VIDEO: MEN talking about their MS, Symptoms and more (Adult discretion advised) – an MS Patient Voices program –
(Adult discretion advised): * This video portrays three Male MS patient advocates, seen speaking with each other quite bluntly about…
Video: Sharing a Journey with a Newly Diagnosed Person with MS, during COVID-19
MS Views Now – with Patient Leader Lina Light Keep in-touch and up-to-date with MS News: Click HERE to Subscribe…
Stuart Schlossman
Accessing MS care in Underserved populations and Rural America – A Compass to Care event
Event Date: February 16, 2021 Published Date: February 18, 2021 Compass to MS Care – Reaching Rural America and Underserved…
Stuart Schlossman
Understanding Specialty pharmacy and the insurance process
Event date: February 8, 2021 Listen with Gary Owens, MD as he presents on: Specialty pharmacy in MS and the…
Stuart Schlossman
MS Patients’ Voices – Men with MS, speak about MS
MS Conversations NOW – Patients’ Voices An AWESOME Event, declared by all who listened live Listen to the questions from…
Stuart Schlossman
Changing public policies and working towards equitable healthcare access for those with MS
Event Date: 01.27.21 Published Date: February 4, 2021 Listen to this video interview with Bari Talente, Executive Vice-President of The…
Stuart Schlossman
Compass to MS Care – Reaching Rural America during COVID
Event Date: 01.19.21 Published Date: 01.25.21 Presented by Ben Thrower, MD – Chief of Neurology at Shepherd Center in Atlanta,…
Stuart Schlossman
A Listing of UPCOMING MS events – Information needed by so many…
Click the various images to RSVP for these upcoming virtual MS events 02.16.21 – Compass to Care Rural America &…
Stuart Schlossman
MS Education: A WHOLE LOT of MS VIRTUAL events to sign-up for in January 2021
Please review all showing below and register for the programs you want to…
Stuart Schlossman
MS Advocacy Hub features The Multiple Sclerosis Foundation and their community resources
Watch this resourceful video interview with Natalie Blake and Derrick Lee of The Multiple Sclerosis Foundation discussing #MSFocus‘s community resources…
Stuart Schlossman
