This isn't a fairy tale. Our lives have been forever changed by Congenital Diaphragmatic Hernia. We're just trying to find a way to make it work.
Monday, April 2, 2012
Humbleing
I talked to our pediatrician today. He's working with Dr Miniati (surgeon and CDH specialist from UCSF) and theyre going to come up with a plan to help Liam. All weekend they kept missing eachother due to crappy cell reception but hopefully tomarrow at Liams appointment Ill have some news. What their plan is and then Ill have to figure out to comply with their plan if its taking Liam to UCSF, which im pretty sure is. Our Ped says he needs to atleast go for a CDH clinic but with all his respitory issues he thinks it'll be more than that. Question is when. Money shouldnt be my worry, it should be my son. We always figure a way to make things work or God finds a way to provide. I pray that we get Liam fixed and that one day I will be able to pay forward all the generosity you all have shown us. Before my son came along I didn't think this world had so many kind and generous people in it. I didn't think there was this much good, this much love left in people. I am an optimist but the amount of feedback we have seen has been truely amazing. From your donations, your prayers, your comments or just following Liams progress its blown me away. Liam's facebook page alone has 103 fans and I couldn't believe at first that 103 people out there care and love my son in their own way. It's still baffeling. I want to thank you for caring, for praying, for loving, for humbleing me. I will do my best to keep this blog going and keep posting updates on Liam and our family. You are truely an amazing group of readers.
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