yvonneadrienne.blogspot.com
Giving Our Angel Wings to Fly...: November 2012
http://yvonneadrienne.blogspot.com/2012_11_01_archive.html
Giving Our Angel Wings to Fly. Hope is the thing with feathers, That perches in the soul, And sings the tune without the words, And never stops at all Emily Dickinson. Gift Ideas for Kids with AS. Books, Books, Books! Wednesday, November 28, 2012. Gluten Free Pie Crust. I have been searching for quite a while for a good looking GF pie crust recipe, and this one looks very promising! I haven't tried it yet though, but it comes from The Renegade Kitchen. Blog, and I always love her recipes! 1/4 tsp Sea Salt.
angelmanannouncements.wordpress.com
Angelman Announcements #2 July 2014 | Angelman Announcements
https://angelmanannouncements.wordpress.com/2014/07/31/angelman-announcements-2-july-2014
Angelman Syndrome related news and events etc. About the Angelman Announcer. Songs and Sensory Clips. Videos – You Tube Channels. Angelman Announcements #1 July 2014. Angelman Announcements – October 2014 →. Angelman Announcements #2 July 2014. July 31, 2014. FAF was founded in honor of Joey Moretti Jr. and all the Angels with Angelman Syndrome. We help raise awareness and fund research for AS. Must be an angel: Brave girl with rare disorder can’t talk or sleep… but can never stop smiling. Gavin, 27, has...
angelmanannouncements.wordpress.com
March | 2015 | Angelman Announcements
https://angelmanannouncements.wordpress.com/2015/03
Angelman Syndrome related news and events etc. About the Angelman Announcer. Songs and Sensory Clips. Videos – You Tube Channels. Monthly Archives: March 2015. Angelman Announcements March 2015. March 31, 2015. Giving Barnsy 18,000 reasons to smile Photos DUBBO residents gave Barnsy a reason to smile on Saturday evening at St Johns Primary School, with more than $18,000 raised for Barnsy and his family. dailyliberal.com.au By Fairfax Regional Media … Continue reading →. Join 19 other followers.
meetthefamiliesofas.blogspot.com
Meet the Families of AS (Angelman Syndrome): Florida Angelman Family Fundraiser for FAST
http://meetthefamiliesofas.blogspot.com/2011/11/florida-angelman-families-fundraiser.html
Meet the Families of AS (Angelman Syndrome). Monday, November 28, 2011. Florida Angelman Family Fundraiser for FAST. Angelman Families get together for a lunch and social fundraiser for F.A.S.T at. BJ's Brewery and Restaurant in Tampa, Florida. On Saturday November 5th many Florida Angelman families came together for a great cause and to hear from Dr. Weeber. The adorable Angels ranged in ages from 3-21. I was laughing and crying with joy as I watched the ceremony online. Click to view: http:/ www.cu...
meetthefamiliesofas.blogspot.com
Meet the Families of AS (Angelman Syndrome): August 2012
http://meetthefamiliesofas.blogspot.com/2012_08_01_archive.html
Meet the Families of AS (Angelman Syndrome). Thursday, August 2, 2012. The Charlie Foundation - To Help Cure Pediatric Epilepsy. As a resource. So I looked them up and gave them a call. I discovered the amazing things they are doing so I had to share with you. As a fellow parent to a child with epilepsy, I wondered how Jim and Nancy could find the time and inspiration to start a foundation. Jim said "It all sort of started with a video they created to help raise awareness about the ketogenic diet and...
meetthefamiliesofas.blogspot.com
Meet the Families of AS (Angelman Syndrome): November 2012
http://meetthefamiliesofas.blogspot.com/2012_11_01_archive.html
Meet the Families of AS (Angelman Syndrome). Tuesday, November 27, 2012. Anticipating the FAST Gala 2012! It's almost here, The 2012 Foundation for Angelman Syndrome Therapeutics Gala! This much anticipated event, which we began immediate countdown after the 2011 Gala ended, will soon be here! Drinks and great conversation 'til 3am with people who "get it" meant the world to me! Many thanks to the team at FAST made up of volunteers, and most are also parents of children with Angelman Sydrome. My son Nath...
meetthefamiliesofas.blogspot.com
Meet the Families of AS (Angelman Syndrome): November 2011
http://meetthefamiliesofas.blogspot.com/2011_11_01_archive.html
Meet the Families of AS (Angelman Syndrome). Monday, November 28, 2011. Florida Angelman Family Fundraiser for FAST. Angelman Families get together for a lunch and social fundraiser for F.A.S.T at. BJ's Brewery and Restaurant in Tampa, Florida. On Saturday November 5th many Florida Angelman families came together for a great cause and to hear from Dr. Weeber. The adorable Angels ranged in ages from 3-21. I was laughing and crying with joy as I watched the ceremony online. Click to view: http:/ www.cu...
meetthefamiliesofas.blogspot.com
Meet the Families of AS (Angelman Syndrome): 90% Improvement in Seizures, My interview with Dr. Ron Thibert!
http://meetthefamiliesofas.blogspot.com/2012/12/90-improvement-in-seizures-my-interview.html
Meet the Families of AS (Angelman Syndrome). Sunday, December 30, 2012. 90% Improvement in Seizures, My interview with Dr. Ron Thibert! I recently had the opportunity to catch up with the Angelman communities very own trusted Neurologists Dr. Ron Thibert! Angelman Syndrome is so rare and when it comes to their brain and seizures, our kids need the best! They need someone who has experience to draw from when deciding the best treatments and medications. Dr Thibert and his team including Dr. Elizabeth ...
meetthefamiliesofas.blogspot.com
Meet the Families of AS (Angelman Syndrome): Anticipating the FAST Gala 2012!
http://meetthefamiliesofas.blogspot.com/2012/11/anticipating-fast-gala-2012.html
Meet the Families of AS (Angelman Syndrome). Tuesday, November 27, 2012. Anticipating the FAST Gala 2012! It's almost here, The 2012 Foundation for Angelman Syndrome Therapeutics Gala! This much anticipated event, which we began immediate countdown after the 2011 Gala ended, will soon be here! Drinks and great conversation 'til 3am with people who "get it" meant the world to me! Many thanks to the team at FAST made up of volunteers, and most are also parents of children with Angelman Sydrome. My son Nath...
meetthefamiliesofas.blogspot.com
Meet the Families of AS (Angelman Syndrome): December 2012
http://meetthefamiliesofas.blogspot.com/2012_12_01_archive.html
Meet the Families of AS (Angelman Syndrome). Sunday, December 30, 2012. 90% Improvement in Seizures, My interview with Dr. Ron Thibert! I recently had the opportunity to catch up with the Angelman communities very own trusted Neurologists Dr. Ron Thibert! Angelman Syndrome is so rare and when it comes to their brain and seizures, our kids need the best! They need someone who has experience to draw from when deciding the best treatments and medications. Dr Thibert and his team including Dr. Elizabeth ...
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