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Step by step to the dream!

Raduga

Charitable foundation · Omsk region

collected

of RUB 96,250

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Vika is an incredibly smiley and affectionate girl. She loves hugging. But there are things that Vika really wants to learn to do, but she can't yet. Her diagnosis is incurable, but chances are the girl can walk on her own without support. To do that, the doctors prescribed Vika to use a special bike simulator. The family didn't have a chance to buy it, although they needed it as soon as possible. Our Center knows that if help is needed quickly, you, people with a good heart and beloved Tooba, will help. Thank you for your help, friends!

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About the campaign

Let's help Vica learn to walk!

While other children are enjoying candy and ice cream, Vica has chicken breast soup on the table without a drop of butter. Only vegetables and only chicken. No sweets and no flour.

Vica has years of therapy and therapeutic procedures ahead of her. Rehab, speech therapist, defectologist, psychologist. Vica's diagnosis is incurable, but it can be controlled.

Doctors don't raise gloomy hands or tell Mom they can't help. This hereditary genetic disease has many symptoms - including dysplasia, obesity, short stature, sometimes infertility, and all because of one chromosome. Often Prader-Willie syndrome is accompanied by mental and speech development delays, but specialists have examples before their eyes when children with this disease even graduated from university.

Now the girl needs to form the correct position of legs when walking and strengthen muscles. In this a velo simulator will help her. But the family does not have the opportunity to buy it, so the family turns to you for help. An incurable diagnosis is not a sentence for a child. It's in our power to tame the disease and make it play by our rules...