Therapy
Hi, I'm new to this so forgive a repeat question. Has anyone used a therapist of some kind following diagnosis? I was diagnosed in August 17 and have a life time experience of MS in my Grandad and 2 Aunties (not both blood relatives). I'm still really struggling to process what's happening to me. I've changed meds so I don't have to be in hospital every month, in the hope that I can have some time not running about it. But I'm always thinking.
@sarah_menday I've had some Physiotherapy to help me move a little easier and some Speech Therapy to try and help me from mumbling and speaking in riddles.
It is a hell of a lot to process, do you mean therapist as in someone to talk to - neuropsychiatric type thing - or a physio or OT type? I too have Ocrelizumab and the freedom from pills l and blood tests is not to be underestimated. I feel less medicalised now, which is lovely.