Sort 453 results by

Page 35

@watsoncraig 

Last reply

watsoncraig

Happy World MS Day

Now let’s get a cure

@jade770 

Last reply

jade770

I'm on the struggle bus

Sorry in advance ... I just need to vent a little and I thought this would be the right place. It's nice to have a group of people that know what you're going through. I'm seriously on the struggle bus. I've been deemed "high risk" for covid so I've been exiled from my home and banished to my nanna'...

@LisaSD 

Last reply

LisaSD

Talking With My Family

I can separate my family into three groups. First up are my siblings and my daddy. Daddy and my older sister will ask sometimes how I am doing, but I feel it is mostly like an obligation to them. My two older brothers never ask and I never bring it up. Next up are my in-laws. They always ask and th...

@dinnerlady 

Last reply

dinnerlady

Treatment help

Hi everyone hope all are keeping safe .Just had a letter from the my M.S. Nurse Informing me my Ocrevus Infusion has been rescheduled to July ( original one cancelled due to virus) I was also told I may be more susceptible to the virus and also may be unable to accept a vaccine for the Virus should ...

@pinkie100 

Last reply

pinkie100

Tysabri - few symptoms but new lesions

I was diagnosed in June 2019 having woken up with pins and needles in my hands in January. No previous symptoms. Pins and needles extended to whole body from chest down and I experienced MS hug a few times. After a couple of months things seemed more or less back to normal and although the pins and ...

@funnybank 

Last reply

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 

Last reply

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 

Last reply

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...