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I’m just getting reestablished on my Plegridy but the flu like aches and fever are challenging! Other than taking regular pain relief is there anything anyone can recommend? I’m only back on it 1.5 months so hoping it’ll all calm down as suggested after 3ish months.

I've recently been diagnosed with MS and am due to start plegridy but feeling quite nervous after reading about all the side effects 😫are there any plegridy users who can tell me a little about their experience on it? Thank you! X

Does anyone take plegridy?

Hi I am due to start on Plegridy this month how have others found it ? Sorry if it’s a silly question just trying to get my head around it all and feeling a bit overwhelmed!

Hi there 😀First time posting on here! Just wondering if anyone on Intramuscular Plegridy (as opposed to subcutaneous) and if anyone gets pains in thighs/legs? Been on this treatment for about a year, side effects not great ☹️, but leg pains in particular getting worse. Wondered if anyone else was a...

I was diagnosed with MS last September. I put my extremely high blood pressure down to a flu jab and COVID jab but it was neither. I had a bad relapse in May 2021 with dizziness, sickness, facial numbness and nearly fell over in Reception at work. My question is that I don’t see many people menti...

Hi i started on my first jab of Plegridy on Thursday just gone, the injection site on my stomach is fine and apart from a headache i dont feel to bad with regards to side effects, however what i did want to ask was if anyone else has had the glands come up in their groin as i noticed this last night...

Hi people. My name is Tivanya. I've been on Plegridy for the last 3yrs and wanted to know if anybody else is taking it and what's your experience, side effects on it. I really suffer when I take it,extreme body pain,hot and cold polar opposite temperatures. But so far its kept the lesions in check...

Does anyone know if it is ok to have injection 12 hours early? I’m flying on the day of meds it will be a nightmare getting the pen through customs … xx

Hi everyone, I'm new here, diagnosed with RRMS 6 months ago. I've just started on Plegridy and wondered if there are others here who can share their experiences using it? I'm currently having an injection site reaction which I know can be quite common so any hints or tips for dealing with these wou...