Deborah Vick

In order to spread awareness about myasthenia gravis (MG), I think it's essential to delve into the perception of MG versus the reality and shed light on the everyday lives...

Living with myasthenia gravis (MG) can mean frequent hospital visits, especially for those of us on immunosuppressants. In my experience, what might seem like a minor infection or cold can...

As we mark another Rare Disease Day®, celebrated globally on the last day of February, it's a time for reflection on the journey of advocacy, connection, and empowerment that many...

Living with chronic illnesses, especially those that remain invisible to the world, is akin to riding the most extreme roller coaster. Picture the tallest, most thrilling roller coaster you've ever...