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When I had Sasha in my first year of life noticed that the child lags behind in growth and naturally ran to the doctors and up to 5 years, doctors diagnosis is not put, saying it is constitutional delay of growth, as I myself not big. Every year I went to the doctors and get bored, saying to them: well, something is definitely wrong, son is up to 3 years differed from their peers. While one doctor we did not assign an analysis, hormonal examination, and this is where it all began...

Tests, insulin-like growth factor reduced, on the basis it was examined in the hospital at the hospital and test with clonidine, the night took a blood test for release of growth hormone because it is produced at night and then the result showed by far not produce its own growth hormone. There was a diagnosis of pituitary dwarfism requires lifelong therapy with growth hormone in the control of the thyroid gland. And this I know as your 6-month pregnant with a second child. The disease is rare and such children shall be obliged to provide the state with artificial growth hormone, in addition, he was not a quality product, but even with breaks in treatment, which in any case do not allow, but unfortunately the government don't have.

We are on the drug under the state program did not grow and in addition to this the blood sugar has increased, in drug treatment, "Somaton" and the growth is stable and all tests were normal, but buying the quality product has no funds. As time goes on, you need to treat now to change the final growth of the baby, it is not only growth, but also the internal organs are reduced in size, which affects the whole body. Also wrote applications in GEC on registration of inefficiency and side effects of the drug, which was given under the state program, but the situation does not change, there is help from the doctor, which shows the dynamics of growth in the drugs, and a conclusion which indicates the selection of preparations taking into account growth allowances, tests, and so on, so you need a quality product.

We have 2 years on treatment, but the money is already there to treat yourself, and the dose of the drug increases with the age, now in a month you need 7 vials "Somaton" (1 apala almost 3,000 UAH) further more, until the closure of growth zones, it is x-rayed hands each year, then for life a transition to the minimum dose to maintain the quality of life. In addition to the use of growth hormone (it's a daily subcutaneous injection at bedtime) more pills, hormonal tests and all of the funds, which are not. With treatment we grow 8-10 inches a year, without treatment grew 3 cm, and the ossification of the skeleton is, at this time to adjust the linear growth required artificial growth hormone. There is a chance to change his son's future, but without the help of people for us to cure such a child does not really! Time goes by, stabbing need every day and have time to grow before the closure of growth zones, I would like to manage to achieve acceptable growth. So pray for help!!!