![Last Wednesday, the Wayland School Committee gathered to discuss a number of topics regarding the health curriculum and Innovation Career Pathway course. Another large topic of conversation was the ways to potentially mitigate distracting cell phone usage. "These [phones] are going to distract your learning and social relationships," Superintendent David Fleishman said. "That's concrete right there."](https://waylandstudentpress.com/wp-content/uploads/2025/06/Screenshot-2025-06-04-at-9.49.31 PM-1200x886.png)
![Troy Hoyt finishes the Boston Marathon, running for the Hoyt Foundation. T. Hoyt is the son of Hoyt Foundation CEO Russ Hoyt.
“[Running a marathon] might seem like a big thing, when it’s presented to you at first, but if you break it up and just keep telling yourself, “Yes, you can,” you can start chipping away at it. And before you know it, you’ll be running the whole 26 miles, and you won’t even think twice about it.” T. Hoyt said.](https://waylandstudentpress.com/wp-content/uploads/2025/04/C36E8761-1CBB-452E-9DF2-543EF7B1095E_1_105_c.jpeg)
Want to make a difference? The Walk to Defeat ALS is a National event sponsored by The ALS Association to promote public awareness about ALS and to raise funds for ALS research and local patient and family service programs.
Amyotrophic lateral sclerosis (ALS), often referred to as “Lou Gehrig’s Disease,” is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. It is a fatal disease, and often patients in the later stages of the disease may become totally paralyzed.
Dana Miller, mother of four, was diagnosed with ALS this past August. Her kids Spencer 12, Hannah 12, Kyle 8 and Marley 5 are organizing a team for The Walk to Defeat ALS called “The Walking Warriors” in her honor.
Please contribute to the cause and participate in Boston’s 1st Annual Walk to Defeat ALS on Sunday, April 26th in Chelsea, MA. Please sign up online and join the team “The Walking Warriors.”
For questions, email Team Captain Spencer Miller at [email protected] or Team Captain Hannah Miller at [email protected].
Meyer Odette • Aug 10, 2024 at 1:53 PM
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 vine healthc entre. 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.