my M.S historyI have had MS for 36 plus years in last 10 years I had facial neuralgia. My doctor has tried kinds of medication, works for awhile then no results. Sent...reactions4repliesPainSymptomsTreatment
HungerHas anyone forgotten to eat? This happens to me alot...I was dxed after I gave birth at 39..Prior I had optic neuritis at 19 which resolved and frequent numbness but...reactions4repliesDiet & NutritionSymptomsMental Health
Nystagmus I recently started experiencing nystagmus as a symptom during this most recent relapse. I've never experienced it before as a symptom and I'm wondering whether it's resolved for others or...reactions2repliesTips & AdviceSymptoms
Pain in my left footI am having a pain in my foot that I just dont know how to explain other than painful and it feels like my foot on the bottom feels like...reactions4repliesSymptomsPain
Undiagnosed/seeking diagnosisI know all the problems about the summer sweating, but I've been sweating from the neck up all times of the year.. They are so powerful that I have to...reactions4repliesSymptomsTips & Advice
Depression: MS? Genetic?Cope or medsI've been told I need to at least try Prozac for probably 10 years (MS diagnosed for 30 years). I'm scared to go down the path of mental drugs but...reactions15repliesMental HealthSide EffectsSymptomsTips & AdviceCoping
1.5 or 3 MRII had one lesion on my brain mri in the callosal septal interface a few months back and none in the spine. I’ve heard spinal ones can be hard to...reactions1replySymptoms
Problems with memoryHi, I'm new to the site since I kind of suspect I may have MS and I wanted to see if someone could help me. I have had some weird...reactions11repliesDiagnosisMental HealthSymptoms
Chronic urticaria with MS pseudoflares I have been going through a very stressful time lately (my husband left me suddenly for another woman), and I developed a urticarial rash during a pseudoflare. However, it didn't...reactions1replySymptoms
Anyone living with NMOSD/ Devics Disease? We want to hear from you 💚Hey there! Jada here, I help run Neuromyelitis-Optica.net and where we support so many living with NMO. We know SO many people have had the NMO misdiagnosed as MS. Sadly...reactionsrepliesAwarenessUndiagnosed/Seeking DiagnosisSymptoms