Seabys journey

Hi, I am Seabys aunt and I created this page to help Seabys parents Paul Clark Jr (PJ) and Jessica Clark with financial burdens as they are already going through what no parent should have to face.
Here is a little bit about Seabys journey. Seaby was diagnosed with Tay Sachs disease on Sept 21st of 2015 at 18 months old. It is a rare genetic neurological disorder with no treatment nor cure. Babies with Tay Sachs develop normally in the first 3/6 months of life. During the next month's the baby will progressively lose the ability to see hear and move. They will stop smiling, laughing, crawling, turning over and reaching out for things. He has lost all of these abilities.
Now at 2 years and 3 months old he is on hospice fighting his battle to survive. On memorial day doctors gave him a 50/50 chance to make it through the night. Thank God he did. Others say that he has maybe 2 months. We all know that God is in control and we still believe in healing. His parents are both out of work. They have tried to get life insurance on him before his diagnosis and was denied. Any donation would help towards any financial burdens and funeral expenses. Your prayers are greatly appreciated. Thanks and God bless! Please share!