Worthy Fundraiser for Oregon Multiple Sclerosis Society JULY 25-27...Hubby & I own a small B&B, DiamondStone Guest Lodge, established in 1994 to give me a productive way to be able to work from home....Reactions 0 reactions Comments0 repliesCoping
JCV positive and Tysabri...My next appointment is in June, meaning I have two more Tysabri infusions before I can change dmd....Reactions 0 reactions Comments5 replies
Frustration with job and disability...I am newly diagnosed in June @ 57yrs and have been out of work since then I used up my sick leave and am now collecting NJ temporary disability...Reactions 0 reactions Comments1 repliesWork & Employment
Question about MS hug...Back in June I started having a relapse which involved amongst other things a loss of sensation in my legs, and over the course of a few months started...Reactions 0 reactions Comments9 repliesSymptoms
Jane...I'm Robins mum, he's 41yrs old, he came home June 2020, he knew he was ill, neither could work out with what, January 2022 confirmed Ms, Ms has affected...Reactions 0 reactions Comments1 replies
What once was simple.....Now, I nearly dread the daunting on-edge task. I find myself in survivor mode with all sense on guard. Where did this all go wrong?...Reactions 0 reactions Comments8 repliesCaregivingSymptomsAwarenessCoping
MS, Work, and Autistic Child...He’s been in ABA therapy for the last few months which is a huge help....Reactions 0 reactions Comments3 repliesWork & Employment
Suspected MS...My names Jade. I've been going to my GP on and off for a couple of years now with varying things....Reactions 0 reactions Comments3 repliesUndiagnosed/Seeking Diagnosis
Loneliness ...She loved the cookies & juice afterwards....Reactions 0 reactions Comments2 repliesPPMSSPMS
Sources for helping maintain residents?...Willing to pay for this but I do have a budget on a fixed income as I am sure everyone here is. Thank you Rob...Reactions 0 reactions Comments0 repliesCoping
2014 North to South Ride for Multiple Sclerosis Awareness...If I improved to wait till June and come back. He said the mass was dimenishing. I continued to improve and made it till the June appointment....Reactions 0 reactions Comments0 repliesCoping
ppms...Had CCSVI procedure in 2013 which made a huge difference in my life until approx. 2019. Now this horrible stuff is really making itself known....Reactions 0 reactions Comments6 repliesCopingExercisePPMS
Employment with MS ...The symptoms are hard on me and the fatigue is huge every day....Reactions 0 reactions Comments11 repliesWork & EmploymentNewly Diagnosed
Do your family or friend's truly understand your MS condition?...I have a friend who continually makes rude remarks to me, for instance: How come you are not up at 6:00 a.m.? In the morning?...Reactions 0 reactions Comments14 repliesCoping
When did you know something just wasn’t right?...My feet burn to the point that I avoid walking or standing, dizziness, huge fatigue like I’ve never felt, quick bladder, IBS, my muscles seem to clench...Reactions 0 reactions Comments4 replies
How do MS attacks look?...hi guys i got diagnosed in june 2022, it all happened because i lost vision in one eye. after they did steroid IVs on me it all went back...Reactions 0 reactions Comments3 repliesTreatmentNewly DiagnosedSide EffectsSymptoms
Confused... Anyone have any input?...I had a CT scan back in June which came back clear. My symptoms Since I was at the hospital I have gotten no better....Reactions 0 reactions Comments1 replies
A Strange Event While I slept...I was diagnosed in June 2023. I had the steroid infusion (which didn't help much, sadly) and I'll start Ocrevus soon....Reactions 0 reactions Comments1 replies
Suggestions for dealing with sensory overload?...The slightest sound can throw me over the edge, and my ability to focus on more than one thing at a time has become impossible....Reactions 0 reactions Comments4 replies