Unique, but not conquered by the disease
Unique, but not conquered by the disease
Completed

Unique, but not conquered by the disease

The project is carried by
Started: 07.09.2023
Ternopil region
Completed
Totally raised
75000.0 UAH
Funded
100%
Total goal
75000.00 UAH

Bilal is 8 years old, аnd he has the rarest chromosomal abnormality, the only case: Emanuel syndrome. The child's body does not perceive ordinary food: the parents immediately have to call an ambulance and save the son in intensive care. We are collecting funds for buying Resource Junior special food for 6 months.

Bilal was born at term, but underweight. He slept constantly, could not suck, food was not digested, the child suffered from vomiting and gastrointestinal disorders. The doctors of the maternity hospital in Zalishchyky could not find the reason for this condition of the newborn and sent him to Ternopil.

The child was immediately taken to the intensive care unit. Mother Mariam managed to teach her son to suck with a nipple and swallow, so that there was no need for droppers and probes. On the 10th day they were discharged home.

At the age of nine months, Bilal and his mother moved to Australia for a year. There, the doctors finally managed to make an accurate diagnosis.

In the case of Bilal Emanuel's syndrome is manifested by hydrocephalus, deafness, lack of speech, heart disease, weak muscle tone. The development of the child corresponds to one year of age. Thanks to the efforts of his mother, Bilal learned to hold his head, sit up and sit, crawl. If nothing bothers, the boy calmly plays with soft toys, watches his favorite cartoons.

The child developed entropion (inversion of the lower eyelid inward) due to blockage and inflammation of the sebaceous gland. Since Bilal has a heart defect, anesthesia is contraindicated for him. With difficulty, parents managed to find a doctor in Ukraine (in Chernivtsi) who is ready to perform an operation on the boy. Its cost is 2 500 euros.

After the boy suffering Covid three times, the condition of the gastrointestinal tract worsened: Bilal even once fell into a coma due to anemia and a deficiency of proteins, fats and carbohydrates. It took a long time to find the right special food. Doctors stopped the choice on the Resource Junior; besides it, the body does not absorb anything.

The financial situation in the family is very difficult, so your help is needed to purchase a six-month supply of special food Resource Junior. Please, help Bilal!

Full name: Bilal Mohammad, 20.05.2015
City: Zalishchyky, Ternopil region
Diagnosis: Emanuel syndrome, profound delay in psychomotor and speech development, open foramen ovale
ID: 8947
Supported
Charity donation
31.12.2023 21:02
2950.13 UAH
Charity donation
31.12.2023 18:54
3000.00 UAH
Charity donation
30.12.2023 23:01
5700.00 UAH
Charity donation
29.12.2023 11:23
200.00 UAH
Charity donation
27.12.2023 13:32
50.00 UAH
All donors

Done - reports are ready,
the project is completed.

Thank you for your support!

Done - reports are ready

Similar projects
Life-giving energy is supplied through drips. 2
Support
Health
Life-giving energy is supplied through drips. 2
At 4.5 years old, Roma had a large part of his small intestine removed, leaving only 12 cm. He receives …
A girl full of life. 2
Support
Health
A girl full of life. 2
Karina is 8 years old. She is an energetic and creative girl who does not let her illness darken her lif…
Prokhor's dream is to get rid of diabetes
Support
Health
Prokhor's dream is to get rid of diabetes
In 2017, the Prokhor family came under fire when they evacuated their great-grandmother from Donetsk. Af…
Dania struggles with autism. 2
Support
Health
Dania struggles with autism. 2
This is not the first fundraiser we have organized for the child, so we are happy to hear about positive…
Show All