Living with multiple sclerosis and rheumatoid Arthritis, Lisa Emrich is an award-winning, passionate patient advocate, health writer, classical musician, and backroad cyclist. Her stories inspire others to live better and stay active. Lisa is author of the blog Brass and Ivory: Life with MS and RA and founder of the Carnival of MS Bloggers. Lisa frequently works with organizations in support of better policies, patient-centered research, and research funding.
Lisa serves on HealthCentral’s Health Advocates Advisory Board, and is a Social Ambassador for the MSHealthCentral Facebook page.
Several medications used for MS are injectable drugs — aka, shots. We’ve been running from shots since we were kids, but they don’t have to hurt as badly as we remember. Here are some simple tips to minimize the pain, while maximizing the treatment.
Multiple sclerosis is a life-altering condition — it's not just going to alter your partner's life, it's going to alter yours, too. However, that doesn't mean it's the end of life and your relationship as you know it. Find ways to be a supportive partner, while keeping your spark alive.
Participating in a research study of any new experimental MS therapy is important, but that’s not the only way to get involved in research. You can also get involved by sharing information about yourself and participating in surveys through programs like iConquerMS™, and more.
Multiple sclerosis symptoms vary so much that no two people with MS are bound to have the same symptoms. Additionally, MS symptoms mimic dozens of other conditions, so it is important to consider that these symptoms may not be MS at all. Here’s how to know the difference.