tag:blogger.com,1999:blog-2480435303065023927.post8872914430104847949..comments2019-09-22T03:57:23.110-07:00Comments on Chronicling The Comerfords: Amelia and the CholesteatomaMrs. Comerfordhttp://www.blogger.com/profile/13132569128279764959noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-2480435303065023927.post-76599128603793756982012-07-02T17:00:54.017-07:002012-07-02T17:00:54.017-07:00Tasha, I will check it out! At this point a secon...Tasha, I will check it out! At this point a second surgery is not planned. We pray it will not come back. We go back in August for a follow up in August then will continue every 6 months afterwards. The pediatric ent said she is the best and earliest case they have seen. We are so thankful for our pediatrician following her instinct. We really feel like the Lord was looking out for her (and Mrs. Comerfordhttps://www.blogger.com/profile/13132569128279764959noreply@blogger.comtag:blogger.com,1999:blog-2480435303065023927.post-11487368433776019312012-07-02T11:08:12.650-07:002012-07-02T11:08:12.650-07:00Hi, I just found your blog. I am setting up a page...Hi, I just found your blog. I am setting up a page about congenital cholesteatoma, and was wondering if you'd like to take a look. It's at http://www.bornwithcholesteatoma.net. I have seen your girl had her surgery and did pretty well, which is great to hear. I haven't heard too many stories like this yet, but so very glad for you. Is a 2nd surgery planned? <br />Blessings to your tygabhttps://www.blogger.com/profile/14194763000087724566noreply@blogger.com