Ok . I read a few pages now and saw a few videos , what a nasty mess , the mean bugs are not really visible and the sickness is too much for a human. Wtf ?
Liar Liar Pants on Fire! 36 years to get a diagnosis and then only an acute positive, but my symptoms are of Late Stage Lyme – The ELISA and the Western Blot came back false neg. The test measures immunity response- the disease affects your immunity so I guess mine didnt respond enough. I had to have my blood sent to a specialty lab to get my diagnosis – insurance wouldn't pay. I had encephalitis, meningitis, trigeminal neuralgia, bells palsy, paralysis, agonizing pain and inflammation, vasculitis, auditory hallucinations (musical) and dejavue for 3-4 years- blindness, deafness, damage to my neck (6 bulging disks and stenosis due to severe inflammation), dizzyness, severe exhaustion, violent shaking episodes, seizures, muscle issues, uncontrolled movements, fainting episodes, flu-like illness, double vision, severe night sweats, confusion, inability to speak or communicate, Inability to walk, struggling to breathe, memory loss, dyslexia, and well way to many to mention with little to NO MEDICAL care as my CBC was normal even though some of these others did show up on a CT and MRI scans. The worst of my symptoms came within a 4-year period that was like a nightmare from hell that would not end. I was misdiagnosed as mentally ill, called a liar, laughed at by drs, and was accused of making up the story for attention. I was finally diagnosed in 2014. I've been on antibiotics for over a year and I'm just now beginning to feel half way normal. My immunity was tested and found to be severely affected. My CBC still read normal and yet my CD-57- which is your immunity was less than 0 on many of the tiers. I have been told that I have permanent damage in muscles, joints and in my brain because I didn't get care quick enough. They also found that I had two copies of a genetic mutation MTHFR which also affected my agility to heal. This illness is a political issue folks. They don't want to acknowledge the severity because then they'd have to give us all treatment – hundreds and thousands of us and the insurance companies don't want to pay. With 300,000+ cases a year- statistically your at risk or someone in your family. Is this how you want to be treated? Other infections, including sinus infections and even acne are treated individually on a case by case basis, but this one obeys the 4 week and your all better rule? That doesn't even make common sense- think about it. Look it up- it can fool and affect your immune system and can change into a cyst form and resist treatment. Its torture to not help some one with this disease and yet Drs have lost their licenses for treating people with Lyme longer than they say they can. We have to change this! Help us change it! – I've been sick with this since I was 9 years old. Just now got an answer- last year- I'm now 45. I still become emotional trying to talk about my ordeal and I doubt I'll ever be able to trust drs again. Lyme Disease patients are human beings, too. More info http://www.ILADS.org. #LymeIsReal#LymeIsHell#Healthcare4thesick
Halperin is a liar. They all knew what really caused AIDS in 1981. Spirochetal disease. And they knew the immune suppressed did not make antibodies against infections. He covers for the suffering of Autism kids, MS, ALS, Alzheimers, Lupus, Parkinson's, Diabetes, Crohn's, Celiac, MD, ALD, ME, CFS, PTSD, ADHD, Kawasaki's, Down's, Arthritis', and hundreds of other lies they don't want you American's to be able to treat the REAL CAUSE. Because they gave it to you for decades in all vaccines.
I have had Chronic Lyme Disease for over 8 years. I was only diagnosed 3 years ago. I have been on and off Antibiotics for 3 years. I am convinced that the antibiotics we have at our disposal are not sufficient to kill the Lyme. Unfortunately, they now know that these bacteria are able to form biofilms to hide under while the antibiotic is in the body. Once it is removed, the bacteria come back out and begin to multiply and take over your body once again. Dr Horowitz is one of the best known doctors that work on Lyme Disease (LLMD). He is very respected for being able to stand up against the government cronies like the CDC and the IDSA who continually try to say that Chronic Lyme does not exist and will go away with just 4-6 weeks of Doxycycline. 1,000s and 1,000s of people have proven that this is not the case – but in their egotistical, stubborn ways, they will not listen to actual patients but just keep reading their books. OUT OF TOUCH and they should be fired! I am moving on to try concentrated herbal remedies which are helping a large number of Chronic Lyme patients.
Sorry but Lyme is not reduced to certain states, it's everywhere! It's the damn crappy out dated testing they're still using! It's been 25 years since I was bitten by a tick on my head, and been suffering ever since, because doctors didn't want to look into Lyme, this time my neuro did one on me, and my 23 and 41 came up positive on my Western Blot. I've been very sick, and still waiting to see an LLMD, because Medicaid doesn't cover these kind of doctors! I'm on Medicaid, because I'm too sick to work a regular job. Really something needs to be done, people are getting sick and some even die from the co infections of the tick, enough is enough!
This show did nothing for the education and awareness of chronic lyme disease. What happened to "first do no harm"? I am not an iv antibiotics treatment advocate as I do not react well yo them, but herbally treating by buhners protocol.
Ok . I read a few pages now and saw a few videos , what a nasty mess , the mean bugs are not really visible and the sickness is too much for a human. Wtf ?
Liar Liar Pants on Fire! 36 years to get a diagnosis and then only an acute positive, but my symptoms are of Late Stage Lyme – The ELISA and the Western Blot came back false neg. The test measures immunity response- the disease affects your immunity so I guess mine didnt respond enough. I had to have my blood sent to a specialty lab to get my diagnosis – insurance wouldn't pay. I had encephalitis, meningitis, trigeminal neuralgia, bells palsy, paralysis, agonizing pain and inflammation, vasculitis, auditory hallucinations (musical) and dejavue for 3-4 years- blindness, deafness, damage to my neck (6 bulging disks and stenosis due to severe inflammation), dizzyness, severe exhaustion, violent shaking episodes, seizures, muscle issues, uncontrolled movements, fainting episodes, flu-like illness, double vision, severe night sweats, confusion, inability to speak or communicate, Inability to walk, struggling to breathe, memory loss, dyslexia, and well way to many to mention with little to NO MEDICAL care as my CBC was normal even though some of these others did show up on a CT and MRI scans. The worst of my symptoms came within a 4-year period that was like a nightmare from hell that would not end. I was misdiagnosed as mentally ill, called a liar, laughed at by drs, and was accused of making up the story for attention. I was finally diagnosed in 2014. I've been on antibiotics for over a year and I'm just now beginning to feel half way normal. My immunity was tested and found to be severely affected. My CBC still read normal and yet my CD-57- which is your immunity was less than 0 on many of the tiers. I have been told that I have permanent damage in muscles, joints and in my brain because I didn't get care quick enough. They also found that I had two copies of a genetic mutation MTHFR which also affected my agility to heal. This illness is a political issue folks. They don't want to acknowledge the severity because then they'd have to give us all treatment – hundreds and thousands of us and the insurance companies don't want to pay. With 300,000+ cases a year- statistically your at risk or someone in your family. Is this how you want to be treated? Other infections, including sinus infections and even acne are treated individually on a case by case basis, but this one obeys the 4 week and your all better rule? That doesn't even make common sense- think about it. Look it up- it can fool and affect your immune system and can change into a cyst form and resist treatment. Its torture to not help some one with this disease and yet Drs have lost their licenses for treating people with Lyme longer than they say they can. We have to change this! Help us change it! – I've been sick with this since I was 9 years old. Just now got an answer- last year- I'm now 45. I still become emotional trying to talk about my ordeal and I doubt I'll ever be able to trust drs again. Lyme Disease patients are human beings, too. More info http://www.ILADS.org. #LymeIsReal #LymeIsHell #Healthcare4thesick
Halperin is a liar. They all knew what really caused AIDS in 1981. Spirochetal disease. And they knew the immune suppressed did not make antibodies against infections. He covers for the suffering of Autism kids, MS, ALS, Alzheimers, Lupus, Parkinson's, Diabetes, Crohn's, Celiac, MD, ALD, ME, CFS, PTSD, ADHD, Kawasaki's, Down's, Arthritis', and hundreds of other lies they don't want you American's to be able to treat the REAL CAUSE. Because they gave it to you for decades in all vaccines.
I have had Chronic Lyme Disease for over 8 years. I was only diagnosed 3 years ago. I have been on and off Antibiotics for 3 years. I am convinced that the antibiotics we have at our disposal are not sufficient to kill the Lyme. Unfortunately, they now know that these bacteria are able to form biofilms to hide under while the antibiotic is in the body. Once it is removed, the bacteria come back out and begin to multiply and take over your body once again. Dr Horowitz is one of the best known doctors that work on Lyme Disease (LLMD). He is very respected for being able to stand up against the government cronies like the CDC and the IDSA who continually try to say that Chronic Lyme does not exist and will go away with just 4-6 weeks of Doxycycline. 1,000s and 1,000s of people have proven that this is not the case – but in their egotistical, stubborn ways, they will not listen to actual patients but just keep reading their books. OUT OF TOUCH and they should be fired! I am moving on to try concentrated herbal remedies which are helping a large number of Chronic Lyme patients.
Sorry but Lyme is not reduced to certain states, it's everywhere! It's the damn crappy out dated testing they're still using! It's been 25 years since I was bitten by a tick on my head, and been suffering ever since, because doctors didn't want to look into Lyme, this time my neuro did one on me, and my 23 and 41 came up positive on my Western Blot. I've been very sick, and still waiting to see an LLMD, because Medicaid doesn't cover these kind of doctors! I'm on Medicaid, because I'm too sick to work a regular job. Really something needs to be done, people are getting sick and some even die from the co infections of the tick, enough is enough!
I had a tick on for hour and I got limes disease after that but I got it off soon enough to never get the symptoms again
Alot of people got lyme without knowing it and it ruin alot of lifes. Only 50% get a rash so it is very hard to know.
Wrote a Lyme disease brochure with the help of 2 Lyme disease specialists. Will email to anyone interested. God bless, Elaine
BS, Lyme doesn't go away in two to four weeks with antibiotics, if you're not diagnosed in time!
This physician has no idea what he is talking bout. very scary. Read the medical journals doctor.
This guy is an idiot
This guy is completely full of shit !!! But to each his own
Wow this doc is clueless.
Omg im not going in my back yard this year I will be inside crafting
This show did nothing for the education and awareness of chronic lyme disease. What happened to "first do no harm"? I am not an iv antibiotics treatment advocate as I do not react well yo them, but herbally treating by buhners protocol.
listened and treated me, I am better today!
Wrote a Lyme disease brochure with the input of 2 Lyme disease specialists. Will email to anyone interested. God bless, Elaine
Elaine, I am interested. I was just diagnosed with Lyme's disease finally yesterday after 28 years of suffering. [email protected]
Thank you.
I would be an invalid at this point.