A re-release from 2017 but still valid. This one addresses CRPS and children, it's always distressing when children develop CRPS and I've seen many with very limiting problems. I've first worked with people with CRPS in the early 1980's when it was called RSD, reflex sympathetic dystrophy, and the key to my success then, and now, isn't just the evidence and approach I take, but my ability to create a really strong therapeutic alliance with my clients, and nowhere is that more important than when working with children. If you want to discuss treatment options to help book a conversation Check out my website there is a page about specialist help for persistent and complex pain conditions I work with https://jillwigmore-welsh.com/specialist-chronic-pain Complex Regional Pain Syndrome, CRPS Chronic Pain & Body Image Treatment in Reading, London and UK wide via webcam I'm in the UK and provide treatment in the UK and for UK registered residents but who travel all around the world. I also provide movement lessons around the world, these are educational and not therapeutic, they provide you with tools to begin safely and kindly reconnecting with your body. If you have CRPS you are welcome to contact me for help, I am particularly interested in working with neurodivergent individuals interested in lifestyle and behaviour change, neuroscience, improving sleep, reducing inflammation, managing anxiety, and improving quality of life.

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