Does anyone have dystonia of the face? If so, can you describe how it feels? I have a constant pressure/pain in the cheekbones & nasal area.
Thank you for your insight. So sorry you have to deal with that!
@A MyParkinsonsTeam Member I do. The dystonia spread to my face. I experienced many years of a crawling like feeling of my muscles in my cheeks and maybe some twitches of my nose and eyes with my jaw popping. Overtime I now experience my jaw clamping shut and getting stuck. My tongue gets stiff. Problems swallowing if I can at all. My neck protrudes forward and gets stuck. This is just some of the symptoms. The levodopa controls this so I can swallow, e-bike my head up and feel normal. When it wears off the symptoms return along with others. It may have started with feelings of muscle pressure before progressing. I would open a dialogue about it with your doctor if you haven’t already.
Does Anybody Have A Problem After They Drink Coffee, It Seems Like It Gives Me Dystonia?
Has Anyone Used A Massage Gun To Relieve Dystonia Pain? What Has Been Your Experience? How About Heat, Say From A Heating Pad?