Artyom was born healthy, he could crawl, at 10 months he began to walk and was able to do all the moves, that were also performed by his peers. He developed well, grew up as a strong and very intelligent kid. But to a great regret, after 18 months, his parents noticed that Artyom had difficulties, he could not run or jump, they also noticed that his legs became weak. Over time, he stopped climbing stairs. They went through numerous visits to doctors, and finally came to the diagnosis ... spinal muscular atrophy type 3 (SMA3).
Now Artyom walks, but very slow. Our only way to keep him on his feet is therapy using "Spinraza", which is very expensive, just unreal money. We sincerely ask you to help ensure this little boy live on his feet ...The disease is progressive and at any moment its condition may worsen. Unfortunately in Moldova there are no medicines to treat and stop this disease progress.
Please consider giving a small donation to help this little prince stay on his feet.
Any help is appreciated. Stay safe.
The recipients of the money are Artyom's parents who are in Moldova waiting for a miracle, and we are here to make it happen.