Hi, does anyone suffer with Dystonia in throat, Consultant struggles to give advise and dismisses it but it is awful.He says it might not be associated with PD. I just wondered if anyone had any treatment that had worked for them? Help xx
Hi Hilly - hopefully our community can offer you some advice, but in the meantime check out our page on Dystonia. https://www.parkinsons.org.uk/information-and-support/muscle-cramps-and-dystonia
We hope this answers some questions you may have.