Breakthrough Relief Through Vagus Nerve Neuromodulation (POTS) (
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- Опубліковано 28 лют 2024
- We go into the biology of rapid heart rate when changing body position (POTS - postural orthostatic tachycardia syndrome) and how vagus nerve neuromodulation could be helping with the condition.
Location: Johnson Falls, Alberta
The vagus nerve neuromodulation apparatus DISCOUNT LINK: nurosym.com/merogenomics
DISCOUNT CODE: longcovid01 (should be automatically applied)
Disclaimer: "The information provided is not intended to replace professional medical advice. The use of Nurosym medical device is a complementary therapy and should not be considered a sole treatment. Consult with your healthcare provider before starting any new therapeutic regimen."
Described content:
POTS + Long COVID: www.heartrhythmjournal.com/ar...
POTS + vagus:
www.sciencedirect.com/science...
POTS + vagus 2: www.heartrhythmjournal.com/ar...
POTS + vagus 3: www.aerjournal.com/articles/n...
POTS + autoantibodies: www.ahajournals.org/doi/10.11...
RAAS: www.merckmanuals.com/en-ca/ho...
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Dr. Raszek Credentials: merogenomics.ca/en/about/
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Absolutely love the way you deliver complicated information with humility and playfulness and the utmost professionalism! One of a kind, best🦄
ooooh unicorn! I like it! :) Thank you for kind words!
My girlfriend’s 16-year-old daughter, got vaccinated and within days she began to experience what the family. Thought was an anxiety attack, while she was playing the piano at church one night she collapsed and she endured a year of of so much stress to the entire family. Doctors could not figure out until now.
Thank you 😢
This is sad. Yes, it can be so challenging sometimes to properly diagnose things. Wish it was easier than it is but sometimes it can be very challenging for doctors to hit on the right test to solve the detective work.
My mom is having the same issues. How is this even diagnosed? The doctors can't "figure" it out
PS - before working with mast cell & POTS clients, I myself had experienced both myself, along with EDS. (They occur together.) I also had a vagal nerve injury and my POTS was hyperadrenergic. This all wraps back to the cell danger response by Naviaux which I mentioned in your last video's comments. I highly recommend investigating. It brings all the pieces together at a deeper root level. All you're discussing, is downstream from the CDR.
Another fellow naviaux fan.
The guy has got to the root cause. The vagus nerve was pretty much a red herring for us CFS/ eds sufferers.
Long COVID, CFS, fibro, lymes ,eds are all intertwined.
The rcccx theory is also part of the picture
I could see CDR downstream of vagus as well, as I see it's bidirectional. Ultimately, the root cause for me are not cells but chemical alteration of environment in which these cells have to survive and respond to. Something akin to change in pH which dramatically affects atomic interactions
See the Lyme book Bitten, by Chris Newby. Read near the end where the description of super-duper-turbo Lyme variants were being produced by Eastern Europeans.
Mr Burgdorfer was concerned, and possibly concealing what could have been playing out just before he died.
Such similar symptoms to long C.
@@Merogenomics I see what you're saying but there is a phenotype to this illness, just as there is with m.e.
It's tissue type. It all starts with a sub clinical or clinical problem with tissue type.
These phenotypes are more susceptible to virus , autoimmunity stress, autism.
I know a guy with eds. He has all the dysautonomia traits but no viral beginning. Just confirmed tissue abnormality.
One cannot ignore this as it's always around ten percent of people who are susceptible and they almost always have these issues.
Dr afrin , a mast cell expert sees this in his clients too.
The poster girl for m.e. Jennifer Brea, has all this dysautonomia until she had spinal surgery on the cci joint in the neck...4 mm misalignment through EDS ligament damage brought on by a virus caused the dysautonomia.
The vessels in her head and the nerves were pinched. As soon as she woke up after surgery her pots had gone.
For at least a subset of people with m.e. and dysautonomia are driven by viral degradation of ligaments that drive strength in the neck. Check out herxstory
For the rest, maybe a lot of long COVID sufferers who haven't had their necks chewed away at for a decade, we need to find away of stenthening tgisxtissue
@@oliverbird6914extremely interesting. I have pots when I move my neck a certain way sometimes I feel like it causes tachycardia and lightheadedness. I have a lot of weird neck pain that was causing ear ringing and lots of headache and pain down back and arms for awhile now. Neurologist says my nerves are fine though after a prickle test...
Thank you for this. I’ve been officially diagnosed with POTS and confirmed lack of blood flow to the brain, along with small fiber neuropathy. Your explanation of the ACE1 and ACE2 and sodium and how that all works is better than anything I’ve seen. I’ve spent hours looking at things and your 33 minutes provided more clear info. Thank you!
Wow, thank you for saying this. I had such a hard time prepping for this video because of the myriad of complexities and I knew it wasn't delivered as smoothly as I like (but then that never happens anyway). I hope life is not affected too much for you
@@Merogenomics I was impressed how much you covered in that beautiful environment. Some searching the brain for info is expected… I’ve been seeing Boston neurologist who seem to be focusing on post covid POTS that haven’t explained as clearly as you did… Sadly for me, my quality of life has demolished. It could always be worse. I am able to work and provide for my family but a lot of the energy I require for my passion of being a gigging musician has been stolen from me. But I’ve been sporadically using a TENs device but your video gave me more hope and I’m going to make it more regular part of my daily routine. Thank you!
Have recommended the device to lots of folks who have long COVID
Let me know please if you ever hear back testimonials! Trying to accumulate what people say!
Oh and thank you for sharing! 😊
Excellent Discussion Dr Raszek
The nervous system regulates the immune system.
Understanding the CDR, explains it all. 😁
And that connection is still fairly new. Not long ago it was believed they are totally independent of each other! 😮
@@Merogenomics There have been many remarkable recoveries (including my own) from many "invisible" (chronic) illnesses including POTS, ME/CFS, MCS, EHS, etc. through the use of neural retraining, which often results in the improved health and vitality of the vagus nerve. So very glad to see you sharing this vitally important information. It has the potential to be life changing for many, many people! 💟🙏
Thank you. I’m trying to get diagnosed for POTS/MCAS because I know it is my issue. Pretty rough.
Tell me how you're attempting to get that diagnosis. For POTS it should be simple. I never looked for mast cells tests yet
@@Merogenomics I just started seeing a Cardiologist. Have an Echo in a week or so. I have been experiencing massive hypersensitivity and histamine issues also that are beyond brutal.
Thank you for sharing this so much more simply than most would and kindly. Some are watching this for the science and many more also here for health personal interest.
thank you for that comment. I studied lots for this video and was very proud of it because as you can see, it is such a difficult subject to explain, plus I loved learning about it myself. I am absolute vagalmaniac right now!
Some reporting POTS after the injections but being misdiagnosed with anxiety. So frustrating. We need proepr well informed investigations. Not just for long covid.
These days I just lump everyone into Long COVID because anyone can get infected anyway. Not sure how you would now start parsing these things out
@@Merogenomics Are there no good tests to distinguish between vaccinal and viral antibodies? I thought that was how they determined the distinction between Long COVID and Long Vaxx. (Compare treatment protocols of the FLCCC)
My life has been put on a standstill acutely with POTS for 5 years. I’m having to lay flat 98% of the day. It’s awful.
I am so sorry to hear this, yes, this sounds really bad. Forgive me for my ignorance as this is all relatively new knowledge to me. But I was discussing deconditioning that can lead to POTS. Do you do limb movements in bed to minimize that effect?
I had POTS (post covid infection) for 2 years. I had to sit to take a shower and can’t stand for long. Now I’m recovering.
Pots are also common in those with hypermobility, it was reported in those who thought they had been impacted by HPV vaccination in Europe.
Yes, the most common cause is heart valve prolapse. Very few people in medical have a clue about this. There are also problems with the brain and neck causing dysautonomia.
Yes indeed, I think because blood vessels are too elastic to properly narrow?
@@Merogenomics Sia has EDS and her song seems to be all about that: ua-cam.com/video/KWZGAExj-es/v-deo.html. Some people with EDS seem to be quite badly affected by the spike protein or some other ingredient.
I was also Injured by the HPV vaccine on January 6th. Got a lot of similar symptoms, I am very sad.
What an excellent presentation and discussion. Thank you. 🙏
So happy you enjoyed it!
If you fall due to the POTS and concuss it can become life threatening. If you crash your car when it hits you after reaching out to lock the door... a real issue. I had a staph infection (systemic) some years ago where every time I looked up, above myself I would be hit with a fear that was overwhelming , similar to a time when I had been in the midst of a tornado event! I immediately felt that horrendous fear yet nothing was happening besides looking up AND having a large amount of debris from the infection loose at a trigger point? I used something I knew was good for FEAR called Tomato flower essence and it really helped calm this response as I was detoxing the bacterial debris. I had no fear, nothing fearful about looking up, it was just a response to debris. Also I learned to do a bowel cleanse when I felt issues building and used ACV/baking soda to change PH. I lived through 2 yrs of off and on sepsis syndrome when many don't.
Last year I had horrible joint pain and decided to see if it was caused by my diet. I cut out all carbs and after 2 weeks started to drop weight rapidly. At the end of that month I was down 45 pounds and looked like a deflated elephant. I do not have a doctor because of covid issues so I must just guess what it going on. I am guessing my blood sugar bottomed out and so my body shed the edema. I had horrible POTS so bad I bound my legs so my blood would slow down going south when I stood. My heart would race and I would nearly faint. I kept to my diet because all my joint pain was gone. It took about a month to settle down and I have no signs of that anymore. I can get right up and walk now.....and without horrible pain. I have my 30 year old body back with 40 years of extra skin hanging on to it. I no longer feel like I will have to have a hip and knee replacement. I wonder how many people out there have POTS because of unregulated blood sugar?
You have to look deeper than that. There's loads of overweight diabetics that don't have this issue.
It's at heartz a tissue type problem
I get very potsy if I am exposed to my allergens.. And it doesn't have to be something i eat. It can be a smell in the air.. And with pots you need to drink enough liquids and eat enough salt too..
Heart murmurs cause it most commonly. I too have found that certain foods can increase pain. I believe a lot of the excess deaths relate to people not having infections and other conditions diagnosed due to most doctors treating every lung condition as a potential covid case and refusing to see them with a cough. Some of the doctors in my town are terrified of covid and getting it over and over again but they are also making a huge amount of money out of it so it suits them financially to act this way.
What a story, wow! Glad you're doing so much better. I would guess besides the benefits of lower sugar uptake, you also no longer consume something that could have been triggering autoantibodies production?
@@Merogenomics That is what I was looking for in your talk. I look forward to hearing much more.
fantastic info including the comment section. wow. thx for bringing us together
Our pleasure! This was really hard to study but hoooo boy, did it blow my scientific mind when I did!
Thank you, so interesting
So glad you enjoyed it
❤ thank You for have You here dr.Mikolaj looks like mine symptoms No I am not worried a lot now. You always explain clearly
So happy this was of help to you!
How about gut and stomach issues? I can't recover even on diet, probiotics, fasting .. Before jabs i ve never had an issue... Now lost 13kg (was really fit, lost all muscle) in few months and pain every day...
Definitely there is connection between the vagus nerve and the gut. It's quite major actually, important brain gut axis. See some of our previous episodes on vagus nerve including the one on long COVID
Thanks
Thank you for the donation!!! Hope this was a valuable topic for you!
Warm? It is wonderful to see the waterfall!😊
Not if your intention was to ice climb it! ;)
@@Merogenomics this is true. Maybe a cold plunge instead!?😄😂💧💦🌊❄️☺️
It's like this ....
I like to dream,
Yes Yes
Right between the
sound machine
On a cloud of sound
I drift in the night
Any place it goes
is right
You don't know what we can see....
Sounds like a vagus nerve neuromodulation attempt 😂
Goes far, flies near...
Acupuncture and natural medicines have been my main support for acute POTS. Was bedbound, now recliner bound. POTS at an acute level is a killer and I have retained my life because I have a excellent natural practitioner. Digestion issues were extreme and nothing worked. So I tried mudras (hand yoga), took 3 months to achieve good results and I continue to do daily. Need no other assistance as they have rebalanced energies through my entire digestive system. Rapid heart rate is keep under control with a heart mudra. I do many others also and they assist all symptoms. Had no idea we have so much healing assistance in our own hands.
Thank you for this great comment! Your practice in my mind most likely was helping with the vagal tone and it is great to hear that people do indeed help themselves dramatically in their recovery process and so that others can try it as well!
I had Covid recently and ever since I have had awful issues - neuropathy, swellings in my veins with pain (moves around), anxiety and palpitations, insomnia…I have two young kids. I am breastfeeding. I am desperate. Have cut out everything but meat and veg and fruit etc no sugar no grains…taking supplements…please point me in the right direction 🙏🏻
I really don't know yet what is the right solution. Personally I advocate for vitamins supplementation to ensure proper levels (they are antivirals in case there is an ongoing issue of persistent infection) and the vagus nerve neuromodulation to help with some of the symptoms. Many supplements have been mentioned by the audience who have suffered with top ones being nattokinase, vitamin D, NAC and bromelain which is why I did my last video on this topic but I haven't seen any scientific evidence yet what helps. At least I have seen some science on the vagus nerve helping with some symptoms. But I am constantly digging for info in this area and what I study, the videos are in the Spike injury help tips playlist of videos so please check it out. I wish you find solution soon and obviously extending wishes of wellbeing to your kids as well!
Me too, same things exactly, same sequence of events. Interesting :) good luck
@melaniemurphyofficial ~ Have you checked out the recovery protocols from the FLCCC? Highly recommended.
I have never had Covid but constant headache, three years and counting, after second Pfizer vaccine. Vagus nerve modulation might help me too?
No episodes? Just constant 24/7 headache?
It could as we know autonomic nervous system can also be affected by shots. So far best testimonials outcomes are improved sleep followed by reduced pain
@Merogenomics what would you do if one day you found the most upstream trigger mechanism for nearly all medical episodes and subsequently could mitigate the episode immediately? I can answer the question; you couldn't do a thing, nobody would believe it. You could help friends and family, maybe some; but that is about it.
Off subject, but are there any studies that Naltrexone could reduce IgG4 antibodies? If not, do you think this is a possibility?
Uff, I would have to dig deep into the proposed molecular mechanism of it but I will not be surprised at all if I were to find out later that the vagus nerve is linked directly or indirectly with IgG4s production, and I am very curious to find out, especially after studying the literature for this video!
Great teacher too, not every intelligent person can do that!
Aw thank you! This was such a difficult topic to break down and disseminate! Next vagus video in the series will also bring lots of info so stay tuned!!!
@Mergonomics can you please create a video on how we can prevent the production of IGg4 (the study you mentioned at 28:00) ?…even if just in theory.
we did, look at the video help for mRNA vaccinated: ua-cam.com/video/CZhYUvJ8kZs/v-deo.html There is more coming!
Could co-v1d 19 induced Anosmia be Trigeminal nerve dysfunction... Especially if numb in just 1 nostril? and what could be potential therapy options to look into (4 years on)
I thought it was established that it can. I would indeed consider vagus nerve neuromodulation and/or look into my vitamin A video (look for it at organic secrets playlist)
@prince-ut2xv ~ My son recovered from anosmia with smell training (yes, it's a thing) ~ It took quite a long while, but now he's almost completely recovered. Wishing you the best of luck!
Enters LOVE : " ... Oh, Dear Doc, ❤ ... We are running not out of Time but of the options available ... "
Ya name'em All❤
what a conundrum? what is better, time or options?
@@Merogenomics Enters Silence : " ... 💓 ... " ( In memoriam of Luc Montaigner & Arne Burkhardt )
Post Moderna shot my heart tends to go into erratic rythms when im sleeping. This symptom aswel as many others include strange muscle twitching all over my body. This device looks interesting. What exactly is vagus nerve stimulation? Is my vagus nerve otherwise stagnant?
your vagus nerve is always working but will have certain biological output range. You can tone it down or increase it, depending on involved inputs
I have this exact symptoms, post second Pfizer vaccine. The muscle twitching is predominantly in my shoulder and tends to get worse and spread if my body is under stress or fatigued. I have a constant dull ache in my left chest area that gets worse in the evening times.
@@jamieenver3074 @micallen2137 ~ Have you tried ionic magnesium for the muscle twitching? It is hugely helpful for me.
So, the Vagus-device is only available in Europe.. not in Canada? If I order from Canada, will it go through customs without hassle ??
I got it into Canada but had to pay small duty fee
@@Merogenomics - oh - good... thank you for letting me know - though I will have to do some major savings to get the funds together... .. hoping it will remain available - I was one of the ridiculed-shamed- and fired-for-nojab- in Sep 2021 and had a whole year of unemployment using up my meagre savings at now age 65... - in spite of having been considered a 'most-valuable-employee' by the managers, with all support denied by the bureaucrats.. thus pretty much bankrupt with no savings and having had to move to eventually find new job last year - but goodness gracious... how lucky and fortunate I feel now to have had the mind to begin questioning already in late February 2020 and having had the conviction to stick to my better knowing and philosophy ... against all pressures like so many of us have done, too - always keep in mind, good people,
You are not Alone,.. We are not Alone,... We may live or we may die for this Cause,... But to the End We shall Stand Together !
Fabulous scene! Canada?
Yes, Alberta Rockies
Lundbreck Falls? I like guessing where you are at:) I’ve never been there in the winter though so I can’t tell for sure.
It seems that Lavender, Bergamot and Ylang Ylang oils can help with slowing heart rate and affects the parasympathetic nerve system. Helps calm, reducing stress and heart rate. Not sure if it could help here.
Thanks for your videos!
Location is now always provided in the video description. Thanks for the info on the oils!!! Very cool
I've been doing VNS for more than 1.5 years. Still have POTS, but my muscle twitching disappeared. It comes back if I stop. Another thing is, colostrum with IgG used to make my reddish complexion normal (milkish), but after a few months it stopped working. I suppose I built tolerance. But any idea why I have a reddish complexion but the colostrum temporarily fixed it?
No idea about the reddish complexion. I often think of my own skin (not that great) and how its make up easily allow bacterial infection. So it could be either something missing in the immune system or moisture of skin allowing microbes to persist more than desired? For me it's a forever struggle
@@Merogenomics @asnoopy ~ My skin/scalp issues improved dramatically after addressing leaky gut with caprylic acid and a high-quality, multi-strain probiotic
Since covid I’ve had tons of problems, getting better but still terrible. Nervous system dysfunction for sure. POTS, dysautonomia, gastroparesis, etc. I also no longer believe buying expensive devices, supplements or paying tons for Drs will help.
Well, I am truly sold on the vagus nerve and you can look into way of naturally improving the vagal tone. I also do recommend looking into vitamin levels. At least it is a safe thing to consider to attempt to help the situation. I understand the hesitation towards the supplements because nothing has officially been cleared for helping with long COVID yet
I am definitely trying natural techniques but I cant digest properly so supplements dont absorb properly
@@Merogenomics
Any studies on auto antibodies for alpha nicotinic receptors?
I would have to check witch receptors were targeted specifically but I thought that was it!
@@Merogenomics were you aware of this article? Frontiers of Medicine Jan 2021 Vol 11 Article 617089
Reaction of Human Monoclonal Antibodies to SARS-CoV-2 Proteins with Tissue Antigens: Implications for Autoimmune Diseases by Vojdani and Kharrazian from Loma Linda Univ and Harvard
HI :) I tried that hat with the X's.. didnt work :( I thought it might bean alpine stitch but that didn't work either... Still working... :D You have me hooked to figure it out!
Haha wow! I will have to tell my mom about it she's going to have a chuckle about this story. The grey hat I'm wearing in other videos is also from her. I had another one that a fan send it but I lost it on a train (and I really liked it too)
I’ve been prescribed a sublingual anti cholinnergic tabs for this. They help to reduce the severity of my parasympathetic response during an “episode .” Can you explain how this drug works with this condition.
It sounds like you have too much parasympathetic nervous system response and as a consequence not enough blood makes it back to the heart for proper cardiac output? It's one of the causes we discussed today
Which sublingual meds did you take. I am taking amitripyline
Hyoscyamine 0.125 SL tabs
@@ealvarez1301 and this resolved your pots and other symptoms
@@ealvarez1301 so this resolved your pots symptoms
RAAS 9:50 potential complication when vagus nerve is activated .
If you put these time stamps together, I will pin your comment to the top of the list :D Thank you by the way for these comments!!
25:45 antibodies targeting autonomous nervous system ...
I have this automatic nervous system de regulation - dysautonomia. I also have small nerve fiber neuropathy SNFN. It is correlated. It also affects my blood pressure. Mine is severe. I can’t leave home. Overstimulation.
Oh this sounds tough. I'm guessing radical blood pressure changes take place? As I'm learning more about these systems and their complexities, it's staggering to take all in. I'd be curious to know more about your condition and what you have to do to help as much as possible
@@Merogenomics give me some time, sir and I will explain my case. It’s quite interesting and genetic. I was planning on responding comprehensibly butI have an infection of the gut.
I’ve been having rapid irregular heartbeat when ever I seem to push my body too far whilst trying to train. Before my second Pfizer jab I was a 30 year old male in peak physical condition. I now have muscle twitching predominantly in my right shoulder and a dull ache in my lower left chest (just under the rib cage) that always tends to get worse as evening time approaches. I’ve had chest scans and an echocardiogram which have all tested postiive results. Can anyone recommend further tests I can go for to try to find some kind of diagnosis?
perhaps heart rate variability to see if dysautonomia is at play?
@@Merogenomics my HRV is in the 30s/40s according to my watch device. Which levels would indicate potential dysautonomia would you say?
@@jamieenver3074jamie, I am in the exact same situation as you, I'd love to know what watch device you're using to check HRV. Btw, same pains, gets worse in the evening, going to a cardiologist soon. Rampant POTS if I'm doing anything besides sitting.
@@TWNPKS99 I use an Apple Watch to track my cardio outputs mostly. Do you also get the muscle twitching? Do you have any other symptoms I haven’t listed? It’s nice to meet people who are in a similar position :)
@@jamieenver3074I used to get muscle and left eyelid twitches, they're gone by now. I live in a country where healthcare is abysmal and you can't get advanced testing done at all, so I've just been spending insane amounts of money on every supplement anyone ever mentioned in relation to healing from the jabs. Will update on the 20th with news from the cardiologist. I've had headaches, red inflamed eyes, ear infections, rhabdomyolysis, and I have some kind of growth on the roof of my mouth, which I'm hoping is just torus palatinus. Panic attacks and anxiety as well, and the POTS. I will look into the Apple Watch, although it's a bit too expensive for my liking. Does it measure HRV as well?
C19 put me in bed for 10 months 😴. Got POTS now and it totally makes sense for the POTS to be as a result of that. I can't work so how much discount does the link give?
I believe it is 5% and we offered higher discount for Patreon users who were willing to be part of the company's research. If that is of interest to you, please contact e
@@Merogenomics Hello Merogenomics, I've been watching your videos for quite some time now, suffering with POTS and a myriad of problems post 2nd Pfizer vaccine, I was about to buy the Nurosym using your discount code, but if it'd be in any way possible to be a part of the company's research, let me know.
I think the issue is clouded by many different factors. Beta blockers are a big one where the body/cardiac is starved for output but does not get it T hen overcompensates causing the person feel very bad temporarily.
I think there are so many layers playing together it is quite overwhelming. Hence this video was so complicated to do
27:44 ability to produce iGg4 antibodies was reduced because they were already suppressing specific cytokines 28:15 vagus nerve modulation can cause significant reduction of auto antibodies
If you have studied this in detail to support these claims further, please send the titles of the papers. I really want to dig deeper into this! I am very fascinated by this outcome
8 hours after the Asterazeneca vaccine, my blood pressure started fluctuating, and i was constantly fainting. After 5 months I was diagnosed with POTS, I couldn't even walk so I had to stay home.
I'm taking midodrine tablets now, but my life is very hard and I'm hopeless. I'm just looking for sth to make me feel normal again. I'm only 24 😢
You could try vagus nerve activation. Someone just left a comment of how certain oils apparently help too. I hope you see improvements soon
Had, what now i identify as POTS, the 4 years prior to cvd. Couldnt stand much longer than 10 minutes at a time. Felt like couldnt get air, body telling me to lay down, pressire in head felt like going to explode. In ER twice for tachycardia. Rate 180, not coming down for 10 minutes plus. My hair was shaking w each beat. Nothing done bc it eventually subsided on its own. Feels terrible.
OH, your description is really scary! I am so glad it's gone!!! I studied it, understood it can be very debilitating but hearing it described like this is something else
@@Merogenomicsthe episodes occurred for years, but started to wonder i was actuslly shutting down altogether. I moved to whole plant-based foods, intermittent fasting, magnesium, and these supplements you've suggested in cycles. Also sleeping disorder. Much stress, loss and loneliness during these years also. still getting better over time.
My daughter recently diagnosed with a connective tissue disorder, which is hereditary, wondering if that elasticity issue you mention plays a role as well. Think many issues came together, so healing is complex also, but possible!
Thank you for all the detailed information you provide on why, what's going on and ways to help ourselves heal. So much accurate detail. Truly, thank you.
This SO fascinating to me, And I am just an ordinary person typically stretched to understand most of what you are saying!! A few questions, and some random thoughts!
~~I know you say this is about long covid and maybe you are not free to say it could also be from the shot.
~~Could it be one OR the other, or both?
~~If the vagus nerve and our innate immune system can be affected by a prolonged negative emotional state, could you possibly develop an auto-immune disorder from it?
~~Might this device aid in many cases someday as well?
~~ I discovered I developed ITP (Idiopathic thrombocytopenia) seemingly out of nowhere 15 years ago at a routine blood test. But looking back it was around one of the most painful, fear filled time in my life that went on for a few years. It does not affect my day to day living in the least but it still not exactly normal. I look forward to your videos.
When I think of Long COVID I really think Long Spike injury, and now remember, any vaccinated person can still be infected and deal with these consequences. So it doesn't really matter where the spike protein came from, what matters is figuring out what has gone wrong. For vagus nerve and autoimmunity, I haven't seen studies but I could see that link absolutely. I suspect it actually plays important role but I need more study time. I would imagine that one day vagus nerve neuromodulation might be approved for many things. Science so far is looking mind blowing. Almost too good to be true. And yes, I could also see your thrombocytopenia linked to potential autoimmune reaction
This is very long and tedious. POTS patients are very desperate. Does it work or not?
According to the data discussed in the video, yes
Could vertigo cause de-conditioning?
Don't know as i haven't gone into that part of biology, the balancing component but on quick view online apparently it could contribute with decreased activity levels
Do you spend a lot of time laying down ?
No. I do not. Just wondered if prolonged incidences of vertigo along with other symptoms could contribute to de-conditioning and evolve into POTS.
👍🏻
☕☕
Been using it for months and it’s done nothing. :(
which company product? this is valuable information
My HRV was extremely low when I paid for a test seperate from Dr order. I told my cardiologist and he said "what is HRV?" ....
😢
Heart rate variability
The point was the doctor didn't know
Hmm, shows you how easy it is to disconnect yourself from different systems specialties? Thinking on a global body wide approach is hard. Look how crazy complicated today's topic was
Are you saying your general practitioner knew what HRV is but your cardiologist didn't?
I am sorry what I am saying is I paid for HRV test without my Dr ordering one because I did research on it and wanted to check. I told my cardiologist about the results and he said what is HRV and when I showed him he said it's not important. He didn't really want to see it or anything because my stress test was ok which was weird. This is also the same cardiologist that saw I had myo and peri with echo a few months before. I explained my pots but he didn't want to hear it or believe it said it's anxiety probably not to worry about it. But I don't worry my heart knocks and alerts me...i can't avoid it.
Sadly my autistic son has a rare Cushings and POTS
I'm very sorry to hear that. Hope it is still easily managed with these complex circumstances
One out of the frontal lobe - Does ear piercing/ wearing heavy earrings have any effect on the body? - involves the earlobe, and heart disease can be seen in those earlobe creases. Just thinking out loud. 🤓
I thought about that too! Could piercing your tragus affect the vagus nerve?
Maybe the researcher who came up with this theory could go back and check clients for piercings? Could it cause the stimulation or inhibit it? People only used to have lobe piercings- now they appear all over the ear. There is some tie-up with ears and hearts. Who knows?! Good luck. That scenery is also spectacular- just saying.
Almost all the women in the Philippines have pierced ears😂
@@clauthequeenTragus piercings? Wonder what is the rate of POTS is among the tragus-pierced Filipino women.
@marysexton7283 ~ My son's eyesight *rapidly* deteriorate after getting one of his ear lobes pierced.
28:46
Did anyone rlse go check on their family members when they heard that woman yell?
I think she was cheering on the achievement of the ice climber who finished very challenging route. You can see him in parts of the video
Who financed this? Phfiser,or who ?
Links are provided in the description, go digging
getting off a bike ride, or the racers that come in from a race running, why if you are standing, and WOMEN have a minstrel cycle that the vagus nerve is all about, 1 of 3 young teen women are SICK iwth side effects, so they really need to get this out to them, I know 3 teens already
the heart rate gets going, veins restrict toward the heart, clever, however if spike proteins are interferring it is like pins and needles this is the pain young women feel, like whole body is being in shock waves, tingling needles pricks,
let us know if solutions are presented please. This sounds bad
Small fiber neuropathy... And probably even autonomous nervous system injured...
@bryalee2782 ~ Are you familiar with the FLCCC recovery protocols? They seem to be helpful for both viral and vaccinal symptoms.