I was misdiagnosed for 21 years, first with MS, then with fibromyalgia. I lost my ability to work, lost my partner ,and lost my home to foreclosure. I'm still suffering the damage to my body and brain, since it is no longer curable at this point. I am so glad to see this finally being discussed!
I'm sorri that happened to you!!... sooOooo important to be in tune wit our bodies.... there are awsum doctors out there but they do need to be sought out.... hope yoi well....
@@ellebenenati7787 - I'm alive only due to studying naturopathy and applying it. I was put on terminal disability in 1994. We have a famous Lyme doc two miles from our home but like most LLMDs he does not take insurance and I can't begin to afford him. He says Lyme is a rich man's game and also that after a certain point it is just not fixable. I am doing well considering the damage. I can do light exercise daily, and the Neurologist says it is a miracle I can even walk with the amount brain damage I have. Back when I got sick in 1986, most doctors had never heard of any of this and the Chamber of Commerce where I live was denying that there were even any deer in our state, a blatant lie!
@meagiesmuse2334 I'm sooOooo happy yoi wit us!!... good on you for seeking out other resources!!... I've been doing homeopathic medicine for sum tyme I was 1first taught by my auntie n then mostly self taught.... sumtymes when western medicine fails us turning to styles of eastern medicine can make all the difference!!... today isn't 1onea my best days, I hurt.... that's another story for another tyme but wanted to say hiii quick!!... ello!!... I will come back here ina couple day's wit sum book titles for you, I still read actual books.... LoL!!... ofcourse you kno what yoi body likes n doesn't allergies ect.... vitamins herbs n minerals can assist aswell crystal therapy is awsum meditation n gentle tai chi movements for yoi body mind n soul.... I was tired of being tired n unintentionally being mislead.... till then be well.... ps: if you watch hockey the panthers are playing north carolina n happy valley is on bbc this eve!!... 🌺🐯💛
@@meagiesmuse2334 What happens if you cut out sugar intake. It seems to be helping me and I just started Methylene Blue but don’t know if it works yet. Only been taking it for a few days.
I got Lyme disease for 3 months, had terrible headaches, lost a tooth and finally got diagnosed by a BioResonance Therapist. After 2 sessions, the bacteria and symptoms were eradicated using frequency therapy.
I’m so sick of media and online sites completely downplaying Lyme. At my worst I had over 100 symptoms. It was horrific for 5-6yrs and no drs helped me.
I had Lyme in the 90's when I lived in Western New York, after a trip to Eastern New York where I did some hiking in the woods. I had the flu-like illness for a few days. I had the bullseye rash. My primary symptom was severe heartburn about a month later. My doctor started treating me for an ulcer. While I was in the waiting room for a follow-up appointment I read an article in a magazine about Lyme showing a picture of the rash. I took the magazine to the consultation, showed the Dr the picture and told him that I had had this rash just before I had the flu-like episode. Long story short, he refused to believe that I had Lyme Disease. He said that because *he* didn't see the rash, he couldn't accept it as a symptom and he said, "There is no Lyme Disease in New York State". At the time, blood tests were very unreliable so even though I had a positive test he still didn't think that was what I had. I finally found a Lyme specialist north of New York City who agreed to see me. I drove 5 hours each way to see him. After telling him my story and taking a blood sample and examining me he told me to call him in a few days. I went home and called him a few days later after he had my blood test back. He said that he couldn't be sure that I had Lyme Disease, but neither could he be sure that I *didn't* have Lyme disease. He treated me with a long course of antibiotics and my symptoms completely resolved. I was fortunate that I had taken the time and effort to track down a specialist who was open minded enough to listen to the patient and to recognize that he didn't have all the answers. I wish I could remember his name, although that was almost 30 years ago.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo. You trust everyone and dats stupid. We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
Yep I’m in that boat. Healthy people can not relate so they like to dismiss it because it makes them uncomfortable. Having empathy for a friend who is suffering is too much for some people and they can be quite cruel about it. Plus, we only make it out of the house on our “good days” so people tend to think we seem fine. They don’t see the bed-ridden migraine days.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel.
I had chronic Lyme Disease for 4 years. Every few months I had flu symptoms and the pain would settle in a different joint. American doctors and insurance companies WILL NOT recongnize chronic Lyme disease, as the insurance companies do not want to be liable for paying for it. I was on a waiting list for 2 years to see a specialist at Tufts. My doctor refused to give me more antibiotics. The only time to truly test for Lyme disease is in the middle of the night, as that is when it is most active in your blood. All other tests come out negative for Lyme. I did all of my research in Europe. In the meantime, I started taking oregano pills (a natural antibotic). I took 9 per day for the first few days and then gradually went down to 2 a day. I took them for about a year, and It finally went away.
Wow, did this really help you? I'm suffering from undiagnosed chronic lymes. I know this is what I have as it started after the classic bullseye tic bite but doc's can't seem to diagnose me. I'm suffering so bad my quality of life is terrible. I need help
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo. You trust everyone and dats stupid. We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
all too common...here in phila pa its everywhere, ticks are infested thoroughly, especially with warm winters now. doctors are the most cocky self absorbed bunch out there, always the last to acknowledge anything new. crazy the situation has only barely changed in 40 years, deny deny deny!!!! it will just go away!!
I’ve had a terrible case of Lyme my whole life and I pray for everyone else who has it because it’s ruined me and I hope I live to see the day a cure is discovered. Most people don’t understand how bad it can be…
Same here it’s bad I lost everything it will not go away everyday is really hard to go through I can’t live like this. My kids were very young they never got a chance to know me and I don’t recognize myself anymore.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel.
DRETIKOCURE on TH-cam thought me that is all about patients and the right person, May God continue to bless You sir for the permanent HPV cure I received after taking your herbs.
It’s nice to see that mainstream Drs are becoming more Lyme literate and finally taking it seriously. They’ve dismissed chronic Lyme and gaslit sufferers for far too long. Better late than never. Now if only they could get informed on the role of environmental toxins in the role of diseases...
Stop using words like informed. They can’t be informed on things not discovered by science yet. There was no science explaining long term Lyme disease before. Now there is. Drs are trained to be like that, it’s highly frustrating for people experiencing things they have no science for of course. They should believe people. But there’s no way to be informed on something not discovered yet by science
Depending on the state you live in has a lot to do with a doctors approach.. In Massachusetts the doctors are on it, they know Lyme's and Triple E" are prevalent there..
Say"EH WAS NAILED TO THE CROSS WITH A CROWN OF THORNS! OH WAS TO THE LEFT AND UH RIGHT. PEOPLE FROM ANOTHER PLANET ARE TRYING TO TAKE OVER EARTH WITH CIRCUMCISION AND EARRINGS! GOD WAS CIRCUMCISED"
I had Lyme disease at 5 years and I ended up being paralyzed. I couldn’t walk, I was taken to the ER and they gave me antibiotics so I was able to walk again! Thank God!!!🙏🏽❤️
My sister was misdiagnosed for MONTHS before finally being diagnosed with Lyme. After 2 years of antibiotics it appears the Lyme is eradicated but she has multiple residual symptoms. Not everyone gets the bullseye around the bite.
All the people I know that have it. My self included never get rid of it. Antibiotics help for about a year at a time and after 3rd round it gets better but it all comes back. I now have Alfagal witch make you allergic from hoofed animal’s and all the derivatives. The allergic reaction in my stomach caused an ulcer and about killed me. Started Methylene Blue a few days ago. From what I understand it surely can’t hurt anything. Tired of being sick and the brain fog is the worst part.
Yes, an inflammatory marker stays high, but why? It is great to see Lyme finally being taken more seriously and getting discussed in the mainstream, but there’s still a long way to go. For instance, why don’t bands 31 and 34 count toward a positive test per the CDC? Because 3,000 people in the 90’s got it in a vaccine? That’s ridiculous. That is one of the biggest reasons people go misdiagnosed, and we need the proper authorities to take action and change this flaw in the medical system.
Tick pics or not, this info could be a game changer for those of us stuck in this situation. Thanks for reporting! Links to original study and sources would be REALLY helpful. Please consider including in description.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo. You trust everyone and dats stupid. We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
No, if you're still suffering, you still have an active infection. There is no test anywhere that proves it was ever 'cured'. ...this is just lazy 100% 'pseudo science', no one is paying proper attention.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉🎉
I was infected around 1987, a harsh learning disability was the worst symptom at the time. In 2008 heart palpitations and panic disorder started, misdiagnosed by many specialists until 2021. My brain MRI results come in soon, I’m anticipating the worst being late for so long. It’s taken everything from me, our government has ignored this and taken everything from me. 💚
I here u Yhere im now Replacing my 2hips & now going for my knees the pain is everywhere I've had lymes 4 or 5 times on the books it never leaves we the people that have been suffering fir yr & still are need to Sue the makers of lymes Fauci Gates In Lymes Connecticut I was a Vibrant strong successful woman that no longer has the true life 🤬 Now replacing body parts when things are better with the pain it's Diet No gluten and Taking The Right Herbs KEEPING Your Vitamin D Up Long time overdue with people suffering with this horrible disease that no doctor likes to help we need to start an organization and Sue the government Gates fauci at the highest levels FOR are pain and suffering I FEEL YOUR PAIN 🙏👍☠️
Misdiagnosed means that there was a mistake or oversight. What happened to you was pure fraud of ALL sectors of medisin covering for a we upon release done in the 1940s that they have no capacity to control.
@@1timeslime971 I hear you TimeSlime. 45 years with Lyme- one year in bed in 1987 and now the last 4 years again. Same Medical Professional (isn't that an oxymoron) diagnosis- your metrics are fine so you are not sick. I totally relate to "welcoming death". With luck we'll get pancreatic cancer.
The suffering is so long and so intense! And the quality of life is practically non-existent. You just hurt and suffer and hurt and suffer, whilst being totally exhausted almost all the time. It's a most horrid disease, and I too had much rather died, than getting it and suffering so badly so long already because of it. But what truly adds insult to injury is the meanness and stupidity of almost all doctors! They can't stoop low enough to reject us and to accuse us falsely. Which causes a different kind of very real pain in the heart. May God revenge us!
Thank you for reporting this news. We need to train more doctors to take this more seriously. It took months to find a doctor to treat me and then it took 6 months to cure me. Lyme disease Can impact someone daily lives in the worst ways.I don't wish it on anyone.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo. You trust everyone and dats stupid. We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
I actually had a doctor here in Oregon tell me that I couldn’t possibly have Lyme disease because they don’t have that here on the West Coast… How ignorant. You didn’t even ask me if I had lived anywhere else. Even if that was true that you can only get it in certain locations,… Doctors are definitely in the dark ages about this. I finally had a doctor that tested me and found the blood markers for it. He said I probably had it since I was around seven or eight years old. and you don’t necessarily have to be bitten by a tick, but that’s an even farther stretch for doctors to acknowledge. It can be spiders and mosquitoes transmitted as well.
@@creativesolutionstoart what an idjut doctor--Lyme is prevalent all over the nation at this point--it only takes one tick bite and in my case, there was no bulls-eye rash. I was lucky--when I first had it, I was in Connecticut and had knowledgeable doctors. After the antibiotics, including intravenous, I was left with fibromyalgia and chronic migraines--the fibromyalgia is now in in recession. The chronic migraines were also in part because there is a genetic disposition in my family, but a good doctor asks these questions....My CT rheumatologist would give me antibiotics when I felt I had symptoms but unfortunately, a lot of doctors are not up to speed on this.
@@FluxyMiniscus the CDC is so captured and corrupt that I can’t fathom why anyone takes them seriously. With their staggering level of corruption disguised as incompetence during the pandemic, they need to be defunded.
It's like the M&M guys meeting Santa Claus! The CDC is uniformed millie tarry covering for a we-upon that was released in the 1940s and got away from them. They HAVE to admit it below the Pahn Day Mik levels that its at to ease it into the public consciousness that its the worst plague that ever faced mankind.
No they’re delaying the inevitable it’s persistent infection there saying it’s due to protein found in the blood that causes prolonged infection so it’s misdirection even worse than before. We have to many biopsy post infection and treatment proof dr Monica embers Tulane university has proof and antibiotics working is proof there is infection there is others dr Kenneth liegner has proof documents extensively
She isn’t addressing the findings that the bacteria has been found to hide in biofilms. Her plan of suppressing people’s immune systems is a dangerous plan for people dealing with chronic Lyme.
depends, if there is not actual infection (lyme bacteria is gone) and the symptoms are due to post trauma inflammatory marker (basically a kind of autoimmune issue) then a targeted immunosuppressant could be the solution...
This is horrible and inaccurate information. Far more than a 5 to 10 percent subset suffers with long term chronic symptoms. Anyone in the Lyme world knows this is a hideous disease that can be chronic for years with difficulty in even treating. They need to be speaking to Lyme literate doctors and actual patients so that the world knows how destructive this disease is. I am living this nightmare.
I was diagnosed with Lyme disease just yesterday, I work in the woods and have had symptoms for more than a year. I didn't have the typical rash or even the typical symptoms. If it wasn't for researching into it myself using google scholar I wouldn't have had any treatment. I have been having symptoms similar to Schizoeffective disorder, lots of sleep paralysis, depression and anxiety. Lyme disease can imitate many disorders and syndromes.
I had the rash and the flu like symptoms. It makes sense once I knew what it was. For almost a decade I was treated for treatment resistant depression. I finally said that I think something is wrong with my immune system, got a bunch of autoimmune testing done, they stuck the lyme disease tests in there, and that was the only thing that came up a strong positive! Since getting doxycycline, it took about 6 months for my antibodies to go down and my psychiatric symptoms to go into remission. My psychiatrist was even considering ECT or ketamine, because I tried almost everything else. I thought the bullseye rash was the strangest mosquito bite I ever saw, I remembered telling my mom about it after I was camping. Then it all started making more sense. I hope you feel better soon! I think lyme disease should be considered before a psychiatric diagnosis like schizoaffective disorder is made. That is a pretty serious diagnosis.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel
Treat it aggressively and do not listen to doctors unless they are dedicated Lyme literate doctors! The vast majority of doctors are clueless, negligent, and cruel when it comes to Lyme! 😱 Research…
It is unfortunate American news always pushes for too short segments. These subjects deserve a bit more time to explain. Forcing to 'wrap it up' just causes for the message to NOT come across.
Thats because it doesn't involve something politically charged, controversial nor money. Its science and health related so it gets the quickie treatment.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo. You trust everyone and dats stupid. We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
Yeah it’s not like they have anything else of any actual importance they need to get to. All they do is spew propaganda to their gullible audience. And no apology or accountability for the damage they did to this country with all their misinformation during the plandemic.
When ppl first complained to doctors about what is now known as Lyme disease they were told their symptoms were psychosomatic, essentially that is all in their head. It took decades before the CDC actually accepted it as a real illness. This drove a lot of people to not talk about having symptoms or go to the doctor because you were immediately labeled as crazy. This has also happened with other diseases, like Morgellans, which in 2009 was finally considered a real medical illness. Prior to the CDC accepting an illness as real, no one is studying it or taking it serious in terms of treatments or cures, so having the CDC recognize an illness is pivotal to the lives of those suffering with these unknown illnesses.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo. You trust everyone and dats stupid. We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
We can thank people like Dr John Aucott at Johns Hopkins and others who bravely researched Lyme and chronic Lyme, (now called Post Treatment Lyme Disease Syndrome), for giving this real disease legitimacy. And we can blame the "Lyme literate" doctors who are making a mint by administering witch doctor treatments to desparate Lyme patients for making the legit doctors skeptical.
The See Dee Sea is uniformed millie tarry services with a Surgeon General. The ONLY reason that they recognize it is because it is so out of control that they can't avoid their intentional release from the 1940s anymore.
I think this is it. This video made me cry. There is hope ! I got lyme disease 7 years ago. My symptoms got worse after covid infection. I was on long term antibiotic treatment ( 6 months ). It got better after treatment , but after some time it returned back. This summer I got infected again with new tick 😢.I met friend few weeks ago. She had lyme as well and she said she had lingering fatigue and joints pain. She also mentioned, that after some time she got immunosupressants for autoimune skin disease and her lyme symptoms miraculously disseapered
Lyme disease is a spirochete like syphilis. The body really hates spirochetes and reacts to them in weird ways, like chankres and in yawyaw it makes weird growths. Spirochetes are normally life long infections so it would make sense the body would continue reacting to Lyme long term
You are 100% correct. NO antibiotic has EVER 'cured' any disease, and it was known in the 1900s that antibiotics turned spirochetes into stealth organisms. So the infections NEVER went away.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉
See this makes sense to me ,iv been into the outdoors for many years and ticks have never been an issue ,i never even checked for any but now every time im outdoors iv always got ticks on me.
I had Lyme for over 50 years, I remember the Erythra Migrans on my abdomen aged 8 after playing in a hay field with friends in S.W England. I developed multiple problems. I had numerous disagreements with the NHS over this (apparently I was imagining the symptoms.) I finally went private and got 3 separate positive test results with full clinical diagnosis. I took antibiotics, used PEMF's, low dose immunotherapy etc for 2.5 years, almost died from Herxheimer reactions several times. I am left dealing with 50 years of damage and inflammation, there is almost nothing I have not tried but I still lose several days a week unable to function above 10%.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉🎉
DRETIKOCURE on TH-cam thought me that is all about patients and the right medication, May God continue to bless You sir for the permanent HPV cure I received after taking your herbs
Chronic lyme is NOT an autoimmune condition - it is persistent infection. There are more than 700 peer-reviewed scientific studies showing this, and I am an example: after 2 1/2 years of intense treatment with multiple simultaneous antibiotics, lyme dna was found in my serum via PCR, the gold standard for detecting infections.
My new meme: All of The Above. Inflammation that fake word that they throw around is an IMMUNE RESPONSE. Chronic inflammation is also lumped with autoimmunity both of which are responses to antibiotics creating 8 different cell wall deficient morphologies but CURING NOTHING.
Yes the video is still missing the point. Its not just an ongoing immune response, its a persistent ongoing infection. Ive witnessed this myself, even have made videos that i posted on my yt channel that clearly show this. The fact that they cant wrap their heads around this simple concept is just baffling.
@@_S13_ I just subbed. Since the advent of clinical medicine no one knows how to destroy a spirochete. They adopt 8 different forms for evasion, so my theory is that unless you hit them with 9 different remedies at the same time to take out all stages you are just playing Whack-A-Mole. So, we examine what I just said: NO ONE since 1900 AD knows how to kyll these things, but they knew back then that even the arsenic, mercury and antimony merely turned them into stealth cell wall deficient forms. Therefore it's not that they can't wrap their heads around it - they KNOW that a Buy Yo We Upon was released in the 1940s. They can't put the Genii back in the bottle. ALL of their efforts are failing. So they hold out the "new research!" and "verge of an answer!" B.S. to keep their victims in a state of perpetual anticipation that something will get better when it can never get better until what I just outlined is arrived at. On top of the 9 remedy approach everyone STILL needs to destroy the filarial worms (Alan MacDonald) that carry the spirochetes inside of them as they bore into the spinal fluid swim up to the brain and unload their neuroborelliosis that is 'another mystery' to these disinfo agents. My most important videos on this topic were removed probably because they were the only truth out there.
Wait a minute! Just because that is the case with you, doesn't exclude other possibilities in others! Don't be like those dumb doctors, who are blinded to several possibilities!
i had babesiosis, a very rare form, and almost died. Had complete renal failure, months of dialysis, and now years later I'm still dealing with joint pain, something I didn't have prior to the lymes. That was second bout of lymes. The first one I recovered fully from. The second? Not so much. Wrecked my life. I was very active and loved that lifestyle
So sorry to read about your sufferings. Yes, it's hardest on the active. You basically can't be you anymore. You still have all the desires, just not the capabilities of living those out. Again, very sorry! Hope one day something is found to give us part of our lives back.
@danielleperry1657 Oh, stop with the trying to make a buck of ill patients! We know you write nonsense and just try to advertise below the surface. May God force you to pay back a 100 times for all you've stolen from people, willing to try your snake oil.
@@mandamoon13 typical antibiotics and typical time. Just the after effects that I’m still dealing with, such as liver and kidney damage and polyarthralgia. I’ve had Lyme disease two other times with no repercussions. Thanks for asking
Northampton integrative medicine in Northampton Massachusetts has been treating chronic Lyme disease for decades. They have a successful track record of helping improve the health and wellness in patients. They have always treated patients that the medical community as a whole turned away. Check them out online.
This makes me so angry. I was diagnosed years back took a round of antibiotics got checked again from the same dr still had a positive test and could t afford the next round. Then I go to Kaiser and another hospital both of which told me I did not have it. I’ve been in with all kinds of symptoms that literally the drs just tell me I have mental health issues..it’s like can you humble yourselves for a moment and remember that maybe you don’t know everything there is to know
They didn't bring up the fact that antibiotics don't tend to get past the blood brain barrier so the lyme can hide out there. Teasel root tincture helped me greatly to get past the blood brain barrier in the treatment of lyme killing it all off. Good luck everybody!
DRETIKOCURE on TH-cam thought me that is all about patients and the right person, May God continue to bless You sir for the permanent HPV cure I received after taking your herbs
@@jonathangraham6412 I have read online that teasel gets past the blood brain barrier since it is natural (whereas antibiotics do not unless given intraveneously). Antidotally, I could feel where it was working because I would get high grade fever localized to where the lyme was (specially in my knee joints and all in my head).
The standard of care set by the IDSA 2006 Lyme disease guidelines is one of medical neglect of persons suffering from chronic Lyme disease. However, such guidelines are indeed useful. They serve to shield from liability physicians who neglect persons with chronic Lyme disease. By misusing CDC case surveillance criteria as the sole basis for a clinical diagnosis of Lyme disease, these guidelines serve the insurance industry very well indeed because such cases represent but the tip of the iceberg of actual cases of Lyme disease, whether acute or chronic. Denial of the possibility of seronegative Lyme disease, likewise serves the insurance industry well and also such simplistic constructs for Lyme disease also serve those physicians who cannot wrap their minds around the true complexity of this illness.T The medical profession and the United States Public Health Service, predecessor to the CDC, have a long history of medical neglect of persons suffering from spirochetal infection. The profession and the USPHS were completely unable to reform themselves from within in this regard. It required moral and political intervention from without to bring the Tuskegee Experiment to an end with Senator Edward Kennedy’s hearings in February and March, 1973 before Committee of Labor and Public Welfare’s Sub-Committee on Health (Jones JH. Bad Blood: the Tuskegee Syphilis Experiment - a tragedy of race and medicine. The Free Press. New York. 1981 pp. 213). The Tuskegee Experiment involved about 400 subjects. Lacking the taint of racism, nonetheless the “mainstream” handling of chronic Lyme disease affects far more people; it would be a fair estimate to say, Tuskegee X 10,000 in the United States alone. Furthermore, the standards held out by the CDC and the IDSA have worldwide influence. Canadians are unable to get care for chronic Lyme disease. We are seeing significant numbers of persons with chronic Lyme disease forced to leave Canada for care. State legislators have begun taking matters into their own hands and the states of Rhode Island, Connecticut, California, New York, Massachusetts and Minnesota have passed laws or promulgated policies protecting physicians who treat persons with chronic Lyme disease. Are these legislators stupid? Are they dupes of Lyme activists? Or can they see what is so obvious to the patients and to any good clinician, that Lyme disease can be a chronic infection that often requires a long-term treatment approach? Furthermore, as the disease spreads and more and more individuals are affected, legislator’s staffers, their wives, their children and they themselves are experiencing the effects of chronic Lyme disease. In the fullness of time, the mainstream handling of chronic Lyme disease will be viewed as one of the most shameful episodes in the history of medicine because elements of academic medicine, elements of government and virtually the entire insurance industry have colluded to deny a disease.
My 14 year old child was complaining of aches and pains and being tired. her pediatrician told us it was in her head and to take her to a child psychologists. He said I can't find anything wrong with her. Take her to a child psychiatrist. The psychiatrist said I can't find anything wrong with her. Has she been tested for Lyme disease? I said of course we live in Connecticut. Lyme CT is where it gets its name. I pulled her medical records and her Yale grad pediatrician never tested her for Lyme. The psychiatrist recommended a neurologist who took18 vials of blood from this poor kid. He sent 6 to Quest, 6 to Lab Corp and 6 to Stonybrook Hospital on Long Island, NY. Stoneybrook was the only place that had the equipment needed and came back with a positive. Now years later she is experiencing the same symptoms and they're telling her she has MS.
they're...anyhow......... healing the gut biome is the only chance she has...start with chevre goat cheese and cantaloupe....low acid, organic foods, no preservatives, filler or gums, only palm and olive oil, t no sugar...lyme loves sugar.
Make sure they also test her vitamin D levels. When I was diagnosed 5 years too late, my vitamin D level was at 6. Magnesium helps the muscle pain and body aches tremendously. I'm so sorry this happened to her. Doctors can be infuriating.
Please look into finding a Functional MD. Standard allopathic MDs are way behind the times. A chronic Lyme patient needs to be tested for environmental toxins and mycotoxins (we often are unable to eliminate chemical toxins from our bodies like healthy people can). I did the GPL-Tox test from Great Planes Lab but there are others as well. Honestly, anyone dealing with MS type symptoms should probably look into doing glutathione IVs anyway. Low carb diets are helpful, as is intermittent fasting. I hope your daughter is able to find answers and make a speedy recovery. 🙏🏼
If who ever pretents to care for lyme sufferers really cared, they would start to do a study checking those people with ongoing symptoms systematically for coinfections like babesia, bartonella, ricketsia, erlichia, anaplasma or reactivated stuff (EBV, chlamydia, mycoplasma). For some reason, there is not one study who ever did that even if it would be highly logical.
caught it in 1990/ 1991 Doctors were clueless. SAW tiny ticks all over--they were crawling up anything that walked through grass of my dad's yard in Orange county, NY. Lymes paralyzed my formerly healthy dog--we had just moved from a city out west. The dog was perfectly fine before, 6 months later she had arthritis so bad she couldn't move her back legs. I was also sick with a rash and "flu" . The vet yelled at me that I was lying she was fine before we moved to NY State. He euthanized my dog. I never got treatment....here I am in utter pain with terrible symptoms that have ruined my life...but of course since I "test negative" no doctors will help me unless I pay thousands out-of-pocket for a "lyme literate" dr.--well, I have no money thanks to lyme ruining my ability to work steady, NYS won't recognize me as disabled...so I have to use herbs just to try and manage it myself. The insurance companies, doctors, CDC--all in it together to hide the truly horrific level of tick borne infections that ARE indeed a CHRONIC infection and at epidemic levels in the Northeast.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉
I got chronic Lyme disease 2years ago. It was an horrific experience..I suffered many symptoms, especially excruciating headaches that never went away and felt like my head was going to explode.. ( I was misdiagnosed 3 times) from time to time I still suffer with fatigue and joint pain. I never got the bullseye mark. I was misdiagnosed with chronic migraines for months before I finally almost lost my mind and got myself to the ER. I sometimes think the bacteria is creeping back on me to cause havoc again in my body. I hope it won’t come back, meanwhile some symptoms come back from time to time..I’m thankful that I was able to be on the antibiotics. Lyne disease is for sure, something I never want to go through again!
My grandson has tested positive for a year. His chronic symptom is daily vomiting multiple times a day. No doctor will link this with Lyme and therefore their only suggestion is anti depressants. They initially gave him one round of antibiotics but he still tests positive and they make no other recommendations. The whole family is frustrated and out of ideas.
Find a good probiotic in the fridge section, preferably powder. Garden of Life 5 day critical care is great. It tastes like banana and you add to water. He may have also developed food allergies and/or food sensivities from the Lyme.
I don't know what state your grandson lives in but Dr Gary Berliner in Dawsonville GA, is a Dr that does believe in Chronic Lyme. You can look him up. Maybe, he could help.
This information is inaccurate, there are thousands of people struggling with chronic Lyme, not just 5 or 10%!! I cannot express how terrible this disease is. Im literally dying from it because it was late stage by the time I got diagnosed, i had it for 30 years before doctors finally dug deep enough to give me answers and no treatment works for me anymore. Its slowly sucking the life from me and its devastating. Someday in heaven God will give me a new body.
They're missing the mark for so many because many still have bartonella or babesia so if you just try to lower inflammation and fix the damage it's not enough. Bartonella and Babesia in so many causes stick around, as does Lyme, so this type of info presented as the "key" will mislead many.
I had it for 2 years before I found out. Lost a $120,000 a year job along the way in 2011. It's now 2023 and I ended up with bells palsy so I went through the Dr. He tested me and I was positive. Weird thing is that he said on the test that's it's not showing I had lymes in the past. I told him that's why I'm here because I know it's my lymes. He gave me 30 days moxicilin and when I went back to Dr I was still positive. Asked him the next step and he said there wasn't anything more he could do for me.
Test again in 6 months. The test is looking for antibodies, not the bacteria itself. Those can take 6-12 months after treatment to start to come down. My test eventually showed less bands positive.
I have full blown Lyme adult female deer tick bite huge bullseye rash all the trimmings and 5 western blot tests over the course of 8 years not one band not one test all complete negative spinal pcr positive don’t trust that test never.
Interferon alpha immune marker. And to imagine for 40 years most doctors denied Lyme existed and to this day there isnt an affordable, accurate and accessable test for it. It should be taught and required all doctors to order at minimum a western blot when patients come in with odd or bazzar symptoms.
Not exactly. If you dig up a few good research papers published in the last 5 years...one on a site called Frontiers, they spell out what's all been explored & is pretty intetesting. Including that detecting it is hard...the tick nymph is poppy seed size...etc.
No, disease is detected then not cured but worsened by doctor's reactions to the disease. Than the patient who is now much worse off for contacting the doctor is not told by doctor that the doctor did it to them but instead that the poisoned-by-doctor patient is imagining it, right?
This is so sad to me. I’ve lost over 12 years of my life from this disease that I will never get back and as the days go by I continue to be sick. I’ve been dismissed by every specialist under the sun and at one point was even convinced it was me causing myself all this pain. I went to alternative medicine after years of no help and spent thousands and thousands of dollars my family didn’t have to try and get better, never happened! I then got diagnosed with stage 3 cancer that it took me longer than it should have to go to the doctor because of being mentally beaten down by all doctors in the past. Having cancer I was believed, treated and supported by the medical community, never was I supported like that with my lyme/viruses. Chemotherapy (suppressing my immune system) relieved a lot of my lyme/viral symptoms and it was amazing! Then once the chemo wore off all symptoms came back with a vengeance. This study is great but hurry up! We need help now!
chronic lymie here....so did I miss it...what was the solution from this information? some of us have an immune protein deficiency and how do we correct that? The other issue with us lyme sufferers getting proper diagnosis in the US atleast is most mainstream aka insurance covered docs will only use the outdated "western blot" test which is known to be the least reliable test for lyme so it causes many false negatives. The most reliable is the "igenex" text but insurance companies won't pay for that one....why ?? why do they want to keep us ill ?? it makes me think its a gmo coverup like covid
DRETIKOCURE on TH-cam thought me that is all about patients and the right medication, May God continue to bless You sir for the permanent HPV cure I received after taking your herbs
I have been sick for over a year and I had been tested for Lyme disease 3 different times and the test results were all negative, until my knee started to swell a month ago. they pulled the fluid out of my knee and low and behold it was Lyme disease. Hopefully untreated for a year isn't too long for me with type 1 diabetes. I've been on the antibiotics for a week now and don't see any improvements yet, in fact I feel worse. wish me luck!
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉
I'd give bee venom therapy a try, it's cheap and easy and seems to be improving for most with Lyme. I'm in Saskatchewan Canada, also have type 1 diabetes and chronic Lyme. It made me suicidal and still have nuero issues but bee venom definitely improved me
But you might ruin the flimsy narrative they’ve worked tirelessly for in order to cover up the real truth. A logical and reasonable person might notice that the first mainland town that this “disease” infected was geographically located right next to Plum Island Animal Disease Center. However, common sense doesn’t live here on Earth anymore. We peons must believe whatever our corporate overlords tell us, otherwise we might not get any of the scraps they throw us.
@@adityaprabhu6 there used to be really great TH-cam videos about it years ago but I’m sure they’ve all been taken down during the censorship campaigns in recent years. Do some research into Operation Paperclip, Erich Traub and Plum Island. Govts have been experimenting with bioweapons far longer than most people realize.
I've been battling chronic Lyme disease for the past 15 years, and it has completely turned my life upside down. To make matters worse, no doctors could diagnose it properly, and hardly anyone believes I'm truly sick, except for my close family members. It's a truly devastating disease.
There are scientists out there working so hard to bring awareness to this disease- only to be criticized and ridiculed when the evidence is right before our eyes
I had Lyme for almost 5 years before getting treatment…treatment lasted 3 years….i have lasting effects from it. I have arthritis in my joints that will never go away, I have a lot of digestive issues due to getting alpha gal as well…so here we are..
Thank you so much! I have suffered from chronic lyme after being diagnosed 2 years after symptoms started. I have been on about 30 antibiotics and I'm still not better...
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo. You trust everyone and dats stupid. We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
That is not fun and so frustrating. Do you by chance have a history of trauma or ongoing stress being dysregulated? Untreated trauma/stress symptoms can contribute to chronic issues and if dealt with, the body can better deal with what has become a chronic health issue. Doctors almost never ask about stress /trauma histories. I have had many chronic health issues, most of them linked back to growing up in a chronically stressful environment. As I dealt with the trauma/stress symptoms by addressing the chronic dysregulation in my nervous system, many of the chronic health issues eased.
There is no known cure for spirochetal disease. I've got the best minds working on it. There are palliatives that work for some but not others. Here's what I posted above in the main comments: More lying Id eye Otts covering for a Pahn Day Mik that is worse that anything anyone is currently being phear phorned into reacting to. It was known in the year 1900 that antibiotics NEVER got rid of ANY disease and it was confirmed by Lida Mattman (now deceased) that the poisons merely create Cell Wall Deficient forms (8 different morphologies) so that with syphilis, lyme, leptospirosis, TB, or leprosy the SYMPTOMS *MAY* go away but the causative agent NEVER DID. Ever. You all are living the aftermath of that LIE. Mel Thornberg (now deceased) said that at best doxycycline *MIGHT* afford some protection from prion formation because it transforms the cell wall competent form to any of the 8 cell wall deficient form and in SOME people the SYMPTOMS might go away but the beast can re-assemble from any of the 8 different morphologies to give what is falsely called a re-currence or re-infection or re-activation. All that antibiotics do is turn people into asymptomatic CARRIERS which is how this got spread worldwide without even requiring ticks from Plum Island. Europe is finally acknowledging that it is spreadable by ALL HUMAN BODY FLUIDS. The use of the word: INFLAMMATION shows that whoever uses it is either at total fuul or purposely spreading disinformation. Inflammation happens under two conditions: tissue injury (which always comes with the introduction of a pathogen as well) and INFECTION. Inflammation is NOT a separate undefined disease or condition or syndrome. Inflammation is an IMMUNE RESPONSE even if it is to the stealth organisms created by Id eye Otts that give antibiotics to something that has NO KNOWN WAY OF DEE STROYING IT. THE REASON IT SHOWS UP IN THE BRAIN (we have Dr. Alan MacDonald to thank for this) is that filarial worms that came in from a tickbite transport the spirochetes inside of it through the cerebral spinal fluid to offload the migrant workers like a coyote emptying a schoolbus once it crosses the border. That is why parasite elimination is essential to mitigating neuroborelliosis. "Markers" and "Genes" and any other nonsense to cover for this out of control threat to hu-manity are purposeful disinformation to keep you from looking at the Millie Tarry We Upon that got away from them and with which they cannot recall despite the use of Glyphosate (patented in 2010 as an 'antibiotic') or any other HUMAN DRUG. There's your "Top Story" that will never be covered by media or medisin because they are all in on the millie tarry coverup.
According to "the quiet epidemic" documentary, two bio markers (proteins 31 and 34) in the standard tests approved by the federal agencies to detect Lyme disease were deliberately omitted. Was this ever rectified??
No they took them out because of the vaccine in the 90s. I guess if you had the vaccine you would pop positive on those bands si they didn’t want false positives if later I guess they got sick from tick bite and everyone got considered because of a few that took the vaccine doesn’t make any sense they made the test even less sensitive there is so much wrong with Lyme it’s to much I wouldn’t be surprised if this was gain of function research from syphills.
Lymes disease hurts your whole body bad, you get a bad fever, nausea and major fatigue and headache! I had it for about 4 mths before I went in, due to my work schedule. So I was pretty sick by the time I finally got to the Dr. It took another 2 months before I could go back to work again, as I ended up on a second dose of antibiotics. I have had problems ever since then, with aching joints and headaches.2006-2023 I know it will be there forever so I just accept it and live life the best I can.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo. You trust everyone and dats stupid. We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
Doctors who take Lyme seriously are rare, certainly in Canada. Our College of Physicians and Surgeons need to be sued for billions. Use the money to research a cure for chronic Lyme.
My 92 year old grandma Contracted Lyme disease. The doctors thought it was a Flu and didn't catch it in time, Sometime later i think like a year or 2 it ended up making its way to the spinal cord, Left her paralyzed in 1 leg and unable to walk. She was still mentally there and happy to be alive! She ended up passing away with no control of that leg.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉🎉
I had Lyme disease when I was around 6, now I’m much older. But overall damage that it caused me were significant, my growth was stunted which mean I would have a height of 5,3 while having full genetics of a 6 foot tall family gene. This caused me to take medical growth hormone prescribed daily until at the age of 15. I maxed out at 5,9 luckily. Though one of the worst things ever was I had permanent damage within my intestines, which made me have to go on celiac diet until it hopefully adjusts. Probably the worst experience was when they were testing me as I remember, putting a needle atleast 6 times into my arm. The fluid was murky and brown. Yes for your information, I got it from Texas when I was visiting close relatives. Symptoms like heart burn, extreme aching, fever, and a big rash where the bite was.
I had a tick bite and the doctor gave me a 2 week course of doxicyclene. Unfortunately neither the doctor nor the pharmacist told me that you must not take any milk with it because milk renders it ineffective. I got a very nasty rash on my hip and quite bad joint pain. I didn't fancy trying the doctor again so I managed to get hold of a 5 week course of doxicyclene and took it 2 hours after a meal and 2 hours before anything else, after 4 weeks my hip was still sore but after 5 weeks the problems had gone. I was lucky, if I had left it to the doctors I could now be a cripple or worse. But I think one reason people have such varied results with the antibiotics is that the doxicyclene is very sensitive to what you have in your stomach, other things affect it too, for example iron.
I'm on my second round of doxycycline also, because they did not tell me how to take it properly the first time. It took 11 years to get diagnosed. 5 years later, still having terrible nerve and joint symptoms. I hope this time works for both of us!
i am hitting my 10th day of Doxy and was given an extra 14 days because of lingering symptoms. no one ever mentioned the proper way to take it, regarding empty stomach, avoiding dairy, etc. frustrating
Lyme debilitated my life only recent am I living a halfway normal life. Years ago was told high protein in blood and urine. This is interesting. NBC please don't stop talking about this!!!!! We need change.
Treating Lyme as a long term disease was not a medical problem but one across insurers. Let’s see them fight this correlation. Let me guess: you need more than 79 people for it to be statistically significant ….
Ok so I had zero symptoms initially, was given an antibiotic...12 years later...I suddenly developed symptoms. I was told this was normal that it goes "dormant" and can resurface many yrs later, with diff. Symptoms. Food intolerances especially to starched & yeast was the only symptoms I experienced those 12 yrs later...and the antibiotic didn't do anything for it. So I was just old to avoid those foods. This broadcast did a very poor job of explaining that.
About 1/3 of ticks (at least at my location) carries lyme. Always carry a tick remover. There are versions shaped as creditcards that fit in a wallet. Highly recommended!
@@jak3589 , here in the northeast US, deer ticks ( which feed on mice in their tiny nymph stage) are the primary Lyme carrier, but other tick species can sometimes carry Lyme. Additional, less common tickborne diseases found here are erlichiosis, babesiosis, anaplasmosis, tularemia and rocky mountain spotted fever. Climate change is causing migration and spreading of species and diseases that previously weren't found here. The longhorn tick is a recent arrival to the region and can cause a severe lifelong allergy to eating meat. Rodents in particular are a major vector for many formerly "exotic" diseases. A man died of hantavirus in Long Island New York a few years ago after sweeping out his garage where evidently mice had been nesting. Hantavirus is a usually fatal respiratory disease (there's no treatment or cure) transmitted in dried mouse urine and which is endemic to the Southwest, especially after El Nino events where the desert blooms and the rodents population swells, but it had never before been found in the northeast.....there is bubonic plague in the west and southwest as well, carried by prairie dogs and other rodents, and I have to wonder how long it'll be before the plague spreads to here.....
My old pharmacist has Lyme disease..got a tick bite in the middle of his back from the deer camp woods.... been all over the country for treatment, no cure...over 20 yrs ago since he was diagnosed with Lyme disease...
So thankful I knew what I was looking at when I was younger when I got the rash. Got treated quickly and never had any problems. But I spend a lot of time outdoors and I warn other people all the time.
I walk my three dogs on local trails every day. I tuck my pants legs into my socks and spray the socks and sneakers with bug repellent (strong DEET formulas will work but permethrin, made from marigolds, is better; it paralyzes ticks and is safe for application on digs and humans). My dogs have light colored fur and white feet and so even tiny ticks tend to be easily visible on them. I'll typically find two or three ticks on each dog when we're out walking (on one occasion it was a dozen plus ticks on each dog and on myself). When we get home,, I strip off my clothes and put them in the dryer while I check myself for hitchhikers. The dogs all get chewable flea and tick meds but those only work on ticks after the ticks start to feed, and since one of our dogs likes to nap on our laps, transfer of a tick from dog to human is a possibility. Ticks love our moist sweaty areas, and I plucked a freshly attached tick from my sensitive nether regions just last week, after the dog and I napped together.
It's been pretty obvious for a while now that chronic lyme is an autoimmune issue. Good to see them further this and r/o active infection. BUT...what is going on with the immune system? Sounds like we are in the second inning for figuring this one out. We have a ton of immune work to do in general for a lot of these emerging autoimmune issues..
what I posted above to diatribe on the autoimmune aspect: More lying Id eye Otts covering for a Pahn Day Mik that is worse that anything anyone is currently being phear phorned into reacting to. It was known in the year 1900 that antibiotics NEVER got rid of ANY disease and it was confirmed by Lida Mattman (now deceased) that the poisons merely create Cell Wall Deficient forms (8 different morphologies) so that with syphilis, lyme, leptospirosis, TB, or leprosy the SYMPTOMS *MAY* go away but the causative agent NEVER DID. Ever. You all are living the aftermath of that LIE. Mel Thornberg (now deceased) said that at best doxycycline *MIGHT* afford some protection from prion formation because it transforms the cell wall competent form to any of the 8 cell wall deficient form and in SOME people the SYMPTOMS might go away but the beast can re-assemble from any of the 8 different morphologies to give what is falsely called a re-currence or re-infection or re-activation. All that antibiotics do is turn people into asymptomatic CARRIERS which is how this got spread worldwide without even requiring ticks from Plum Island. Europe is finally acknowledging that it is spreadable by ALL HUMAN BODY FLUIDS. The use of the word: INFLAMMATION shows that whoever uses it is either at total fuul or purposely spreading disinformation. Inflammation happens under two conditions: tissue injury (which always comes with the introduction of a pathogen as well) and INFECTION. Inflammation is NOT a separate undefined disease or condition or syndrome. Inflammation is an IMMUNE RESPONSE even if it is to the stealth organisms created by Id eye Otts that give antibiotics to something that has NO KNOWN WAY OF DEE STROYING IT. THE REASON IT SHOWS UP IN THE BRAIN (we have Dr. Alan MacDonald to thank for this) is that filarial worms that came in from a tickbite transport the spirochetes inside of it through the cerebral spinal fluid to offload the migrant workers like a coyote emptying a schoolbus once it crosses the border. That is why parasite elimination is essential to mitigating neuroborelliosis. "Markers" and "Genes" and any other nonsense to cover for this out of control threat to hu-manity are purposeful disinformation to keep you from looking at the Millie Tarry We Upon that got away from them and with which they cannot recall despite the use of Glyphosate (patented in 2010 as an 'antibiotic') or any other HUMAN DRUG. There's your "Top Story" that will never be covered by media or medisin because they are all in on the millie tarry coverup.
My immune system needed to be boosted, not suppressed like it would be if this was autoimmune. I have been tested for about 20 autoimmune diseases now, the only test that ever came up positive as a differential diagnosis was my lyme Western Blot. Sometimes an inflammatory marker here and there is high. My immunoglobulins are low, so I started IG replacement therapy this year.
As an overweight female of course it's all in my head and not real. Just lose weight and take antidepressants or anxiety meds. I just want to be able to walk more than 100 feet without pain and cramps. Five years ago I moved most of our house and ran steps frequently until Lyme happened.
There are 8 different cell wall deficient morphological forms created by the insane use of antibiotics. ALL are persistent and ALL can re-assemble into the cell wall competent form.
Not only do l suffer from Chronaic 🎉Lymes after an initial outbreak in 1997, but l developed chronic symptoms following Covid. I have Rheumatoid Arthritis and there are alot of autoimmune disorders in my family. Possibly those of us who develop chronic Lymes complications are already suffering undiagnosed autoimmune disease?
I was a deerstalker for 20 years in Oxfordshire. I seem to have escaped Lyme, despite having occasional tick bites. I read that the best knowledge on this is in Germany as they are keen stalkers and recognise the problem.
Living in Germany with Lyme disease for over a decade. It's a myth, that German doctors know this. In fact, German doctors are about the worse one can have. They are lazy, incompetent and full of prejudice. They truly know how to add insult to injury. And with me it even was certain, that it was Lyme disease, due to ACA on my skin and blood tests. There is a tiny minority of Lyme literate doctors here, most of which you have to pay out of your own pocket. Yet, even they have no clue on how to cure my late stage Lyme disease, after I relapsed after a move. I'm basically left to rot. Don't even go to doctors anymore, cause I cannot handle anymore heart breaking meanness. May God revenge me!
So, auto-immune reaction of the central nervous system. Some have successfully treated it with accupuncture - triicking the signals and allowing the inflamed part to recover.
I woke up in my bed and found a tick attached to my arm ( i have a dog). I'm terrified, I'm from a 3rd world country and life just started to look good for me.
Except for decades the government for infectious disease doctors to deny chronic Lyme, make testing and treatment in absence of classic rash difficult and often past the window to be most effective.
@@sillygirl3284 i went to see specialist after all symptoms were gone.she told me she didnt think i had lymes musta been glandular fever,im like ffs i had the bullseye rash and a lot of the symptoms on line .shes like dont believe everything you read online only use n.i.c.e site which is the uk goverment site thats all factual information on there.i came away from there having lost all faith in doctors and specialist govt trained .id now rather follow a chiropracrer on yt to help with my health lol
Oh, that is interesting (not to dismiss the tragedies). IgG4 is alleged to be elevated in patients with Lyme's disease. IgG4 is a tolerance antibody to reduce severe reactions. But it can serve to protect pathogens, too, which get the green light to create havoc. So when you mentioned an entire 2 months of antibiotic treatment can sometimes be helpful, the IgG4 tolerance hypothesis is supported. Antigen tolerance may be the mystery cause. IgG4 antibody is created for antigens when the body fluids contain elevated "allergy interleukins" that stem from an allergic reaction. Interesting. At the same time, being bitten by a lone star tick can create mammalian meat allergy. This is often confused with Lyme's disease, but a mere change in a low allergen, sometimes low salicylate, plant-based diet can profoundly help.
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I was misdiagnosed for 21 years, first with MS, then with fibromyalgia. I lost my ability to work, lost my partner ,and lost my home to foreclosure. I'm still suffering the damage to my body and brain, since it is no longer curable at this point. I am so glad to see this finally being discussed!
I'm sorri that happened to you!!... sooOooo important to be in tune wit our bodies.... there are awsum doctors out there but they do need to be sought out.... hope yoi well....
@@ellebenenati7787 - I'm alive only due to studying naturopathy and applying it. I was put on terminal disability in 1994. We have a famous Lyme doc two miles from our home but like most LLMDs he does not take insurance and I can't begin to afford him. He says Lyme is a rich man's game and also that after a certain point it is just not fixable. I am doing well considering the damage. I can do light exercise daily, and the Neurologist says it is a miracle I can even walk with the amount brain damage I have. Back when I got sick in 1986, most doctors had never heard of any of this and the Chamber of Commerce where I live was denying that there were even any deer in our state, a blatant lie!
@meagiesmuse2334 I'm sooOooo happy yoi wit us!!... good on you for seeking out other resources!!... I've been doing homeopathic medicine for sum tyme I was 1first taught by my auntie n then mostly self taught.... sumtymes when western medicine fails us turning to styles of eastern medicine can make all the difference!!... today isn't 1onea my best days, I hurt.... that's another story for another tyme but wanted to say hiii quick!!... ello!!... I will come back here ina couple day's wit sum book titles for you, I still read actual books.... LoL!!... ofcourse you kno what yoi body likes n doesn't allergies ect.... vitamins herbs n minerals can assist aswell crystal therapy is awsum meditation n gentle tai chi movements for yoi body mind n soul.... I was tired of being tired n unintentionally being mislead....
till then be well....
ps: if you watch hockey the panthers are playing north carolina n happy valley is on bbc this eve!!... 🌺🐯💛
@@meagiesmuse2334
What happens if you cut out sugar intake.
It seems to be helping me and I just started Methylene Blue but don’t know if it works yet. Only been taking it for a few days.
I got Lyme disease for 3 months, had terrible headaches, lost a tooth and finally got diagnosed by a BioResonance Therapist. After 2 sessions, the bacteria and symptoms were eradicated using frequency therapy.
I’m so sick of media and online sites completely downplaying Lyme. At my worst I had over 100 symptoms. It was horrific for 5-6yrs and no drs helped me.
I'll say it people hate medical doctors and their higher ups
How did you get better?
@@DJBILINGUALcan u mention some symptoms?
@@chrisluisangel wrong tag
@@DJBILINGUALooops
I had Lyme in the 90's when I lived in Western New York, after a trip to Eastern New York where I did some hiking in the woods. I had the flu-like illness for a few days. I had the bullseye rash. My primary symptom was severe heartburn about a month later. My doctor started treating me for an ulcer. While I was in the waiting room for a follow-up appointment I read an article in a magazine about Lyme showing a picture of the rash. I took the magazine to the consultation, showed the Dr the picture and told him that I had had this rash just before I had the flu-like episode. Long story short, he refused to believe that I had Lyme Disease. He said that because *he* didn't see the rash, he couldn't accept it as a symptom and he said, "There is no Lyme Disease in New York State". At the time, blood tests were very unreliable so even though I had a positive test he still didn't think that was what I had. I finally found a Lyme specialist north of New York City who agreed to see me. I drove 5 hours each way to see him. After telling him my story and taking a blood sample and examining me he told me to call him in a few days. I went home and called him a few days later after he had my blood test back. He said that he couldn't be sure that I had Lyme Disease, but neither could he be sure that I *didn't* have Lyme disease. He treated me with a long course of antibiotics and my symptoms completely resolved. I was fortunate that I had taken the time and effort to track down a specialist who was open minded enough to listen to the patient and to recognize that he didn't have all the answers. I wish I could remember his name, although that was almost 30 years ago.
Good for you and your persistence.
I was on a college soccer team and our goalie was from Old Lyme Conn. He knew the kid who got the first known case. I think he said he was a wrestler.
How much time passed between hiking and the antibiotics?
@@OurNewestMember Hard to remember exactly, but 6-10 weeks.
Yep, similar story here…the idiotic doctor refused to acknowledge I had/have Lyme disease
I had an ex who had Lyme. No one supported her or believed her. She was always dizzy, had migraines and just other bad symptoms.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo.
You trust everyone and dats stupid.
We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
Yep I’m in that boat. Healthy people can not relate so they like to dismiss it because it makes them uncomfortable. Having empathy for a friend who is suffering is too much for some people and they can be quite cruel about it. Plus, we only make it out of the house on our “good days” so people tend to think we seem fine. They don’t see the bed-ridden migraine days.
@Jerry Howard obvious scam is obvious 🤡
So crazy and terrifying how SOO many people trust the cdc😂🤡 those who dismiss everything are “trusting the science” 🤓🤡🌎
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel.
I had chronic Lyme Disease for 4 years. Every few months I had flu symptoms and the pain would settle in a different joint. American doctors and insurance companies WILL NOT recongnize chronic Lyme disease, as the insurance companies do not want to be liable for paying for it. I was on a waiting list for 2 years to see a specialist at Tufts. My doctor refused to give me more antibiotics. The only time to truly test for Lyme disease is in the middle of the night, as that is when it is most active in your blood. All other tests come out negative for Lyme. I did all of my research in Europe. In the meantime, I started taking oregano pills (a natural antibotic). I took 9 per day for the first few days and then gradually went down to 2 a day. I took them for about a year, and It finally went away.
Wow, did this really help you? I'm suffering from undiagnosed chronic lymes. I know this is what I have as it started after the classic bullseye tic bite but doc's can't seem to diagnose me. I'm suffering so bad my quality of life is terrible. I need help
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo.
You trust everyone and dats stupid.
We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
Wow I wish I could tolerate that many oregano pills.
all too common...here in phila pa its everywhere, ticks are infested thoroughly, especially with warm winters now. doctors are the most cocky self absorbed bunch out there, always the last to acknowledge anything new. crazy the situation has only barely changed in 40 years, deny deny deny!!!! it will just go away!!
@@funeats8201I know, right!? I can barely tolerate ONE! 😂
I’ve had a terrible case of Lyme my whole life and I pray for everyone else who has it because it’s ruined me and I hope I live to see the day a cure is discovered. Most people don’t understand how bad it can be…
Same here it’s bad I lost everything it will not go away everyday is really hard to go through I can’t live like this. My kids were very young they never got a chance to know me and I don’t recognize myself anymore.
And you both were treated with antibiotics/Doxycycline?
@@jenniferhodgson7640 idk, I was born with it.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel.
DRETIKOCURE on TH-cam thought me that is all about patients and the right person, May God continue to bless You sir for the permanent HPV cure I received after taking your herbs.
It’s nice to see that mainstream Drs are becoming more Lyme literate and finally taking it seriously. They’ve dismissed chronic Lyme and gaslit sufferers for far too long. Better late than never. Now if only they could get informed on the role of environmental toxins in the role of diseases...
Stop using words like informed. They can’t be informed on things not discovered by science yet. There was no science explaining long term Lyme disease before. Now there is. Drs are trained to be like that, it’s highly frustrating for people experiencing things they have no science for of course. They should believe people. But there’s no way to be informed on something not discovered yet by science
Especially with mold
Depending on the state you live in has a lot to do with a doctors approach.. In Massachusetts the doctors are on it, they know Lyme's and Triple E" are prevalent there..
Say"EH WAS NAILED TO THE CROSS WITH A CROWN OF THORNS! OH WAS TO THE LEFT AND UH RIGHT. PEOPLE FROM ANOTHER PLANET ARE TRYING TO TAKE OVER EARTH WITH CIRCUMCISION AND EARRINGS! GOD WAS CIRCUMCISED"
How about the governments role in creating Lyme.. can we talk about that, also?
I had Lyme disease at 5 years and I ended up being paralyzed. I couldn’t walk, I was taken to the ER and they gave me antibiotics so I was able to walk again! Thank God!!!🙏🏽❤️
God gave you lime disease, thank science, that’s what saved you
You should thank the doctors
@@sarajuanaict Indeed. God gave her lyme disease and paralysis. Science and doctors cured it.
@@sarajuanaict You mean for creating Lyme disease?😂
@@johngrasso1483 😹
My sister was misdiagnosed for MONTHS before finally being diagnosed with Lyme. After 2 years of antibiotics it appears the Lyme is eradicated but she has multiple residual symptoms. Not everyone gets the bullseye around the bite.
I wouldn't stop treatment if I still had the symptoms Make sure she's seeing a good limes doctor or a infectious disease specialist
All the people I know that have it. My self included never get rid of it. Antibiotics help for about a year at a time and after 3rd round it gets better but it all comes back.
I now have Alfagal witch make you allergic from hoofed animal’s and all the derivatives. The allergic reaction in my stomach caused an ulcer and about killed me.
Started Methylene Blue a few days ago.
From what I understand it surely can’t hurt anything.
Tired of being sick and the brain fog is the worst part.
What was your sister symptoms
@@rexhorning7228How is the methylene blue working out?
It kills the bacteria without the biofilm but the ones with biofilm still remain causing inflammation and the symptoms
Yes, an inflammatory marker stays high, but why? It is great to see Lyme finally being taken more seriously and getting discussed in the mainstream, but there’s still a long way to go.
For instance, why don’t bands 31 and 34 count toward a positive test per the CDC? Because 3,000 people in the 90’s got it in a vaccine? That’s ridiculous. That is one of the biggest reasons people go misdiagnosed, and we need the proper authorities to take action and change this flaw in the medical system.
Everything does not always fully resolve with Antibiotics. Lyme hides.
Tick pics or not, this info could be a game changer for those of us stuck in this situation. Thanks for reporting! Links to original study and sources would be REALLY helpful. Please consider including in description.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo.
You trust everyone and dats stupid.
We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
No, if you're still suffering, you still have an active infection. There is no test anywhere that proves it was ever 'cured'. ...this is just lazy 100% 'pseudo science', no one is paying proper attention.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉🎉
Thanks so much *MR OBALAR* on TH-cam for curing me from Herpes, keep saving lives.❤😊❤
I was infected around 1987, a harsh learning disability was the worst symptom at the time. In 2008 heart palpitations and panic disorder started, misdiagnosed by many specialists until 2021.
My brain MRI results come in soon, I’m anticipating the worst being late for so long. It’s taken everything from me, our government has ignored this and taken everything from me. 💚
I here u Yhere im now Replacing my 2hips & now going for my knees the pain is everywhere I've had lymes 4 or 5 times on the books it never leaves we the people that have been suffering fir yr & still are need to Sue the makers of lymes Fauci Gates In Lymes Connecticut I was a Vibrant strong successful woman that no longer has the true life 🤬 Now replacing body parts when things are better with the pain it's Diet No gluten and Taking The Right Herbs KEEPING Your Vitamin D Up Long time overdue with people suffering with this horrible disease that no doctor likes to help we need to start an organization and Sue the government Gates fauci at the highest levels FOR are pain and suffering I FEEL YOUR PAIN 🙏👍☠️
@@debraparella4877 It's called Lyme, not lymes. Capital L and no s.
🙏
Misdiagnosed for 30 years . A slow unforgiving death
Misdiagnosed means that there was a mistake or oversight.
What happened to you was pure fraud of ALL sectors of medisin covering for a we upon release done in the 1940s that they have no capacity to control.
Yep, misdiagnosed also….I was in remission then got covid and I now welcome death
@@1timeslime971 I hear you TimeSlime. 45 years with Lyme- one year in bed in 1987 and now the last 4 years again. Same Medical Professional (isn't that an oxymoron) diagnosis- your metrics are fine so you are not sick. I totally relate to "welcoming death". With luck we'll get pancreatic cancer.
The suffering is so long and so intense! And the quality of life is practically non-existent. You just hurt and suffer and hurt and suffer, whilst being totally exhausted almost all the time. It's a most horrid disease, and I too had much rather died, than getting it and suffering so badly so long already because of it.
But what truly adds insult to injury is the meanness and stupidity of almost all doctors! They can't stoop low enough to reject us and to accuse us falsely. Which causes a different kind of very real pain in the heart. May God revenge us!
Same thing I’m bed ridden 8 years know I only think of ending this I lost all hope.
Thank you for reporting this news. We need to train more doctors to take this more seriously. It took months to find a doctor to treat me and then it took 6 months to cure me. Lyme disease Can impact someone daily lives in the worst ways.I don't wish it on anyone.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo.
You trust everyone and dats stupid.
We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
@Jerry Howard hey can I get the deets?
I actually had a doctor here in Oregon tell me that I couldn’t possibly have Lyme disease because they don’t have that here on the West Coast… How ignorant. You didn’t even ask me if I had lived anywhere else. Even if that was true that you can only get it in certain locations,… Doctors are definitely in the dark ages about this. I finally had a doctor that tested me and found the blood markers for it. He said I probably had it since I was around seven or eight years old. and you don’t necessarily have to be bitten by a tick, but that’s an even farther stretch for doctors to acknowledge. It can be spiders and mosquitoes transmitted as well.
Can you please tell me how you were cured? I've had Lyme for 5 years.
@@creativesolutionstoart what an idjut doctor--Lyme is prevalent all over the nation at this point--it only takes one tick bite and in my case, there was no bulls-eye rash. I was lucky--when I first had it, I was in Connecticut and had knowledgeable doctors. After the antibiotics, including intravenous, I was left with fibromyalgia and chronic migraines--the fibromyalgia is now in in recession. The chronic migraines were also in part because there is a genetic disposition in my family, but a good doctor asks these questions....My CT rheumatologist would give me antibiotics when I felt I had symptoms but unfortunately, a lot of doctors are not up to speed on this.
Oh so they’re finally agreeing that Chronic Lyme actually DOES EXIST!
Yep, MSM is always a day late and a dollar short
@@funeats8201 CDC also has denied Chronic Lyme for years
@@FluxyMiniscus the CDC is so captured and corrupt that I can’t fathom why anyone takes them seriously. With their staggering level of corruption disguised as incompetence during the pandemic, they need to be defunded.
It's like the M&M guys meeting Santa Claus!
The CDC is uniformed millie tarry covering for a we-upon that was released in the 1940s and got away from them. They HAVE to admit it below the Pahn Day Mik levels that its at to ease it into the public consciousness that its the worst plague that ever faced mankind.
No they’re delaying the inevitable it’s persistent infection there saying it’s due to protein found in the blood that causes prolonged infection so it’s misdirection even worse than before. We have to many biopsy post infection and treatment proof dr Monica embers Tulane university has proof and antibiotics working is proof there is infection there is others dr Kenneth liegner has proof documents extensively
She isn’t addressing the findings that the bacteria has been found to hide in biofilms.
Her plan of suppressing people’s immune systems is a dangerous plan for people dealing with chronic Lyme.
They won’t ever address it or ever have an honest debate, these people are 🤡 demons
Agreed very very dangerous to suppress immune system against Lyme
Don’t take immunosuppressants if you have Lyme, you need to bolster your immune system to manage it
depends, if there is not actual infection (lyme bacteria is gone) and the symptoms are due to post trauma inflammatory marker (basically a kind of autoimmune issue) then a targeted immunosuppressant could be the solution...
This is horrible and inaccurate information. Far more than a 5 to 10 percent subset suffers with long term chronic symptoms. Anyone in the Lyme world knows this is a hideous disease that can be chronic for years with difficulty in even treating. They need to be speaking to Lyme literate doctors and actual patients so that the world knows how destructive this disease is. I am living this nightmare.
I was diagnosed with Lyme disease just yesterday, I work in the woods and have had symptoms for more than a year. I didn't have the typical rash or even the typical symptoms. If it wasn't for researching into it myself using google scholar I wouldn't have had any treatment. I have been having symptoms similar to Schizoeffective disorder, lots of sleep paralysis, depression and anxiety. Lyme disease can imitate many disorders and syndromes.
I had the rash and the flu like symptoms. It makes sense once I knew what it was. For almost a decade I was treated for treatment resistant depression. I finally said that I think something is wrong with my immune system, got a bunch of autoimmune testing done, they stuck the lyme disease tests in there, and that was the only thing that came up a strong positive! Since getting doxycycline, it took about 6 months for my antibodies to go down and my psychiatric symptoms to go into remission. My psychiatrist was even considering ECT or ketamine, because I tried almost everything else. I thought the bullseye rash was the strangest mosquito bite I ever saw, I remembered telling my mom about it after I was camping. Then it all started making more sense. I hope you feel better soon! I think lyme disease should be considered before a psychiatric diagnosis like schizoaffective disorder is made. That is a pretty serious diagnosis.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel
Treat it aggressively and do not listen to doctors unless they are dedicated Lyme literate doctors! The vast majority of doctors are clueless, negligent, and cruel when it comes to Lyme! 😱 Research…
What other symptoms did you have?
It is unfortunate American news always pushes for too short segments. These subjects deserve a bit more time to explain. Forcing to 'wrap it up' just causes for the message to NOT come across.
Thats because it doesn't involve something politically charged, controversial nor money. Its science and health related so it gets the quickie treatment.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo.
You trust everyone and dats stupid.
We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
Yeah it’s not like they have anything else of any actual importance they need to get to. All they do is spew propaganda to their gullible audience. And no apology or accountability for the damage they did to this country with all their misinformation during the plandemic.
I mean why would you think the media is your friend. America has never been for you
They are just a bunch of propaganda outlets. They work for the 5 corporations in a trenchcoat that are masquerading as the usa
When ppl first complained to doctors about what is now known as Lyme disease they were told their symptoms were psychosomatic, essentially that is all in their head. It took decades before the CDC actually accepted it as a real illness. This drove a lot of people to not talk about having symptoms or go to the doctor because you were immediately labeled as crazy. This has also happened with other diseases, like Morgellans, which in 2009 was finally considered a real medical illness. Prior to the CDC accepting an illness as real, no one is studying it or taking it serious in terms of treatments or cures, so having the CDC recognize an illness is pivotal to the lives of those suffering with these unknown illnesses.
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo.
You trust everyone and dats stupid.
We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
A judgemental doctor is a sick patient's worst nightmare.
I have Morgellons/Lyme 😢😢
We can thank people like Dr John Aucott at Johns Hopkins and others who bravely researched Lyme and chronic Lyme, (now called Post Treatment Lyme Disease Syndrome), for giving this real disease legitimacy. And we can blame the "Lyme literate" doctors who are making a mint by administering witch doctor treatments to desparate Lyme patients for making the legit doctors skeptical.
The See Dee Sea is uniformed millie tarry services with a Surgeon General.
The ONLY reason that they recognize it is because it is so out of control that they can't avoid their intentional release from the 1940s anymore.
I think this is it. This video made me cry. There is hope ! I got lyme disease 7 years ago. My symptoms got worse after covid infection. I was on long term antibiotic treatment ( 6 months ). It got better after treatment , but after some time it returned back. This summer I got infected again with new tick 😢.I met friend few weeks ago. She had lyme as well and she said she had lingering fatigue and joints pain. She also mentioned, that after some time she got immunosupressants for autoimune skin disease and her lyme symptoms miraculously disseapered
What were your symptoms? How did you find out had it?
Lyme disease is a spirochete like syphilis. The body really hates spirochetes and reacts to them in weird ways, like chankres and in yawyaw it makes weird growths. Spirochetes are normally life long infections so it would make sense the body would continue reacting to Lyme long term
Very cool. Thanks for sharing.
You are 100% correct. NO antibiotic has EVER 'cured' any disease, and it was known in the 1900s that antibiotics turned spirochetes into stealth organisms. So the infections NEVER went away.
They pretend it's gone after 30 days antibiotics. What tests are they using to prove that? It's BS.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉
Read the book “ Bitten: The secret history of Lyme disease and biological weapons”
I was waiting for you!! Read the book. Thank your government for Lyme!
FINALLY!!!! I'm going through this entire comment section and you are the FIRST to tell the ONLY truth in this matter.
See this makes sense to me ,iv been into the outdoors for many years and ticks have never been an issue ,i never even checked for any but now every time im outdoors iv always got ticks on me.
Lyme specialists have been talking about this for years, but nobody cares what Lyme specialists have to say about Lyme.
I had Lyme for over 50 years, I remember the Erythra Migrans on my abdomen aged 8 after playing in a hay field with friends in S.W England. I developed multiple problems. I had numerous disagreements with the NHS over this (apparently I was imagining the symptoms.) I finally went private and got 3 separate positive test results with full clinical diagnosis. I took antibiotics, used PEMF's, low dose immunotherapy etc for 2.5 years, almost died from Herxheimer reactions several times. I am left dealing with 50 years of damage and inflammation, there is almost nothing I have not tried but I still lose several days a week unable to function above 10%.
Limbic system rewire
Oh my goodness. What were your herx reactions like? I’m so sorry😞 I’m just now being treated after having it for over 10 years not knowing
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉🎉
For me .. Popcorn is terrible for lyme inflammation!
Collagen just about cripples me .
TQ I will look at this.@@bloodcamarosexmagik4223
I caught it last year in July, and it’s ruined my life.
The CDC and ISDA need to start recognizing it for what it is.
DRETIKOCURE on TH-cam thought me that is all about patients and the right medication, May God continue to bless You sir for the permanent HPV cure I received after taking your herbs
biofilm , it's a satanic cult, Eben back in the day doctors spread bubonic plague and allegedly the 1918 influenza, just research biofilm
watch my public playlist
They do, they are just paid off by insurance and pharma as well as government
They know. th-cam.com/video/zoxszhv9D1k/w-d-xo.htmlsi=ZNuFW5iwtRFHh42D
Chronic lyme is NOT an autoimmune condition - it is persistent infection. There are more than 700 peer-reviewed scientific studies showing this, and I am an example: after 2 1/2 years of intense treatment with multiple simultaneous antibiotics, lyme dna was found in my serum via PCR, the gold standard for detecting infections.
My new meme: All of The Above. Inflammation that fake word that they throw around is an IMMUNE RESPONSE. Chronic inflammation is also lumped with autoimmunity both of which are responses to antibiotics creating 8 different cell wall deficient morphologies but CURING NOTHING.
Yes the video is still missing the point. Its not just an ongoing immune response, its a persistent ongoing infection. Ive witnessed this myself, even have made videos that i posted on my yt channel that clearly show this. The fact that they cant wrap their heads around this simple concept is just baffling.
@@_S13_ I just subbed.
Since the advent of clinical medicine no one knows how to destroy a spirochete. They adopt 8 different forms for evasion, so my theory is that unless you hit them with 9 different remedies at the same time to take out all stages you are just playing Whack-A-Mole.
So, we examine what I just said: NO ONE since 1900 AD knows how to kyll these things, but they knew back then that even the arsenic, mercury and antimony merely turned them into stealth cell wall deficient forms. Therefore it's not that they can't wrap their heads around it - they KNOW that a Buy Yo We Upon was released in the 1940s. They can't put the Genii back in the bottle. ALL of their efforts are failing. So they hold out the "new research!" and "verge of an answer!" B.S. to keep their victims in a state of perpetual anticipation that something will get better when it can never get better until what I just outlined is arrived at. On top of the 9 remedy approach everyone STILL needs to destroy the filarial worms (Alan MacDonald) that carry the spirochetes inside of them as they bore into the spinal fluid swim up to the brain and unload their neuroborelliosis that is 'another mystery' to these disinfo agents.
My most important videos on this topic were removed probably because they were the only truth out there.
Wait a minute! Just because that is the case with you, doesn't exclude other possibilities in others! Don't be like those dumb doctors, who are blinded to several possibilities!
@vaccinefraud5570 you sound like you know
.. how do I get rid of it ?
i had babesiosis, a very rare form, and almost died. Had complete renal failure, months of dialysis, and now years later I'm still dealing with joint pain, something I didn't have prior to the lymes. That was second bout of lymes. The first one I recovered fully from. The second? Not so much. Wrecked my life. I was very active and loved that lifestyle
So sorry to read about your sufferings. Yes, it's hardest on the active. You basically can't be you anymore. You still have all the desires, just not the capabilities of living those out.
Again, very sorry! Hope one day something is found to give us part of our lives back.
@danielleperry1657 Oh, stop with the trying to make a buck of ill patients! We know you write nonsense and just try to advertise below the surface.
May God force you to pay back a 100 times for all you've stolen from people, willing to try your snake oil.
How did you get rid of the babesiosis? How long did you have it?
@@mandamoon13 typical antibiotics and typical time. Just the after effects that I’m still dealing with, such as liver and kidney damage and polyarthralgia. I’ve had Lyme disease two other times with no repercussions. Thanks for asking
How'd you find out you had babesiosis, what were your symptoms?
Northampton integrative medicine in Northampton Massachusetts has been treating chronic Lyme disease for decades. They have a successful track record of helping improve the health and wellness in patients. They have always treated patients that the medical community as a whole turned away. Check them out online.
This makes me so angry. I was diagnosed years back took a round of antibiotics got checked again from the same dr still had a positive test and could t afford the next round. Then I go to Kaiser and another hospital both of which told me I did not have it. I’ve been in with all kinds of symptoms that literally the drs just tell me I have mental health issues..it’s like can you humble yourselves for a moment and remember that maybe you don’t know everything there is to know
They didn't bring up the fact that antibiotics don't tend to get past the blood brain barrier so the lyme can hide out there. Teasel root tincture helped me greatly to get past the blood brain barrier in the treatment of lyme killing it all off. Good luck everybody!
DRETIKOCURE on TH-cam thought me that is all about patients and the right person, May God continue to bless You sir for the permanent HPV cure I received after taking your herbs
Thanks At this point I'll try anything
It's definitely worth a shot. For me, teasel root tincture started working within a day. @@debraparella4877
How do you know if helped the blood brain barrier? Were you experiencing neurological symptoms?
@@jonathangraham6412 I have read online that teasel gets past the blood brain barrier since it is natural (whereas antibiotics do not unless given intraveneously). Antidotally, I could feel where it was working because I would get high grade fever localized to where the lyme was (specially in my knee joints and all in my head).
The standard of care set by the IDSA 2006 Lyme disease guidelines is one of medical neglect of persons suffering from chronic Lyme disease. However, such guidelines are indeed useful. They serve to shield from liability physicians who neglect persons with chronic Lyme disease. By misusing CDC case surveillance criteria as the sole basis for a clinical diagnosis of Lyme disease, these guidelines serve the insurance industry very well indeed because such cases represent but the tip of the iceberg of actual cases of Lyme disease, whether acute or chronic. Denial of the possibility of seronegative Lyme disease, likewise serves the insurance industry well and also such simplistic constructs for Lyme disease also serve those physicians who cannot wrap their minds around the true complexity of this illness.T
The medical profession and the United States Public Health Service, predecessor to the CDC, have a long history of medical neglect of persons suffering from spirochetal infection. The profession and the USPHS were completely unable to reform themselves from within in this regard. It required moral and political intervention from without to bring the Tuskegee Experiment to an end with Senator Edward Kennedy’s hearings in February and March, 1973 before Committee of Labor and Public Welfare’s Sub-Committee on Health (Jones JH. Bad Blood: the Tuskegee Syphilis Experiment - a tragedy of race and medicine. The Free Press. New York. 1981 pp. 213).
The Tuskegee Experiment involved about 400 subjects. Lacking the taint of racism, nonetheless the “mainstream” handling of chronic Lyme disease affects far more people; it would be a fair estimate to say, Tuskegee X 10,000 in the United States alone. Furthermore, the standards held out by the CDC and the IDSA have worldwide influence. Canadians are unable to get care for chronic Lyme disease. We are seeing significant numbers of persons with chronic Lyme disease forced to leave Canada for care.
State legislators have begun taking matters into their own hands and the states of Rhode Island, Connecticut, California, New York, Massachusetts and Minnesota have passed laws or promulgated policies protecting physicians who treat persons with chronic Lyme disease. Are these legislators stupid? Are they dupes of Lyme activists? Or can they see what is so obvious to the patients and to any good clinician, that Lyme disease can be a chronic infection that often requires a long-term treatment approach? Furthermore, as the disease spreads and more and more individuals are affected, legislator’s staffers, their wives, their children and they themselves are experiencing the effects of chronic Lyme disease.
In the fullness of time, the mainstream handling of chronic Lyme disease will be viewed as one of the most shameful episodes in the history of medicine because elements of academic medicine, elements of government and virtually the entire insurance industry have colluded to deny a disease.
My 14 year old child was complaining of aches and pains and being tired. her pediatrician told us it was in her head and to take her to a child psychologists. He said I can't find anything wrong with her. Take her to a child psychiatrist. The psychiatrist said I can't find anything wrong with her. Has she been tested for Lyme disease? I said of course we live in Connecticut. Lyme CT is where it gets its name. I pulled her medical records and her Yale grad pediatrician never tested her for Lyme. The psychiatrist recommended a neurologist who took18 vials of blood from this poor kid. He sent 6 to Quest, 6 to Lab Corp and 6 to Stonybrook Hospital on Long Island, NY. Stoneybrook was the only place that had the equipment needed and came back with a positive. Now years later she is experiencing the same symptoms and they're telling her she has MS.
they're...anyhow......... healing the gut biome is the only chance she has...start with chevre goat cheese and cantaloupe....low acid, organic foods, no preservatives, filler or gums, only palm and olive oil, t no sugar...lyme loves sugar.
Make sure they also test her vitamin D levels. When I was diagnosed 5 years too late, my vitamin D level was at 6. Magnesium helps the muscle pain and body aches tremendously. I'm so sorry this happened to her. Doctors can be infuriating.
@@jillelizabeth478 Thank you. I'll make certain they do that.
Please look into finding a Functional MD. Standard allopathic MDs are way behind the times.
A chronic Lyme patient needs to be tested for environmental toxins and mycotoxins (we often are unable to eliminate chemical toxins from our bodies like healthy people can). I did the GPL-Tox test from Great Planes Lab but there are others as well. Honestly, anyone dealing with MS type symptoms should probably look into doing glutathione IVs anyway. Low carb diets are helpful, as is intermittent fasting. I hope your daughter is able to find answers and make a speedy recovery. 🙏🏼
Better Health Guy and Mark Hyman have good Lyme videos on their TH-cam channels.
Stephen Harrod Buhner’s books and teachings…he passed last year…. Everyone must read all his on Lyme’s.
First, please call it Lyme not Lyme's; the former is correct. Using the latter will not help your credibility with doctors or scientists.
If who ever pretents to care for lyme sufferers really cared, they would start to do a study checking those people with ongoing symptoms systematically for coinfections like babesia, bartonella, ricketsia, erlichia, anaplasma or reactivated stuff (EBV, chlamydia, mycoplasma). For some reason, there is not one study who ever did that even if it would be highly logical.
caught it in 1990/ 1991 Doctors were clueless. SAW tiny ticks all over--they were crawling up anything that walked through grass of my dad's yard in Orange county, NY. Lymes paralyzed my formerly healthy dog--we had just moved from a city out west. The dog was perfectly fine before, 6 months later she had arthritis so bad she couldn't move her back legs. I was also sick with a rash and "flu" . The vet yelled at me that I was lying she was fine before we moved to NY State. He euthanized my dog. I never got treatment....here I am in utter pain with terrible symptoms that have ruined my life...but of course since I "test negative" no doctors will help me unless I pay thousands out-of-pocket for a "lyme literate" dr.--well, I have no money thanks to lyme ruining my ability to work steady, NYS won't recognize me as disabled...so I have to use herbs just to try and manage it myself. The insurance companies, doctors, CDC--all in it together to hide the truly horrific level of tick borne infections that ARE indeed a CHRONIC infection and at epidemic levels in the Northeast.
thank you for this segment because this is a serious disease being overlooked by many medical professionals
and the media
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉
I got chronic Lyme disease 2years ago. It was an horrific experience..I suffered many symptoms, especially excruciating headaches that never went away and felt like my head was going to explode..
( I was misdiagnosed 3 times)
from time to time I still suffer with fatigue and joint pain. I never got the bullseye mark. I was misdiagnosed with chronic migraines for months before I finally almost lost my mind and got myself to the ER. I sometimes think the bacteria is creeping back on me to cause havoc again in my body. I hope it won’t come back, meanwhile some symptoms come back from time to time..I’m thankful that I was able to be on the antibiotics. Lyne disease is for sure, something I never want to go through again!
Blaming Interferon alpha for Lyme is like blaming cholesterol for heart disease.
Exactly!!
Can you make it to where kids can figure this out too, please
My grandson has tested positive for a year. His chronic symptom is daily vomiting multiple times a day. No doctor will link this with Lyme and therefore their only suggestion is anti depressants. They initially gave him one round of antibiotics but he still tests positive and they make no other recommendations. The whole family is frustrated and out of ideas.
get chevre goat cheese and cantaloupe in his gut soon.... this will help remedy the vomiting.. and heal the gut biome so he can fight this himself.
Find a good probiotic in the fridge section, preferably powder. Garden of Life 5 day critical care is great. It tastes like banana and you add to water. He may have also developed food allergies and/or food sensivities from the Lyme.
I don't know what state your grandson lives in but Dr Gary Berliner in Dawsonville GA, is a Dr that does believe in Chronic Lyme. You can look him up. Maybe, he could help.
@@littlefootinalaska6253 my grandson lives in Northern Minnesota
@@littlefootinalaska6253 thanks for the tip
This information is inaccurate, there are thousands of people struggling with chronic Lyme, not just 5 or 10%!! I cannot express how terrible this disease is. Im literally dying from it because it was late stage by the time I got diagnosed, i had it for 30 years before doctors finally dug deep enough to give me answers and no treatment works for me anymore. Its slowly sucking the life from me and its devastating. Someday in heaven God will give me a new body.
You’re so right! God bless you 🙏🏼
They're missing the mark for so many because many still have bartonella or babesia so if you just try to lower inflammation and fix the damage it's not enough. Bartonella and Babesia in so many causes stick around, as does Lyme, so this type of info presented as the "key" will mislead many.
Whats the cure
@@jonathangraham6412 There is no cure for chronic Lyme but it can be put in remission.
@@jonathangraham6412 keto diet and fasting i would say is your best bet but cinnamon bark tea also worked for me .
I had it for 2 years before I found out. Lost a $120,000 a year job along the way in 2011. It's now 2023 and I ended up with bells palsy so I went through the Dr. He tested me and I was positive. Weird thing is that he said on the test that's it's not showing I had lymes in the past. I told him that's why I'm here because I know it's my lymes. He gave me 30 days moxicilin and when I went back to Dr I was still positive. Asked him the next step and he said there wasn't anything more he could do for me.
Test again in 6 months. The test is looking for antibodies, not the bacteria itself. Those can take 6-12 months after treatment to start to come down. My test eventually showed less bands positive.
I have full blown Lyme adult female deer tick bite huge bullseye rash all the trimmings and 5 western blot tests over the course of 8 years not one band not one test all complete negative spinal pcr positive don’t trust that test never.
do dark field microscopy. there will be your answers
Interferon alpha immune marker. And to imagine for 40 years most doctors denied Lyme existed and to this day there isnt an affordable, accurate and accessable test for it. It should be taught and required all doctors to order at minimum a western blot when patients come in with odd or bazzar symptoms.
I’ve had it in Australia for 26 years
The list of symptoms is huge and the seizures are gnarly as
Thanks so much *MR OBALAR* on TH-cam for curing me from Herpes, keep saving lives.❤😊❤
So long term lyme has always been a side effect of doctors' reaction to the disease?
Not exactly.
If you dig up a few good research papers published in the last 5 years...one on a site called Frontiers, they spell out what's all been explored & is pretty intetesting. Including that detecting it is hard...the tick nymph is poppy seed size...etc.
No, disease is detected then not cured but worsened by doctor's reactions to the disease. Than the patient who is now much worse off for contacting the doctor is not told by doctor that the doctor did it to them but instead that the poisoned-by-doctor patient is imagining it, right?
This is so sad to me. I’ve lost over 12 years of my life from this disease that I will never get back and as the days go by I continue to be sick. I’ve been dismissed by every specialist under the sun and at one point was even convinced it was me causing myself all this pain. I went to alternative medicine after years of no help and spent thousands and thousands of dollars my family didn’t have to try and get better, never happened! I then got diagnosed with stage 3 cancer that it took me longer than it should have to go to the doctor because of being mentally beaten down by all doctors in the past. Having cancer I was believed, treated and supported by the medical community, never was I supported like that with my lyme/viruses. Chemotherapy (suppressing my immune system) relieved a lot of my lyme/viral symptoms and it was amazing! Then once the chemo wore off all symptoms came back with a vengeance. This study is great but hurry up! We need help now!
@cdc is it real now because all my doctors who dismissed me told me you the CDC told them that my symptoms weren’t real! Help us
chronic lymie here....so did I miss it...what was the solution from this information? some of us have an immune protein deficiency and how do we correct that? The other issue with us lyme sufferers getting proper diagnosis in the US atleast is most mainstream aka insurance covered docs will only use the outdated "western blot" test which is known to be the least reliable test for lyme so it causes many false negatives. The most reliable is the "igenex" text but insurance companies won't pay for that one....why ?? why do they want to keep us ill ?? it makes me think its a gmo coverup like covid
DRETIKOCURE on TH-cam thought me that is all about patients and the right medication, May God continue to bless You sir for the permanent HPV cure I received after taking your herbs
They keep us ill because thats where the money is,simple!!!
@thisandthat808 - See if you can find a copy of the book "Plum Island". That will explain it and sadly it's worse than you think. A bioweapon.
38 yrs of TBI! Great info! Thanku!
I have been sick for over a year and I had been tested for Lyme disease 3 different times and the test results were all negative, until my knee started to swell a month ago. they pulled the fluid out of my knee and low and behold it was Lyme disease. Hopefully untreated for a year isn't too long for me with type 1 diabetes. I've been on the antibiotics for a week now and don't see any improvements yet, in fact I feel worse. wish me luck!
❤ Very normal to feel worse at the beginning when you start antibiotics, it is called a Herxheimer reaction and you can look it up online.
It's good that you feel worse when taking any effective Lyme treatment. The dying borrelia are toxic till they are removed from the body. Drink lots.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉
I'd give bee venom therapy a try, it's cheap and easy and seems to be improving for most with Lyme. I'm in Saskatchewan Canada, also have type 1 diabetes and chronic Lyme. It made me suicidal and still have nuero issues but bee venom definitely improved me
Look up high dose intravenous vitamin c.
I'm amazed. A calm, intelligent discussion about a disease with no histrionic.
Did you know it was created in a military lab. Yup, just another bio weapon released ages ago .
This is false, lymes was found in a 15,000 year old frozen ice man. Stop the conspiracies....
The MSM will not cover that fact
But you might ruin the flimsy narrative they’ve worked tirelessly for in order to cover up the real truth. A logical and reasonable person might notice that the first mainland town that this “disease” infected was geographically located right next to Plum Island Animal Disease Center. However, common sense doesn’t live here on Earth anymore. We peons must believe whatever our corporate overlords tell us, otherwise we might not get any of the scraps they throw us.
Explain + give links?
@@adityaprabhu6 there used to be really great TH-cam videos about it years ago but I’m sure they’ve all been taken down during the censorship campaigns in recent years. Do some research into Operation Paperclip, Erich Traub and Plum Island. Govts have been experimenting with bioweapons far longer than most people realize.
I've been battling chronic Lyme disease for the past 15 years, and it has completely turned my life upside down. To make matters worse, no doctors could diagnose it properly, and hardly anyone believes I'm truly sick, except for my close family members. It's a truly devastating disease.
There are scientists out there working so hard to bring awareness to this disease- only to be criticized and ridiculed when the evidence is right before our eyes
I had Lyme for almost 5 years before getting treatment…treatment lasted 3 years….i have lasting effects from it. I have arthritis in my joints that will never go away, I have a lot of digestive issues due to getting alpha gal as well…so here we are..
I wonder if having the MTHFR gene mutation plays a part in chronic Lyme. Many, including myself have the mutation, and remain ill.
Thank you so much! I have suffered from chronic lyme after being diagnosed 2 years after symptoms started. I have been on about 30 antibiotics and I'm still not better...
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo.
You trust everyone and dats stupid.
We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
That is not fun and so frustrating. Do you by chance have a history of trauma or ongoing stress being dysregulated? Untreated trauma/stress symptoms can contribute to chronic issues and if dealt with, the body can better deal with what has become a chronic health issue. Doctors almost never ask about stress /trauma histories. I have had many chronic health issues, most of them linked back to growing up in a chronically stressful environment. As I dealt with the trauma/stress symptoms by addressing the chronic dysregulation in my nervous system, many of the chronic health issues eased.
@@annemurphy8074 I was going through the care and death of my mother when I was first diagnosed. I'm sure that didn't help the situation any...
You need to go see an infectious disease doctor. Also Marty Ross, MD he is helpful on TH-cam and there's a few others but I can't remember their names
There is no known cure for spirochetal disease. I've got the best minds working on it. There are palliatives that work for some but not others. Here's what I posted above in the main comments:
More lying Id eye Otts covering for a Pahn Day Mik that is worse that anything anyone is currently being phear phorned into reacting to. It was known in the year 1900 that antibiotics NEVER got rid of ANY disease and it was confirmed by Lida Mattman (now deceased) that the poisons merely create Cell Wall Deficient forms (8 different morphologies) so that with syphilis, lyme, leptospirosis, TB, or leprosy the SYMPTOMS *MAY* go away but the causative agent NEVER DID.
Ever.
You all are living the aftermath of that LIE.
Mel Thornberg (now deceased) said that at best doxycycline *MIGHT* afford some protection from prion formation because it transforms the cell wall competent form to any of the 8 cell wall deficient form and in SOME people the SYMPTOMS might go away but the beast can re-assemble from any of the 8 different morphologies to give what is falsely called a re-currence or re-infection or re-activation. All that antibiotics do is turn people into asymptomatic CARRIERS which is how this got spread worldwide without even requiring ticks from Plum Island. Europe is finally acknowledging that it is spreadable by ALL HUMAN BODY FLUIDS.
The use of the word: INFLAMMATION shows that whoever uses it is either at total fuul or purposely spreading disinformation. Inflammation happens under two conditions: tissue injury (which always comes with the introduction of a pathogen as well) and INFECTION.
Inflammation is NOT a separate undefined disease or condition or syndrome. Inflammation is an IMMUNE RESPONSE even if it is to the stealth organisms created by Id eye Otts that give antibiotics to something that has NO KNOWN WAY OF DEE STROYING IT.
THE REASON IT SHOWS UP IN THE BRAIN (we have Dr. Alan MacDonald to thank for this) is that filarial worms that came in from a tickbite transport the spirochetes inside of it through the cerebral spinal fluid to offload the migrant workers like a coyote emptying a schoolbus once it crosses the border. That is why parasite elimination is essential to mitigating neuroborelliosis.
"Markers" and "Genes" and any other nonsense to cover for this out of control threat to hu-manity are purposeful disinformation to keep you from looking at the Millie Tarry We Upon that got away from them and with which they cannot recall despite the use of Glyphosate (patented in 2010 as an 'antibiotic') or any other HUMAN DRUG.
There's your "Top Story" that will never be covered by media or medisin because they are all in on the millie tarry coverup.
Thank you for sharing this awareness. Too many people continue to suffer and their condition which is often extreme, ignored or seen as fake.
According to "the quiet epidemic" documentary, two bio markers (proteins 31 and 34) in the standard tests approved by the federal agencies to detect Lyme disease were deliberately omitted. Was this ever rectified??
No they took them out because of the vaccine in the 90s. I guess if you had the vaccine you would pop positive on those bands si they didn’t want false positives if later I guess they got sick from tick bite and everyone got considered because of a few that took the vaccine doesn’t make any sense they made the test even less sensitive there is so much wrong with Lyme it’s to much I wouldn’t be surprised if this was gain of function research from syphills.
Follow the money. Insurance and pharma own CDC and government. It's about profit.
Lymes disease hurts your whole body bad, you get a bad fever, nausea and major fatigue and headache! I had it for about 4 mths before I went in, due to my work schedule. So I was pretty sick by the time I finally got to the Dr. It took another 2 months before I could go back to work again, as I ended up on a second dose of antibiotics. I have had problems ever since then, with aching joints and headaches.2006-2023 I know it will be there forever so I just accept it and live life the best I can.
No you don't need to accept it. Try lamotium. Oregano oil. Saunas help with detoxification as well.
FINALLY they're taking chronic Lyme seriously
@jerryhoward6937 Diz iz political yah an ya gots ta close da borders yah. Diz shitz crazy yo.
You trust everyone and dats stupid.
We wuz in your hood an days surround me ands tooks mah wallet and I hadda walk alls dah way home, and nobody help me tah get there!
Don’t hold your breath. I’ll believe it when I see it.
Doctors who take Lyme seriously are rare, certainly in Canada. Our College of Physicians and Surgeons need to be sued for billions. Use the money to research a cure for chronic Lyme.
@@garsonprice3441what province are you in?
@@Bigshoots11
New Brunswick. The province with no medical care.
My 92 year old grandma Contracted Lyme disease. The doctors thought it was a Flu and didn't catch it in time, Sometime later i think like a year or 2 it ended up making its way to the spinal cord, Left her paralyzed in 1 leg and unable to walk. She was still mentally there and happy to be alive! She ended up passing away with no control of that leg.
So sorry to hear that. God bless you both.
DRETIKOCURE assured me of getting healed and surprisingly after 21days of taking the Roots medication I was tested for HSV Negative, Thanks Dr Etiko I will keep letting the world know about your TH-cam channel🎉🎉🎉
biofilm, certain enzymes could have helped with antimicrobials etc
Terrible; I’m so sorry.
I had Lyme disease when I was around 6, now I’m much older. But overall damage that it caused me were significant, my growth was stunted which mean I would have a height of 5,3 while having full genetics of a 6 foot tall family gene. This caused me to take medical growth hormone prescribed daily until at the age of 15. I maxed out at 5,9 luckily. Though one of the worst things ever was I had permanent damage within my intestines, which made me have to go on celiac diet until it hopefully adjusts. Probably the worst experience was when they were testing me as I remember, putting a needle atleast 6 times into my arm. The fluid was murky and brown. Yes for your information, I got it from Texas when I was visiting close relatives. Symptoms like heart burn, extreme aching, fever, and a big rash where the bite was.
I had a tick bite and the doctor gave me a 2 week course of doxicyclene. Unfortunately neither the doctor nor the pharmacist told me that you must not take any milk with it because milk renders it ineffective. I got a very nasty rash on my hip and quite bad joint pain. I didn't fancy trying the doctor again so I managed to get hold of a 5 week course of doxicyclene and took it 2 hours after a meal and 2 hours before anything else, after 4 weeks my hip was still sore but after 5 weeks the problems had gone. I was lucky, if I had left it to the doctors I could now be a cripple or worse. But I think one reason people have such varied results with the antibiotics is that the doxicyclene is very sensitive to what you have in your stomach, other things affect it too, for example iron.
I'm on my second round of doxycycline also, because they did not tell me how to take it properly the first time. It took 11 years to get diagnosed. 5 years later, still having terrible nerve and joint symptoms. I hope this time works for both of us!
i am hitting my 10th day of Doxy and was given an extra 14 days because of lingering symptoms. no one ever mentioned the proper way to take it, regarding empty stomach, avoiding dairy, etc. frustrating
Doxycycline is the only one they use for central sensitisation to
I’m terrified of Lyme disease.
Lyme debilitated my life only recent am I living a halfway normal life. Years ago was told high protein in blood and urine. This is interesting. NBC please don't stop talking about this!!!!!
We need change.
biofilm
Treating Lyme as a long term disease was not a medical problem but one across insurers. Let’s see them fight this correlation. Let me guess: you need more than 79 people for it to be statistically significant ….
Ok so I had zero symptoms initially, was given an antibiotic...12 years later...I suddenly developed symptoms. I was told this was normal that it goes "dormant" and can resurface many yrs later, with diff. Symptoms. Food intolerances especially to starched & yeast was the only symptoms I experienced those 12 yrs later...and the antibiotic didn't do anything for it. So I was just old to avoid those foods. This broadcast did a very poor job of explaining that.
or maybe you got infected again.
Nooo
It really goes dormant for years until a trigger reactivated it. My trigger was mononucleosis
Sounds like a freakin dream compared to many😂 be thankful that’s all you got bro, be well 🙏🏽
What other symptoms you have?
How do I get this new information for my daughter in law
#MrEbose has herbal products that can help treat Lyme disease
About 1/3 of ticks (at least at my location) carries lyme. Always carry a tick remover. There are versions shaped as creditcards that fit in a wallet. Highly recommended!
Are lyme ticks found only on the east coast?
@@Xylophone8 i am in the Netherlands, that's the number here. Varies from place to place
@@fatvegan4621 i think they are everywhere.
The female deer tick is the one that causes the disease.
@@jak3589 , here in the northeast US, deer ticks ( which feed on mice in their tiny nymph stage) are the primary Lyme carrier, but other tick species can sometimes carry Lyme. Additional, less common tickborne diseases found here are erlichiosis, babesiosis, anaplasmosis, tularemia and rocky mountain spotted fever. Climate change is causing migration and spreading of species and diseases that previously weren't found here. The longhorn tick is a recent arrival to the region and can cause a severe lifelong allergy to eating meat. Rodents in particular are a major vector for many formerly "exotic" diseases. A man died of hantavirus in Long Island New York a few years ago after sweeping out his garage where evidently mice had been nesting. Hantavirus is a usually fatal respiratory disease (there's no treatment or cure) transmitted in dried mouse urine and which is endemic to the Southwest, especially after El Nino events where the desert blooms and the rodents population swells, but it had never before been found in the northeast.....there is bubonic plague in the west and southwest as well, carried by prairie dogs and other rodents, and I have to wonder how long it'll be before the plague spreads to here.....
Prosím přidejte nastavení českých titulků....
Suffered for years with undiagnosed symptoms from a tick that was on back of knee all night.
Undiagnosed and misdiagnosed for over 11 years... Even after being aggressively treated, some symptoms remain. I am glad to see this video.
My old pharmacist has Lyme disease..got a tick bite in the middle of his back from the deer camp woods.... been all over the country for treatment, no cure...over 20 yrs ago since he was diagnosed with Lyme disease...
biofilm and it can change form spirochete to something or other
@@Whyaretaxespayingforcorr-cc8sr spirochete to l shaped persister bacteria.
Hydromycin a clinical trail in Australia last may this may 2025 clinical trial UMASS ,mass general,and some were in Maryland
They dont know still???
So thankful I knew what I was looking at when I was younger when I got the rash. Got treated quickly and never had any problems. But I spend a lot of time outdoors and I warn other people all the time.
@jerryhoward6937 Why would I want a pay cut?
@@saywhatnow57 , you're replying to a spam-bot. Just report it to TH-cam.
I walk my three dogs on local trails every day. I tuck my pants legs into my socks and spray the socks and sneakers with bug repellent (strong DEET formulas will work but permethrin, made from marigolds, is better; it paralyzes ticks and is safe for application on digs and humans). My dogs have light colored fur and white feet and so even tiny ticks tend to be easily visible on them. I'll typically find two or three ticks on each dog when we're out walking (on one occasion it was a dozen plus ticks on each dog and on myself). When we get home,, I strip off my clothes and put them in the dryer while I check myself for hitchhikers. The dogs all get chewable flea and tick meds but those only work on ticks after the ticks start to feed, and since one of our dogs likes to nap on our laps, transfer of a tick from dog to human is a possibility. Ticks love our moist sweaty areas, and I plucked a freshly attached tick from my sensitive nether regions just last week, after the dog and I napped together.
She snickered at "Tick Pics" 😂
thank you nbc. raise awarness please to this evil disease many are suffering from 😭
It's been pretty obvious for a while now that chronic lyme is an autoimmune issue. Good to see them further this and r/o active infection. BUT...what is going on with the immune system? Sounds like we are in the second inning for figuring this one out. We have a ton of immune work to do in general for a lot of these emerging autoimmune issues..
From what I've read, researchers say Lyme could trigger and autoimmune response but others are less committed to that.
what I posted above to diatribe on the autoimmune aspect:
More lying Id eye Otts covering for a Pahn Day Mik that is worse that anything anyone is currently being phear phorned into reacting to. It was known in the year 1900 that antibiotics NEVER got rid of ANY disease and it was confirmed by Lida Mattman (now deceased) that the poisons merely create Cell Wall Deficient forms (8 different morphologies) so that with syphilis, lyme, leptospirosis, TB, or leprosy the SYMPTOMS *MAY* go away but the causative agent NEVER DID.
Ever.
You all are living the aftermath of that LIE.
Mel Thornberg (now deceased) said that at best doxycycline *MIGHT* afford some protection from prion formation because it transforms the cell wall competent form to any of the 8 cell wall deficient form and in SOME people the SYMPTOMS might go away but the beast can re-assemble from any of the 8 different morphologies to give what is falsely called a re-currence or re-infection or re-activation. All that antibiotics do is turn people into asymptomatic CARRIERS which is how this got spread worldwide without even requiring ticks from Plum Island. Europe is finally acknowledging that it is spreadable by ALL HUMAN BODY FLUIDS.
The use of the word: INFLAMMATION shows that whoever uses it is either at total fuul or purposely spreading disinformation. Inflammation happens under two conditions: tissue injury (which always comes with the introduction of a pathogen as well) and INFECTION.
Inflammation is NOT a separate undefined disease or condition or syndrome. Inflammation is an IMMUNE RESPONSE even if it is to the stealth organisms created by Id eye Otts that give antibiotics to something that has NO KNOWN WAY OF DEE STROYING IT.
THE REASON IT SHOWS UP IN THE BRAIN (we have Dr. Alan MacDonald to thank for this) is that filarial worms that came in from a tickbite transport the spirochetes inside of it through the cerebral spinal fluid to offload the migrant workers like a coyote emptying a schoolbus once it crosses the border. That is why parasite elimination is essential to mitigating neuroborelliosis.
"Markers" and "Genes" and any other nonsense to cover for this out of control threat to hu-manity are purposeful disinformation to keep you from looking at the Millie Tarry We Upon that got away from them and with which they cannot recall despite the use of Glyphosate (patented in 2010 as an 'antibiotic') or any other HUMAN DRUG.
There's your "Top Story" that will never be covered by media or medisin because they are all in on the millie tarry coverup.
The persistent infection causes persistent immune activation and autoimmunity. The root cause must be removed.
It's usually trigger autoimmun response.. Because it's a chronic infection
My immune system needed to be boosted, not suppressed like it would be if this was autoimmune. I have been tested for about 20 autoimmune diseases now, the only test that ever came up positive as a differential diagnosis was my lyme Western Blot. Sometimes an inflammatory marker here and there is high. My immunoglobulins are low, so I started IG replacement therapy this year.
I had to be rushed to hospital, fever 106, anaplasmosis from tick bite, never even heard if it - same treatment doxycycline
As an overweight female of course it's all in my head and not real. Just lose weight and take antidepressants or anxiety meds. I just want to be able to walk more than 100 feet without pain and cramps. Five years ago I moved most of our house and ran steps frequently until Lyme happened.
No paper link?
If that inmune marker is there, is because the bacteria is pretty persistent.. is obvious is still lingeing in th ebody.. the infection
There are 8 different cell wall deficient morphological forms created by the insane use of antibiotics. ALL are persistent and ALL can re-assemble into the cell wall competent form.
@@vaccinefraud5570 what is cell wall deficient morphological forms?
My ancestors in Bavaria survived the plague, so now I'm more susceptible to inflammatory incidents. Funny how that worked out.
I've only known one person that has Lyme's disease & when he had seizure from it. insane!😮
Lyme not lymes
Not only do l suffer from Chronaic 🎉Lymes after an initial outbreak in 1997, but l developed chronic symptoms following Covid. I have Rheumatoid Arthritis and there are alot of autoimmune disorders in my family. Possibly those of us who develop chronic Lymes complications are already suffering undiagnosed autoimmune disease?
what antibiotic? is normally used for the Borrelia burgdorferi?
I was a deerstalker for 20 years in Oxfordshire. I seem to have escaped Lyme, despite having occasional tick bites. I read that the best knowledge on this is in Germany as they are keen stalkers and recognise the problem.
Living in Germany with Lyme disease for over a decade. It's a myth, that German doctors know this. In fact, German doctors are about the worse one can have. They are lazy, incompetent and full of prejudice. They truly know how to add insult to injury. And with me it even was certain, that it was Lyme disease, due to ACA on my skin and blood tests.
There is a tiny minority of Lyme literate doctors here, most of which you have to pay out of your own pocket. Yet, even they have no clue on how to cure my late stage Lyme disease, after I relapsed after a move. I'm basically left to rot. Don't even go to doctors anymore, cause I cannot handle anymore heart breaking meanness. May God revenge me!
How can we participate in research????????
Why don't they actually link the study? Over the last couple years that have lost credibility over their ability to interpret….
So, auto-immune reaction of the central nervous system.
Some have successfully treated it with accupuncture - triicking the signals and allowing the inflamed part to recover.
It's been said that Lyme disease was developed by the U.S. Govt. in a lab in Lyme Conn. Any Feedback?
Really? Don't you think there's enough wacky conspiracy theories circulating in the media? Jesus Christ Almighty!
Yes that is completely true the government even admitted to it of course it wasn't publicized very widely.
Thanks for the need to know!!!!strong reporting;
🤣"We are on a roll with the early morning rash and the tic pictures. Thanks for hanging in there with us."🤣
I woke up in my bed and found a tick attached to my arm ( i have a dog). I'm terrified, I'm from a 3rd world country and life just started to look good for me.
Thanks so much *MR OBALAR* on TH-cam for curing me from Herpes, keep saving lives.❤😊❤
It's good that have a sorta cure fore lime disease and have a treatment I know alot of people suffer from this disease
Except for decades the government for infectious disease doctors to deny chronic Lyme, make testing and treatment in absence of classic rash difficult and often past the window to be most effective.
@@sillygirl3284 i went to see specialist after all symptoms were gone.she told me she didnt think i had lymes musta been glandular fever,im like ffs i had the bullseye rash and a lot of the symptoms on line .shes like dont believe everything you read online only use n.i.c.e site which is the uk goverment site thats all factual information on there.i came away from there having lost all faith in doctors and specialist govt trained .id now rather follow a chiropracrer on yt to help with my health lol
Oh, that is interesting (not to dismiss the tragedies). IgG4 is alleged to be elevated in patients with Lyme's disease. IgG4 is a tolerance antibody to reduce severe reactions. But it can serve to protect pathogens, too, which get the green light to create havoc. So when you mentioned an entire 2 months of antibiotic treatment can sometimes be helpful, the IgG4 tolerance hypothesis is supported. Antigen tolerance may be the mystery cause. IgG4 antibody is created for antigens when the body fluids contain elevated "allergy interleukins" that stem from an allergic reaction. Interesting. At the same time, being bitten by a lone star tick can create mammalian meat allergy. This is often confused with Lyme's disease, but a mere change in a low allergen, sometimes low salicylate, plant-based diet can profoundly help.