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Faith, Hope and Joy

We are a family of five. Mum, Dad and three beautiful little girls, two of whom have diastrophic dysplasia, a rare form of dwarfism. This blog was started during my pregnancy with my second daughter and mainly talks about the ways in which dwarfism affects our lives.

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Faith, Hope and Joy | madeline-hope.blogspot.com Reviews
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We are a family of five. Mum, Dad and three beautiful little girls, two of whom have diastrophic dysplasia, a rare form of dwarfism. This blog was started during my pregnancy with my second daughter and mainly talks about the ways in which dwarfism affects our lives.
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2 our medical story
3 resources
4 more letter writting
5 dear minister
6 adequate spinal monitoring
7 yours sincerely
8 nicole
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Faith, Hope and Joy | madeline-hope.blogspot.com Reviews

https://madeline-hope.blogspot.com

We are a family of five. Mum, Dad and three beautiful little girls, two of whom have diastrophic dysplasia, a rare form of dwarfism. This blog was started during my pregnancy with my second daughter and mainly talks about the ways in which dwarfism affects our lives.

INTERNAL PAGES

madeline-hope.blogspot.com madeline-hope.blogspot.com
1

Faith, Hope and Joy: February 2014

http://madeline-hope.blogspot.com/2014_02_01_archive.html

We are a family of five. Mum, Dad and three beautiful little girls, two of whom have diastrophic dysplasia, a rare form of dwarfism. This blog was started during my pregnancy with my second daughter and mainly talks about the ways in which dwarfism affects our lives. Wednesday, February 26, 2014. Unlike Maddy, Briella has been "blessed" with the typical diastrophic clubbed feet. Currently, the most effective treatment for clubbed feet is the Ponseti method. Please keep us in your thoughts and prayers ove...

2

Faith, Hope and Joy: October 2014

http://madeline-hope.blogspot.com/2014_10_01_archive.html

We are a family of five. Mum, Dad and three beautiful little girls, two of whom have diastrophic dysplasia, a rare form of dwarfism. This blog was started during my pregnancy with my second daughter and mainly talks about the ways in which dwarfism affects our lives. Wednesday, October 22, 2014. Today Maddy had her first try of a wheelchair. Maddy was SO excited by it and kept saying "I love it! I'll be careful not to run anyone over. It's much faster than walking! Tuesday, October 14, 2014. And an MRI o...

3

Faith, Hope and Joy: Resources

http://madeline-hope.blogspot.com/p/resources.html

We are a family of five. Mum, Dad and three beautiful little girls, two of whom have diastrophic dysplasia, a rare form of dwarfism. This blog was started during my pregnancy with my second daughter and mainly talks about the ways in which dwarfism affects our lives. Here's a list of some sites that I've found useful in my pregnancy journey:. Poor Prenatal Diagnosis help:. A website set up to help parents of children with DD. Although the medicine is not comprehensive, it has a lot of practical help ...

4

Faith, Hope and Joy: November 2014

http://madeline-hope.blogspot.com/2014_11_01_archive.html

We are a family of five. Mum, Dad and three beautiful little girls, two of whom have diastrophic dysplasia, a rare form of dwarfism. This blog was started during my pregnancy with my second daughter and mainly talks about the ways in which dwarfism affects our lives. Tuesday, November 25, 2014. After a quick check by the surgeon and anesthetist, we were free to go home for the night. Unlike Maddy, they were happy to not draw blood from Briella before the surgery - which I was thankful for as my girls...

5

Faith, Hope and Joy: Like us on Facebook!

http://madeline-hope.blogspot.com/2015/03/like-us-on-facebook.html

We are a family of five. Mum, Dad and three beautiful little girls, two of whom have diastrophic dysplasia, a rare form of dwarfism. This blog was started during my pregnancy with my second daughter and mainly talks about the ways in which dwarfism affects our lives. Tuesday, March 24, 2015. Like us on Facebook! Life in Australia is hectic! Instead, I had the brilliant(? Looking forward to seeing you there! Subscribe to: Post Comments (Atom). Like us on Facebook! Like us on Facebook! Like us on Facebook!

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Like A Rox: November 2013

http://roxannaj.blogspot.com/2013_11_01_archive.html

The Magic Mushroom II. So, I am still sick. Imagine that. It is mainly sinuses. I woke up with my tongue really dry this morning. Not sure how that happened. Maybe because I slept with my mouth open? It felt like a cat's tongue. You know the roughness? Or am I the only one that thinks that? My MIL had no clue what I was talking about. haha. We slept in today. Love Saturdays for that reason! We got ready and went to lunch at Chick-fil-A. Isn't my hubby crazy? And if I need to drive, I'll be able too!

nossopequenogigante.blogspot.com nossopequenogigante.blogspot.com

Nosso Pequeno Gigante: Fevereiro 2013

http://nossopequenogigante.blogspot.com/2013_02_01_archive.html

Segunda-feira, 25 de fevereiro de 2013. No dia 28 de novembro de 2012 nosso pequeno gigante comemorou seu terceiro aniversário. São nessas datas que paramos para pensar um pouco mais sobre o que esses três anos de vida do Guilherme representaram para nossa família e somente a palavra AMOR pode explicar o privilégio que temos em conviver com nosso amorzinho por esse tempo. Filho, amamos você! Links para esta postagem. Santa Maria, RS, Brazil. Visualizar meu perfil completo. Blogs de Amigos com DD. Nanismo...

doesithaveaname.wordpress.com doesithaveaname.wordpress.com

Not as sneaky as I’d like to think | No Day But Today

https://doesithaveaname.wordpress.com/2015/05/10/not-as-sneaky-as-id-like-to-think

No Day But Today. Twenty Years from now you will be more disappointed by the things you didn't do than by the ones you did do. So throw off the bowlines. Sail away from the safe harbor. Catch the trade winds in your sails. Explore. Dream. Discover. – Mark Twain. Not as sneaky as I’d like to think. Remember that 5k that I was going to run? I’m sorry though, what? I should do it? I am praying/hoping/having faith that I am loosening things on earth. What is loosened may not necessarily be financial and ...

seeingjosh.wordpress.com seeingjosh.wordpress.com

A Fake What…? | Seeing Josh

https://seeingjosh.wordpress.com/2013/03/04/a-fake-what

About – a bit of History. Life goes on with glasses. The Post-Op Debrief →. A Fake What…? March 4, 2013. Once the swelling goes down, in about two weeks, he’ll be fitted for a contact lens and the fun and games will begin! This entry was tagged Aphakia. The Post-Op Debrief →. 3 thoughts on “ A Fake What…? March 5, 2013 at 2:16 pm. You’re in my thoughts! All the best with it all…. March 6, 2013 at 9:41 am. How did it go yesterday guys? We have been thinking of you and hope that it went as best as it possi...

oursonkai.blogspot.com oursonkai.blogspot.com

Our.Son.Kai: October 2013

http://oursonkai.blogspot.com/2013_10_01_archive.html

At 26 gestational weeks, after an amniocentesis and genetic testing, he was diagnosed with Diastrophic Dysplasia, a rare type of dwarfism. Now 6 years old, our son Kai is happy, healthy, and full of mischief. The purpose of this blog is to lend support and encouragement to others in similar situations and to share the tremendous experiences we've had and will continue to have as we raise our little, little boy. Friday, October 11, 2013. Oh, you're a stay-at-home Mom? What do you DO all day?

oursonkai.blogspot.com oursonkai.blogspot.com

Our.Son.Kai: February 2012

http://oursonkai.blogspot.com/2012_02_01_archive.html

At 26 gestational weeks, after an amniocentesis and genetic testing, he was diagnosed with Diastrophic Dysplasia, a rare type of dwarfism. Now 6 years old, our son Kai is happy, healthy, and full of mischief. The purpose of this blog is to lend support and encouragement to others in similar situations and to share the tremendous experiences we've had and will continue to have as we raise our little, little boy. Monday, February 27, 2012. The World Forestry Center. There was a bat exhibit. First you put o...

oursonkai.blogspot.com oursonkai.blogspot.com

Our.Son.Kai: Worth a Read

http://oursonkai.blogspot.com/2013/10/worth-read.html

At 26 gestational weeks, after an amniocentesis and genetic testing, he was diagnosed with Diastrophic Dysplasia, a rare type of dwarfism. Now 6 years old, our son Kai is happy, healthy, and full of mischief. The purpose of this blog is to lend support and encouragement to others in similar situations and to share the tremendous experiences we've had and will continue to have as we raise our little, little boy. Friday, October 11, 2013. Oh, you're a stay-at-home Mom? What do you DO all day?

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We are a family of five. Mum, Dad and three beautiful little girls, two of whom have diastrophic dysplasia, a rare form of dwarfism. This blog was started during my pregnancy with my second daughter and mainly talks about the ways in which dwarfism affects our lives. Wednesday, April 27, 2016. Please do not hesitate to contact me to discuss these issues further,. Tuesday, February 16, 2016. Getting Political part 2. Within a few days of writing my letter. Madeline has certainly benefited from the letter ...

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