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Hi everyone, sorry I’ve not been on the website for a while but a few months ago i was diagnosed with PPMS and it’s knocked me for six. I went to the doctors complaining of various symptoms and he referred me to a consultant at Stoke hospital, after several tests it came back with MS. It was hard at first to take in but now I’m getting use to the idea. Every day is hard the symptoms are ridiculously horrible. It’s making it harder because i live on my own and with being in a wheelchair as well it just seems to keep me down, being down means depression and anxiety. I don’t know if anyone has MS but if you could post ideas and help that would be nice. Take care NC