babyhazels.blogspot.com
Baby Hazel and Family: October 2008
http://babyhazels.blogspot.com/2008_10_01_archive.html
Baby Hazel and Family. This blog is about the life of Hazel who was diagnosed with Williams Syndrome and the progress she is making in the world. This blog is about me, Hazel who has Williams Syndrome. View my complete profile. Growing Up With Emma and Tatum. Jen's Two In Pink. Keeping up with the Johnsons. Williams Syndrome Web Watch. Saturday, October 4, 2008. Subscribe to: Posts (Atom).
babyhazels.blogspot.com
Baby Hazel and Family: June 2009
http://babyhazels.blogspot.com/2009_06_01_archive.html
Baby Hazel and Family. This blog is about the life of Hazel who was diagnosed with Williams Syndrome and the progress she is making in the world. This blog is about me, Hazel who has Williams Syndrome. View my complete profile. Growing Up With Emma and Tatum. Jen's Two In Pink. Keeping up with the Johnsons. Williams Syndrome Web Watch. Tuesday, June 16, 2009. Subscribe to: Posts (Atom).
babyhazels.blogspot.com
Baby Hazel and Family: January 2010
http://babyhazels.blogspot.com/2010_01_01_archive.html
Baby Hazel and Family. This blog is about the life of Hazel who was diagnosed with Williams Syndrome and the progress she is making in the world. This blog is about me, Hazel who has Williams Syndrome. View my complete profile. Growing Up With Emma and Tatum. Jen's Two In Pink. Keeping up with the Johnsons. Williams Syndrome Web Watch. Wednesday, January 13, 2010. Hazel and Cedar relaxing. Maddie and Isabelle, best friend cousins. Hazel's sedated echo and renal ultrasound went well. Dr.Baker was ...
babyhazels.blogspot.com
Baby Hazel and Family
http://babyhazels.blogspot.com/2010/01/maddie-and-isabelle-best-friend-cousins.html
Baby Hazel and Family. This blog is about the life of Hazel who was diagnosed with Williams Syndrome and the progress she is making in the world. This blog is about me, Hazel who has Williams Syndrome. View my complete profile. Growing Up With Emma and Tatum. Jen's Two In Pink. Keeping up with the Johnsons. Williams Syndrome Web Watch. Wednesday, January 13, 2010. Maddie and Isabelle, best friend cousins. Subscribe to: Post Comments (Atom).
samsmom-ourwsjourney.blogspot.com
Our WS Journey: February 2007
http://samsmom-ourwsjourney.blogspot.com/2007_02_01_archive.html
This is our family's journey through all the ups and downs of raising a child with a rare genetic disorder. Monday, February 19, 2007. Well, here goes another sleepless night! Instead of the 4 or 5 I might get during the day. Maybe someday he will be able to get to sleep during the night. I hope! He is such a precious little boy. I count myself very lucky to have him. I just wish he would sleep! Oh well, maybe someday. Links to this post. Thursday, February 15, 2007. Links to this post. Links to this post.
samsmom-ourwsjourney.blogspot.com
Our WS Journey
http://samsmom-ourwsjourney.blogspot.com/2007/02/this-is-sam.html
This is our family's journey through all the ups and downs of raising a child with a rare genetic disorder. Sunday, February 11, 2007. We have since learned that he has supra-valvular aortic stenosis, (SVAS), narrowing of his aortic valve, possible coronary narrowing, scoliosis, pronounced Kyphosis, among other issues. So far it feels like I am on a never ending roller coaster ride, but then I look into those beautiful blue eyes and he gives me that bright smile and it makes it all worthwhile.
ellaandemerson.blogspot.com
Life with Ella and Emerson: April 2007
http://ellaandemerson.blogspot.com/2007_04_01_archive.html
Life with Ella and Emerson. This is a blog dedicated to my beautiful daughters, Ella and Emerson. Emerson was diagnosed with a rare, genetic disorder called Williams Syndrome when she was 5 months old. Wisconsin, United States. View my complete profile. Just one of those days. Emmy and her Microphone. Good Morning, Sunshine! WS Awareness Event 2008. Tuesday, April 10, 2007. Abi- What a Easter you guys had, yikes! I can't wait to hear from you guys and will love your blog whether you post daily or monthly.
ellaandemerson.blogspot.com
Life with Ella and Emerson: One Last Plea...
http://ellaandemerson.blogspot.com/2008/09/one-last-plea.html
Life with Ella and Emerson. This is a blog dedicated to my beautiful daughters, Ella and Emerson. Emerson was diagnosed with a rare, genetic disorder called Williams Syndrome when she was 5 months old. Wisconsin, United States. View my complete profile. Junior Kindergarten - Mixed Emotions. Forever in our hearts. Tuesday, September 30, 2008. Here is my e-mail: nbeaumier@yahoo.com. Thank you, Thank you, Thank you! Posted by Nicole 6:48 PM. I love the picture, she is just so cute! Hey if you need more pics...
ellaandemerson.blogspot.com
Life with Ella and Emerson: March 2007
http://ellaandemerson.blogspot.com/2007_03_01_archive.html
Life with Ella and Emerson. This is a blog dedicated to my beautiful daughters, Ella and Emerson. Emerson was diagnosed with a rare, genetic disorder called Williams Syndrome when she was 5 months old. Wisconsin, United States. View my complete profile. Just one of those days. Emmy and her Microphone. Good Morning, Sunshine! WS Awareness Event 2008. Wednesday, March 21, 2007. She is now giggling more, especially for daddy, and is great at giving wet and sloppy kisses. Ella gives Emerson so much love and ...
ellaandemerson.blogspot.com
Life with Ella and Emerson: Just one of those days...
http://ellaandemerson.blogspot.com/2009/06/just-one-of-those-days.html
Life with Ella and Emerson. This is a blog dedicated to my beautiful daughters, Ella and Emerson. Emerson was diagnosed with a rare, genetic disorder called Williams Syndrome when she was 5 months old. Wisconsin, United States. View my complete profile. Emmy and her Microphone. Good Morning, Sunshine! WS Awareness Event 2008. Junior Kindergarten - Mixed Emotions. Monday, June 08, 2009. Just one of those days. Emerson has also started calling out "Hi, Grandma! Posted by Nicole 7:45 PM. Girl I broke out la...