Arthurchik continues to struggle with great perseverance for every new step in his development. If he stops to do it, he will provoke a step backward. Many people have already known the story of our son. Due to hypoxia, the baby had a severe brain damage, which resulted in epilepsy, spastic tetraparesis, infantile cerebral paralysis.
And today I want to tell a little about this disease because in October we celebrate the International Day of infantile cerebral paralysis.
It was October 4th this year. This project was launched by Australia with America and supported by 270 organizations and hospitals from 46 countries. This date is designated specifically so that healthy people have an idea of the disease and about people with this disease.
An infantile cerebral paralysis is a group of motorized motor disorders. The disease occurs due to perinatal damage of the nervous system during pregnancy, at time of childbirth or in the first months of life.
The main number of children with infantile cerebral paralysis is harmed at time of childbirth.
Such patients are born in all countries of the world.
Almost always there is no any fault of his parents or himself in the fact that the baby has such an ailment.
Infantile cerebral paralysis is just three letters, of which are hundreds of thousands of broken fates.
With the apparition of such a situation in the family, the life of the parents is changed radically, it becomes completely different. All their time they are engaged in caring for a child, holding a massage and exercise therapy, training with other specialists, traveling to rehabilitation centers, and between all of these - raising funds for treatment.
Among the kiddies, there are those who walk independently or with minimal support and can serve themselves. There are those who can’t keep their heads, sit and walk, and who are forever chained to a wheelchair.
All parents are real fighters. And our children with infantile cerebral paralysis are real heroes. Because their childhood is injections, hospitals, stretches, exercises through the pain. It is obligatory to do exercises. It is not possible to be without them
The most important thing is that the deterioration is not progressing, it is necessary to be treated all life.
Look into the eyes of these children, how many are in them the desire to be friends, to love, to learn, to rejoice. There are many talented children among them. Their parents also want to be proud of their children, just like you are of yours. They are proud because their children come through the obstacles despite their desire and impossibility at first sight.
Look around you. Do not let your children offend children with infantile cerebral paralysis, do not push them off and their parents. They are hurt very much.
Thank God, we with Arthurchik meet only kind and sympathetic people who are always ready to help, who do not divide people into "special" and healthy ones.
Unfortunately, Arthurczyk is still not sitting independently or walking, he is constantly suffered from dystonic attacks, but we believe, thanks to our efforts, aspirations, actions, that our son will have new steps in his development.
Sessions with the osteopath, which we have been going through on an ongoing basis since May, are yielding results. Special nutrition significantly strengthened Arthur’s immune system.
We have a planned examination in the Kharkov genetic center in November - 200-250 USD(tests and medications), weekly trips to the osteopath in Dnipro - 180 USD (for 2 months).
The amount is 380 USD is overwhelming for our family.
Therefore, we turn to you, our good acquaintances and strangers.
We are very grateful to you for all your kindness, for that you do not leave us alone with our misfortune, for that you help us to move forward.
Thank you all very much! The deepest gratitude to everyone!
