I’m new to this group but not to MS. I was officially diagnosed with RRMS in 1993 when I was 37yrs old. My neurologist thinks it probably started in 1988 (based on my symptoms) when I was pregnant. So I’ve had MS for approximately 29-34. I’m currently in SPMS which started probably 10-15 years ago. I’ve had very three…
Diagnosed 2011 primary progressive. Added more symptoms. Borderline stage 4 kidney (not diabetic or have any history) scarring of lungs (not smoker or covid) and my personal favorite VERTIGO! Nothing like falling.
So, I’m 39 years old and was just diagnosed with PPMS and I’m scared out of my mind. I e had some issues like the MS hug, issues with muscles locking, this odd sensation when I bend my neck it feels like I’m being electrocuted. Honestly I don’t even know the proper terms for anything, which is sad cause I used to work as a…
Hi all, is anyone on this app? I joined it several weeks ago and I have gotten a lot of information regarding MS. It has quickly become another tool in my tool belt. I joined this group a little bit ago however do not see much activity. I've been on MFP for many years. If you are active and would like a fitness and diet…
Hello all. I’ve been diagnosed with RRMS for 7 years. First Copaxone, then Tecfidera, now Ocrevus. Last time I was active here on MFP I lost a good 40+ lbs (still needed to lose more, but lost motivation). Unfortunately, I got out of the swing of it, and allowed my food addiction to take over again. But I’m back on it, and…
I have been recently diagnosed with MS and am looking for an active group.
The scale has been creeping up since I got my motorized wheelchair and I want to get back to feeling comfortable and attractive. Let's motivate each other!
I have been walking anywhere from 9 to 18 miles a week for the last year. It's helped me physically with weight loss, general health (lower blood pressure, slower resting heart rate) but most importantly, it's helped me mentally. I feel stronger, more in control of myself. But for the last week I have been tired. Like my…
I am newly diagnosed. I have tried Copaxone and I thought I would die on it. So now I want to try a diet. This Wahl's diet looks scary. Anybody have any luck with it?
Hi all, so good to see there's an MS group here. I was diagnosed a few months back but it's only just hit me. Especially since I'm having trouble walking and trouble with balance. Fell over only yesterday! And I am putting weight on, finding it hard to exercise, taking stupid amounts of medication. But the biggest problem…
