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I have a remedy that works 100% ot the time

My wife is 82 yrs old. She has Parkinson's. As well as Lyme. Her doctor was faced with old age problems as well as Parkinson's and Lyme. What is the cause of her problem?? Still working through it all.

WHY no mention at all of Vitamin D3 blood levels? Everyone should know that a high Vitamin D3 blood level, 80 ng/ml to 100 ng/ml, should help regulate the immune system reducing or eliminating cytokine storms (rogue antibodies causing disease states). This would be the FIRST thing I would look for. If you are going to build a house the first thing you need is a strong foundation. Patients need to have a GOOD foundation of high Vitamin D3 levels in the blood before you move forward with additional treatments. To do otherwise is malpractice and ignorance. I strongly suggest getting all patients up to a good Vitamin D3 blood level as a first step. Healthy Vitamin D3 levels equal a healthy immune system. Follow up with a supplemental minerals and vitamins to round out the patients nutrition. (Vitamins A, B complex, C, Omega-3, folate, magnesium, potassium, selenium, iodine, steroids, etc.) Stop looking for zebras when you see horse hoof prints!

Lyme disease is an autoimmune disease. We KNOW that low Vitamin D3 blood levels cause a severe deficit in the immune system, causing autoimmune states, and that restoring higher, proper Vitamin D3 blood levels regulate the immune system to a proper state of function. It seems to me that Long Covid is an autoimmune disease and ALL autoimmune disease are caused largely, not entirely, by malnutrition. Low Vitamin D3, low Vitamin C, low B12, low Thiamine - B1, low Omega-3, low steroid levels, low minerals like magnesium, potassium, selenium, folate, low iron, low iodine, etc...causing an entrance scenario ready for infection and inflammation. I also feel that current recommendations for Vitamin D3 blood levels are still MUCH too low. (100ng/ml sounds about right for a base level) Also how do you feel about Dr. Paul Marik's MATH+ protocol for Covid and Sepsis which includes steroids, ascorbic acid, thiamine and heparin amongst other essential vitamins and minerals. It seems even more appropriate now with the discovery of low steroid levels in long Covid patients. Finally is there any value to be gained in treating severe long Covid patients with IGIV and PLEX (immunoglobulin and plasmapheresis) as front line GBS (Guillen-Barre Syndrome) patients are initially treated to save their lives? Many thanks! www.ncbi.nlm.nih.gov/pmc/articles/PMC8912998/ covid19criticalcare.com/protocol/math-covid-hospital-treatment/

7 long years 😢 lost everytime

What about the people that test negative but still have a tick-borne disease?

Well that was pretty uninformative

No one mentioned that even the CDC, (on their website) mentions in the first paragraph or two, that Lyme Disease IS diagnosed by “SYMPTOMS”. Yet most medical people, even when shown this, REFUSE to go by that, instead, they INSIST on going by the current 2 blood lab test for Lyme Disease, EVEN THOUGH those 2-tests are each known to be only 45-50% accurate at best! I had this very experience my self, and I shown medical people the CDC website, and STILL, despite having so many Lyme symptoms (but I never saw a tick or a bit), they refused to give me a Lyme diagnosis. One medical person when shown the CDC website, and then asked if they knew the 2 blood lab tests for Lyme were on about 45-50% accurate, said “yes”, but still, they refused to give me a diagnosis of Lyme, despite agreeing that my symptoms match Lyme disease (and in the chronic stage). WHY does this happen. Well, not many are talking about this part either, that more and more states are taking medical licenses away from medical people for things like prescribing antibiotics for Lyme disease for more than a couple weeks, or treating for Lyme without a positive Lyme blood lab test. This issue needs to be brought out to the general public, and to the entire medical community, and told, this is WRING! I personally believe this is why the medical provider I saw who knew the 2 blood lab tests are only about 45-59% accurate, yet agreed my symptoms matched Lyme disease (& a chronic Lyme disease stage at that), told me that without a positive Lyme test, they would NO give me a Lyme disease diagnosis, and would NOT treat me at all for Lyme disease. They even refused to give me any antibiotics. Lastly, Lyme disease is NOT the only health condition diagnosed by symptoms, yet Lyme disease is NOT being diagnosed by symptoms by most medical providers (regardless of their specialty, or being a “Dr”, a “D.O.”, or a “N.P.”). Patients NEED to seek out LYME LITERATURE MEDICAL PROVIDERS!!! PERIOD!!! This should NOT be the case!!! I finally had to seek out a Lyme Literate medical provider (an hour from my home), but had to wait to save up for that initial 4-hour first appt (as ALL their appts are pay by cash, no insurance, as most insurance does not cover most Lyme treatment protocols, OR the true length of time needed for those protocols/treatments). It took me a year to save up, and once I had the funds saved, I then made my 1st appt to see my Lyme Literate Medical Provider, but, the. I had to wait at least 3 additional months for a first appt opening with them. By the time I finally had that first appt, I had already been not able to work for a month, due to my health condition worsening, and now, 3+ years later, I’m still not well enough to work, in any capacity. p.s. I live in Wisconsin, a Highly Infected Tick State, yet our medical people here know very little about Lyme Disease, and symptoms to look for, especially beyond if a patient saw a tick, or a bullseye rash (which is only seen in about 45% of the cases at best), AND they don’t know to dig feeling besides checking if your knees hurt or are swollen, if you have swollen neck glads (but they only check a could neck glad spots). I had swollen neck glads, but not where they checked. I showed them, but it was dismissed! They may also asked if you had any face paralysis, but that too is iffy, and not all Lyme patients, even in the chronic stage, have this. Then when you try going elsewhere to get diagnosed, they say, oh, you were checked for Lyme, test was negative, you don’t have it, and as the patient, you can’t even get them to re-address looking to see if what you have is truly Lyme disease. Yep, I’ve experienced this too. To many times actually! ALL medical people need to also be educated that treating Lyme disease is not a one size fits all treatment for people, especially in the chronic Lyme stage! Also, each patient MUST HAVE a treatment plan tailored to them, AND, this plan will need to be constantly changing! Expect that! Most medical people are sadly NOT trained in Supplements and Herbals, and this MUST CHANGE! Our medical people should not be captive prostitutes for serving Only BIG Pharma! They also MUST change their industry to ALL OF THEM being Functioning Medicine TRAINED people, AND this must change with Both their Initial medical school education training and certification, AND ALSO needs to be included in their every 2-year Continual Education (CE) requirements (INCLUDING having correct and continually updated Lyme education required CE training EVERY 2-years, -Regardless of what state they are in)! A couple years before getting really sick from Lyme disease, I ended up switching to a Whole Food Plant-Based diet, with extremely limited amounts of sugar (I don’t add it to anything, once in a while,a small bit sneak into something I buy, but I’m aware of it from the label ingredients). I try to avoid oils too. I of course avoid all dairy, including eggs, cheese and milk. My diet changed to this because I was developing food sensitivities to so many things and so many ingredients. It also caused me to have to read all food, beverage, vitamin and prescription ingredient labels. I have to avoid gluten, whey, soy, maltodextrin, dextrose, and of course, sugar as that feeds the bacteria. I’ve even had to let my pharmacist know of all the food ingredients I react to, and like I said, I even have to read vitamin and supplement labels now. I strongly suggest to everyone to also read all your ingredient labels, and be sure to look too at the section called “Other Ingredients”, and for everyone to tell their pharmacist too about every food sensitivity, and food allergy you have! Oh, and awareness needs to be shouted too through the medical community, and the public, that Lyme disease in the chronic stage Lyme disease patient, and in other chronic health condition patients, do see a higher number of suicides than in initial acute stage health conditions.

Many auto antibodies are being produced with lyme and will cause other issues. Anti nuclear, Anti mitochondrial, Anti cardiolipin, two types to thyroid, GAD 65, Beta 2 glycoprotein 1, Anti parietal cell etc etc. Lyme will turn on Type 1 diabetes for instance. Common Variable immune deficiency occurs so we have low immunity coupled with auto immunity. Mannose binding lectin deficiency, and MGUS a marker for Multiple Myeloma is also present in certain cases. Low IgA as well. We are learning how dendritic cells are damaged and Complement is crippled etc. We need the NIH and NIAID to fund research on our broken immune systems,

pubmed.ncbi.nlm.nih.gov/28216098/#:~:text=Deficiency%20and%20altered%20function%20due%20to%20gene%20mutations,thrombotic%20disorders%2C%20in%20which%20autoantibodies%20play%20a%20part.

Oh honey, I understand.

Hi ALL, I am a WelshMan now 52 Years OLD and got VERY SICK [Over-Night] In 2010 @ just 38. I HAD a great Job/Family/Social-Life etc and it ALL went Literally OVER-NIGHT in May 2010. I WAS Very Fit/Strong/Healthy as i had been Training with my Royal-Marine Friend for over a Year and put on a LOT of Weight [Health Weight] I had been working as a Mobile Crane Operator for 5 Years and just Finished an 7 Month Contract so Decided to Take 2 Weeks off Work and Enjoy myself. I had planed on Riding my Ninja600 In the Morning [Upto 12pm] Then Girlfriend/Children in Car and Out. I did this 1st 2 Days BUT as soon as i opened my eyes on the 3rd Morning I JUST KNEW there was SOMETHING WRONG as i could;nt even get myself out of bed, My Girlfriend HAD to help me. I finally get Diagnosed with Chronic Pain And Fatigue Syndrome 2 YEARS Later. I have been through HELL and Back, My family thought i was MAKING it up and LEFT [That Stung=Still Does] My Girlfriend of 5 Years Looked after me another 10 Years [Together 15 Years] It;s been 14 Years now and i was getting somewhere just before CV19 Hit. I have had 3 BAD Resp-Infections/Broke 2 Ribs Coughing and the Medics would;nt take me to Hospital Because there was 22 Ambulances WAITING OUTSIDE for Beds [The NHS for you] I HOPE that telling this BAD story somehow Reaches SOMEONE/ANYONE Because i NEVER thought i;d make 2 Years lets alone 14. I HAVE had many Up;s and DOWNS but NEVER give up on life/Living as there COULD be Something just around the corner, Thanks for Reading.

ummm, first thing a patient should know is that your doctor knows NOTHING about tick borne disease and that these people's stories of missed diagnosis is the norm. Do your best to get any antibiotics from your know nothing doctor and then find a "Lyme literate" physician who will be in private practice and treats tick borne diseases as the focus of their practice - negative lyme tests are also routine and common - your medical center doctor will also deny this, while your lyme literate physician will be well aware.

same story going on for 40 years now - physician's these days STILL have no clue about tick born disease and still are completely confident that they know all there is to know . . . this is the result of decades of misinformation from the so called "authorities" on Lyme that have insisted that these diseases are no big deal, easy to diagnose, easy to treat and easily cured . . . wrong on all counts. And, any physicians and scientists who have disagreed with the "authorities" are slandered, slurred and penalized if they speak up . . . sound familiar?

I was bitten by multiple ticks in June 2018 … Immediately, my Doctor prescribed 3 weeks of Doxycycline and another 3 weeks of Doxycycline 2 weeks later as a preventative measure .. I was tested for Lyme’s Disease twice within the first 6 months & the results were both “ NEGATIVE “ … In that first 4 months I was extremely fatigued & had lost 30 lbs … Then the God-Awful pain came 😰😰😰… It took me right to deaths door 😱😱😱 In my desperation, I sought out a Lyme Disease Specialist ( A Naturopathic Doctor ) & his prognosis was that I most likely did have Lyme’s Disease along with multiple co-infections as well 😖😖😖 He sent my blood samples to The Armin Lab in Germany for an accurate assessment… They, within a few week, notified myself & my Doctor that his prognosis was accurate 😳😳😳. They decided to test me for 15 Tick-Borne Pathogens & discovered that I was “ Positive “ for Borrelia along with 12 co-infections 😱😱😱… As pharmaceuticals were ineffective, I started a strict protocol of extremely powerful herbal medicines … It’s primarily Stephen Buhner’s Protocol with a few additional remedies…I have also developed a severe sensitivity to certain foods where I was actually going into a anaphylactic reaction… So I have had to alter my diet as well … I have currently continued this regimen for 5 years now & I’ve been pain free for 1 year now 👍👍👍 I’ve got my life back 🥹🥹🥹 I truly hope that this information may be beneficial to other victims of Lyme’s Disease & it’s horrific co-infections … Lyme Disease is an world-wide epidemic & requires public awareness to have any positive impact on the lives that it destroys 😰😰😰 Unfortunately, hundreds of thousands of victims have been undiagnosed and/or misdiagnosed 😱😱😱 This is unacceptable 😰😰😰 Lyme’s Disease might very well be The Next Pandemic 😖😖😖

What a shame with this Doctors very dissapointing

Please say what did help you to cure to others try to help

This is a terrible desease and Doctors are non educated giving time to borrelia grow in your body like crazy

Only fools live with Lyme when the remedy is so quick and easy. As an energy healer with 45yrs. experience, I am able to eliminate Lyme in minutes. All you have to do is to call me toll free from the US and Canada and I will treat you for free.

I can help you. If you call me, toll free from the US and Canada, I will treat you for free.. as an energy healer, I can eliminate it in minutes, and have done it hundreds of times without a failure.

How abput giving last 45 minute appt of the days ctors day and how about HE STAY A BIT LONGER SEEING THERE ISNT A NEXT PATIENT . A NOVEL IDEA!

Lyme is easily eliminated, energetically, in minutes. Drugs will not cure it.

Please have Dr Steven Phillips and Dr Joseph Jemsek share their findings.

4:00

Long covid is reaction to spike protein. Covid isn't the only cause of spike reaction. It isn't even the main cause of spike reaction.

Lyme disease is a much worse problem because the CDC and IDSA have financial conflicted interests in the faulty Lyme disease tests that have a 50% false negative failure rate. The CDC and IDSA are corrupt and it's hurting people.

Can blood gene test tell if I have Lyme disease or not? I have morgellons 2 years. I had blood gene test which cover 17500 pathogen no speical finding. But fibers in different length in different shape and different color constantly come out of my skin.

The other question is, why would a doctor even ask whether their patients were right? It's really, are they crazy or are they lying. Thank you for this presentation!

We grew up in Central NY, ran around in the fields & orchards with no shoes and no one ever got bit by a tick. Can a scientist with integrity please ask the question why?

Why they not trying to find the frequency to kill that bacteria?

His website doesn’t work

Ty for sharing!❤ I now remember the weird mind thing. I have been " sick as a dog" since April, after a tick bite. I had the bullseye rash and I seen it move through my body. I took pictures of it all and also wrote down my symptoms. I lost my appetite, I was soooo sick, tossing cookies and really sick. I've lost 15 lbs and still losing😢. Igenx is the best place to go for the best testing for true results, imo. It's not covered by insurance, which hurts, bc now I have to wait to save up the $300 or so to order the test. In September/October I realized all my symptoms and pictures are in line with Lyme disease. You are in my prayers, God Bless ❤

All lymies should be gluten free

The conventional testing does not work. I got tested properly by holistic drs and found everything I have, and its all etiological. But treatments for the immune system and these disease are very difficult.

Great video! Thank you! PLEASE READ THIS BECAUSE: I found a product people could try. I’d also love to help (or be a Guinea pig) in any way I can: PLEASE!! I’m now 69, single (it’s very hard, especially when no one understands Lyme.), and have been sick and in horrific pain for 21 years. I luckily was able to teach high school for 40 years before I had to retire because I was so sick. I have an extensive education, raised two children mostly alone, and now I live in Rochester, MI, an upscale city northeast of Detroit. I’ve been an advocate for several invisible illnesses; breast implant illness (which caused several autoimmune diseases, several major operations within 10 months, hideous infections, sepsis, and a stroke), autoimmune encephalitis, (which my adult son has due to Lyme meningoencephalitis at age 7, which caused him brain damage and disability), mold toxicity (which we both had from different houses), and now Lyme. I have several coinfections of Lyme including a live Babesia Mycroti for which I am being treated, but went through all the malaria symptoms! I realize I’ve had it since I was a child with horrific leg pain, stiff necks, boils, lethargy, malaise, etc. yet, no one considered Lyme back then. I’ve had to change my entire lifestyle and diet as well. I lost almost my own life during an operation. and everyone in my life, SO MUCH MONEY, and I have ADHD, brain and neurological issues, and CPTSD, because of the medical system for lying to women and allowing breast implants which immediately put me in danger of every disease imaginable. (Black box warning now!), dismissing mold toxicity, and chronic Lyme disease. I could be a poster child. BUT: Try: Biotics Research: Ultra Vir-X, a supplement I got online from an integrative health doctor in Michigan, Dr. Brownstein, who has now gotten into Lyme protocols. He’s written books on other things, and is well-known in his field. I was thinking about the viral particles, and tried this. My leg pain that was the worst, has substantially subsided! If you’ve read this far, I you probably have Lyme or know someone who has it. I hope to God you get better! My sincerest wish is to hope that generations to come (including my 8 year-old granddaughter) never have to experience any of these traumatic and life-changing illnesses! Much love…🩷

~ Igenex Lab is 93 - 98% accurate. ELISA is a total waste of time and resources. ~ Lyme and coinfections are always persistent. Tamping it down with inadequate treatment is typical standard of care and makes the microbes stronger. Bartonella is incredibly resistant to treatment due to inadequate treatment. ~ Lyme literate doctors are the ONLY way for mainstream medicine to learn. ~ CDC so called standards are killing people. ~ Steroids destroy the immune system, which has been disabled by the evolving microbes, especially bartonella. ~ Get Lyme literate doctors involved; examples include Neil Nathan, Richard Horowitz, Daniel Kinderlehrer, Tom Moorcroft and others are outstanding researchers and practitioners that others can learn from. ~ Wake up! People are suffering and dying.

Could shock treatments kill this.

Thank you for sharing this!

Helping a friend with her yard, I acquired Lyme. I worked in Pharma, and after complaining about not feeling well, a colleague suggested I get a Lyme test. It came out a false negative. 3 or 4 months later, one of our Pharmaceutical doctors insisted I get retested again (different) lab. It was positive. I month of taking Doxycycline, and I felt like a different person. I did however lose my gallbladder. It was filled with calcified small, Spiro-??? I now take a Lyme tonic to be on the safe side....

Curious if you have now found any treatment/relief?

Thanks to CDC for not believing Lyme is a long term condition. Yes, if Lyme is caught very early it can be treated with a short term treatment of Doxycycline. But for many of us, we are diagnosed late into the illness because many doctors know absolutely nothing and you are either misdiagnosed or shunned into believing it is emotional. Quest and LabCorp tests are terrible with 48 to 50% false negatives, and on top of this, when you are diagnosed late in the game, the standard protocol does nothing for your infection. Doctors wash their hands with you and you are left alone suffering. The only possibility is LLMD doctors, but they don't accept insurance and are very very expensive. For common people, we can't afford long term treatment. I don't understand why nothing is being done about it. On record, there are 300 to 400k people being diagnosed each year. But what about all the false negatives. There is closer to around a million new cases each year. Wake up CDC!

Just went to a neurologist for bad brain fog and memory issues....was told its due to anxiety. Didn't do that well on memory test though so she ordered a pet scan. Gonna prove her anxiety diagnosis out of the water.

I love medical science, biology, anatomy, immunology, physiology etc…but it is extraordinarily difficult to think clinically when what you are seeing has been completely debilitating within you. It has contributed to years of my life being missed

I know for an absolute FACT that on MANY MANY occasions, some lab workers do NOT take their job seriously and just want the paycheck without having to actually do the testing.

Thank you for a fascinating lecture. Very complex. I must admit though, speaking as one who actually has Lyme arthritis, I have to disagree in part. My father was an immunologist, so I am not entirely without knowledge. As a Lyme patient, I am driven by a desire to completely understand my condition. So, what I must say, is, I do not for one minute believe in the concept of auto immunity. I think that what you are witnessing is not a wayward immune system destroying it's host but rather the ongoing progression of the infestation. After many years with this disease, I still have all the symptoms you show in your slides. I think that this is due to the actions of the parasite, very much active within my tissues. So my body's 'auto immune' response is actually the normal response to inflammation. My cytokines are reacting to a needed demand to deal with the invaders, NOT fighting ghosts. In these long Lyme cases what you have to do is inspect the victim's spinal fluid for signs of spirochete activity. Not assume that the antibiotics have done their job and declare " why is the body eating itself " . No , it is still mounting a rear guard battle for homeostasis. Doing what it is supposed to do. One should investigate the work of Alan Mc Donald. He was a pathologist who had access to dead subjects. He found spirochetes everywhere ! Significantly in spinal fluid. They are to be found in synovial fluid too, I am sure. I am sure they are still wandering about my body. They have this ability to wander and to disguise themselves and to hide under a biofilm. Therefore I say, NO, not auto immunity but self survival. NB I also have Neuro Lyme Disease . Not nice.

I’m so sorry about your mom. I was lucky and only spent 8K for treatment. Thank you so much for sharing your story. ❤

I was given LIthium Orotate 5 mg x 2 per day for moods with Lyme by my LLMD. I had no side effects. No withdrawal and very safe. It's been very effective for me.

Excellent, realistic, accurate, and informative on so many levels. One of the best presentations on Lyme I have seen.

I heard that male tics don’t carry disease and I’d like to know if that true information please?

The SOI is expensive anyone interested search Genesis Cummings Georgia