I've gone back to the neurologist today. The result of the MRI is correct.
I have improved somewhat from what I'm taking clonazepam. My neurologist says it's all because of clomipramine is causing me dyskinesia. While taking clomipramine should I take clonazepam, although it would be best to change antidepressant. I hope to continue to improve and that the diagnosis is correct
Well, according to the internet dyskinesia is permanant, however that is incorrect. I took care of a patient who developed severe dyskinesia secondary to inappropriate prescribed respiridol. After discontinuance of the drug the dyskinesia resolved in eight months.
Hello, thank you very much to both of you for your answers.
I visited a neurologist, his diagnosis was dyskinesia caused by medications. I've been taking topiramate and Clomipramine for many years and am currently in the process of withdrawal of both.
It is a diagnosis that does not convince me because i have understood the dyskinesia are involuntary movements. I do not notice my continuous movements of mouth or lip, just what happens is that my lip is in that position comfortably and unconscious. I am able to place it in the correct position easily.
It is quite true that i allways move the jaw and play with her and my teeth, but I allways thought it was because of bruxism
What do you think ? Can it be dyskinesia correct diagnosis?
He sent me take clonazepam for a while and has sent me a brain MRI
Thanks
The liklihood this is a cranial nerve palsy. What is unclear is the etiology of the palsy. Yes, botox could be the cause. Usually the disfiguration resolves by itself in one to three months. Your problem is a limited variation of Bell's palsy. A neurologist should be able to provide helpful, but usually there is not much to do. They used to suggest prednisone, but it isn't that helpful. You have my sympathies.
Wow! That's a lot to go through.
It's quite possible that you had a mild stroke somewhere in the past.
It's also quite possible that the botox may have caused this.
There are many possibilities.
I would suggest seeing the neurologist first, and see what he/she recommends.