It can't be left like that

The maximum power of the oxygen device is not enough for Dima – he needs a stronger one. The boy is 24, but he depends entirely on his mother's care and good support of the people. Dima was born with cerebral palsy and all his life consists of a struggle: his own – for himself, his family and doctors – for him… It has never been easy. But the last year has been extremely difficult even for them. 

A year ago, doctors had to perform a tracheostomy on Dima – a special hole in the neck directly to the trachea – only like this the guy can breathe now. At first it seemed that it wouldn't be for a long time. And the first oxygen device with a capacity of 5 l/min. was taken temporarily. But now Dima needs oxygen concentrator support all the time. And that, first, device is not enough, at its maximum it extracts the level of oxygen in the boy's blood only up to 89% on the best days. Obviously, it is already required to look for the device with more power. A medical suction pump is also needed to clear the airways from the sputum (the boy cannot cough up so well on his own). And, of course, for the device – a stock of catheters for sanitatin. 

In addition, during a conversation with the boy's mum, we learned that their home is often cut off from electricity. But there lives a person whose life is critically dependent on medical equipment that works "from the socket"! In particular, the oxygen apparatus. When the light is turned off Dima suffocates. We can't leave it like that, so the first purchase under this project should be an electricity generator. 

In fact, all the needs on which funds are raised within this project are vital for Dima. And Tetiana, the mother, has nowhere to address, except to us.