littlemisshandy.com

littlemisshalfpint.wordpress.com

Little Miss Half Pint | I want to be the girl with the most cake….

Little Miss Half Pint. I want to be the girl with the most cake…. Move Over Barbie… There is a New Doll in Town. December 10, 2011 in Art. I was introduced to The Kouklitas dolls. Last year and fell head over heels. Handmade by artist Andrew Yang, these incredible 27 dolls can only be described as ‘Couture Rag Dolls’. Each doll is truly a work of art… Yang fashions the dolls from muslin and hand paints their delicate faces. They are both captivating and haunting. Ben Eastaugh and Chris Sternal-Johnson.

littlemisshalfway.wordpress.com

littlemisshalfway

December 2, 2011. Time for an upgrade. I’m leaving this blog and starting a new one, bringing some of the old posts with me. From now on, you can find me at my new blog, Maybe, Matilda. Look at you, you’re growing old so young. September 15, 2011. Dishpan hands and an aching back. She never could have imagined this. All she had ever wanted,. One more year and the light through the cracks in the windows. Might shine a little more. Two more years might mean less of the tension hardening his jaw,. I have ga...

littlemisshamilton.blogspot.com

Little Miss Hamilton x 2

Little Miss Hamilton x 2. Saturday, September 3, 2011. Football (and baton) edition. Football with Ellie was not so fun last year- -but times have changed! At the last minute today I decided to take Ellie to the State game, my parents had an extra ticket and I thought it would be a good opportunity for Ellie to see Zoe twirl. She loved it. She cheered when everyone else cheered, kept a watchful eye on the wolf mascots (all mascots are freaking her out right now) and loved seeing Zoe. We have had to major...

littlemisshammer.blogspot.com

The Grand mel Adventure

The Grand mel Adventure. My home is Colorado.and her proud mountains tall.". Tuesday, April 9, 2013. Virtually, not physically, don't worry! Check out my new page at www.thestokedlife.com. Links to this post. Monday, January 28, 2013. Learning to Walk Again. Instead of just gathering my "worst things" I've decided to view them as challenges and my anticipated reward having overcome the challenge. 1 The Complainers/Excuse makers. Result: A renewed sense of passion and drive. Having the opportunity to see ...

littlemisshamr0ck.skyrock.com

littlemisshamr0ck's blog - # Little Miss Shamr0ck # - Skyrock.com

Little Miss Shamr0ck #. Un bl0g p0ur t0us les m0ments passes en Irlande. Et p0ur t0us les gens qu on a renc0ntres la bas. N0s plus belle ph0ot0s. N0s plus beau s0uvenirs. 11/07/2007 at 8:20 AM. 20/02/2008 at 12:47 PM. Subscribe to my blog! 3 eme artcile sur. AUSSI DE KILKENNY mdrr. EME SI ON SE VOIT TRES PEU. VEC QUELQUES PASSAGES SUR MSN. EMPECHE QUE VOUS ME MANQUEZ. UOIQU'IL EN SOIT.[/. N JOUR PEUTETRE ON SE REVERRA. T ENCORE UNE FOIS. JE OUS EST FAITE EN STAR CAR JE M'ENNUIYAIS]. Beaucoup de temps c'e...

littlemisshandy.com

Price Request - BuyDomains

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littlemisshandy.net

Little Miss Handy

littlemisshannah.com

Little Miss Hannah - Fight against Neuronopathic Gaucher's Disease type 2/3 — Our Fight against Gaucher's Disease type 2 or 3

Our Fight against Gaucher's Disease type 2 or 3. If you have a child with GD23. GD23 Research & News. So Long, Farewell…. My Little Miss Hannah. I am coming up on two years since my sweet little girl passed away. Two years. How could two years have passed yet I still feel as raw and affected as if it was yesterday. I am content with this “new me.” Happy? That weighs on me. I am forever a “grieving mother” but I don’t wear this on the outside the large majority of the time. People do...However, I want the...

littlemisshannah.org

Little Miss Hannah Foundation — Support for Families of Children Diagnosed with Rare, Life-Limiting, or Complex Medically Conditions. Childhood Rare Disease Advocacy.

Skip to primary navigation. Little Miss Hannah Foundation. Support for Families of Children Diagnosed with Rare, Life-Limiting, or Complex Medically Conditions. Childhood Rare Disease Advocacy. Medical-Therapy Equipment Assistance Program. Childhood Rare Disease Advocacy. Family Support and Activities. One Child at a Time. One Child at a Time. Our Mission: Enhance the quality of life for children diagnosed with rare and complex medical conditions in Southern Nevada. Little Miss Hannah Foundation. We are ...

littlemisshannah.wordpress.com

Little Miss Hannah | In search of a diagnosis for our little girl…

In search of a diagnosis for our little girl…. December 30, 2008 by Overloaded Mama. If you haven’t already updated your RSS feeders and email notifications for the new blog location, just click or fill out below. Thanks so much 🙂. Subscribe to Little Miss Hannah by Email. Posted in Living Life. Hannah’s blog has a new home. December 27, 2008 by Overloaded Mama. You can find future updates at http:/ www.littlemisshannah.com. If you have us on your blogroll or links list, please update our information.

littlemisshannie.blogspot.com

The Key to Me

Monday, February 16, 2015. I need to write. I just don't know where. Sunday, June 2, 2013. The End’s Not Near, It’s Here (Again). I’ve been reflecting on this little ole blog. I haven’t written here in ages. Much has changed in my life since I started writing here so, so long ago. When I first started blogging, I was just a wee one in high school and now? Now I’m on the cusp of my final semester of classes for my undergraduate degree. Where did the time go? Thank you for the last 4 years. Thank you for b...