Shift.ms

18 Jun 2022 10:58 EditedLast reply 21 Sep 2022 18:58

Ocrevus & progression

For those of you well established on Ocrevus, has it ever exasperated your symptoms in any way or presented anything new? I recently had an infusion following a 7 month delay and am now experiencing bladder incontinence (new), leg tremors (not new, but much worse), a funky eye brow tremor and a ge...

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@HelenD

18 Jun 2022 10:58Last reply 20 Sep 2022 21:37

Ocrevus & progression

For those of you well established on Ocrevus, has it exasperated your symptoms in any way or present anything new? I recently had an infusion following a 7 month delay and am now experiencing bladder incontinence (new), leg tremors (not new, but much worse), a funky eye brow tremor and a general ...

35

@Sez81

6 May 2022 23:43Last reply 7 May 2022 01:20

Symptoms coming back...not diagnosed.

I first posted here in 2020 when I was having intense symptoms. Wasn't taken seriously and told it was either related to my epilepsy or anxiety. Many of my symptoms stayed but weren't as intense but recently ones that pretty much went away have come back and some other things I've noticed as well....

Auckland, New Zealand

2

@TonyMS47

18 Mar 2022 13:17Last reply 18 Mar 2022 13:45

Drs

I tell you, trying to get hold of my doctors is proving extremely difficult. My Primary Doctor and my Neurologist. It's like they've disappeared off the face of the earth. I did let them know that I was going through some rough symptoms earlier in the week and I have heard nothing. #Disconcerting.

St. Louis, MO, USA

1

@TonyMS47

18 Mar 2022 13:16

Drs

I tell you, trying to get hold of my doctors is proving extremely difficult. My Primary Doctor and my Neurologist. It's like they've disappeared off the face of the earth. I did let them know that I was going through some rough symptoms earlier in the week and I have heard nothing. #Disconcerting.

St. Louis, MO, USA

@monty1952

12 Oct 2019 05:11

Life and Times of an MS., Sufferer.

Life & Times of an MS Sufferer….. By Roger Deuxmont · March 31, 2019 Life & Times of an MS Sufferer….. These pages are dedicated to the following people, my father Leslie 1911-1980, my father was an indirect casualty of the smoking lobby, succumbing to the effects of lung cancer at the ag...

@milliepipkins

19 Apr 2019 09:46Last reply 19 Apr 2019 18:54

Me again

Apologies for the influx of posts. I have been experiencing pins and needles in my back, similar to that of when I had my lumbar puncture. I'm putting it down to the treatment and fatigue etc but it's a very disconcerting feeling. Has anyone else experienced this? And if so, do you have any way to h...

5

@Katy79

20 Mar 2016 09:47Last reply 23 Mar 2016 08:01

All new

Hello, this is my first post. I'm currently somewhere between a CIS diagnosis and MS (having been told I meet the revised McDonald criteria for MS based on my MRI and current (very mild) sensory CIS). I don't (think) I know anyone with MS and just want to reach out and share my story and feelings ...

22

@John1985

9 Mar 2016 14:52Last reply 10 Mar 2016 13:35

Eye Problems!

Hi all, I was wondering if anyone would know, I've recently started having problems with one of my eyes - it comes and goes but I've noticed it shortly after lunch my right eye seems to get blurry and it seems like I've got retina burn where I've just looked at a bright light, that is the basic k...

3

@Wilf

9 Aug 2014 17:26Last reply 10 Aug 2014 10:51

Life decisions affected by MS

I've had a week of making life decisions based on my MS. It's been a bit disconcerting, I know it's necessary but it makes me feel sad, just more reminders of something I'd rather ignore. I'm a scientist but quit my job and career in 2012 because I felt the stress was affecting my health. Of course...

3

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