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@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?

@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...

@pauley 

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pauley

Thankful

Hi there, I just finished my 1st cycle of Mavenclad treatment...free now for 4 weeks before the next lot No real side affects...just a little exhausted...more than the usual kind I could feel burning sensation while swallowing the medication..make sure anyone taking this medication has plenty of w...

@Henrietta 

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Henrietta

Newly diagnosed - which DMD?

Diagnosed yesterday (by phone of course, thanks COVID) with RRMS. Was expecting it so not surprised. Now have to decide between Aubagio and Tecfidera. I’m tending towards Tecfidera but would welcome feedback / opinions / advice. Thanks 😊

@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...

Curled fingers

Three fingers on my hand keep curling under. Anyone else have this problem

@newbie 

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newbie

DMT and work

Hi all, hope you are keeping well and safe in these unusual times. I am newly diagnosed in March, first symptoms 18 months ago and 1 minor relapse 6 months ago. Other than that I am lucky not to have any symptoms of note. I discussed with my MS nurse DMT drugs early March and my neurologist recom...

@hope33 

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hope33

Petition Request-Covid19 and employment

From MS Society With shielding set to be paused in all four nations of the UK in August, we want the UK Government to support people with MS who can’t safely go back to work. We’re campaigning with Age UK, the Trade Union Congress (TUC) and 9 other charities. Together, we’re calling for the furlou...

@Rachel_Hilton_1 

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Rachel_Hilton_1

Starting anew?

I’m struggling at the moment. As we went into lockdown, my partner of 11 years decided to tell me he effing hates living with me and dumped me, the same week as I had to have my 19 year old dog put to sleep. He knew from the outset of the relationship that I had ms and it is a degenerative disease...

@Mich 

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Mich

Copaxone rashes

Hi all, I started on copaxone 4 weeks ago. The first two weeks went really well & I had no side effects. Since then every time I have injected I’ve come out in a hot red swollen rash, which has then turned into a hard lump, like a marble (sometimes bigger) in the injection site. Has anyone e...