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There is definite evidence that chronic symptoms can be attributed to Lyme spirochetes. See Monica Embers Tulane primate study published in 2012 and Invisible International free CME online that includes many researchers and veterinarians on Lyme. See many research articles in lymedisease.org on research. See "Dr Neil Spector 2017 Focus on Lyme" youtube. Even Allen Steere and Gary Wormser now know that the lyme spirochete causes chronic disease as shown by Jac(fob Lemieux including by Allen Steere and Gary Wormser as coauthors of the recently published in 2023 "Whole genome sequencing of human Borrelia burgdorferi isolates reveals linked blocks of accessory genome elements located on plasmids and associated with human dissemination" that explain why some people have severe disease. Like syphilis which is also a spirochete that reaches the brain, lyme can be severe. Unlike syphilis, it has no accurate test with CDC admitting 21-70% sensitivity in early and mid-Lyme so more than half are misdiagnosed. Patients are not treated when tests are negative and not treated when tests are positive "false positive" claimed. "Cure Unknown" by Pamela Weintraub, a medical journalist whose family came down with Lyme documents the Lyme Wars leave patients with no care and go after doctors who try to help them. Yes, there are quacks but there are also people who commit suicide from pain from long Lyme or a coinfection such as Bartonella. Fallon, et al Columbia 74% higher suicide rate in population study in Denmark. See Bartonella Babe Jake Picker 30 yr old who recently chose ass't suicide legal in Calif, a beautiful soul who tried to educate. It is worse than Tuskegee and Wiki should doccument it and remove outdated info. I hope you look carefully at all this. I did not know it until several people I know in NE Ohio were affected in some way as millions are now. Darry Hall of Hall and Oates called it a "scandal" how patients are treated as lyme loonies and I completely agree. See "Lyme the 1st Epidemic of Climate Change" by MB Pfeiffer, an investigative reporter. See Shania Twain, see Kris Kristofferson. See Senator Tina Smith who cosponsored the Kay Hagan Tick act who saw 23 doctors and spent $240,000 before being diagnosed. Doctors do not know it is prevalent and the WB, Eliza tests do not work early when it is most treatable. Kids end up in wheelchairs. Willie Burgdorferi who discoverd Lyme says it is chroni. Feel free to email me. I feel sad that I did not know this despite 28 yrs in the medical field. Teri Sanor, MD 170.250.215.18 ( talk) 01:13, 9 April 2024 (UTC)
Not done: please provide
reliable sources that support the change you want to be made. '''[[ User:CanonNi]]'''( talk| contribs) 01:18, 9 April 2024 (UTC)
| This
edit request has been answered. Set the |answered= or |ans= parameter to no to reactivate your request. |
This article is outdated. Even hardliners like Allen Steere and Gary Wormser who denied patients had long lyme now know that Lyme can cause severe and fluctuating symptoms. They are co-authors of the 2023 Lemieux "Whole genome sequencing of human borrelia isolates reveals linked blocks of accessory genome elements located on plasmids and associated with human dissemination" showing viruses within the spirochetes and genes associated with the probability of invasive infection and severe symptoms.
Gary Wormser testified against physicians who tried to help Lyme patients. Lyme is a clinical diagnoses since it needs treated early to prevent dissemination. Now he knows better from this research. They left patients without any treatment which is like Tuskeegee experiment only many more. CDC now estimates 476,000 cases/yr and funding is only $63/per pt. Lyme is a spirochete like syphilis yet 3x more common. HIV/AIDs funding is 2.9 billion which is $82,000/per pt.
The western blot and eliza test miss half the ases in the early and mid-stages.
CDC and IDSA used to say that most patients get a rash yet less than half get a target rash as even Steere's early research showed.
Even with facial droop and musculoskeletal severe symptoms, the guidelines say no treatment is needed unless there are 5 bands.This is arbitrary based on a surveillance definition that is highly specific and poorly sensitive. Over 50 journal articles document Lyme disease despite negative tests.
Even a positive test of 5 bands was often not treated "false positives" so the patients with long symptoms had no treatment then either. Cases like Dr Neil Spector, a successful breast cancer researcher who was repeatedly misdiagnosed leading to his lyme carditis and a heart transplant. He switched careers and noted Lyme disease was in the Dark Ages for research (see Dr Neil Spector 2017 Focus on Lyme") and says syphilis has already confirmed that spirochetes go into the tissues and brain. Kris Kristofferson's dementia was from Lyme. J. Miklossy's research on oral spirochetes and lyme spirochetes found "Alzheimer's disease-a neurospirochetosis. Analysis of the evidence following Koch's and Hill's criteria" and that biofilms of the spirochetes cause the brain plaques, tau and amyloid years ago.
NIH and NINDS funds research based on what individual researchers want to study. Almost all say "more research is needed" yet there is no follow up to advance the field.
$3 billion dollars donated to Alzheimer's disease every year, yet there is not 1 trial on clinicaltrials.gov and in RePORTER, the only researcher advancing the field that I found was Monica Embers at Tulane. Either prove or disprove that dementia can be from oral treponema spirochetes and Lyme spirochet
Invisible International free CMEs shows that veterinarians are ahead of physicians. They do not have the Lyme Wars. They see dogs and treat them. Tulane's Monica Embers gives free education there and has shown monkey brains contain intact Lyme spirochetes, DNA and RNA. That was in 2012 yet no follow up until she did it and found that monotherapy antibiotics is not enough to eradicate Lyme infections.
Wormser did a study years ago showing Lyme patients do not have long symptoms yet selected only patients who had the target rash and got antibiotics within 4 days. It is easily treated then. That is not the population with severe symptoms.
NIH funded in 1997 Lyme and deafness by the Institute for Deafness yet there are no published results, 2 more studies were funded, no published results. Much of neuroborreliosis has no published results despite giving taxpayer dollars. No results mean the field cannot advance.
Senator Tina Smith who signed the 2019 Tick Act was misdiagnosed by 21 physicians and spent 1/4 million dollars on unnecessary tests before Lyme was diagnosed. It costs the USA $75 billion dollars a year because disabled adults cannot work and disabled children cannot attend school regularly so need a 504 Education plan. I was an RN and MD for 28 years combined and knew nothing of this until 4 people I know had Lyme or a coinfection and it is truly a scandal how they were treated. A 14yo went from straight As to disability, a young boy is deaf in 1 ear, a man had joint surgery on his hand and on RA meds until his lyme coinfections were treated with antibiotics for 6 months and then did not need the other 4 hand joints surgery, is off all RA meds and still his pcp and rheumatologist did not research any of this.)
All who sent out misinformation owe people that suffered so much. Mark Ruffalo, the Hulk says it was "brutal, brought me to my knees" Olivia Goodreau was so disabled her parents had to lift her into a wheelchair (much like the children in Lyme 42 years ago) yet was misdiagnosed by dozens of physicians. At 12 yrs old she started LivLyme when she heard that a boy and his mom were living in a car to afford their Lyme treatment. Her book "But She Looks Fine" is true. If they had the late stage sores that syphilis spirochetes have, it would never have come this far. CDC needs to count all cases which it does not do now, it uses a percentage based on if it expects LYme ie in Lyme NE, 1 in 7 cases are counted and in other states much less are counted since they feel clinicians are overdiagnosing it. See lymedisease.org for details. It is the largest lyme database in the world. Public service announcements could be easily changed to say it is a clinical diagnosis, any mental change should be evaluated for infections, the tiny nymph could be shown since many do not see it or the rash. Suicide is 70% higher if Lyme per Fallon research of 6 million in the Danish population. Dr Swedo of NIMH has been trying for years to get education out about strept,lyme and other infections as cause of severe psych problems especially in OCD patients.
Forward this to anyone who will help prevent these tragedies. Teri Sanor, MD OhioMD ( talk) 02:28, 21 April 2024 (UTC)
Not done: it's not clear what changes you want to be made. Please mention the specific changes in a
"change X to Y" format and provide a
reliable source if appropriate. '''[[ User:CanonNi]]'''( talk| contribs) 02:32, 21 April 2024 (UTC)
| This is the
talk page for discussing improvements to the
Chronic Lyme disease article. This is not a forum for general discussion of the article's subject. |
Article policies
|
| Find medical sources: Source guidelines · PubMed · Cochrane · DOAJ · Gale · OpenMD · ScienceDirect · Springer · Trip · Wiley · TWL |
|
Archives:
1,
2Auto-archiving period: 60 days
|
|
| The
contentious topics procedure applies to this page. This page is related to
pseudoscience and
fringe science, which has been
designated as a contentious topic. Editors who repeatedly or seriously fail to adhere to the purpose of Wikipedia, any expected standards of behaviour, or any normal editorial process may be blocked or restricted by an administrator. Editors are advised to familiarise themselves with the contentious topics procedures before editing this page. |
| This page is not a forum for general discussion about Chronic Lyme disease. Any such comments may be removed or refactored. Please limit discussion to improvement of this article. You may wish to ask factual questions about Chronic Lyme disease at the Reference desk. |
| This page is not a forum for general discussion about various personal beliefs about Lyme disease. Any such comments may be removed or refactored. Please limit discussion to improvement of this article. You may wish to ask factual questions about various personal beliefs about Lyme disease at the Reference desk. |
|
| This article is rated B-class on Wikipedia's
content assessment scale. It is of interest to the following WikiProjects: | |||||||||||||||||||||||||||
| ||||||||||||||||||||||||||||
|
| Ideal sources for Wikipedia's health content are defined in the guideline
Wikipedia:Identifying reliable sources (medicine) and are typically
review articles. Here are links to possibly useful sources of information about Chronic Lyme disease.
|
Italic text
| This
edit request has been answered. Set the |answered= or |ans= parameter to no to reactivate your request. |
There is definite evidence that chronic symptoms can be attributed to Lyme spirochetes. See Monica Embers Tulane primate study published in 2012 and Invisible International free CME online that includes many researchers and veterinarians on Lyme. See many research articles in lymedisease.org on research. See "Dr Neil Spector 2017 Focus on Lyme" youtube. Even Allen Steere and Gary Wormser now know that the lyme spirochete causes chronic disease as shown by Jac(fob Lemieux including by Allen Steere and Gary Wormser as coauthors of the recently published in 2023 "Whole genome sequencing of human Borrelia burgdorferi isolates reveals linked blocks of accessory genome elements located on plasmids and associated with human dissemination" that explain why some people have severe disease. Like syphilis which is also a spirochete that reaches the brain, lyme can be severe. Unlike syphilis, it has no accurate test with CDC admitting 21-70% sensitivity in early and mid-Lyme so more than half are misdiagnosed. Patients are not treated when tests are negative and not treated when tests are positive "false positive" claimed. "Cure Unknown" by Pamela Weintraub, a medical journalist whose family came down with Lyme documents the Lyme Wars leave patients with no care and go after doctors who try to help them. Yes, there are quacks but there are also people who commit suicide from pain from long Lyme or a coinfection such as Bartonella. Fallon, et al Columbia 74% higher suicide rate in population study in Denmark. See Bartonella Babe Jake Picker 30 yr old who recently chose ass't suicide legal in Calif, a beautiful soul who tried to educate. It is worse than Tuskegee and Wiki should doccument it and remove outdated info. I hope you look carefully at all this. I did not know it until several people I know in NE Ohio were affected in some way as millions are now. Darry Hall of Hall and Oates called it a "scandal" how patients are treated as lyme loonies and I completely agree. See "Lyme the 1st Epidemic of Climate Change" by MB Pfeiffer, an investigative reporter. See Shania Twain, see Kris Kristofferson. See Senator Tina Smith who cosponsored the Kay Hagan Tick act who saw 23 doctors and spent $240,000 before being diagnosed. Doctors do not know it is prevalent and the WB, Eliza tests do not work early when it is most treatable. Kids end up in wheelchairs. Willie Burgdorferi who discoverd Lyme says it is chroni. Feel free to email me. I feel sad that I did not know this despite 28 yrs in the medical field. Teri Sanor, MD 170.250.215.18 ( talk) 01:13, 9 April 2024 (UTC)
- Not done: please provide
reliable sources that support the change you want to be made.
'''[[ User:CanonNi]]'''( talk| contribs) 01:18, 9 April 2024 (UTC)
| This
edit request has been answered. Set the |answered= or |ans= parameter to no to reactivate your request. |
This article is outdated. Even hardliners like Allen Steere and Gary Wormser who denied patients had long lyme now know that Lyme can cause severe and fluctuating symptoms. They are co-authors of the 2023 Lemieux "Whole genome sequencing of human borrelia isolates reveals linked blocks of accessory genome elements located on plasmids and associated with human dissemination" showing viruses within the spirochetes and genes associated with the probability of invasive infection and severe symptoms.
Gary Wormser testified against physicians who tried to help Lyme patients. Lyme is a clinical diagnoses since it needs treated early to prevent dissemination. Now he knows better from this research. They left patients without any treatment which is like Tuskeegee experiment only many more. CDC now estimates 476,000 cases/yr and funding is only $63/per pt. Lyme is a spirochete like syphilis yet 3x more common. HIV/AIDs funding is 2.9 billion which is $82,000/per pt.
The western blot and eliza test miss half the ases in the early and mid-stages.
CDC and IDSA used to say that most patients get a rash yet less than half get a target rash as even Steere's early research showed.
Even with facial droop and musculoskeletal severe symptoms, the guidelines say no treatment is needed unless there are 5 bands.This is arbitrary based on a surveillance definition that is highly specific and poorly sensitive. Over 50 journal articles document Lyme disease despite negative tests.
Even a positive test of 5 bands was often not treated "false positives" so the patients with long symptoms had no treatment then either. Cases like Dr Neil Spector, a successful breast cancer researcher who was repeatedly misdiagnosed leading to his lyme carditis and a heart transplant. He switched careers and noted Lyme disease was in the Dark Ages for research (see Dr Neil Spector 2017 Focus on Lyme") and says syphilis has already confirmed that spirochetes go into the tissues and brain. Kris Kristofferson's dementia was from Lyme. J. Miklossy's research on oral spirochetes and lyme spirochetes found "Alzheimer's disease-a neurospirochetosis. Analysis of the evidence following Koch's and Hill's criteria" and that biofilms of the spirochetes cause the brain plaques, tau and amyloid years ago.
NIH and NINDS funds research based on what individual researchers want to study. Almost all say "more research is needed" yet there is no follow up to advance the field.
$3 billion dollars donated to Alzheimer's disease every year, yet there is not 1 trial on clinicaltrials.gov and in RePORTER, the only researcher advancing the field that I found was Monica Embers at Tulane. Either prove or disprove that dementia can be from oral treponema spirochetes and Lyme spirochet
Invisible International free CMEs shows that veterinarians are ahead of physicians. They do not have the Lyme Wars. They see dogs and treat them. Tulane's Monica Embers gives free education there and has shown monkey brains contain intact Lyme spirochetes, DNA and RNA. That was in 2012 yet no follow up until she did it and found that monotherapy antibiotics is not enough to eradicate Lyme infections.
Wormser did a study years ago showing Lyme patients do not have long symptoms yet selected only patients who had the target rash and got antibiotics within 4 days. It is easily treated then. That is not the population with severe symptoms.
NIH funded in 1997 Lyme and deafness by the Institute for Deafness yet there are no published results, 2 more studies were funded, no published results. Much of neuroborreliosis has no published results despite giving taxpayer dollars. No results mean the field cannot advance.
Senator Tina Smith who signed the 2019 Tick Act was misdiagnosed by 21 physicians and spent 1/4 million dollars on unnecessary tests before Lyme was diagnosed. It costs the USA $75 billion dollars a year because disabled adults cannot work and disabled children cannot attend school regularly so need a 504 Education plan. I was an RN and MD for 28 years combined and knew nothing of this until 4 people I know had Lyme or a coinfection and it is truly a scandal how they were treated. A 14yo went from straight As to disability, a young boy is deaf in 1 ear, a man had joint surgery on his hand and on RA meds until his lyme coinfections were treated with antibiotics for 6 months and then did not need the other 4 hand joints surgery, is off all RA meds and still his pcp and rheumatologist did not research any of this.)
All who sent out misinformation owe people that suffered so much. Mark Ruffalo, the Hulk says it was "brutal, brought me to my knees" Olivia Goodreau was so disabled her parents had to lift her into a wheelchair (much like the children in Lyme 42 years ago) yet was misdiagnosed by dozens of physicians. At 12 yrs old she started LivLyme when she heard that a boy and his mom were living in a car to afford their Lyme treatment. Her book "But She Looks Fine" is true. If they had the late stage sores that syphilis spirochetes have, it would never have come this far. CDC needs to count all cases which it does not do now, it uses a percentage based on if it expects LYme ie in Lyme NE, 1 in 7 cases are counted and in other states much less are counted since they feel clinicians are overdiagnosing it. See lymedisease.org for details. It is the largest lyme database in the world. Public service announcements could be easily changed to say it is a clinical diagnosis, any mental change should be evaluated for infections, the tiny nymph could be shown since many do not see it or the rash. Suicide is 70% higher if Lyme per Fallon research of 6 million in the Danish population. Dr Swedo of NIMH has been trying for years to get education out about strept,lyme and other infections as cause of severe psych problems especially in OCD patients.
Forward this to anyone who will help prevent these tragedies. Teri Sanor, MD OhioMD ( talk) 02:28, 21 April 2024 (UTC)
- Not done: it's not clear what changes you want to be made. Please mention the specific changes in a
"change X to Y" format and provide a
reliable source if appropriate.
'''[[ User:CanonNi]]'''( talk| contribs) 02:32, 21 April 2024 (UTC)