Let us not give Yeremiy to an evil disease

At a time when other parents could enjoy the first months of fatherhood,  Yeremiy's father and mother were constantly looking for the cause of the baby's cough. They were discharged from the hospital and admitted again. And it was like that for up to 11 months. The family was in shock after the diagnosis of cystic fibrosis: the disease is serious and incurable. The parents decided that they would never give their son to the disease.

Now the boy is 5 years old, he is his mother's joy. He knows letters, many words in English, a lot of poems and songs. It would seem that he is an ordinary child, but coughing and hospitalization have not disappeared anywhere. But now there is hope that he would have a full life if treated properly. Yeremiy has a fixed schedule: pills, inhalations, vitamins, exercises to make it easier to cough up phlegm. None of this should be missed, otherwise thick sputum will accumulate in the bronchi and it will become harder to breathe, and food will not be digested. With cystic fibrosis all the body's secretions are thicker than normal, so the respiratory and digestive systems suffer the greatest blow.

Yeremiy needs to get regular tests and adjust his treatment, so he often goes to another city to see his doctor. So that the child does not miss important inhalations on the road or in the hospital, we and his parents ask for your help to buy him a portable inhaler. This inhaler can be used right on the road.

A home trampoline can be just a simple toy at first glance, but in fact it is a necessary thing for  Yeremiy. The more the boy jumps and moves on it, the better sputum will leave his lungs. A trampoline right at home will be a huge miracle for Yeremiy and will help him in his physical therapy.

Let's create a miracle for the family of  Yeremiy by purchasing what is necessary for the treatment of the boy.