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I had my annual check up with my consultant 2 hours ago at RUH Bath. Here is a brain dump of our discussion, while it's fresh in my mind, in case it helps anyone else with RRMS/SPMS who takes a T Cell based DMD: - Lymp count was 1.3 and right where they want it. - The very slow annual increase in...

2 different things here. Thought combine in one post to make easier for me. 1. Does anyone else find that there legs randomly cross over one another at random times while sitting or lying down. Then trying to un cross them is difficult Just not sure if its something to do with spasticity or what. ...

I thought I knew #ChronicPain ( and I don't mean being unable to score some sticky Icky) Then, during a month long attack of #sciatica (not my first) I developed a fucked ankle (not a medical term) - presumably #MS #spasticity in the peroneal muscle (shin/calf - not per_I_neal!). Can't walk (got t...

I noticed that several people have posted that they receive deep tissue massage for their leg aching/burning. Did your neurologist suggest this? My doctor has never brought up the possibility of ‘medical massage’ for relief, but it sounds wonderful. Just curious if it gives you some relief? Ho...

This may be a lot and I want to apologize in advance but I’ve reached a point where I have nothing in my mind worth two cents (to me at least)…. I’m one of those people who grew up in a very strict, culture/religious immigrant family. Life went quick. I grew up quick. First daughter and all that. ...

Anyone else experience joint paint to the point they can’t move until it goes away on its own ? The last week I’ve woken up with my right knee feeling stiff where it hurts to put pressure on it when I stand but normally goes away after 1 min. Then today I woke up around 5am (not totally sure ) with ...

For the last six years or so I have had a multitude of issues hysterectomy do to adenomyosis parathyroid condition resulting in surgery the diagnosed with fibro one doctor said she thinks I may have ms due to my wide spread symptoms I am on a waiting list for an mri but here is some of my symptoms b...

Hi, I've been having stiffness and pain in my neck and shoulder area, my ms neurologist prescribed me Baclofen but it is not helping at all. I'm in tears writing this, can I take more pills or should I go to the e.r? Idk what to do but it hurts so much.

So 4 days In and my symptoms are worse than where be4 I went on infusion and new spasms in hands feet and keeping me awake still head killing me

Hello All, Im seeking some guidance on how one might feel when moving to ocrevus from tysabri, is it better similar or you feel no difference at all? Does it improce symptoms is it good in the long run? Will one feel better? Thanks