“Some Days We”… is the Title of a Book, to help parents educate their children about MS and/or any chronic illness
About the Book: Follow Wyatt and his Mom, Anne, as they navigate through the unpredictable obstacles of a chronic illness,…
A Patient’s story: Disclosing MS On the Job: Why I Did, and Why I Didn’t
By TK Sellman · November 17, 2020 The question regarding disclosure of your MS at your workplace is really a…
Stuart Schlossman
Living with MS: African-American Perspectives – National MS Society
Click HERE to Subscribe for the MS Beacon Newsletter Living with MS: African-American Perspectives Visit our MS Learning Channel on…
Stuart Schlossman
An MS Patients’ story: How the Pandemic Has Changed How I Manage My Chronic Illness
Written by Amy Mackelden on November 4, 2020Medically reviewed by Arefa Cassoobhoy, MD, MPH The COVID-19 pandemic has impacted people…
Stuart Schlossman
MS Twins – Coast 2 Coast —- Twin patients’ story
twinscoast2coast Introduction to Our Journey with Living with Multiple Sclerosis Throughout our entire lives we were known as the “Haber”…
Stuart Schlossman
Before She Was Diagnosed With Multiple Sclerosis, This Dancer and DJ Saw 14 Specialists
Misdiagnosed, again and again and….. It took three years and countless doctors and physical therapists for Diane Palaganas, 36, to…
Stuart Schlossman
Video Game Treatment May Improve Cognitive Function, Study Shows
August 25, 2020 By Trevis Gleason New research indicates that a novel, video-game-style intervention may be beneficial to people with MS…
Stuart Schlossman
What’s the Plan for People With MS, Post-COVID-19 Pandemic?
As much of the world is trying to find a way to reopen, people with disabilities are being left behind.…
Stuart Schlossman
Exercise… a must for both, MS patients to partake in doing and healthcare providers to promote
September 2020 Written by: Jeffrey A Segal CSCS, NSCA-CPT, CPTS Exercise is an essential component of the…
Stuart Schlossman
Seeing both sides with an invisible disability
August 8, 2020 | By Dan Digmann I fear that others living with an invisible disability are going to hate me for what…
Stuart Schlossman
