PHILADELPHIA: Amyotrophic Lateral Sclerosis, also known as Lou Gehrig’s disease, is a very rare terminal disease with about 5000 patients diagnosed every year in the US. It affects the patient’s nervous system, weakening muscle tissue and impacting physical function and mobility.
Every month, the ALS association hosts the ‘Walk to Defeat ALS’ in hopes of raising awareness and funds to help support those affected by the disease, and hopefully one day find a cure.
The walk is relatively popular, averaging around 500-10,000 participants. Each walk has specific ‘teams’ you can join or donate to, that are formed to support a person who has the disease.
This year on November 18th, the “Walk to Defeat ALS” will be held at Citizens Bank Park. Everyone is welcome to join and if you are interested check-in begins at 9:00 AM, and the walk starts at 10:00 AM.
There are many ways that you can help:
- If you are unable to attend the walk you can donate here. You can donate to specific participants, teams, or the association.
- If you want to volunteer there are many different aspects of the walk that you can help with. From clean up to set up, find the job that suits you. Make sure to fill out this survey, so that you can be registered for volunteer work in this event.
Participating in community service is one of the most effective ways to enhance your well-being and offer hope for a better tomorrow. Such opportunities don’t come by often, so everyone who is interested should take part take. Having an opportunity like this appear isn’t a common occurrence, and everyone interested should participate. Let’s all come together and work towards a brighter future for all.
Elizabeth Chucks • Oct 6, 2025 at 9:42 pm
I was diagnosed with Bulbar ALS. I had weakness in my arms legs and hands. I lost all of my strength. I had to keep pliers and wrenches scattered around to open things. I couldn’t walk very far, and I lost my balance easily. I had trouble swallowing and drool sometimes. It impacted all my voluntary moves. My hands shake when I eat or write. this year my PCP decided I try alternative treatment as Riluzole caused severe side effects I started on ALS/MND protocol from Limitless health centre which has made my coordination issues go away. That was the biggest thing that convinced me I was on the right track. Everything before that was just small improvements and was up and down at times. I have gained strength in all muscle, but my right wrist and left shoulder are the slowest to improve. My left wrist is almost back to 100%. we got the treatment from limitlesshealth center . c om This is a game changer for people with ALS.
Maggie Patel • Apr 1, 2025 at 12:52 pm
I was diagnosed with MND. I had weakness in my arms, legs, and hands. I lost all of my strength. I had to keep pliers and wrenches scattered around to open things. I couldn’t walk very far, and I lost my balance easily. I had trouble swallowing and drooling sometimes. It impacted all my voluntary moves. My hands shake when I eat or write. This year my family doctor decided I try alternative treatment as Riluzole caused side effects for me. I started on the ALS/MND protocol from the Uinehealth Center. Since starting the treatment, my symptoms have greatly improved. I now write and eat without my hand shaking, I can feel my strength again with no case of muscle weakness, I’m getting active again. This is a game changer for people with motor neurone disease. Google uine healthcentre . co m. This protocol has truly transformed my daily life, allowing me to reclaim activities I once thought were lost forever. I encourage anyone facing similar challenges to explore their options and seek support, as there is hope beyond the diagnosis.
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Meyer Odette • Aug 10, 2024 at 12:07 pm
My husband had ALS/MND programme about 4 months ago. he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. It doesn’t make the ALS go away but it did give him better quality of life. we got the treatment from vinehealthcentre. com
Meyer Odette • Aug 2, 2024 at 3:22 am
Last year, my 68-year-old partner was diagnosed with Lou Gehrig’s disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither the riluzole nor the medical staff did much to aid him. He would not have survived if our primary care physician hadn’t given him attentive care and attention, as the hospital center didn’t provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms. This year our family physician suggested using vinehealthcentre. com ALS/MND treatment, which my husband has been receiving for a few months now. I’m delighted to say that the treatment greatly reduced and reversed his symptoms of ALS, he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband’s tale; in the end, you have to do what suits you the best.
Julie Hilditch • Nov 25, 2023 at 5:09 am
I stopped most of my ALS medications due to severe side effects and I started on ALS herbal treatments from Natural Herbs Center (Visit naturalherbscentre. com), the treatment has made a very huge difference for me. My symptoms including weakness, difficulty swallowing and slurred speech disappeared after few months on the treatment. I am getting active again since starting this treatment.