husband has become very active