Lisa recently turned 5 years old. From the first minutes of her life, the girl has been struggling with a rare genetic disease – ichthyosis. Her skin is unable to retain moisture, it constantly flakes off, becomes cracked, which causes itching, pain and discomfort to the child.
The baby was diagnosed immediately. After the birth, she spent 2 months in hospitals – doctors selected the appropriate therapy, while simultaneously teaching her mother to take care of her daughter.
"It was hard at first, I was afraid to hurt her. Then I learned how to treat my skin, drip my eyes, clean my ears, we started going to rehab, and the state of "not understanding what to do next" changed to "you can live with it," Maria recalls.
Lisa is a very active, cheerful girl, loves to draw, sing and dance.
To date, ichthyosis is incurable, but regular skin hydration can improve the overall condition and avoid complications. Lisa needs special care products every day: balms, oils, shampoos, and eye drops, because ichthyosis also affects the conjunctiva of the eyes.
Therefore, we are opening a collection that will help create a year's supply of necessary medical devices for Lisa. Give the girl the opportunity to live a full life!
Verified by Tooba
Verified by Tooba
