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@funnybank 

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funnybank

hearing loss

I've looked it up and apparently, it's a rare effect of MS only 6%. And doctors prefer to say that is probably caused by another factor. I've just lost hearing in my second ear, the first went 12 years ago in very similar sudden onset. I'm on steroids but I have to say this has really knocked all h...

@laurainiho 

Last reply

laurainiho

Re starting treatment

Hello, So I got diagnosed with rrms last August, started on ocrevus in October. I was supposed to have the next infusion in March but it was cancelled because of coronavirus. My ms nurse rang me yesterday to say my treatment is happening next month- great! But due to covid19 I will have to isolate...

@watsoncraig 

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watsoncraig

Wobble

The next Zoom meeting that we Falkirk MSrs are having is Sunday June 14th at 11am. This is open to all, MSrs, family or carers regardless of where you are. We have no affiliations and just shoot the 💩 with no agenda nor “top table”.All that’s required is that you drop me a message with an mail addr...

@Sophietest 

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Sophietest

Shift.ms is LIVE

Daniel & Kevin are live on the Shift.ms Facebook page talking about diagnosis, MS and relationships. Tune in and ask them your questions here: https://www.facebook.com/shift.ms/videos/969374456852750/?v=969374456852750&notif_id=1590677836563640&notif_t=live_video

@CarolO 

Last reply

CarolO

Treatment plan

Only recently diagnosed (7 months ago) & I’d like opinions on my medication please. My MS nurse prescribed 10mg of Baclofen,one to be taken each night along with 30mg of Duloxetine,one at night for a week building up to two twice a day. I stopped both after a week as was experiencing such a mugg...

@Alex1723 

Last reply

Alex1723

Paramedicine with MS

Hi guys, I have always wanted to be a paramedic (am currently an RN) but have recently been tentatively diagnosed with MS. I am wondering if anyone has successfully gained employment as a paramedic with a known diagnosis of MS or whether I need to put this dream to bed. Thank you :)

@ncm22 

Last reply

ncm22

How long have you had ms ??

Hi everyone. I have had relapsing remitting ms since 2010, symptoms since 2007. Main symptom numbness from waist down on movement. I have had numbness for 10 plus years. I also get tremors from waist down, usually controlled by medication. I get other sensory issues. I didn't start medication till...

@Massery 

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Massery

Staying useful

How do you stay useful when you have a crippling disease like ms?’s

Staying useful

How do you stay useful when you have a crippling disease like ms?’

@juliacemilligan 

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juliacemilligan

Ballet

Don't know if anyone is interested in ballet but I found this when looking for activities for my work to post about. It's at the Royal Opera House streaming from the 29th of May until the 11th June. A new ballet by Cathy Marston telling the true story of Jacqueline du Pré, the prodigiously gifted ...