Rett Syndrome Research Trust Blog Welcome to the RSRT Blog. RSRT is a nonprofit organization fighting to reverse the devastating symptoms of Rett Syndrome and related MECP2 disorders.
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Wednesday, March 16, 2011. Today was one of those lucky days. The weather, food and friends were just what I needed! Here are pics from the all 3 years! Posted by Carrie and Avery. Thursday, December 23, 2010.
What is bracelets for Rett? Wednesday, September 19, 2012. Monday, April 16, 2012. Lemonade? Im so sorry for my lack of being here! Did you know that 1 in 88 kids have autsim? Did you know that.
Wednesday, December 21, 2016. Molly Barker, Founder Girls on the Run International and The Red Boot Coalition. Team GP2C has a new team member for the Disney Princess Half Marathon in February! Molly Barker is the founder of Girls on the Run International, the program that uses running to empower girls. She will help us power the flower on the course to raise awareness for Rett Syndrome! In addition, we are honored to have her as our guest speaker for our team dinner.
Kate Foundation for Rett Syndrome Research. Monday, November 18, 2013.
Providing services to people with Developmental Disabilities since 1994. History of the Baker Act. History of the Baker Act. In 1971 the Florida Legislature passed into law the Florida Mental Health Act, which went into effect July 1 of the following year. It substantially strengthened the due process and civil rights of persons in mental health facilities.
Take a look around! We have a ton to share with you! And please share with us! Everything here is hopefully something that will help your little girl fight a stronger fight against Rett Syndrome. Girl Power 2 Cure items. Gluten and Dairy Free Recipes. Welcome to Rett Girl! .
Create your own video slideshow. A new video channel on YouTube.
This blog is to raise global awareness of Rett syndrome. Please join and share this blog with everyone. Monday, June 29, 2015. 8 Million For Research and Two Clinical Trials. Is publishing this finding today. You may be asking yourself, why does this matter? .
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Rett Syndrome Research Trust Blog Welcome to the RSRT Blog. RSRT is a nonprofit organization fighting to reverse the devastating symptoms of Rett Syndrome and related MECP2 disorders.DESCRIPTION
Welcome to the RSRT Blog. RSRT is a nonprofit organization fighting to reverse the devastating symptoms of Rett Syndrome and related MECP2 disorders.PARSED CONTENT
The site had the following in the homepage, "Welcome to the RSRT Blog." I noticed that the web site stated " RSRT is a nonprofit organization fighting to reverse the devastating symptoms of Rett Syndrome and related MECP2 disorders." They also stated " LI scientists Find Possible Treatment for Rett Syndrome. July 31, 2015 in Research. Tags Cold Spring Harbor Laboratory. Writing in the current issue of the Journal of Clinical Investigation, Tonks and colleagues report on a possible but still distant drug intervention. Tonks and research associate Navasona Krishnan ha."ANALYZE MORE BUSINESSES
Thursday, June 18, 2009. Cocktails for a Cure 2009. Click on the picture above to enlarge the invitation. Cocktails for a Cure - Saturday June 20, 2009. O n the top right side of this page or. To check on the items to be auctioned.
Thursday, August 23, 2007. Islip Terrace Grapes and Grains. Friday, August 17, 2007. Signed Jersey, Ball and Bat. ROGER CLEMENS - Signed Ball. NOLAN RYAN - Signed Ball. METS PACKAGE - Darryl Strawberry, Bud Harrelson and 1986 Mets. JOHN STARKS - Signed Mini-basketball. 6 zones fully equipped by Water Works. Plates, Cups, Aluminum. Trays donated by Tommy and Toni Krisa. Farmingdale, NY 11735 - 2618.
Wednesday, June 3, 2009. Yankees Bucket - Tickets Field Level Yankees vs. Red Sox - The Krisa family. Johnnie Walker Blue Label Whisky. Giants Tickets - The Mittleman family. Garden, Cupcake and Holiday - Ginny Franzen. Lottery Tickets - Pamela Joachim. Beach Bag with Umbrella - Donna and Bob Merkert. Vera Bradley Beach Bag - The Huber family. Handy Man for a Day - Michael Funk. Jewelry - The Amabile family.
This blog is to raise global awareness of Rett syndrome. Please join and share this blog with everyone. Monday, June 29, 2015. 8 Million For Research and Two Clinical Trials. Is publishing this finding today. You may be asking yourself, why does this matter? .
Our Rett Syndrome Journey with Erin. I Am The Disabled Child. Rett Syndrome in South Africa. To those parents learning about Rett Syndrome for the first time, take heart, you are not alone.