Living Well with MS: A 6-Week Group Coaching Series

The annual Brian Mason Respite Weekend is fast approaching, and we’re excited for another wonderful event! With many new faces joining us, we felt it was the perfect time to reintroduce the man who inspired it all. It is our distinct pleasure to present Brian Mason, a truly dedicated philanthropist whose unwavering commitment has profoundly impacted the Multiple Sclerosis Alliance of Virginia.

Brian is the visionary force behind the “Brian Mason Respite Camp,” an initiative born from his desire to offer a much-needed sanctuary for individuals living with MS and their caregivers. This camp provides a vital break from daily challenges, fostering a sense of community, respect, and love. His enduring support for the MS Alliance of Virginia, inspired by the passion of President Suzanne O’Connell, stems from a recognition of the Alliance’s crucial role in addressing the daily, on-the-ground needs of individuals with MS. Brian’s continued sponsorship isn’t just motivation; it’s a deep “connection” and a profound commitment to instilling “HOPE” in the hearts of everyone touched by MS.

MSAV:  To begin, could you tell us a bit about what initially inspired your journey into philanthropy?

BRIAN:  I was President of the YARC (Youth Association for Retarded Children… not politically correct verbiage now) my junior and senior years in high school. I developed a passion for helping people less fortunate and for those who couldn’t help themselves. We participated in Special Olympics and took the children to places they otherwise wouldn’t have been able to see or experience. It was challenging (especially for teenagers), but the incredible feeling we received from watching the children’s faces was irreplaceable.

MSAV:  The “Brian Mason Respite Camp” has become a beacon of hope and enjoyment for so many. Could you share the original vision and story behind how the camp first came to be?

BRIAN:  The Respite Camp’s original purpose was to offer a getaway for people who suffered with MS and their caregivers. We wanted to first serve the most afflicted who may not otherwise get a vacation or time away from their home. We wanted caregivers to receive a much-needed break from the daily grind by having nurses and volunteers to take the burden away for a few days. We wanted to celebrate the ones who so bravely handled the day-to-day struggles and celebrate the caregivers who seldom received a thank you. It eventually evolved into something similar to today’s version with workshops and speakers. I’m very proud of the benefit it has been and continues to be for so many. It’s a magical experience as it makes everyone there feel respected and loved because it’s all about them as they associate with people who are experiencing the same affliction.

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