Our life, our experience, our history, about my daughter with a rare chromosome disorder. She is missing a small portion of her 8th chromosome, which is called a deletion. She also has a small part of XP added to that. Her karotype or diagnosis is deletion 8p23.3 with extra xp22.2 to the terminal deletion (a new chromosome test summer 2011 changed her karotype to deletion 8p23.2 with extra xp 22.12, essentially meaning more missing chromosome 8 and more added xp). #herrarelife
Saturday, February 14, 2009
Yawning
So funny. A couple of nights ago, Bill was in the kitchen, tired after taking care of us all. We had the stomach flu. He let out one of those deep yawns. The kind that tells everyone in ear shot that you are exhausted. A few seconds went by and Sadie makes exactly the same yawning sound. I giggled a little and told Bill, I think Sadie just yawned like you. I asked her to yawn again...She did it 3 times. It was the cutest thing.
Wednesday, February 11, 2009
Life
School is going great and everyone is impressed with Sadie's ability to sit for longer periods of time. She has gone back to her old eating habits...barely eating. We took her off the periactin for a short break because of the sleepy/grumpy side effects. Sadie's geneticist said that was fine. Usually people are on it for 2-3 weeks and then off again for a week or two. I feel my stress level going up again though worrying about her weight. She gained about 1 1/2 pounds during the 3 weeks that she was on the medication. But being back in school has brought the stomach bug to our house. Shelbi and I caught it a few days later. Sadie and Shelbi's stomach bug wasn't as bad as mine, they are both on children's probiotics, so I think that helped them. Sadly, I'm pretty sure Sadie lost most of what she gained. She will start the periactin again this week.
Other than the stomach bug, everything is the same around here. Chasing Sadie around the house to keep her out of trouble and Shelbi is following suit and helping me. Taking and picking Sadie up from school hasn't been that challenging. Maybe I'm just getting used to it?! Daddy's been helping take on Tuesday and Thursday. Thanks Daddy!
Other than the stomach bug, everything is the same around here. Chasing Sadie around the house to keep her out of trouble and Shelbi is following suit and helping me. Taking and picking Sadie up from school hasn't been that challenging. Maybe I'm just getting used to it?! Daddy's been helping take on Tuesday and Thursday. Thanks Daddy!
Monday, February 2, 2009
Another morning at the hospital
This morning we took Sadie to have her blood drawn for the Angelman Syndrome UBE3A test, AGAIN! They screwed up the paperwork for the 1st test and therefore it had to be drawn again.
As expected, the lab tech blew the first vein and was unable to get enough blood out of her other arm. They had to call in the "Vat" team (i think i spelled that wrong, and i don't know what it stands for except they are supposed to be able to draw blood when the "regular tech" can't do it). Finally, after the 3rd attempt and endless poking with the needle, they were able to get 2 1/2 tubes.
Now for the 3-4 week wait AGAIN.
The UBE3A test is sequencing the genes on the 15th chromosome. It would be like getting number cards 1 to 1000 and you have to make sure each is in the proper numeric sequence. If 53 and 58 are switched that means they are out of sequence. If her genes are not sequenced correctly, she will have 2 documentable diagnosis. The gene sequence test will indicate if she has Angelman Syndrome.
As expected, the lab tech blew the first vein and was unable to get enough blood out of her other arm. They had to call in the "Vat" team (i think i spelled that wrong, and i don't know what it stands for except they are supposed to be able to draw blood when the "regular tech" can't do it). Finally, after the 3rd attempt and endless poking with the needle, they were able to get 2 1/2 tubes.
Now for the 3-4 week wait AGAIN.
The UBE3A test is sequencing the genes on the 15th chromosome. It would be like getting number cards 1 to 1000 and you have to make sure each is in the proper numeric sequence. If 53 and 58 are switched that means they are out of sequence. If her genes are not sequenced correctly, she will have 2 documentable diagnosis. The gene sequence test will indicate if she has Angelman Syndrome.
Subscribe to:
Posts (Atom)
Time is a Thief
I don't remember the first time I heard the sentiment, "time is a thief." Recently it is heavy on my mind. I haven't post...
-
and the flu panic begins... http://www.cloroxclassrooms.com/downloads/teacher_brochure.pdf
-
Sadie has been having spasm type clinch arm and mouth type movements that last about 2 seconds randomly starting in June. For the past mont...
-
Today I was feeling the need to read other stories about other children with chromosome disorders. I googled blogspot to see if I could find...