“L’ union fait la force”
Support groups are very useful source of information and very important to subscribe if you have a rare condition; your participation will help them to have a voice..
1-The Dystonia society:http://www.dystonia.org.uk/
2-The Hyperhydrosis UK support group: http://www.hyperhidrosisuk.org/
3-The Parkinson’s disease society: http://www.parkinsons.org.uk/
4- The British Neurotoxin network where the treatment centres for Botox per conditions is accessible online to everybody ( non Members)
5–The American blepharospasm society , the BEBREF: http://www.blepharospasm.org/
6–The National spasmodic torticollis association, the NSTA: http://www.torticollis.org/ and the http://www.spasmodictorticollis.org/