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A Physician's TMS story - RSI, Hyperacusis and much more.....

WARNING: I just wrote a small novel below. I did it for you....I hope it helps. Feel free to ask me any questions.


I hope you can find your peace. I am about two months in to the TMS thing, and I am just now into day 3 with noticeably lowered back pain....nearly gone but still there. But even this improvement has blown my mind and shown me that I am no exception to TMS healing, because I was worried about that after two months of no progress. I am still not going to get too excited until at least a month has gone by and Im still doing good.

I do get what you are saying about people posting on here about feeling good, and then wondering if they were just having a few good days and then either don't get back on here to post that they relapsed, or get back on here to post that they are having a few bad days. This TMS thing is truly hard to believe....but ironically enough.....fully believing is the only way you can heal yourself and end the torture of chronic back pain.

My story: Im a normal dude, 36 year old male living in Austin TX. I grew up playing sports my whole life, hockey and soccer mostly. Ive been dealing with chronic back pain since I was 18....18 years now, which is half my life. It started when I was 18 one day when I was helping a friend move, all I did was twist to the left to set down a light box....and felt a sharp pain in my low back that progressively got worse throughout the day until I could hardly stand up and was in a lot of pain. That was the start of my downward spiral, filled with "flare ups" (what I call those painful swelling episodes that would last for a week or longer, after feeling like I had pinched a disc or something and included a lot of swelling). Flare ups have been causing me much fear throughout the years, because if I get one, it means that I will be in immense pain for at least a week, can't get off the couch, and having to miss work, pissing off my boss, coworkers....causes my wife and I to get behind on bills, etc. I work in restaurants as a server, so you can't just call out sick...the place depends on you to be there. I can't count the times I have missed work....it is embarrassing too to be known as the guy who is always in pain. Your coworkers don't care what you have going on.....nobody understands.

I used to get so mad and jealous when I would see a fat person outside running or getting exercise. How can that person with all that weight move like that, yet here I am a relatively fit guy suffering so much?

My back pain progressively got worse over the years, flare ups started happening multiple times a year instead of maybe once a year, and the pain would be worse and worse and would last longer and be harder to get over....until my back would just hurt all the time. Chronic. No more exercise. Just miserable.

I developed plantar fasciitis in my right foot 5 years ago and that flares up here and there. Ive had acid reflux problems for about 10 years that comes and goes.

The worst thing that has ever happened to me happened about 3 years ago when I developed prostatitis, inflammation and swelling of the prostate. Very very painful, and it wouldn't go away. Ive had minor pain there before, but this time it just came on strong and wouldn't go away.....nonstop suffering. I didn't have insurance so I would just go the ER. Their stupid decisions revolved around me taking very powerful antibiotics that absolutely destroyed me from the inside out....even though all of my bloodwork, CT scans, MRI's, every damn test showed no sign of infection. I was going to the ER about every 3 or 4 days, begging them to do something, but they had no idea what was going on. Sometimes I couldn't pee, I had to have a catheter for a little while....torture. I racked up over $30,000 in hospital bills......and still couldn't get an answer. The doctors were scratching their heads.

One of the strangest things that I noticed was that the pain would jump around...it was mostly in the prostate area, but would travel all around my abdomen, up to my chest where I had to have tests done for heart issues (always came back normal). Pain was always somewhere in my body but never in multiple places at once. I asked the doctors so many times about this....it was the question I asked more than anything else: WHY IS MY PAIN MOVING AROUND???

Never got an answer. The doctors were stumped.

I suffered all day and night for 3 months....eating antibiotics which destroyed my insides. I thought that if I died then it wouldn't be so bad. I would never do anything to hurt myself, I love life, but the thought of living in endless pain just becomes unbearable. It was terrifying. I was a mess. The only time I got some form of relief was when I took a scalding hot bath.......and funny enough those baths would eventually lead to the answer of what was going on with me. Let me explain.....

A friend of mine down here studies Oriental Medicine. I was talking to her about my problems one day and she asked if anything gives me relief....I mentioned the hot baths....and she said if the heat helps then it must be a MUSCLE problem. I started searching online for answers to that. My investigating led me to a whole underworld of guys who were suffering from chronic prostatitis, and there were these two doctors who had been studying this mysterious problem for a while, Dr Wise and Dr Anderson. The even wrote a book on it called A Headache In The Pelvis. Their conclusion: some guys just happen to store their stress and tension in the network of muscles and ligaments that make up the pelvic floor. These muscles constrict around the prostate and cause prostatitis. Some people store stress in their shoulders, Im one of the guys that stores it in his nether-regions. The pain started to go away about a month after my discovery. It was the sweetest relief ever. I was terrified that I was going to be like that forever. Thanks to my friend who said that heat helps muscle pain.

Ive seen multiple urologists since then who have backed this dignosis for me. I saw a urologist just a couple months ago who said that only less than 1% of guys who have prostatitis actually have a bacterial infection......the other 99%+ have a chronic stress-storing problem down there. Unreal.

Also worth noting that throughout this prostatitis episode I remember thinking how my back pain had pretty much gone away.

But as always the back pain continued.....

I had an MRI done about 5 years ago for my low back....it showed a couple herniated disks, and my L5-S1 had some degeneration. I saw one of the top spine surgeons in Austin and begged him to operate on me so I could finally lead a somewhat normal life. He showed me the MRI and said that although I do have some herniated disks, none of them were touching a nerve. He didn't know why I was in so much pain. I left feeling so depressed that I couldn't get this surgeon to cut open my spine and pull some stuff out or fuse something together....anything! Thank god he didn't.

I continued to suffer. The surgeon prescribed physical therapy which didn't help. I did acupuncture, ice, heat, blah blah blah....you know the drill. I even used some student loan money to do the Egoscue method, which is an expensive form of physical therapy where you see a therapist who studies your posture and gives you exercises that you do every day that work the muscles of your body into shape and fixes your posture problems. Egoscue helped, and I haven't had a flare up in the past year of Egoscue.......but it could never get rid of that one painful spot on my low back. That one damn spot. To the right of my spine on my pelvic bone. That damn spot that would never go away no matter how good I was feeling.

Im in school for computer programming, Im on the computer a lot. I developed a pain in my right hand last January (5 months ago). That pain spread all over my hand, to my wrist. I diagnosed myself (correctly) with having a Repetitive Strain Injury (RSI). I started using the mouse with my left hand.....the same pain spread to that hand and all over that wrist. The pain would move up into my forearms and would hurt so bad that I would go get massages just on my forearms alone. My masseuse was puzzled.

I saw an orthopedic doctor, he gave me a cortisone shot in my right wrist.....didn't help. Saw him again and told him the pain was in both hands and would move around and back and forth but never really in both hands at the same time. It would take turns. This animal of a doctor was like "well, lets just shoot up the left hand with cortisone". Yeah asshole, lets just shoot up my whole body. He was your typical American doctor, didn't think or listen, ready to just shoot anything up with a needle full of drugs. He probably kept a needle in a holster on his hip, at the ready. I refused his shot but did try out a strip of Prednisone ( a steroid).....didn't help.

I got really depressed about it. My future as a computer programmer, the thing I had been studying and racking up student loan debt for was now going to go to waste. I need a job that is easy on my back, sitting and/or standing hurts it, and one that I don't have to use my hands. Hmmmmmmm..........I got nothing.

ENTER SARNO.

In my desperation, I googled "RSI hand pain that moves from hand to hand". I found the blog of a guy who worked for Google, and had the same exact story of mine. Programmer, hand pain started in right, moved back and forth to the left, moved all over. He saw some of the worlds top surgeons, tried every treatment possible to no avail. A friend suggested the MindBody Prescription and his 2 year RSI was gone in 2 weeks.

I found my answer.

Now, I had heard of Sarno before, and had seen numerous posts in forums throughout the years from my numerous health issues, stories of people who were claiming to have been cured of this or that after reading Sarno's books.....and I always just thought it was bullshit. How could you not? I had accidentally even bought Healing Your Back Pain about 7 years ago, before getting home and reading the first chapter and putting that bullshit down. MY PAIN WAS REAL. Not in my head.

It took me reading that Google guys story (and no other option left) to realize this could be the answer to my problems. His page also had a link to Harvard's study of RSI's and Sarno's work....on it was a 10 question quiz to see if you could have TMS....one of the questions: do you have a history of prostate issues or prostatitis?

DING DING DING! WE HAVE A WINNER!

I was finally convinced that I had my answer. I stayed up all night reading success stories, I found the TMS wiki. I laughed and cried at the same time, as I had finally found my damn answer. It had been there all along. I fit the personality type for TMS perfectly....it desribes exactly who I am. In April I made an appointment with Dr Sklar (a TMS doctor in Fort Worth TX, who worked for a while under Dr Sarno), and he confirmed that I have TMS through a series of physical and mental tests. I knew it. Still somewhat hard to believe.

My 5 month long RSI hand pain was reduced by 50% in a couple days. It went completely away until the stressful end of my school year in May, which coincides with the busiest time of year at my work. Super stressful. After that was over though it kept getting better. I have been writing this story now for maybe an hour and a half, I have a little bit of pain in my right hand. If I had tried this 2 months ago, I would've been able to write for maybe 5 minutes tops. Back then, the pain would start as soon as I touched my keyboard. So things are definitely improving, and up until I discovered Sarno things were getting progressively worse and worse. Im feeling great in my hands, but not at 100%......I would say 75% better though. I don't expect it to go away overnight.

The main problem is the back pain. After reading Healing Your Back Pain, my back pain was unchanged. I started reading the MindBody Prescription a couple weeks ago, and again no relief in back pain.

Today is Tuesday, I finished reading The Mindbody Prescription late last Saturday night. I woke up Sunday and throughout the day I noticed that I pretty much had no back pain.....90% pain free. I told my wife about it and said I wasn't going to get to excited yet, but thats what was going on. How funny it would be, I thought, that my back pain waited to go away until I finished reading the book. How ridiculous. But thats what happened. I thought that pain free Sunday was a fluke, a good day, but I don't have "good days".....as in ever. That one spot, that one damn spot....was always hurting no matter how good of a day I was ever having.

But that one spot, that one damn spot, is still hardly noticeable and its been 3 days now. Its only 3 days, but for someone who has had chronic low back pain and specifically that one damn spot for as long as he can remember......3 days is an eternity. Ive been running a mile a day for the last 3 days. Before, if I ran for two minutes then I would be hurting for a week. I don't run.....until now, that is. If I want to run then I am going to run. I know what is going on and Im not scared anymore. Ive been lifting weight the past couple of weeks, pretty intensely too, and even that would have been impossible in the past. This is the greatest discovery of my life. It's still early, so maybe I will keep posting an update to see how I progress....or you can feel free to hit me up if you need a confidence boost. Im a normal dude, and my story is real. I almost can't believe it, and I won't be able to fully believe it until enough time has passed. I was excited when these books and stories helped my RSI, got worried when my back pain was still there, but now that my back is seeing improvement......I am utterly blown away that it is happening to me. If this fixes me, I will make it my life's mission to spread the word in hopes of saving others from misery and depression.

MY ADVICE TO YOU

First, and most important, you have to fully 100% know that your brain and psychological issues are causing your pain. The pain is real, it's just being caused by unknown forces. YOU HAVE TO KNOW THIS IS WHAT IS GOING ON.

The thing I read that changed my mind on this, and I can't remember where I read it, is that stress and tension narrow your blood vessels, this is scientifically known, and that when your blood vessels get narrowed, not enough blood is getting to certain parts of your body....this causes pain. Stress is dangerous. Stress causes heart attacks. Stress causes a certain someone to suffer chronic prostatitis. Stress causes people to have a mental breakdown. Stress is a killer....and if stress can cause all this, its not far fetched to think that it could cause some back pain.

Our bodies are amazing, and they are amazing at healing and regenerating....it's just what it does. If you break a bone in your body, it is healed in 6 weeks, and the pain only lasts a couple days. Why would some mysterious back pain, that doesn't show anything on MRI's and CT Scans, cause pain for 18 years????

If its nerve pain, then the nerve would've gone dead a long time ago. It just doesn't keep going. Something else has to be going on.....and it's called TMS. Im convinced of it.


Dr Sarno says that knowledge is the penicillin of TMS. That means reading about it, and reading about it, and re-reading about it. Learning and learning and having this knowledge become part of your being. THIS IS VERY VERY IMPORTANT. I cant stress this enough. You have to immerse yourself in this culture. Have no doubts that it is anything else but TMS. You will not get better until this happens. You can't get better until this happens. Judging from your post, you haven't fully accepted this. You have to stop all treatments for back pain too....acupuncture, physio, etc.

Just read and read and read. And when you're ready, start a journal and try to discover what repressed emotions you might have. This is where I am at....I just started journaling last night.

You just have to believe. Everything depends on that.

Im done here. Hit me up if you need support....we can work on it together. Good luck.
 
Beezy,
Thank you so much for writing your story down. You have been through so much. I'm so happy for you that you are turning the corner. It is vey empowering when you start to make progress and realize where the key to recovery lies.
Keep us all posted.
Alicia
 
Beezy I feel like we are brothers from another mother!!lol
Only I was 25 when I bothered to question the pain 'experts' and discovered Sarno, it truly is a life changing initial moment but that first epiphany can be replaced by fear when the pain doesn't go away instantly . I'm finding it really difficult to try and get family and friends to conceptualise what I am going through.
I know my main issue but feel powerless to overcome it, it truly is a battle for your life!

I like to think of this whole experience as the Pebble process. I am currently thrashing around the around getting chunks taken out but by the end I will be smooth and the bumps will be gone! :D
 
Thank you for this. I am not at the point of giving up yet, although sometimes I do get the wind taken out of my sails when my pain acts up.

I relate to what you are saying about going in to a surgeon and begging them to operate. That was my mentality the first time around. These authoritative doctors on the cutting edge of medical technology were going to run a few tests, find out my problem and fix it. So needless to say, that turned out to be a bitter disappointment. I realized I was all alone then and no one could fix me. It was just so crushing.

I actually just went into a doctor today. I haven't been to one in the better part of a year since it all failed so badly when I was first in pain and I've accepted the TMS explanation. I only went in today specifically to get bloodwork done to see if I have rheumatoid arthritis. That is one of those things TMS can't fix (as I've read Sarno himself say).

The doctor I went to see is someone I trust who I have been unable to see ever since my pain started because of insurance issues. I was excited to get the insurance issues resolved and go back to him and see what he had to say about all this. He took one look at my scans, poked at my body here and there and just flatly said "You don't have RA. Doing blood work will be a waste of time. What you need is better physical therapy. Go to my guy and he will sort you out. Your last PT was a hack and you just need someone better."

I have to admit I got excited and have made an appointment. I had given up on all physical cures and even now I'm not placing faith in PT curing me. But as my doctor told me, not all PT is the same. You need a real expert and not just some hack to get fixed up. We will see. It could fail again, but it's true my first attempt at PT was pretty half assed.

I still believe in TMS, but the truth is my body is not the same as it was two years ago. I have lost mobility and strength. I have desperately wanted to get stronger and more fit just in general, but my pain stops me from vigorous exercise. I could use the PT just as a way to get stronger under a medically supervised and encouraging environment. I will go to the PT but I will take it with a grain of salt. I will not think of it as a salvation, but just as another tool. And I will continue to try to push through psychological barriers in the meantime.
 
Thank you for this. I am not at the point of giving up yet, although sometimes I do get the wind taken out of my sails when my pain acts up.

I relate to what you are saying about going in to a surgeon and begging them to operate. That was my mentality the first time around. These authoritative doctors on the cutting edge of medical technology were going to run a few tests, find out my problem and fix it. So needless to say, that turned out to be a bitter disappointment. I realized I was all alone then and no one could fix me. It was just so crushing.

I actually just went into a doctor today. I haven't been to one in the better part of a year since it all failed so badly when I was first in pain and I've accepted the TMS explanation. I only went in today specifically to get bloodwork done to see if I have rheumatoid arthritis. That is one of those things TMS can't fix (as I've read Sarno himself say).

The doctor I went to see is someone I trust who I have been unable to see ever since my pain started because of insurance issues. I was excited to get the insurance issues resolved and go back to him and see what he had to say about all this. He took one look at my scans, poked at my body here and there and just flatly said "You don't have RA. Doing blood work will be a waste of time. What you need is better physical therapy. Go to my guy and he will sort you out. Your last PT was a hack and you just need someone better."

I have to admit I got excited and have made an appointment. I had given up on all physical cures and even now I'm not placing faith in PT curing me. But as my doctor told me, not all PT is the same. You need a real expert and not just some hack to get fixed up. We will see. It could fail again, but it's true my first attempt at PT was pretty half assed.

I still believe in TMS, but the truth is my body is not the same as it was two years ago. I have lost mobility and strength. I have desperately wanted to get stronger and more fit just in general, but my pain stops me from vigorous exercise. I could use the PT just as a way to get stronger under a medically supervised and encouraging environment. I will go to the PT but I will take it with a grain of salt. I will not think of it as a salvation, but just as another tool. And I will continue to try to push through psychological barriers in the meantime.


Thats great that it turned out not to be RA! Congrats on that!

Funny enough...the night I discovered that Google guy's story (the one that convinced me that I have TMS)....that night I had convinced myself that I have RA because: I felt like I had arthritis for one, and for two I read that RA attacks both sides of your body. If you have pain in your right foot, then your left foot will also have pain. I was convinced I had RA, and I got online and read horror story after horror story and convinced myself that I was going to be living a life of agony and hardcore medication. That same night my hands hurt more than ever before....the stress and worry was causing it, I would later find out. I would do a routine of cold then hot. I kept a huge bucket of water in the bathroom that I would fill with ice, and then fill the tub with hot water.....and would alternate dunking up to my elbows in each. I usually got short term relief from this. After reading about RA that night, even the hot and cold technique couldn't help. I was mortified.

And then I found Google guy's story.....and my journey of TMS began.


Take what I am about to say how you will....as obviously I am no expert in this TMS stuff....but I have dedicated almost all my free time over the past two and a half months or so reading about it, and thinking about it, and reading success stories. One of the main things you have to do is to:

STOP ALL ACTIVITIES RELATED TO TREATING YOUR BACK AS AN INJURED BACK WITH SOMETHING PHYSICALLY WRONG WITH IT. Those aren't my words, those are John Sarno's words. Im sure it's hard to believe a guy like me who is so new to this game.....but it is one of the main things that Sarno talks about. As long as you are treating your back as an injured thing, with a structural abnormality......you will not get better. Im sorry to put it like that, and I know you are hurting, but you have to give up all treatments that treat your back like there is something wrong with it.

I understand that you want to treat this PT as using them to just help you work out and get in shape, but they aren't going to treat it like that....they are going to treat you as an injured person with an injured back and they need to gently get you back into shape. Your brain will still be winning as long as you are staying in the realm of an injured person. And again, not to sound harsh, but as long as you are wanting to try stuff like this tells me that you haven't fully, 100%, beyond a shadow of a doubt, accepted TMS as what is going on with you. And you will not see any improvement until you forget all those forms of treatment, 100% fully ACCEPT that you have TMS, and read and read and read about TMS. Just read nonstop about it. Information is the key....it is the answer....it is the penicillin for your suffering.

But who am I to advise you? It's your life, and maybe this is just something you need to try out. So try it out.....but if it doesn't help, then you know what you need to do. Consider it as something you need to mark off your list as stuff you've tried out. You can only fully be ready to accept TMS when you are ready, and that may mean trying out all kinds of stuff until TMS is the only thing left.

I talked about the Egoscue physical therapy that I did. Well, after I discovered TMS and read about how you have to give up all treatments related to your back pain, I walked into my next appointment with my Egoscue therapist and told him that I was going to be stopping Egoscue....I was going to be stopping the exercises that I had been spending an hour on every single day....I was going to be stopping the treatment that I had shelled out $2500 for, and I still had 5 visits left on my package that might be going to waste. I stopped all that because Sarno emphasizes that over and over and over. I trust in this stuff....and I took a leap to do it right. So far it seems to be working. I just ran another mile today, and I still have very little pain. It just feels different....it feels like something is going on....and it's good.

Again, you can't take my words for it.....you can only come to this conclusion on your own. If anybody else could chip in Im sure they would say the same thing.

But try what you must and see how it goes. I hope it works for you, I hope it does what it was meant to do. But if it doesn't, I hope you can fully get into the TMS thing and see where that road takes you.
 
Thats great that it turned out not to be RA! Congrats on that!

Funny enough...the night I discovered that Google guy's story (the one that convinced me that I have TMS)....that night I had convinced myself that I have RA because: I felt like I had arthritis for one, and for two I read that RA attacks both sides of your body. If you have pain in your right foot, then your left foot will also have pain. I was convinced I had RA, and I got online and read horror story after horror story and convinced myself that I was going to be living a life of agony and hardcore medication. That same night my hands hurt more than ever before....the stress and worry was causing it, I would later find out. I would do a routine of cold then hot. I kept a huge bucket of water in the bathroom that I would fill with ice, and then fill the tub with hot water.....and would alternate dunking up to my elbows in each. I usually got short term relief from this. After reading about RA that night, even the hot and cold technique couldn't help. I was mortified.

And then I found Google guy's story.....and my journey of TMS began.


Take what I am about to say how you will....as obviously I am no expert in this TMS stuff....but I have dedicated almost all my free time over the past two and a half months or so reading about it, and thinking about it, and reading success stories. One of the main things you have to do is to:

STOP ALL ACTIVITIES RELATED TO TREATING YOUR BACK AS AN INJURED BACK WITH SOMETHING PHYSICALLY WRONG WITH IT. Those aren't my words, those are John Sarno's words. Im sure it's hard to believe a guy like me who is so new to this game.....but it is one of the main things that Sarno talks about. As long as you are treating your back as an injured thing, with a structural abnormality......you will not get better. Im sorry to put it like that, and I know you are hurting, but you have to give up all treatments that treat your back like there is something wrong with it.

I understand that you want to treat this PT as using them to just help you work out and get in shape, but they aren't going to treat it like that....they are going to treat you as an injured person with an injured back and they need to gently get you back into shape. Your brain will still be winning as long as you are staying in the realm of an injured person. And again, not to sound harsh, but as long as you are wanting to try stuff like this tells me that you haven't fully, 100%, beyond a shadow of a doubt, accepted TMS as what is going on with you. And you will not see any improvement until you forget all those forms of treatment, 100% fully ACCEPT that you have TMS, and read and read and read about TMS. Just read nonstop about it. Information is the key....it is the answer....it is the penicillin for your suffering.

But who am I to advise you? It's your life, and maybe this is just something you need to try out. So try it out.....but if it doesn't help, then you know what you need to do. Consider it as something you need to mark off your list as stuff you've tried out. You can only fully be ready to accept TMS when you are ready, and that may mean trying out all kinds of stuff until TMS is the only thing left.

I talked about the Egoscue physical therapy that I did. Well, after I discovered TMS and read about how you have to give up all treatments related to your back pain, I walked into my next appointment with my Egoscue therapist and told him that I was going to be stopping Egoscue....I was going to be stopping the exercises that I had been spending an hour on every single day....I was going to be stopping the treatment that I had shelled out $2500 for, and I still had 5 visits left on my package that might be going to waste. I stopped all that because Sarno emphasizes that over and over and over. I trust in this stuff....and I took a leap to do it right. So far it seems to be working. I just ran another mile today, and I still have very little pain. It just feels different....it feels like something is going on....and it's good.

Again, you can't take my words for it.....you can only come to this conclusion on your own. If anybody else could chip in Im sure they would say the same thing.

But try what you must and see how it goes. I hope it works for you, I hope it does what it was meant to do. But if it doesn't, I hope you can fully get into the TMS thing and see where that road takes you.

I am just not sure sometimes. I can't even start the PT for a couple weeks because this particular therapist happens to be going on vacation.

The thing is, over the past year and a half, my pain has gotten better. Then worse. Then better again. Then worse than before. Then completely gone! Then back again in a few weeks. It is exhausting. I feel like I tried the stopping all physical treatments thing before and I was still not able to get out of pain.

I have read healing back pain, the mindbody prescription, to be or not to be pain free (marc sopher) and am currently working on the great pain deception and the divided mind. I feel like I could write my own TMS book at this point. I see them go over the same points again and again. I have a really firm grasp of the concept. But it just doesn't take.

I just can't break the mental barrier. At times I have felt really convinced there is nothing wrong with me. It has felt like a white light moment. But it just doesn't last. One day I go to sit up out of bed and feel that old familiar throbbing around my illiac crest as weight is applied to it. And my heart just sinks.

Today I am in worse pain than I've been in a while. Probably because of the stress and worry, as well as the old idea that maybe it's physical creeping back in. Maybe I never even should have gone to the doctor.

Thank you for listening though. It means a lot.
 
@mirepoix , I feel that "mental barrier" that you describe from time to time, too. I have the knowledge and know what I need to do, but I can't make the leap to actually doing it. To me it is like being in a rut where spinning my wheels just makes it worse. Perhaps this is the feeling of being stuck in old neural pathways and not having the will or energy to forge a new one. What helps me at these times is to stop thinking about it---all of it--my pain, TMS, my life story, etc. and just live. It's counterintuitive, I know. We have a problem, so we try to think harder to solve it. But sometimes you just have to stop thinking, and let all the knowledge you have acquired seep into your unconscious. Take a break from it all. Try to find some joy in life. Be good to yourself and those around you. Just be.
 
Breezy - thanks for this excellent post. You should copy this and create a separate thread so it gets the attention it deserves. I too suffered for many years and like you, felt giddy when I discovered Sarno because I instinctively knew I had stumbled on the answer to my pain. The excitement you felt dissolved the fear you had for many years, allowing healing to begin. For me I recall enormous relief that I could heal myself and get off the medical merry-go-round. My Dr Sarno discovery came at a time when I was ready to accept TMS, and I felt empowered; having previously resigned myself to just coping/living with my pain.

I'm delighted for you - thanks for sharing.

Alicia thanks for your wonderful contribution here. It will help countless sufferers.

Mirepoix, TMS healing takes time, but importantly don't calendar-watch because this adds to frustration. Embrace TMS healing 100% and do the mental work to settle your tired nervous system down. This is something you need to work at every day...affirmations, post-it notes, mirror work (yes, talk to yourself) - whatever you can connect with - embrace it now and don't beat yourself up - us TMSers are experts at that, but it's that trait that gets us in a TMS pickle and hampers healing. Have faith in TMS healing because it's the truth.

Irish - I notice on this and other posts that you long to have your family and friends acknowledge and understand what you've been going through. Accept that they possibly will never understand. It frustrates me that my Dad and some of my sisters suffer with TMS, yet they will never get it - despite me showing them my story on the wiki. Just accept their resistance or lack of understanding, and use that energy on you and healing.
 
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I am often asked what “my story” is. Everyone who has suffered from Tension Myositis Syndrome (TMS) or a Psychophysiologic Disorder (PPD) has a long, tortuous story to tell - that is, if they are lucking enough to have found a TMS-trained physician or therapist who has helped them step off the Merry-Go-Round Epidemic of Chronic Pain in the 21st Century.

So, I’m posting “My Story” today. My goal in posting such an honest account of my experience is to allow others who suffer from TMS/PPD a window into another’s experience, so that they may see themselves and find hope that they too can recover. PPD is a trickster. It can make you believe you will never get better, that every one will get better but you. Often, it helps to see that someone else had the very same symptom and recovered.

I can’t say when my story began. As I look back, there were signs in my childhood that my body was crying out. But, the big problems that I could no longer ignore started in 2003 while working in a fast-paced, high stress medical practice - too little time with patients, too much time at the computer and doing paper work, too little sleep. I developed pain in my elbows which quickly blossomed into disabling “repetitive strain injury” which resulted in my having to stop work. For the next 10 years, I stumbled from treatment to treatment trying to figure out what was wrong with my arms and meanwhile, collecting more symptoms as time went on. Well-intentioned practitioners offered me their expert treatments, doing their best to help me, to no avail. Some treatments would help for awhile, but the symptoms would always return - or would go away only to make way for another, new symptom to appear. I was only able to return to work for brief stents, ultimately being brought to my knees again by the intense computer usage - or so I believed. I spent a great deal of money trying to find the answer since most of my care occurred in the alternative medicine world. It was exhausting. It was devastating. It was terrifying. It affected every aspect of my life - my work, my family, my marriage, my social life, my health. I could list all the things the pain prevented me from doing, but just know that every aspect of my life was adversely affected. Eventually, one of my physical therapist referred me to Dr. Howard Schubiner’s website, www.unlearnyourpain.com . I am eternally grateful for this. I knew immediately that this was my problem - my mind was causing all of these physical symptoms. Even with 9 years of medical training in both psychiatry and internal medicine, this never occurred to me. What a huge relief it was for me to find someone who knew the truth, to tell me the truth ! This affirmed my experience and gave me a way forward - a way home. Considering what I had gone through the prior ten years, the treatment was a cake walk. Though it took time to undo all the fear and autonomic nervous system activation I had built up over a lifetime, recovery was steady. In a year, I began training for my first triathlon which for me, was a celebratory marker for my healing.

Below are the TMS symptoms I had and the treatments I underwent. The quotes contain diagnoses I was given.


My TMS Symptoms:

Bilateral forearm pain, tingling, numbness, subjective weakness (“repetitive strain injury”)
Trapezius/neck muscle tightness, swelling, tingling, sensitivity to touch (“long neck syndrome”)
Tinnitus
Hyperacusis (sound sensitivity)
Ear pain, popping, pressure changes
Temporomandibular Joint pain (“TMJ”)
Teeth sensitivity
Jaw clinching resulting in multiple cracked teeth
Tension headaches
Upper back muscle spasm
Lower back muscle tightness
Buttock Pain (“sacroiliac joint pain” and “pyriformis syndrome”)
Lower back and leg pain (“sciatica”)
Ankle pain (“peroneal tendonitis”)
Knee pain (“chondromalacia patella”)
Femoral Muscle strain
Ham string strain
Achilles tendonitis
Plantar Fasciitis
Rectal muscle spasm (“endometriosis”)
Constipation
Nighttime urinary frequency
Skin Rashes
Multiple food sensitivities
Eye twitches
Bilateral hand tremor
Chronic cough
Dizziness
Generalized Anxiety
Panic Attacks
Insomnia


Workups, specialists and treatments I underwent:

Orthopedic Surgeon - normal lab work, nerve conduction studies, and cervical MRI
Neurologist
Ear, Nose and Throat specialist
Psychiatry
Dentistry - retainer
Acupuncture x 3 different practitioners
Alternative medicine physician x 2 - prescribed bio-identical hormones, vitamins, supplements and herbs
Physical Therapy x 4 different practitioners
Massage - several practitioners over the years
Myofascial Release x 2 different practitioners
Non-TMS Psychotherapy
EMDR
Mindfulness Meditation and Yoga
Food Sensitivity Antibody Testing - I was told I was sensitive to 13 different foods. My diet became impossible.

What I find most concerning about this experience is that it not unusual. Many people suffer from chronic pain today and they are all on the Chronic Pain Merry-Go-Around - cycling through the hope and disappointment over and over again with each attempt at a new treatment.

My goal is to reach as many chronic pain sufferers as possible - to help them step out of the pain-hope-disappointment cycle and get back to the lives they left behind.

Alicia B. Batson MD
Center for the Treatment of Psychophysiologic Disorders, PLLC
2021 Richard Jones Road, 340B
Nashville, TN 37215
615-788-3557

http://aliciabatsonmd.com/

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Alicia, Thank you for your post. It really helped to hear your story. Without people sharing their symptoms, I would not be doing so much better. When I am fully recovered I will be sure to do the same.
 
Hi, I have recently started seeing a tms therapist for chronic neck pain and headaches. I have also developed tinnitis the past few months. I also believe that I now have symptoms of hyperacusis and you are the only person on the board that also listed this symptom. It is really scary and I would love to get more info on your symptoms of it and if it went away with your other tms symptoms. It is really starting to scare me.
 
Hi lasleysl, I am so sorry you are going through all of these symptoms. I just wanted to share with you that I have had many symptoms associated to tms including head pain, neck pain, muscle twitching and anxiety. I found a link to Dr. Joe Dispenzas meditation on the forum 3 weeks ago and his teachings have made a dramatic difference in my recovery. The meditation alone was not the most helpful at first, but once I watched and listened to many of his interviews and seminars on youtube it really started to help me. I attended his weekend workshop and I am now almost symptom free! I sincerely hope his work will help you too. I know how tortuous fear can be. You will find your way, keep searching and learning.
 
Hi, I have recently started seeing a tms therapist for chronic neck pain and headaches. I have also developed tinnitis the past few months. I also believe that I now have symptoms of hyperacusis and you are the only person on the board that also listed this symptom. It is really scary and I would love to get more info on your symptoms of it and if it went away with your other tms symptoms. It is really starting to scare me.
Hi lasleysl,
Yes, hyperacusis can be very difficult and life-altering. Mine went away completely with all of my other symptoms once I did the emotional work, learned to turn off my fear thoughts and self-destructive thoughts and ultimately calm down my autonomic nervous system. The TMS Recovery Program by Alan Gordon on this website was critical to my recovery. It gradually got better over some months and then was gone.
 
Hi Alicia Just come across your post as I am trying to do something as a practitioner for others what I never received myself. i.e. an understanding of TMS or MindBody syndrome as Howard Schubiner calls it (and his book 'Unlearn your pain' is a great self-help starter for people who can't yet afford or don't want to work with a practitioner. My story is similar although my physical symptoms were more like fibromyalgia/ chronic fatigue with all over joint pain, extreme fatigue, anxiety, insomnia, etc, etc.

I suffered for about 2 years before I got help - and then (we're talking around 2000) the only thing on offer was anti-depressants, painkillers and other drugs to suppress symptoms. My 'a-ha' moment was going for counselling and finding out I hadn't dealt with the loss of my father 15 years before. Coupled with the recent loss of my relationship and my A-type personality style, I was driving myself into the ground. Seems like quite a few of the correspondents on here are similar. My realisation was to work on admitting to myself I was lonely and I was in conflict with myself for not wanting to admit I was lonely (having always been the 'strong one' in my family.

I now offer TMS treatment to people in the UK and elsewhere (by Skype) via journaling, and a specialist trauma transformation programme using hypnotherapy/ EFT (Emotional Freedom Technique) and EMDR (Eye movement desensitisation) all of which help considerably. Although not medical, I was a biochemist and health researcher for many years and very steeped in the scientific model so this has been a really big leap for me. . I am just about to publish a book which details my story because I thought maybe it's more powerful when it's someone who has been sceptical and now sees the truth of this - I also include a lot of the science too so people can see why this happens. I've got a trauma and chronic pain survey on this site too for anyone who would like to take part in scientific research.

Anyone out there who is looking for help - don't think about it just do it. Get yourself skilled in the understanding that virtually all of the chronic syndromes we see are learned responses to trauma by the brain. We can unlearn them but we need to do the work. Well done Alicia for being honest and showing us that no matter what your background, experience or levels of expertise you can do something... Good work!
 
Thanks pworby for your post. It sounds like you have accomplished quite a lot and are helping many people. I tell patients that TMS is the best diagnosis to have because it is fully treatable. If you haven't already posted your story, it would be very helpful to do so. I find that those with fibromyalgia and chronic fatigue are some of the most resistant to the diagnosis and can have a harder time recovering. Your story would be inspiring I'm sure. Best to you !!
 
I've just uploaded my story (highly shortened version) Sorry I didn't sign off with my full name. I'm a newbie on the site! Patricia
 
Yes Fibro/ CFS have been described as the 'poster children' of TMS type syndromes. They get quite deeply rooted in the pain cycle and people get stuck there. it seems the medical profession aren't helping either as the prognoses for these modern diseases are so poor. People are basically told, it's for life get used to it. I try to get them out of that frame of mind but it's an uphill battle because not only modern medicine but also the online support groups support the idea its incurable. hence I can only help a small proportion of people who are willing to believe they can recover. It's so important to start with that belief.
 
Yes Fibro/ CFS have been described as the 'poster children' of TMS type syndromes. They get quite deeply rooted in the pain cycle and people get stuck there. it seems the medical profession aren't helping either as the prognoses for these modern diseases are so poor. People are basically told, it's for life get used to it. I try to get them out of that frame of mind but it's an uphill battle because not only modern medicine but also the online support groups support the idea its incurable. hence I can only help a small proportion of people who are willing to believe they can recover. It's so important to start with that belief.

This is the great tragedy of modern medicine and one many Doctors should be embarrassed about. it highlights the growing disconnect between Physician and Patient only aided by the internet and people trying to self diagnosis or find hope elsewhere.
My pain specialist(third one) told me its just a part of life for some people and didn't offer any indication there may be a psychosomatic element at all.
Incredibly discouraging and no wonder depression and suicide is a major risk factor for those with chronic pain.
 
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