Who will help Dmytryk, if we don't?

From birth we are fighting for Dima's health. From the first days of the predictions were terrible we put diagnoses: Syndrome Lipella-Crinone-Weber, macrocephaly, and next to them stood the question marks, so we don't find anything better and went to Kyiv, and there again the institutes, clinics and everything new diagnoses : Proteus syndrome, partial gigantism of both feet and macrodactylia, and besides lactose intolerance. The only thing that they advised us to have to have surgery as long as the child will grow. But there's another way out.

In March this year was supposed to be routine surgery to remove the flanks of the toes on both feet. But what will be the result of how to heal after the operation (foot increased by adipose tissue), they could not say. Will the child go? We looked for a year and finally found parents of children with similar diseases, because they are all individual, they helped us to contact the clinic in Germany in March 2015 they are waiting for us on the survey.

Dima in his 2 years very active, loves to play, run, jump, begins to speak and even read. He is very cheerful and kind, but we hate to see his manner of walking and the views of other children. Now he started to grow and his feet began to grow very quickly. We hope that the situation after the examination and treatment will improve. And much experience that our family does not have enough funds to put the boy on his feet!

Therefore, parents are asked to all the caring people to help them recover their little Dmytryk!

Name: Dmytro V. Voznyy, born 08/11/2012

Location: Khmelnytskyi region

Diagnosis: Syndrome – Weber-Klipell-Trenonne Syndrome?, Proteus – Syndrome?, Ollie Disease?, partial gigantism of both feet?, congenital malformation of both feet and left n/limb, makrodaktaliya p.right1-2, makrodaktaliya. 1-3 p.left