Hi folks,
I'm fairly new to TMS, having recently discovering it almost by accident. I've read through most of Dr Sarno's work (actually, I listened because one of my more recent symptoms is blurry vision and reading has become more difficult) and found myself relating so hard it almost hurt! However, there's is one complication to my health journey - an enormous one, in my mind - and I'd love some feedback on my overall history and, in particular, the complication (which I'll get to below).
I don't want this to become too long-winded, so am going to summarize in note form, eliding much detail, and focusing more on recent events. But please feel free to ask me for more information should you think it relevant.
Personality: quiet, introverted, achievement-oriented, perfectionist in many areas of life including work, definitely relate to the "goodly" character traits Sarno describes, feel utterly outraged and depressed when people treat each other poorly.
Age 0-18: Wonderfully healthy, at least physically. I was the kid who was rarely ill, and bounced right back when I was. I was very active and ate a balanced diet (thanks to my Mum). However, I was brought up in an incredibly strict fundamentalist Christian home, and my father in particular was emotionally abusive. Even in my earliest memories of him (I was about 5) I recall that I was afraid to interact with him. I was also "lovingly" punished by spankings with a wooden spoon and, during my teens, a horse whip (yes, a horse whip, intentionally purchased by my dad for the purpose of punishment). I'm not sure if that counts as physical abuse, but I sure didn't appreciate it.
19: Fell very ill with glandular fever and tonsilitus not long after leaving home. Took me a couple weeks to get out of bed, but I rushed back to work and my life as soon as I could, probably earlier than I should have.
23: Married my girlfriend of 4 years.We're still married nearly 20 years later (with two kids, one of whom is now a legal adult).
23-24: Began seeing doctors due to fatigue that wouldn't quit. Began scaling down physical activity as a result. Began getting occasional back spasms, where muscles in my back would lock up in extreme pain, disabling me for a day or two at a time. Always triggered by a seemingly innocuous movement.
26-31: Progressively got worse fatigue and neurological issues like vertigo. At my worst I felt like I was living through a dreamlike haze, all my senses becoming blunted and distorted. I didn't know what to do because I had seen so many doctors to no avail, so I did what I could to push through by increasing caffeine and sugar. My body eventually collapsed with neurological symptoms so severe that I almost suicided, and it took improved nutrition and around 3 years to "fully" dig myself out of that hole, though to this day I occasionally feel "flashbacks" of those symptoms, but to a far lesser degree of severity.
31-41: Life plodded on. I finally saw a doctor who "diagnosed" me with CFS and cautioned me against stress, but I didn't take it seriously enough. I became more and more hesitant to do physical activities, travel, eat foods that would trigger me etc, and lost myself more and more in work (somehow not seeing it as "stress"). I'd occasionally wake with a terrible hollow-feeling ache in my hips, and have to roll over to relieve the pain. Sometimes I'd wake with my calf muscles in the most excruciating cramp.
After finishing up an enormously stressful job where I was somehow blamed for all the bad outcomes I had warned management would ensure their own decisions, I experienced debilitating fatigue and muscle pains during my notice period. My Rheumatoid Factor was slightly elevated (though it had never been checked previously so who knows what my baseline was), and my then GP suggested I might be developing RA. This sent me into an emotional doom spiral. Fast forward six months and I had basically fully recovered from the RA-like symptoms and in fact was more active than I had been in years. I was far from perfect, but I was pretty good.
42: After much deliberation, I couldn't make a decision about Covid vaccination and put the decision in my GP's hands. Time was a factor because my dear Grandma was dying in a nursing home, and they of course had vaccination requirements for visitors. My GP was adamant I should get vaccinated and refused to entertain an exemption despite my clear history of CFS and a generally sensitive body. The first Pfizer was fine but the second sent my health into a crumbling, spiralling mess and I've been struggling to recover ever since (19 months now). Incessant muscle twitching, full body weakness and shaking, tachcardia, bradycardia, POTs symptoms, blurry vision, fatigue, internal tremors, involuntary movements, parasthesia, tinitus, ear pressure/popping/clicking, anxiety, depression, suicide ideation etc etc etc - I seem to have experienced every symptom under the sun.
I've been under the care of various physicians and of course changed my GP since I couldn't bear to even see the one who recommended vaccination. They've identified immune system dysregulation and it's abundantly clear to me that autonomic dysfunction is at the core of my health woes (I do have some diagnostics to show this as well, not that I needed them). My HRV has been terrible - as low as 7ms - though slowly improving over the months since vaccination. My Rheumatoid Factor has actually elevated even further, though now it's considered "in range" because they recently went and changed the ranges!
My symptoms always worsen at night. Even if I go to sleep feeling relatively OK, I'll often be woken with varying symptoms in the dead of night - feverish, hot tight feet, a feeling of my blood being stingy and "poisoned" for lack of a better description, GI upset, or random pains like a throbbing ache in my lower back. Even if I do sleep the night through, there is very little restorative feel to the sleep.
So that's a high-level timeline, and my dilemma is likely obvious to anyone paying attention to what's being said about vaccine injuries outside the narrative that continues to deny I exist, along with many thousands of others like me. Whilst I'm supremely confident that TMS explains everything up until my vaccination, I don't know about how to eliminate physiological causes of everything thereafter. Sarno himself makes a very strong point to work with physicians to rule out any structural issues, but no one knows how to do that yet. Some physicians are offering compelling evidence that spike protein is at the core of injury woes, and have no definitive protocol for eliminating it from the system. Since these vaccines are so novel and no one is being funded to investigate adverse events (because they don't happen, remember!?), it's simply too early.
I'm aware there is also an emotional component to my vaccine injury. I can't help but dwell on the fateful decision and all the things that led up to it, beating myself up for not trusting my gut. And of course, there's the toll that the gaslighting and censorship takes on us injured folks.
So my dilemma is: how do I move forward with TMS given that there may be structural, physiological reasons for my body's inability to regain homeostasis? How can I remain informed on the latest research and treatment options whilst pursuing a TMS-based approach at the same time? Are these even compatible goals?
Thanks for any help or advice you can offer.
I'm fairly new to TMS, having recently discovering it almost by accident. I've read through most of Dr Sarno's work (actually, I listened because one of my more recent symptoms is blurry vision and reading has become more difficult) and found myself relating so hard it almost hurt! However, there's is one complication to my health journey - an enormous one, in my mind - and I'd love some feedback on my overall history and, in particular, the complication (which I'll get to below).
I don't want this to become too long-winded, so am going to summarize in note form, eliding much detail, and focusing more on recent events. But please feel free to ask me for more information should you think it relevant.
Personality: quiet, introverted, achievement-oriented, perfectionist in many areas of life including work, definitely relate to the "goodly" character traits Sarno describes, feel utterly outraged and depressed when people treat each other poorly.
Age 0-18: Wonderfully healthy, at least physically. I was the kid who was rarely ill, and bounced right back when I was. I was very active and ate a balanced diet (thanks to my Mum). However, I was brought up in an incredibly strict fundamentalist Christian home, and my father in particular was emotionally abusive. Even in my earliest memories of him (I was about 5) I recall that I was afraid to interact with him. I was also "lovingly" punished by spankings with a wooden spoon and, during my teens, a horse whip (yes, a horse whip, intentionally purchased by my dad for the purpose of punishment). I'm not sure if that counts as physical abuse, but I sure didn't appreciate it.
19: Fell very ill with glandular fever and tonsilitus not long after leaving home. Took me a couple weeks to get out of bed, but I rushed back to work and my life as soon as I could, probably earlier than I should have.
23: Married my girlfriend of 4 years.We're still married nearly 20 years later (with two kids, one of whom is now a legal adult).
23-24: Began seeing doctors due to fatigue that wouldn't quit. Began scaling down physical activity as a result. Began getting occasional back spasms, where muscles in my back would lock up in extreme pain, disabling me for a day or two at a time. Always triggered by a seemingly innocuous movement.
26-31: Progressively got worse fatigue and neurological issues like vertigo. At my worst I felt like I was living through a dreamlike haze, all my senses becoming blunted and distorted. I didn't know what to do because I had seen so many doctors to no avail, so I did what I could to push through by increasing caffeine and sugar. My body eventually collapsed with neurological symptoms so severe that I almost suicided, and it took improved nutrition and around 3 years to "fully" dig myself out of that hole, though to this day I occasionally feel "flashbacks" of those symptoms, but to a far lesser degree of severity.
31-41: Life plodded on. I finally saw a doctor who "diagnosed" me with CFS and cautioned me against stress, but I didn't take it seriously enough. I became more and more hesitant to do physical activities, travel, eat foods that would trigger me etc, and lost myself more and more in work (somehow not seeing it as "stress"). I'd occasionally wake with a terrible hollow-feeling ache in my hips, and have to roll over to relieve the pain. Sometimes I'd wake with my calf muscles in the most excruciating cramp.
After finishing up an enormously stressful job where I was somehow blamed for all the bad outcomes I had warned management would ensure their own decisions, I experienced debilitating fatigue and muscle pains during my notice period. My Rheumatoid Factor was slightly elevated (though it had never been checked previously so who knows what my baseline was), and my then GP suggested I might be developing RA. This sent me into an emotional doom spiral. Fast forward six months and I had basically fully recovered from the RA-like symptoms and in fact was more active than I had been in years. I was far from perfect, but I was pretty good.
42: After much deliberation, I couldn't make a decision about Covid vaccination and put the decision in my GP's hands. Time was a factor because my dear Grandma was dying in a nursing home, and they of course had vaccination requirements for visitors. My GP was adamant I should get vaccinated and refused to entertain an exemption despite my clear history of CFS and a generally sensitive body. The first Pfizer was fine but the second sent my health into a crumbling, spiralling mess and I've been struggling to recover ever since (19 months now). Incessant muscle twitching, full body weakness and shaking, tachcardia, bradycardia, POTs symptoms, blurry vision, fatigue, internal tremors, involuntary movements, parasthesia, tinitus, ear pressure/popping/clicking, anxiety, depression, suicide ideation etc etc etc - I seem to have experienced every symptom under the sun.
I've been under the care of various physicians and of course changed my GP since I couldn't bear to even see the one who recommended vaccination. They've identified immune system dysregulation and it's abundantly clear to me that autonomic dysfunction is at the core of my health woes (I do have some diagnostics to show this as well, not that I needed them). My HRV has been terrible - as low as 7ms - though slowly improving over the months since vaccination. My Rheumatoid Factor has actually elevated even further, though now it's considered "in range" because they recently went and changed the ranges!
My symptoms always worsen at night. Even if I go to sleep feeling relatively OK, I'll often be woken with varying symptoms in the dead of night - feverish, hot tight feet, a feeling of my blood being stingy and "poisoned" for lack of a better description, GI upset, or random pains like a throbbing ache in my lower back. Even if I do sleep the night through, there is very little restorative feel to the sleep.
So that's a high-level timeline, and my dilemma is likely obvious to anyone paying attention to what's being said about vaccine injuries outside the narrative that continues to deny I exist, along with many thousands of others like me. Whilst I'm supremely confident that TMS explains everything up until my vaccination, I don't know about how to eliminate physiological causes of everything thereafter. Sarno himself makes a very strong point to work with physicians to rule out any structural issues, but no one knows how to do that yet. Some physicians are offering compelling evidence that spike protein is at the core of injury woes, and have no definitive protocol for eliminating it from the system. Since these vaccines are so novel and no one is being funded to investigate adverse events (because they don't happen, remember!?), it's simply too early.
I'm aware there is also an emotional component to my vaccine injury. I can't help but dwell on the fateful decision and all the things that led up to it, beating myself up for not trusting my gut. And of course, there's the toll that the gaslighting and censorship takes on us injured folks.
So my dilemma is: how do I move forward with TMS given that there may be structural, physiological reasons for my body's inability to regain homeostasis? How can I remain informed on the latest research and treatment options whilst pursuing a TMS-based approach at the same time? Are these even compatible goals?
Thanks for any help or advice you can offer.