History and appeal from the words of the mother:
” “A certificate from the maternity ward states that the child was born from the first delivery, full-term, no resuscitation, 53 cm tall, weighing 3 kg 540 g, with an Apgar score of 9, discharged on day 4. At 3 months of age, the child received a routine DPT vaccination, after which Nicole was admitted to the infectious diseases department with an atypical reaction the same day with a temperature of 39.8°.
Until 7 months, she was developing normally, and a child pediatrician was constantly being monitored for a period of time, recruiting the child and growing up on the development table without any special features. At 7 months we contacted the child neurologist N. I. Novikova. Because of the fact that the child does not bother to go back, and during the hour of the shower she falls over and does not straighten her back. After which the referral to the child neurological department in Poltava was withdrawn.
After profile monitoring according to the protocol, including EEG and neurosonography, a diagnosis of CNS HIP in the postnatal period was made. At the age of 12 months, the baby still hasn’t developed her first babies, and the skills of living and sitting independently were also just a day.
Two months later, the child began to hear pendulum sounds. After which, independently, without direction, they went to the ophthalmological department of OKHMADIT. After fasting, Nicole was diagnosed with high myopia and astigmatism.
We spent the entire hour waiting for the local neurologist. It gave the same results and we had to go back to the neurologist in Kiev. After the lack of diagnostics and the cold, in 2016, with a confirmed diagnosis of cerebral palsy, we turned to Poltava. There we were diagnosed with disability and prescribed treatment with the drugs Neuroxon, Cerebrocurin and Cortexin. These drugs themselves act as hydrolysis to renew damaged parts of the brain as a result of hypoxia. All faces were bathed in moist cat.
Beginning in 2016 and today, we have undergone painless rehabilitation in various centers of Ukraine, including waste from the human cat. Once all the protections were exhausted, they rushed to the local administration with groans and encouragement. There were no vids. And we were completely deprived of all the problems that the rent had brought us.
Near the fall of 2022, Nicole underwent achyloplasty near the Dnipro metro station, and in the summer of 2023, they were judged, in what kind of life and camp the child became miserable. At the beginning of 2023, Nicole was hospitalized at the regional pediatric neurological department, where an MRI was performed, which revealed the destruction of the myelin alba of the cerebrum. This is a genetic breakdown, which is why we are diagnosed with a very rare metabolic neurodegenerative disease - leukodystrophy. The disease is not severe and with such a diagnosis, children rarely survive until the 16th century.
To confirm the diagnosis, two metabolic panels were created, their range ranged from 28 to 32 thousand. UAH It is necessary to create a third panel in order to determine the type of illness, and then to exclude the possibility of conducting a course of immunoglobulin therapy. This procedure will help you stream white speech.
Nicole's condition is getting worse every day. She has started to lose her skills in chewing, standing, swallowing, holding objects in her hands, and her speech has become slurred. Any contribution, regardless of the size, will be extremely valuable and will help Nicole to get a chance for the future. ”
At the moment, the fundraising for the full extended genome sequencing of the leukodystrophy, leukomalacia and epileptic model panel is open for a total amount of UAH 12 556.
LET'S CREATE GOOD TOGETHER!!!
For Nicole's sake, we will have to violate one of the foundation's principles. Due to the full-scale war, international laboratories have terminated their contracts with Ukrainian ones, and we will have to transfer the money for the tests not to an international organization, but to Tatiana's Shut card, which in turn will provide us with a payment screen to confirm payment for the tests.
