I’ve just come back from 2hrs of Reiki and massage and feel wonderful. I have always enjoyed going for the odd massage as a treat but only felt so emotionally and physically disjointed on diagnosis (30th March 2012) that I went for a trial, and go back whenever I can afford it as it’s so helpful!
I just wondered if anyone else found these types of ‘alternative therapies’ useful? I’ve looked into them on the MSTrust and MS Society and the main message I’ve picked up is they need further research to understand the true benefits. Is anyone doing this type of research?
I think it would be really beneficial for everyone to have access to this should they want to. My OT says its not available as part of ‘normal’ treatment for symptoms.
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