Aisha managed to cope with the disease and quit intravenous nutrition

AiF. Dobroe Serdce

Foundation Moscow

Your support has helped Aisha grow and develop normally. Due to special nutrition, the length of her small intestine has more than doubled. This made it possible to completely avoid feeding through a vein. Thank you for your help. Aisha has a rare disease in which there are no nerve tissues in the colon. After several surgeries, she developed intestinal insufficiency. The girl needed constant parenteral and enteral nutrition, as well as infusion therapy and supplies. - I want to express my gratitude to everyone who helped us in a difficult moment, - says Aisha's mother Aminat. – They refused to give us all this for free, but we couldn't have done it on our own. Recently, the child underwent colon surgery, and now he is working normally. At the same time, the small intestine grew from 70 to 160 cm, which made it possible to completely abandon the droppers, on which they used to spend 22 hours a day. Now Aisha eats special mixtures through gastrostomy. They also try ordinary food – she likes pumpkin puree and squash. This summer I tried apple and melon for the first time. In November, they will travel to Moscow to consult with gastroenterologists. In the meantime, Aisha is trying to catch up with her peers: at the age of 1.4, she actively moves around the apartment in a walker, speaks syllables. Thank you for not passing by and feeding Aisha with your kindness and care.

Report

Campaign information

To cope with the disease, Aisha needs a supply of intravenous feeding mixtures.

After the intestinal surgery, little Aisha is fed not with porridge from a spoon, but with special solutions - through a dropper. Regular food is not absorbed by her body, and intravenous food along with the consumables for the droppers is too expensive for the family. Aisha's parents are doctors, but even they cannot save their daughter without our help. The fact is that without intravenous nutrition, the child has no chance of recovery. This is all due to a rare disease due to which there are no nerve endings in the intestinal walls, so the organ cannot function properly. Aisha has already undergone several operations. First, part of the intestine was removed, then the organ was reconstructed. Now it takes time for the intestine to work and learn to take nutrients from baby food. In the meantime, instead of regular food in the girl's diet, intravenous mixtures based on glucose, proteins, fats, important microelements and vitamins. Aisha spends 22 hours a day on a dropper. And it is important for her family to know that there is a supply of nutrient solutions and all necessary consumables in the house. Let's help!

Donors

619
Сокол Сапсан

Сокол Сапсан

50 ₽ • 1 year ago

Рамазан

Рамазан

100 ₽ • 1 year ago

Ghost Toober

Ghost Toober

138 685 ₽ • 1 year ago

Дикая Собака Динго

Дикая Собака Динго

500 ₽ • 1 year ago

Большая ДрофаУссурийский тигрВадим УсмановN N
619 helping

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