Little Dima cannot without water

The Petersburg charity foundation "Alyosha" continues fund raising for little Dima from Izhevsk which passes treatment in the city on Neva. In March to the boy three years will be executed. It has a serious genetic illness a lamellyarny ichthyosis. As well as at "children butterflies", at suffering from an ichthyosis skin is affected. The child cannot simply live without water and moisturizing cream. In Russia the disease is not treated. Hope for doctors from Freiburg. Inspection and treatment cost – two million rubles. While it was succeeded to collect only 260 thousand.

Alyosha Charity foundation repeatedly requested to "Fontanka" the help to Dima.

At present collected 261 thousand rubles. Remained 1 740 000. Funds need to be raised until the end of spring.

we Will remind p history of the boy according to his mother:

"The child need to be smeared

to 5 times per day with special medical cosmetics. Cream constantly we change since skin gets used and it is humidified less, – mother Natalya tells. – According to the preferential list we do not receive anything since these cream are cosmetics … We bathe on 2-3 times a day with addition of special means for moistening. In eyes we put gel for moistening mucous on 4 times a day, at night Dima sleeps with half-open eyes and a mouth therefore we bring cream and at night too that the child did not dry up and did not scratch till it bleeds. Because of a permanent care of the child I cannot send him to kindergarten and go to work. The disease is not treated in Russia, and the University clinic of Freiburg (Germany) invited us to diagnostics and carrying out genetic dough, after delivery of all analyses, treatment for the sum about 2 million rubles which we not in forces to pay will follow also. To us not to do without assistance, very much we hope for your kind hearts. In advance many thanks".

Dima's Page and ways of the help on BF "Alyosha" site.