Noahs Mommy and Daddy

It's has been the longest 18 days of our entier life. Noah Lee was Diagnosed with A.L.L Lukeimea on January 4, 2016. We thought that this was the hardest thing to deal with. We were sent to Riley Hospital the next day with the thought that we would only be here for a few days to a week. In this time period he developed phenomenon and Metaphenome Virus. He has no immune system because of the Lukeimea and the Chemo. He continued to get worse over the past 11 days. On the 12th day they paralyzed his body and put him on life support. After 7 days of no changes and things only getting worse the doctors and my husband I made the decision to try the last option we have. He was placed on a machine called an ECMO. It takes the blood in his body and takes it out and puts it in a machine and put oxygen in it. It gives his lungs the rest that it needs to try and heal itself. They survival rate is not the greatest at only 25%. We have to give Noah this chance. He is a fighter since before his was born and he will fight with everything he has now. We have had to stop working for the time being until we know what is going on. We travel back and forth from Fort Wayne to Indy. We are living off of a credit card and the last of our paychecks right now. We are right now coming into a very hard financial crisis. We are running out of options to continue to stay with him all the time. I am also getting ready to give birth to our 2nd son on February 6th. We have done are best to not ask for help, but at this point we have ran out of options. If you can spare anything at all we would greatly appreciate it. Continue to pray and think of us as we go though this. Thank you so much.