Date:   1/3/2017 11:17:46 AM ( 8 y ago)
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URL:   https://www.curezone.org/forums/fm.asp?i=2349557

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Hi.

I have a nasty parasite resistant to Albendazole. After 50 doctors and 20 years with bad symptoms, including severe muscle tightness and pain-mostly in back bicepts, and diaphragm, and some Sugar imbalances. Also, night sweats, fever, and chills (when it got severe), I finally tested positive for Trichinosis, a food borne roundworm that gets into and lives in skeletal muscle. It has made my life hell. Before we found this, I was on Rifampin and Metrodazole thinking it was Bartonella with Giardia, and the meds stopped the illness but never cured it. Albendazole keeps me from having the symptoms too, but doesn't kill most of muscular trichinosis. I recently found a doctor-peer-reviewed article that Emodeside works on muscular trichinosis. They just finished a clinical trial in London with healthy individuals in Oct 2016. They found Emodepside safe. There is no report completed and published yet. The trial I found is on clinical trials government website.
Albendazole causes bone marrow suppression and I was getting colds and flu's and my hair started coming out (not noticeable, but lots on the brush) after 5 mths on it, so I had to get off it. Back on Rifampin and Metronidazole. I am trying to find out when Emodepside will be available to humans. Hope this helps. By the way, Emodepside comes from a fungus called Mycellia sterile that grows on the Japanese Camillia plant. They use a metabolite (a chemical daughter is what they call it) called PF1022 to make it.
A note: If you have vision issues not from one of the meds, it is probably Toxoplasmosis. Causes a lot of the same issues as Trichinosis but somewhat different. They both cause Sugar imbalance, weight gain, and diabetes. Toxoplasmosis causes blindness but is reversible. Treated with 6-8 weeks of Clindamycin.
Have you heard any new info of release of Emodepside for humans in any country yet?
 

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