MSAA Gives ThanksIt is the season of giving and gratitude, and the Multiple Sclerosis Association of America (MSAA) cannot help but reflect on the wonderful amount of support we receive from our... By Multiple Sclerosis Association of America - MSAA1 min readBookmark for laterReactions0reactionsComments0 comments
Stories Are What Bring Us TogetherWhere would we be without stories? Stories are what bring us together. Stories are what give us insight into the real world of living with MS. It's through stories that... By Editorial Team 1 min readBookmark for laterReactions0reactionsComments5 comments
The Impact of Leg WeaknessA long time ago, while still in college, I awoke one morning and as I tried to leave my bed, I fell flat on my face. My legs seemingly gave... By Devin Garlit3 min readBookmark for laterReactions0reactionsComments29 comments
Never-Ending ConcernWe are now entering what some are calling the post-COVID, or after-COVID, era. I am seeing the shorthand PCE or ACE more often. This means that rather than facing a... By Anita Williams2 min readBookmark for laterReactions0reactionsComments5 comments
Find Your Fit!You’re here at MultipleSclerosis.net, reading this site for any number of reasons, and those reasons can be widely varied. It is always helpful to know where we fit in the bigger... By Laura Kolaczkowski2 min readBookmark for laterReactions0reactionsComments2 comments
Care Giving With Good CareLet me begin by saying kudos to all of the conscientious, caring, willing, thoughtful, hard-working, compassionate, skilled, and helpful Certified Nursing Assistants (CNAs), Home Health Aides, and Personal Care Attendants. If... By Dianne Scott2 min readBookmark for laterReactions0reactionsComments5 comments
Life After DisabilityBeing diagnosed with multiple sclerosis in my early 20’s was an unexpected shock. Getting diagnosed with an incurable disease at any age is a life-changing event. As surprising and terrifying... By Devin Garlit4 min readBookmark for laterReactions0reactionsComments18 comments
Community Spotlight: A Glimpse Into Martin's MS JourneyMartin, a valued member of our MultipleSclerosis.net community, graciously agreed to spend some time chatting with us about his life with MS. We covered a lot of different topics during... By Editorial Team 1 min readBookmark for laterReactions0reactionsComments1 comments
Doing My Best for a LivingWhen meeting someone for the first time or seeing someone after many years, it's natural to ask questions to become acquainted or reacquainted. Areas of interest may revolve around family... By Dianne Scott2 min readBookmark for laterReactions0reactionsComments20 comments
The Good StuffThere are days when I'll suddenly stop and realize how good I truly feel. I may be exhausted to the core, and I know I need to rest, but I... By Calie Wyatt3 min readBookmark for laterReactions0reactionsComments5 comments
MS and Cog Fog...What Was I Thinking About?I am sure most, if not all, of us have enjoyed that moment of “what was I going to do?" or "what was I thinking?” That puzzled look, scratching your... By Mike Russell3 min readBookmark for laterReactions0reactionsComments28 comments
The Mystery of Missing My MedicationA few days ago, I was sitting around my house and realized that I wasn’t feeling quite right. My head felt fuzzy and I was markedly more tired than I... By Devin Garlit3 min readBookmark for laterReactions0reactionsComments68 comments
Cat Feeders to the Sleep RescueTips, tricks, and tools to make life easier are always popular. Here’s my latest idea to share. My husband and I have two sweet kitties. They are 14 years old... By Lisa Emrich3 min readBookmark for laterReactions0reactionsComments4 comments
You Had One Job: When Healthcare Gets in the Way of HealthcareBefore I start, I just wanted to make it clear that I am pretty much just venting in this post. Maybe you can relate? (I hope not). Maybe this will... By Matt Allen G4 min readBookmark for laterReactions0reactionsComments23 comments
What I Thought Was Eczema Turned Out to Be ShinglesEditor’s Note: This article was written by Patient Leader Cora Lyn Sears and originally appeared on our partner site AtopicDermatitis.net. She describes her experience of having shingles while living with... By Editorial Team 3 min readBookmark for laterReactions0reactionsComments0 comments
HSCT Part 4: The Treatment ItselfPreparations for my trip to Mexico caused so many emotions: worry, excitement, anxiety, and a feeling that I just had to take a breath and get it over with. My 'Hail... By Jenny Angus5 min readBookmark for laterReactions0reactionsComments6 comments
Put Your Best Artwork Forward With MSAA’s Art ShowcaseGet your art materials ready! The Multiple Sclerosis Association of America (MSAA) is now accepting submissions for the 2023–2024 Art Showcase! Since 2009, MSAA has held an annual Art Showcase... By Multiple Sclerosis Association of America - MSAA1 min readBookmark for laterReactions0reactionsComments7 comments
Serving Others Despite MSOne thing I genuinely hope to have in life is a servant's heart. To me, having a heart of service means feeling excited when I see others flourish. To feel... By Calie Wyatt2 min readBookmark for laterReactions0reactionsComments11 comments
My Shingles SurpriseRecently, members of our community discussed shingles. Shingles symptoms are uncomfortable, and can be more severe when combined with autoimmune diseases. It is always an unwelcome surprise when shingles erupt... By Editorial Team 2 min readBookmark for laterReactions0reactionsComments0 comments
Doctor Versus Insurance Company: Patient Put in the MiddleEarlier this summer I received an email from my neurologist's office about an insurance problem. Uh oh, that can’t be good. Upon first reading, my thought was: “What the heck... By Lisa Emrich2 min readBookmark for laterReactions0reactionsComments41 comments