miraclesformiles.blogspot.com

Miracles for Miles

I found out on September 5, 2014 that my son, Miles, will be born with Spina Bifida. He is due in February 2015. Here is his story from the beginning. Sunday, February 8, 2015. If I Were Being Honest. Many parents of special needs children share this poem. I didn’t read that anywhere in the poem. It’s getting hot. We are getting uncomfortable. Where are we landing? We are in Haiti. Oh hells no. I did NOT buy that ticket. Saturday, January 17, 2015. Whose Side Am I On Anyway? This has been a fascinating p...

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I found out on September 5, 2014 that my son, Miles, will be born with Spina Bifida. He is due in February 2015. Here is his story from the beginning. Sunday, February 8, 2015. If I Were Being Honest. Many parents of special needs children share this poem. I didn’t read that anywhere in the poem. It’s getting hot. We are getting uncomfortable. Where are we landing? We are in Haiti. Oh hells no. I did NOT buy that ticket. Saturday, January 17, 2015. Whose Side Am I On Anyway? This has been a fascinating p...

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Miracles for Miles | miraclesformiles.blogspot.com Reviews

https://miraclesformiles.blogspot.com

I found out on September 5, 2014 that my son, Miles, will be born with Spina Bifida. He is due in February 2015. Here is his story from the beginning. Sunday, February 8, 2015. If I Were Being Honest. Many parents of special needs children share this poem. I didn’t read that anywhere in the poem. It’s getting hot. We are getting uncomfortable. Where are we landing? We are in Haiti. Oh hells no. I did NOT buy that ticket. Saturday, January 17, 2015. Whose Side Am I On Anyway? This has been a fascinating p...

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miraclesformiles.blogspot.com

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Miracles for Miles: January 2015

http://www.miraclesformiles.blogspot.com/2015_01_01_archive.html

A family's precious life. Their youngest son born with Spina Bifida and experiences the worst complications possible. They learned their third son will be born with the same disability. They chose joy. Saturday, January 17, 2015. Whose Side Am I On Anyway? I had switched teams. I’m back on the team of hope, joy, faith and insurmountable love. I know now that God wasn’t going to let me have Miles until I learned this lesson. Location: Phoenix, AZ, USA. Monday, January 12, 2015. A Little Patch of Grass.

2

Miracles for Miles: Whose Side Am I On Anyway?

http://www.miraclesformiles.blogspot.com/2015/01/whose-side-am-i-on-anyway.html

A family's precious life. Their youngest son born with Spina Bifida and experiences the worst complications possible. They learned their third son will be born with the same disability. They chose joy. Saturday, January 17, 2015. Whose Side Am I On Anyway? I had switched teams. I’m back on the team of hope, joy, faith and insurmountable love. I know now that God wasn’t going to let me have Miles until I learned this lesson. Location: Phoenix, AZ, USA. January 17, 2015 at 11:11 PM. Sharon M. Himsl. Januar...

3

Miracles for Miles: December 2014

http://www.miraclesformiles.blogspot.com/2014_12_01_archive.html

A family's precious life. Their youngest son born with Spina Bifida and experiences the worst complications possible. They learned their third son will be born with the same disability. They chose joy. Thursday, December 4, 2014. Just an Ordinary Girl. 8220;Do you wonder as you watch my face. If a wiser one should have had my place? But I offer all I am. For the mercy of Your plan. Help me be strong”. 8220;Breath of Heaven” Amy Grant. I have traveled many moonless nights. Cold and weary with a babe inside.

4

Miracles for Miles: The Day We Got The News

http://www.miraclesformiles.blogspot.com/2014/09/the-day-we-got-news.html

A family's precious life. Their youngest son born with Spina Bifida and experiences the worst complications possible. They learned their third son will be born with the same disability. They chose joy. Saturday, September 6, 2014. The Day We Got The News. The tech left us alone in the room for about 15 minutes as we sent texts to family, overjoyed to be having a second boy! How disabled is she? Shortly after those question she said it, “There is a Spina Bifida.” I just stared at her. ...No, he doesn't&#4...

5

Miracles for Miles: If I Were Being Honest

http://www.miraclesformiles.blogspot.com/2015/02/if-i-were-being-honest.html

A family's precious life. Their youngest son born with Spina Bifida and experiences the worst complications possible. They learned their third son will be born with the same disability. They chose joy. Sunday, February 8, 2015. If I Were Being Honest. Many parents of special needs children share this poem. I didn’t read that anywhere in the poem. It’s getting hot. We are getting uncomfortable. Where are we landing? We are in Haiti. Oh hells no. I did NOT buy that ticket. Subscribe to: Post Comments (Atom).

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My Not-So-Little Guy & My Little Punky Pie: PR Friendly

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Have a product or service you would like our opinion on? My Not So Little Guy and My Little Punky and Pumpkin Pies would love to review and share your product! The mama, Stephanie. 8211;42, female. A kindergarten teacher turned SAHM who loves taking pictures, music, education, couponing/bargains/frugal shopping, party planning, hockey, baking, marching band, anything to do with my kids,. Matching my girls' clothes, and. The husband (George)–41, male. My Not So Little Guy (Andrew)–16, male. She's a happy ...

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My Not-So-Little Guy & My Little Punky Pie: The Husband

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And I met through a mutual friend, the internet, in 2007, only to discover we actually. Have a mutual real life friend. We knew fairly quickly we had something special together. After all, when you start "dating" someone who lives 1800 miles away from you, all you. Is communicate and learn about one another. We met in person on June 17 of that year, Father's Day. We spent most of that summer together- one of the perks of being a teacher, as I was able to stay in Pittsburgh. But, God did. The day we met).

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My Not-So-Little Guy & My Little Punky Pie: The Mama

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I'm a 42 year old wife to the love of my life, my best friend, George. We've been together for 9 years and married 5 and half. Our love story is very full of peaks and valleys and it's made us strong together. We are miscarriage survivors and we have a spunky 5 year old girl, Lily and our grand finale, baby girl Violet. I'm honest, loyal, patient, loving, emotional, authentic and playfully sarcastic. I'm a former kindergarten teacher, an event planner and even pursued a singing career in Nashville. I emb...

littlepunkypie.blogspot.com

My Not-So-Little Guy & My Little Punky Pie: Let Freedom Ring!

http://littlepunkypie.blogspot.com/2015/07/let-freedom-ring.html

Tuesday, July 14, 2015. I'm not sure why so many townships in PA celebrate the 4th of July on random days other than the 4th, but ours chooses a Sunday around the 4th. This year was July 5. The festivities started off with a local parade that Andrew. S high school marching band participates in. This was Andrew. S first year marching since the kids don't march their rookie year and last year we were already in AZ visiting family. I love parades and the girls are loving them too! And I kept our place.

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My Not-So-Little Guy & My Little Punky Pie: Happy to be with You on the 4th of July!

http://littlepunkypie.blogspot.com/2015/07/happy-to-be-with-you-on-4th-of-july.html

Monday, July 13, 2015. Happy to be with You on the 4th of July! July started off much better- It was great to reconnect with our friends we hadn't seen in too long! Fourth of July was hot and muggy, but really fun! We went to a picnic at our friends' family's house. This is a tradition with their family and the second time we've gone. This was, however, the first year we've made it in time for the parade! We arrived and got to catch up, ate, the kids got to play, and then we headed to the parade. I'm hon...

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My Not-So-Little Guy & My Little Punky Pie: The Kids

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Is my Not-So-Little Guy. ;). Yeah, the 16-year-old, first born, my first baby, my guinea pig for parenting. He loves lacrosse, hockey, legos, Star Wars, video games, robotics, math, reading, fishing, social studies, Greek mythology, swimming, Harry Potter books and movies and his favorite color is green. His favorite food is a cheeseburger and he's loved them since he was 1. He is in his 3rd year of marching band this year and it makes my bandgeek heart so happy that he loves it as much as I did! Is our ...

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My Not-So-Little Guy & My Little Punky Pie: #RacetotheEdge with Netflix

http://littlepunkypie.blogspot.com/2015/07/racetotheedge-with-netflix.html

Friday, July 31, 2015. I know I say this all the time, but it is without question that Netflix. Is our tv go to. We do not miss cable at all and live network tv is pretty much nil in the summer, so Netflix. Is absolutely solidified as a part of our family even more! Original shows like Orange is the New Black and House of Cards. I also really. Love that there are Netflix. We were all excited! Is always using her imagination, creating, and exploring! So, when Netflix. Shared the Dragons: Race to the Edge.

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They told us there was no hope of our son living a normal life. We know they are wrong. He was born with severe brain damage on both sides of his brain. He is behind but he's already doing things the doctors said he would never do. This site is for all those who have brain injured children and were told to prepare for the worst. My husband and I wanted to write this to give hope to those parents who were told there was no hope. Proudly powered by Weebly.

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Miracles for Miles

I found out on September 5, 2014 that my son, Miles, will be born with Spina Bifida. He is due in February 2015. Here is his story from the beginning. Sunday, February 8, 2015. If I Were Being Honest. Many parents of special needs children share this poem. I didn’t read that anywhere in the poem. It’s getting hot. We are getting uncomfortable. Where are we landing? We are in Haiti. Oh hells no. I did NOT buy that ticket. Saturday, January 17, 2015. Whose Side Am I On Anyway? This has been a fascinating p...

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Click here to edit subtitle. Thank you Generous People. Please come in and sign our. Leave Mitchell with your best wishes, let him know he's not. The Trust fund has been developed, cheques may be made out to The Mitchell Condren Family Trust Fund as of August 2012. Thank you for your support. Please mail your donations to Beverly Johnston C/O Mitchell, at 5615 Blind Line, Burlington, Ontario. Here to edit text. Mitchell June 3, 2012. This is Mitchell Condren at his grade 8 graduation June 2011. These bra...

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We strive to create awareness, education and support. No one should ever walk this journey alone. Miracles for Mito: In the spirit of strength. Miracles for Mito’s mission is to ensure that no individual or family has to be alone while trying to understand a complicated mitochondrial diagnosis. We will create partnerships worldwide to help understand and share the most recent research, patient therapies and resources available in the Rocky Mountain Region. What is a mitochondrial disease? Heather Schicht...

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