| New Diagnosis
Well even though I just started to work with another dr (my 5th in the last 2 yrs) and he is in the process of making me upper and lower over dentures (my teeth are prepped for crowns) that will also function as a splint since the back teeth will basically be flat planes, I had previously made an appt with a neuro/facial pain specialist at Columbia Presbyterian in NYC almost 2 months ago and just came back from the appt.
He diagnosed me with Oromandibular Dystonia accompanied by acute myial (sp?) facial spasms and pain. Is this just fancy wording for severe tmd or tmj? I did a little research when I came home and the symptoms are pretty much like those usually used to define tmj. Anyone familiar with it?
He said I definitely needed to be treated with botox injections which initially paralyze the muscles and then allow them to relax. It needs to be done multiple times until the muscles forget the contractions they are currently doing. Only at that point would any type of teeth or splint work to keep or maintain the muscles in a relaxed state. It kind of makes sense since I have already tried 4-5 different splints and at least 5 different sets of overdentures with no relief whatsoever. He said his patients usually do not see much relief until about 5-6 monthly injections, some take as long as a year, but all eventually get better. The longer the muscles are in a constant contraction the longer it takes to get them to relax and go back to a normal position. I have been dealing with this for 2 1/2 yrs so I guess I still have a long journey ahead of me. He said he has a 99% success rate which I have heard from other drs as well, but also said this includes patients that simply stop coming for treatments - so he is not sure whether they were successful or not (bells and whistles went off in my head - like "warning Will Robinson - danger" - if any one can remember Lost in Space, which is how I often feel, btw.) He said I would have to go back to PT as well. He did not pressure me at all - said to take as much time as I needed to decide if I wanted to try it. If I did want to give it a try, he would want to do another MRI on the brain, neck and spine since it has been more than 2 yrs since they were done and he wants to see if any other degenerative changes have developed since then, given that I have not had the proper treatment.
So any thoughts, comments, or input on all of this. Since I have tried everything that has been suggested I am inclined to try this as well - I simply am at my wits end from the constant pain and desperate for even just a little relief. Thanks.
|