Explanation of colored fibers in skin by angrymorg ..... Morgellons Disease Forum
Date: 12/2/2010 2:10:34 AM ( 15 y ago)
Hits: 3,651
URL: https://www.curezone.org/forums/fm.asp?i=1732530
Finally got in touch with old college professor. He is no longer in the scientific research field...an unfortunate loss. Also had to stop the Conspiracy thing...son is with the U.S. Intelligence Agency now and reports regularily to Pres. Obama. Nothing like having to bite my tongue for help, but this guy comes severely connected to the Science field. So here's what he had to say about the Morgellons delema. Said the only thing that can produce fibers that would be in various colors is FUNGUS!!!!! Not to say there aren't underlying bacteria involved or something parasitic. He told me Kaiser Permente was useless to determine anything about this disease. He said the only research they would take part in would be to find numbers infected and investigate the costs of medical expenses involved (how ironic they would be the first involved). He said the Military Institute of Pathologist is exceptional in disease research and should have been able to find the cause and cure fairly quickly. Basically, he told me something is bad wrong that nothing is being done regarding the CDC. He also said it is not logical for a physician to diagnose delusional or any other mental condition for someone who has chronic lesions that don't heal. He said lesions are connected to things like diabetes, cancers, and more serious illnesses especially when they don't heal over long lengths of time. That it is a sign of serious infection and he is baffled that we are not getting anyone to issue further and more in-depth testing. In other words....again....something is not right about this situation. He suggested bringing in a microscope or magnifier with you on the appointment to force the physicians to look at your skin. Reason for this...he said 99.9% of medical doctors don't even probably have a microscope in their office. He said the delusional diagnoses is saying, "Your doctor doesn't believe you!" He advised me to look into a faculty member at a University for further assistance in testing skin, soil, water, etc. He said no private lab will do anything without huge funds for research, but a University may take it on out of curiosity. He said they also, if from a prominent school may also give us the reinforcement we need to pursue things legally to change the way the disease is viewed. Another suggestion was to form a National organization which would allow us more media coverage contacts and allow us personal meeting with governmental officials. In other words, we would be taken more seriously rather than a single individual just whining...which is what he said we are probably all being viewed as when we call the local health agencies and CDC as of now. He said grouping would pay off over time. Those intested in participating in the formation of a National organization please email me.
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