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Abdulaziz received medical assistance in the treatment of biphosphonatamia.

Deti-babochki

Charitable foundation · Moscow

collected

of RUB 186,145

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The boy has two rare incurable diseases: epidermolysis bullosa, in which the skin is vulnerable like a butterfly's wing, and imperfect osteogenesis, which made his bones brittle, "crystal". Abdulaziz was hospitalized and treated under the supervision of a doctor with the necessary qualifications. Thanks to you, the benefactors, it will strengthen the child's bones, reduce the risk of fractures and reduce pain.

Also, with the money collected, we were able to provide dental care to another small ward of the Nikita foundation. The boys' parents thank everyone involved in the collection!

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About the campaign

Abdulaziz has a genetic skin disease. He needs medicine to protect his skin and help from a specialist.

Abdulaziz has two rare incurable diseases: epidermolysis bullosa, in which the skin is vulnerable, like a butterfly's wing, and osteogenesis imperfecta, which made his bones brittle, "crystal".

Now Abdulaziz needs treatment with bisphosphonates. This is the gold standard for the treatment of osteogenesis imperfecta. The drug zoledronic acid will strengthen the child's bones, reduce the risk of fractures and reduce pain, which Abdulaziz has almost come to terms with.

In the region where the boy's family lives, there is no doctor with the necessary qualifications to administer the medicine, so we are raising funds for the arrival and accommodation of a medical specialist, as well as for targeted assistance with medicines, bandages and skin care ointments for Abdulaziz.

Let's help the boy together!