gran maul seizureHas any one had a gran maul seizure because of MS. I had won I had one after 26 years living with MS...Reactions0reactionsComments3 repliesAwareness
Equity and MSI'm an engineer looking beyond the bench towards where I can have a greater impact to help people with MS, and was wondering what were the current biggest barriers for...Reactions0reactionsComments1 repliesAwareness
Christina Applegate.I propose someone invite Christina Applegate write stories on this site, that would be fun....Reactions0reactionsComments3 repliesAwareness
Ms cool down It's really hard for me I n this heat it really adds more fatigue,we have tried provigel I had every side effect has anyone else tried this...Reactions0reactionsComments1 repliesAwareness
Medical bracelets A friend of mine suggested I get one so as I'm not mistaken for someone who is intoxicated. Does anyone wear one? What are the costs? Thanks....Reactions0reactionsComments7 repliesAwareness
MS Caregiving ResearchHello Everyone! My name is Jacqueline Mercado, and I am a PhD candidate at the School of Rehabilitation Services & Counseling at The University of Texas Rio Grande Valley. I...Reactions0reactionsComments1 repliesCaregivingAwarenessCoping
Dealing with optic neuritis?!Need suggestions on getting an eye doctor to accept and understand my right eye blurriness is caused by my persistent optic neuritis (courtesy of my MS). Even putting it in...Reactions0reactionsComments7 repliesCopingAwarenessCommunity Resources
Pain rating scale 0-10We’ve all been asked to rate our pain. I find the chart with the round emoji-like faces to be lacking and not helpful. Since I tend to underrate my pain...Reactions0reactionsComments11 repliesAwareness
Every MS Superhero Needs a SidekickWe want to know about your sidekick. Are they your best friend, your doctor, family member, or a pet? Share here what makes them the perfect sidekick to you. Feel...Reactions0reactionsComments536 repliesAwarenessCaregivingFriends & Family
Part of my story and in need of physical help So I was diagnosed in May of 2020, but I've probably had MS since 2017 as subtle RRMS. It progressed to SPMS in 2018 or 2019, so a lot of...Reactions0reactionsComments1 repliesAwareness