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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

Hi, Hoping to get some advice about some recent reactions I've had to taking Plegridy. The last two times I've taken the injection I've had a really intense neurological 'episode' a few hours afterwards: sudden drop in body temperature (33.8 degrees on the thermometer) whole body shaking because of...

Does anyone take plegridy?

Good morning MS community 🤗. I was diagnosed in July with relapsing ms and have had it for four years before diagnosis. I am due to start my injections once the nurse has visited to show me correctly how to do the injection. I had worries about medication (family all have died of liver cancer or p...

Hello! First experience of DMTs. My MS team have just prescribed Plegridy. What’s everyone’s experience on this one? Open to all the good, bad and ugly feedback. Thanks in advance!

Hi.. I’m currently on plegridy injection, does anyone else have varied side effects every time you inject (fortnightly). Some weeks I’m fine and other weeks I have flu-like reactions and massive headaches for days and it wipes me out and I’m bedbound because of the side effects. Thank you

Hey everyone, im having my Treatment changed from Avonex to Plegridy and i was wondering if anyone has ever done that shift before and if you encountered any horrible side effect.. im changing treatments because im currently on weekly injections and the injection sites are really painful so my MS nu...

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, I’ve just started Plegridy (began in January and built up to full dose now) and I’ve noticed injection site reactions which is annoying but I was expecting. I’ve also noticed quite severe pains in my knees at times. It seems like it might be linked to the Plegridy as it started shortly afterward...

Hi, relatively newly diagnosed (April this year). Has anyone else experienced an ongoing splitting headache from either plegridy or ms? I'm trying to figure out what is causing it but don't know where to start, not hoping someone else has has similar experience, but if you have I'd like to hear abou...