PDF Ebook Why Can't I Get Better?: Solving the Mystery of Lyme and Chronic Disease-
Superbe Why Can't I Get Better?: Solving The Mystery Of Lyme And Chronic Disease- publication est toujours étant le pal mieux pour passer peu de temps dans votre bureau, le temps du soir, bus, ainsi que partout. Ce sera un bon moyen de regarder simplement, ouvert, et aussi lire le livre Why Can't I Get Better?: Solving The Mystery Of Lyme And Chronic Disease- en ce moment - là. Comme l'a reconnu, la rencontre ainsi que des compétences ne viennent pas toujours avec le plus d' argent pour les obtenir. La lecture de ce livre avec le titre Why Can't I Get Better?: Solving The Mystery Of Lyme And Chronic Disease- va certainement vous faire savoir beaucoup plus de choses.
Why Can't I Get Better?: Solving the Mystery of Lyme and Chronic Disease-
PDF Ebook Why Can't I Get Better?: Solving the Mystery of Lyme and Chronic Disease-
Trouver le secret pour améliorer le mode de vie en lisant ce Why Can't I Get Better?: Solving The Mystery Of Lyme And Chronic Disease- Ceci est une sorte de livre que vous avez besoin actuellement. Par ailleurs, il peut être votre publication préférée à lire après avoir cette publication Why Can't I Get Better?: Solving The Mystery Of Lyme And Chronic Disease- Demandez-vous pourquoi? Eh bien, Why Can't I Get Better?: Solving The Mystery Of Lyme And Chronic Disease- est un livre qui a diverses notamment avec les autres. Vous pourriez ne pas devez comprendre qui est l'auteur, exactement comment le travail est très populaire. Comme mot sage, jamais évaluer les mots de qui parle, mais faire les mots que votre peu coûteux à votre vie.
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Détails sur le produit
Relié: 384 pages
Editeur : St Martin's Press; Édition : 1 (2 décembre 2013)
Langue : Anglais
ISBN-10: 1250019400
ISBN-13: 978-1250019400
Dimensions du produit:
16,4 x 4,2 x 24,4 cm
Moyenne des commentaires client :
5.0 étoiles sur 5
2 commentaires client
Classement des meilleures ventes d'Amazon:
495.386 en Livres (Voir les 100 premiers en Livres)
Ouvrage très complet qui rassemble en un lieu les questions que je pouvais me poser. Sa lecture a permis que je m'identifie au diagnostique et que je comprenne les enjeux des multiples prescriptions et recommandations médicales.
If you have ME"cfs", Fibromyalgia, ALS, MS or are undiagnosed with serious physical and mental fatigue, pain and/or neurological symptoms and tired of going from doctor to doctor looking for an answer, GET THIS BOOK! Sorry to shout, but this is very important.I have been sick for 12 years with an ME"cfs" diagnosis. Only two years ago did I find out the CDC's recommended test, which they and the Infectious Disease Society of America claim is 100% accurate (sensitive and specific) is actually only 40 - 60% accurate (depending on the study). I then did an Igenex PCR test, which is much better (but not 100% accurate either- but at least they admit it), which CDC and IDSA warn against. Thanks to the Igenex test, I found out I have Lyme Disease. And thanks to Medicare, which pays for this expensive test, because they deem it "medically necessary."There are an estimated 1 Million people in the United States that contract Lyme each year, but most are not diagnosed. Many are misdiagnosed with the above-listed diseases. This is a huge epidemic.Dr. Horowitz's book is fun to read (for a medical book) and tells you what you need to know to get diagnosed and begin healing. Dr. Horowitz is recognized as the top Lyme doc in the world and this is his first and only book. Just released recently, it is up to date.Oh yeah, also get this book if you know you have Lyme! :)Enjoy and happy healing everyone!
Yet another book that fails to acknowledge the high treatment failure rate for patients with advanced Lyme disease who are treated using the very methods described in this book. I am looking at the section where the author wrote: "Her [the patient's] inflammation was a red flag, so I decided to send a cytokine panel to LabCorp to eveluate her for other markers of inflammation. Her TNF-alpha came back within normal limits, but her IL-6 returned extremely elevated." But such testing reveals nothing about intra-CNS inflammation, and the patient's TNF-alpha levels within the CNS could have (and probably were) extremely elevated. Thus, using inherently inaccurate lab tests to measure inflammation plays an important role in the treatment approach advocated in this book. Perhaps I've missed something, but all I see in this book are claims of success, and no acknowledgement that many patients ( very likely) deteriorated as a result of repeated Herxheimer reactions, which exacerbate excitotoxicity and oxidative stress, and also exacerbate immune system dysregulation. Aggressive antimicrobial therapy and the ineffective prophylactic measures for Herx-like reactions that are described in the book utterly destroyed my health due to excessive herxing. I had probably been infected for 28 years when diagnosed and treated. I was actually in remission for nearly two years before treatment. As a result of the kind of treatment described in this book, I'm disabled and have been struggling to survive. And I know of many people who have had the same experience. But reading this book, an unsuspecting patient is led to believe that "everything will be okay," as stated in the preface. The treatment success rate for this disease complex is zero percent, if success is defined as cure. Using iv glutathione (one of the anti-inflammatory protocols used by the author) provides only short-term relief, probably because 20% of it is metabolized as extracellular glutamate, which causes excitotoxicity. And curcumin only suppresses quinoliic acid in vitro; it is completely ineffective at reducing elevated quinolinic acid levels within the central nervous system. Yet the author advocates its use for this purpose. Many patients with advanced Lyme disease end up in worse shape after being subjected to aggressive antimicrobial treatment. Some patients do improve, but those are the ONLY patients described in this book. So the book provides a an extremely skewed picture. Of course, that doesn't change the fact that the IDSA is a mafia. But many people who oppose the IDSA have put on blinders, and fail to convey the potential and often high risks of aggressive antimicrobial treatment to patients. The claim in this book "that with each protocol we were seeing a 70% success rate, and 30% were relapsing" is truly irresponsible. The author is claiming he can cure a disease that is incurable (as acknowledged to me by email from Drs. Burrascano,. Liegner, etc.). Yes, some people will respond to say they were cured. Just like Pam Weintraub thought she was cured when she wrote the first edition of Cure Unknown. And they will discover afterwards that they will eventually relapse. If the book honestly stated that symptoms can be managed using these methods in only a very small percentage of patients with advanced, long-term (20+ years of infection) Lyme disease, that would be a good start at providing informed consent. The author is nowhere close to solving the mystery of Lyme and chronic disease. He can probably alleviate the symptoms of a majority of people who have been infected for five years or so, and a small minority of people infected for longer than roughly 15 years. But he can cure nobody except perhaps somebody who had just been bitten by a tick.
If you have ME"cfs", Fibromyalgia, ALS, MS or are undiagnosed with serious physical and mental fatigue, pain and/or neurological symptoms and tired of going from doctor to doctor looking for an answer, GET THIS BOOK! Sorry to shout, but this is very important.I have been sick for 12 years with an ME"cfs" diagnosis. Only two years ago did I find out the CDC's recommended test, which they and the Infectious Disease Society of America claim is 100% accurate (sensitive and specific) is actually only 40 - 60% accurate (depending on the study). I then did an Igenex PCR test, which is much better (but not 100% accurate either- but at least they admit it), which CDC and IDSA warn against. Thanks to the Igenex test, I found out I have Lyme Disease. And thanks to Medicare, which pays for this expensive test, because they deem it "medically necessary."There are an estimated 1 Million people in the United States that contract Lyme each year, but most are not diagnosed. Many are misdiagnosed with the above-listed diseases. This is a huge epidemic.Dr. Horowitz's book is fun to read (for a medical book) and tells you what you need to know to get diagnosed and begin healing. Dr. Horowitz is recognized as the top Lyme doc in the world and this is his first and only book. Just released recently, it is up to date.Oh yeah, also get this book if you know you have Lyme! :)Enjoy and happy healing everyone!
Book came on time & in perfect condition. I was diagnosed at age 5 with Rheumatoid Arthritis & had a couple unexplainable medical problems but was overall a healthy child. I suffered from eating disorders from 14 until I just say 21 because I don't know exactly when at 20yrs old I overcame, by then just Bulimia. I accomplished that in under a year after 7 & 1/2 weeks of inpatient treatment & continued outpatient therapy only to find myself with debilitating horribly awful lower abdominal & back pain attacks along with diarrhea at times up to 30X a day. That happened in less than a year of eating normally & I was diagnosed with Crohn's Disease. Many more chronic illnesses were to follow that I tried everything modern medicine & alternative treatments had to offer. Autoimmune diseases being my biggest problem. I had Graves Disease that went undiagnosed for I don't know how many years which after a few years on medication I was told my best option was to radioactively ablate (kill) my thyroid with no mention of the word Hypothyroidism. I have never even had a year of being healthy & quite honestly I don't know what that would feel like. I thought I finally discovered my problem after around 7yrs of seeing one specialist after another with no improvement but a ton of different diagnosed diseases & medical conditions. I thought it was under treatment of Hypothyroidism & found a doctor that treated in an entirely different way than the Endocrinologist & D.O. I had been seeing. I felt as though someone has turned the lights back on but I was far from healthy but was told I had a year ahead of me to heal my immune system. After only 3 months I had a horrible setback that left me in more pain than I had ever been & unable to even sit or stand for any amount of time, constant headaches that were coming from my neck feeling as though it had turned to stone, dizziness, lightheaded, extremely low blood pressure & much more. Finally the new doctor tested me for Lyme which came back positive for 3 bans or strains. I haven't been able to get my thyroid hormone levels back to what they were for those 3 months so that causes fatigue, pain & a list of symptoms too long to write. I have done a lot of research & joined the Lyme Disease Group on Facebook which is where I first heard of Dr. Horowitz. Anyone that has Lyme Disease should read his book because there is a war going on between the Infectious Disease MDs & ilads which Dr. Horowitz is one of the cofounders of. He has dedicated his career to helping people with Chronic Lyme Disease & all that comes with it, which is what I have but is not recognized by modern medicine. Lyme has become an epidemic & many people are misdiagnosed with everything from MS to Bipolar Disorder. Many people think you must get the bullseye rash to have Lyme but many such as myself do not. I have been in treatment for 9 months now & have never been so sick. I have tested positive for one coinfection but blood tests are unreliable so a good LLMD, Lyme Literate MD, should be able to treat them according to symptoms which currently I don't have a good LLMD. I have heavy metal poisoning also which is common since the bacterial infection that is Lyme weakens your immune system leaving you defenseless to fight off common toxins we all come in contact with. Lyme can trigger autoimmune diseases so I believe I was infected as a child but I will never know when. I have found a good LLMD but can't make the 7 plus hour round trip until my thyroid hormone levels are better which takes months when they are as off as mine are. I have been told too many times to count that I'm not in the medical books, I do the exact opposite of what the medical books say & the best is, this is just impossible. For those suffering from chronic illnesses that never get better despite doing everything & anything to get better I highly recommend this book & going to ilads.org to find a LLMD to get tested. They call Lyme "The Great Imitator" because it can mimic so many diseases. I have a long road ahead of me & there is no cure for Chronic Lyme but I'm told there is a life to be lived as a survivor. I haven't done much living for the past 24yrs, just a lot of existing. Lyme is curable if caught & treated correctly but sadly most people that go through their local hospital or Infectious Disease MD are not cured & told they have to live with the effects of Post Lyme Syndrome, I believe that is correct. To be left with catch all diagnosis of Chronic Fatigue Syndrome, Fibromyalgia, sleep disorders, depression, anxiety..... My memory has been affected along with depression & anxiety. Lyme attacks your entire body including your mind.
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