@Redhead 

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Redhead

Makes You Realise

Hi, I'm new to all this. Newly diagnosed with RRMS and awaiting medication. Taken them ages to get me to this point. I really didnt realise that so many people were in the same boat. It will be nice to chat with other people who understand.
@grandma

Hi and welcome, I'm one of the old codgers, had the beast for 25 years, had rrms for 24 years, was on Avonex, it turned into spms laser yr (but they did tell me that was going to happen in 10-15 yrs, and it took 23 so not complaining) am now on Tecfidera. We all quite nice and safe here, you can ask anything you want, someone will know the answer, and if we don't 'we know a man who does' usually Stumbler who will be along in due course. You have had a major shock being diagnosed, sit back, have a cuppa, don't rush things, don't make any major changes (house, job, etc.,) you need time to digest this info. Having an ms diagnosis is no longer the life sentence it used to be, dmt's are so widely available and used these days, and if one doesn't work they will try another. Keep your chin up, we're always here for a natter, a moan, a celebration, a cry, whatever you want. We don't judge, you won't be doing or saying we haven't said or done already. And remember with ms there us no such thing as a silly question😍

@Redhead

Thank you xx