My mum has had Parkinsons for 6 years now. She started sublingual B1 therapy 3 months ago, and I have seen an improvement in her sleeping, urinary frequency and energy. But her biggest problem is dystonia. Her right hand is clenched, if we try to manipulate it in any way she shakes. I have tried a hand splint, she doesn't like them because she can't get up with it on. In the past she took Mucuna puriens, which released her from a nasty spasmed piriformis. But if she takes it now all her symptoms get worse.
Has anyone had experience with micro dosing of dopamine?
Is there a dystonia recovery program that would help? Or a hand splint that they have found useful?
Any tips would be so appreciated