Healing Back Pain: The Mind-Body Connection Mass Market Paperback – February 1, 2010

I have read every Sarno book multiple times as well as listened to the audio versions of each many times. I truly believe his TMS theory is spot on. I wanted to share my story because I believe it aligns with everything he describes. I also know that I benefit from reading other people's reviews when they share their personal experiences with chronic pain and TMS because it helps strengthen my belief in TMS when I hear others just like me. I hope this helps someone. So here is my story. It is VERY long, but nobody is making you read it! I believe the details are all very relevant to my complete chronic pain story.I am a 43 year old male with a long history of continuous health issues for the better part of the past 25 years of “adulthood”. Only recently have I realized that these might all be related and the result of a deeper stress/tension induced psychosomatic issue. I have read 100’s of similar stories of people with “TMS” or other stress induced disorders over the years, and I believe my symptoms and traits perfectly match the typical profile.Summary of my personality traits: perfectionist, overachiever, people pleaser, want to be liked, want recognition/approval/validation, chronic worrier, anxious.Probable sources of unconscious anger & fear: years of constant, relentless worrying about career and job security, afraid of failing in my education or in my jobs, fear that work is too hard and I won't be able to handle it, fear of losing my loved ones, guilt/shame, messes/disorder (neat freak), and frustration over my chronic health issues.At the end of this, I will talk about my latest issues and current battles with all of this, but first, here is a summary of my history that may put things in better context:1974-1992: Childhood through end of high school. Perfect childhood, parents, family, and middle class life. No traumas- physically or emotionally. Driven, perfectionist, afraid to fail. Graduated 2nd in my class of 300 students in school. Put a lot of pressure on myself to be “the best” and make everyone happy and get praise and admiration from people.1990’s: Developed Allergies. Controlled by shots & medications. (mold, pollen, dust)1992: 18 years old and started college. Chemical Engineering student and member of rowing team. Difficult courses and studies, and very busy schedule with sports. Started to develop constant sore throats and “sinus infections”. Many months of every kind of antibiotic. Always sick.1993: Had tonsils removed. Sore throats were better, but still always getting sick.1993: For 6-9 months had what was diagnosed as Carpal Tunnel syndrome from one really long day scooping Italian ice non-stop for 10 hours in my summer job.1994: Sinus surgery. Stopped getting sick as much.1994: After feeling a “pop” and a jamming feeling in my lower back while on a rowing machine one day, I had an “injury” and Back Pain for the first time in my life. Until then, I was in great physical condition with strength training, running, and rowing almost daily. From that day, I developed chronic low back pain which lasted 2 miserable years.-Pain was in lower back. Mostly on left and right sides of spine in the small of the back in the boney parts around the Hip/SI joint areas. Sometimes pain would be bad in the center and hurt to touch the spine, but also moved side to side throughout the day. Pain never went into legs or any numbness/tingling/burning. It was a constant, dull, but torturous aching. The pain was the worst when sitting. I couldn’t sit for a minute. I spent two years of college with an ice pack on my back to get through class to numb the pain. It also hurt to stand for too long. The only relief was walking or lying on my back, but even that hurt to some extent.-The only thing that helped with the pain was ice (which just numbed it temporarily) and Ultram (tramadol) which I lived on like candy for 2 years.-I had X-Rays, MRIs, CT Scans, Nuclear Bones Scans, and went to probably 8 different co-called “best doctors” in FL and NJ. Nobody could find anything wrong on the images or exams. Best they could say was “soft tissue” inflammation or strain.-I did months of Physical Therapy with stretching, core strengthening, walking, stairs, massage, heat/ice, and TENS unit.-I tried acupuncture (at two different places) and 3 or 4 different chiropractors in NJ and FL.-Nothing ever helped and the pain was 24/7 causing so much rage and frustration, Depression, and hopelessness. I wanted to die every day. It was so hard to go to class all day, study Chemical Engineering, and my life (which was supposed to be full of possibilities) was upside down and miserable.-Cortisone injections didn’t help, nor did any other OTC NSAID or Rx medicine.-I did meditation and self-hypnosis.-Found out about Dr. Sarno and TMS, and read all of his books at the time, and was 100% convinced I had TMS! As an Engineer with a logical, rational mind, it made perfect sense to me. Unfortunately, I was just unable to undo the pain even the slightest bit.1996: A “so-called” top in the nation spine surgeon in North Jersey (Dr. Casey Lee) said my L3/4 disc was destroyed. He said I probably broke the vertebrae above (or below?) the disc when I “injured” it that day, and the broken bone probably destroyed the disc. Nothing bulging or herniated, but rather he said the disc has small nerves in the annulus and that was causing the pain which was “referred” to the area a few inches below it in my back. He performed a discography(discogram) the confirmed his diagnosis. For the first time I had hope that someone figured it out, and I was confident this was the answer. He proceeded to perform a discectomy and interbody spinal fusion (no metal, just hip bone graft). I had to take off a semester from college and took about 4 months to recover before I went back to finished my final semester before graduation. The surgery was a success by every measure. In fact, recent MRIs this year (2017) were reviewed by a chiropractor, and he said that he and his partner have reviewed 1000’s of MRIs over the decades, and this was by far the most impressive fusion they had ever seen!1997: I went back to college after the recovery, and slowly rebuilt my strength and was in great shape again. For the next 20 years, I was pain free (for the most part). I definitely thank Dr Lee for the surgery. It was a success both medically and for getting rid of my pain. I was pretty much able to do anything, but I was always cautious not to lift anything too heavy. I did however lift weights regularly for years with no problems.A few times over the years, I would have the occasional back spasm or muscle strain that would go away in a few days. No big deal.A couple times over the years I had pain very similar to the pain that I had prior to my fusion surgery, which made me wonder- how could that be possible? How could I have the SAME EXACT pain in the SAME EXACT location if the problem (the disc) was removed? After a week or two, I got worried, and I immediately read Dr Sarno’s books and people’s reviews on amazon all day for weeks, and I was convinced it was TMS. Eventually the pain went away. That had me 100% a believer in the TMS diagnosis now. This made me think I probably never even needed surgery. Was it just a placebo? I couldn’t change the past, so I didn’t dwell on that thought to much.2001- 2008 – I had a lot of career changes and stressful jobs during this time. Always still trying to be perfect and successful (like I was “supposed” to be). Always fearing losing my job as the main income provider in my family (with a wife and 2 small boys). I was in the computer/tech industry which was constantly downsizing and laying off people every few months. Lot of worrying and stress daily from that.2006/2007: After 15 years of contact lenses, I developed Dry Eye Syndrome and have never been able to wear contacts since.2008: Fell into a severe depression with anxiety. Spent 4 months on long term disability. Tried every antidepressant, anti-psychotic, anti-anxiety medicine in every class of meds. Eventually got better and returned to work. Been on antidepressants ever since then.2010-2012: For about two years, I had a constant strange Stomach “tension” or nervous/butterflies feeling. Nothing would relieve it. No medication or therapy. It was not painful at all. Just a strange feeling of nervousness in my stomach which was distracting and uncomfortable. It felt like nerves. Doctors said it was not a digestive issue.2012-2014: For no reason, out of nowhere one day, I got terrible Elbow Tendonitis pain, and the stomach issue went away! I never did anything to injure the elbow. Pain was awful. Couldn’t even lift a gallon of milk. Did a few months of PT everyday with no improvement. Spent two years getting many cortisone shots in my elbows. Elbow(s)? Oh, did I forget to mention that the pain would go away after a cortisone shot and then my other elbow would hurt just as bad a couple of months later!!! So I would need a shot in that elbow! This went back and forth from elbow to elbow, shot after shot for almost two years. Sometimes they would work, and sometimes not. Then one day the pain just stopped and never again!2015: Lots of uncertainty about my job (my company was closing locations and might be forced to move away from our families). I developed bad anxiety with shaking arms and legs when I would lay in bed in the morning. Never had a panic attack, but just chronic general anxiety. Wound up out of work again for 4 months in a treatment program on long term disability again.2015-2016: Developed IBS (Irritable Bowel System) with diarrhea. Many docs, colonoscopy showed a perfect colon, yet now all of a sudden I had constant diarrhea for a year! Put me on medicine (Viberzi) which helped a little.2016: Spent about a year of intense job searching because the end was near at my job. No luck. Very discouraging. A few months later in mid-2016, the anxiety got really debilitating, and once again, I was out for 4 months in a program on disability. I should mention that for the past 8 years since 2008, I saw a great psychiatrist and therapist for the depression/anxiety. Did a lot of CBT/DPT therapies. Meditation, deep breathing, mindfulness, etc. My doctor and therapist and I believed that the job environment was toxic (60+ hour weeks, high stress because it was in nuclear power, and the impending thought of having no job in a couple of years). The belief was that if I got a new job, the anxiety would go away.November 2016: Finally got a new job!!! Was SOOOO happy for once! I felt hope and relief. I felt like my problem was solved and I could finally relax and be happy for the first time in a long time!December 2016: Started the new job. It was great. Great people, boss, the type of work, hours, etc. Couldn’t ask for anything more. Only downside was an increase from 20 mins to 60 mins each way in commute, but I was willing to live with that for all of the positives that came with it. Not a problem. I was a few weeks into my new job and all was wonderful for once! My job is not strenuous. I just sit at a computer all day in a nice ergonomic chair.A few weeks into the job, before I could barely enjoy the relief of years of anxiety, and my low back started hurting. I didn’t think anything of it. Started a little achy. Felt like I might have just strained something from bad posture as I was leaning forward and twisting to the side a lot reading and typing a bunch of reports for a few weeks. A few weeks later and it was very sharp and “spasming” on the lower right side. I could barely bend down to tie my shoes. It hurt to even breathe. I thought I must have done something serious, but how? I did nothing to injure it!! I was able to do so many physical things prior to this with no pain. What caused this?Oh, by the way, I forgot to mention that the IBS that I had every day for the past year miraculously stopped ever since the back pain started! Another ailment/pain replaced by another once again!So I started the doctor/treatment/medication routine. A few weeks later, it developed into more of a dull, nagging ache. Moved from left to right sides throughout the day. I would describe it as having two dull knives stuck into my low back all day. Pain never goes into buttocks or Leg. No numbness/tingling. Unbearable pain to sit for any period of time. Relieved only when walking and lying on back. In the beginning, heat helped. Then it no longer helped. Then ice helped numb the pain for a few months. Now neither really help.I spent the next 2 months reading every TMS, mind body syndrome book, audiobook, website, testimonials etc. I was convinced this was TMS and nothing really wrong. Unfortunately nothing changed. I believed 100% in it but just like back in 1994, no luck. I immerse myself in the TMS readings all day and night, buy into fully, but never helps. I want it to help so bad, but I never feel any sign of relief to give me hope.Went to 4 MD’s and chiropractor in the 6 months since Dec 2016. An MRI showed L2/3 disc degeneration and a couple of “mild” disc bulges. Initially tried OTC NSAIDs, Flexeril, methylprednisolone, ice, heat, bed rest, pain ointments/creams, etc. Tried yoga/stretching. That didn’t help, and one day I bent and twisted the wrong way at Yoga, and got a really sharp jolting pain, and never went back. I have tried about 5 different lumbar support pillows/devices at work, in my car, and at home. They don’t help at all.The first Spinal Orthopedic Surgeon at a reputable, established Ortho/Pain center basically said it is probably soft tissue strain or an annual disc tear (but never even said which disc). She sent me for PT. I tried physical therapy – core strengthening, stretching, TENS, etc. No improvement.I then tried a supposedly reputable Chiropractor with decades of experience and he said I had two bulging discs that were pressing into nerves and causing the pain. He was 100% sure. So he started me on a fancy “VAX-D” Spinal Decompression table. I went every day for 30 mins each for about 4 weeks (~17 treatments) along with some PT there afterwards (core strength, massage, TENS). No relief at all, so I stopped going.This was really affecting my ability to work or be useful at home to my family or around the house. I have spent every waking moment at home on the couch or bed or floor.I went to a Physiatrist (gave me Ultram, Flexiril, Valium) and said probably soft tissue strain. After more weeks, no improvement. He sent me to a “top” Spine Pain Specialist MD. He scanned the MRIs and a quick evaluation and said it is most likely your facet joints (arthritic). Sounded 100% sure that was it. No question. He said we need to inject anesthetic into the medial branch nerves of the vertebrae (a medial branch block). If the pain was reduced significantly enough for a few solid hours, then it would confirm that the pain is indeed from the facet joints and the next step would be radiofrequency ablation (RFA) where they would burn those medial branch nerves to provide 3-18 months of relief until they grown back. He did the lower 3 lumbar/sacral vertebrae one week and then the upper 3 lumbar vertebrae another week. The first procedure seemed to provide some relief for a few hours, but second procedure didn’t help at all.That brings me to this past week at my follow-up again. He said they need to repeat the first procedure again!!! This was needed to confirm it works (that the relief I experienced wasn’t a fluke) before proceeding with the nerve ablation. This seemed to be his practice of ensuring success but also apparently required by my insurance (BCBS) before they will cover the ablation procedure. He said if it is confirmed, then an ablation would be recommended. If not, however, then he said it is probably the L2/3 degenerative disc causing a “referred” pain to the area a few inches down lower in the back where I feel it. That would require more consults with a separate surgeon, a discography (discogram) diagnosis procedure, and then potentially a surgery (fusion or artificial disc replacement). I do NOT want any of that!So here I am today in May 2017. 6 months of the SAME EXACT pain as 23 years ago! Just like back then, only ice, laying down, and Ultram provide any relief. Lately the Ultram (50 or 100 mg, 1-3 times per day), or the ice, or lying down don’t really help anymore. I try not to take the Ultram because I don’t want to go down the opioid addiction/narcotic path. I may be take 1 to 4, 50mg pills a week.I am 3 weeks away from that 3rd nerve block procedure. I am frustrated on how this has dragged on for 6 months now with NO IMPROVEMENT. I can’t believe I am still in pain. How could this be? The pain consumes me every waking moment (and even disturbs my sleep at times lately). Every once in while I have a better hour or day, and think I am turning the table, but then the next hour or day, I am back in the normal state of pain and misery. I really think if I didn’t have a family, I would not be alive at this point because it seems so hopeless and the thought of living the rest of my life with this constant pain is unthinkable. Because I love my family, I decided to be positive and beat this. I have to. I started a strict self-PT program this week. Every day walking 20-30 mins, and 10 mins of core strength and stretching.I go back and forth lately between thinking something must be really physically wrong to cause this kind of 24/7 horrible pain vs. the TMS psychosomatic pain theory. I don’t know what to believe. I am currently re-reading everything by Dr. John Sarno, “The Great Pain Deception” by Steve Ozanich, and now “Crooked” by Cathryn Jakobson Ramin, Dr. David Schechter’s work, etc. They are all AWESOME books and I believe they describe me on every page. I just don’t know how to undo this? Are my neural pathways so strong now that I cannot reverse this after 6 months?So here’s why I think I have TMS… 25 years of constant pains or sicknesses. Always something getting my constant attention on my body- instead of letting my unconscious fear and anger surface which would be emotionally painful to face. There has never NOT been something wrong with me since I became an “adult”. It all started in college when life got stressful. One ailment moves to the next, and the next.... Pains move from Arm to Arm, side to side in lower back. How can a real physically induced problem do that? Either something is hurt or it isn’t.It is frustrating seeing 5 different medical professionals/doctors and getting 5 different diagnoses! It seems like they just guess and try things until something works. I feel like a guinea pig while they just try to make money and push meds and procedures on me. I am sure they are well-intended, but it doesn’t feel right. Each time I had confidence in their diagnoses, but each time they failed to result in any improvement.I find it hard to believe that my discs are the problem. I have seen WAY WORSE spines on MRIs! The two discs are barely bulging (probably how everyone’s discs look over 20 years old), and one degenerative disc which wasn’t even that bad from what I have also seen. Even the first two docs or radiology report said NOTHING about the discs!So I’m really wondering now where to go from here. I am reading all these books and believe so much in TMS and feel like that has to be it. However, I just don’t know how to change it? I would love a TMS expert or Mind-Body Doc to read my story and let me know what they think. How do you ignore the pain and tell yourself nothing is wrong when it hurts you 24/7? How do you unlearn that and reverse that? Would love to hear from you all. Thanks for your time. james.e.kerr (at) comcast.net

This editorial quote is key to understanding: "He's not saying that your pain is all in your head; rather, he's saying that the battle going on in your mind results in a real physical disorder that may affect muscles, nerves, tendons, or ligaments. An injury may have triggered the disorder, but is not the cause of the amount or intensity of the resulting pain." I can't begin to even place into words how life-changing this book was and how grateful I am that celebrities have been cured through him because that's how I heard about the book (as well as the doctor being written up in Forbes as "America's best doctor and his miracle cures")for years and, as a last ditch effort to help my chronic acute pain that I'd recently developed, even though mine was far more than back pain, I decided to read it.Let me start from the beginning, having gone through a criminal act done to me a couple years ago which resulted in temporary PTSD I thought I'd worked through, to me throwing myself more heavily into work and having recently bought my fourth company, then having minor surgery in which I was not properly anesthetized, then having a reaction to sulfa,to someone close to me giving me some digs now and again that I did not confront, I can look back now on the triggers that added up to things that I needed to deal with that would create mental and bodily stress. Collectively and individually.But I didn't think the book fit me because the pain was real and I was hospitalized twice for it, completely unable to function. My pain was not just in my back although it eventually settled there. It began as full-body acute level 9 crippling can't-function pain--part of that likely began as the sulfa allergy I had to an antibiotic, although the doctors had never seen it at the level I had it and were surprised a sulfa reaction could be so crippling although they admitted it had been documented as a possible reaction in others, but was rare. Although they tried drugs for fibromyalgia, they had no effect and eventually I was on hydrocodone, a 2nd pain killer, and steroids. With hospital visits in between for greater help. And still in crippling pain. I am very much against pain killers for anything more than a few weeks so I was very troubled, of course.Eventually I was diagnosed with an auto-immune disease which they felt was likely lupus. An appointment was made with a rheumatologist to work out which one I actually had. It had been a month of crippling pain that let up for a couple days then came back. And it was acute. I eventually only wound up sleeping an hour every night.I remembered this book and finally, before my specialist visit to work out how I would be treated for the rest of my life to MASK my pain, I bought it. And then I read this book as I laid in bed, awake all night as usual. Remembering Ellen Degeneres having talked about the mind-body connection and her body shutting her down due to back pain when she was doing too much or not dealing with enough mentally, and Howard Stern's years of chronic pain that this doctor eliminated, and a few others...it was my last hope before serious drugs or surgery and a lifetime of pain pills or even a wheelchair to simply cope. I was at the point where I could no longer walk up and down the stairs in my home for any reason. My joints suddenly made creaking noises, proving it's not all in the mind but can be very much created there, leading the doctor to diagnose this as a joint-related disease, my muscles (my main source of pain) felt like I'd been beaten for days, I could feel everything on my body in greater detail--the ring on my finger, scratchy clothing, dry feet--like overactive pain receptors-- I could not work, (but I am self-employed!) I could not function. And just thinking maybe my body was doing this to myself was not enough to make it go away. I had my diagnosis.And then...that was it. It was gone. I closed the last page and I was well. That does not even seem logical does it? It's what happened.I was told I had an autoimmune disease and that my body was attacking itself and my life was going to be changed forever.I had loved ones taking care of me. And then I closed the book--got up, and walked downstairs, pain-free, effortless. Later that day, I was actually able to get on my treadmill for the first time in what felt like forever since it was once a very important part of my daily routine. I was normal. My life was back in full swing after being told it was gone for good--and everyone around me just had dropped jaws.The reality was that tension caused an oxygen deprivation to my muscles and blood vessels which is not something anyone can find or understand. And every time I'd ever had a massage I was told I had no tension. Once I recognized not only this reality but thought about the stresses leading up to it, and fully understood the process of why it happens, my body was not able to create the pain in order to mask the emotions because I knew what it was doing. Knowing what it was doing cured it. But the thing is, before I opened the book I thought about that being the case having HEARD about the book and that was not enough--I needed to fully read and understand the physical steps as to why it happens and internalize and believe them and THAT is when the cure seeped in, likely about 1/3 of the way through the book--to the point where I could close the book and then actually go workout that same DAY because i was NORMAL again. The night before I read this book I was in so much pain that I was ready to just check myself into the hospital and go stay there, medicated because I could no longer take the level of pain and I was simply constantly in a fetal position, in tears.Here is the interesting thing. When they ran the test for lupus I was told "If it comes out negative I don't want you to get too excited. This test has a very high false negative rate." Looking back, because I was told if the pain did not subside (which it did not) that it meant I did have the auto-immune disease in spite of the negative reading, I believe that it may be that there are not false negatives at all. But in Western medicine, if one is in acute ongoing pain, you have to label it something and mask it with meds. My body WAS attacking itself but not due to lupus. Due to trying to mask emotions it did not want to have brought to the surface. But that's not recognized in Western medicine where we treat the symptoms but not get to the root, especially embracing the idea that my body could create these issues due to psychological tension. Not when I am not a typical psychological "case" but a woman who is seen as "with it" enough to run 4 companies, a charity, and a social club and who STUDIED psychology in graduate school, no less! The fact is, that's not "with it" in reality, but even more of a mask and a tad over-driven. Because it's true that I prefer to work harder when I don't wish to deal with something. It seemed like a positive "outlet" but in reality it masked what I needed to deal with.I was a people pleaser, I was a "yes man", I was a work perfectionist but considered myself very laid back because I never was angry. I now know for me that is not a good thing...I was angry inside. (Actually many people with this are angry outside, but that was not me. I was always the calm one no matter what I faced in life) And rather than acting out, my body internalized it all. I now speak up and speak out, I now deal with my emotions. And I am now pain-free 100% OVERNIGHT to the shock of my family doctor and the emergency room physicians who grew to know me and my condition.We don't treat the issue in Western medicine or equate psychology with physical ailments--we simply treat the ailments. I was on high level pain killers and it would still come back. I asked my doctor before reading the book if the recent stress could cause this and he said no, it was physical and my immune system was confused and attacking my body and the flare up was triggered by the sulfa allergy but was dormant until then. They just are not trained to fully grasp the mind-body connection. And understanding what was happening DID make it go away because it was 100% my body telling me "lay down and don't think! Here! concentrate on this pain for awhile so that you don't bring those painful emotions to the surface and go batty! That will take your mind off of that stuff that is under the surface!"I have never felt the kind of pain I was in and I actually have a high tolerance for pain--I can have surgery and be back on my feet working in no time, I am tough and can deal with it--but I was 100% crippled and in bed and non-working and disabled with a diagnosis of it being the rest of my life.The more I read the more I thought of others I knew who came down with crippling back pain and how things like surgery did not help and they could not work. What's interesting is that this doctor realized that some people showed the same back deformaties in x-rays but had no pain and he looked to why for some it was crippling and for some it was nothing in spite of whatever x-rays or tests showed. Or why some got better and others did not since the body typically heals itself. I knew someone who had surgery after surgery after surgery. I can now understand why that never helped. The mind is more clever. You have to understand what it's doing to stop it.This literally changed what was about to be a lifetime of being crippled in some regard according to my doctor...I was told to accept it. Thankfully, instead I accepted with an open mind, reading this book. The irony is that before I read the book, I would have a few good days but once I was given the diagnosis that I for-sure had an auto-immune disease, that's when the pain got worse than ever. My body had tricked me.I took back that power.