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 (MSAA) is hosting a number of educational events... By Multiple Sclerosis Association of America - MSAA1 min readBookmark for laterReactions0reactionsComments0 comments
Please Don’t Tell Me What I Can and Can’t DoWhen it comes to living with Multiple Sclerosis (MS), this is definitely one of my top 5 things that angers me above all else; when someone tells me that I... By Matt Allen G3 min readBookmark for laterReactions0reactionsComments27 comments
Patient 'Splaining and How to Make It EffectivePatient ‘splaining. We all do it. Heck, it’s part of the job description of a chronically ill person. When the doctor asks how I’ve been doing, I always answer with... By Kim Dolce3 min readBookmark for laterReactions0reactionsComments4 comments
Cutting to the Chase About Self-Harm & MSContent note: The following article mentions details surrounding the author's experiences with self-harm. If you or a loved one are struggling, consider reading our mental health resources page or calling... By Devin Garlit5 min readBookmark for laterReactions0reactionsComments16 comments
The Yin and Yang of MS: Love and HateOne day, while feeling especially reflective and pondering over the plethora of aspects that living with Multiple Sclerosis brings, I wondered how much of a challenge it’d be to ascertain... By Dianne Scott2 min readBookmark for laterReactions0reactionsComments10 comments
The Joy Of Evoked PotentialsThe process of diagnosing someone with Multiple Sclerosis is not easy. There is no one test that guarantees you have MS. Instead, doctors rely on a series of tests and then... By Devin Garlit3 min readBookmark for laterReactions0reactionsComments20 comments
When Did I Become A Caregiver?In the three decades of my marriage to Cathy Chester, an award-winning healthcare blogger and MultipleSclerosis.net contributor, there have been times when I had to increase my role as a... By Gary Chester2 min readBookmark for laterReactions0reactionsComments6 comments
Empowered to Live Beyond Effects of MSI’m not sharing with you an essay dedicated to celebrating my MS Diagnosis Day anniversary, but let me get this out of the way: I was diagnosed on February 14... By Dan and Jennifer Digmann2 min readBookmark for laterReactions0reactionsComments1 comments
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 with our disease. In this chapter, I want... By Devin Garlit3 min readBookmark for laterReactions0reactionsComments0 comments
How Social Media Has Always Helped Me Overcome MSI am young. I was born in 1990, but that means I am just “old enough” to remember when this “internet thing” started to really take off. Nothing like the... By Matt Allen G4 min readBookmark for laterReactions0reactionsComments2 comments
Frustrated Friends & Family: The Impact Of Their CommentsSince I’ve been sharing my battle with MS, I’ve been fortunate to talk to many people about their own struggles (which is great, because I see everything I write as... By Devin Garlit3 min readBookmark for laterReactions0reactionsComments41 comments
MS Brought Me Home Instead of...“This is not a great way to start the new year.” This text was the cold response received after advising my employer I’d be unable to return after the Christmas... By Dianne Scott3 min readBookmark for laterReactions0reactionsComments40 comments
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 amputee? A morbidly obese person? Or your own... By Kim Dolce4 min readBookmark for laterReactions0reactionsComments3 comments
First Steps: Confessions of an HSCT SurvivorConfessions? Survivor? Oh puh-leeze. So melodramatic, Dave. I know, right? But when I was preparing to get an autologous hematopoietic stem cell transplant (HSCT) in 2010 for my aggressive multiple... By Dave Bexfield — ActiveMSers4 min readBookmark for laterReactions0reactionsComments18 comments
Still Learning How To Live With MSSunday I had a very busy schedule. Something I don't normally do. Because of extreme fatigue, I limit myself in the amount of errands I perform in a day. It... By Nicole Lemelle2 min readBookmark for laterReactions0reactionsComments37 comments
Phone Representative: A Part Time Job That Comes With MSLet me first explain what is going on, after that I promise I have a point. I am really frustrated right now. Well, I have been for a while now actually... By Matt Allen G7 min readBookmark for laterReactions0reactionsComments10 comments
With My MSiversary Approaching I Feel...InvincibleAs I sit here, I realize I’m closing in on my MSiversary next week (a full 18 years since I was officially diagnosed with MS). That’s a pretty big deal... By Devin Garlit3 min readBookmark for laterReactions0reactionsComments3 comments
Dating with a Disease - Part One: Can/Should I?OK, with everything I’ve written about over the years, you had to know I’d cover this part of my life too. Not because I enjoy talking about me, but because I... By Devin Garlit4 min readBookmark for laterReactions0reactionsComments15 comments
The Anguish Of AnxietyAs I’m sitting on the couch, seemingly staring at nothing, my roommate (who I did not even notice enter the room) asks me what’s wrong. It is physically difficult to... By Devin Garlit3 min readBookmark for laterReactions0reactionsComments33 comments
A Different Kind of DadI’ve been asked to write a little something about parenting with MS from the male perspective – although there are a few parents amongst the contributors here, I’m the only... By Steve Woodward3 min readBookmark for laterReactions0reactionsComments1 comments