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ME caused by squeezed nerve?

Hip

Senior Member
Messages
17,858
This TMJ thing is poppycock.

So are you saying that that Uzma Qureshi's cure from her probable ME/CFS illness through TMJ treatment was just imagined? To me it would not seem inconceivable that, in some small subset of patients with ME/CFS or ME/CFS-like conditions, their illness arises from or is exacerbated by some physical dysfunctions of the nerves.

It should be noted that higher levels of substance P are found in TMJ dysfunction patients. Substance P is released into the cerebrospinal fluid when the trigeminal nerve (which runs through the lower jaw) is stimulated.

Substance P is also found raised in the cerebrospinal fluid of fibromyalgia patients, and may be driving the symptoms of fibromyalgia. Substance P stimulates pain receptors in the body.

Now since temporomandibular joint disorder is a comorbid condition found in fibromyalgia, it is quite feasible that the substance P released by the TMJ dysfunction may be exacerbating the fibromyalgia, and thus TMJ treatment may lead to some remission from fibromyalgia.
 
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Sushi

Moderation Resource Albuquerque
Messages
19,935
Location
Albuquerque
@Sushi I know there are no autonomic specialists in my area (as we've already discussed this!) but did yours recommend any treatment or suggestions after determining that you had vagus nerve dysfunction? All of my doctors agree that I have autonomic dysfunction with varying degrees of BP dropping when I stand and tachycardia/POTS stuff. But other than Beta blocker & Florinef, no other real suggestions.

Yes, he treated me for several years (until I left that city) but the meds he used were tailored to my test results and couldn't be taken as general treatment guides for dysautonomia. I don't have POTS, beta blockers aren't suitable for me--just an example of how individualized treatment has to be.

About the only things that are right for most dysautonomia patients are more fluids and electrolytes. There are about 15 (off the top of my head) meds that are used in treatment and the wrong one is worse than none at all!

Sushi
 

Hip

Senior Member
Messages
17,858
It is possible to test vagus nerve functioning, however. Yet it wouldn't be possible to link dysfunction to a specific cause, like an infection. There have been some (I knew such a person) who, when a vagus nerve stimulator/pacer (not the correct word!), was implanted, either temporarily (think wires coming out the mouth! :jaw-drop:), or surgically, found that the majority of their symptoms resolved. There have also been some who got worse, hence the wires out the mouth approach.

Those implantable vagus nerve stimulators can work very well for severe depression, I read; and I have always wondered if they could help ME/CFS. The only trouble is that the surgery and the implantable stimulator device will set you back $50,000.

However, a new cheap, hand-held vagus nerve stimulator called the Gammcore that does not require surgery is soon to become available, and this will be worth trying.
 
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Hip

Senior Member
Messages
17,858
Since many people on PR (and elsewhere) with ME/CFS have been helped by anti-virals and you said that av's do not penetrate the Vagus nerve, does that somewhat disprove this theory in your opinion? I do not have enough of a science background to give an opinion!

No, the antivirals can penetrate the vagus, but do so poorly. So according to Michael VanElzakker, this may explain why antivirals can be helpful, but do not cure ME/CFS.

I think the most interesting aspect of VanElzakker's theory of ME/CFS is not the specifics of vagus infections, but the idea that a chronic low level infections somewhere in the body may constantly induce the state of sickness behavior. Sickness behavior can explain how many the symptoms of ME/CFS arise. This paper compares the symptoms of sickness behavior to the symptoms of ME/CFS, and finds similarities and differences.
 

Sushi

Moderation Resource Albuquerque
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19,935
Location
Albuquerque
Those implantable vagus nerve stimulators can work very well for severe depression, I read; and I have always wondered if they could help ME/CFS. The only trouble is that the surgery and the implantable stimulator device will set you back $50,000.

However, a new cheap, hand-held vagus nerve stimulator called the Gammcore that does not require surgery is soon to become available, and this will be worth trying.

That is really interesting, Hip. My friend had severe dysautonomia with an onset after being given 4 instead of 3 Hep B vaccinations. The vagus nerve stimulator removed the dysautonomia symptoms nearly instantly.

Sushi
 

Hip

Senior Member
Messages
17,858
My friend had severe dysautonomia with an onset after being given 4 instead of 3 Hep B vaccinations. The vagus nerve stimulator removed the dysautonomia symptoms nearly instantly.
Wow, that's amazing. I wonder if vagus nerve stimulation might help POTS, which I have.
 

Sushi

Moderation Resource Albuquerque
Messages
19,935
Location
Albuquerque
Wow, that's amazing. I wonder if vagus nerve stimulation might help POTS, which I have.

It might, I wonder about the availability of the units you linked? And the price, and whether a doc could prescribe one for a patient to try without buying, or to use in his/her office?

Sushi
 

Hip

Senior Member
Messages
17,858
I wonder about the availability of the units you linked? And the price, and whether a doc could prescribe one for a patient to try without buying, or to use in his/her office?

I think the Gammacore manufacturer is talking about pricing per electrical stimulation dose. The idea is that you would pay for say 300 electrical doses, and the stimulator unit would keep working until you had used up all of the 300 electrical stimulation doses it dispenses. Each stimulation lasts for 90 seconds, and presumably you'd only need to apply these stimulations a few times throughout the day. So I imagine the device itself will be cheap, and they will make money when people charge up the device with additional doses. I read this in this article about the Gammacore VNS device.

You apply the Gammacore device to the jugular vein area of your neck, where you can feel the pulse. The vagus nerve runs through this zone. You are supposed to do this only on the right side of the neck, not the left side (because stimulating the left side vagus nerve may have some untoward effects on the heart).
 
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2) If there is Vagus nerve infection, do anti-virals treat it? (assuming you identify correct pathogen)
CMX001 is lipophilic; i.e. it is drawn to fats. It crosses the blood brain barrier readily. I imagine it would have some effects on the peripheral nerves, too. It is "only" effective against herpes virus / double stranded viruses, though I imagine knocking those out would enable one's immune system to handle e.g. enteroviruses more readily. I found the typical "viral half life" under antiviral treatment is about a year.

The vagus nerve idea is promising, though I wonder if it is more often a problem due to the gut-vagus connection.
 

Sushi

Moderation Resource Albuquerque
Messages
19,935
Location
Albuquerque
@Hip
Leave it to medical device manufacturers to invent creative pricing! It sounds interesting but also something to be a bit cautious of. I won't be first in line!

Sushi
 

WillowJ

คภภเє ɠรค๓թєl
Messages
4,940
Location
WA, USA
Did anyone ever hear about this? What's your thought? I have to admit I have more or less decided not to go for it, but thought just to hear with you guys.

I think it would be like any other physical/ manual/ chiropractic/ etc therapy: some people would get some benefit, and some would not (or would feel worse).

I would think it would be a bad idea to go to someone who treated necks on the side. Pretty sure the normal way to do this is with compressed sound. Here's a description:
http://forums.phoenixrising.me/index.php?threads/chiropractic-treatments-need-advice.12751/

(apologies if that's already been posted, as I've not read the entire thread)

Ps, I think there is one published study on this in CFS
 
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Wayne

Senior Member
Messages
4,308
Location
Ashland, Oregon
Below is a part of a post I did on another thread regarding some of my experiences after getting an Atlas Profilax treatment (which I believe Optimist's original post was referring to). I believe my atlas "repositioning" released a lot of pressure on my cranial nerves, especially my vagus nerve. Thought it was pertinent to this thread because of the ongoing discussion about vagus nerve issues.
---
Here’s what I believe happened. The 12 major cranial nerves exit the brainstem through the opening in the atlas. If the atlas is out of alignment, these nerves can become impinged, and nerve flow to the rest of the body is inhibited. The vagus nerve is the longest of the cranial nerves, traversing through the TMJ, through the thyroid, the heart, stomach, GI system, and ending in the colon. If these organs/areas aren’t receiving enough nerve energy because of a crimped vagus nerve, they’re not going function properly or efficiently.

Here’s my theory as to why some people notice significant improvements from AP, and others don’t. — The opening in the atlas through which the cranial nerves go through is different in size from one person to the next. If the opening is large, the atlas can be out of alignment by quite a bit without impinging on the cranial nerves. If the opening is small, only a small misalignment can cause significant cranial nerve dysfunction. — A former NFL football player was temporarily paralyzed from a rather insignificant blow, and it was determined that the opening in his atlas was much smaller than normal, which significantly raised his potential for a serious injury. He promptly retired.

I feel certain most, if not all of my cranial nerves became impinged from a serious head injury/whiplash I experienced at age 15, which corresponded with the decline in my overall health. I am even more certain that at least my vagus nerve was majorly impacted. To have all this pressure relieved from a single treatment felt almost miraculous to me. I can easily see why others wouldn’t have a similar experience, because even if they had a seriously misaligned atlas, they may not have had seriously crimped nerves. The following is a list of improvements I jotted down a few months after receiving my AP treatment in the summer of 2007:
...............................................................

Symptom Improvements since Atlas Profilax Treatment 7-9-07

Primarily Neurological Symptom Improvements

Sensory Overload - 25-50%

Excessive Neuronal Firing - 25-50% (I feel Perque B-12 is very good for this also)

Anxiety – 25-50% (Didn’t even fully realize my levels of anxiety until they lessened significantly)

Vertigo / Neurally Mediated Hypotension – 25-50%

Environmental Illness (EI) / Multiple Chemical Sensitivity (MCS) – 25-35%

Cognitive Function / Ability to take make mental notes – 25-35%

Ability to Organize - 15-20%

TMJ (Moderate to begin with) - 20%-25%

Ability to relax – 25-35%

Severe adrenal exhaustion / dysfunction – approx. 25%

Sense of Balance – 25-50%

Sleep – approx. 15-20%

Primarily Physical Symptom Improvements

Physical / muscle strength – 25-30%

Viral overload symptoms – 50-75%

Digestion – 50%+

Generalized Pain and Headache reduction - 25-50%

Detoxification Capabilities – 25-50%

Postural Corrections, from my neck, down my entire spine to my hips, knees and even feet – I can’t even put a percentage on this – A growing sense of wholeness seems to pervade my entire postural structure. My chest cavity seems to have risen. When I walk these days, I feel like I’m almost gliding.

Overall energy level – approx. 10-25%

I feel taller and I am taller by 1/4"-1/2"

Spiritual/Energetic Improvements of Note

Overall Sense of Well Being – 25-50% (I especially notice this when I’m walking)

Greater sense of patience

Greater sense of rhythm

Feel less dense, a greater sense of fluidity
 

Wayne

Senior Member
Messages
4,308
Location
Ashland, Oregon
A brief comment on TMJ issues: I once read that 70% of all the nerve impulses exiting the brain pass through the TMJ. If this area is crimped, it's easy for me to imagine varying degrees of health impairment resulting from inadequate nerve flow to critical areas of the body.
 

ukxmrv

Senior Member
Messages
4,413
Location
London
If one peels of all mystic, weird stuff and dig around the purely scientific issues. there might actually be something to this squeezed nerve thing. I haven't been (cap)able to read through all that's been posted, but according to the articles @Hip refers to - having an alignment of the atlas bone and a correction of the jaw could be a possible symptom reliever.

According to the link provided by @khr (yes, that was the guy) and which I have briefly skimmed now, he seem to suggest that there is need of rebuilding some muscles, and a few other things too...

I wonder how this would relate to the Rituximab study?

I don't think that it is a question of "peeling away the mystical stuff" - that's another important part of the scam that hooks one in.

All the best scamsters who have claimed to be able to cure me have all had a hook that involves something plausible. It's part of the spiel. There needs to be something that sounds scientific or has a possibility there for the best ones to appeal to those of us who have done our homework. We are the more desirable victims. More of a challenge.

We say "OK he might be a bit flaky but he could be on to something under neath it all". It really hits after when we realise it is a scam. Not only did we go with the treatment but we didn't listen to our inner voice.

I'm speaking as well as someone who went though all the TMJ stuff in the 80's as well and got fleeced. Saw it happen to others in my support group.
 
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adreno

PR activist
Messages
4,841
Those implantable vagus nerve stimulators can work very well for severe depression, I read; and I have always wondered if they could help ME/CFS. The only trouble is that the surgery and the implantable stimulator device will set you back $50,000.

However, a new cheap, hand-held vagus nerve stimulator called the Gammcore that does not require surgery is soon to become available, and this will be worth trying.
Wouldn't a TENS or similar device possibly work for this, if placing the electrodes correctly?
 

Hip

Senior Member
Messages
17,858
Wouldn't a TENS or similar device possibly work for this, if placing the electrodes correctly?

I think the problem with your average TENS unit is that it uses DC current or low frequency (less than 300 Hz) AC current, and this apparently is not good for deeper penetration. You need higher frequency AC (several kHz) for good skin penetration. A strong enough DC current causes pain and irritation as it passes through the skin, but higher frequency AC can pass through the skin without eliciting pain, due to a capacitance effect of the skin which passes the current more easily.

If you look at this brochure, the Gammacore appears to use a 5000 Hz AC current, which is pulsed into short bursts — ie, pulsed current (PC); and a peak to peak voltage of up to 48 volts. I believe the reason pulsed current is used is also related to the skin capacitance effect. There is some info on the rationale for using pulsed alternating current in this paper.
 

Hip

Senior Member
Messages
17,858
CMX001 is lipophilic; i.e. it is drawn to fats. It crosses the blood brain barrier readily. I imagine it would have some effects on the peripheral nerves, too. It is "only" effective against herpes virus / double stranded viruses, though I imagine knocking those out would enable one's immune system to handle e.g. enteroviruses more readily. I found the typical "viral half life" under antiviral treatment is about a year.

The vagus nerve idea is promising, though I wonder if it is more often a problem due to the gut-vagus connection.

CMX001 sounds like a promising candidate.

The actual reasons that antivirals are much less effective for infections within nerve ganglia are listed in this post.

Another issue is working out what virus might be infecting the vagus nerve. It could be an enterovirus rather than a herpes family virus, in which case all the herpes antivirals are not going to be much use. Dr Chia says that enterovirus infections in the stomach can enter into the vagus nerve (as this nerve innervates the stomach), and it then takes just three days for the enterovirus infection to travel the entire length of the vagus nerve, from stomach to brain (and it may then enter the brain too). Chia found 82% of ME/CFS patients have enterovirus infections of the stomach, so enterovirus infections would be a prime suspect for a vagus nerve infection in ME/CFS.
 
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Hip

Senior Member
Messages
17,858
I found this about vagus nerve stimulators, where it says that the Gammacore stimulates both sympathetic and parasympathetic, hence a problem :
Neurostimulation Devices in Migraine treatment.

That link does say that the Gammacore stimulates both sympathetic and parasympathetic, but I don't think that can be correct, for the following reason:

Most of the parasympathetic nervous system runs through the vagus nerve, and the vagus lies not far beneath the skin in the neck, hence the vagus will be easily reached and stimulated by an electrical current passed through the skin of the neck. (The vagus nerve is the only nerve running from the head to the rest of the body that lies outside the spine).

By contrast, all of the sympathetic nervous system runs through the spine, which is encased in bone and is deeper inside the neck, and will thus presumably more protected from this electrical current passed through the skin.

The Vagus Nerve Running Outside The Spine, Through The Neck
Vagus Nerve in Head and Neck.jpg



The Parasympathetic (Left) and Sympathetic (Right) Nervous Systems
sympatheticandparasympatheticnervoussystem.jpg

In the above diagram, note how most of the parasympathetic nervous system
runs through the vagus nerve and the cranial nerves, with only a tiny part of the
parasympathetic running through the spine (this part exits at the very bottom of
the spine, in the sacral nerves); by contrast, all of the sympathetic nervous system
is routed through the spine.
 
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