The Mysterious Chronic Lyme Disease Nightmare: Why It’s So Hard to Detect and Treat | |
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Uncle Gintel
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Anonymous Coward User ID: 74387734 United States 06/15/2021 10:54 AM Report Abusive Post Report Copyright Violation | My living nightmare started in February of 2019. That’s when my 2-year struggle with Lyme disease began. I never even saw the tiny, poppy-seed-sized tick that got me. And I never saw a bullseye rash. It was six months before I got a diagnosis. By then, the microscopic spirochetes that cause the illness had worked their way into my joints. A simple two-week course of antibiotics would not fix my problem. I didn’t know it then, but I had entered a struggle where constant joint pain, crushing insomnia, and a never-ending flu-like brain fog would haunt my every step. Quoting: Coastie Patriot Today, I’m older and a little wiser. After countless prescriptions and doctors’ appointments, and interviewing several of the top Lyme researchers in the field, I know a lot more about Lyme disease and ticks than I ever wanted to. I’m also largely symptom free. But it didn’t come easy. The good news for you is, I can pass those years of knowledge on to you in a few minutes, so you can arm yourself against this damaging disease. The Trouble With Detecting Lyme Disease The real problem with Lyme isn’t that it’s hard to cure. It’s not — if you know you have it in the first month. In that case, a quick course of the right antibiotics is enough to cure you permanently. Or at least until you get another tick bite. The problem is what happens if you don’t catch it in time. “We typically see manifestations of chronic symptoms occurring when there’s any sort of delay in diagnosis or treatment,” says Dr. Shannon Delaney, Lyme researcher at Colombia University. Those chronic symptoms show up in what’s called post treatment Lyme disease syndrome (PTLDS). They happen in about 20% to 30% of Lyme sufferers, making Lyme the painful elephant in the outdoor-lover’s living room. Many victims turn to Lyme specialists or “Lyme literate doctors.” Others suffer in silence. Still others may not even know they have it. There’s also no test that proves you’re cured. So, if you get the “cure” but you’re still sick, what then? The answer is a deep, wide trail of suffering for millions much more in article and a very good read [link to www.outdoorlife.com (secure)] I studied Lyme disease years ago. The problem is insurance companies will only pay for a two week course antibiotics. Most people have a delayed diagnosis. The gold standard is a two month course of antibiotics. Research like your life depends on it. |
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Old Alpinist
User ID: 80128077 United States 06/15/2021 11:09 AM Report Abusive Post Report Copyright Violation | Girlfriend grew up eastern shore MD. Has been dealing with it 20 years now. Incredible difficult. Have to go through specialist by out of pocket expenses to treat. Some meds are covered. OP PM me if have any questions "assuming to know is a disease of the mind. Recognize that you are sick" Toa de Ching |
Icey
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Uncle Gintel
User ID: 77733820 United States 06/15/2021 12:29 PM Report Abusive Post Report Copyright Violation | I will say this one more time bc somehow you missed the answer to your fucking question. The Plum Island level 4 bioweapons research lab is located just offshore from Lyme Connecticut. You can look out and see it. Lyme disease is named after Lyme Connecticut. I grew up there, everyone kinda knew something drifted across the water. The facility was shut down just a few years ago. The kept it offshore bc many off the pathogens are so bad it is illegal to bring them onto the US mainland. Last Edited by Uncle Gintel on 06/15/2021 12:31 PM |
Offender
User ID: 78384741 United States 06/15/2021 12:57 PM Report Abusive Post Report Copyright Violation | Hey OP,I have late stage lyme and I have found a cure and is working miracles on me. 1/4 teaspoon Borax in one liter of water with 2 cap fulls of food grade H2O2 3.5%.I use one scoop of gatorade powder to hide the taste.Taken 5 days a week with 2 days off.Drink plenty of water.It works!!! Doses are smaller for woman and they can only take an 1/8 teaspoon Borax daily.This also cures lupus,fibromyalgia,MS,Chronic fatigue syndrome,and all forms of arthritis and many other things. Good luck to you!!! CHEERS |
Anonymous Coward User ID: 80026877 United Kingdom 06/15/2021 01:21 PM Report Abusive Post Report Copyright Violation | Hey OP,I have late stage lyme and I have found a cure and is working miracles on me. Quoting: Offender 1/4 teaspoon Borax in one liter of water with 2 cap fulls of food grade H2O2 3.5%.I use one scoop of gatorade powder to hide the taste.Taken 5 days a week with 2 days off.Drink plenty of water.It works!!! Doses are smaller for woman and they can only take an 1/8 teaspoon Borax daily.This also cures lupus,fibromyalgia,MS,Chronic fatigue syndrome,and all forms of arthritis and many other things. Good luck to you!!! CHEERS Thank you I have suffered chronic late Lyme for 12+ years. In recent weeks this method has come to me 3 times from 3 different locations... I had already brought the borax and was still in considering it mode.... I have my 3 time rule.. see it 3 times it's a sign .. I will be starting tomorrow when the H2O2 gets here... I will report back any results ... |
Anonymous Coward User ID: 78825402 United States 06/15/2021 03:29 PM Report Abusive Post Report Copyright Violation | My living nightmare started in February of 2019. That’s when my 2-year struggle with Lyme disease began. I never even saw the tiny, poppy-seed-sized tick that got me. And I never saw a bullseye rash. It was six months before I got a diagnosis. By then, the microscopic spirochetes that cause the illness had worked their way into my joints. A simple two-week course of antibiotics would not fix my problem. I didn’t know it then, but I had entered a struggle where constant joint pain, crushing insomnia, and a never-ending flu-like brain fog would haunt my every step. Quoting: Coastie Patriot Today, I’m older and a little wiser. After countless prescriptions and doctors’ appointments, and interviewing several of the top Lyme researchers in the field, I know a lot more about Lyme disease and ticks than I ever wanted to. I’m also largely symptom free. But it didn’t come easy. The good news for you is, I can pass those years of knowledge on to you in a few minutes, so you can arm yourself against this damaging disease. The Trouble With Detecting Lyme Disease The real problem with Lyme isn’t that it’s hard to cure. It’s not — if you know you have it in the first month. In that case, a quick course of the right antibiotics is enough to cure you permanently. Or at least until you get another tick bite. The problem is what happens if you don’t catch it in time. “We typically see manifestations of chronic symptoms occurring when there’s any sort of delay in diagnosis or treatment,” says Dr. Shannon Delaney, Lyme researcher at Colombia University. Those chronic symptoms show up in what’s called post treatment Lyme disease syndrome (PTLDS). They happen in about 20% to 30% of Lyme sufferers, making Lyme the painful elephant in the outdoor-lover’s living room. Many victims turn to Lyme specialists or “Lyme literate doctors.” Others suffer in silence. Still others may not even know they have it. There’s also no test that proves you’re cured. So, if you get the “cure” but you’re still sick, what then? The answer is a deep, wide trail of suffering for millions much more in article and a very good read [link to www.outdoorlife.com (secure)] i am the op and i dont want to see unappreciative and at one point it was thought i had lyme, I very well may as i hunt and fish and forage alot. I knew going in people would think this as most of my lyme posts get this. this is an article from the OUTDOOR LIFE hunting and fishing magazine.didnt want to mislead any one I know how horrible it is an i also knew year ago when i was stationed in BOSTON and people told me about PLUM island and seeing deer swim from plum to LYME. one of the dr here locally diagnoses everyone with it .. I didnt trust that so i went to another dr in aanother town and her schtick is mold, she mentored the other doctor and now the old doc is diagnosing a friend with lyme and mold. I dont deny it exist and think is a weapon fm plum island. just some doctors have figure out a way to make alot o money of people too again i dint want to mislead anyone .. sorry for anyone that has it and being an outdoorsman always paranoid aboit those super small bastads i cant see. they can lay dormant for 18 years and feel virbation or catch a hint of co2 and reactivate HATE EM!!! |
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Treerat
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Anonymous Coward User ID: 81605431 United States 10/01/2022 02:20 PM Report Abusive Post Report Copyright Violation | You have to do an "antibiotic challenge" for five days to two weeks prior to the test to kill off some to reactivate immune recognition and must use the IGenex test to get results. Many of you probably also have bartonella. If you have foot fevers, restless leg syndrome, or ever get very sore tender feet upon waking, or sudden out of the blue bouts of despair or rage, bartonella is your culprit though many with less severe bartonella infection may not get these manifestations. The #1 thing that helped me the most was glutathione IV pushes (I am MTHFR genetic mutant prob like many of you). Also Byron White Formulas A-Bart tincture helped me a great deal, now available for purchase online from Dr. Daniels store. |
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Anonymous Coward User ID: 78178088 United States 10/01/2022 02:30 PM Report Abusive Post Report Copyright Violation | My living nightmare started in February of 2019. That’s when my 2-year struggle with Lyme disease began. I never even saw the tiny, poppy-seed-sized tick that got me. And I never saw a bullseye rash. It was six months before I got a diagnosis. By then, the microscopic spirochetes that cause the illness had worked their way into my joints. A simple two-week course of antibiotics would not fix my problem. I didn’t know it then, but I had entered a struggle where constant joint pain, crushing insomnia, and a never-ending flu-like brain fog would haunt my every step. Quoting: Coastie Patriot the organisms were DESIGNED to be super tiny so as to be VERY difficult to diagnose. the scum doctors are coached to NOT diagnose lyme disease. the doctors keep it all a secret. one doctor DID diagnose it...in our DOG. he retired right after that, or something happened to him? anyways. like the spike protein, they actually have several variants. that's why they are always talking about variants, they created variants of their own bioweapons. it's possible there could be variants of lyme, I don't pretend to know. but I knew a whole shitload of people with Lyme disease, it makes them go crazy too fasting is the ONLY cure for it. |
Anonymous Coward User ID: 78178088 United States 10/01/2022 02:34 PM Report Abusive Post Report Copyright Violation | I went to the doctor about lyme, told them about my mom,dog being diagnoses, my grandma had lyme symptoms, my aunt, cousin. so first time I went, it was this cute doctor, and then this other cute doctor, then they brought in the bull dyke, she WREAKED of being some sort of FBI doctor or some shit, to cover up the Lyme, so I went to the doctor and the treatment was SO strange. Like they just treated me like...I was a terrorist. highly suspicious,they refused me treatment, or anti biotics, then they squirted water in my ears and charged me $500, then froze my credit score for not paying, after telling me it was free, so then I become homeless because i have no credit score, every single apartment complex literally laughed in my face, because they are all demons who love being in on it. If Putin melted their faces off I would shit on their scorched faces. |
Treerat
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