Fighting Dystonia, Chronic Lyme Disease & EDS Type 3… any questions?

So Dystonia Awareness Week 2015 has officially drawn to close for another year. It’s been great seeing pictures of people dressing in green and wearing green wigs to promote awareness on social media. I must admit I’m still struggling to get parts of the green dye out of my hair, I may have vague tints of green streaks for a few more weeks but that’s not for lack of trying.

Whilst Dystonia Awareness Week may officially have drawn to a close, our annual fundraiser for The Dystonia Society has yet to take place. We shall be throwing this in June, and shall be announcing the upcoming date this week. So keep your eyes and ears peeled! We hope to see as many of you as possible for tea, cake and some awareness!

I am thrilled to report that over the awareness week almost 1500 people viewed my blog. Of which 937 were new visitors. This completely hit last years numbers out the window. Hopefully everyone learned something new or helpful.

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