cobbiemommy Posted October 30, 2011 Report Posted October 30, 2011 One of son's blood tests from one year ago, stated he had Chlaymidia Pneumonia (CPN). Has anyone here treated for this and if so, what did you do?
JuliaFaith Posted October 30, 2011 Report Posted October 30, 2011 Ds was diagnosed with this, in addition to, mico pneu. This was after several neg. tests results from prior doctor. My son's ND has him using a nebulizer (~$100 from compounding pharmacy) with liquid iodine from Tri-Quench - Scientific Botanicals (3-4 drops). She told him to do this once at night for 1 year. He is almost at the 1 year mark so will see if done yet. From what I hear these pnuemonias are difficult to get rid of. This is just one of many treatments he does daily.
jenf Posted October 31, 2011 Report Posted October 31, 2011 Hi Cobbiemommy, I have Cpn and have found the website http://www.cpnhelp.org/ to be helpful. Treatment can vary, but it mirrors long term Lyme treatment. There's a bunch of research that's been done at Vanerbilt University on Cpn as it relates to those diagnosed with MS, so that may be helpful to you. The wife (Sarah) of the micobiologist who discovered the link can be found on the This is MS forum, under the "Antibiotics" section. If you need any other info, pm me and we can discuss more in detail. Jen
philamom Posted October 31, 2011 Report Posted October 31, 2011 My dd's C. Pneumoniae IGG is 1:128 (ref range is <1:64). Her IGM and IGA are in normal range. She is not being treated for it...I will inquire why at our next LLMD appointment.
sophia smith Posted November 1, 2011 Report Posted November 1, 2011 No..I never treated such pneumonia before this..Even I am listening this 1st time...I am sure there will be best treatment available..You have to see expert doctor as soon as possible...
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