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Hazat Özkan and his family in Izmir's Shimmer Muscle Atrophy (SMA) face the joy of leaving the days behind the announcement of the "initiation of individual drug supply requests" from the Ministry of Health covering patients with Type 2 SMA and Type 3 SMA.
According to AA; Hatice Özkan, a 37-year-old woman living in Narlıdere, where she is diagnosed with "SMA", also known as "muscular disease" at the age of 10 and has two years of life, is an example to everyone with loyalty to life.
Özkan, who began education with the support of his mother Hatice Özkan, kept her in contact with her computer chief and graduated from the Department of Justice of the Faculty of Economics at Anadolu University with distance studies and Atatürk University, the Department of Justice . the patient is happy to receive the requests.
"I was very happy when I learned the news"
Hatice Özkan, announced the news with a friend, wrote a message while using the computer and said he was very happy.
A disease without treatment for many years as he and his family saying Özkan, "the Health Ministry has previously given medicines for the treatment of SMA Type 1. Patients will be covered now. I used my hand before, like swallowing and chewing I could I will be very happy if you will perform these functions again. " he said.
Ozkan, who share the same fate with the beginning of the request, expressed that he is very pleased.
Ozkan said he had been looking forward to starting demand and using the drug. He thanked all the authorities.
Mother returned to Özkan said that her daughter had a hard time because of the years spent unfortunately.
Ozkan said that the news he had heard on TV: "I am very happy that I have waited many years for the approval of the Ministry of Health and I thank all those who have contributed." I hope that hands and girls holding their hands on their own can do something in my days that I want to see. "He said.
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