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@Feroze_Rossan 

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Feroze_Rossan

MS

I am MS person for 20 years and still suffering from drop leg,spasm

@Henrietta 

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Henrietta

Diagnosis - the long and winding road

2001 Optic neuritis. Go blind suddenly - and fortunately temporarily - in one eye. Ophthalmologist sends me to neurologist. The neurologist tells me in a jovial tone to say that I have had optic neuropathy to insurers - if I say optic neuritis they’d put me down as having MS. MRI done. No follow up...

Meeting

Meeting on the Sunday 30th Holiday Inn Bromsgrove B61 9 AB 12.00 start but turn up when you can, lets hope this one happens as the last went to Corona shut down www.wholesorts.com my bi monthly blog, take a read you may find it interesting Hopefully see you there and invite other MSers too

@Artistjd 

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Artistjd

Shift ms app

Is there an app for shift ms so that I can put an icon on my iPad home screen?

August

A meeting will be held at the Holiday Inn Bromsgrove B61 9AB hopefully this will go ahead and any spike in this virus will not affect us like before Any MSer is welcome as the last one was informative and fun it will start at 12 but your welcome to come early. Also take a read of my recently posted ...

@Peggy7 

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Peggy7

Wedding

Hi all, I rarely say anything on here but I am getting a little nervous instead of being excited. It’s my son’s wedding on the 8th August (30 guests only) it’s being held in a stunning listed property, the problem is I have Secondary Progressive MS and the toilets are downstairs with no lifts, I hav...

@Moglula 

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Moglula

Copaxone and depression?

I've had depression for a long time and have been on antidepressants for about 3 years now (Citalopram). My mood has been pretty stable in that time, but since starting Copaxone 3 weeks ago my depression seems to have returned with a vengeance, and I'm really struggling to shift my low mood. Readi...

@Sophietest 

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Sophietest

VOTE for Shift.ms - pls 🙂

Please VOTE for Shift.ms to win ➡️ https://buff.ly/2CcRgUc ⬅️ 'Best non-fiction' at Webfest Berlin. The 'Animated Symptoms' series has been nominated - a series that shows real stories & experiences told by people living with symptoms of MS. You can watch it here: https://www.youtube.com/playli...

@Isa_Elfers 

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Isa_Elfers

Cymbalta

Hi all, first post. I'm 22 and slogging through the long and troublesome diagnostic process to figure out what's going on. My strong suspicion is MS, but my objective clinical indicators are either barely there or nonexistent ⁠— I have small demyelinated lesions and speckled ANA blood titer, but tha...

@A_Girls_Gotta_Eat 

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A_Girls_Gotta_Eat

Diet and MS

Hey guys I’m in need of urgent help! I’ve had extreme bloating and abdominal discomfort for as long as I can remember ! The doctors have ran all the tests and don’t know what’s wrong :( I was wondering if anyone follows a certain diet that might help with this because I have a feeling it’s connected...