Hello, I’m Katie, this is the first time since my MS diagnosis that I have reached out for help, advice from people who understand. I was diagnosed with RRMS in April 2020 and with Covid and other things I was lost in the hospital system for a long time and didn’t get referred to see an MS nurse until late 2021. I started off on Avonex and lasted about 3 months but was so sick on it I came off it. I’m currently on Copaxone but finding the 3 injections a week mentally and physically very tiring and the site reactions seem to be getting worse. I’ve been offered Plegridy, 1 injection a fortnight but as it’s the same ingredient as Avonex I’m worried it will make me sick. Does anyone out there have experience of Plegridy? How did you find it? Thank you and take care x
Hi Katie, I dont have any experience of DMDs, but hopefully someone else will reply.
I just wanted to say hi. x
Boudsx