"We thought we'd have to teach our son about the world. Turns out we have to teach the world about our son. They see a boy who cannot speak. We see a miracle who doesn't need words." -unknown
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Our Journey With One of God's Miracles | ourjourneywithoneofgodsmiracles.blogspot.com Reviews
https://ourjourneywithoneofgodsmiracles.blogspot.com
"We thought we'd have to teach our son about the world. Turns out we have to teach the world about our son. They see a boy who cannot speak. We see a miracle who doesn't need words." -unknown
ourjourneywithoneofgodsmiracles.blogspot.com
Our Journey With One of God's Miracles: August 2015
http://ourjourneywithoneofgodsmiracles.blogspot.com/2015_08_01_archive.html
Our Journey With One of God's Miracles. We thought we'd have to teach our son about the world. Turns out we have to teach the world about our son. They see a boy who cannot speak. We see a miracle who doesn't need words." -unknown. Sunday, August 30, 2015. A Day at Dreamcatcher Ranch. Through an organization called a A Kid Again. We had a great day at Dreamcatcher Ranch. The Mosaic Mansfield Church. Noah got to ride a horse named Ricochet . He seemed to really like it. Tuesday, August 25, 2015. We rode d...
Our Journey With One of God's Miracles: July 2015
http://ourjourneywithoneofgodsmiracles.blogspot.com/2015_07_01_archive.html
Our Journey With One of God's Miracles. We thought we'd have to teach our son about the world. Turns out we have to teach the world about our son. They see a boy who cannot speak. We see a miracle who doesn't need words." -unknown. Thursday, July 30, 2015. What a fun day we had at Cedar Point. We had fun seeing all the dinosaurs. The best part it was free. It was Scott's company picnic. Noah doesn't do well in the heat. I gave him lots of water but he still was still pretty miserable. Today marks 5 years...
Our Journey With One of God's Miracles: November 2014
http://ourjourneywithoneofgodsmiracles.blogspot.com/2014_11_01_archive.html
Our Journey With One of God's Miracles. We thought we'd have to teach our son about the world. Turns out we have to teach the world about our son. They see a boy who cannot speak. We see a miracle who doesn't need words." -unknown. Sunday, November 30, 2014. What does ABR therapy look like? If you ever wonder what ABR therapy looks like here's your chance. Click on the last sentence and then enter this code NS2014684. There are 7 videos of our exercises for the next 6 months. Enjoy. What a Crazy Week.
Our Journey With One of God's Miracles: March 2015
http://ourjourneywithoneofgodsmiracles.blogspot.com/2015_03_01_archive.html
Our Journey With One of God's Miracles. We thought we'd have to teach our son about the world. Turns out we have to teach the world about our son. They see a boy who cannot speak. We see a miracle who doesn't need words." -unknown. Sunday, March 22, 2015. We decided to stick around long enough to send the walkers/runners off. The masked man in the orange shirt is Stan Roberts. He runs for Noah because he can't run himself. He is such an inspiration to myself and others. Thanks, Stan! Noah is Doing Great!
Our Journey With One of God's Miracles: Having A Great Summer
http://ourjourneywithoneofgodsmiracles.blogspot.com/2015/08/having-great-summer.html
Our Journey With One of God's Miracles. We thought we'd have to teach our son about the world. Turns out we have to teach the world about our son. They see a boy who cannot speak. We see a miracle who doesn't need words." -unknown. Thursday, August 6, 2015. Having A Great Summer. We've been having a great summer. I can't believe it's almost over. Noah and Issiah decorated a flower pot for the Richland County Fair. If you go to the fair this week you'll have to look for it. Welcome to the Circus. What a b...
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Missy's CP Journey: Settling into Year 6
http://missyscpjourney.blogspot.com/2013/03/settling-into-year-6.html
Follows the journey of Missy a young determined girl who has to fight the challenge of Cerebral Palsy everyday. Missy smiles at everyday and reminds all around her to just get on with life. Saturday, March 16, 2013. Settling into Year 6. So with the same Teacher, Miss H continuing to be Missy's aid and all Year 6 in the one class this year, it's sure to be a great final year at Primary School. A week long excursion is planned for Term 3 which will be a highlight. April will see us go to Sydney again with...
Missy's CP Journey: March 2013
http://missyscpjourney.blogspot.com/2013_03_01_archive.html
Follows the journey of Missy a young determined girl who has to fight the challenge of Cerebral Palsy everyday. Missy smiles at everyday and reminds all around her to just get on with life. Wednesday, March 27, 2013. Sydney Royal Easter Show. Sticking to our annual tradition of attending the Sydney Royal Easter Show, we made the trip again. Posted by Written by Missy's proud mum. Saturday, March 16, 2013. Settling into Year 6. We continue to have meetings at our Local High School to go over property issu...
Missy's CP Journey: April 2013
http://missyscpjourney.blogspot.com/2013_04_01_archive.html
Follows the journey of Missy a young determined girl who has to fight the challenge of Cerebral Palsy everyday. Missy smiles at everyday and reminds all around her to just get on with life. Saturday, April 20, 2013. More than a badge. Missy showing off her badge. So what a wonderful honour it was for Missy to be voted by her peers to be their representative. Mum, Missy and our Mayor at the SRC Presentation. To be chosen by your peers to be the “go to person” with ideas and be responsible to r...It would ...
Missy's CP Journey: Everyone needs a friend to lean on
http://missyscpjourney.blogspot.com/2012/11/everyone-needs-friend-to-lean-on.html
Follows the journey of Missy a young determined girl who has to fight the challenge of Cerebral Palsy everyday. Missy smiles at everyday and reminds all around her to just get on with life. Friday, November 16, 2012. Everyone needs a friend to lean on. Posted by Written by Missy's proud mum. Subscribe to: Post Comments (Atom). Leonid Blyum - ABR Founder. Everyone needs a friend to lean on. Carcoar Cup Running Festival. Interesting Blogs I follow. Our Journey With One of God's Miracles.
Missy's CP Journey: The Miracle of Unbroken sleep
http://missyscpjourney.blogspot.com/2013/01/the-miracle-of-unbroken-sleep.html
Follows the journey of Missy a young determined girl who has to fight the challenge of Cerebral Palsy everyday. Missy smiles at everyday and reminds all around her to just get on with life. Monday, January 14, 2013. The Miracle of Unbroken sleep. At our last ABR Clinic in Sept 2012 we were offered the trial of a new product developed by Advanced Biomechanical Rehabilitation founder Leonid Blyum. The balls and eggs in the picture are ABR Tools with varying consistence that we use in a number of precise ar...
Missy's CP Journey: July 2012
http://missyscpjourney.blogspot.com/2012_07_01_archive.html
Follows the journey of Missy a young determined girl who has to fight the challenge of Cerebral Palsy everyday. Missy smiles at everyday and reminds all around her to just get on with life. Sunday, July 22, 2012. Posted by Written by Missy's proud mum. Tuesday, July 3, 2012. Back in a post in May, I mentioned the changes in Missy's arm, shoulder and hand functions. These negative changes in Missy's function brought some very dark days for me especially and but of course huge frustration for Missy. Suppor...
Missy's CP Journey: More than a badge.....
http://missyscpjourney.blogspot.com/2013/04/more-than-badge.html
Follows the journey of Missy a young determined girl who has to fight the challenge of Cerebral Palsy everyday. Missy smiles at everyday and reminds all around her to just get on with life. Saturday, April 20, 2013. More than a badge. Missy showing off her badge. So what a wonderful honour it was for Missy to be voted by her peers to be their representative. Mum, Missy and our Mayor at the SRC Presentation. To be chosen by your peers to be the “go to person” with ideas and be responsible to r...It would ...
Missy's CP Journey: November 2012
http://missyscpjourney.blogspot.com/2012_11_01_archive.html
Follows the journey of Missy a young determined girl who has to fight the challenge of Cerebral Palsy everyday. Missy smiles at everyday and reminds all around her to just get on with life. Friday, November 16, 2012. Everyone needs a friend to lean on. Posted by Written by Missy's proud mum. Friday, November 9, 2012. Carcoar Cup Running Festival. In it's second year the Carcoar Cup has doubled in entries and is a great social get together although many people put many hours of training into their run.
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Bi-annual Blogging Competition Winners | ABR Blogging Campaign Blog
https://abrbloggingcampaign.wordpress.com/2012/09/12/bi-annual-blogging-competition-winners
ABR Blogging Campaign Blog. Bi-annual Blogging Competition Winners. September 12, 2012 at 4:09 am · Filed under Uncategorized. We are pleased to announce 2 winners for bi-annual Blogging Competition for Dec 2011 and Jul 2012. Noah: http:/ ourjourneywithoneofgodsmiracles.blogspot.com/. Harrison: http:/ harrishope.blogspot.sg/. Congratulations to the both of you! You will receive 3 months of Machine use ABSOLUTELY FREE! To the other parents, do not be discouraged! ABR Social Media Coordinator. Enter your e...
Missy's CP Journey: July 2013
http://missyscpjourney.blogspot.com/2013_07_01_archive.html
Follows the journey of Missy a young determined girl who has to fight the challenge of Cerebral Palsy everyday. Missy smiles at everyday and reminds all around her to just get on with life. Sunday, July 28, 2013. Oh it's been so long. Sorry I haven't posted for so long, life gets in the way of writing sometimes. A Morning cuddle with Taz. Posted by Written by Missy's proud mum. Subscribe to: Posts (Atom). Leonid Blyum - ABR Founder. Oh its been so long. Interesting Blogs I follow. FOR THE LOVE OF CORBIN.
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ourjourneywithjoy.blogspot.com
Our Journey with our baby girl Joy
Our Journey with our baby girl Joy. On April 24, 2012, when we were 16 weeks pregnant with our fifth child we discovered at an ultrasound that our baby has Anencephaly. The next day we discovered that this sweet baby was going to be our first girl! This blog is our journal of our journey with our sweet baby girl Joy. Our friends blog for their baby Alexis. Our first post about Joy. Monday, November 10, 2014. Wednesday, November 5, 2014. 3 I have a more time consuming church calling. 5 My absolute favorit...
ourjourneywithlittlebit.blogspot.com
And Baby Makes Three
And Baby Makes Three. Saturday, July 3, 2010. Let's start with February. February 1st Bryson turned 4m old. He was wearing 6-9m clothes already. He was still VERY blond. His eyes were still VERY blue. Sweet Aidan, we think of you ever day. Bryson loves his gift from you- Goodnight Moon- and we read it each night before we go to bed. We love you little Angel. That's all for now. Saturday, July 03, 2010. Friday, July 2, 2010. I've been a HORRIBLE Blogger. Let's see.9 months old. Has 4 teeth- 2 top, 2 bottom.
Our Journey with Multiple Myeloma
Our Journey with Multiple Myeloma. Wednesday, March 4, 2015. Six Months of a Year of Firsts. Message to my honey:. Tomorrow, you will have been gone six months. Six months. Six months. Six months. It seems impossible that I've lived, without you, this long. This wasn't supposed to be.or maybe it was. We vowed "til' death do us part".I just never realized how hard that would be. I'm going through this "year of firsts.". I touch the urn and feel like I'm still touching you. My birthday.I added another ...
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ourjourneywithoneofgodsmiracles.blogspot.com
Our Journey With One of God's Miracles
Our Journey With One of God's Miracles. We thought we'd have to teach our son about the world. Turns out we have to teach the world about our son. They see a boy who cannot speak. We see a miracle who doesn't need words." -unknown. Monday, March 26, 2018. Hey World , Meet Boris. Noah is so excited that his new companion dog came today. His name is Boris. He is a Yorkie/Dachshund mix. It was so hard to see Bindi leave but we are excited to see Boris and Noah's relationship grow. Links to this post. Morgan...
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ourjourneywithoutnaps.blogspot.com
Our journey without naps
Aug 13, 2015. Look, no more training wheels! Posted by Our Journey Without Naps. Aug 3, 2015. Posted by Our Journey Without Naps. Aug 2, 2015. More county fair fun! Posted by Our Journey Without Naps. Jul 26, 2015. Hot and humid fun at the county fair. Posted by Our Journey Without Naps. Jul 19, 2015. Posted by Our Journey Without Naps. Subscribe to: Posts (Atom). 12/9/10- 25lbs 3oz and 32 inches long. 9/9/10- 23lbs 13oz and 31 1/4 inches long. 3/9/10- 21lbs 7oz and 28 inches long. More county fair fun!
Our Journey with Pulmonary Atresia
Our Journey with Pulmonary Atresia. Our son's/family's journey with a congenital heart defect called Pulmonary Atresia. This blog is to keep our families and friends updated on "our journey". We want to thank everyone who has prayed for us and supported us through the journey. Sunday, March 6, 2011. HAPPY 1st BIRTHDAY LEO. I know its been awhile but here's some updated pictures of Leo. Tuesday, November 16, 2010. Today is Leo's curcumcision :( We are nervous but feeling good. I will update later today.
ourjourneywithradar.blogspot.com
Finding Our Way
Lets Get Caught Up. North Star's Mushlit Family. View my complete profile. Wednesday, May 20, 2009. Let's Get Caught Up. Last year was the first time I went into Jason's class with the purpose of educating his classmates during autism awareness month- April. His class is great and the kids are really receptive. I read a simple book and we spoke a bit. This year I returned and Radar came with me. There are no photos since I had Radar on a leash and that kept my hands busy! One of the first things I did wa...
ourjourneywithscoliosis.blogspot.com
Our Journey With Juvenile Scoliosis
Our Journey With Juvenile Scoliosis. The journey with our daughter's scoliosis. From the diagnosis aged 6, to the different avenues of treatment she has and is currently going through. 15 November, 2009. 26 July, 2009. Progress from wearing SpineCor brace. 12 July, 2009. SpineCor and Biobloc update. At this stage we're all set for her tonsils/adenoids to be removed on Tuesday. She says that she's a bit scared but she's being very brave. I'm certainly not looking forward to it, I'm sure things wil...
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