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Life with Jessica | Ramblings on raising a child with Cornelia de Lange Syndrome

Ramblings on raising a child with Cornelia de Lange Syndrome

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Life with Jessica | Ramblings on raising a child with Cornelia de Lange Syndrome | cdlsva.wordpress.com Reviews
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Ramblings on raising a child with Cornelia de Lange Syndrome
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Life with Jessica | Ramblings on raising a child with Cornelia de Lange Syndrome | cdlsva.wordpress.com Reviews

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Ramblings on raising a child with Cornelia de Lange Syndrome

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SOOC Saturday ~ Spring | Life with Jessica

https://cdlsva.wordpress.com/2010/04/10/sooc-saturday-spring

Ramblings on raising a child with Cornelia de Lange Syndrome. A Bit About Jess. April 10, 2010. Change is the constant, the signal for rebirth, the egg of the phoenix”. Happy Saturday, happy Spring! Posted in SOOC Saturday. Laquo; SOOC Saturday Hidden Worlds. I love this image, I love how her little hands are cupping the egg ever so gently. This is a fantastic image! On April 10, 2010. Wow, I love the hands, how they are holding the egg. Beautiful! On April 10, 2010. Thanks for stopping by my blog! You a...

2

sooc9509 | Life with Jessica

https://cdlsva.wordpress.com/2009/09/05/sooc-saturday-5/sooc9509

Ramblings on raising a child with Cornelia de Lange Syndrome. A Bit About Jess. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out. You are commenting using your Google account. ( Log Out. Notify me of new comments via email. Mom's a Nerd.

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iPod Touch – there really is an app for everyone… | Life with Jessica

https://cdlsva.wordpress.com/2009/10/08/ipod-touch-there-really-is-an-app-for-everyone

Ramblings on raising a child with Cornelia de Lange Syndrome. A Bit About Jess. October 8, 2009. IPod Touch – there really is an app for everyone…. And Jessica found hers…the Atomic Fart app😀. Posted in Fun stuff. Cornelia de Lange Syndrome. Laquo; An Official Teenager! SOOC Saturday “X” Marks the Spot. We always enjoy your videos! By: Heidi @ ggip. On October 8, 2009. I can’t hear it – but I imagine that it is quite hilarious! On April 8, 2010. Leave a Reply Cancel reply. Enter your comment here. Get e...

4

SOOC Saturday ~ “X” Marks the Spot | Life with Jessica

https://cdlsva.wordpress.com/2010/02/13/sooc-saturday-x-marks-the-spot

Ramblings on raising a child with Cornelia de Lange Syndrome. A Bit About Jess. February 13, 2010. SOOC Saturday “X” Marks the Spot. Who knows what treasures lie beneath the frozen tundra that is our yard. We shall find out come spring! PS – we are soooo tired of snow! Posted in SOOC Saturday. Laquo; iPod Touch – there really is an app for everyone…. SOOC Saturday Hidden Worlds. Oh my that is a lovely picture. Loads loads and loads of snow. Glad to see you back! By: floortime lite mama. Yes, the soggy re...

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See you in September… | Life with Jessica

https://cdlsva.wordpress.com/2009/08/17/see-you-in-september

Ramblings on raising a child with Cornelia de Lange Syndrome. A Bit About Jess. August 17, 2009. See you in September…. School will be back in session soon…so maybe I’ll be able to start blogging regularly again! Thought I’d share this video of Jessica “entertaining” her grandparents and uncle. She sings “It’s a Small World”, the end of “The Star Spangled Banner” and says the Pledge of Allegience…all in Jessica language of course! Notice how she initiates the applause at the end of each tune. Notify me o...

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Megzys World: Making a Mommy

http://megzyworld.blogspot.com/2008/12/making-mommy.html

CLICK HERE FOR THOUSANDS OF FREE BLOGGER TEMPLATES. Monday, December 1, 2008. So my friend Kadi from the. Is mentoring a young mother to be. She has taken a young girl under her wing who is newly pregnant. She is journaling the whole expereince on her new blog Making a Mommy. Thanks for the link. I'm sure it's such an interesting experience. December 1, 2008 at 7:43 PM. Subscribe to: Post Comments (Atom). My name is Megan and I am a proud mother to two great boys, Reece and Mason! View my complete profile.

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Megzys World: Win a $10.00 Starbucks Gift Card!!

http://megzyworld.blogspot.com/2008/11/win-1000-starbucks-gift-card.html

CLICK HERE FOR THOUSANDS OF FREE BLOGGER TEMPLATES. Wednesday, November 26, 2008. Win a $10.00 Starbucks Gift Card! Click Here For Details. November 27, 2008 at 9:18 AM. Subscribe to: Post Comments (Atom). My name is Megan and I am a proud mother to two great boys, Reece and Mason! My youngest son Mason has Cornelia de Lange Sydrome. Please visit CDLSUSA.ORG to learn more! I just graduated Nursing School this past May. I am looking forward to the new adventures that lie ahead! View my complete profile.

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Megzys World: The Most Wonderful Time of The Year!!

http://megzyworld.blogspot.com/2008/12/most-wonderful-time-of-year.html

CLICK HERE FOR THOUSANDS OF FREE BLOGGER TEMPLATES. Friday, December 26, 2008. The Most Wonderful Time of The Year! I could just eat both of them up! How ADORABLE x's 100! These made my night! December 26, 2008 at 9:20 PM. I'm so glad you posted some photos! I love the ones of both boys together. Hope you had a happy holiday! December 27, 2008 at 7:43 AM. I, too, was so excited to see these photos when I checked on you. The boys are cuties. Happy New Year. December 27, 2008 at 12:45 PM. Mommy to an angel.

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Maddy's Farm

http://maddysfarm.blogspot.com/2001/10/welcome-to-maddys-new-blog-i-decided-to.html

Monday, October 22, 2001. Welcome to Maddy's new blog! I decided to start here, since I don't really have time to update her web site on a regular basis. Besides, the web site seems to always be down. I'll leave it up, but for now all updates will happen here instead. Maddy will turn five years old on November 22! We're planning on redecorating her room for her birthday. Right now, she still sleeps in a crib. Nana and Grandpa bought her a toddler bed for her birthday (shhhh! She doesn't know about it yet!

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About | Caitlin & Life with CdLS

https://sgisti.wordpress.com/about

Caitlin and Life with CdLS. This is an example of a WordPress page, you could edit this to put information about yourself or your site so readers know where you are coming from. You can create as many pages like this one or sub-pages as you like and manage all of your content inside of WordPress. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out.

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Megzys World: November 2008

http://megzyworld.blogspot.com/2008_11_01_archive.html

CLICK HERE FOR THOUSANDS OF FREE BLOGGER TEMPLATES. Wednesday, November 26, 2008. Win a $10.00 Starbucks Gift Card! Click Here For Details. Monday, November 24, 2008. In Memory of Nicholas. Please pray for the family and friends of little Nicholas. Nicholas was a very special little boy with. His mother notified our online support group the other day that he passed away while napping on the couch. He will forever hold a place in our hearts. Did YOU See It? I didit was as if I was 10 all over again! Rush ...

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Journey of Hope: June 2011

http://journeyofhopekurth.blogspot.com/2011_06_01_archive.html

Wednesday, June 15, 2011. So long, Dr. Brown. I dreamed about this day, toying with it in my brain. What would it be like? What would I do with all that extra time? Fool around on Facebook? Play with the kids more? Alas, it's here. Earlier this month, for the first time in THREE AND A HALF YEARS, we are bottle-free. Hope has been off bottles since January and Oscar finally got the hang of sippy cups about two weeks ago. Dr. Brown has finally left the building. Subscribe to: Posts (Atom). Walk with the Ri...

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Journey of Hope: October 2007

http://journeyofhopekurth.blogspot.com/2007_10_01_archive.html

Wednesday, October 31, 2007. I'm Joel. She's Mo. We're newspaper journalists from suburban Detroit. Enough about us. The cute girl is Hope. She is awesome. Hope was born on Halloween in 2007. She was teensy. 3 pounds, 15 ounces at 37 weeks, most of which was a magnificent shock of red hair and big, beautiful eyes. Doctors didn't need long to diagnose her with Cornelia de. Syndrome. They had experience: Our son, Will. 18, another birth defect. That triggered numerous ultrasounds and echocardiograms. We we...

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Información en Español. Annual Report and Financials. Connect with a Family. Información en Español. CdLS Advocacy and Awareness. CdLS Centers for Excellence. Celebration and Memorial Gifts. Stocks, Trusts and Other Gifts. 21st Century Conference Fund. Connect with a Family. Dress Down for CdLS. Team CdLS 5k Club. Yard Sale Across America. We're Here for You. The CdLS Foundation staff is here to listen and help. Call 800.753.2357 Monday through Friday, 8:30 am to 5 pm, eastern time.

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CdLS Foundation: The Water Cooler

CdLS Foundation: The Water Cooler. December 17, 2010 · 12:56 pm. The CdLS Foundation blog is moving …. The CdLS Foundation blog is moving to http:/ blog.cdlsusa.org. On our brand new Web site. Be sure to check it out at http:/ www.CdLSusa.org. December 7, 2010 · 3:11 pm. Happy Holidays from the CdLS Foundation. Http:/ myemail.constantcontact.com/Happy-Holidays-from-the-CdLS-Foundation.html? November 23, 2010 · 11:21 am. Making a giant impression …. October 25, 2010 · 3:32 pm. The 40 page book has lots of...

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Life with Jessica | Ramblings on raising a child with Cornelia de Lange Syndrome

Ramblings on raising a child with Cornelia de Lange Syndrome. A Bit About Jess. April 10, 2010. Change is the constant, the signal for rebirth, the egg of the phoenix”. Happy Saturday, happy Spring! Posted in SOOC Saturday. February 20, 2010. SOOC Saturday Hidden Worlds. 8220;To see a world in a grain of sand and heaven in a wild flower; hold infinity in the palm of your hand and eternity in an hour”. February 13, 2010. SOOC Saturday “X” Marks the Spot. PS – we are soooo tired of snow! October 8, 2009.

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The Williams Family Blog

The Williams Family Blog. Friday, September 4, 2009. Thursday, March 19, 2009. Spencer turns 6 months old. Wednesday, January 14, 2009. Christmas 08 and early 09. Dawn, Charlie, Logann and Spencer. Monday, December 22, 2008. Sunday, December 7, 2008. This past month was busy and fun. We finally got our first snow on Thanksgiving night. As you can see from the photos, Logann. Is quite the snow bunny. She turned 3 on the 11 th. Spencer now smiles, coos, says ah-goo and tolerates his sister. Logann's. Went ...

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The worldwide website about. Cornelia de Lange Syndrome. Cornelia de Lange Syndrome. Cornelia de Lange Syndrome. Last modified by Gerritjan Koekkoek. Select the pages to export:. World of the Cornelia de Lange syndrome. An International source of information about the rare genetic condition, Cornelia de Lange Syndrome (CdLS). Here you can find people who know about CdLS as well as answers to your questions about the condition. Here you can find hope. CdLS is a rare and complex syndrome! All of the inform...

cdlsworld.org cdlsworld.org

Cornelia de Lange Syndrome - CdLS World

The worldwide website about. Cornelia de Lange Syndrome. Cornelia de Lange Syndrome. Cornelia de Lange Syndrome. Last modified by Gerritjan Koekkoek. Select the pages to export:. World of the Cornelia de Lange syndrome. An International source of information about the rare genetic condition, Cornelia de Lange Syndrome (CdLS). Here you can find people who know about CdLS as well as answers to your questions about the condition. Here you can find hope. CdLS is a rare and complex syndrome! All of the inform...