eightball776
Well known member
I know TMJ is super common & probably should be on page #1 when compiling symptoms for a TMS diagnosis. I've been dealing the symptoms in varying severity and since adolescence. Stress and clenched jaw muscles of course always exacerbate things, even when I'm not grinding (that's stopped years ago) or tight in the jaw joints, it separates & clicks whenever I try to open my mouth wide enough to say, eat a large sandwich or get a minor dental procedure. Dental bills are wiping me out financially, and I'm typing this with a retainer/fake tooth that's been in my mouth for 6-7 months now while I wait for another implant. I have a lisp & my entire jaw has visibly shifted. Now I can't stand to be in the dentist chair more than 20-30 minutes at the most, and my teether are continuing to rot & break & fall out at an alarming rate.
The underlying autoimmune disease and lifelong corticosteroids are a big part of it as well, as what I'm describing is very common in people like me. Of course a large percentage of those people are also suffering from MBS, stemming from the stress and psychological impact of dealing with incurable chronic illness, and perhaps even more so from what it takes to deal with the impossibly broken, unaffordable, and inadequate healthcare system.
With all that said, I find myself in a place where I am seeking a more aggressive, invasive treatment for it now. This is coming from someone desperately fighting to stay off of the operating table for a number of other issues. There are very few specialists, available options are extraordinarily expensive with low chances of being covered by insurance, and that's if I am lucky enough to even find one who accepts is. I guess I'm posting here looking for someone in a similar situation. I see the parallel between this and say, someone considering spinal surgery for chronic LBP. After all of these years, and about as much experience dealing with TMS as you'll find here, I am still feeling like treating the symptoms is the only path I have.
Now am I spending 30 minutes doing jaw exercises while meditating and wearing my appliance religiously these days? No ... it's just that those things haven't moved the needle even a little. Now the severity of the symptoms definitely changes, but not the range of motion or clicking/separation when I open my mouth...and I definitely focus on it more when it's tense, or when other symptoms are less prominent, but it's not like a TMS flare of the back where I can loosen up and "just do it" like Dr. Sarno always advised. If I try to eat a tough steak, flaring or not, I'm going to be in pain when I'm done, if I can get through the meal at all.
Sorry, I tend to be a little too verbose... using this forum as a journal or therapeutic outlet.. but if anyone is still reading & has any ideas...
Thank you
The underlying autoimmune disease and lifelong corticosteroids are a big part of it as well, as what I'm describing is very common in people like me. Of course a large percentage of those people are also suffering from MBS, stemming from the stress and psychological impact of dealing with incurable chronic illness, and perhaps even more so from what it takes to deal with the impossibly broken, unaffordable, and inadequate healthcare system.
With all that said, I find myself in a place where I am seeking a more aggressive, invasive treatment for it now. This is coming from someone desperately fighting to stay off of the operating table for a number of other issues. There are very few specialists, available options are extraordinarily expensive with low chances of being covered by insurance, and that's if I am lucky enough to even find one who accepts is. I guess I'm posting here looking for someone in a similar situation. I see the parallel between this and say, someone considering spinal surgery for chronic LBP. After all of these years, and about as much experience dealing with TMS as you'll find here, I am still feeling like treating the symptoms is the only path I have.
Now am I spending 30 minutes doing jaw exercises while meditating and wearing my appliance religiously these days? No ... it's just that those things haven't moved the needle even a little. Now the severity of the symptoms definitely changes, but not the range of motion or clicking/separation when I open my mouth...and I definitely focus on it more when it's tense, or when other symptoms are less prominent, but it's not like a TMS flare of the back where I can loosen up and "just do it" like Dr. Sarno always advised. If I try to eat a tough steak, flaring or not, I'm going to be in pain when I'm done, if I can get through the meal at all.
Sorry, I tend to be a little too verbose... using this forum as a journal or therapeutic outlet.. but if anyone is still reading & has any ideas...
Thank you