hacked By Fallag Gassrini


Hacked By Fallaga Team | El Gass bou3asba

HaCkeD by Fallaga Team<br />

Hacked By Fallag Gassrini

Fuck MuhmadEmad Fuck MuhmadEmad Fuck MuhmadEmad Fuck MuhmadEmad Fuck MuhmadEmad
This Kids Know just Using MyTools Then he Call him self Pro xD LOL Fuck son of bitsh
THIS IS MY DICK FOR UR MUM AND UR SISTER SUCK IT MADAKER
Long Life Tunisia Long Life Palestine Long Life Fallaga Team

Gassbot@gmail.com
FUCK You All Mafakerz !

Morgellons Syndrome And What You Can Do About It



by Amir Alwani
PotentNews.com
November 29, 2012

As many of us now know, a vast amount of airplanes are currently spraying most of the Earth’s population with aluminum, barium, strontium, etc.  Less discussed components of the spray programs include lab-created synthetic life-forms and other biological materials such as red blood cells, fungus, and self-replicating nano-fibers.  Massive and diverse geo-engineering operations are indeed occurring.  Moreover, a peculiar syndrome called Morgellons has emerged and has now been linked to these eugenics/transhumanist operations.

While this is alarming, humanity should at some point face the ugly details of this dilemma.  This is an agenda partly involving a nano-technology infestation in our bodies.  Potent News Blast #10 seeks to shed some light on this often neglected issue:

 

 

What You Can Do About It

As creepy as all this is, there is room for hope.


August 17-19 of 2012 represented the coming together of some of the most prominent chemtrail researchers at a historic conference and fundraiser event in L.A., California titled Consciousness Beyond Chemtrails.  The event was also the premier of the documentary film Why In The World Are They Spraying? and even well known public figures like Cynthia McKinney and Rosanne Bar spoke at the conference to show their support.  DVDs of the fundraiser are still available and all proceeds apparently go to Morgellons research, namely Morgellons Research Group and Carnicom Institute.

A recent Carnicom Institute newsletter has also mentioned that there currently is a petition on the White House official website asking the Obama Administration to honestly investigate Geo-Engineering, HAARP & Chemtrails.  Since its inception 2 weeks ago, it has accumulated over 4000 signatures (with the goal being 25,000 by Dec. 14, 2012).

[UPDATE: Here’s a new petition which calls on Congress to put a stop to the secretive and deadly geo-engineering program(s).]

The general increase in awareness on this subject is refreshing.  Even as far back as two years ago chemtrail protests were happening in places like the UK and Italy.  Now similar chemtrail rallies have popped up in places like Greece and New Zealand.  The movement is gaining ground.

But what can be done about chemtrails and Morgellons to yield immediate effects for our bodies here and now?  To answer that question I’ve included some very instructive videos that summarize Gwen Scott’s excellent dietary suggestions and also Ken Rohla’s fascinating research into orgonite.

 

Maps of Morgellons Research Foundation Registrants in the United States

 

The Morgellons Research Foundation (MRF) has received registrations from people reporting this condition from all fifty U.S. states. The MRF has also received registrations from people reporting this condition from 45 other countries, most notably Canada, Australia, England, South Africa and the Netherlands.

U.S. Families Registered


Note: The maps below are based on U.S. families who felt that they fit the criteria for Morgellons disease, and were motivated to register with the Morgellons Research Foundation. These are all self-reported cases, and likely do not represent the true number of families affected by this illness. Although this is clearly not a methodical study of an officially defined disease, we feel that the numbers below justify an official, unbiased investigation of this situation.

morgellons disease Usa


 

 

California Families Registered

Note: Although California represents 12% of the US population, 24% of all families in the U.S. who have registered with the Morgellons Research Foundation reside in California.

 

CA


 

 

Texas Families Registered

 

geogra1

 


 

 

Florida Families Registered

FL

 


 

 

 

 

Morgellons Disease symptoms


Morgellons Disease

Most individuals with Morgellons disease report disturbing crawling, stinging, and biting sensations, as well as non-healing skin lesions, which are associated with highly unusual structures.

Symptoms

These structures can be described as fiber-like or filamentous, and are the most striking feature of this disease. In addition, patients report the presence of seed-like granules and black speck-like material associated with their skin. Fig 1. and Fig 2. below show Fibers emerging from a lesion on child’s lip at 200x.

morgellons disease symptoms

morgellons disease symptoms

Fig 1. 200x.

morgellons disease symptoms

morgellons disease symptoms

Fig 2. 200x.

 

Although skin symptoms are of particular interest to this foundation and are extremely troubling to patients, they are also a vital clue that something is terribly wrong with the body. More significant than skin symptoms, in terms of the diminished quality of life of the individual with this illness, are symptoms unrelated to skin, to include Chronic Fatigue Syndrome (CFS), Fibromyalgia (ME), joint pain, and significant problems with concentration and memory.

Remarkably, not all people with this disease have overt skin lesions, as some individuals report intact skin. The troubling sensations and accompanying physical structures, are the consistent clues to this infectious process.

 


 

 

How can these unknown fibers be described?
The unknown fibers associated with skin lesions can be described as coenocytic (aseptate), smooth-walled, branching, filamentous objects.

 

SETHS-HAIR

The elongated fibers are often twisted into balls or what appear to be bundles of fibers, as they grow within the skin. Many people refer to these bundles as fiber balls, fuzz balls, or lint balls. The fibers are clearly hyphae-like structures, and yet, do not fall within the description of known hyphae or pseudohyphae. The fibers are most often white, but are also consistently seen as blue, black, and rarely red.

 


These fibers exhibit a high degree of autofluorescence and are not textile derived. Fig 3. below shows striking autofluorescence of fibers from the skin lesion on the child’s lip.

Fig 3. Autofluorescent fibers.

Fig 3. Autofluorescent fibers.

Nothing was added to skin sample, except Gel/Mount mounting media and coverslip. Image is an overlay of red and blue images. Imaging was done using an Olympus Provis Microscope which employs standard wavelengths for rhodamine (Excitation 550 nm/ Emission/565 nm ) and Fluoroscein/alexa 488 (Excitation 494 nm/Emission 519nm).

Frequently Asked Questions


Frequently Asked Questions

  1. What is Morgellons disease?
  2. Where did the name “Morgellons” come from?
  3. What is it like to have Morgellons disease?
  4. What is the source of the skin lesions and fibers?
  5. Could this be bio-terrorism?
  6. Is there a cure?
  7. Does anyone care?
  8. What is the treatment?
  9. Who suffers from Morgellons disease?
  10. How is the CDC responding to this crisis?
  11. How are physicians responding to this crisis?
  12. How can I help?
  13. How can I receive the latest news and developments in research?


  • What is Morgellons disease?
    Morgellons disease is a poorly understood condition which a growing number of physicians believe to be a chronic infectious disease. The disease can be both disabling and disfiguring. The symptoms include itching, biting and crawling sensations, “filaments” or fibers which emerge from the skin, skin lesions which range from minor to disfiguring, joint pain, debilitating fatigue, changes in cognition, memory loss, mood disturbance and serious neurological manifestations. Although the Centers for Disease Control and Prevention (CDC) is currently investigating the disease, it is not yet fully recognized by the medical community. At this time, the cause of Morgellons disease is unknown and there is no known cure. Morgellons Disease is best explained in detail by our Case Definition.Back to top

  • Where did the name “Morgellons” come from?
    The name comes from a condition involving “black hairs” emerging from the skin of children that was documented in France in the 1600’s. It is unknown whether that description is related to the illness we are now describing. However, the similarities were such that the name seemed a unique label for an illness not described by any other medical label, and thus became a much-needed niche for patients otherwise falling outside the present medical paradigm. The name “Morgellons” was intended to be used as a temporary label.Back to top

  • What is it like to have Morgellons disease?
    It is difficult to understand the tremendous suffering caused by this disease. Many patients report feeling abandoned by the medical community, as they experience increasingly bizarre, disfiguring and painful symptoms, while often being unable to receive medical treatment for their condition. A large number of patients become financially devastated and without health insurance because they can no longer work. Most people who suffer from Morgellons disease report feeling frightened and hopeless.Back to top

  • What is the source of the skin lesions and fibers?
    So far, we have no idea whether Morgellons skin lesions and related material such as colored fibers are (1) biological agents, (2) produced by such agents, (3) are products of the body’s attempt to rid itself of pathogens, or (4) an aberrant body system unrelated to any agent. Serious efforts are finally now underway to characterize the dermal-related material that should solve part of the puzzle.To date, various clinicians have seen,and occasionally identified, certain common dermato-pathogens OR organisms not found on humans but on animals or on inert material. This suggests the possibility that the skin immunity of Morgellons is seriously deficient, allowing numerous animal or plant parasites to live on human skin. Experience and information from registrants leads us to believe the skin phenomena of Morgellons is not specifically dangerous, although possibly frightening and uncomfortable. The same information sources lead us to observe that treatment addressing the more global symptom set also resolves the skin symptoms and signs. The treatment presently most successful is antibiotics addressing one or more candidate infectious bacteria or protozoa.Back to top

  • Could this be bio-terrorism?
    NOTHING that we know from credible sources even suggests this. The cause is likely known bacteria missed by science because of incorrect early assumptions, much like Marshall’s finding Helicobacter pylori, a common “good” stomach parasite turned out to be the primary cause of certain ulcers and gastritis…NOT stress and pizza.Back to top

  • Is there a cure?
    Most Morgellons patients, if found positive for Chlamydophila pneumonia, a Babesia species or a Borrelia species pathogenic to humans and given appropriate antibiotics long enough, resolve most symptoms. Research and clinical experience are still too early, and numbers treated too few as yet, to know whether present treatment success will mean total, once-and-for-all cure. Many Morgellons patients are improving significantly.Back to top

  • Does anyone care?
    WE care! With each successive month, more professionals are becoming aware of Morgellons and treating it. The US Centers for Disease Control and Prevention (CDC) has now undertaken the task of helping to further characterize the illness. Eventually, the truth, whatever it may be, will prevail, and with ultimate answers will come ultimate caring.Back to top

  • What is the treatment?
    The concept we now find most useful has, as mentioned above, lead us to effective treatments. This MRF will continue to move through the necessary steps of fully characterizing the illness, understanding its biological mechanism, determining any involved agents, and identifying them in detail…and finally, refining treatment for rapid and complete recovery. We ARE moving rapidly now. We ARE seeing effective…though not yet always complete…treatment. Funds to bring in additional researchers, collaboration with credible institutions and individuals, and eventually entry of the NIH and full medical community, are the fuel needed to end the existence of this nemesis. If you wish to contribute towards these efforts, you are most welcome. Please visit our Advocacy/Volunteer page.Back to top

  • Who suffers from Morgellons disease?
    There are more than 13,000 families who report that they suffer from this disease, but it is believed that the actual number may be much higher. Many of these reports involve multiple family members, including numerous children suffering the effects of the disease. According to reports from parents, many of these children are no longer able to play sports or attend school, due to fatigue, pain and difficulty with mental concentration. Adults are equally affected by this illness and many eventually become unable to work.Back to top

  • How is the CDC responding to this crisis?
    The CDC is currently conducting an epidemiologic investigation of the disease. CDC has awarded a contract to Kaiser Permanente’s Northern California Division of Research to assist them in this investigation. You can read more about the investigation on the CDC website. Private research is needed to augment this government investigation and help bring us faster scientific answers. For the history of CDC action with regards to Morgellons disease, please see our CDC Timeline.Back to top

  • How are physicians responding to this crisis?
    Some physicians are attempting to treat patients with this illness, though they do not understand its cause. Since the disease cannot be found in medical textbooks, many other physicians dismiss these symptoms as psychosomatic, and may misdiagnose their patient with “delusional parasitosis,” a mental condition where people imagine that they are infested with parasites.Back to top

  • How can I help?
    Please consider making a donation. Research is desperately needed to understand the cause of the disease and to find a cure. The MRF has been approached by several institutions that are interested in conducting research. Although the MRF has given seed money to three institutions, at this time, the MRF lacks sufficient funds to fully support these researchers.You can also check out our advocacy pages for ways to get involved and help the cause.Back to top

  • How can I receive the latest news and
    developments in research?

    When you register, you will be placed on our Newsletter mailing list. We also are taking note of the states where patients and their family and friends are living. If you would like to see the states where we see the greatest number of reports of Morgellon disease, go to the geographical maps.Back to top