Hi there new to here, was diagnosed with PPMS last September, it affects my left side, been told about MS society but taken me til now to really fife this a try. So just seeing what happens if can speak to people similar 
xx
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Hi Anna just to say hello.
I am new to MS, just been confirmed before christmas Waitingvti start DMT.
How are you doing?
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Hi Anne, pleased to meet you!
I’ve had PPMS 25 years.
I am happy to chat with you.
Boudsx
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Hi there how are you? I’m still trying to take it all in tbh was a shock diagnosis
I am good thanks how are u?
Hi my names Kelly it just wouldn’t let me use that as username lol I got diagnosed last September still trying to take it all in. But be good to chat to you all.
Hi Anne, I’m doing quite good thanks. Just back rom a 3 nighter in a fab hotel good. Blackpool. They have all the kit I need. It did me good!
Take your time to assimilate the diagnosis. Have you got some good support? Without mine, life would be much worse.
Boudsx