Guest guest Posted December 22, 2006 Report Share Posted December 22, 2006 Hi brianne19802004, There are several surgeries that are common with BPEI. Without knowing which surgery you're referring to, it's hard to provide much specific information. There are a number of resources on the Intarweb that describe the surgeries. For example: http://www.emedicine.com/ent/topic97.htm describes ptosis repair surgery. And here's a random article that Google threw at me: http://www.ijo.in/article.asp?issn=0301-4738;year=1983;volume=31;issue=4;spage=3\ 39;epage=341;aulast=Betharia Can you say what operation the surgeon has been talking about? Rob W p.s. Please turn off your caps lock. In Internet fora, upper-case is usually used for SHOUTING. brianne19802004 wrote: > HI EVERYONE, > FIRST LET ME SAY I WAS SO GLAD TO FIND A SUPPORT GROUP FOR THE FAMILIES > OF CHILDREN WHO HAVE BLEPH. MY SON WAS DIAGNOSED WHEN HE WAS A WEEK > OLD. NO ONE IS MY FAMILY OR HIS FATHERS SIDE HAS THIS SYNDROME. MEHKAI > IS GETTING READY TO TURN 3 AND WE ARE HEADING UP TO CHICAGO IN JANUARY > TO DISCUSS SURGERY OPTIONS. THE SURGEON HAS ALREADY TOLD ME HE NEEDS > THE SURGERY MY BIGGEST FEAR IS THE SURGERY AND POSSIBLE COMPLICATIONS. > I HAVE RESEARCHED MY HEART ON THIS SYNDROME BUT I HAVENT FOUND MUCH ON > THE SURGERY DOES ANYONE HAS ANY SUGG. ON WEBSITES FOR ME TO LOOK AT I > WOULD GREATLY APPRECIATE IT. AGAIN IM SO GLAD I FOUND THIS GROUP AND > ITS NICE TO KNOW IM NOT ALONE IN THIS. > THANKS AGAIN Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 27, 2006 Report Share Posted December 27, 2006 Hello ne, I wanted to just let you know that my daughter is 5 months old and had a sling surgery at 3 months of age. The surgery was performed at Riley Hospital for Children in Indianapolis, Indiana. The doctor was wonderful and I could not have asked to better results. You can see before and after pictures of Avery's surgery. If you have any questions or know what surgery your child is scheduled for, please let me know. Thanks, Nicki > > HI EVERYONE, > > FIRST LET ME SAY I WAS SO GLAD TO FIND A SUPPORT GROUP FOR THE FAMILIES > > OF CHILDREN WHO HAVE BLEPH. MY SON WAS DIAGNOSED WHEN HE WAS A WEEK > > OLD. NO ONE IS MY FAMILY OR HIS FATHERS SIDE HAS THIS SYNDROME. MEHKAI > > IS GETTING READY TO TURN 3 AND WE ARE HEADING UP TO CHICAGO IN JANUARY > > TO DISCUSS SURGERY OPTIONS. THE SURGEON HAS ALREADY TOLD ME HE NEEDS > > THE SURGERY MY BIGGEST FEAR IS THE SURGERY AND POSSIBLE COMPLICATIONS. > > I HAVE RESEARCHED MY HEART ON THIS SYNDROME BUT I HAVENT FOUND MUCH ON > > THE SURGERY DOES ANYONE HAS ANY SUGG. ON WEBSITES FOR ME TO LOOK AT I > > WOULD GREATLY APPRECIATE IT. AGAIN IM SO GLAD I FOUND THIS GROUP AND > > ITS NICE TO KNOW IM NOT ALONE IN THIS. > > THANKS AGAIN > Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.