Hatice Özkan and his family at the type 2 Atrophy Muscular Atrophy (SMA) in Izmir have the joy of leaving hard days after the announcement of "starting individual claims for drug supply" by the Ministry of Health; n covers type 2 SMA and type 3 patients.
According to AA; Hatice Özkan, a 37-year-old living in the Narlıdere area, where she is diagnosed with "SMA", also known as "muscle disease" when she was 10 months old and He has two years of life, sets an example to everyone with loyalty to life.
Özkan, who started her education with the help of her mother Hatice Özkan, kept her in touch with her computer head and the Department of Justice Department completed the Faculty of Economics of Anadolu University with a distance education and Department of Justice, Department of Justice. It also worked individually for SMA Type 2 and Type 3. the patient is willing to accept their applications.
"I was very happy when I learned the news"
Hatice Özkan wrote the news with the help of a friend message when using the computer and said he was very happy.
A disease without treatment for many years is that he and his family declare Özkan, "The Ministry of Health had given drugs for the type of SMA type 1. Patients will be covered now. I have I used to use my hands from before, such as swallowing and baking, I would be happy to fulfill these functions again, "he said.
Ozkan, who shares the same fate as he started the application said he was very satisfied.
Ozkan said he was still dissatisfied to start the application and use the medication. He thanked each authority.
Mum returned Özkan said her daughter had a tough time because of the inconvenience years spent.
Ozkan said the news he had heard on television, "I am very pleased, we have been waiting for the Ministry of Health's approval for many years. Thanks to everyone who contributed. I hope that my hands and women who hold their hands alone do something at my own time I want to see it. " he says.
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