For those who are not familiar with Morgellon disease, it may seem like a disease that comes out of science fiction, but for those suffering from bazaars and painful symptoms it is too realistic is.
People who explain the symptoms of Morgeron's disease as early as 1985 have been reported, but this fiber disease is better known around 2000.
What makes this skin disorder so mysterious? People suffering from this disease explain a series of embarrassing symptoms.
The website Morgellons UK reported that people with Morgellon have problems with their systemic system (skin, including hair, scales, feathers, nails and their accessories), the cardiovascular system, the endocrine system and the digestive system ing.
With such a series of symptoms, it is not obvious why it is difficult to obtain a correct diagnosis.
One of the main symptoms is that the bug sensation creeps under the skin.
The symptom that makes this disease unique is a filament that protrudes from lesions formed in various parts of the body. In fact, the other name of this disease is fibrosis or Morgellons fiber disease.
In 2006, Dr. Randy Wymore asked a Tulsa police researcher to inspect the fiber taken from one of these lesions. According to his findings, comparing this filament with 100,000 fibers and other similar samples, the FBI file was included, but none of them matched.
The results of this study seem to cause these filaments extracted from the lesion to pause the idea that garments or other materials can rub against the skin.
In addition to the problem for the physician to correctly diagnose this disease, there is no diagnostic symptom standard or agreed standards.
In fact, the medical community can not agree whether the disease is a new disease, or whether people exhibiting these symptoms have a common cause of symptoms, or whether they share a common risk factor.
Researchers have no idea whether this disease is contagious or not. In some families, only one person reports symptoms, but other families may have more than one person. Interestingly, it has also been reported in dogs and horses.
Dermatologists and psychiatrists do not regard this disease as new and continue to see it as evidence of other medical conditions such as Leigh's disease. They often diagnosed this condition as delusive parasitosis. It's all in the patient's head.
In some surroundings, parents who took the child to the doctor are diagnosed with Munshausen.
The reasons why the medical community is not interested in this disease are puzzled by people trying to find answers to skin problems.
Thankfully, research has begun. The disease management center started collaborative research with Kaiser Permanente. This research is in progress and results have been published to date.
This study is the ray of people suffering from Mongolians.
Mayo Clinic gave the best advice when they suggested treating the symptoms. If there is no proven treatment for this disease, it seems to be the best way to treat Mongolian disease.
