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Anyone who uses the term “PTLDS” is disqualified.

So how is she today ?

th-cam.com/video/owJ8aOBvEv0/w-d-xo.htmlsi=wwUQZmEZaWKE4J9W

Hi😊

He's wrong. Infection starts sub 12 hours at best as evidenced in the 2018 study.

Great talk! Babesia air hunger presents as yawn attacks sometimes (@Judy).

Yes fyi 8yr old was in utero after a lymes bout for year so far the gorl born has been sum po tom free or no problems.maybe the lymes was successfully cured b4 pregnancy althuogh mother had vertigo.which she had before preg that could be related to a severe car accident yea4s b4.whst a mess.just cant Drs treat with a bactiracide right away.?

Ya there is testing up the kazoo but i think LYMESshould be the first one to test.i agree to treat stmptons for releif first

Medicsl marijuana sound like an appropriate help for symptoms as as the rest od antibiotics

Im scared because my dauggter had lymes a few years before she got pregnant. She was treated but I never beleived she was cured.im worried about the baby who is 8 so symptoms but i always wonder i pray she is safe from it .

My heart goes out to u xxx

Is there any concern with eating lyme infected meat?

My brother was the first person diagnosed with Lyme in northern Ontario. It was back in the eighties. He was a biologist and had to really advocate for himself to get the diagnosis. But he was right.

Thank you for sharing your story! God bless you!

Boy I would love to tell you my lyme story.

Thank you for caring❤

35:50- therapie

What repellent does she mention?

What antibiotic intra venos helped?

One of the best descriptions for Lyme is what you said, "Something doesn't feel right." You experienced heavy-hitter symptoms right away.

Did sanoviv help?

Yep. For 40 years the CDC denied the existence of chronic Lyme disease. Just 2 years ago around April, they recanted their statements. They now recognize it. It is CRUCIAL to get the antibiotics when you are in the acute stage. That is when you will be successful in kicking the bacteria out of your system.

Lyme is horrendous! I thank God every day that I managed to heal myself. I contracted Lyme in 2015 and I wouldn't wish it on my worst enemy. I couldn't walk, couldn't lift my arm and I couldn't sleep because of the severe pain 24 hours a day. After a few weeks in hospital the doctor's told me that they couldn't do anything to help me and that my body would have to heal itself. After 3 months in hell I was on the verge of taking my own life just to end the pain. What saved me was reading a book by Professor Buhner's called 'Healing Lyme' and followed his protocol to the letter. When I told the doctor's what I was going to do that they laughed at me. What else was I supposed to do? It was a very slow process because first you have to kick start your immune system and second you have to fight the bacteria of which actually hides from your immune system - known as 'pathogenic bacteria'. What is different about the Lyme bacteria to other bacteria is that it eats the magnesium in your body whereas most bacteria eat iron. Without magnesium your muscles can't work. Little by little I began to improve but I won't lie, it was the fight of my life. All in all it took about one year for all the symptoms and the pain to stop. Only then could I begin to build up my strength again. Today, 2024, I play golf and I am a 8 handicap. If I ever contracted Lyme againI don't think I could go through it a second time and would probably just end my life. That's how vicious it is. For anyone reading this who has Lyme - don't give up - your body can kill it. It takes a special diet, special herbs and sheer will power. It will be the fight of your life but if you want your life back that is what you must do. Anyone interested; I made a video of my Lyme recovery journey and posted it on my youtube channel vlog

There are herbs, vitamins and supplements that can help you improve. In addition you should check for coinfections that you may not have been treated for yet.

I got lyme play golf on Jekyll Island GA . Took 5 almost 6 years to get diagnosed. It's been a struggle ever since. I too, have brain pressure, anxiety, pain, my eyes were perfect now I can read the E at the top of the eye chart with my right eye but not with my left. I an alone a lot bc I feel so hopeless. I understand his tears. But I get up everyday, exercise, try as hard as I can. I have been bit a few other times in last several years and bullseye everytime. It is scary bc no one understands and no doctor is educated enough to help.

Erythema can present after a short time. Did you say 6 months?? Every one of these CNY lectures contains errors.

Please update or remove the misinformation about time of Borrelia transmission, we now know it can be INSTANT. primary literature, FACT, evidence is there that a tick can be 'primed' pre bite. Lazy lack of research. Same as the Wes guy who states even longer time period!!!

wow! * Borrelia transmission can be instant with tick bite, this is proven and in primary literature now, please update

I was bit in summer of 2023 by deer tick that tested positive for lyme bacteria. --I am suffering constantly with dizziness and vertigo, visible muscle and soft-tissue loss, causing weakness and pain. I was as active and healthy as can be before this happened, but am currently housebound for a year. --I'm still looking for proper testing and treatment.

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!