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The Bradys: July 2015
http://lynetteandjon.blogspot.com/2015_07_01_archive.html
Monday, July 27, 2015. Cake and Ice Cream. Another homeschool activity. It happened to be right after Pioneer Day but I didn't have the materials I wanted to incorporate it all so it was just learning about ice cream. And, we saw Curious George make an oven to cook something outside so we wanted to see if it would work. I had them each prepare their own baggies of ice cream and then we shoved them all into the same #10 can. I knew I saved these for a good reason! Here are our cakes in their "oven". The k...
The Bradys: Country Life
http://lynetteandjon.blogspot.com/2015/07/country-life.html
Sunday, July 5, 2015. Subscribe to: Post Comments (Atom). Ella's Four Year Questionnaire. Tidbits of my life. A football, swimming, cooking, teeth, election week. More about our life. Oliver's Birthday Bonanza, Part Two. The House of Payne. Multiply Life By the Power of Four. Spinal Muscular Atrophy Research News. Researchers Targeting Astrocytes Discover Treatment Benefits in SMA-Induced Mice. Happy 3rd Birthday Aviator. Where did March go? The 200 for SMA - Help Us Raise $1,000,000 for SMA in 1 Year!
The Bradys: January 2015
http://lynetteandjon.blogspot.com/2015_01_01_archive.html
Saturday, January 3, 2015. I always feel like a girl will want to know way more about what my pregnancy was like with them than boys will and I have completely failed at documenting things about this pregnancy. So here goes, pregnancy with baby #4 up to 30 weeks. Mom, why haven't you done it yet? I'll do it Mom." "Uh, Mom, just DO it! Yes, it took me a good 20 minutes but it did happen and I have even done it two other times! Might as well get it right the fourth time, right? For New Years Eve, we had th...
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: 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.
Alesia - my fight for life: "I can read? yes I can read!"
http://www.ana-alesia.ro/2012/01/i-can-read-yes-i-can-read.html
Alesia - my fight for life. Thursday, January 19, 2012. Yes I can read! My Dear Friends,. Long time no news, hope you didn't miss me to much! I have been busy learning the alphabet and, yes, now I can read and pronounce, with style :), all the letters from the alphabet. Check this out:. Is this amazing or what? March 11, 2012 at 5:26 AM. Subscribe to: Post Comments (Atom). View my complete profile. View my page on. Yes I can read! THANK YOU for help! Received as Royal gift.from a Prince. Kaitlyn Hatchard...
Alesia - my fight for life: Last day of school...let the vacation begin
http://www.ana-alesia.ro/2014/06/last-day-of-schoollet-vacation-begin.html
Alesia - my fight for life. Thursday, June 26, 2014. Last day of school.let the vacation begin. Alesia graduated first year of school. Together with teacher Sorina studied mathematics, read, wrote and discussed about stories, created beautiful crafts and enjoyed every day of school. In fact I am sure Alesia would like the school to continue during summer but for now vacation is good too. I have got a first grade graduation diploma and a story book. See you in 2nd grade! June 27, 2014 at 12:25 AM. Receive...
Alesia - my fight for life: Noi Orizonturi Familia - Thank you!
http://www.ana-alesia.ro/2011/04/noi-orizonturi-familia-thank-you.html
Alesia - my fight for life. Thursday, April 7, 2011. Noi Orizonturi Familia - Thank you! And to improve quality of life for Alesia. We thank to all of you that directed their 2% for Alesia already! Noi Orizonturi-Familia" is a not-for-profit association in Romania, whose goal is to enhance the quality of life for all members of the community. More about their projects can be found on their website:. Http:/ www.noiorizonturifamilia.ro/. Thank you Christian, Cristina and Noi Orizonturi Familia. Received mo...
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Spinal Mouse ®
What is Spinal Mouse? Spinal Mouse is a device that, combined with a computer program (PC), assesses the curvatures of the vertebral column without applying harmful radiation. Spinal Mouse checks: spine alignment, measuring segmental and global angles in the sagittal and frontal planes posture and spinal mobility spine functions and performance Measurements are: quickly and easily performed accurate and [.]. What is Spinal Mouse? Posture and spinal mobility. Spine functions and performance. The spine is ...
SpinalMouse, spinal assessment, spine, medical solutions in San Diego, California
Welcome to SpinalMouse Solutions . . . The SpinalMouse is the Future of Spinal Assessment. The SpinalMouse is more than just a computer-assisted device that measures and graphically reports on functionality and range of motion of the axial spine. It is an accurate, efficient, and cost-effective way to measure the range of motion of virtually all major “movable” joints of the body, as well as the spine. You can contact us directly by using the information listed below:. 8501 Spotted Fawn Court.
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Spinal Muscular Atrophy Research News
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ACT for SMA - Ally Cadence Trust for Spinal Muscular Atrophy
0800 23 43 762. 0333 44 43 762. By SMA Type 1 ". By SMA Type 1 ". 0800 23 43 762. 0333 44 43 762. 0800 23 43 762. 0333 44 43 762. Supporting families affected by SMA Type 1 ". Other types of SMA. How You Can Help. How Your Money Helps. Other types of SMA. How You Can Help. How Your Money Helps. Ally Cadence Trust for Spinal Muscular Atrophy. The Ally Cadence Trust is a UK Registered Charity,. The History behind the Ally Cadence Trust. Sign up for our newsletter. Make a monthly donation.
spinalmuscularatrophysupport.com
ACT for SMA - Ally Cadence Trust for Spinal Muscular Atrophy
0800 23 43 762. 0333 44 43 762. By SMA Type 1 ". By SMA Type 1 ". 0800 23 43 762. 0333 44 43 762. 0800 23 43 762. 0333 44 43 762. Supporting families affected by SMA Type 1 ". Other types of SMA. How You Can Help. How Your Money Helps. Other types of SMA. How You Can Help. How Your Money Helps. Ally Cadence Trust for Spinal Muscular Atrophy. The Ally Cadence Trust is a UK Registered Charity,. The History behind the Ally Cadence Trust. Until a few weeks before she was diagnosed, and after the diagnosis th...
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