So little for us and yet so much for him

There was excitement in her voice as we discussed the possibility of her son's face being whole, but I could also hear the concern in her questions. Perhaps it was a dumb question on my part, but I asked her if she (Ate Vergie) was interested in having her son's face fixed. I've learned never to assume anything. I thought to myself, "It's possible that she could be against modern medicine or too afraid to have her son go under the knife". After I brought it up, Ate Vergie and Ate Sylvia asked me a few questions. Would he feel pain or would the doctor make him sleep during the procedure? Would the doctor just numb his lip? Would they use needles or would he just have to breath in the anesthesia? "It's too mahal (expensive)! How can we afford the medicine?" I told her, "akong bahala sa gastos" (I will take care of the expenses) if she is interested. I'm kind of taking this by faith because I don't know exactly how much it will cost, but I heard that there is one group that comes to Manila about once a year and does the surgery for about $300-$400. That's no small amount for a missionary salary, but it is still relatively small. How could Jessica and I not do that? Relatively so little for us and yet so much for him. I haven't done the math, but I wouldn't be surprised if I found out that we spend that much on coffee each year. This surgery could be life changing for Angelo. It would spare him from years of ridicule and hurt, adverse hygiene and medical issues, open up better possibilities for work and most of all, be a life long testimony to the love of Christ.

Angelo was born four years ago with a cleft palate. His tita (aunt) told me how he never cried as a baby and still doesn't speak. Ate Vergie said that he makes some sounds and he clearly understands what is being said to him. She hopes that he will be able to talk after his mouth is fixed. Angelo's father seems to have had a nervous break down and is out of work and seems to have given up on life at the moment. Maybe God will use this surgery to give Angelo's dad some hope and remind Him that He loves him.

I'm hoping that this surgery will have several other effects as well. First, Angelo has asthma. He is one of many kids and adults living under the bridge who have asthma. I'm guessing that the fumes from the exhausts of the thousands of cars passing over their bridge each day has a lot to do with it. This is especially dangerous for Angelo because I don't think he can use a conventional inhaler for his asthma. He is not able to form a seal around an inhaler with his mouth due to the section of lip that is missing. I think this could potentially be life threatening for Angelo if an asthma attack makes it difficult for him to breathe. His family can't afford a trip to the hospital, but they do have access to an inhaler...An inhaler which I'm guessing would have little effect at this time because of his deformity.

Second, I hope that God helping him through us will not only be a testimony to Angelo and his family, but to that whole community under the bridge. Several of them have and are reading bibles that I was privileged to give them. I was just talking with some of them today and they can see how God has not forgotten them. They see how He has sent me and other people over the years to help them as He cares for them. I have found a few possibilities of some local churches that might be able to help me minister to them. Their hearts have become more and more prepared for this. I get excited as I think about the possibilities. Join me in praying that we can help correct Angelo's deformity and get a local church involved with loving and teaching these precious people. Click here to read what happened next.