tag:blogger.com,1999:blog-5189235178576919403.post5116532683969998204..comments2023-10-24T05:55:46.244-04:00Comments on The Smithson Family: Lainey's Cystic Fibrosis StoryThe Smithson Familyhttp://www.blogger.com/profile/00459233993191994420noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-5189235178576919403.post-17976955183906176682010-08-28T02:02:20.914-04:002010-08-28T02:02:20.914-04:00My daughter and your daughter have the same mutati...My daughter and your daughter have the same mutations! Wow! I don't feel so alone anymore.Amandanoreply@blogger.comtag:blogger.com,1999:blog-5189235178576919403.post-35397726448195273522010-06-19T02:11:37.356-04:002010-06-19T02:11:37.356-04:00I was surfing through blogs and came upon yours. I...I was surfing through blogs and came upon yours. I have been looking for other families that are dealing with CF. Your story sounds so familiar. My son was born Feb '08 also with meconium ileus. He had surgery at 3 days old and stayed in the NICU for 3 months. He had many complications associated with CF other than the meconium ileus. His mutation combination is nowhere on file in the world. One mutation had very little info while the other has none. We are very fortunate to be close to a CF research clinic and have great doctors. I hope your little princess stays as healthy as possible. Lung infections are scary.Bridgette Knowlsonhttps://www.blogger.com/profile/14882123722949488354noreply@blogger.com