Click Here to Read Brady's Story
Wednesday, April 04, 2007
Brady is star of the month.
Just wanted to let everyone know that Brady is Star of the month for a developmental toy company,DbD Toys. You can check him out at http://www.dbdtoys.com/index.html He's such a little cutie,but Im a little partial,lol. Hes doing really well these days. We finally got him off the klonipin,his sensory issues from being outside are gone,hes sleeping well and back to his happy self again,whooo hooo!! His bahavior has greatly improved since he stopped the klonipin,it just amazes me the effects that meds can have on people. Anyway thank goodness that is over.
Oh I also wanted to give a shout out to big brother,he made all A's at school,way to go,were so proud of you Peyton!! He got a fish aqarium with some really cool fish,for all his hard work. I have two of the best boys in the world,yeeeeeesss Im the gloating mother,lol. Anyway thats about it,have to get some sleep now. Hugs all.

posted by angelwings @ 2:05 AM
   3 comments
3 Comments:
  • At 8:01 AM, Blogger Zachary Rouleau said…

    Hey guys! Glad to see that Brady is a real star instead of an Angel, lol. Just kidding! Way to go Peyton, you did great job!

    Audrey

     
  • At 11:20 PM, Blogger Unknown said…

    Way to go Brady! We knew you were a star already!

    And Stephanie - he IS a real cutie pie! No reason to be "partial" when it's true! LOL!

    I love reading about his progress and how far he's come. Keep posting.

    Hope is doing great also! They are looking for some standers for her. I'll email you privately to tell you more!

    Shona Watson

     
  • At 4:33 AM, Blogger Unknown said…

    Yay for Brady!! Love seeing his smiling face as a star!!

     
 
Home        Post        Edit        Post a Comment
 


What is Angelman Syndrome?

                 

About Brady

Read Brady's Story Here   

I am 11yrs old and I have Angelman Syndrome. I may have this syndrome, but I dont let it hold me back. I love life and live it to the fullest every single day. My mom says that our research organization, Foundation for Angelman Syndrome Therapeutics, is working really hard on a treatment or even a cure for me and my friends. I am thankful to have 25 words but I look forward to the day that I can carry on long conversations and talk so much that everybody has to ask me to please be quiet for a few minutes :) Anyway, mom says Im awesome and super funny and I have to agree,lol.

See my complete profile

Home      Post        Edit

Our blocks are in!!
  This is an essay by Soeren Palumbo who is a senior...
  Update on Paint a Block Fundraiser.
  Latest Update.
  Vacation photos 2/07.
  Update
  Update on Brady.
  Brady walking the treadmill!
  We are doing two fundraisers this year,the online ...
  We are doing two fundraisers this year,the online ...
 
Archives
Interactive Seizure Diary

This downloadable Interactive Seizure Diary helps you track your seizure activity and medication routine. You can also record doctor appointments and notes about how you are feeling. Before a doctor appointment, print the information and share it with your physician.

Angelman Forum & Chat

The AS Forum was created in April 2005 and provides an easy way for family members and carers of people with Angelman Syndrome (AS) to exchange information with each other.

Cure Angelman Syndrome

The Foundation for Angelman Syndrome Therapeutics (or FAST) is an organization of families and professionals dedicated to finding a cure for Angelman Syndrome and related disorders through the funding of an aggressive research agenda, education, and advocacy.

Angelman Links
Angelman Blogs
All About Epilepsy