There are a lot of other DMSO articles in the cue, but I made a decision I needed to do a much more comprehensive review of the literature first (manually going through ~300,000 studies and sorting the 6,000 comments I've received) as certain studies needed to write the future articles cannot be found in any other manner. I'm hoping to have the next one done at the end of February or start of March.
Thank you so much for your support and understanding.
Additionally since many of you have asked where I am at on the DMSO project, I feel like I have now gone through over 90% of the available literature. At this point I need about a week to do:
I enjoyed and learned a lot from your thoughtful write ups!! Thanks!
It is extremely hard to find an effective solution for MRI contrast agent Gadolinium toxicity which can be worse than cancer. I don't know if DMSO can help. Or anything else.
There are other alternatives, as Doc has said - but - getting your radiologist to use them is the issue. "Oh, this is what we use," "this is all we have"
If they ever ask me about contrast, I will likely decline. Watching a friend who took the contrast last year for a cardiac thing, and - she's not been well, since.
AMAZING. I am 100% sure that the link between previous injuries (that involve scarring) are hot zones for gasoline on the fire spots wrt spike and the inflammatory response. This is also why I believe cell turnover is key to "healing". Sweating, movement, fascia release, nerve flossing - all vital. If everyone had access to a sauna, red light lamps (+ natural UV light and clean food and water, there would be almost no disease states in humans. Even in the face of the psychos weaponizing ticks .
Have you ever heard of Canadian doctor Adeel Khan? If not please have a watch & listen.
I found him when I was researching possible treatments for my jab injured son. (FYI: He had to flee Canada in order to practice this type of Regenerative Medicine.)
I'm not sure what he meant by "It's not CANADA but it's the next best thing" ? I live in Canada and our health care system is as bad or worse than any LOL.
I think local anaesthesia acts as a reset button in terms of being a biophysical hard reset button on peripheral nociceptive circuits? ie: temporarily short-circuiting aberrant, self-sustaining electrical storming in inflamed nerves and dorsal root ganglia. This would extinguish maladaptive positive-feedback loops of neurogenic inflammation, central sensitization wind-up, and glial over-activation which would subsequently allow the system's intrinsic homeostatic mechanisms to reboot toward normalized membrane potentials, restored microvascular perfusion, damped cytokine cascades, and accelerated tissue repair without the persistent "phantom alarm" of chronic pain signaling.
I am curious as to the connection to general vs. local experiences... do we local consciousness, for example? And if so, is this why local anaesthetics "work" as reset/heal mechanism?
The way I often describe the process to patients is that it's like rebooting a computer that crashed, and when it resets everything works normally. The classic way this is explained is that every nerve has a firing threshold, and when they get overly stressed, they can switch to becoming hypersensitive to firing and hence cause a lot of issues from firing a lot, whereas when the anesthetic wears off, they reset to the normal firing.
The condition which maps the most closely to a classic neural therapy lesion is complex regional pain syndrome since it has all the pain plus localized dysautonomica.
I have wondered about gas anesthetics. Overall, I don't think they help with these issues, which may in part be due to them being CNS toxins rather than something that just temporarily sedates the nerve and wears off.
Sorry, one more comment add-on. :) Since local cellular bioelectric contributions [linearly] add up to form emergent "general" fields that orchestrate multicellular life, then perturbing one part (e.g., via ion channel drugs) could propagate system-wide changes (see: Michael Levin's work)
I'm reachin' a bit here, but the body connection thing seems key. Why the hell isn't biophysics common learning ground anyway? And the fact that we comprise a massive load of other organisms with their own [electrical/biophysical] signatures - why the hell aren't we almost only focused on the environment created by these organisms within us that effectively IS us? We're so dumb sometimes. :)
We have to wait until the aliens arrive and demonstrate how so much of modern "medicine" is blood letting and sorcery. It's absolutely fascinating to consider the ramifications(ethical of course...not profit oriented like the medical mafia overlords) of these areas of discipline. It's utterly confounding how any so called science can be so myopic in its understanding of the body despite the hollow boasting of yet one more toxic creation to lower a meaningless metric or mask a root cause. Thanks for the contributions of both you and MWD.
I had good sustained results with trigger point injections with local anaesthetic, with or without steroid, for nerve pains, including postoperative neuromas, very common after c-sections.
Jumping in here, Jesdica and AMD. Dont understand most of what you're talking about as am not a learned person, but wondering if this may be the way to deal with Trigeminal neuralgia??? The prescribed drugs are just SO evil.
Jumping in here, Jesdica and AMD. Dont understand most of what you're talking about as am not a learned person, but wondering if this may be the way to deal with Trigeminal neuralgia??? The prescribed drugs are just SO evil.
Human healing is so complex! I’ve been working on it personally for 45 years! 25 of those as a physician. Most of my training was learning and growing through 20 years of epilepsy and 300 seizures.
I was one of the first individuals offering PRP in the country. Fortunately, I was more drawn to the cases that did not progress, rather than the successful ones. There are downsides to not being satisfied with results! I’ve neurotically created procedures, pathways, paradigms, structures, approaches, ways of embracing the human body, mind, heart spirit as an integrated quantum bioenergetic, wonder, etc. i’m sure we could have many long discussions on this and many other topics.
Currently, cervical dystonia, complex, regional pain, syndrome, complex, PTSD, craniocervical, instability, lumbar discs, neuropathy, Ehler’s Danlos Syndrome, fluoroquinone toxicity, are my most common cases.
Having performed stem cell therapist for longer than nearly anybody else in the country, the most significant challenge facing this emerging field is autologous versus allogeneic therapies. I’ve given whole weekend conferences on why allogeneic therapies are a problematic set of approaches from immune, infectious,, genetic, and survivability approaches. Many people will discuss outcomes/decrease in symptoms. However, healing and decreasing symptoms often are quite divergent in their course forward.
Harmonizing structural, neurologic, physiologic, emotional, energetic, spiritual, and timing aspects of care is extremely complex. We have nine providers collaborating together at our center – most of us working together for the last 10 years – to encourage a person to embrace their own healing journey. The reduction in interference patterns – from Energetic/quantum to emotional to cellular – thank you for highlighting the cell danger response – to neurologic, and structural is extremely important trophic effects to occur in structure. The neurological layer alone is seven segments of interrelated healing care!
Thank you for the thoroughness of your articles! One small inclusion: the most commonly used anesthetic for subcutaneous Neuroprolotherapy is procaine. It is the only anesthetic that has parasympathetic effects.
Finally, perhaps the most important tool in all of our bag of tricks is called Stellate ganglion block. I was fortunate to be the third physician in the country doing them under ultrasound guidance for PTSD. I’ve been doing this for over 15 years. The calming effects to the sympathetic system, the opening it gives parasympathetic healing, the relaxation of emotional trauma, and the quantum energetic effects from resetting the ganglia widely opens the door for more significant healing.
Thank you for the article on regenerative therapies for pain!! I was almost unable to walk because of knee pain, facing life in a wheel chair and was not going to have a knee replacement. Family members had done that and still experienced so much pain. So I had stem cell transplant on the worst knee and PRP on the one with less pain. It improved greatly but I still had some pain, some days in both knees on walking. So I did a second round of PRP on both knees and I can walk pain free now. I cannot walk long distances - which for me is taking short jaunts into more than 3 stores in a day - but it does not hurt while I am walking. I notice that pain that night in bed but it is not severe at all. I use DMSO on it then to help with pain. But I am careful to not walk too far. I'm 75 and had the stem cell transplant and first PRP in 2021 and the second round of PRP in 2024. Now my husband is having knee pain so he is willing to do this same routine!!
My aunt had stage 4 osteoarthritis in her hip ie bone on bone and she had several prp and stem cell injections but it didn’t work for her. So she had hip replacement 2 years ago and says she has never been better.
Injecting sugar as a local irritant also matches Naviaux saying that when his autistic patients get a fever their autism symptoms reduce or go away dramatically. Autism and fever don't coexist at the same time, presumably, because they are different parts of the CDR and the body must prioritize one over the other.
My friend and I highly suspect that the chronic CDR illness happen when the 'memory cell's in the immune system are imprinted with the body-in-CDR template. We figure that they live about 3-6 months as per the internet description of T and B cells, which matches Naviaux's timeline for when a stressor can go chronic when uncured, which means new memory cells being formed are being signaled an unhealthy state for your body as the default which then causes your body to 'ignore' or even maintain your CDR cells unless something novel happens because they never knew you when you were healthy.
Amazing article. Hurt my brain on a few points. Incredible how the body handles waste it cannot dispose and that whole interconnected repair function that you eloquently described. Trying a few things with DMSO, and a few more yet to do. Thanks for the education: you are marvellous.
FWIW, I’ve received a couple PRP type treatments after tooth extraction to heal more sufficiently. They take my blood first, centrifuge it (I think) and create a fibrous plug/clot of sorts they place into the extraction site after removal. It’s worked amazingly well according to my dentist. To shift gears slightly I’m wondering if you have any opinions around hernias more specifically lower abdominal type hernias and whether or not healing is possible without surgical intervention. I’m considering some approaches, including BPC 157 and or Comfrey along with DMSO… I’m not planning anything outlandish, but can’t help thinking about alternative approaches to the typical surgical mesh approach. Thank you for your Substack, wonderful content.
Correctly done prolotherapy can halt progression. Beyond that gets kind of complicated, but some surgeons (if you can find them) will do repairs without mesh.
I've had a similar hernia for years and have decided to just keep stuffing it back in every night before bed so there are no adhesions. I've built a homemade truss that holds it back enough to go about my day without even remembering the hernia is there. The reasons for this decision were that mesh repairs have about a 40% failure rate, and one slip by the surgeon with the scalpel or surgical robot and you're wearing a colostomy bag for the rest of your life, this happens more than surgeons would like to admit. There have even been multiple incidences locally of hernia surgeons nicking a vein or artery and sending the unsuspecting patient home bleeding into their abdominal cavity...which required life saving heroics surgery to save the patient later. As the Doc here says, surgical skill levels vary drastically, possibly fatally.
The only reputable place I could find that will still stitch up a hernia without mesh is Shouldice hospital in Canada. I've been to Shouldice for a different hernia years ago, and I really like them, but that's not guaranteed to work either. Have a look at their google reviews for the pros and cons there, the reviews highlight a lot of what you won't find otherwise, good and bad.
Here's a page from my long neglected website on Shouldice and that first hernia:
P.S. My holistic vet saved both rear knees on my Golden Retriever using prolotherapy. She had fixed her own knees wrecked from years of semi pro basketball playing the same way. She also picked up on the DMSO smell on my dog and we talked a bit on how DMSO had been her saving grace as an athlete for all the injuries.
I had 2 no mesh hernias repairs 4 years ago. The one that was the big problem for me was a ventral. The inguinal wasn't a big issue yet. But since I traveled that far, Ft.Meyers from Minnesota, and the recovery period about the same....
Anyway, thankful I got them both fixed. Haven't had any complications. Great people to work with. They specialize in no mesh.
I recently had PRP injection in my right shoulder due to a tear in my rotator cuff area that was causing much pain. After the PRP injection, it was quite painful for about 15 minutes, but then the pain was reduced and still much less painful. I still have pain with some movements, but it doesn’t ache like previously. I was told it would take a week of two to determine how much it helped. My question is how do you know if you had a cheap PRP kit that was ordered, my kit cost $500 since it’s not covered by insurance.
Hi Ruth . I had a bad fall and stretched the ligaments in my bicep and had a tear in rotator cuff that had happened 15 years ago and took 5 years to get back to 85%. Arm was useless . No doctor visits . After 2 months and about 10 or 15 % healing I took barbera oneills advice and put potato poultices on each injury . Dr. Berg talked about collagen with peptides so I started that simultaneously. The result were almost instantaneous. I could tell after 2 days my arm was healing . It's been 4 weeks with my regimen and I know its just a matter of another 4 weeks or so and ill be back to normal . 32 dollars for the collagen and 4 pounds of potatoes.
Hi Ruth . I took about 4 heaping tablespoons of collagen . The Australian lady Barbera Oneil has videos on t he poultice . My arm is rapidly improving and the rotator cuff went from searing pain to pinching but has full mobility .
Sadly for me, even at only 10%, DMSO severely irritates my skin. And I find no Regenerative Medicine doctors anywhere nearby Holladay TN. I've called QC Kinetix, they are unaffordable for a retired trucker with VA and Medicare.
Try 1%. Approximately 1 drop of DMSO in a tsp. of distilled water. Then increase the dose slowly. Once you see irritation, back off by 1 drop or so. Anything over 5% can irritate the skin. Learn more at https://raindrop.io/glycop/2-dmso-and-msm-18528209
Thanks for your meticulous work that pushes so courageously back against what I term the Iatrogenesis Mafia (pHarmaceutical industry, medical establishment, regulatory agencies).
I note you mention hormesis but not Chlorine Dioxide and if I am accurate you have not written much on the Universal Antidote, anything on this coming up in the future especially after Pierre Kory’s new book: The War on Chlorine Dioxide?
By Curious Outlier:
“When people with diseases caused by mitochondrial dysfunction (e.g. diabetes, cancer, chronic fatigue, and dementia) take chlorine dioxide, they quite often have a reversal of these problems. The known mechanism of action for reversing these diseases caused by mitochondrial dysfunction is ROS-induced mitochondrial hormesis.”
Ok, looking forward to you publishing your understanding of the Universal Antidote as you seem to have the ability to ferret out really useful information backed by science.
I consider of all the substances and machines that can help us obtain Health Freedom, Chlorine Dioxide is the main one since it seems to live up to its NASA bestowed handle of the "Universal Antidote" and is so inexpensive compared to most others (second might be DMSO).
Again, thank you for your great, good work to help us exit the Iatrogenesis Mafia's Morgue.
Consider using AK and test the concentration of eATP in the effected tissue(by holding that tissue frequency near the organ, the eATP vial, and using homeopathic vials with concentrations from most to least). Then make up homeopathic vials for each remedy/procedure and see which solution works best by using the concentration kit to see if eATP is more dilute to non existent. Use vials for the different stages of CDR. Test to see if the cells normalize. Your writing is tremendous and provokes ideas of testing. Sincerely, Dan Eyink MD
Thanks - I was asked can one use DMSO after a Penile implant - could it damage the cylindar implants in the penis or it is safe and will promote healing and health . edit -Materials = Silicone: The main body of the cylinders, which gives the implant a natural, pliable feel.
Dacron/Lycra Fabric: A woven fabric layer incorporated into the silicone, strengthening the cylinders and preventing aneurysmal ballooning.
Parylene Coating: A micro-thin coating applied to the silicone surface to reduce surface friction, decrease fatigue, and increase the longevity of the device.
InhibiZone Antibiotic Surface Treatment: A proprietary coating containing Rifampin and Minocycline to protect against post-operative infection.
Doc - what do you think about using prolotherapy on knee replacement? I've had it imaged, and the implant and bone are happily growing together & the joint itself is strong - but the soft tissue around is a mess of pain.
I asked my most recent prolotherapy doc (she's a by-the-book doc) and she said NO that she would never, the needle would go too close to the implant. I suspect that my original shot doc - who is more of a cowboy (but I feel like a piece of meat on his table) might do it if I asked.
I have NOT used DMSO subcutaneous injections around the knee - also afraid to shake loose any - whatever is in there.
Wondering your opinion?
ALSO (sorry to ask two) - I think I traced my headaches back to head injury. X-rays as an infant to eliminate port wine stain (they did that in the 60's) - I have a dent in my skull where they did that. And a concussion in the 70's, I still have a bump from that. HOW do you do regenerative medicine on skull & brain?
Thank you for your invaluable work exposing the truth and your deep dives into forgotten/suppressed effective treatments that can help heal the body.
"The rate of autoimmune complications is very high, and concerns about these effects have led to various hypotheses over why it is happening."
The mRNA transfection platform itself is irreparably flawed & inherently dangerous and the platform itself IS the primary problem.
The mechanism of action (using mRNA instructions to turn one’s own cells into foreign non-self “spike protein factories”) IS the primary mechanism of harm. This triggers an immune system attack response, starting with the Killer T-Lymphocyte cells which will target & destroy one's formerly healthy cells, ANYWHERE in the body, that are now expressing non-self proteins...starting a cascade of damage at the deepest biological/cellular level.
Due to the proven systemic biodistribution properties of the (toxic & inflammatory) lipid nanoparticles, the encased (designed to be long-lasting) n1-methyl pseudouridine modified mRNA can go anywhere in the body, including crossing the blood-brain & placental barriers. The LNP "delivery vehicles" traveled to different parts of the body in different people.
Expressing any foreign non-self protein is fatal to the cell doing the expressing.
Some people will express lots of foreign proteins in vulnerable locations.
Others express less in less vulnerable areas.
The location of expression defines the adverse event: if you get foreign protein expression in your heart cells, you could get myocarditis & experience cardiac arrest; if the expression is in your brain, spinal cord, or peripheral nervous system, you could get one or more of a variety of neurological conditions; if in your eye, possible blindness; if in your ovaries, possible infertility; if in the placenta, possible miscarriage, stillbirth, or birth defects; if in the endothelial cells that line your blood vessels, possible vascular &/or microvascular injuries like clots/microclots or the long white fibrous clots, leading to strokes, heart attacks, or pulmonary embolisms…
If the expression of foreign proteins is in your own immune cells, you could experience immune dysfunction, dysregulation, & suppression including repeated infections, immune tolerance of a pathogenic foreign protein due to antibody subclass switch to IgG4 & increased IgG4-related diseases, T cell exhaustion, interference with & suppression of innate immunity, persistent systemic inflammation, dysregulation of toll-like receptors and reduced cancer surveillance or the suppression of tumor-suppressing immune system activities & cell-signaling (increasing your risk of fast-growing and aggressive cancers). And more…
Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs.
These modified mRNA-LNP genetic transfection injections never would have passed proper safety studies required for gene therapy products. Safety studies (including biodistribution, immunogenicity, immunotoxicity, genotoxicity, carcinogenicity, reproductive toxicity, shedding, long-term effects, & more) that were bypassed because of the mislabeling as “vaccines”. (And because of the EUA & “countermeasure” designations under the Project BioShield Act & PREP Act).
The danger is NOT limited to just getting more COVID “boosters”. ANY mRNA gene “therapy” product that transfects your cells & instructs those cells to produce non-self proteins (ANY non-self protein) will trigger an immune system attack response against your own cells & tissues. This makes EVERY mRNA-based transfection product harmful by design.
This immune response to one's own cells being instructed to express non-self proteins (ANY non-self protein) triggers autoimmune responses, & then T-cell exhaustion & immune system dysfunction, regardless of whether or not the foreign protein is toxic itself.
"While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system.
This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart.
Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues."
As you and your readers know, the immune dysfunction & collapse that has manifested in an unprecedented number of people worldwide, accompanied by surges in autoimmune conditions, chronic infections, cancers, & cardiometabolic disease is unfortunately very real.
This is not speculation. This is measurable — in lymphocyte counts, antibody profiles, T-cell exhaustion markers, & verified clinical outcomes, including deaths.
AND, as you have documented, shedding from these mRNA transfection injections IS an extremely serious concern, with some people being affected more than others.
NO ONE should have ever had the “choice” of taking these gene “therapy” transfection injections because the modified mRNA-LNP genetic transfection technology platform is fundamentally flawed & dangerous by design.
These transfection injection bioweapons NEVER should have been injected into a single human being.
It is not enough for there to be no mandates. It is not enough for the injurious and even deadly COVID modified mRNA transfection shots to be recalled. For the sake of humanity, the mRNA-LNP genetic transfection platform, and ALL of its iterations, must be banned.
If you have had a DMSO report you'd like to share, please do so here:
https://www.midwesterndoctor.com/p/the-remarkable-history-and-safety/comments
When they are posted in other places, despite my best efforts, they frequently get missed and don't make it up there.
Additionally, the most current information on using DMSO can be found in this article:
https://www.midwesterndoctor.com/p/dmso-heals-the-eyes-and-transforms
There are a lot of other DMSO articles in the cue, but I made a decision I needed to do a much more comprehensive review of the literature first (manually going through ~300,000 studies and sorting the 6,000 comments I've received) as certain studies needed to write the future articles cannot be found in any other manner. I'm hoping to have the next one done at the end of February or start of March.
Thank you so much for your support and understanding.
Additionally since many of you have asked where I am at on the DMSO project, I feel like I have now gone through over 90% of the available literature. At this point I need about a week to do:
•This one (currently on 2021): https://pubmed.ncbi.nlm.nih.gov/?term=(DMSO%5Btiab%5D%20OR%20%22dimethyl%20sulfoxide%22%5Btiab%5D%20OR%20dimethylsulfoxide%5Btiab%5D%20OR%20dimethylsulphoxide%5Btiab%5D%20OR%20%22dimethyl%20sulphoxide%22%5Btiab%5D)%20NOT%20(DMSO%5Bti%5D%20OR%20%22dimethyl%20sulfoxide%22%5Bti%5D%20OR%20dimethylsulfoxide%5Bti%5D%20OR%20%22dimethyl%20sulphoxide%22%5Bti%5D%20OR%20dimethylsulphoxide%5Bti%5D)&filter=years.2021-2021&size=50&page=6
• https://pubmed.ncbi.nlm.nih.gov/?term=%22Dimethyl+Sulfoxide%22%5BMeSH+Terms%5D+NOT+%28DMSO%5Btiab%5D+OR+%22dimethyl+sulfoxide%22%5Btiab%5D+OR+dimethylsulfoxide%5Btiab%5D+OR+%22dimethyl+sulphoxide%22%5Btiab%5D+OR+dimethylsulphoxide%5Btiab%5D%29&ac=yes&cauthor_id=None&user_filter=&schema=none&page=1&whatsnew=None&show_snippets=on&sort=relevance&sort_order=desc&format=summary&size=200 (much shorter to do)
•Possibly do a second pass through the first one to catch what I missed.
•5000 more results in CNKI
• https://scholar.google.com/scholar?q=intitle%3A%28DMSO+OR+%22dimethyl+sulfoxide%22+OR+dimethylsulfoxide+OR+%22dimethyl+sulphoxide%22+OR+dimethylsulphoxide%29&hl=en&as_sdt=0%2C33&as_ylo=2025&as_yhi=2025 (title only searches for 2025 I held off doing until the end of the project so they would all be indexed and searchable)
•The big thing I am trying to figure out is if I want to do this one (it's the last thing left outside of those and will probably take about a week to a month depending on how thoroughly I do it): https://scholar.google.com/scholar?hl=en&as_sdt=0%2C5&q=intext%3A%22dmso%22+-intitle%3ADMSO+-dimethyl+-dimethylsulfoxide+-cryo*+-synthesis+-oxidation+-Swern+-PCR+-NMR+-photoresist+-ligand+-extraction+-polymerization+-catalysis+-pKa+-swelling+-battery+-reduction+-chromatography+-solubility+-film+-gel+-solvation+-simulation+-dissolution+-electrolyte+-complex+-nanoparticle+-composite+-fabrication+-coating+-adsorption+-perovskite+-electrochemical+-deposition+-corrosion+-separations+-crystallization+-formulation+-dispersion&btnG=
I enjoyed and learned a lot from your thoughtful write ups!! Thanks!
It is extremely hard to find an effective solution for MRI contrast agent Gadolinium toxicity which can be worse than cancer. I don't know if DMSO can help. Or anything else.
There are other alternatives, as Doc has said - but - getting your radiologist to use them is the issue. "Oh, this is what we use," "this is all we have"
If they ever ask me about contrast, I will likely decline. Watching a friend who took the contrast last year for a cardiac thing, and - she's not been well, since.
Amazing article - the scarring part is the most fascinating to me and I will follow up.
Thank you Jessica; I hope you are doing well!
AMAZING. I am 100% sure that the link between previous injuries (that involve scarring) are hot zones for gasoline on the fire spots wrt spike and the inflammatory response. This is also why I believe cell turnover is key to "healing". Sweating, movement, fascia release, nerve flossing - all vital. If everyone had access to a sauna, red light lamps (+ natural UV light and clean food and water, there would be almost no disease states in humans. Even in the face of the psychos weaponizing ticks .
Hi Jessica
Have you ever heard of Canadian doctor Adeel Khan? If not please have a watch & listen.
I found him when I was researching possible treatments for my jab injured son. (FYI: He had to flee Canada in order to practice this type of Regenerative Medicine.)
https://www.illusionconsensus.com/p/ep-45-new-hope-for-vaccine-injuries
Also: "It's not CANADA but it's the next best thing".
Dr. Khan has partnered with a Florida clinic. God BLESS Dr. Joe Ladapo & Governor Ron DeSantis. 👍👍👍🙏
https://youtube.com/shorts/eXhfKeHpmeo
I'm not sure what he meant by "It's not CANADA but it's the next best thing" ? I live in Canada and our health care system is as bad or worse than any LOL.
I live here too. 😥
I think local anaesthesia acts as a reset button in terms of being a biophysical hard reset button on peripheral nociceptive circuits? ie: temporarily short-circuiting aberrant, self-sustaining electrical storming in inflamed nerves and dorsal root ganglia. This would extinguish maladaptive positive-feedback loops of neurogenic inflammation, central sensitization wind-up, and glial over-activation which would subsequently allow the system's intrinsic homeostatic mechanisms to reboot toward normalized membrane potentials, restored microvascular perfusion, damped cytokine cascades, and accelerated tissue repair without the persistent "phantom alarm" of chronic pain signaling.
I am curious as to the connection to general vs. local experiences... do we local consciousness, for example? And if so, is this why local anaesthetics "work" as reset/heal mechanism?
The way I often describe the process to patients is that it's like rebooting a computer that crashed, and when it resets everything works normally. The classic way this is explained is that every nerve has a firing threshold, and when they get overly stressed, they can switch to becoming hypersensitive to firing and hence cause a lot of issues from firing a lot, whereas when the anesthetic wears off, they reset to the normal firing.
The condition which maps the most closely to a classic neural therapy lesion is complex regional pain syndrome since it has all the pain plus localized dysautonomica.
I have wondered about gas anesthetics. Overall, I don't think they help with these issues, which may in part be due to them being CNS toxins rather than something that just temporarily sedates the nerve and wears off.
Hmm... gonna think on that.
My comment to Jessica about trigger point injections and sustained benefits...
Sorry, one more comment add-on. :) Since local cellular bioelectric contributions [linearly] add up to form emergent "general" fields that orchestrate multicellular life, then perturbing one part (e.g., via ion channel drugs) could propagate system-wide changes (see: Michael Levin's work)
In practice that is what you often see.
I'm reachin' a bit here, but the body connection thing seems key. Why the hell isn't biophysics common learning ground anyway? And the fact that we comprise a massive load of other organisms with their own [electrical/biophysical] signatures - why the hell aren't we almost only focused on the environment created by these organisms within us that effectively IS us? We're so dumb sometimes. :)
My longstanding hypothesis is that it's because biophysics does not lead to the development of profitable drugs.
Touché!!
We have to wait until the aliens arrive and demonstrate how so much of modern "medicine" is blood letting and sorcery. It's absolutely fascinating to consider the ramifications(ethical of course...not profit oriented like the medical mafia overlords) of these areas of discipline. It's utterly confounding how any so called science can be so myopic in its understanding of the body despite the hollow boasting of yet one more toxic creation to lower a meaningless metric or mask a root cause. Thanks for the contributions of both you and MWD.
I had good sustained results with trigger point injections with local anaesthetic, with or without steroid, for nerve pains, including postoperative neuromas, very common after c-sections.
Jumping in here, Jesdica and AMD. Dont understand most of what you're talking about as am not a learned person, but wondering if this may be the way to deal with Trigeminal neuralgia??? The prescribed drugs are just SO evil.
I see there are several potential causes of your condition:
compression by a blood vessel
Multiple sclerosis
myelin sheath damage
A tumor pressing against the trigeminal nerve
stroke or facial trauma.
injury of the nerve due to surgery
Perhaps, if its known, that can better determine if success can be reached with these tretments discussed in this article.
I certainly will send some positiove vibes your way as I cant even claim to understand how uncomfortable and stressful that must be.
Jumping in here, Jesdica and AMD. Dont understand most of what you're talking about as am not a learned person, but wondering if this may be the way to deal with Trigeminal neuralgia??? The prescribed drugs are just SO evil.
Well done!
Human healing is so complex! I’ve been working on it personally for 45 years! 25 of those as a physician. Most of my training was learning and growing through 20 years of epilepsy and 300 seizures.
I was one of the first individuals offering PRP in the country. Fortunately, I was more drawn to the cases that did not progress, rather than the successful ones. There are downsides to not being satisfied with results! I’ve neurotically created procedures, pathways, paradigms, structures, approaches, ways of embracing the human body, mind, heart spirit as an integrated quantum bioenergetic, wonder, etc. i’m sure we could have many long discussions on this and many other topics.
Currently, cervical dystonia, complex, regional pain, syndrome, complex, PTSD, craniocervical, instability, lumbar discs, neuropathy, Ehler’s Danlos Syndrome, fluoroquinone toxicity, are my most common cases.
Having performed stem cell therapist for longer than nearly anybody else in the country, the most significant challenge facing this emerging field is autologous versus allogeneic therapies. I’ve given whole weekend conferences on why allogeneic therapies are a problematic set of approaches from immune, infectious,, genetic, and survivability approaches. Many people will discuss outcomes/decrease in symptoms. However, healing and decreasing symptoms often are quite divergent in their course forward.
Harmonizing structural, neurologic, physiologic, emotional, energetic, spiritual, and timing aspects of care is extremely complex. We have nine providers collaborating together at our center – most of us working together for the last 10 years – to encourage a person to embrace their own healing journey. The reduction in interference patterns – from Energetic/quantum to emotional to cellular – thank you for highlighting the cell danger response – to neurologic, and structural is extremely important trophic effects to occur in structure. The neurological layer alone is seven segments of interrelated healing care!
Thank you for the thoroughness of your articles! One small inclusion: the most commonly used anesthetic for subcutaneous Neuroprolotherapy is procaine. It is the only anesthetic that has parasympathetic effects.
Finally, perhaps the most important tool in all of our bag of tricks is called Stellate ganglion block. I was fortunate to be the third physician in the country doing them under ultrasound guidance for PTSD. I’ve been doing this for over 15 years. The calming effects to the sympathetic system, the opening it gives parasympathetic healing, the relaxation of emotional trauma, and the quantum energetic effects from resetting the ganglia widely opens the door for more significant healing.
Thank you for living your calling!
Ronald W Hanson Junior, MD
Thank you for the article on regenerative therapies for pain!! I was almost unable to walk because of knee pain, facing life in a wheel chair and was not going to have a knee replacement. Family members had done that and still experienced so much pain. So I had stem cell transplant on the worst knee and PRP on the one with less pain. It improved greatly but I still had some pain, some days in both knees on walking. So I did a second round of PRP on both knees and I can walk pain free now. I cannot walk long distances - which for me is taking short jaunts into more than 3 stores in a day - but it does not hurt while I am walking. I notice that pain that night in bed but it is not severe at all. I use DMSO on it then to help with pain. But I am careful to not walk too far. I'm 75 and had the stem cell transplant and first PRP in 2021 and the second round of PRP in 2024. Now my husband is having knee pain so he is willing to do this same routine!!
Glad that prp and stem cells worked for you.
My aunt had stage 4 osteoarthritis in her hip ie bone on bone and she had several prp and stem cell injections but it didn’t work for her. So she had hip replacement 2 years ago and says she has never been better.
Injecting sugar as a local irritant also matches Naviaux saying that when his autistic patients get a fever their autism symptoms reduce or go away dramatically. Autism and fever don't coexist at the same time, presumably, because they are different parts of the CDR and the body must prioritize one over the other.
My friend and I highly suspect that the chronic CDR illness happen when the 'memory cell's in the immune system are imprinted with the body-in-CDR template. We figure that they live about 3-6 months as per the internet description of T and B cells, which matches Naviaux's timeline for when a stressor can go chronic when uncured, which means new memory cells being formed are being signaled an unhealthy state for your body as the default which then causes your body to 'ignore' or even maintain your CDR cells unless something novel happens because they never knew you when you were healthy.
Amazing article. Hurt my brain on a few points. Incredible how the body handles waste it cannot dispose and that whole interconnected repair function that you eloquently described. Trying a few things with DMSO, and a few more yet to do. Thanks for the education: you are marvellous.
FWIW, I’ve received a couple PRP type treatments after tooth extraction to heal more sufficiently. They take my blood first, centrifuge it (I think) and create a fibrous plug/clot of sorts they place into the extraction site after removal. It’s worked amazingly well according to my dentist. To shift gears slightly I’m wondering if you have any opinions around hernias more specifically lower abdominal type hernias and whether or not healing is possible without surgical intervention. I’m considering some approaches, including BPC 157 and or Comfrey along with DMSO… I’m not planning anything outlandish, but can’t help thinking about alternative approaches to the typical surgical mesh approach. Thank you for your Substack, wonderful content.
Correctly done prolotherapy can halt progression. Beyond that gets kind of complicated, but some surgeons (if you can find them) will do repairs without mesh.
I've had a similar hernia for years and have decided to just keep stuffing it back in every night before bed so there are no adhesions. I've built a homemade truss that holds it back enough to go about my day without even remembering the hernia is there. The reasons for this decision were that mesh repairs have about a 40% failure rate, and one slip by the surgeon with the scalpel or surgical robot and you're wearing a colostomy bag for the rest of your life, this happens more than surgeons would like to admit. There have even been multiple incidences locally of hernia surgeons nicking a vein or artery and sending the unsuspecting patient home bleeding into their abdominal cavity...which required life saving heroics surgery to save the patient later. As the Doc here says, surgical skill levels vary drastically, possibly fatally.
The only reputable place I could find that will still stitch up a hernia without mesh is Shouldice hospital in Canada. I've been to Shouldice for a different hernia years ago, and I really like them, but that's not guaranteed to work either. Have a look at their google reviews for the pros and cons there, the reviews highlight a lot of what you won't find otherwise, good and bad.
Here's a page from my long neglected website on Shouldice and that first hernia:
https://www.davebross.com/Health/Hernia.html
P.S. My holistic vet saved both rear knees on my Golden Retriever using prolotherapy. She had fixed her own knees wrecked from years of semi pro basketball playing the same way. She also picked up on the DMSO smell on my dog and we talked a bit on how DMSO had been her saving grace as an athlete for all the injuries.
Thanks so much for the insight!
You're welcome, always glad to save someone some research legwork.
I had 2 no mesh hernias repairs 4 years ago. The one that was the big problem for me was a ventral. The inguinal wasn't a big issue yet. But since I traveled that far, Ft.Meyers from Minnesota, and the recovery period about the same....
Anyway, thankful I got them both fixed. Haven't had any complications. Great people to work with. They specialize in no mesh.
Dr. Tomas, U First Health
I recently had PRP injection in my right shoulder due to a tear in my rotator cuff area that was causing much pain. After the PRP injection, it was quite painful for about 15 minutes, but then the pain was reduced and still much less painful. I still have pain with some movements, but it doesn’t ache like previously. I was told it would take a week of two to determine how much it helped. My question is how do you know if you had a cheap PRP kit that was ordered, my kit cost $500 since it’s not covered by insurance.
Hi Ruth . I had a bad fall and stretched the ligaments in my bicep and had a tear in rotator cuff that had happened 15 years ago and took 5 years to get back to 85%. Arm was useless . No doctor visits . After 2 months and about 10 or 15 % healing I took barbera oneills advice and put potato poultices on each injury . Dr. Berg talked about collagen with peptides so I started that simultaneously. The result were almost instantaneous. I could tell after 2 days my arm was healing . It's been 4 weeks with my regimen and I know its just a matter of another 4 weeks or so and ill be back to normal . 32 dollars for the collagen and 4 pounds of potatoes.
Collegen with peptides, how much did you take daily? Interesting about that and the poultice. Thanks
Hi Ruth . I took about 4 heaping tablespoons of collagen . The Australian lady Barbera Oneil has videos on t he poultice . My arm is rapidly improving and the rotator cuff went from searing pain to pinching but has full mobility .
Wow. That’s impressive. I’ll order the collagen and see how it does. The PRP injection has helped a lot.
Sadly for me, even at only 10%, DMSO severely irritates my skin. And I find no Regenerative Medicine doctors anywhere nearby Holladay TN. I've called QC Kinetix, they are unaffordable for a retired trucker with VA and Medicare.
Dwayne - I have the same issue. But it disappears when I followup the DMSO with caster oil.
Thanx, I'll try it. Stuff is sho'nuff MESSY.
Try 1%. Approximately 1 drop of DMSO in a tsp. of distilled water. Then increase the dose slowly. Once you see irritation, back off by 1 drop or so. Anything over 5% can irritate the skin. Learn more at https://raindrop.io/glycop/2-dmso-and-msm-18528209
Thanx.
There is a practice called Performance Medicine with a few locations in TN that might be able to help you.
Thanx. I'm in W. TN they're in E. TN.
It's not E Tennessee. It's in Florida.
Watch Dr. Khan's vids for more data:
https://youtube.com/shorts/eXhfKeHpmeo
Thanks for your meticulous work that pushes so courageously back against what I term the Iatrogenesis Mafia (pHarmaceutical industry, medical establishment, regulatory agencies).
I note you mention hormesis but not Chlorine Dioxide and if I am accurate you have not written much on the Universal Antidote, anything on this coming up in the future especially after Pierre Kory’s new book: The War on Chlorine Dioxide?
By Curious Outlier:
“When people with diseases caused by mitochondrial dysfunction (e.g. diabetes, cancer, chronic fatigue, and dementia) take chlorine dioxide, they quite often have a reversal of these problems. The known mechanism of action for reversing these diseases caused by mitochondrial dysfunction is ROS-induced mitochondrial hormesis.”
https://curioushumanproductions.substack.com/p/how-chlorine-dioxide-can-reverse
Have to write about ozone first. Views CDS as less urgent since Pierre Kory has already written about.
Ok, looking forward to you publishing your understanding of the Universal Antidote as you seem to have the ability to ferret out really useful information backed by science.
I consider of all the substances and machines that can help us obtain Health Freedom, Chlorine Dioxide is the main one since it seems to live up to its NASA bestowed handle of the "Universal Antidote" and is so inexpensive compared to most others (second might be DMSO).
Again, thank you for your great, good work to help us exit the Iatrogenesis Mafia's Morgue.
Consider using AK and test the concentration of eATP in the effected tissue(by holding that tissue frequency near the organ, the eATP vial, and using homeopathic vials with concentrations from most to least). Then make up homeopathic vials for each remedy/procedure and see which solution works best by using the concentration kit to see if eATP is more dilute to non existent. Use vials for the different stages of CDR. Test to see if the cells normalize. Your writing is tremendous and provokes ideas of testing. Sincerely, Dan Eyink MD
Please write a thesis about methylene blue and its ability to improve mitochondria respiration..
See the Truth About Methylene Blue & Nitric Oxide Signaling: Science Vs. Fads In Health Trends https://raindrop.io/glycop/2016-18528107/search/sort=score&perpage=30&page=0&search=methylene
Many thanks,
Randy
Thanks - I was asked can one use DMSO after a Penile implant - could it damage the cylindar implants in the penis or it is safe and will promote healing and health . edit -Materials = Silicone: The main body of the cylinders, which gives the implant a natural, pliable feel.
Dacron/Lycra Fabric: A woven fabric layer incorporated into the silicone, strengthening the cylinders and preventing aneurysmal ballooning.
Parylene Coating: A micro-thin coating applied to the silicone surface to reduce surface friction, decrease fatigue, and increase the longevity of the device.
InhibiZone Antibiotic Surface Treatment: A proprietary coating containing Rifampin and Minocycline to protect against post-operative infection.
Can DMSO help with MCAS? Do you have any insight regarding histamine/ MCAS? Have you written on it?
Erin, consult with a naturopathic doc and see if DMSO would help. You need a physician that understands you as an individual. This article may be helpful at https://drrobssolutions.com/blogs/mcas-and-breast-implant-illness/understanding-mast-cell-activation-syndrome-mcas-complete-guide-to-symptoms-triggers-treatment
Doc - what do you think about using prolotherapy on knee replacement? I've had it imaged, and the implant and bone are happily growing together & the joint itself is strong - but the soft tissue around is a mess of pain.
I asked my most recent prolotherapy doc (she's a by-the-book doc) and she said NO that she would never, the needle would go too close to the implant. I suspect that my original shot doc - who is more of a cowboy (but I feel like a piece of meat on his table) might do it if I asked.
I have NOT used DMSO subcutaneous injections around the knee - also afraid to shake loose any - whatever is in there.
Wondering your opinion?
ALSO (sorry to ask two) - I think I traced my headaches back to head injury. X-rays as an infant to eliminate port wine stain (they did that in the 60's) - I have a dent in my skull where they did that. And a concussion in the 70's, I still have a bump from that. HOW do you do regenerative medicine on skull & brain?
Great article. How does neurotherapy treat tinnitus exactly and where would the injection sites be for such treatment??
Thank you for your invaluable work exposing the truth and your deep dives into forgotten/suppressed effective treatments that can help heal the body.
"The rate of autoimmune complications is very high, and concerns about these effects have led to various hypotheses over why it is happening."
The mRNA transfection platform itself is irreparably flawed & inherently dangerous and the platform itself IS the primary problem.
The mechanism of action (using mRNA instructions to turn one’s own cells into foreign non-self “spike protein factories”) IS the primary mechanism of harm. This triggers an immune system attack response, starting with the Killer T-Lymphocyte cells which will target & destroy one's formerly healthy cells, ANYWHERE in the body, that are now expressing non-self proteins...starting a cascade of damage at the deepest biological/cellular level.
Due to the proven systemic biodistribution properties of the (toxic & inflammatory) lipid nanoparticles, the encased (designed to be long-lasting) n1-methyl pseudouridine modified mRNA can go anywhere in the body, including crossing the blood-brain & placental barriers. The LNP "delivery vehicles" traveled to different parts of the body in different people.
Expressing any foreign non-self protein is fatal to the cell doing the expressing.
Some people will express lots of foreign proteins in vulnerable locations.
Others express less in less vulnerable areas.
The location of expression defines the adverse event: if you get foreign protein expression in your heart cells, you could get myocarditis & experience cardiac arrest; if the expression is in your brain, spinal cord, or peripheral nervous system, you could get one or more of a variety of neurological conditions; if in your eye, possible blindness; if in your ovaries, possible infertility; if in the placenta, possible miscarriage, stillbirth, or birth defects; if in the endothelial cells that line your blood vessels, possible vascular &/or microvascular injuries like clots/microclots or the long white fibrous clots, leading to strokes, heart attacks, or pulmonary embolisms…
If the expression of foreign proteins is in your own immune cells, you could experience immune dysfunction, dysregulation, & suppression including repeated infections, immune tolerance of a pathogenic foreign protein due to antibody subclass switch to IgG4 & increased IgG4-related diseases, T cell exhaustion, interference with & suppression of innate immunity, persistent systemic inflammation, dysregulation of toll-like receptors and reduced cancer surveillance or the suppression of tumor-suppressing immune system activities & cell-signaling (increasing your risk of fast-growing and aggressive cancers). And more…
Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs.
These modified mRNA-LNP genetic transfection injections never would have passed proper safety studies required for gene therapy products. Safety studies (including biodistribution, immunogenicity, immunotoxicity, genotoxicity, carcinogenicity, reproductive toxicity, shedding, long-term effects, & more) that were bypassed because of the mislabeling as “vaccines”. (And because of the EUA & “countermeasure” designations under the Project BioShield Act & PREP Act).
The danger is NOT limited to just getting more COVID “boosters”. ANY mRNA gene “therapy” product that transfects your cells & instructs those cells to produce non-self proteins (ANY non-self protein) will trigger an immune system attack response against your own cells & tissues. This makes EVERY mRNA-based transfection product harmful by design.
This immune response to one's own cells being instructed to express non-self proteins (ANY non-self protein) triggers autoimmune responses, & then T-cell exhaustion & immune system dysfunction, regardless of whether or not the foreign protein is toxic itself.
https://www.youtube.com/watch?v=SDFUymH-9W8
https://entwine.substack.com/p/the-platform-is-deadly
https://robertchandler.substack.com/p/vaccinated-dead-kruger-lang-morz
https://x.com/newstart_2024/status/1981375686251069797
"While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system.
This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart.
Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues."
As you and your readers know, the immune dysfunction & collapse that has manifested in an unprecedented number of people worldwide, accompanied by surges in autoimmune conditions, chronic infections, cancers, & cardiometabolic disease is unfortunately very real.
This is not speculation. This is measurable — in lymphocyte counts, antibody profiles, T-cell exhaustion markers, & verified clinical outcomes, including deaths.
https://johncatanzaro.substack.com/p/the-profound-risks-of-gene-transfer
AND, as you have documented, shedding from these mRNA transfection injections IS an extremely serious concern, with some people being affected more than others.
https://www.midwesterndoctor.com/p/what-weve-learned-from-a-year-of
https://pierrekorymedicalmusings.com/p/shedding-of-covid-mrna-vaccine-components
https://www.thefocalpoints.com/p/breaking-study-pfizer-mrna-found
AND...if all of this is not already horrific enough, there are legitimate concerns that the blood supply is contaminated:
https://x.com/Safe_Blood3/status/1942237297035899370
https://vesavanhatupa.substack.com/p/a-call-to-action-lets-end-the-silence
https://laurakasner.substack.com/p/the-devil-was-hard-at-work-trying
https://laurakasner.substack.com/p/results-of-the-2024-worldwide-embalmer
https://laurakasner.substack.com/p/a-horrifying-breakthrough-in-the
NO ONE should have ever had the “choice” of taking these gene “therapy” transfection injections because the modified mRNA-LNP genetic transfection technology platform is fundamentally flawed & dangerous by design.
These transfection injection bioweapons NEVER should have been injected into a single human being.
It is not enough for there to be no mandates. It is not enough for the injurious and even deadly COVID modified mRNA transfection shots to be recalled. For the sake of humanity, the mRNA-LNP genetic transfection platform, and ALL of its iterations, must be banned.