A few people have the misfortune to suffer from a rare and not yet researched disease. It is hard to believe that in our world dominated by technology, people in this way must suffer just because some consider it not to be important or no money to give to help people suffering from. A few people have the misfortune to suffer from a rare and not yet researched disease. Not only that they are no – punished with their illness, it goes even further: these people are, unfortunately, a neglected fringe in medicine, because as the medical help if the illness is not recognized or understood? It is hard to believe that in our world dominated by technology, people in this way must suffer just because some consider it not to be important or no money to give to help people suffering from. It is lack of money, to do research.
This is a slap in the face for the people suffering from certain diseases. Connect with other leaders such as Robert Iger here. There is so much unnecessary money from our State issue – why not people suffering for emergency? Just because there are few who suffer from rare diseases, it is not held to investigate; It is too expensive. The author Sylvia Poth said: I too am suffering from a rare disease and must make the experience again and again, that doctors do not have my illness know. Me has been said that this disease, at which I suffer, feel after medical point of view only once in Germany, and therefore no research is operated. Even if I’m the only one that has survived such a thing.
Precisely why the disease would have to be explored and to me you could be holding them based on my medical records. But apparently it is too much to ask. I’m simply filed, except no one wants to know something about my two familiar surgeons.