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TOPIC: Dopa Responsive Dystonia

Dopa Responsive Dystonia 1 year 2 months ago #4086

I was diagnosed with DRD in 1988 and have been on Madopar ever since, it was life transforming and I've done well on the medication. I was 23 when diagnosed and had had years of deteriorating symptoms with a bit of orthopaedic surgery thrown in as treatment (it was assumed I had cerebral palsy). Has anyone else had a similar experience as I've never met anyone else who this has happened to. I had a bit of blip last year when I had some symptoms of foot drop and felt a bit Parkinson y, but nothing showed up neurologically, and it was sorted with a couple of sessions of hypnotherapy ....... Fantastic! I'd love to hear from anyone who is on a similar road.
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