Hey ya’ll
Just wanted to introduce myself and also try to get some insight on my current situation if I can...first time posting and sorry it’s so long, but I’m really going through it right now.
First a bit of background info – I’m in my mid forties and have been dealing with TMS off and on for a a few decades, definitely no stranger. Low back stuff/sciatica is the usual thing, but I’ve also had some knee and hamstring/hip stuff as well, so it can come at me multiple ways. I’m an athlete and I do a physical job, so I get banged up all the time and it’s hard to separate normal aches and pains, acute injuries that need addressed and TMS manifestations.
A common pattern with me is I develop some kind of actual acute physical issue and treat it with PT initially, but then at some point TMS brain takes over it and turns it into an ongoing, arduous thing long after the physical element is basically fine. I never know when this transition occurs and I don’t want to risk aggravating a real physical problem, so I always have to go through the motions of regress, get frustrated, find a new PT, have initial success, regress again, get frustrated, repeat. This will go on for months till I wise up and start thinking in a more TMS-related direction. But even then it’s a slow process to internalize it, I’m always stubborn to accept TMS. The good news with me is once I’m confident it’s TMS, symptoms tend to clear up right away, that’s all I need is the knowledge. The bad news is it takes me a long time to be convinced, and I usually need a real doctor to tell me - this often comes after spending months on wasted PT and expensive imaging. But traditionally I do really need that, I need to be reassured by somebody with proper medical authority that I’m not causing any damage by returning to training.
So anyway...I got the back stuff under control, I don’t think TMS can fool me with that again, it’s been great. Anybody here ever suffer tennis elbow as a manifestation of TMS though? I got a bad case of it right now and its just killing me. Based on what I’ve learned about it tennis elbow seems to have been designed in a lab to be uniquely torturous for TMS sufferers – almost like AIDS for someone who already has an autoimmune disorder. I first developed it a year and a half ago and I’ve had 4 major flare ups since then – this last one has been going on since december.
I saw a bad orthopedist for a while who gave me too many cortisone shots without bothering to tell me that too many cortisone shots are bad for tendons. Now the skin is all white and the fat pads have sunken, so I’m freaked out I’ve done too much irreparable cortisone-related damage to the tendon, so that didn’t help. Then I got a new orthopedist, who is marginally better for at least telling me not to do anymore cortisone, but he also told me the thing was pretty bad and might rupture one day and would likely need surgery eventually regardless. I’m very susceptible to suggestion and hate it when doctors say things like that – I once had a doctor tell me I’d for sure need back surgery and I got very depressed and had 3 more months of severe symptoms, then I saw another doctor who looked at my imaging and said “looks OK to me” and within 3 weeks I was symptom free. So that didn’t help either.
So anyway, I started PT for the elbow in January, and have simultaneously been rehabbing a shoulder sprain from last year that didn’t heal properly on the same arm – the hope being that fixing both means the whole arm will improve. The shoulder mostly has improved though it still has some work ahead; the elbow has been very up and down. My initial PT discharged me and cleared me for activity because I was symptom free for a couple weeks but as soon as I started lifting weights again I had a bad flare up, so I found a new PT. At first things with that PT went well, but she’s been pushing me lately to up the weights again and so I’m having another bad flare up and its as bad as it’s ever been – even tying my shoelaces aggravates it slightly and I just don’t know what to think about it anymore I’m beyond frustrated.
So that’s where I’m at. It’s miserable. I haven’t been able to work lately, I work with my hands and have to move heavy things so a weak and painful forearm tendon is a debilitating. So I’m running out of money and that’s stressful. Plus I have severe ADHD and absolutely need intense physical activity to regulate my brain chemistry, and when I’m hurt and can’t get it I start to spiral and ruminate, so that’s also bad. And I got pretty high anxiety right now because I was planning a big move but have had to delay it till I feel confident I can generate income again so in the mean time I’ve been stuck in limbo bumming around my mom’s house while I’m out of work and in arm rehab and am increasingly depressed about that situation. So I got a lot of stressors currently. Plus the world completely sucks right now generally and I don’t want to deal with it, so...I’m sure on some unconscious level I like having reasons to be cranky and stay home
There’s also that same pattern developing of start a treatment, then it fails, then try another one, it works at first but then fails and I get more and more frustrated, so that tracks with TMS. But then again I don’t know...the symptoms have been very consistent, and every time I try to push it a bit I get a flare up, always in the same place, it’s pretty acute. I did have an MRI on it last year, and was told it looked normal – severe inflammation but no damage, so nothing to worry about. But that was last year; it might be worse since then. I’m just scared to death of a tendon rupture - if that is in fact a real risk and not just a ghost story from a shitty doctor with bad bedside manner, but I absolutely CANNOT do that surgery on my good arm, I’ll be out of a job, maybe out of a career and unable to even wipe my own ass for months, I just can’t do it.
So...anybody have anything at all to offer? I know I can’t get a diagnosis from strangers on a forum, but what are the armchair opinions? Anyone have a similar experience they can relate? Or a suggestion of how to approach it and move forward? Anybody know of any specialists to reach out to? I would love to find another TMS doctor I can meet with if anyone can point to one or at least a list/directory so I can find one on my own. I had been living in NY and saw Dr. Rauschbaum who took over sarno’s old clinic, then after he retired I saw Dr. Gzwozds in New Jersey. I live in Pittsburgh now, I have no idea if there’s anyone around here that does TMS. I’ll drive a little if I gotta. Telehealth would be fine too if I could find someone who will do it, think they’d need to be in PA as well though. I’ll drive back to Jersey if I have to, but it’d be a 2 day trip so only if there’s no better option.
And if it DOES turn out to be TMS, then...I’m going to need some better strategies to deal with it moving forward, because apparently it’s just never going to relent.
Ok, thanks in advance to anybody who reads all this and replies.
Just wanted to introduce myself and also try to get some insight on my current situation if I can...first time posting and sorry it’s so long, but I’m really going through it right now.
First a bit of background info – I’m in my mid forties and have been dealing with TMS off and on for a a few decades, definitely no stranger. Low back stuff/sciatica is the usual thing, but I’ve also had some knee and hamstring/hip stuff as well, so it can come at me multiple ways. I’m an athlete and I do a physical job, so I get banged up all the time and it’s hard to separate normal aches and pains, acute injuries that need addressed and TMS manifestations.
A common pattern with me is I develop some kind of actual acute physical issue and treat it with PT initially, but then at some point TMS brain takes over it and turns it into an ongoing, arduous thing long after the physical element is basically fine. I never know when this transition occurs and I don’t want to risk aggravating a real physical problem, so I always have to go through the motions of regress, get frustrated, find a new PT, have initial success, regress again, get frustrated, repeat. This will go on for months till I wise up and start thinking in a more TMS-related direction. But even then it’s a slow process to internalize it, I’m always stubborn to accept TMS. The good news with me is once I’m confident it’s TMS, symptoms tend to clear up right away, that’s all I need is the knowledge. The bad news is it takes me a long time to be convinced, and I usually need a real doctor to tell me - this often comes after spending months on wasted PT and expensive imaging. But traditionally I do really need that, I need to be reassured by somebody with proper medical authority that I’m not causing any damage by returning to training.
So anyway...I got the back stuff under control, I don’t think TMS can fool me with that again, it’s been great. Anybody here ever suffer tennis elbow as a manifestation of TMS though? I got a bad case of it right now and its just killing me. Based on what I’ve learned about it tennis elbow seems to have been designed in a lab to be uniquely torturous for TMS sufferers – almost like AIDS for someone who already has an autoimmune disorder. I first developed it a year and a half ago and I’ve had 4 major flare ups since then – this last one has been going on since december.
I saw a bad orthopedist for a while who gave me too many cortisone shots without bothering to tell me that too many cortisone shots are bad for tendons. Now the skin is all white and the fat pads have sunken, so I’m freaked out I’ve done too much irreparable cortisone-related damage to the tendon, so that didn’t help. Then I got a new orthopedist, who is marginally better for at least telling me not to do anymore cortisone, but he also told me the thing was pretty bad and might rupture one day and would likely need surgery eventually regardless. I’m very susceptible to suggestion and hate it when doctors say things like that – I once had a doctor tell me I’d for sure need back surgery and I got very depressed and had 3 more months of severe symptoms, then I saw another doctor who looked at my imaging and said “looks OK to me” and within 3 weeks I was symptom free. So that didn’t help either.
So anyway, I started PT for the elbow in January, and have simultaneously been rehabbing a shoulder sprain from last year that didn’t heal properly on the same arm – the hope being that fixing both means the whole arm will improve. The shoulder mostly has improved though it still has some work ahead; the elbow has been very up and down. My initial PT discharged me and cleared me for activity because I was symptom free for a couple weeks but as soon as I started lifting weights again I had a bad flare up, so I found a new PT. At first things with that PT went well, but she’s been pushing me lately to up the weights again and so I’m having another bad flare up and its as bad as it’s ever been – even tying my shoelaces aggravates it slightly and I just don’t know what to think about it anymore I’m beyond frustrated.
So that’s where I’m at. It’s miserable. I haven’t been able to work lately, I work with my hands and have to move heavy things so a weak and painful forearm tendon is a debilitating. So I’m running out of money and that’s stressful. Plus I have severe ADHD and absolutely need intense physical activity to regulate my brain chemistry, and when I’m hurt and can’t get it I start to spiral and ruminate, so that’s also bad. And I got pretty high anxiety right now because I was planning a big move but have had to delay it till I feel confident I can generate income again so in the mean time I’ve been stuck in limbo bumming around my mom’s house while I’m out of work and in arm rehab and am increasingly depressed about that situation. So I got a lot of stressors currently. Plus the world completely sucks right now generally and I don’t want to deal with it, so...I’m sure on some unconscious level I like having reasons to be cranky and stay home
There’s also that same pattern developing of start a treatment, then it fails, then try another one, it works at first but then fails and I get more and more frustrated, so that tracks with TMS. But then again I don’t know...the symptoms have been very consistent, and every time I try to push it a bit I get a flare up, always in the same place, it’s pretty acute. I did have an MRI on it last year, and was told it looked normal – severe inflammation but no damage, so nothing to worry about. But that was last year; it might be worse since then. I’m just scared to death of a tendon rupture - if that is in fact a real risk and not just a ghost story from a shitty doctor with bad bedside manner, but I absolutely CANNOT do that surgery on my good arm, I’ll be out of a job, maybe out of a career and unable to even wipe my own ass for months, I just can’t do it.
So...anybody have anything at all to offer? I know I can’t get a diagnosis from strangers on a forum, but what are the armchair opinions? Anyone have a similar experience they can relate? Or a suggestion of how to approach it and move forward? Anybody know of any specialists to reach out to? I would love to find another TMS doctor I can meet with if anyone can point to one or at least a list/directory so I can find one on my own. I had been living in NY and saw Dr. Rauschbaum who took over sarno’s old clinic, then after he retired I saw Dr. Gzwozds in New Jersey. I live in Pittsburgh now, I have no idea if there’s anyone around here that does TMS. I’ll drive a little if I gotta. Telehealth would be fine too if I could find someone who will do it, think they’d need to be in PA as well though. I’ll drive back to Jersey if I have to, but it’d be a 2 day trip so only if there’s no better option.
And if it DOES turn out to be TMS, then...I’m going to need some better strategies to deal with it moving forward, because apparently it’s just never going to relent.
Ok, thanks in advance to anybody who reads all this and replies.
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