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Cystic fibrosis and Pulmonary Adenocarcinoma lung cancer both metabolic and dietary acidic conditions of the interstitial fluids of the interstitium

Joint Meeting on 2nd Annual Congress on Bacterial, Viral and Infectious Diseases & 6th International Conference on Rare Diseases & Orphan Drug

Robert O Young

PH Miracle Center, USA

Keynote: J Infect Dis Ther

Abstract
Cystic Fibrosis (CF) and Pulmonary Adenocarcinoma (PAC) have similar symptomologies and are chronic, progressive and frequently fatal acidic conditions of the respiratory system (lungs), lymphatic system (lymph nodes), intestines, pancreas, urinary tract system, reproductive organs and the skin as the alkaloid glands (the salivary glands, stomach and small and large intestines) produce and secrete alkaline compounds, such as sodium bicarbonate to buffer and preserve the alkaline design of the body and the specific organs and glands affected. These metabolic and dietary acidic conditions resulting in the build-up of mucous can affect any organ or organ system but primarily affects the respiratory, lymphatic system, digestive and reproductive tracts in children and young adults with CF and the lungs and surrounding lymph nodes in PAC. I have suggested from my own clinical research that both of these conditions are the result of Latent Tissue Acidosis (LTA) in the interstitial fluids of the Interstitium or the fluids that surround every cell, created from metabolism, diet, thoughts and environment and may be successfully treated and reversed with an Alkaline Lifestyle and Diet (ALD).
Biography

Robert O Young is currently working as a Professor at Capital University in Washington, DC. He has completed his MS in Nutrition from the American College in Birmingham, Alabama and DSc with emphasis in Chemistry and Biology and also s PhD from Clayton College of Natural Health.

E-mail: phmiracleliving@aol.com

 

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