ur family has been in big trouble. Our son Artem 4g 8, he is seriously ill (severe cerebral palsy) When in the last months of pregnancy I wriggle stopped Artyom shared her concerns with your doctor. "He slept, not get upset, beating of the heart good, as I could not believe the doctor with experience! After birth, it became clear that Artem suffered from a severe lack of oxygen and thus ceased to grow. After delivery, without first intensive care, my kid left at love with a young nurse, and only through 10:0, which has changed the doctor's Office, my son had it: put a neck corset, give oxygen. But it was getting late, gone, bleeding swelling of the brain.
That had to go through our family during those six weeks, that Artsyom was hospitalized, not words. But our little one survived, and now we are fighting hard for his recovery. As the blind kittens, my husband and I were looking for doctors and hospitals. Take one loan after another paid consultations of specialists, physical therapists from other cities. In our city there is not even a normal child neurologist. With the first month and a half Artem constantly screamed, tremor and spastic was such a strong that he could lie on his back, spastic was even in the larynx. Feeding it a harsh ordeal for him and me, he strongly cried constantly davilsâ and srygival. At your own risk I had to fill him in her mouth to eat from a spoon. During sleep it vskidyvalsâ and screamed wildly. All these symptoms were like convulsions. But in spite of all the suffering endured by our son, from birth, a very expressive eyes, he captures the mind follows the subject, eyes "speaks". His eyes, that is our hope. It is as if looking at me and said, "No Mommy, I need popravlûs′! I am strong, I've got everything all you get! And I believe we will succeed. "
When we asked the advice of the regional hospital, we conducted a survey on EEG. EPI-hearths were found. As it turned out after four years, on the grounds that the alleged hotbeds of EPI-no treatment which designate us doctors were absolutely contraindicated in our case. Thus, without noticing positive results from repeated treatment, we went On to survey the I.M.T. Moscow. Where we finally have a diagnosis actually symptomatic epilepsy and was led to an anticonvulsant therapy.
Over time I have learned a lot. Taken Away By Artem LFK. Very good, but briefly, Artsyom Vojto, methodology which helped me trained in Moscow. During the year, we worked to log into. We constantly take baths, drink herbal infusions. Positive results are there but they are minimal. Artem started watching cartoons, understand some of my request, for example: keep your head, look, are good to eat. In the locomotive engine development progress, we have not yet achieved, but really this desire.
In order to achieve good results over time, Tëme must be constant costly survey, treatment and rehabilitation. To our regret, we have no money, but we have high hopes of a miracle. We believe in good and benevolent people. Not pushing hands, we are looking for a way out of this psychologically and financially difficult situation. In our family it is Artem has two sons 16 and 3 years. We have to seek assistance from the different funds that would support us financially. And one of those funds was Help. Fes. With the money raised, we were able to deliver the Artem to rehabilitation in Evpatoria. Because of the large order of many foundations are denied care, but we do not despair and do not lose hope. Passing through all these hardships, fighting for the health of our son, we decided to seek assistance through the forums.
WE, PARENTS OF ARTEM, INVITE ALL PEOPLE WHO READ OUR LETTER. PLEASE HELP!!! We still have time and still can change the destiny of our baby! With your help, Artem necessarily will get better! Thanks in advance to all who are ready to help our son to learn to live a full life!!!
WITH HOPE AND RESPECT TO YOU! Parents Artem Str.
PLEASE HELP OUR ARTEM!!!
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Here parents of children with Cerebral Palsy can post questions about caring for their child and get advice on special needs and care.
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