"I carried my baby in the womb for 9 months, waiting impatiently for him to come into this world and meet his older sister. When I first hugged him, I found out what happiness is. Four years after the birth of our daughter Emilia, God blessed us with a new child, a boy. When I brought Robert home, we were the happiest people in the world. But after I found out the diagnosis, I felt to the marrow of my bones what this disease means, it takes my child away. I found out what endless pain is. The only thing I felt was injustice... not to us, but to him! For him, the struggle for life began. Robert must fight to breathe, eat, move every part of the body. I felt this injustice and was worried about his future, especially in a society where it is very difficult for people with disabilities. I do not know why life gave us this challenge, but I look into his eyes, and I know that Robert came to this world to do miracles. This is a huge sum of money, but I, as a mother, continue believe that if 2.1 million people will donate at least a dollar, Robert has a chance to live. " - Irina Grabazei, mother of Robert.

Robert was born on October 1 in Chisinau and brought great happiness to his family. A month later, after 3 genetic tests, his parents learned the terrible news - their little boy was diagnosed with spinal amyotrophy, type 1. This disease affects neurons of the spinal cord, sometimes the brain and leads to their death. But Robert has good chances for treatment. It is very expensive, but the hope is the vaccine that can stop the disease, it costs $ 2,100,000. The treatment should be made in the United States and it can help defeat this disease. Any donation is vital to this little boy!