Hey everyone! I have decided to make a blog called “10 Ways to Respect Children and Adults With Tourette’s Syndrome”.
I feel like it’s not just important to tell others what shouldn’t be said, but that it’s also very important to follow this up with things that should be said and things that are helpful and supportive. This is important so that others without Tourette’s don’t shy away from talking about it all together, but instead know ways they can acknowledge Tourette’s by being helpful, supportive and accepting without being offensive.
So counting down toward No. 1, here is No. 4:
Not limiting them to a diagnosis. Instead, giving them the tools and support to reach their highest potential.
Look for No. 3 tomorrow. And in case you missed the ones that came before, here’s a list:
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