Knowing that the lack of awareness among the public and among health professionals comes at a high cost, and instead of allowing the diagnosis to define him, Michael chose to turn his experience into an opportunity for advocacy and support. With unwavering determination, he set out to raise awareness about AS, educate others about the condition, and provide support for those navigating similar challenges.
One of the most significant milestones in Michael’s advocacy journey is the “Let’s Get Loud for AS” Fundraiser Gala. Each year, Michael and his team work passionately to organize an unforgettable evening that serves as a platform to raise funds for research, support programs, awareness, and community initiatives. More than just a fundraiser, the gala is a celebration of resilience and hope.
“I’m so proud and humbled that I’ve created this “Let’s Get Loud for AS Fundraiser Gala”… I’ve been diagnosed with ankylosing spondylitis (AS) since 2018, and I’m very happy and proud to say that the wonderful treatments and the assistance of the CSA and my rheumatologist… have really helped me to live a better life with ease.”
As we join together to observe World AS Day, let’s get loud and continue to advocate for a world where everyone living with AxSpA can thrive.
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