If someone looks at this pretty boy, he will not immediately see that he is terminally ill (in our country). Oleksii has a genetic disease, progresses and according to the statistics of doctors, such children do not live long. The boy was born without signs of illness. Up to 6 months developed as an ordinary baby. But after a common cold, began to sit badly. Parents turned to the pediatrician, she sent to the neurologist and began tests, consultations with doctors... At issue was the diagnosis: Verdneg-Hoffman Spinal Muscular Atrophy. His mother really hoped that it was not this disease, but a genetic analysis was made, and it was confirmed.
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.
This isn't the first time you've helped Artur. He is very worried that hurts, going through that makes mommy sick, "I see how mommy again quietly wipe tears. I'm asking why she's crying. Mom thinks I'm too young to understand and meet that speck of dust got in her eyes. But I'm an adult, even if I'm small, but the man-she cries because soon I need to go to rehab, and she was able to collect only on the road and accommodation and need more than 12 000 thousand for treatment... I so want her not to cry, I try, I listen to her but...".
On March 9, 2017, Ira gave birth to her first and only son Danichka with a weight of 4 200 kg and 53 cm. Apparently, due to a rather large weight, he was born with cephalhematoma on her head. After 4 days in the hospital, the baby was sent to the hospital to remove the cephalhematoma. His mom was uncomfortable, because after the maternity hospital everyone is met with festive balloons and is happily going home, and she and her husband drove many kilometers, and again 4 walls, again a hospital...
12 years ago, a sweet, beautiful girl was born, who completely changed the life of her mother and her dreams. The whole family was very happy when Yulia was born, they were very happy with her, but soon this joy turned into tears, pain, and despair... When 9 months drew attention to the fact that my daughter does not develop as her peers and does not stand on his feet, relatives sounded the alarm. Doctors during the examination, was diagnosed with cerebral palsy.
Vladislav will soon be 19 years old... It is a cool adolescence, each of us remembers these bright youth years. But Vlad is different. His most vivid memories are associated only with trips to rehabilitation courses. Still, Vlad did not speak, cannot maintain itself handles, does not sit independently, does not go... Vladyslav is appointed four times a year to undergo rehabilitation courses.
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...
UPD: our Stepan became an angel. The disease named CMA was stronger. The UBB team brings our most sincere words of sympathy to Stepan's relatives and thanks to all the Donors who supported the boy.
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).
"I wish all children were healthy and my son is among them! He's such a little angel and from the very childhood knows what trouble is. Though it is still small already understands that's not like all healthy children. You should have seen his eyes when he looks at kids who run and play.
Again and again, I have to ask for help! I am a single mother of two boys living in a town Stebnyk, Lviv region. I am very happy that I have such "men", but still, I have the PAIN is a disease, my son! Due to the negligence of doctors pain the hospital my son at birth received a traumatic brain injury (in a very serious state of asphyxia, with extensive bruising of the brain), was infected by Streptococcus and at the age of 14 days have surgery (removal of umbilical vein) – the consequence was a terrible disease of cerebral palsy.
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.