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| Has anyone visted Morgellonswatch.com, recently? Careful inspection of their most recent entries may reveal a small-positive adjustment in their disposition. Previously, one may reckon outlandish claims of folie de deux: Nurses and teachers, (void of any psychiatric history) would look at environmental dust on skin, and compulsively pick to prurigo. Furthermore, one bloke alleged the possibility of medical technicians injecting fibers under themselves to gain support for this "internet disseminated somitzation disorder". Much is to be realised and revealed to these vocal skeptics; however the tone has shifted towards better recognition of sufferers experiencing real physical pathologies. The narrator even recently reprimands a recent article in an Annapolis newspaper implying our experience as mass hysteria. He continues to support the null hypothesis; How could he have single-handedly ascertained no common exposure pattern in geographical clusters. Credible scientific and medical journals have alluded to incidents of mass porphyria and toxicity epidemics. Rest-assured, many of these historical and potential contemporary exposure patterns, should prove treatable. And there may or may not be elements of opportunistic, non-communicable infections, resulting from such exposures. No doubt, it appears so from my experience. Let's strive, on our end to maintain broad perception and avoid the "polarity mistake" of our traditional skeptics, along with some organizations alleging support of our cause, driven by ulterior motives. I digress again. Let's consider some very arrogant statements made by critics may have been driven by ignorance. While this group stands quite away from describing our picture, it is progress. E |
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| well morgellons watch was founded by a retired computer programmer in la who wished to prove his point of morgellons disease was right that it does not exist, to merely prove an argument like on a high school debate team. on a debate team, it is not even who is right but who argues better. the folks who make up their message board, many of them consist of dermatologists biomedical, sceptics a few small number of the sick with morgellons disease seeking help. yes they have softened their view because of folks like me who are living proof it is systematic and not just skin. that there is physical neurological damage and not just mental. that environmental factors can come ito play. if you want to feel real good go to morgellons.com look under publications and dr. harvey letter to the editors of a prominent dermatology magazine. will be the most recent one. the problem is, on morgellons watch they are discovering there are rational folks out there who have physical stuff going on. they are even awknologing not all of us need psych drugs. and their power compared to ours is waning because the truth shall come to light over time (LC). |
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| We will win! PS: Can't testify to the validity of this site; however, it appears the CDC has publicized a request for proposal for a private contractor to investigate Unexplained Dermopathy. The contract is to be awarded by August 31 2007. This is the source: http://www.fbodaily.com/archive/2007...O-01342706.htm Hopefully, more progress for everyone in the right direction. The seven month project scope further implies why we should all continue to work in synergy to push one another towards remission. |
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| i like your thinking, evdown this a goal i want too, for those who come here to find remission. frankly this is the best place to find it, without having to worry about being harrased by advertizers. a place we can come, talk and heal and share our findings. (LC) |
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