Help not to starve

Now many families had to "tighten the belt" and limit the costs. Probably you are among them. Millions have lost their earnings and nobody knows when or how it ends... But there is something that remains unchanged: we still have each other. We cannot temporarily hug each other, but we can still save each other. Now it is difficult for all ordinary families. But there are those among us for whom it is even more difficult: families where the baby or mom or dad are seriously ill. 

Earlier they had to choose often what to buy: medicine or food? They have nowhere else to tighten the belt. Make a small contribution to this project – together we can help them
not to starve. 

Our patients are families that bring up children with severe congenital cystic fibrosis, as well as adults with this disease. One of its phenomena is malnutrition problems, most patients have a deficiency of body weight. At the same time, they are vulnerable to infectious diseases and the weight influences whether they have the strength to fight another exacerbation. The program of supportive treatment for the person with cystic fibrosis contains many requirements for a diet, nutrition should be full, of high quality, with high calories. Yes, this is important to anyone. But for a person with cystic fibrosis – especially. It is dangerous for them to save on food.

They are saving anyway, because such are the realities. But let's help them just a little! Now they need the strength to stand it.