isabelgracevsepilepsy.blogspot.com
Isabel Grace, Beating Epilepsy One Day At A Time: October Update
http://isabelgracevsepilepsy.blogspot.com/2011/10/october-update.html
Isabel Grace, Beating Epilepsy One Day At A Time. Wednesday, October 5, 2011. He would also like to admit her to CHKD at some point to get a 3-4 day EEG. Dr. F is amazed that Isabel is not a zombie with all of the meds that she is on, in fact she is just the opposite, she is a nut! That girl has more energy than Caden half the time! In other news speech therapy is going very well! Subscribe to: Post Comments (Atom). Lilypie Third Birthday tickers. Vitamin B6- 1 25mg tablet crushed daily.
isabelgracevsepilepsy.blogspot.com
Isabel Grace, Beating Epilepsy One Day At A Time: GI
http://isabelgracevsepilepsy.blogspot.com/2012/02/gi.html
Isabel Grace, Beating Epilepsy One Day At A Time. Wednesday, February 8, 2012. Although I've been through the anethesia route many times with Caden, it's harder to think of my baby girl going under although I'm sure she will be just fine. Please send some good thoughts our way! Subscribe to: Post Comments (Atom). Lilypie Third Birthday tickers. Keppra-We have been using this since day 1. It has not caused any side effects. She is currently taking 4.0mL 2x a day. Vitamin B6- 1 25mg tablet crushed daily.
isabelgracevsepilepsy.blogspot.com
Isabel Grace, Beating Epilepsy One Day At A Time: New Year/New Updates
http://isabelgracevsepilepsy.blogspot.com/2012/01/new-yearnew-updates.html
Isabel Grace, Beating Epilepsy One Day At A Time. Wednesday, January 4, 2012. We also went to see hematology due to her lack of clotting when she got her blood drawn and her easy bruising. After a long talk with the doctor and a few tubes or blood we found out that she has low Factor VI or Hemophilia C. It's definitely not a huge concern but something that we will need to follow up with in February when we see hemo again. I feel so bad for brushing off her pain for so long. January 6, 2012 at 7:11 PM.
isabelgracevsepilepsy.blogspot.com
Isabel Grace, Beating Epilepsy One Day At A Time: February 2012
http://isabelgracevsepilepsy.blogspot.com/2012_02_01_archive.html
Isabel Grace, Beating Epilepsy One Day At A Time. Wednesday, February 8, 2012. Although I've been through the anethesia route many times with Caden, it's harder to think of my baby girl going under although I'm sure she will be just fine. Please send some good thoughts our way! Subscribe to: Posts (Atom). Lilypie Third Birthday tickers. Keppra-We have been using this since day 1. It has not caused any side effects. She is currently taking 4.0mL 2x a day. Vitamin B6- 1 25mg tablet crushed daily.
isabelgracevsepilepsy.blogspot.com
Isabel Grace, Beating Epilepsy One Day At A Time: I Saw This One Coming...
http://isabelgracevsepilepsy.blogspot.com/2011/11/i-saw-this-one-coming.html
Isabel Grace, Beating Epilepsy One Day At A Time. Friday, November 4, 2011. I Saw This One Coming. As soon as Isabel walked through the door yesterday I said to Brian that I think a seizure is coming soon. The last few days she has been miserable. She also has been waking up shaking very badly, which has recently subsided a bit. Last night she cried non-stop from the minute she got home until the seizure started, why is that? Subscribe to: Post Comments (Atom). Lilypie Third Birthday tickers. Tegretol- W...
isabelgracevsepilepsy.blogspot.com
Isabel Grace, Beating Epilepsy One Day At A Time: March 2012
http://isabelgracevsepilepsy.blogspot.com/2012_03_01_archive.html
Isabel Grace, Beating Epilepsy One Day At A Time. Friday, March 2, 2012. Thankfully Isabel's surgery went off with out any problems. They scheduled it for 1:00 in the afternoon so getting her to abstain from food and drink was definetly the hardest part. About an hour before the surgery the anesthesiologist brings in a picture of all of the different flavors of anesthesia that they have. Of course they are pictures of FOOD! Isabel starts freaking out screaming, "Nana, Nana! About a week later we got a ca...
isabelgracevsepilepsy.blogspot.com
Isabel Grace, Beating Epilepsy One Day At A Time: January 2012
http://isabelgracevsepilepsy.blogspot.com/2012_01_01_archive.html
Isabel Grace, Beating Epilepsy One Day At A Time. Friday, January 27, 2012. A Day At CHKD. Overall it was a long day, but CHKD make the experience enjoyable for Izzy and for that we love them! Wednesday, January 4, 2012. I feel so bad for brushing off her pain for so long. I just wish that she could catch a break. Through it all she is such a trooper.she always has a smile on her face. She is teaching me an invaluable lesson and I will never forget it, she truely is my hero. Subscribe to: Posts (Atom).
isabelgracevsepilepsy.blogspot.com
Isabel Grace, Beating Epilepsy One Day At A Time: October 2011
http://isabelgracevsepilepsy.blogspot.com/2011_10_01_archive.html
Isabel Grace, Beating Epilepsy One Day At A Time. Thursday, October 20, 2011. She is not severely disabled as you called her! You can bet that this is not the last time that they hear from me! Wednesday, October 5, 2011. He would also like to admit her to CHKD at some point to get a 3-4 day EEG. Dr. F is amazed that Isabel is not a zombie with all of the meds that she is on, in fact she is just the opposite, she is a nut! That girl has more energy than Caden half the time! Subscribe to: Posts (Atom).
isabelgracevsepilepsy.blogspot.com
Isabel Grace, Beating Epilepsy One Day At A Time: Surgery and PT
http://isabelgracevsepilepsy.blogspot.com/2012/03/surgery-and-pt.html
Isabel Grace, Beating Epilepsy One Day At A Time. Friday, March 2, 2012. Thankfully Isabel's surgery went off with out any problems. They scheduled it for 1:00 in the afternoon so getting her to abstain from food and drink was definetly the hardest part. About an hour before the surgery the anesthesiologist brings in a picture of all of the different flavors of anesthesia that they have. Of course they are pictures of FOOD! Isabel starts freaking out screaming, "Nana, Nana! About a week later we got a ca...
