Help the Goss Family Fight Biliary Atresia

My name is Sara. I have only known Chelsey and Johnluke for a handful of years, but in those years they have become my family. Kyle has known them a very long time. In the time that we have known them they have been nothing but the most selfless and caring people. They are always first to step up and help anyone no matter what they have going on in their own lives. This last week their world has been flipped upside down. Their 2 month old son, Lincoln has been diagnosed with Biliary Atresia

(http://baaware.org ) , which is an extremely rare liver disease that currently has no cure. The only treatments are the Kasai procedure and in most cases a liver transplant. They have been in Children's hospital for a week and little Lincoln had the Kasai procedure last night. He was in surgery for 5 hours and everything went well, but they have a long road ahead to battle this disease. They also have an 11 year old son and 6 year old daughter, which due to COVID restrictions they have been unable to be with during their hospital stay. Lincoln is expected to go home just before Christmas. The stress this family is going through is unimaginable. Johnluke has had to drive back and forth to the hospital due to only one parent being allowed to sleep at the hospital. Gas bills are stacking up. Food bills are stacking up. Medical bills will start pouring in. Money is the last thing they should have to be worrying about, as their son's care is going to need all the focus and attention they have. If you have the ability to give to them, please please do so. If you would rather help in another way, such as meals when they get home, please reach out to me. If you would rather donate via Venmo, please reach out to me. If you are not able to donate, please please share. This family deserves the world and my heart has been broken for them. One day at a time. Thank you for reading.