Health Minister Endang Rahayu Sedyaningsih visit Gullain disease patients Barre Syndrome (GBS), Safa Azalia (4) at St. Carolus, Jakarta, Monday, August 1, 2011.During his visit, the Minister of Health admitted that the disease is a rare type of disease.
"It is indeed rare. The trouble is that we as yet have a cure. So that could be done until now only treat it, keeping alive on a ventilator but did not know when it ends well," said Endang.
Therefore, Endang proposed Public Health Service, Health Center or IHC needs to take measures for dissemination to the public. However, Endang said the disease is difficult to prevent. "Difficult, yes, because rare. When there are symptoms of the best step is immediately brought to the hospital, the nearest health center," he said.
Associated with the patient, Azka (in Bogor) and Safa, Endang promised to pay more attention to both. It's just that given the enormous cost while the patient's recovery time limit of GBS is unknown, Endang said the government could not bear the self-financing.
"Maybe We Can help it is only partly Because of our budget is limited, it may not help thisThat Continues, what about other diseases. We were really asking for help andhimbauannya to Philanthropists and Journalists to help, '"Endang said.
As is known, Muhammad Azka Arriziq (4) and Safa Azalia (4.6) suffering from GBS positive. According to health experts, GBS should be wary because it included a rare disease. If you had the disease then the lifetime of GBS patients will live with GBS. Can lead to death if mishandled.
The disease is found since the year 1916 by two doctors of France, Jean-Charles Alexander Barré and Georges Guillain, but GBS patients are still rare in Indonesia even the world.
From medical recap, in GBS patients a year and most of 1:40.000 just less informed what it is so often mistaken for GBS disease or cikungunya weak wilt. Whereas if delayed treatment, patients with GBS within hours of being confronted with the abyss of death

Tidak ada komentar:
Posting Komentar