Access Even More Information About Multiple Sclerosis With MSAA’s Digital Educational Program GuidesThe Multiple Sclerosis Association of America (MSAA) is here for you throughout your MS journey, and has made it even easier for you to learn about important topics related to... By Multiple Sclerosis Association of America - MSAA1 min readBookmark for laterReactions0reactionsComments0 comments
The Day the Poltergeist Moved In, Set Up Shop, and Wielded a Nightmare: Part 2I call my disease a poltergeist because it felt as though this entity, with enormous power, engulfed me, controlling my every thought, need, want, and desire. I had spent decades... By Jenny Angus3 min readBookmark for laterReactions0reactionsComments6 comments
Are You Even Listening?My MS flips the script and tolerates heat much better than cold. I, therefore, spend a lot of time outdoors during the summer months, and this year was no different... By Fredric Andersson4 min readBookmark for laterReactions0reactionsComments5 comments
Am I Getting Old or Is It MS?Oh boy, am I having a fun time these days. I have a new game I get to play every day now. It starts in the morning and ends at... By Anita Williams2 min readBookmark for laterReactions0reactionsComments36 comments
Shaking in a New SymptomYou might remember Mariah Carey's song about moving on from a failed relationship. She soulfully sang that she was striving to "Shake, shake, shake, shake, shake it off..." And there... By Dianne Scott3 min readBookmark for laterReactions0reactionsComments20 comments
Community Views: What is Life Like With PPMS?Primary progressive multiple sclerosis (PPMS) is MS that develops slowly and steadily worsens over time. PPMS does not go through periods of relapse or remission like other forms of MS... By Editorial Team 2 min readBookmark for laterReactions0reactionsComments20 comments
Using an E-reader to Improve My Reading With MSEver since I was a young child, one of my most enduring passions has been reading. Even after I was diagnosed with multiple sclerosis, reading was an integral part of... By Devin Garlit4 min readBookmark for laterReactions0reactionsComments7 comments
How to Choose an MS Medication in 3 Not-So-Easy StepsSo, you’ve decided to take a disease-modifying therapy (DMT) to try to keep your MS at bay. As a caregiver, I have been actively involved in researching and discussing therapeutic... By Gary Chester3 min readBookmark for laterReactions0reactionsComments4 comments
Taking a SeatWhen it comes to leaving my house and engaging in various activities, whether it be meeting friends, running errands, or going to a doctor's appointment, I find my success can... By Devin Garlit3 min readBookmark for laterReactions0reactionsComments21 comments
Contemplating the Medication VacationWhen first diagnosed with MS, my first big question was which disease-modifying therapy (DMT) I would start. My neurologist gave me a list of options: injectables (the interferon class and... By Tamara K Sellman3 min readBookmark for laterReactions0reactionsComments3 comments
Take the Managing Treatment and Medication SurveyThe Managing Treatment and Medication Survey is now closed. Thank you for your interest! Treatment is a big part of managing a chronic (long-term) health condition like multiple sclerosis (MS)... By Editorial Team 1 min readBookmark for laterReactions0reactionsComments2 comments
The Day the Poltergeist Moved In, Set Up Shop, and Wielded a Nightmare: Part 1I was an athlete and knew how to grind through a lot of pain during training. When I began to experience all these insane abnormalities and rapid decline in body... By Jenny Angus3 min readBookmark for laterReactions0reactionsComments11 comments
Saying Yes to Sex After an MS Diagnosis: Part IThis article is one in a series about the positives of saying 'yes' to sex after a devastating MS diagnosis. My approach will continue to be explicit, frank, and heartfelt... By Kim Dolce3 min readBookmark for laterReactions0reactionsComments4 comments
MS Comic: MakeupIn this comic, Brooke shares her journey with makeup application and the struggles MS created. She persevered and found a way to still partake in this form of self-expression! Have... By Brooke Pelczynski1 min readBookmark for laterReactions0reactionsComments6 comments
Five Resources for African-Americans Living With MSI have written before about my multiple sclerosis advocacy on behalf of African-Americans. My focus is primarily on the equity in research, but that doesn’t mean my support ends there... By Anita Williams2 min readBookmark for laterReactions0reactionsComments5 comments
The Difficulties of Maintaining Friendships With MSOne of the common gripes I often hear from those with multiple sclerosis is about the toll it takes on relationships. This disease can have a very negative effect on... By Devin Garlit3 min readBookmark for laterReactions0reactionsComments69 comments
To Medicate or Not to Medicate: Helping Patients ChooseIn March, the Food and Drug Administration (FDA) approved a new medication for the treatment of relapsing-remitting and secondary-progressive multiple sclerosis. It was the seventh FDA approval of an MS... By Gary Chester3 min readBookmark for laterReactions0reactionsComments14 comments
Out and About in Spite of MSBeing primarily homebound is not what I signed up for. Getting out, for me, can definitely be tiring and requires quite the effort. When I was no longer able to... By Dianne Scott3 min readBookmark for laterReactions0reactionsComments12 comments
Has Anyone Seen My Attention Span?I thought I left it on my desk. Maybe under that stack of papers. Or, maybe I left it outside on the patio table where I tried to do some... By Tamara K Sellman3 min readBookmark for laterReactions0reactionsComments10 comments
“You Used to Be So Happy” - My Emotional Journey With MSI believe I have dealt with a form of depression my whole life. I only called it something different back then. I called them “funks” and treated them like a... By Moyna John2 min readBookmark for laterReactions0reactionsComments25 comments