This is my son Yohance, for 3 years now, he have lost his ability to walk and in 2 years his ability to talk. He was diagnosed with EPILEPSY and ENCEPHALOMALACIA, as a result of him having ADEM in 2016. He have no control of his movements, that is why he need utmost care. He have daily, frequent seizures ranging from 2-10 or more times daily. He have quite a few medication and supplements for him to hopefully control his condition and atleast be in good health. It has always been our struggle as a family, foremost emotionally to see our handsome, bright and good kid have come to this. We try to keep ends meet, even though my husband has work abroad, there are just times that we fell short financially, there are still tests that we have put off and travel to better hospitals that we just have to set aside at the moment and we just pray for the best for our little man. Lately, it saddens me that his wheelchair broke, it was not part of our monthly budget and it’s quite expensive, and we have to source it out of town. For now, we are hoping for anyone’s kindness that we may be able to gift him with a new ride on his coming birthday on September the 20th. God bless your good heart.