PLEASE SUPPORT FOR HIRA BABY!

PLEASE SUPPORT FOR HIRA BABY!

Hi, I'm writing here to ask you for your signature for my nephew, Hira, a half month old. I would like to thank everyone in advance for reading and sharing my time.

Unfortunately, babies with hypophosphatasia and infants who do not start treatment can live for a few years at most. Unfortunately, we learned this with a very painful experience because we lost Hira's older brother from the same disease.

That's why I want your signature so that a parent doesn't bury their second son. Please support us for the necessary treatment.

Hypophosphatasia is a rare disease.

None of us can choose the family we will be born into. Had Hira been the daughter of a wealthy family, a long life would have been waiting for her. He and his brother were going to have little fights in between, playing games together.

However, if he doesn't get treatment now, his life will end like his brother after a few years. Because Hira's father is a construction worker and her mother is a housewife. I can't digest this. Believe me, it's not easy.

Turkey is a big country. A great state. I would like to think that the Ministry of Health will not allow a lost family to lose their second child according to the same illness. So I invite everyone who reads these lines to help.

Hira may not have chosen the family she was born to, but that's why we have to keep her from dying. Please support for the necessary treatment.

I would like to thank everyone who feels our sorrow and is there with their support.