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The parents were waiting for Misha with love and hope. But during childbirth, doctors had to make a vacuum. It was a critical moment in the life of the family. Brain malformations appear after a difficult birth. In Misha only 20% of the brain is “active”. When he was 1.5 years old, he held his head a little and started shouting the first sounds, but everything stopped, now he can’t do that either.

The child has localized symptomatic epilepsy, microcephaly, tetraplegia, optic nerve atrophy, he does not see, does not focus his gaze, does not sit and does not even smile at his mother, just hugs. Parents control seizures with medication, and therefore they were allowed to go with Misha for rehabilitation in the village. Modrychi, where they chose a special course for such children, with epileptic seizures and convulsions.

Doctors hope that he will be able to hold his head and sit at least a little on his own, because now he is constantly on the handles, in a wheelchair can withstand up to 15 minutes, sometimes even swallowing saliva is a problem for him.

The course is designed for 15 days, on dobro.ua we collect half – UAH 30,000, and we ask for help from everyone to help Misha smile at his mother for the first time in his life.Misha’s first smile
Перша посмішка Мишка

Name: Molodetskyi Matvii, 26.07.2017
Diagnosis: hypoxic-ischemic brain damage, cerebrospinal fluid dysciculation, atactic syndrome, developmental delay

Matvii was born prematurely, the little one had a respiratory arrest, the beginning of his life he was in intensive care. This beginning of life has led to a lot of diagnoses, significant developmental delays and various defects that loving mom and dad are trying to correct as much as possible now, while there is time when Matthew is still small and still amenable to treatment and correction. The boy has hypoxic-ischemic brain damage, cerebrospinal fluid discipline, atactic syndrome, developmental delay.

He is not like his peers, but with every rehabilitation you help Matvii, he has made progress. After the last course of treatment, he pleased his mother – managed to climb the small steps. And more and more new sounds and exclamations appear, because before the child was just silent. Thus, doctors advise to carry out intensive medical therapy for three years, during the time when the body is formed there is hope for a full course, speech, movement.

Matvii and his mother really want to go to the next rehabilitation, where they will have classes and consultations with speech therapists, masseurs, neurologists, correctional teachers and other specialists who help the child have a full future through a comprehensive program.

Let’s again help Matvii get treatment, and after this course, he will definitely give us good news, and mom a joyful smile from new skills and achievements.
Нехай Матвій сміється. 3

Julia Palamarchuk
Diagnosis: “Necrotic enterocolitis, cerebral palsy, spastic tetraplegia, in the phase of lying with head control”
Julia Palamarchuk was born one of the twins ahead of schedule, and this affected the condition of the children. Her brother passed away on the 20th day, but Julia continued to fight for both health and life.

“In one year she was diagnosed with cerebral palsy, spastic diplagia. Now she is already 3 years old, but she does not sit, does not stand, does not walk … The child’s diagnosis “Necrotizing enterocolitis, cerebral palsy, spastic tetraplegia, in the lying phase with head control,” says the child’s mother.

Relatives, if possible, work with the girl at home, but she needs intensive and specialized rehabilitation in order to get closer to a full life.

But such treatment for the family needs exorbitant funds – 39 thousand hryvnia. They ask caring people to help them raise funds.

“I’m the mother of a special boy, Dima. Despite the diagnosis of cerebral palsy, he is really special. When I look into his beautiful eyes and charming smile, I for a moment forget about all the problems”, so begins the appeal to all the mother of 5-year-old Dima. Father left them when Dima was 8 months old. And now she and Dima live in the great-grandmother’s old house in a village in Cherkasy region, every day in the dream that the baby will take his first step.

The boy has atrophy of the optic nerves of both eyes, he does not sit, does not walk, almost does not roll over. Every mother of a special child knows how hard it is to treat cerebral palsy and how much strength and patience it takes, but she can’t lose hope, rehabilitation and treatment courses at medical centers are very important for children like Dima. Such a course of treatment in Truskavets significantly increased this year – 18 140 UAH – the cost of treatment for Dima in August.

After the last rehabilitation, Dima tried to sit down on his own and roll over, such rehabilitation cannot be stopped. This year, the state allocated a meager amount for treatment courses for children such as Dimka. Therefore, your help will be able to bring Dima’s mother closer to the realization of a dream, so that her only child walks herself. The kid is really a very cute and kind child, he loves to ride on a swing and play with pets. And every time a mother looks into the eyes of her only child, she dreams of one thing – so that he can walk!