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.
Interview with Brian Mason
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.
MSAV: What first brought the Multiple Sclerosis Alliance of Virginia to your attention? Was there something specific about our mission or work that resonated with you?
BRIAN: Suzanne’s vision first brought me to the MS Alliance. She has a passion for helping others. The Alliance fills the void left by other MS organizations. They are predominantly devoted to research and have a “big picture” mentality which is extremely important, but as hard as they try, they can’t meet the everyday needs at the ground level. The day-to-day needs are maybe the most important when dealing with MS.
MSAV: Could you tell us about how your association with our President, Suzanne O’Connell, began? How did that relationship develop and lead to the MSAV becoming the fortunate beneficiary of your generosity?
BRIAN: Suzanne is a remarkable person, a diamond. She has a quality most people must learn; hers is natural. She has the ability to understand and feel the needs of others. I feel very honored to know her.
MSAV: The Smith Mountain Lake 4-H Center provides such a serene and suitable environment for the camp. What led you to select this specific venue? What qualities of the 4-H center made it stand out as the ideal location?
BRIAN: Pure luck. We needed something large enough and suitable for people with special needs. In hindsight, it was divine intervention!
MSAV: What motivates you to continue your generous sponsorship of the MS Respite Camp year after year?
BRIAN: I wouldn’t call it motivation; I would call it connection. I feel connected to everyone who has MS, and I’m passionate about giving those who suffer the most a break and the feeling of being wanted and, more importantly… HOPE!
MSAV: From your perspective, what do you hope participants experience and gain from attending the Brian Mason Respite Camp?
BRIAN: Being wanted… being needed, and knowing that they are appreciated and loved. They can accomplish anything, and they are not alone.
MSAV: Are there any particular moments, memories, or stories from past camps that have been especially meaningful or impactful for you personally?
BRIAN: I have enjoyed and cherished all of them. I feel so good when I receive a thank-you note or card or email and read about how special the camp was for them. It’s beyond rewarding!
MSAV: Is there anything else you would like to share about your involvement with the camp, or your broader commitment to supporting individuals living with MS?
BRIAN: I would like to thank you for taking the time to ask me about the camp and thank Suzanne and the Alliance for their commitment to helping all who suffer with MS. Always remember, “Hope” is a good thing… maybe the best thing!