heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: CHD-UK...A website with lots of information on CHD
http://heterotaxypolysplenia.blogspot.com/2012/02/chd-uka-website-with-lots-of.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Thursday, February 9, 2012. CHD-UK.A website with lots of information on CHD. In honor of CHD awareness week. I am posting a link to a website that I wanted to share with all of you. Http:/ congenital-heart-defects.co.uk/WhatisCongenitalHeartDefects.aspx. Subscribe to: Post Comments (Atom). Ava - The story of a baby ...
heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: Brady's full sentence
http://heterotaxypolysplenia.blogspot.com/2010/03/bradys-full-sentence.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Saturday, March 27, 2010. Last night, we took the kids to the YMCA for family swim. We had so much fun and the kids loved it. Today, Brady said to his dad, "Lets go swimming". Can you believe Brady said a full sentence. Well he did! I am so excited! I just wanted to share that with all of you. Drawing Heart Project -...
heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: Another Pneumonia/Influenza A
http://heterotaxypolysplenia.blogspot.com/2009/06/another-pneumonia.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Friday, June 19, 2009. Subscribe to: Post Comments (Atom). With awareness comes understanding and with understanding comes change. From a special friend in Canada (Laura). But I believe god only gives us special little ones when we are special too. Hold onto that my dear friend.”. Helping Hallie - A very special litt...
heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: Aiden's Angels, Inc.
http://heterotaxypolysplenia.blogspot.com/2012/03/taken-directly-from-aidens-angels-inc.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Tuesday, March 20, 2012. Aiden's Angels, Inc. Aiden is a 2 year old little boy with Heterotaxy and CHD. His mom is a nurse, his dad a pharmacist. The non-profit organization to help families in the Central Kentucky area with children born affected by congenital heart disease. Aiden's Angels, Inc. 8220;God must trust ...
heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: Angel Flight and Angel Bus
http://heterotaxypolysplenia.blogspot.com/2011/06/angel-flight-and-angel-bus.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Wednesday, June 22, 2011. Angel Flight and Angel Bus. Angel Flight is a non profit organization that arranges free air transportation for any serious medically related need. Angel Bus is a non profit organization that arranges free ground transportation for any serious medically related need. Ava - The story of a bab...
heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: A great Article...A must read...
http://heterotaxypolysplenia.blogspot.com/2011/07/great-articlea-must-read.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Sunday, July 17, 2011. A great Article.A must read. See link below.It's an article on Heterotaxia, Congenital Heart Disease, and Primary Ciliary Dyskinesia. Http:/ circ.ahajournals.org/content/115/22/2793.full. Subscribe to: Post Comments (Atom). With awareness comes understanding and with understanding comes change.
heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: Chloe started 1st Grade & Junes encountrer with Swine Flu
http://heterotaxypolysplenia.blogspot.com/2009/09/chloe-started-1st-grade-junes_02.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Wednesday, September 2, 2009. Chloe started 1st Grade and Junes encountrer with Swine Flu. Subscribe to: Post Comments (Atom). With awareness comes understanding and with understanding comes change. From a special friend in Canada (Laura). HELP SPREAD THE WORD ABOUT HETEROTAXY AROUND THE WORLD. Drawing Heart Project ...
heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: (PDD NOS) Autism & Brady
http://heterotaxypolysplenia.blogspot.com/2009/08/autism-brady.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Friday, August 14, 2009. PDD NOS) Autism and Brady. Http:/ www.autismvotes.org/site/c.frKNI3PCImE/b.4432481/k.90A7/Massachusetts.htm. Http:/ www.autismvotes.org/atf/cf/%7B2A179B73-96E2-44C3-8816-1B1C0BE5334B%7D/Arguments for private insurance %20coverage.pdf. And good luck with your new non-profit! HELP SPREAD THE WO...
heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: Rhode Island Rare Disease Foundation - October's Newsletter
http://heterotaxypolysplenia.blogspot.com/2012/11/rhode-island-rare-disease-foundation.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Friday, November 2, 2012. Rhode Island Rare Disease Foundation - October's Newsletter. Chloe was featured in Rhode Island Rare Disease Foudation October Newsletter http:/ us5.campaign-archive1.com/? Subscribe to: Post Comments (Atom). With awareness comes understanding and with understanding comes change. Fishing for...
heterotaxypolysplenia.blogspot.com
Finding Answers to Heterotaxy, Polysplenia Syndrome: Today
http://heterotaxypolysplenia.blogspot.com/2010/03/today.html
Finding Answers to Heterotaxy, Polysplenia Syndrome. A 10 year old girl living with Heterotaxy - Polysplenia. Join me in my quest to find answers to my questions as I learn about heterotaxy. Monday, March 1, 2010. My daughter Chloe is special not because of her syndrome but because of who she is as a person. My daughter is my champ; I have such admiration for her! Subscribe to: Post Comments (Atom). With awareness comes understanding and with understanding comes change. 8220;God must trust that you are t...
SOCIAL ENGAGEMENT