Annual Patient Workshop
Treating
Autoimmune and
Inflammatory
Diseases with
Inflammation
Therapy
When: Sunday
February 16, 2014
Where: Hilton
Dallas-Ft. Worth
Lakes Executive
Conference Center
For details and
registration
information
click here
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Therapy Tip
Injected medications may contribute to chronic disease because the filters that are used when making them aren't small enough to block Cell Wall Deficient bacteria. However, for some patients, getting an annual flu shot or the Pneumovax injection is important to attempt to prevent acute infections. Patients at high risk for succumbing to an acute viral or bacterial infection should consider these vaccinations.
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Recovery Reports
We are contacted daily by people with chronic illnesses who are looking for an effective treatment. Many ask us to provide evidence of efficacy in the form of statistics or stories. If you have recovered your health or had significant symptom improvement with Inflammation Therapy (or a similar treatment), please help us 'pay it forward' by telling your story. We will post it in the public section of our website to encourage others. Any report, short or long, with or without objective data (e.g., lab results, imaging reports) would be helpful. Please
send your story to
our email .
Thank you!
To see the latest recovery reports,
click here.
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CIR Library Access
Access to our free, extensive, easy-to-read Library of Information
(see this sample page)
and Physicians' Reference Library is available to anyone, without enrollment in our counseling program. If you're interested in using this resource, please send a request to our email
address along with your doctor's name and fax number (in the US or Canada) or his/her email address, so we can notify your doctor that you have access to this information.
A list of the articles in our libraries is available at this link.
Physicians may use CIR libraries even if they don't have a patient enrolled in our counseling program. Interested medical practitioners should contact CIR and ask to register.
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CIR is an IRS-recognized 501(c)3 non-profit charitable organization.
Donate to CIR
in support of our educational and research efforts.

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Contact Us
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you may phone us toll free from anywhere in the US and Canada
1-888-846-2474
Skype
Chronic.Illness.Recovery
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Greetings!
"It is undoubtedly true that the same drug, microbe, emotional irritant, or physical injury may produce a disease of adaptation in one person and be tolerated with impunity by another"...Hans Selye was right in the 1930s when he said it would take many generations before the details of disease from systemic cellular stress are elucidated.
Our world is complicated, full of toxins, meds, and chemicals no doubt breeching our barrier to a formidable foe. The devil's in the details of a very big problem: we host a microbial soup and our immune system needs help. We're on it...
Sincerely, your CIR team
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Patient Workshop - Sunday, February 16, 2014
| Featured Speaker
Meg Mangin, RN has provided skilled nursing services in a variety of medical specialties. She served on a National Institutes of Health State of the Science panel and an NIH Data, Safety and Monitoring Board. She was one of the earliest adopters of Inflammation Therapy and participated in its early research. She led a team of online nurses in counseling hundreds of patients on their road to recovery and was a presenter at Days of Molecular Medicine in Karolinska, Sweden, the Understanding Aging Conference in Los Angeles and the International Conference on Autoimmunity in Porto, Portugal.
Ms. Mangin is the author of Observations of Jarisch-Herxheimer Reaction in Sarcoidosis Patients and a co-author of a chapter in the 2006 medical textbook Vitamin D: New Research, published by Nova. Her latest paper is a review of Vitamin D, Intracellular Bacteria and the Immune System. Ms. Mangin will present Vitamin D and Dysregulated Vitamin D Metabolism.
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About Inflammation Therapy
| Effects of Intracellular Pathogens
The human body is colonized by a vast number of microbes and microbial colonies gain many advantages by parasitizing immune cells and altering nuclear receptor activity. Tissue invasion provides a privileged niche with access to host protein and iron, sequestration from immune response, and a means for persistence. [1] Macrophage microbicidal mechanisms are thought to be responsible for the control and elimination of intracellular pathogens; 1,25(OH)2D production and action in macrophages activates toll-like receptors to increase expression of the AMP cathelicidin and kill the infectious invaders. [2, 3] Consequently, when immune defenses are stimulated Th17 cells mobilize host immunity and contribute to the development of harmful chronic inflammatory conditions. [4, 5] The Human Microbiome project, which is cataloguing all the microorganisms associated with mankind, has revealed that over 90% of the cells in the human body are not human in origin. The millions of genes carried in the human microbiota greatly outnumber the 23,000 genes in the human genome. When host conditions are favorable, non-pathogenic bacteria in the microbiome may become pathogenic using a panoply of tactics to cause interferences within host cells. Intracellular pathogens are described as often entering an unusual biologic state designated "persistence" and in this form have been associated with engendering several chronic diseases. [6-8] Phagocyte-inflicted tissue damage plays an important role in many chronic diseases. [9] In the arms race of host-microbe co-evolution, successful microbial pathogens have evolved innovative strategies to evade host immune responses and persist in intracellular cytoplasm. For example, 'crosstalkmanipulation' (the proactive microbial interference strategies that instigate, subvert or disrupt the molecular signaling crosstalk between receptors of the innate immune system) undermines host defenses and contributes to microbial adaptive fitness. [10, 11] Pathogenic microbes also induce stress responses which protect the cell from lethal factors, express proteases that degrade AMPs, use biofilms as a shield, modulate host cell motility to facilitate establishment of an infection, and secrete substances that block the VDR. [12-16] Genetic foreign and host protein interactions alter gene transcription and translation mechanisms and many species survive by horizontal gene transfer. [6, 17, 18] Autoimmune patients acquire a distinct pathogenic microbiota and multi-morbidity often results. [19, 20]Intracellular bacteria modulate cytokine production; and in monocytes and macrophages, cytokine activation markedly inhibits 1,25(OH)2D/VDR gene transcription. [21, 22] When the immune system is fighting a persistent microbe, it continually releases inflammatory molecules in an effort to kill the pathogen. [23] This dysfunctional immunological response produces low-grade inflammation which is a component of many chronic and autoimmune diseases. - Kozarov E. Bacterial invasion of vascular cell types: vascular infectology and atherogenesis. Future Cardiol. Jan 2012;8(1):123-38.
- Nauciel C. Immune Defenses against Intracellular Bacterial Infection. In: Paradise LJ, Friedman H, Bendinelli M, eds. Opportunistic Intracellular Bacteria and Immunity. New York, NY: Kluwer Academic Press; 2002.
- Liu PT, Stenger S, Li H, et al. Toll-like receptor triggering of a vitamin D-mediated human antimicrobial response. Science. Mar 2006;311(5768):1770-3.
- McGeachy MJ, McSorley SJ. Microbial-induced Th17: superhero or supervillain? 2012. J Immunol Oct;189(7):3285-3291.
- Oswald-Richter KA, Beachboard DC, Seeley EH, et al. Dual analysis for mycobacteria and propionibacteria in sarcoidosis BAL. J Clin Immunol. Oct 2012(32(5)):1129-40.
- Smillie CS, Smith MB, Friedman J, Cordero OX, David LA, Alm EJ. Ecology drives a global network of gene exchange connecting the human microbiome. Nature. Oct 2011;480(7376):241-4.
- Branton WG, Ellestad KK, Maingat F, et al. Brain Microbial Populations in HIV/AIDS: α-Proteobacteria Predominate Independent of Host Immune Status. PLOS one. 2013;8(1):e54673.
- Eishi Y. Etiologic aspect of sarcoidosis as an allergic endogenous infection caused by Propionibacterium acnes. Biomed Res Int. 2013:2013:935289.
- Labro M. Interference of antibacterial agents with phagocyte functions: immunomodulation or "immuno-fairy tales"? Clin Microbiol Rev. 2000;13(4):615-650.
- Khan N, Gowthaman U, Pahari S, Agrewala JN. Manipulation of costimulatory molecules by intracellular pathogens: veni, vidi, vici! PLoS Pathog. 2012;8(6):e1002676.
- Hajishengallis G, Lambris JD. Microbial manipulation of receptor crosstalk in innate immunity. Nat Rev Immunol. Mar 2011(11(3)):187-200.
- Dörr T, Vulić M, Lewis K. Ciprofloxacin Causes Persister Formation by Inducing the TisB toxin in Escherichia coli. PLoS Biol. 2010;8(2):e1000317.
- Chakraborty K, Ghosh S, Koley H, et al. Bacterial exotoxins downregulate cathelicidin (hCAP-18/LL-37) and human beta-defensin 1 (HBD-1) expression in the intestinal epithelial cells. Cell Microbiol. Dec 2008;10(12):2520-37.
- Thornton RB, Rigby PJ, Wiertsema SP, et al. Multi-species bacterial biofilm and intracellular infection in otitis media. BMC Pediatr. Oct 2011;11:94.
- Fuks JM, Arrighi RB, Weidner JM, et al. GABAergic signaling is linked to a hypermigratory phenotype in dendritic cells infected by Toxoplasma gondii. PLoS Pathog. Dec 2012;e1003051(8(12)).
- Godchaux W3, Leadbetter ER. Sulfonolipids of gliding bacteria. Structure of the N-acylaminosulfonates. J Biol Chem 1984. October Mar;259(5):2982-90.
- Goodacre R. Metabolomics of a superorganism. J Nutr. Jan 2007;137(1 Suppl):259S-266S.
- Riley DR, Sieber KB, Robinson KM, et al. Bacteria-human somatic cell lateral gene transfer is enriched in cancer samples. PLOS Comp Bio. 2013(tbc).
- Giongo A, Gano KA, Crabb DB, et al. Toward defining the autoimmune microbiome for type 1 diabetes. ISME J. Jan 2011;5(1):82-91.
- Anderson G, Horvath J. The growing burden of chronic disease in America. Public Health Rep. May-Jun 2004;119(3):263-70.
- Wang KX, Chen L. Helicobacter pylori L-form and patients with chronic gastritis. World J Gastroenterol. May 2004;10(9):1306-9.
- Jones G, Prosser DE, Kaufman M. 25-Hydroxyvitamin D-24-hydroxylase (CYP24A1): Its important role in the degradation of vitamin D. Arch Biochem Biophys. Jul 2012;523(1)(9-18):9-18.
- Allie N, Alexopoulou L, Quesniaux VJ, et al. Protective role of membrane tumour necrosis factor in the host's resistance to mycobacterial infection. Immunology. Dec 2008;125(4):522-34.
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Quotes |
When I started treatment there was a lot happening and quickly. Some of it is scary and that is precisely why this counseling service is so vital. ~Flyboy
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