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Saturday, January 29, 2005 |
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Getting Ear Tubes
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| Just wanted to let everyone know that Brady is getting his second set of tubes in his ears.We took his brother to the doctor and on the way to the doc brady was messing with his ear.So on a hunch I had his ears checked too.When the doc was done checking them,he said that they both need tubes.Peyton because we have been treating them for about 3 mths,and Bradys because of still having fluid in his ears,and because they dont want to risk him loosing his hearing on top of everything else.We talked to his ped.and he sent us for a second opinion,and that doc confirmed it.They are scheduled Feb.4 to get tubes.But hey,at least they get to do it together hugh!Just pray for them and us.We will have 2 little ill boys on our hands.I will update and let everyone know how it goes. |
posted by angelwings
@
11:09 PM
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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
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ANGELMAN SYNDROME
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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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