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Wednesday, July 20, 2005 |
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Losing our Speech Therapist
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| Okay just had to post this.We just found out that we are losing Bradys speech therapist.She is going to be moving.We are so sad.She has been such a blessing for our family and has gotten Brady doing things I wasnt sure he ever would.She has taught us that even if he doesnt ever speak,he can still communicate.She has been not only a therapist,but a friend to our family and we are going to miss her so much.We recently lost a great physical therapist also,because Brady turned 3yrs old and aged out of early intervention.I suppose we should get used to this,but I dont know that we ever will!So Lisa and Joey I have to say thank you so much for all your hard work and words of encouragment. We are going to miss you guys. |
posted by angelwings
@
6:58 PM
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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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Seizure free for 3 Weeks!
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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
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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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