@jack13 

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jack13

May not be me but fnd

Been to see my neurologist to day. He's going to test me for me but he Thinks i may have fnd. As anyone had the same said to them.
@jack13

I'm sorry I me t MS

@grandma

Hi Jack and welcome, Im glad you've found us. You are in what we call Limboland, not yet diagnosed but still suffering allthe the wierd symptoms. Sit back, have a cuppa, do t stress, stress is one if the worst things if it us ms, it only exacerbates it and can bea major factor in relapses so do take care. If it does turn out to be ms, then you will have dozens of questions , take your time, write all your questions down, you wont remember when you get to see the neurologist. You can always comr here for a chat, a moan, a celebrate, a cry, whatever , we don't judge, you can say almost anything (barring slander!) and always remember, if it is ms, there is no such thing as a silly question Im one of the old codgers, had the beast for 25 years, and even though there were no DMT's in those days, I hate to say this, but if it is ms, you have a huge choice of DMT'd these days,l depending on age, type of ms etc.,something that was notavailableall all those years ago.Keep posting, we don't know all the answers, but "we know a man who does" usually Stumbler who will be along shortly. 😍