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Thursday, September 07, 2006 |
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One Year!
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Just wanted to let eveyone know that today marks one year that Brady hasn't had a seizure! It has been such a journey getting to this point,and I wasn't sure that we would ever make it to this point. We are thrilled,but really scared at the same time.I can only hope and pray that he will make it through another year without a seizure.
Anyway just wanted to update everyone and ask you to continue prayer for our little man,that is what will keep him well!God bless you all. |
posted by angelwings
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10:01 PM
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WOW Brady! I am so proud of you Big Boy! You need to continue on this way! We will fight those seizures together! Good luck!
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Way to go Brady! I pray that the seizures NEVER come back! Angel hugs!
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| 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
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Brady's new Tricks
Update on Brady
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| Archives |
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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.
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Angelman
Forum & Chat |
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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.
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Cure Angelman Syndrome |
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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.
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| Angelman Links |
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WOW Brady! I am so proud of you Big Boy! You need to continue on this way! We will fight those seizures together! Good luck!