Diagnosis: Cerebral spastic infantile paralysis, a double gemiplegichesky form in the form of spastic tetraparesis with a delay of stato-motor and psycho-speech development.
Hello, my name is Olga. I am mother of the wonderful, beautiful and lovely kid Chichko Vanya, I write you in hope about the help to my sonny.
Now we are 2 years old our diagnosis – Cerebral spastic infantile paralysis, a double gemiplegichesky form in the form of spastic tetraparesis with a delay of stato-motor and psycho-speech development.
Pregnancy proceeded without complications till 30 weeks, but on the 30th week the stomach bottom has begun to hurt, me have put on preservation, next day I had a loss of loops of an umbilical cord, doctors have performed operation Cesarean section to rescue me and the child. Childbirth was heavy the child was born very small and weak, didn’t breathe, the body weight of 1 kg 300 гр., height is 47 cm, a surrounding goal. 28 cm, surrounding гр. 28 cm, scale Apgar 4-6 points.
Reanimation in the rodzal, IVL, transfer to OPN for the 9th days where it was treated with the diagnosis Atelektatichesky pneumonia. Hypoxemic – hemorrhagic encephalopathy in the form of IVK 1-2st. Prematurity of 30 weeks. Konyyugatsionny jaundice. Vanyusha grew and developed as all children, despite difficult delivery, but in 11 months to us have made the scary diagnosis to cerebral spastic infantile paralysis.
After constant courses of massage and LFK I began to hold the head, keeps sitting, but because of a strong spastika he doesn’t sit, keeps on all fours, takes itself toys. At verticalization an emphasis on socks. Steps with support by hands.
But treatment which we pass now to us doesn’t yield big results, we have found more effective methods of rehabilitation.
Many think, about children with cerebral spastic infantile paralysis “yes same not cancer”, it is possible to pass and help someone to another to whom it is more urgent and more necessary. Unfortunately, this terrible delusion. Cerebral spastic infantile paralysis as well as cancer have a restriction on time. And the less kid, the is more than chances to put him completely on legs and further to forget about the terrible childhood forever. But if time is missed, the child has already not so elastic muscles, to treat him to become more difficult and more expensive, and such children from a baby carriage change in for disabled and on it all dreams are finished because from 6-7 years it is almost incurable. But if to think that they in a wheelchair will just sit, it is one, but they will live with awful pains until the end of life. Therefore parents of kids with cerebral spastic infantile paralysis desperately fight for the children in the very first years of their life then not to roll the adult child on a carriage to the death.
Real and effective help to us is ready to be given in hospital of diseases of a brain of the city of Yuncheng, People’s Republic of China.
All sum to me isn’t feasible in full therefore I address you. Remained to time very little, in October wait for us in clinic therefore one hope for your help! Please help!