“A cure for MS would mean freedom and peace of mind. It would ease the worry of how this disease is going to affect my life as it progresses.” — Rob C., Doug the Pug’s dad On this Giving Tuesday, we’re honoring Rob — and everyone living with the uncertainty, strength, and resilience that MS demands. Today, you can help honor that strength and ease that uncertainty. Every gift to the National MS Society will be 2x matched, doubling your impact on life-changing research, accessible care, and hope

After seven months of unexplained numbness in her left arm, blurry vision, fatigue, and a body that felt increasingly unfamiliar, Arius went through it all — MRIs, bloodwork, nerve tests, hospital visits, even a spinal tap — searching for answers. On March 2, 2021, the answer finally came: multiple sclerosis. What looked invisible from the outside had been a constant, exhausting battle on the inside. The relief of finally having answers mixed with the grief of hearing the truth she had feared fo

Have you ever wondered what it’s really like to join an MS clinical trial... or if it could be right for you? In a special episode of RealTalk MS, Dr. Aaron Boster, who’s cared for people with MS for over 20 years and led more than 65 clinical trials, breaks it all down. From what each trial phase means, to how safety is monitored, to the real-world impact participation can have, Dr. Boster explains it with clarity, compassion, and honesty. Clinical trials aren’t just about research — they’re ab