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@pinkcandystick 

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pinkcandystick

Swatting MS with a stick!

Hi friends. It's been a while since I posted so I'll give you a quick run down. I went off all ms meds in sept of last year due to having a 1 in 100 chance of contracting PML. Then in december I had a flair up that had me in bed until march. It was horrific to say the least. So in march I started my...

test post

@millar tis is a test and i didn't get a drop down of names - and it think's i'm in Northampton
Northampton, United Kingdom

@Ray_Thomas 

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Ray_Thomas

Eyes

Hi Since my last relapse , a year ago in May - my eyes have been a real problem. not double vision as such.., I assume its just a mild version of my vertigo , that never went away It's worse if i have been in a room for a while then go out side ! looking around and left to right quickly is a no no...

June/July

www.wholesorts.com June/July posting, difficult to write when we are restricted but here it is, please read and if you enjoyed it feel free to share www.wholesorts.com

A Vaccine is 12-18mo Away, At Best

I am not trying to be a party pooper here. Why would I? I wrote a bit about them here https://shift.ms/topic/doms-covid-diary-sat-25th-apr This is an excellent piece from a pharmaceutical market analyst. These folk really don't care about you or me, they are in it for the money. End of. Have a re...

Chapter 1 day 2

Much better today than yesterday Apart from being a little bit tired my treatment is going well

Newbie here!!

Hello I've been recently diagnosed, I'm still getting my head round it, fed up with the chronic pain, I'm working mum with two kids. My MS Nurse is coming to see me next week. I feel like people that don't have MS don't really get it. If I say I'm tired they say oh I am too, erm it's not the same!!...

@melmel1 

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melmel1

Anyone in same boat?

So I was diagnosed with MS in 2018 by a general neurologist after all the tests and on and off symptoms for years, I have 5 lesions on brain 1 on the spine, since then been with a MS specialist who did not want to put me on disease modifying drugs as he wanted to watch me further he believes it's M...

@lilyloo 

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lilyloo

Like minded people needed.....

Hi....my name is Lisa. I'm 50. Until the diagnosis with this life changing disease I was a gym goer....almost every day .... Ran from work....I never really sat down. I have progressive ms. Last year I had a stem cell transplant in the hope my disease would be halted.....it hasn't worked. Its still ...

@wobbleone 

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wobbleone

GP recommendations

Hi, hope everyone is doing well ? Just wondering if anyone has a recommendation for a good GP in the Chester/Cheshire west area of the country. Many thanks 😊