26JulWalk of Hope for ALS
The 24th Annual Walk of Hope for ALS will be held on Saturday, September 6th, 2025 in Wakefield, MA. The 3.5-mile Walk begins and ends at the lower Common.
This family-friendly event raises funds that directly benefit ALS (Lou Gehrig’s Disease) research at the UMass Chan Medical School.
Gather family and friends, create your team and join us as we raise funds for ALS research. You can walk as a team or as an individual. We encourage you to join in this celebration of hope by walking, and raising money, for those who are living with ALS, or in memory of those who are no longer with us.
Angel Fund President Rich Kennedy and Dr. Robert Brown will kick off the walk at 11 a.m. Walkers will walk the 3.5 miles around LakeQuannapowitt.
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Steven Westermann
I was diagnosed with bulbar ALS in May 2024. I live in Texas, and I’m 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. I’m 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 uine healthcentre. ne t This is a game changer for people with ALS.
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