Ride to Defeat ALS is a community fundraising event that creates the hope and action needed to create a world without this devastating disease. Each ride brings together a diverse group of individuals and teams dedicated to taking the challenge for those who bravely fight ALS and creates hope for a future without it.
Riders enjoy supported routes with rest stops, support vehicles ready to provide a lift, course marshals along the course, and a finish line celebration with entertainment and refreshments. Participants also have the ability to earn unique Ride to Defeat ALS cycling items like jerseys, shorts, water bottle, and more – based on their fundraising efforts.
Sunday, September 18, 2022
Start /Finish: The Longfellow Club, 524 Boston Post Road, Wayland, MA.
Event URL: https://secure2.convio.net/alsa/site/TR?fr_id=16384&pg=entry
Bike New England 
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.
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My husband has Bulbar ALS, he is about 63 years old it was diagnosed 2 years ago. It was getting more difficult to live for him, because of stiff muscles he couldn’t even move. Riluzole and tofersen medicines were given, but didn’t give much relief. He couldn’t eat food without choking. I thought this might be the last stage and the medications he was given did not help at all, so I started to do alot of research on Ayurveda treatments, I was introduced to Natural Herbs Centre and their ALS/MND Ayurveda Protocol. He started on the Ayurveda Treatment last year, his symptoms gradually diminished including his vocal cord spasm, Muscle Weakness, speech and Difficulty with swallowing. Reach them at naturalherbscentre.com , he is getting active again since starting this treatment, he is able to walk again ( down the street and back ) he has also resumed exercising to strengthen muscles and lo longer require a feeding tube!! God Bless all ALS Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.
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