LittleLab4CF

CF diagnosis at 52yrs by sweat chloride test and clinical presentation. Genetically a carrier of S1235R. Insufferable Know-it-all. Enjoying every minute of my life. I am a polymath, a gift tempered by dyslexia, CF and really bad handwriting. A child with a doctorate in genetics and a strong engineering background I have had such fun and excitement in the pleasure of learning and the outright thrill of experience.

I divide my time between CF research and robotics.

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67yr. old man, DX CF 2002 by sweat test. Heterozygous S1235R revealed by genetic testing in 2003 & 2012 accepted secondary mutation. 7T, 7T polymorphism established to be virulent. Classification review in 2017 remains CF diagnosis.

Complete pancreatic atrophy, Bronchiectasis, MRSA, osteoporosis, small duct disease, charming personality.

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