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http://www.facebook.com/darith1.lyme
D&L THOMAS
TICK BORNE DISEASE ADVOCATES
THROUGH CHALLENGE and Lyme Disease
Blog
Checking out Dajanoli Outdoors
Posted on October 21, 2020 at 7:43 PM |
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We now Have a place where you can enjoy the shopping of outdoor products at Dajanoli Outdoors at www.dajanolioutdoors.com. We are happy to bring you some nice products and if you are looking for something. Just ask and perhaps we can find that for you. Check us out. Thanks |
A Journey of Mazes
Posted on May 7, 2020 at 12:30 AM |
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I am sorry to say the tentacles of medical corruption have eliminated the YOutube video. Hello all, What a beautiful day. A bit chilly, A bit damp, A bit bored, but now a bit hopeful. With the following film. Maybe with truth and courage and Facebook's support. We can educate the world, of the world. Let us go to the movies. https://youtu.be/fsi9csLNb-Y I am sorry to say the tentacles of medical corruption have eliminated the YOutube video. |
An update
Posted on January 16, 2020 at 10:13 PM |
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I am the author of Journey Through Challenge and Lyme in advocacy that tries to stay with the symptoms of vector-borne diseases depression, neuropathic pain, anxiety, as we all face this pandemic from Lyme, Bartonella, Babesiosis and many others. We hope you can find something that will help your decision making to better health. I feel there is some progress being made in this dreadful disease and there is much work to be done still in the future. The suffering still suffers, the ignorant is still doubtful of problems. The profit takers are still clinging to their profit margins. Knowing the sky will likely fall when Tick born diseases are eradicated, elimanating the high percentage of infectous diseases that move so much money. |
DAJANOLI OUTDOORS
Posted on November 20, 2019 at 7:00 PM |
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Welcome to my store at at www.dajanolioutdoors.com. I will integrate this project to help finance the Lyme diseases advocacy and lighten the load on my disability as I receive little to nothing for support of my projects. |
Update to Disulfiram experience
Posted on September 30, 2019 at 5:22 PM |
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I have improved just starting and stopping at the one month period. Have not started back yet but will start much slower when I do. I have been off for about two months now. I really need to slow down because my previous heart issues will stop me if I don't. But I am doing things again and I believe the DSF had helped greatly in the low dosages that I was taking. I believe a major herx is why I had trouble, and now I am glad I took the DSF. I start with a quarter 250mg pill every day for two weeks. done great, then half 250 mg pill for two weeks. I started nerve jerking and synapses in the nervous system that I was not able to rest with. That meant my heart was likely doing the same thing. So I stopped. I just may be one of those highly sensitive individuals that respond to lower dosage. Thank you all here for sharing and caring. keep talking. |
My Disulfiram Experience
Posted on August 23, 2019 at 10:03 AM |
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Hello all, I am still here after my first month of Disulfiram. For me, this has been an experience that has helped me with some issues and I believe added some issues. I will explain here.
I hope this helps, David R Thomas – Tick-Borne diseases advocate |
Inquiries of Longihornis Tick
Posted on May 29, 2019 at 3:09 PM |
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I have been getting more than a couple of concerned inquiries about the Longihornis Tick. Or Asian Tick. I have also been reading up on the Longihornis Asian Tick. Appears any human infections are considered accidental. This Tick carries the SFTS ( Severe Fever Thrombocytopenia Syndrome) ( A dog disease )Only deadly to 20 to 30% of those that get it. (I suspect cross-contamination.) |
Baby steps in a big way
Posted on November 10, 2017 at 6:50 AM |
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Loraine Johnson's response to CDC article
Posted on June 19, 2017 at 7:08 AM |
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In Response to the CDC's recent published article against the Lyme world From Loraine Johnson - To All, Lorraine Johnson posted their response. It was filed by Raphael B Stricker, MD. (see below). Much appreciation is due to them,Jill ---- read bellow ----Last night Ray filed our pub-commons response to the Christina Nelson MMWR piece, detailing the previous ethics case. This can now be cited. https://www.ncbi.nlm.nih.gov/pubmed/28617768 Lorraine Johnson, Raphael B. Stricker, MD.Lymedisease.org, PO Box 1352, Chico, CA 95927; ILADS, PO Box 341461, Bethesda, MD 20827The article by Marzec et al. published in MMWR purports to show the dangers of treatment in patients diagnosed with chronic Lyme disease (1). Recent reports from the Centers for Disease Control and Prevention (CDC) indicate that more than 300,000 new cases of Lyme disease are diagnosed each year in the USA (2). The MMWR article from the CDC describes five anecdotal cases of treatment complications in these patients while ignoring the significant morbidity related to denial of treatment for chronic Lyme disease (2,3). The resultant biased report raises scientific and ethical issues about the CDC's role in promoting the best care for patients with tickborne diseases.The MMWR piece resulted from anecdotal reports gathered by Dr. Christina Nelson of the CDC. The article notes that the information was gathered because “clinicians and state health departments periodically contact CDC concerning patients who have acquired serious bacterial infections during treatments for chronic Lyme disease.” However, an ethics complaint filed against Dr. Nelson by the Lyme disease patient advocacy group LymeDisease.org suggests that these adverse event reports were in fact specifically solicited by Dr. Nelson via emails distributed in 2014 (4). Dr. Nelson asked clinicians from the Infectious Diseases Society of America (IDSA) to provide anecdotal evidence of harm to patients from intravenous antibiotic therapy related to Lyme disease, and she apparently offered coauthorship of her article as an incentive to describe these adverse events. She did not ask for consequences of failing to treat these patients, nor did she solicit commentary from practitioners who treat chronic Lyme disease according to the guidelines of the International Lyme and Associated Diseases Society (ILADS).The risk of any medical treatment is extremely context-sensitive. A crucial question is whether the risks of treatment are warranted given the potential benefits, the availability of other treatment options, the severity of the patient's presentation, and the risk tolerance of the individual patient. By asking for an assessment of treatment risks only, Dr. Nelson is framing the issue in a manner that excludes the other half of the equation in a risk/benefit assessment. She is also ignoring an issue that is critical to patients who suffer a profoundly diminished quality of life due to their illness, namely the risk of not treating (5,6). Moreover, by failing to mention that these adverse event reports were rare and specifically solicited, she implies that these rare occurrences are a common concern. In reality, studies of the risks and benefits associated with intravenous antibiotic treatment for Lyme disease indicate that the risks of adverse events are no greater than the risks of intravenous therapy in other unrelated diseases (7,8).By asking the question only of those on one side of the controversy, Dr. Nelson is further demonstrating favoritism and a lack of impartiality on the part of the CDC. Accordingly, Dr. Nelson's solicitation of anecdotal adverse events for case studies of Lyme disease is a highly inappropriate partisan act of favoritism toward the IDSA viewpoint at the expense of critical stakeholders - Lyme disease patients and their treating physicians - and an attack on the ILADS viewpoints. References 1. Marzec NS, Nelson C, Waldron PR, et al. Serious bacterial infections acquired during treatment of patients given a diagnosis of chronic Lyme disease - United States. MMWR Morb Mortal Wkly Rep. 2017 Jun 16;66(23):607-609. 2. Stricker RB, Johnson L. Lyme disease: Call for a ‘‘Manhattan Project’’ to combat the epidemic. PLoS Pathog. 2014;10(1): e1003796. 3. Stricker RB, Fesler MC. Chronic Lyme disease: A working case definition. Chronic Dis Int. 2017; 4(1): 1025. 4. Leland DK. TOUCHED BY LYME: CDC ignores ethics, attacks “chronic Lyme”. Available at https://www.lymedisease.org/touchedbylyme-cdc-ignores-ethics/. Accessed June 16, 2017. 5. Johnson L, Aylward A, Stricker RB. Healthcare access and burden of care for patients with Lyme disease: a large United States survey. Health Policy. 2011;102: 64–71. 6. Johnson L, Wilcox S, Mankoff J, Stricker RB. Severity of chronic Lyme disease compared to other chronic conditions: a quality of life survey. Peer J. 2014;2:e322. 7. Stricker RB, Green CL, Savely VR, Chamallas SN, Johnson L. Safety of intravenous antibiotic therapy in patients referred for treatment of neurologic Lyme disease. Minerva Med. 2010;101:1–7. 8. Stricker RB, Delong AK, Green CL, et al. Benefit of intravenous antibiotic therapy in patients referred for treatment of neurologic Lyme disease. Int J Gen Med. 2011; 4: 639–646. |
Lyme,Opioid, Heroin ???
Posted on June 16, 2017 at 2:54 PM |
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Hello all, In a response to being asked of the Attorney General to sign on to the severe Opioid/heroin epidemic in Pa. I replied with. --- Hello Mr. Shapiro, I am grateful that you are taking an interest in the opioid and heroin epidemic on every front. but there is one front that you are totally not listening to. This is the pain and suffering that is raping the nation of good people and driving them to something that works. Your fight for Opioid and Heroin control will not get better until we get this Lyme and Late Stage Lyme, Chronic Lyme issue under control. Why would I say something so ridiculous? Late stage lyme pain is Hell and the meds out there now are not enough. The pain is 10x worse than any Non-Lyme Literate Doctor can fathom. You, sir, need desperately to sit down with a table of Lyme Literate individuals and sufferers LLMD's and discuss this epidemic that you keep blaming on the Pharma companies. All Pharma is, is a supplier of a badly ignored situation. Take the opioid and heroin away and start burying the dead. Many will be young people middle aged, people. All we will have if we continue the direction your heading is more suffering. It is the Lyme sufferers that need help. We need to get this SB-100 voted on and passed to give the medical community some leverage and freedom to treat these sufferers without threats of losing their license. I hope this helps in your and my fight to get this terrible drug problem under control. |
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