Click Here to Read Brady's Story
Thursday, July 31, 2008
Well its been another busy day here at our house. Brady decided to climb up and get a jar of peanuts,and shatter the jar on the tile floor,guess he couldn't get the lid off, :) I walked back in to find him rubbing his feet and hands around in the glass. I put him in the high chair to assess the damage,he had some small cuts on his toes and hand,but otherwise he was ok, very lucky. So I managed to get that cleaned up, there must have been a million pieces of glass everywhere.
Well I have been really busy this afternoon,so we were cooking a late supper. Brady was playing in the living room,right next to the kitchen,and we called ourselves watching him. Anyway his brother said "uh mom,either Brady has jelly in his ear,or hes bleeding. Yep, it was blood. He had blood dripping down his ear and neck,coming from inside his ear. So we turned all the food off,and headed to the ER,not knowing what had happened. Brady made lots of new friends in the waiting room,even convinced two nice ladies to buy him two bags of chips,which he ate all of. He had everyones attention there,he was being such a monkey. Of course everyone wanted to know what happened,why his ear was bleeding,and probably why he was so dang happy with blood running out of his ear,lol. We finally seen the doc,and just as we had suspected,he had stuck something down in it,and cut the center part of the inside of his ear. The doc said his ear drum looked fine,thank goodness. But we have no idea what he stuck in his ear,luckily whatever it was,was not there anymore. He has never stuck anything up his nose or in his ears,so I guess this is a new bad habit to worry about :o We walked all around the living room,but didn't find anything. Oh,in case your wondering,we did finish supper and ended up eating at midnight. Of course the kitchen cleaning has to wait til we wake up in just a little while.
All is well now though,were home, and Brady is happy as a lark. He hasn't touched his ear at all,so it must not be bothering him. Oh well,there went another ten years off mommy,lol.
Now were just gonna hang out and wait til he decides to sleep,which I pray is soon. I will keep you guys posted on how things progress.

posted by angelwings @ 1:33 AM
   0 comments
0 Comments:
 
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

Still goofing!
  Just goofing off.
  We have had such a good day here,other than having...
  Well were doing good here. Brady has had a busy we...
  Well its been a busy week! We had to go to the hea...
  Just wanted to let everyone know that Brady is doi...
  Well its been a busy weekend here. Brady spent mos...
  Well we made it back from the doc today and they s...
  Were heading out to the ENT to have Brady's nose a...
  YEY!!!!!!! We have our papi's and Brady couldn't b...
 
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