Our aim is to share information about Tourette Syndrome with the public, eliminating or minimalizing the social isolation of people with TS. Our objective is to improve quality of life of those with TS. We offer our members the following:
a membership card
a website with the latest information on TS including latest research
a forum
PR through TV, radio and press articles.
brochures and other publications (including books) regarding TS
cooperation with public authorities and other organisations
annual General Meeting of the members attended also by doctors, psychologists and experts.
A directory with contact details of other members of the Association
a list of recommended doctors in the Region
training sessions for the members and volunteers and meetings with parents
support group
One of achievements of our Association is involving people to work voluntarily for the benefit of the organisation. With a help of our volunteers we want to support people suffering from tics and their families. Our plan for the nearest future is to continue our educational campaign,to organise series of events, such as family picnics or meetings. We have already established a support group and a forum. In our annual report we provide information about all our activities. If we are visible, the society will have to recognise that we exist – us, people with Tourette Syndrome.
Die Tourette-Gesellschaft Polen e.V. unterstützt die Tourette-Syndrom Betroffenen und ihre Angehörigen, indem sie eine Plattform für gegenseiteige Kontakte schafft und das Wissen über die Natur der Erkrankung und ihre Behandlungsmethoden zusammenträgt und an die Öffentlichkeit bringt.
Für die Umsetzung dieser Ziele betreibt die Gesellschaft Beratungs-, Informations- und verlegerische Tätigkeit . Der Verein arbeitet mit Spezialisten und Institutionen aus dem Bereich der Edukation, des Gesundheitswesens und der Forschung zusammen.![]() |
Die Tourette-Gesellschaft Polen e.V. ist als gemeinnütziger Verein anerkannt |