My daughter had KD last year and found this forum to be a wealth of help and advice.
However being based in the UK I was looking for some local support.
I found it at www.kssg.org.uk
I am now actively involved in raising our profile via social media and we have a group on Facebook https://www.facebook.com/pages/Kawasaki ... 8930243761 and we will be holding a family day in Spring 2013.
If you are based in the UK and have had experience with KD please get in touch with us and help us raise awareness and offer support.
Discuss upcoming parent, research, and physician events
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