If you’ve been diagnosed with Multiple Sclerosis—or someone close to you has—it’s natural to start asking questions about the role of genetics. “Could I pass this on to my kids?” or “Did I get this because my parent had it?” are common concerns, especially for families trying to make sense of something as unpredictable as […]
If you’re experiencing strange sensations, persistent fatigue, or vision problems and wondering what’s going on, you’re not alone. Multiple Sclerosis (MS) is often called the “disease of a thousand faces” because it shows up differently in everyone—and those early signs can be confusing, subtle, and easy to dismiss. For people living with MS or those […]
If you’ve recently typed “MS specialist near me” into a search engine, chances are you’re either newly diagnosed or reevaluating your current care. Either way, it’s a smart move. Multiple Sclerosis is a complex, unpredictable disease that affects everyone differently, and having the right doctor can make all the difference. You deserve more than a […]
Multiple Sclerosis (MS) is notoriously unpredictable, often showing up in ways that seem small but are, in fact, significant. One of the lesser-known red flags? Changes in your feet. Tingling, numbness, pain, or a strange sense that your foot isn’t quite doing what it’s supposed to—these can all be signs of MS in the feet. […]
Living with Multiple Sclerosis can feel incredibly isolating. Whether you’re newly diagnosed or have been managing MS for years, the need for connection, understanding, and community doesn’t go away. You might be searching “MS support groups near me” after a particularly tough day, looking for someone who just gets it—someone who understands the physical, emotional, […]
Happy Holidays!!! 🥳 🕎 🎄 This is my 13th year putting out an FUMS Holiday Gift Guide!! This year I wanted to do something a little different. I really like the number 6 (I don’t know why) so – I’m giving you my top 6 picks for this year. Six things that have really […]
This annual Multiple Sclerosis Holiday Gift Guide is a HIT every year. I’ve updated it this year (for the 13th time – what??) with new products that either I’ve come across or have been suggested by others in the FUMS community. NEW THIS YEAR: Kathy’s Top 6 Picks – other recommendations follow […]
Hi FUMS’ers, It’s the last day of July. I say this all the time but – how did that happen? This summer is FLYING by. While summer represents a notion of relaxation and frolicking in the surf, for those of us with MS, it’s much more associated with heat exhaustion and the onset of new […]
Hello. My name is Kathy and I’ll be your server. On today’s menu you’ll find some tasty questions about Dementia and MS, a lovely pairing of DMTs, a side of smoldering MS, your choice of B-cell metabolism or a single drop of blood as a predictor of MS, a perfectly aged bottle of obesity drugs, […]
It’s starting to heat up here in Virginia. How about where you are? Extra water consumption, cooling vests, and misting fans are about to be my daily habits again. I would LOVE to hear how you approach the heat of summer. Leave a comment and let me know what you do to stay cool […]