Restore Funding for Tourette Services in Pennsylvania

The Tourette Sevices needs funding from this state! It is more than a vital services!

Please give funding for Tourettes

For my son...bravest strongest person I know! May you never have to feel the way he does daily!

My son was diagnosed with Tourette Syndrome at the age of 10 years in 1989. We struggled because I could find no information on Tourette Syndrome even doctors I took him to were unfamiliar with Tourette Syndrome. Until I went to a neurologist office and saw a card with the Tourette Syndrome office in Gettysburg contact information. My son is now 39 years old he has a Masters degree in Fine Arts. Mary Lou Reaver through the Gettysburg Tourette Syndrome office assisted us tremendously in turn I was able to then go into my community and help others, educate the police and the school district please think about giving the funding.

My son has Tourette syndrome and a collection of other comorbities (ADHD, OCD, anxiety, depression, mood disorder, learning and social skills deficits, sensory processing problems, and dyspraxia). We have found the resources from PA Tourette Syndrome Alliance invaluable.

Please fund the tsa .

In honor of my son

My 10 yr old grandson has Tourette's. What a wonderful group!

Please keep funding in your budget to support those with Tourette syndrome!

PATSA was the most necessary support for my son and one of the reasons he was able to succeed throughout school and is now in college. This organization provides support and necessary guidance to help our kids thrive.

Mother of a sweet child with tourettes, he is 13 and trying real hard to educate people. Just yesterday a substitute teacher yelled at him for his tics. We all have to work together to educate everyone we can about this disease.

Our community will always support those with Tourette’s syndrome together we can help and make a difference.

We desperately need this funding. Our families need your support. Thanks

So unfair and so sad that this is happening.

Please do not eliminate funding for PATSA. Their services are crucial to those with TS and their families.

Don't know where we would be without the services provided by the Tourettes Association. Please for the sake of all the families dealing with Tourettes Syndrome, do not take away funding for a syndrome that is very complicated and emotionally and physically debilitating.

These services have been so important for my Grandson.

These services are critical to my family.

I believe funding for Tourette’s is very important to those living with the syndrome.

It's ridiculous they cut funding.there is so little done for tourettes and tourettes awareness as it is