Guest guest Posted March 8, 2011 Report Share Posted March 8, 2011 Hi all, I'm wondering if anyone is familiar with Klinghardt's KPU/HPU theory/protocol (http://planetthrive.com/2010/04/hpukpu-protocol-for-lyme-and-autism/). I am unable to do a search in the messages here for some reason, so I apologize if it's been discussed before. Klinghardt found that his lyme and autism patients who did not progress in their recovery many times had an underlying condition known as hemopyrrollactamuria (HPU), also known as kyptopyrroluria (KPU). HPU is a severe but reversible deficiency of zinc, biotin, manganese, vitamin B6 (or P5P), and arachidonic acid. When treated for this condition, his patients were then able to move forward in their treatment with success. I suspect I might fall into this category. I am wondering if this condition is caused by mercury poisoning. When I started this chelation protocol in 2002, I had normal mineral transport. Years later when retested, I had severe mineral deficiencies including taurine, magnesium, B6, and others. Just wondering if anyone is doing the HPU protocol concurrently with this chelation protocol, or if the chelation protocol alone will address any HPU issues without extra supplementation. Quote Link to comment Share on other sites More sharing options...
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