Meet Kathy: The MS Warrior with a Smart-Ass Attitude
Hi, I’m Kathy Reagan Young!
I’m a wife, a mom, a friend, a writer, a marketer, a reader, a crab eater, a beer and wine drinker (with an occasional taste for Jameson), a singer/songwriter, an activist, and an advocate. Oh, and - did I mention? I have MS.
But let’s be clear: I’m not just living with MS—I’m talking back to it. I’m a patient who’s lost her patience with this disease. I’ve dealt with the symptoms, the flares, and the indignities that come with MS, and yet, I still find plenty to laugh about. My attitude? I tell MS exactly where to go, every single day. I give it the finger and say “FUMS” because that’s what it deserves. And I’m here to help everyone with MS feel empowered to do the same thing.
My mission? To provide information, inspiration, and motivation to everyone dealing with Multiple Sclerosis. I share my journey and the latest news in MS through my weekly FUMS 6-Pack newsletter, articles in other publications, and on the FUMS social media accounts. And I always “find the funny” in it all.
And yes, I do it all with a smart-ass attitude, middle finger extended, with my battle cry “FUMS” always on my lips!
Hot off the Press
I'm so excited to bring this new book to you.
Adria P.
MS Patient
I LOVE IT. There is just the right combination of facts and funny. Truly, this is an uncomfortable topic to discuss at any level, and the information given is thorough, clear, and easily understandable - with a few chuckles thrown in. I'm a firm believer in not taking anything too seriously, and while this subject matter has the potential to be big problems for us MS’ers, I learned a lot and am Kegel-ing away. Thank you again, best wishes and best of luck! And, always, FUMS.
Nancy P.
MS Patient
Thank you so much for all your hard work. The book is going to be a wonderful resource for those of us who struggle with these lovely issues. I’d recommend this ebook to anyone suffering from these issues.
Sharon Keverline
MD, FACOG
The authors have tackled a subject that is extremely common but oftentimes not addressed by patients or health care professionals. Perhaps this reticence is because patients are embarrassed and/or members of the medical community are unaware that treatment options exist. This book breaks down both of those barriers. Using humor and accessible language it addresses sensitive issues while providing guidance on how to achieve symptomatic improvement.
Kerri C.
MS Patient
I really liked the book. It was quick and easy reading for my MS brain, and was informative with a good laugh here and there. If you didn't want to put it on your coffee table, it would be great bathroom reading material! I will definitely recommend this book, not to just MS’ers, but anyone with undercarriage issues.
About FUMS
FUMS: Empowering the MS Community with Support, Resources, and a Sassy, Smart-Assy Attitude
FUMS is more than just a website—it's a movement, a mindset, and a community built around empowering those living with Multiple Sclerosis (MS). Founded in 2010 by Kathy Reagan Young, FUMS was born out of a need for a positive, uplifting space in the MS world. Diagnosed with MS in 2008, Kathy realized there was a gap in the resources available—everything felt too clinical, too heavy, and too depressing. She decided to create something different.
The FUMS Mission - it’s simple: to provide information, inspiration, and motivation to help people with MS live their best lives. With the right information, and the right support, and the right attitude (FUMS), you can take control of your MS journey.
What We Offer:
Weekly FUMS 6-Pack Newsletter: This newsletter delivers the top MS news directly to your inbox every week. From new research to inspiring stories, paid MS gigs, clinical trial opportunities, and product/service recommendations, you’ll always be in the know without having to search for the information yourself.
Resources and Support: From blog posts that tackle the everyday challenges of living with MS to downloadable guides and tools, and an engaged, supportive community, FUMS is a hub for practical advice and emotional support.
The FUMS Philosophy: FUMS is built on the belief that attitude is everything. We encourage our community to “speak to this stupid disease as it deserves: tell it F-U-M-S every day!” Through humor, grit, and a refusal to let MS win, FUMS empowers people to face MS head-on and live life on their own terms.
Where I’ve Been Featured
FUMS: Taking a Stand Against MS
"MS doesn’t get the last word - we do. Let’s live boldly, laugh loudly, and support each other in our fight. Together, we can be strong and talk to this stupid disease as it deserves: FUMS!"
Kathy XXO
How Can We Do a Fab Collab?
Explore opportunities for newsletter sponsorships, content creation, or consulting to connect with the MS community. Let's talk about how I can support you and your business.