War on ALS
The Death Ride Tour/ Fall Blaze expands the popular Colorado Death Ride tour series to New England. The three-day tour rolls through western Massachusetts and southern Vermont October 6 – 9, 2017 (Columbus Day weekend). Profits support the Blazeman Foundation for ALS and the ALS Association and their research to combat amyotrophic laterals sclerosis (ALS) a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Register at http://www.deathridetour.com
Website: http://www.deathridetour.com
Dates: October 6 – 9, 2017
Starting Town: Northampton, MA
Beneficiaries: Blazeman Foundation for ALS and the ALS Association
Route: https://ridewithgps.com/routes/17807179
Route at RideWithGPS
View and print cue sheet
View and print map
GPX file
TCX Course


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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