milestrip blogspot.com

Miles New Ear

lt;img srcquot;httpimg.photobucket.comalbumsv381mpcmommyMilestree.jpgquot; altquot;Image hosted by Photobucket.comquot;gt; lt;brgt; This blog was originally set up for our friends and family to receive updates on Miles39; ear reconstruction surgery. We have since started using it for general updates on both our boys, but you39;ll still find lots of information on microtia surgery. See the side bar below for direct links to posts you39;ll find most relevant. Thanks for visiting! Please

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LINKS TO WEB SITE

The adventures of Trey and Matthew

The adventures of Trey and Matthew. Adventures in ear reconstruction surgery and enjoying the adventures of 2 beautiful boys. Update on Trey with a baha Oticon Ponto. He is very happy about his ear. This blog is to share .

Anises Adventure

Our journey with Atresia and Microtia and the adventures of Atresia Repair Surgery. Tuesday, September 14, 2010. Monday we wake up and head downstairs and the 1st thing Anise asks for.

Langer Loksh

Foundation for Faces of Children. Bringing Up a Child Whose Face Looks Different. Other Groups that Help with Hemifacial Microsomia.

Mission Little Brother

Monday, August 16, 2010. We are considering having the BAHA implant - maybe next year? Here are some pictures of the first day of school - my how they grow! Friday, January 01, 2010. Tuesday, December 22, 2009.

Sydneys Ear Reconstruction

Sydney is our beautiful little girl born in 2004. Sydney was born with Treacher-Collins Syndrome. In September 2008, she underwent the first of three ear reconstruction surgeries under the care of Dr. John Reinisch at Cedars-Sinai Medical Center in Los Angeles. Her final surgery took place in May 2009. This blog is a chronicle of that journey. Wednesday, December 23, 2009. Sunday, July 26, 2009. No more earrings for now. Tuesday, July 7, 2009. 6 weeks post op- stage 2.

The Antonio Family

Tuesday, April 14, 2015. We recently took Miles to McAllen, TX to compete in the State Scholastic Grade Championships. He did very well, losing only the first two games and then going on the win the next 5 in a row. His best performance at a weekend tournament this size yet. After the tournament, we rented a cottage in Corpus Christi and had a 3 day vacation to do some beach time and sight seeing. He ended up tying for 9th place and came in 29th out of 150.

Robbies Little Nubby

Wednesday, October 3, 2012. Robbie had his fracture repair surgery on June 7th again in LA. Everything went well and he recovered and bounced back really fast. Things have been going really good and we are hoping for the best with this implant and continue to move forward. Robbie goes to the ENT for his first cleaning since the surgery and a hearing test. Keeping our fingers crossed that his hearing is the same or better. Tuesday, March 6, 2012.

Belle Josh

Thursday, December 27, 2007. May 2007 - Ear Doing Great. Here we are 7 weeks post Stage 2 Medpor surgery and the ear is looking great. You can still see the spot that was slow to heal, but it appears to be healing. Click on the pages listed below in the Blog Archive. Stage 2 - Three Weeks Later. May 2007 - Ear Doing Great. Atresia and Microtia Yahoo Group.

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Miles New Ear

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lt;img srcquot;httpimg.photobucket.comalbumsv381mpcmommyMilestree.jpgquot; altquot;Image hosted by Photobucket.comquot;gt; lt;brgt; This blog was originally set up for our friends and family to receive updates on Miles39; ear reconstruction surgery. We have since started using it for general updates on both our boys, but you39;ll still find lots of information on microtia surgery. See the side bar below for direct links to posts you39;ll find most relevant. Thanks for visiting! Please

CONTENT

This web page milestrip.blogspot.com states the following, "Thursday, March 18, 2010." We saw that the webpage said " Miles got a Hearing Aid." It also said " Last Fall, we finally got a loaner hearing aid for Miles to try out. Actually, we got two. He got to try a BAHA and a BCHA for a total of 3 months. A BAHA is a bone anchored hearing aid. You can either wear it on a softband or get a permanent implant so it attaches to your skull. I dont have a picture of him with it, but it looked like this, but red. He doesnt wear it much at home and I dont push him too much. But his teacher reminds him to wea."

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Miles Tucker

University of Massachusetts, Amherst.