Hi all…just joined, not done anything like this before so it’s a bit scary. I had my diagnosis in January of this year, RR MS and was completely overwhelmed but glad to put a name to what’s been happening to me. 2018 marked a significant change for me and was probably the start of my MS but who knows…I’ve had lots of support and returned to full time work. I walk on 2 sticks and a stroller. I have given up driving but in the process of being assessed. I live on my own. I think I have a positive, open mind but it’s not always that way which is why I’m here.
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Hi Sooty
Welcome to the group that no one would choose to join, but we are here and life goes on.
The forum has lots of lovely people always willing to offer advice when they can, or lend an ear.
Take care and ask away with any questions when you’re ready.
Pam x
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Just to say welcome
Thank you.
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I’m new here too! Feels like a big empty space at the moment, but friendly. I’m secondary progressive now having been diagnosed 30 years ago. Had three kids since then so I can give great hope to others! However some of the more gruesome effects are raising their ugly heads and I’m delighted to find so much wisdom, compassion and humour. Looking forward to populating this space with friendly chat.