Sofia has ichthyosis - due to a genetic breakdown, her skin cannot retain moisture, flakes, itches 24/7 and becomes covered with painful cracks.
Thanks to the support of the Butterfly Children Foundation, the girl lives a normal life: she goes to kindergarten and dances. Previously, Sofia's skin needed to be treated 7 times a day, now 3-4 are enough.
But in order not to lose this progress, she periodically needs rehabilitation from specialized experts. Qualified care for children with rare genetic skin diseases, such as ichthyosis, is provided in several federal medical institutions in Moscow and St. Petersburg.
We are opening a collection for air tickets for Sofia and four more wards of the foundation. It is necessary to pay for the children and their accompanying persons so that they can be hospitalized and rehabilitated on time. These trips will help improve the skin condition of the wards and maintain the achieved result.
