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@Gabrielle_Wagner 

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Gabrielle_Wagner

Over it all

I don't feel good....My left leg has been having spasms all day, my right hand and arm is acking and I'm feeling depressed about all of it. I don't want to go to the hospital with all covic 19 going on....so what do I do...just be in pain? Signed I'm really just over the whole Multiple Sclerosis...S...

@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...

@Andre_Cyr 

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Andre_Cyr

Wheelchair access

The government paid $6,000 on repairs and I'm still not getting it used and I was prescribed an electric wheelchair with the automatic legs and backing all three different prescriptions I was diagnosed with secondary Progressive. Don't understand Ontario Health Care coverage ODSP?

@mser79 

Last reply

mser79

Ocrevus- fatigue following infusion

Hello. Just wondering what people's experience of fatigue following Ocrevus infusion was? We were planning on trying to take a trip away (in the UK) immediately after the second infusion. Trying to understand if that's advisable given energy levels? Thanks

@Isa_Elfers 

Last reply

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...

@Moglula 

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Moglula

Started Copaxone - tips from MS Nurse!

I’ve just started Copaxone and did my first injection with the MS Nurse a few days ago. I just wanted to share some of the advice she gave me in case it’s of use to anyone else, as some of it I hadn’t seen mentioned before. Firstly, she said she doesn’t like the CSYNC autoinjector because it leave...

@michael_washburn 

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michael_washburn

Dementia due to MS?

After nearly 3 years of searching for answers to my wife's rapid cognitive decline, multiple tests and MRIs and second opinions it is clear she has a the syndrome of Dementia. Our local neurologist as well as the team at UCLA agree that the cause is MS. Images show significant brain atrophy. I ...

@Kel_B 

Last reply

Kel_B

Toe pain

Does anyone else get the terrible MS related toe pain ? Omg it is awful 😔

@BeeFirefly 

Last reply

BeeFirefly

Seeking advice

Hi there im just wanting some advice and help really. In a nut shell I am 25 years old and had this illness since just shy of my 16th birthday (great gift that was) anyway last year after my birthday i suffered a miscarried (first time pregnant as well) and that sent me down a dark dark hole anyway ...

@Hlyndar89 

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Hlyndar89

Travel and Covid19

What are people’s views on travel at the moment? I’m due to go to Amsterdam with my friend for a few days in August. Obviously I’ll be vigilant with hand washing and social distancing where possible but I can’t imagine the place will be heaving with folk like it usually is. Am I being too fearless? ...