It's been almost 20 years since I first got my tourettes diagnosis, and I found out last month that TS is a disability. There are resources I should have had access to for the past two decades that I did not because I never knew, and no doctor or school councilor ever told me, so I'm posting this to get the word out. Please share it around if you can. If you have tourette syndrome, you are legally protected under the ADA and there are accommodations and support that you have a right to.














