The project «The life as a miracle» of the charity foundation «Family. Traditions. Mercy»

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Endzhe Galimullina

Village: Baltasi, Republic Tatarstan

DOB: 31 October 2010

Diagnosis: Glycogenosis 1А, hypoglycaemia

The help is rendered: 3 821 100 rub.

When: 15 October 2011 г.

Documents

In order to avoid copying of documents by swindlers, we have made decision not to publish official documents on a web-site (accounts on payment, abstracts of medical record etc.), and to give the necessary information on demand.

The second child

Endzhe Galimullina has glycogenosis of 1А type. It means that her sugar regularly falls to the lowest values. That she has the strict diet — in two hours in the afternoon and in an hour at night she needs to eat the dissolved corn starch. In the long term it means strong backlog in physical development, and frequent spasms and the losses of consciousness arising against falling of sugar, through any time, most likely, will cause cerebration infringement. Behind examples far it is not necessary to go — Endzhe has an older brother, Idris is suffering same illness. That Idris and Endzhe have genetic, instead of the casual mutation, was possible to find out only after a birth of the girl. A unique way to get rid from glycogenosis is to make liver transplantation. The «Cliniques Universitaires St. Luc» is ready to accept the babe. On operation 94 000 euros are necessary.