At the ParkOur resident comic artist, Brooke, shares her experience laying in the park with a friend looking at the clouds, only to have...reactions4comments
Dating with a Disease - Part Two: DisclosingIn the first part of this series, I talked about those tough questions involved in deciding if we really want to date...reactionscomments
The Emotional Toll of Chronic IllnessTrigger WarningThe content includes information related to mental and emotional distress and it might be upsetting to some people. If you or...reactionscomments
Just Trying to Get Through the DayWhen someone asks how you are, what do you say? Fine, thanks.Still sucking air.I’m swingin’! Does that question drive you batty? Do...reactions12comments
MS & Insomnia: Current ResearchMany people with MS complain of insomnia. Either they can’t fall asleep when they go to bed, or they awaken frequently at...reactions1comment
Your Bowel Issue Questions Answered by Your Pelvic Floor FriendsKathy Reagan Young of FUMSnow.com and Erin Glace, Pelvic Floor Dysfunction PT, are back in this video to answer YOUR questions about...reactions4comments
Funky Hacks for Life with MSContributing video producer Kathy Reagan Young shares some some tricks for life with MS to help with cog-fog, fatigue while out and...reactions1comment
Curating Hope With Monday MorningsMonday, the day people throughout the world dread. The beginning of many people’s work week, and often times, it is the end...reactionscomments
You've Got a FriendYou just call out my name And you know wherever I am I'll come running to see you again Winter, spring, summer...reactions2comments
I Relate More to My Elderly Neighbors Than to People My Own AgeWhenever people asked me what that first MS attack felt like, I was frustrated and at a loss. I threw out words...reactions23comments
Your Shortcomings Can Be Your SuperpowersWarning: This may be a trigger post for some. Negativity. Why it is so popular, I will never understand. I used to...reactions14comments
The Caregiver as RefereeThe role of caregiver to MS patients is multi-faceted. Provider. Support system. Cheerleader. Head chef and bottle-washer. Trusted advisor. If you care...reactionscomments
Why We Need to Go Outside Every Day If We Have MSI recently ran across a discussion in a forum on the subject of local workshops for forest bathing. (Yes, this is the...reactions7comments
The Joy of Getting an MRIThat title is extremely sarcastic, folks! While many of us with Multiple Sclerosis have a wide range of symptoms, there are certainly...reactions52comments
Join MSAA for a Live Relapse Management Webinar in Honor of MS Awareness MonthEach year, March is nationally recognized as Multiple Sclerosis Awareness Month. In honor of this month, the Multiple Sclerosis Association of America...reactionscomments
MS and the Terrible 2'sBeing a mom is the hardest yet most rewarding thing I’ve ever done. I love being a mom more than I can...reactions5comments
It's Normal to Grieve For What You've LostAs traumatic as a multiple sclerosis diagnosis was for me, the trauma soon faded and the losses that followed lingered much longer in my...reactions5comments
MS and Workplace AccommodationsLiving and working with multiple sclerosis can be a real challenge. Luckily, the Americans with Disabilities Act (or ADA for short) requires...reactions3comments
What Multiple Sclerosis Looks LikeTry to imagine what disease looks like. Any disease. Diabetes, for example. When you hear the word, what do you envision? An...reactions3comments
I'm No Longer a Victim of MSI decided over the past few years that I would no longer allow myself to play the victim of MS. Throughout my...reactionscomments
