Baby Roberto's surgery

Our little bundle of joy has gone through so much since the day he was born. July 29th of 2015 Roberto JR was born because of a car accident we were in, since that day he stayed in the hospital NICU. We spent every hour we could with our baby boy, my husband and I both worked so me being there all day couldn't happen. Aug 14th he was able to come home, his brother and the whole family were happy. A couple weeks later he went right back into the hospital for a fever that would not break. He was released days later. When we took him for his 3month check up his doctor told me to sit down, she had to talk to me, mind I wanted my husband there with me because I didn't know what was going on. She explained that the babies head wasn't growing anymore, that he never had a soft spot in his head, I knew something was wrong with him, because his head was starting to form differently. We were referred to a specialist, I didn't know what to do or think, my husband said everything will be okay. The specialist asked for a 3D CT Scan of his head, to confirm what he thought might be wrong. Sure enough his front fibrous sutures were closed. He has Craniosynostosis. He will have to undergo surgery to reconstruct his forehead and his skull. As of March 29th he is now 8 months old. Trying to gather up money here and there for the surgery has been so hard with everything that we are going through its been really hard on us.  We honestly would have never asked anyone to help us but we are having a rough time. Anything honsetly helps us, the money is not going to us it will be going straight to his surgery bill. May 20th 2016 is his surgery day, he will have to stay once again in the hospital for 4 days to a week which means I will be off work until he is discharged and able to be his normal self again. My husband will be the only one working at this point. Donate anything it will really help us out, not only will we appreciate all the support and help you guys give us but our lord will also bless you in a millions way we can not. 

Thank you so much everyone for your help!!! The Silva family