Finally doctors emphatic about the cure and solely on pain management. I was exposed to white coats with no Hope when it came to first wife’s Lung Cancer. I knew that’s more that could have been done and Howard’s work crosses into Lung Cancer too. Thank you!
Is your course still available ?? I have chronic fibromyalgia. Am currently reducing methotrexate and prednisone, which I have been on for over a couple of years. I can relate to the function of the brain and believe my upbringing has a lot to do with my pain.
Sadly, the medical industry makes many diagnoses that they give a name to. By calling it by a syndrome name, they can offer a prescription. Western medicine sadly resolves all pain issues with either drugs or surgery. They ignore any solution that isn’t resolved by these two avenues.
I wish I knew about this course three years ago I’ve been in chronic pain forever with trigeminal neuralgia worsened by TMJ I got 10 after surgery on my jaw bone, I’ve had chronic pain this is unlike anything I’ve ever experienced and I even had neuropathic pain with a IC, Many years. Is there anyway I can purchase a copy of this course since it’s already done and gone?
As mom of kids ; I have pain this 2 years from Doctor to doctor even I did spinal surgery with no results , and I’m still with pain and pressure around my pelvic , tailbone, rectum and anus , buttocks; with hernia disc and imbalance of muscles when sitting and high tension in my head …. All these symptoms pain stoped me to come back to work and to get job and I become with no income …. And I hope one of Doctor for TMS pain free body helps me for free because of my bad financial situation please!! I live in Illinois 😢🙏🏻
Hi ,I too have severe rectum ,tailbone,sacrum ,spine ,torso pain ever since I was forced cold turkey off ativan in May 2017 ! How are you doing now ? Hugs sent it’s HELL
@@sweetmountainbaby I can’t believe you got that after going cold turkey off Ativan. I had all of that stuff too it’s probably 80% better but I had it for decades. I didn’t know about TMS because I stopped researching everything because it just made me worse and I stopped going to therapy because I became broke and lost my insurance a while back now I am on disability and have Medicare. I found it made me a lot better. But I know getting off benzos can be really hard my aunt was on Them for many years and I take them for relaxation to try and help my TMJ and trigeminal neuralgia which is my worst issue after a surgery on my jaw. Again many many years ago. Wondering if you feel any better I did find when I was at the height of my pain the internal pelvic floor therapy helped me but I had to go through for therapists to find the one who was able to help me. They don’t all do it the same she just pressed on a trigger point and held it until it released and then she did it again, and then I gynecologist did trigger point injections which helped even more. Not sure if you tried those things or how you’re doing but thought I would mention that. It’s not permanent but it does give you relief so you’re not going crazy. I hope you’re doing better if you decided to do TMS I would love to hear how you’re doing and my doctor is retiring after working with her for 18 years how in the world do I find a doctor to treat me like she did I have no idea everybody is so fearful now.
This is so important. Seeing the prevalence of "long covid" I wonder how much of this is MBS at play? Seems like a good possibility especially given the stressful emotions going on around contracting the virus. The stress and anxiety around covid is as contagious as the virus itself to begin with, and I could imagine that once one "recovers" medically their brain still triggers the pathways of the covid symptoms. Interesting too that they are calling "long covid" as similar to Chronic Fatigue Syndrome, Fibromyalgia etc....hmmm.
what about vax injury - caused me severe neuroapthy all over - can it start because of that cause or say covid itself and then get turned on and stay "on" with syptoms until we get it out of the loop of pain/fear ??
I had an extreme inflammatory response to the shot. I only received one and I went through a LOT. Saw a bunch of doctors and specialists, had an endoscopy and colonoscopy, tons of bloodwork….all anyone could find was inflammation. You are not alone. Some doctors try to use medical gaslighting, remain strong. Work on lowering your inflammation and keeping your mental health doing as good as possible. You can get through and over this!
You know this is the thing, I have had IBS and then fibromyalgia for most of my adult life. So then listening to this I would think ok yes this would be a good treatment for me. However all the years they have been saying this isn't autoimmune disease but UK study last year now saying that it is autoimmune. So what do we say now!!!
Hi I am responding to a Question you posed in a post after watching a TMS video. You said I’ve had IBS and fibromyalgia for most of my adult life, me too, they said it wasn’t auto immune and now they are saying it’s auto immune. I didn’t know they were saying it’s auto immune now because I stopped researching. But I always knew it was autoimmune, I had a holistic doctor that said fibromyalgia lupus it’s all the same it’s the body attacking itself. They thought I had lupus in the beginning turned out I didn’t. Many of the symptoms were so similar at that point I had a lot of joint pain unlike Now. So I’m just wondering how are you doing and did you ever work the program I just started a few weeks ago really researching it, I don’t research illnesses because I find my symptoms are so much better when I stay off of finding answers. But I kind of regret that because I didn’t know all this information was out there. Just so if you had any improvement or even if you didn’t would love to hear how you’re doing now. I agree that it’s so confusing, About the auto immune part but they do say autoimmune issues are usually TMS.
