Seizures in ms...My husband has PPMS diagnosed in 2017. He has just had a seizure and I was wondering how common it is in MS....reactions1replyPPMS
Here's to Hoping the Weight is Over...Is it possible to be hopeless and optimistic at the same time? Welcome to my world when it comes to weight loss as a woman who uses a wheelchair and...reactions64comments
Any relief?...I figured I would ask. I have not been formally diagnosed but I have a appointment this morning with my neurologist to review my MRI. I was able to get...reactions2repliesUndiagnosed/Seeking DiagnosisPainTreatment
Mysterious Chest Pain...I have a symptom where when I lay down flat on my back, the left side of my chest feels like I’m having a heart attack. The same thing happens...reactions8repliesPainCoping
My legs are burning with every step that I take!...I try to mask the pain, but honestly my legs are on fire! Moving and stationary, every position I'm in my legs are burning. The spasticity is awful. I'll move...reactions3repliesCopingSymptomsUndiagnosed/Seeking Diagnosis
Positive acceptance of this monster...First time posting but have been reading the forums for a while now, so here goes. I was diagnosed in 2015 and it didnt really register and properly kick in...reactions5repliesMental HealthCopingDepressionAwareness
Does anyone have occasional violent room going round?...Each time I have been lying in bed, looking at the ceiling, when suddenly I have felt as if the room was swirling and the ceiling fan has shot across...reactions11repliesFatigueSymptoms
Shaking and jerking ...My hands shake and at times my left leg will jump....reactions3repliesCopingSymptoms
Weird hair and spider feelings on my hand...I have had MS for 10 years and have been experiencing weird feelings of a hair wrapped around my one of my left fingers or a spider crawling on my...reactions3repliesSymptoms
Do you Age out of needing DMT's?...Hi, I am going on 55 and have had MS for 10 years. My MS has been stable for a few years other than constant low grade spasticity in the...reactions1reply
Recovering from Hurricane Helene...Currently live in Coastal Georgia where we (mostly) sustained minimal damage from the storm (can't begin to say how grateful I am for that). Power and internet were offline, lost...reactions34repliesWeatherCopingAwareness
MS Fatigue...I want to do so much more than I am able to do because of MS fatigue. I simply give out. My saying is “I have hit my Brick wall!”...reactions2repliesFatigue
Online support groups new York ...Does anybody have any information regarding online support groups for multiple sclerosis in the New York area or close by? Thank you...reactions1reply
What are some resources for getting information for getting a good case worker ...Does anyone have a special non family or friend member that helps you get to your appts and help with various things ? Thanks...reactions2replies
The emotional toll ...Sad to say that last night, after hours of my zings and zappers and spasticity going absolutely haywire... I was so exhausted and couldn't relax, I wanted sleep but couldn't...reactions3repliesCopingSymptomsUndiagnosed/Seeking Diagnosis
Managing fatigue ...My fatigue is getting worse. I don’t know what else to do. I’ve talked to my neurologist couple times she doesn’t feel it’s related to my MS, which I don’t...reactions7repliesSymptomsDepressionFatigue
Fatigue ...Fatigue and my legs hurt have stopped me daily. There are times when I can't hardly walk....reactions2replies
having a relapse...Wondering whether others would do a prednisone treatment or get a covid vaccine first...reactions1reply
Frequency urinating...I kept a log and I recently went 24 times/day (5am-10pm). My urologist says it’s bc of the nerves in my bladder telling my brain that my bladder is full...reactions11repliesPPMS
How Speech Therapy Helped Me...Back in the spring of 2023, I told my new MS specialist that, for years, I’d been having problems voluntarily swallowing at times. This mostly occurred at night, while lying...reactions4comments
