Palatal Myoclonus Sufferer
 

Hello. I am a palatal myoclonus sufferer for almost 6 years now but it has developed so gradually that I realized something was going wrong when I was 14. Doctors could diagnose my disease 4 years ago. I live in Turkey by the way. I researched everything about PM, went to lots of doctors but nothing worked to cure me. All the doctors say that they do not know the possible reason that cause my PM and there is no cure about it so I should forget it and try to focus on other things, according to them. I am sick of living desperately right now. I give up trying to search the treatment options and then I get hope again to be cured, I cry then I try to forget all those things. It is a vicious cycle for me. It is a shame for medicine that they could not even find a root cause of PM. They do not know anything. I wonder if anyone suffers from PM here? Anyone who got relief about PM? It would be great to hear some hopeful news.