Liam Morel spread his wings to meet with Jesus Today. After a long battle with a genetic disorder called GM1 type 1, He passed in peace at the hospital, giving his last farewells around 4am. Liam  celebrated his 3rd birthday at the hospital when he passed away.

 GM1 is a lysosomal storage disorder that destroys neurons in the brain and spinal cord. It is a disease without cure and progressive. When Liam was diagnosed the doctors told me that he was not going to spend more than 2 years. As Liam's parent it took us years to understand this disease. We saw how this disease took away everything from our son including his life. As days passed, we saw how Liam lost his ability to sit, stand, eat, and including breath within his fist 2 years of his life. Eventually, as the days passed by, Liam spent his finals day with a tract vent on his neck breathing through tube. 

We are glad to share that Liam's legacy stand as a testimony to bring hope for a cure to the generations of kids suffering from this genetic disease. On Saturday Feb 13 we  got the chance to make a video so that big pharmaceutical  companies can use Liam's story to bring a cure to GM1. 

This gofundme campaign will cover the funeral cost for Liam Morel. As Liam's parent we will be in charged of all funeral expenses and help is greatly appreciated.