Don't Take Life For GrantedDo you remember a time when you awakened from a late afternoon nap and it was dusk? You needed to close the blinds, but it hit you suddenly that not... By Dianne Scott2 min readBookmark for laterReactions0reactionsComments10 comments
New Year, New Goals- How I'm Decluttering My LifeThe holidays always have a way of leaving me feeling overwhelmed afterwards…Overwhelmed by being tired, but mostly overwhelmed because I feel like once we get home with all of our... By Calie Wyatt4 min readBookmark for laterReactions0reactionsComments0 comments
Why I Can’t Physically Take Naps AnymoreOK, time for a nap!” “No, no, no, but I’m not tired! I don’t want to take a nap!” Do you remember that? Being a kid and not wanting to... By Matt Allen G3 min readBookmark for laterReactions0reactionsComments19 comments
It's Not Because I'm Naughty...I think all of us at one time or another in life wonder why we are faced with certain ailments and problems. Sometimes things happen we just cannot understand. Whether... By Calie Wyatt4 min readBookmark for laterReactions0reactionsComments2 comments
Accommodations Done Right: My Trip To The Eagles GameA lot has changed for me over the years that I’ve been battling MS. The disease has affected so many important aspects of my life that this one feels almost... By Devin Garlit4 min readBookmark for laterReactions0reactionsComments0 comments
Winning: My Battle with MSI’ll let Jennifer tell you about her MS diagnosis, but here’s a little bit about what happened to me in December 1999 … and it still is happening. I didn’t... By Dan and Jennifer Digmann3 min readBookmark for laterReactions0reactionsComments17 comments
A Holiday Reminder for Our Friends and FamilyWe are now in the thick of what most consider the holiday season. This time of year can be especially rough for people suffering from a chronic illness like MS. You... By Devin Garlit4 min readBookmark for laterReactions0reactionsComments11 comments
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 past articles I’ve tried to help explain why... By Calie Wyatt3 min readBookmark for laterReactions0reactionsComments0 comments
X’s and O’sWhether it's... Dinner rolls and stuffing, it’s still bread; Forks and spoons it's still cutlery; Motrin and Aleve they’re still pain relievers; An apartment and a house, they are still... By Dianne Scott2 min readBookmark for laterReactions0reactionsComments7 comments
Five Ways to Help You Feel Good During the Holiday SeasonThe holidays can be a time of great stress for many in the Multiple Sclerosis community. Difficult symptoms make us sad as we're forced to sit back and watch others... By Cathy Chester3 min readBookmark for laterReactions0reactionsComments7 comments
His Side of The Story: An Interview with My HusbandI wrote an article a while back about the importance of finding that special someone. I talked about how despite my illness and some beasts along the way I was... By Calie Wyatt4 min readBookmark for laterReactions0reactionsComments4 comments
Footwear and LossIs it right to grieve material loss when so many other much more important things are happening to my body with MS? It struck me that slowing down, not doing... By Laura Kolaczkowski2 min readBookmark for laterReactions0reactionsComments26 comments
10 Things You Should Know About Clinical TrialsEach year thousands of clinical trials occur. Learning about clinical trials can feel like you are learning a new language. The good news is that there are lots of resources... By Editorial Team 4 min readBookmark for laterReactions0reactionsComments0 comments
Getting Ready for the Day Has Become Pretty DifficultAs I have mentioned in the past, I am very routine oriented. Nowadays this helps me remember to do everything that I need to do but even before Multiple Sclerosis... By Matt Allen G5 min readBookmark for laterReactions0reactionsComments11 comments
Gabapentin Abuse and the Fear of Losing Access to MedicationThe glutton for punishment that I am, I had the news on over the weekend when a potentially disturbing story (ok, one of many disturbing pieces) came on. Crammed in... By Devin Garlit4 min readBookmark for laterReactions0reactionsComments23 comments
Would Life With MS Be Better Without So Many People in It?It would be easy for introverts and embittered, abandoned souls in general to conclude that life would be easier without so much social contact. Lots of MS patients complain about hostile... By Kim Dolce4 min readBookmark for laterReactions0reactionsComments0 comments
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 or fall All you have to do is... By Kim Dolce3 min readBookmark for laterReactions0reactionsComments2 comments
Challenges of Being an MS CaregiverIn our MS In America 2017 survey, we gathered insights and information from people living with multiple sclerosis (MS) as well as their caregivers. As a chronic and progressive disease... By Emily Downward3 min readBookmark for laterReactions0reactionsComments1 comments
Four Keys to Succeed in MS Caregiving RelationshipsOK. We get it. For those of us living with Multiple Sclerosis, most are quick to say that the disease doesn’t define who we are. I have MS, MS does... By Dan and Jennifer Digmann4 min readBookmark for laterReactions0reactionsComments2 comments
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 such as fatigue and weakness only to hear... By Kim Dolce5 min readBookmark for laterReactions0reactionsComments23 comments