Hello everyone! My heart brake founding out about this terrible and inimmaginabile rare disease SMA that affected a 15 months old my brother. There is a treatment that has a ridiculous cost of $2.3 million dollars. The child is fighting for life every day with less and less strength, the ONLY and Only hope is that treatment. Please I beg you people any donation even the smallest one is a chance for saving his life GOD BLESS YOU!!! Here below is the letter for parent. "Hello everyone... We are parents of little boy Arsenka. 21.01.2021 r. - a day that became a fracture in our lives. A confirmation of our son's terrible diagnosis has arrived. SMA is a disease we haven't heard of before, and a disease we've learned so much in 2 days. Shock, tears, disappointment, a condition that cannot be conveyed in words. The smile of our son helped us to master ourselves, his look in which there is the thirst for life. * SMA is a rare nerve-muscle disease accompanied by motorcycle loss and progressive muscle atrophy, leading to early death. ! We really need the support of each of you! We believe that the world is filled with good people and your good will return to you."