Natural Sarcoid Treatment

Sarcoidosis Remission and Aden Protocol

Eliminate the primary triggers of your disease in 2 weeks (based on a breakthrough in research of underlying chemical triggers of the disease) and get on fast track to remission. Shift the chemical imbalance inside a small organ in your abdomen. This imbalance was proven to be one of the 3 primary triggers of the disease. This new-found connection changed everything. Relieve your pain almost instantly. Dissolve and Eliminate granuloma from your lungs and any other affected organs. Cleanse Your body of all the polluting residue in 3 weeks.

Sarcoidosis Remission and Aden Protocol Summary


4.6 stars out of 11 votes

Contents: Ebook
Author: Danielle May
Price: $37.00

My Sarcoidosis Remission and Aden Protocol Review

Highly Recommended

This is one of the best ebooks I have read on this field. The writing style was simple and engaging. Content included was worth reading spending my precious time.

All the testing and user reviews show that Sarcoidosis Remission and Aden Protocol is definitely legit and highly recommended.

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Chinese Secrets To Sarcoidosis Healing

The most important aspects of the program describes in the ebook are: It is research based and scientifically proven. The explanations are simple , adjusted to the Western view, specific and precise. It will allow you to discover and put a stop to the. habits, diet and lifestyle choices that are keeping. you sick and making your healing a mission impossible. It reveals all the culprits that I identified to be the. reason why people in China don't get sarcoidosis. My practices proved that once these aggravating agents are removed from your life, self-healing aided with herbs and remedies becomes simply inevitable. It reveals the remedies made from the herbal healing. agents and supplements that boost the self-healing and speed up the recovery. It will save you thousands of dollars. in drugs, doctor appointments and expensive surgeries. More here...

Chinese Secrets To Sarcoidosis Healing Summary

Contents: EBook
Author: Abe Hsieh
Official Website:
Price: $29.00

Sarcoidosis Freedom Cookbook

This e-book is a 143 pages long downloadable ebook with hundreds of delicious recipes. But these recipes are not only delicious but have another crucial feature they use only the ingredients that are carefully chosen to meet all the criteria that are critically important in our pursuit of health and sarcoidosis remission. This is how The Sarcoidosis Freedom Cookbook will change your life: You will never eat a meal that triggers your sarcoidosis again. And you very likely did it today. You will gently soothe your endocrine system and shift the ravaging chemical imbalance that is eating away your organs. Kick start the boost of self-healing chemicals that will repair your organs before it's too late. Enjoy delicious meals while knowing every second that you are doing good to your body and getting closer to remission. You won't have to think about where to start in your healing, you will have all the work done for you. When you wake up in the morning you'll feel light and positive, knowing that healing chemicals in your body are doing their work every second. You won't have to spend endless hours in front of your computer or buy nutrition books to know what is completely safe for you. Never again buy another book about diet and health, because you have it all right here and written just for your condition, not general and vague. Start your healing today, without any procrastination. Once again, feel that health and energy you so desperately pursue. More here...

Sarcoidosis Freedom Cookbook Summary

Contents: 143 Page Ebook
Author: Danielle May
Official Website:
Price: $17.00

Idiopathic Diseases Sarcoidosis

Sarcoidosis is a chronic, idiopathic, granulomatous disease with a strong predilection for African American and Puerto Rican women in their third or fourth decades of life. Patients most often present with pulmonary symptoms, including shortness of breath, hemoptysis, nonproductive cough, and dyspnea on exertion however, the spectrum of patient presentation can range from asymptomatic to involvement of any organ system. When neurologic involvement is present, the term neurosarcoidosis has been used. Neurologic involvement can be central or peripheral. Diabetes insipidus, basal leptomeningitis, and peripheral neuropathy are frequent manifestations (76). An estimated 12 of all patients with sarcoidosis and 50 of patients with neurosarcoi-dosis have facial paralysis, which remains the most frequent neurological presentation of the disorder. The paralysis can be either unilateral or bilateral in up to 33 of patients. Any case of bilateral facial paralysis deserves consideration of...


This is an idiopathic chronic granulomatous disease that occasionally affects the larynx. Peak onset is from the age of 20 to 40 years. There is a higher incidence in African Americans, Puerto Ricans, and Scandinavians, and it is sometimes familial. The pathogenesis of sarcoidosis is unknown. One theory is that it results from a mycobacterial infection. It is usually systemic, most commonly including the lungs and hilar lymph nodes. Isolated local involvement is rare, so head and neck manifestations are virtually always in the context of disease in other sites. A review of 2319 patients seen at the Mayo Clinic for sarcoidosis found head and neck involvement in 9 of cases. Of these, the eyes and lacrimal system were involved in 40 , the nose in 13 , and the larynx in 6 (10). Symptoms of laryngeal involvement include hoarseness, dysphagia, stridor, and dyspnea. On physical examination, supraglottic involvement appears as a pale and diffusely enlarged, sometimes nodular epiglottis. Vocal...

Clinical Manifestations

Uveitis occurs in a wide variety of systemic diseases including those described herein and in other chapters of this book. Several associated diseases are of primary clinical interest, although individually they are relatively uncommon or even rare in the usual practice of a head and neck specialist. Sarcoidosis is a common cause of anterior, intermediate, and posterior uveitis, which is covered in more detail later in this chapter. Other diseases causing uveitis are described in other chapters of this book and include Behcet's disease, relapsing polychondritis, syphilis, Lyme disease, cat-scratch disease, tuberculosis, fungal infection, and infection with the human immunodeficiency virus, cytomegalovirus, and herpes viruses.

Complications And Prognosis

FIGURE 2 (A) Conjunctival nodule related to sarcoidosis. Note the circumscribed epithelioid inflammatory nodule, without necrosis (noncaseating). (B) Histopathology of a similar nodule. Note inflammation in surrounding areas, including plasma cells. There are no giant cells. Source (A) Courtesy of Dr. Glenn Jaffe, Duke University Eye Center. (B) Courtesy of Dr. Alan Proia, Duke University School of Medicine, Department of Pathology. FIGURE 2 (A) Conjunctival nodule related to sarcoidosis. Note the circumscribed epithelioid inflammatory nodule, without necrosis (noncaseating). (B) Histopathology of a similar nodule. Note inflammation in surrounding areas, including plasma cells. There are no giant cells. Source (A) Courtesy of Dr. Glenn Jaffe, Duke University Eye Center. (B) Courtesy of Dr. Alan Proia, Duke University School of Medicine, Department of Pathology.

Affected Organs And Cell Types In Polyomavirusassociated Disease And Persistent Virus Infection

Pregnancy is the most common condition of altered immunocompetence that has been linked to Polyomavirus activation (Coleman et al., 1980 Lecatsas et al., 1981). The onset of virus excretion is related to time of gestation, most often occurring late in the second and during the third trimester. Once established, excretion continues intermittently to term and might even extend into the postpartum period (Coleman et al., 1980 Gardner and Knowles, 1994). Serologic studies revealed that excretion in pregnant women is usually the result of virus activation of a persistent infection. Although activation of infection had no clinical significance (Arthur et al., 1989), women excreting polyomaviruses had more illness before and during pregnancy and may have underlying diseases such as diabetes and sarcoidosis (Gardner and Knowles, 1994). When BKV and JCV viruria were differentiated, BKV excretion rates of 15-25 were observed (Jin et al., 1993 Markowitz et al., 1991). The incidence of JCV...

TABLE 5 Extraglandular Manifestations in Primary SS

Diagnosis of SS also requires exclusion of other conditions that can mimic it. These include previous radiation therapy to the head and neck, amyloidosis, sarcoidosis, lymphoma, graft versus host disease, hepatitis C virus infection, HIV-diffuse infiltrative lymphocytosis syndrome, medication-induced dryness, and uncontrolled diabetes mellitus.

Inflammatory Autoimmune

Sarcoidosis is an autoimmune disorder of unknown etiology. It affects multiple organ systems and is characterized by an accumulation of T-lymphocytes and mononuclear phagocytes causing noncaseating epithelioid granulomas. Its appearance in the oropharynx mimics that of infectious adenotonsillitis. Sarcoid frequently involves

Other Manifestations

A complete discussion of the clinical features of sarcoidosis is beyond the scope of this chapter. Briefly, sarcoidosis most commonly affects the lungs, where it may be asymptomatic or cause symptoms of dyspnea, dry cough, wheezing, and chest pain. Lung rales are heard in less than 20 of patients. The diagnosis may be aided by chest radiograph and highresolution chest CT scan showing bilateral, symmetrical lymphadenopathy with or without pulmonary interstitial opacities. Sarcoidosis may also affect other organs (Table 4). Laboratory findings include anemia, leucopenia, thrombocytopenia, hypercalcemia, elevated erythrocyte sedimentation rate, hypergammaglobulinemia, and a positive test for rheumatoid factor (due to chronic immune stimulation). The serum levels of ACE are elevated in 75 of untreated patients with sarcoidosis, but a positive test is not diagnostically specific, and its value in monitoring disease activity is controversial (30,33). TABLE 4 Other Organ Systems in...


The diagnosis of tularemia is based on paired antibody agglutination titers. Biopsy specimens of affected lymph nodes will show abscess formation with caseating necrosis. In the latter stages of the disease, the histologic picture will demonstrate granulomatous inflammation similar to mycobacterial infection or sarcoid.