This is Kolia Tkachov, our ward is not the first year. The baby was born with a "whole bouquet" of diagnoses, and such happiness as a healthy, carefree childhood, alas, did not get him from birth... The child has to fight for every skill, for the first step, for "skillful hands"... And now not the first year we together with parents observe and rejoice, as one more child on the earth becomes independent and happy. And we, ordinary people, involved in this miracle.
Charitable Fund "Hope for Life"hope-life.com.ua
Charitable Fund "Hope for life" was established in March 2014 to address urgent social problems, although we started to help in 2011. The main objective of the Fund is a charitable activity in the public interest.
With your help Vika was provided with special food for 2 years. She is stronger and already studying in the second grade (teachers come to her home). But... without food a girl can not lose weight. She has a very dangerous disease – spinal muscular amyotrophy. She cannot walk, cannot sit without support, cannot lift the arms of gravity and generally cannot raise her hands up. All this is due to weak muscles. But her condition can be improved if you take medicine, vitamins and a complex of amino acids. Victoria also needs special food, because she is very ill gaining weight.
We want to introduce you once again to this cheerful, open and shy girl who lives in the small town of Boryslav. Mom tries very hard to put her daughter on her feet, to realize her dream, that she should be healthy. Her mother remained an orphan, so she has no one to whom she could go for help. Angelina had an uncle who loved her very much and helped with treatment. But he went to Kiev to the Maidan, then went to the National Guard to protect us from the enemy, and died under the Sloviansk. Angelinka is treated with a birth...
The young girl, Anastasia Lokaychuk needs to be treated by foreign doctors! She has the following diagnoses: spastic tetraparesis, optic atrophy, toxoplasmosis chorioretinitis both eyes, shunted, spasms cystic formation in the head. Doctors suggest that it is congenital, as the mother in pregnancy time has not discovered the infection toxoplasmosis. During his 10 years, she underwent 10 operations that have been associated with failure of the shunt.
Stepan is a fighter for life, he was born before the line. His immature lungs did not open during childbirth, during the resuscitation, a stroke occurred... Only by two months, the baby was able to breathe independently. But the restless happiness of parents did not last long. Against the background of not passing general weakness and lethargy, there were sudden problems with breathing. Then again there was resuscitation and now with a tracheostomy (this is a hole in the neck that allows breathing).
From the letter of the boy's mother:
"Help the boy live fully, for him every centimeter is important! Thank you in advance for the indifference to someone else's misfortune! When I gave birth to Sasha, already in his first year of life, I noticed that the child is lagging behind in growth. Before 5 years doctors did not make any diagnoses and said that this is a constitutional delay in growth because I myself am not very high.
When I had Sasha in my first year of life noticed that the child lags behind in growth and naturally ran to the doctors and up to 5 years, doctors diagnosis is not put, saying it is constitutional delay of growth, as I myself not big. Every year I went to the doctors and get bored, saying to them: well, something is definitely wrong, son is up to 3 years differed from their peers. While one doctor we did not assign an analysis, hormonal examination, and this is where it all began...
A letter from mom:
"10 years ago Angelina was born in a difficult birth, during which received a birth trauma. After that, the girl was in the intensive care unit and a month she was discharged home. When she turned six months, I noticed that my baby's strange behavior, she started having seizures. She could not hold her head and don't react to anyone. When we went to the Lviv city hospital, we made the diagnosis: psychomotor retardation, cerebral palsy, microcephaly.
"Dear God! Save and help everyone who supported my son, thanks to whom we can treat Kolia. God! Please hear their prayers as they heard mine...". With these words of prayer, Kolia's mom starts every morning. She thanks everyone who helps to fight for the health of her son... But the woman still needs assistance, it is impossible to cope on her own, unfortunately...
I see how mommy again quietly wipe tears. I asked why she was crying. Mom thinks I'm too young to understand and meet that speck of dust got in her eyes. But I'm an adult, I maybe small but I'm a man – she's crying because soon I need to go to rehab and she was able to assemble just for travel and accommodation and we need more of 10 000 for treatment... I wish she didn't cry, I try, I listen to it...but... let me Remind You the story about me with the words of my mom:...