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Mary's Blog: Mary Returns to School!!!
http://miracleformary.blogspot.com/2011/09/mary-returns-to-school.html
Tuesday, September 13, 2011. Mary Returns to School! So Mary started back to pre-school for the 3rd year in a row! Yes, she is absolutely ready for Kindergarten, but since she isn't 5, she gets another year of pre-K. I think Mary could probably teach the class! This picture is actually of Jackson's first day of preschool, but it was so cute, I couldn't resist posting it! A picture of Mary with her class out of the Nature Observation Deck! Mary and her friend Aoife! One very happy girl! Researchers Target...
Mary's Blog: FLU + SMA = NOT a good combination
http://miracleformary.blogspot.com/2011/10/flu-sma-not-good-combination.html
Sunday, October 23, 2011. FLU SMA = NOT a good combination. The intubation went fine, but she has still be having some trouble with low O2 saturations, so she had been on 60-80% O2 all day. But she is resting comfortably now, and thankfully there is no pneumonia in her lungs. Please keep up the prayers for Mary! Subscribe to: Post Comments (Atom). FLU SMA = NOT a good combination. Petition to cure SMA. Mission: Moris' Down Under. Try to remember the kind of September. Spinal Muscular Atrophy Research News.
Mary's Blog: Spring Break Trip to Lakeshore!
http://miracleformary.blogspot.com/2014/04/spring-break-trip-to-lakeshore.html
Thursday, April 10, 2014. Spring Break Trip to Lakeshore! Since before we moved to Alabama last summer, Mary has been telling us she wants to play wheel-chair soccer. Well, we've been here for about 8 months and Mary finally got her wish! Mary had the opportunity to learn some power chair soccer skills and techniques with a coach at the Paralympic training center at the Lakeshore Foundation in Birmingham. We went to a spring break camp there, and some of the pictures are below:. June 3, 2014 at 10:58 AM.
Mary's Blog: A better day.....
http://miracleformary.blogspot.com/2011/10/better-day.html
Tuesday, October 25, 2011. Please pray that the extubation goes well and we can get home before Halloween! Subscribe to: Post Comments (Atom). FLU SMA = NOT a good combination. Petition to cure SMA. Please take 30 seconds and sign the Petition to Cure SMA. This landmark legislation will help SMA afflicted kids as well as a host of other neuromuscular diseases. Please help us and pass the word along! Acts of Kindness: Research Named For Gwendolyn. Mission: Moris' Down Under. How many kids do you have?
Mary's Blog: February 2012
http://miracleformary.blogspot.com/2012_02_01_archive.html
Monday, February 13, 2012. RSV Again = 3 More Weeks In PICU. Mary has been in the UMDNJ Hospital for the past 2 weeks with another bout of RSV and a few other viruses ( Enterovirus. Rhinovirus, and a few others), she is also battling Clostridium difficile or. She was intubated on January 31st, and extubated on February 8th, and then re-intubated on the 10th. Needless to say, Mary has had a pretty rough few weeks. Here is the video:. Please continue to pray for Mary's speedy recovery. Petition to cure SMA.
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Mission: Moris Family Journey: December Recitals
http://themorisfamily.blogspot.com/2012/12/december-recitals.html
Mission: Moris Family Journey. The Journey of an Army Family on a Mission for God and Country. Sunday, December 16, 2012. The one thing exciting about early December for me is watching my darlings celebrate their hard work in recitals! Emma just completed her first year of Piano lessons. She's worked very hard and I am so proud of her! She loves her teacher, Ms. Marah and she seems to be a natural at performing for an audience! John, Heather, Emma, Lily and Jana. Subscribe to: Post Comments (Atom).
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1): Home for Christmas 2010!
http://alifeforkaitlyn.blogspot.com/2011/01/home-for-christmas-2010.html
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1). Hello and welcome. My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, swallow and clear my airway. Friday, January 7, 2011. Home for Christmas 2010! Just in time for Christmas!
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1): Happy Mother's Day
http://alifeforkaitlyn.blogspot.com/2011/05/happy-mothers-day.html
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1). Hello and welcome. My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, swallow and clear my airway. Monday, May 9, 2011. Our doctors felt that the scans wouldn't be much help? I'm no...
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1): Feeding Intolerance or Bacterial Overgrowth in the Small Bowel ???
http://alifeforkaitlyn.blogspot.com/2010/11/feeding-intolerance-or-bacterial.html
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1). Hello and welcome. My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, swallow and clear my airway. Sunday, November 21, 2010. Kaitlyn had a few days before we started treating for b...
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1): November 2011
http://alifeforkaitlyn.blogspot.com/2011_11_01_archive.html
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1). Hello and welcome. My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, swallow and clear my airway. Monday, November 21, 2011. Oh my dear.what has it been? Where did we leave off?
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1): January 2010
http://alifeforkaitlyn.blogspot.com/2010_01_01_archive.html
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1). Hello and welcome. My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, swallow and clear my airway. Monday, January 25, 2010. Help Kaitlyn Get Her Wheels! As Kaitlyn's condition is d...
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1): March 2011
http://alifeforkaitlyn.blogspot.com/2011_03_01_archive.html
Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1). Hello and welcome. My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, swallow and clear my airway. Thursday, March 24, 2011. It was so good of her to see us! If her hypercalcemia is...
Mission: Moris Family Journey: Winter Weather in the Borderland
http://themorisfamily.blogspot.com/2013/01/winter-weather-in-borderland.html
Mission: Moris Family Journey. The Journey of an Army Family on a Mission for God and Country. Thursday, January 3, 2013. Winter Weather in the Borderland. My girls have never lived in a place where snow is a normal part of winter. We have so many mismatched and random snow clothing that is really quite comical. In these pictures, you see the matching hats and gloves that I got on clearance at Gymboree in preparation to go to Nana and Papa's house for Christmas :-). Lily is the original snow bunny: she l...
Mission: Moris Family Journey: Emma's Sweet Heart
http://themorisfamily.blogspot.com/2012/12/emmas-sweet-heart.html
Mission: Moris Family Journey. The Journey of an Army Family on a Mission for God and Country. Thursday, December 13, 2012. Last night, after we dropped off your friend, you asked to share your Awana bucks with her because you knew she wouldn't have as much as you and you didn't want her to feel bad. Mommy's eyes were misty with tears and I heard your heart. Of course I said yes. We walked into the house and you said, "I wonder what my sisters would like from the Awana store? There's Strong and there's M...
Mission: Moris Family Journey: August 2012
http://themorisfamily.blogspot.com/2012_08_01_archive.html
Mission: Moris Family Journey. The Journey of an Army Family on a Mission for God and Country. Tuesday, August 28, 2012. Day Zero - the hardest part is over. God, we love you. We love our Country. We will do what you've asked of us in a way that honors and glorifies You. God, you love him, you know him, made created his inmost being. We surrender all to you today. We will be still and know You are God. Day Zero - the hardest part is over. God, you love him, you know him, made created his inmost being.
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miracleformadison.blogspot.com
Miracle for Madison & Friends
Friday, May 20, 2016. Pre-order SMA Awareness Leggings. Can you help make Madison's fashion design dream come true please? Only 21 more pre-orders needed! 9 pre-ordered so far) by June 1! Pre-order here: https:/ www.lbwear.com/product-category/sma-pre-order/. These are perfect for any adult or little girl and can be ordered in capri and/or full length. Wednesday, December 24, 2014. Merry Christmas from our family to yours! Thank you for your gift of friendship and support! 8206;SMA awareness. Madison he...
Miracle for Madison & Friends
What is the Miracle for Madison Fund? Official SMA Awareness Ribbon - Creation and Meaning. Resources for SMA Clinical Trials. Madison in the News. Pictures of Madison and Friends. Official SMA Awareness Ribbon Merchandise. Official MFM&F and SMA Ribbon Merchandise on Zazzle. More Official Miracle for Madison Merchandise. Angels at the End Zone 2000 through 2007. 9th Annual Angels at the End Zone. 10th Annual Angels at the End Zone. Official SMA Awareness Ribbon on Facebook. Follow Us on Facebook. Madiso...
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Miracle for Manami - Home
Thank you for visiting our site. We want to tell you about an exciting opportunity we have discovered for our daughter with Cerebral Palsy. Create a free website. Start your own free website. A surprisingly easy drag and drop site creator. Learn more.
Miracle for Mark
Thursday, June 16, 2011. Blog Post # 19. Mark Alfred Riddle completed his mortal life early Saturday morning, June 11, 2011. He had, with great courage and faith, battled for many months a very aggressive form of cancer. Mark was born on May 12, 1946 and spent his youth in Provo and Orem where he attended BY High. In 1989 he was formally accredited as a Japanese-to-English translator by the American Translators Association. For most of his working career, Mark was an educator. Additionally he taught ESL ...
Mary's Blog
Friday, September 23, 2016. An excerpt from a paper I'm writing. I'm thinking and praying for one of my fellow dads, Travis who is in the hospital right now fighting for his beautiful daughter, Stella's life. Be strong Travis, she is strong, she will be ok. We are all praying with you. The Father will watch over her and bring her back to health. In the final year of my Troop Command I had a child, and I came to realize adversity like I never imagined I would. I have given her CPR on the pavement of a bus...
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Welcome to MiracleForMcKaylee.com | Support Mac Today!
Welcome to MiracleForMcKaylee.com! Support the Borklund family with prayers, donations, and encouragement. From here, you can buy a t-shirt. And get updates, as well as read McKaylee's story and post a note on CaringBridge. Let them know today that you love and support McKaylee! Watch Mac on YouTube! Watch Mac on a St. Jude Commercial!
A Miracle For Megan
A Miracle For Megan. Tuesday, June 30, 2015. Copy of an email sent to provider looking for updates on Megan. Sorry for the delayed respond time. It has been a rollercoaster around here between Maxim, nurses, all-nighters and Megan's GI and seizures. Maxim is patching our nights but at this point each week I have been up 1 - 2 nights per week all night long which knocks me out for the following day to be good for anything. Work and dr. appts have been being juggled around this. There are no plans for anyo...
Miracle For Michael - Home
3rd Golf Tournament Photos. 4th Golf Tournament Photos. Miracle for Michael is a small non-profit organization designed to help Michael and other children with special needs obtain desperately needed therapies and treatments that are not covered by insurance. Create a free website.
Miracle for Mom – CURE PSP
PSP Links & Information. VISIT US ON FACEBOOK. News & Events. Pics & Video. Janice Lee Murphy Obituary. Janice Lee Murphy Obituary Janice Lee Murphy passed away peacefully at home, with her family by her side, on October 6, 2014. Janice is survived by her loving husband, Dick. Miracle For Mom dine-out at South City Kitchen Vinings. Miracle For Mom dine-out supporting CurePSP South City Kitchen Vinings Thursday, Sep. 18 at 7pm I hope you will join Miracle For Mom for a special night at South. CBS Atlanta ...
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