Timeline


Apr-11 Homestudy began
Jul-11 Signed with Holt
6/28/11 Found Jospehine, but another family is
currently reviewing
7/13/11 Received information for Josephine
to review
07/20/11 Asked for additional information about
Josephine's development
08/20/11 Filed I800A
08/23/11 Received additional information from her
orphanage and asked to hold her for me
08/24/11 Josephine went off Great Walls list to Holt
08/26/11 Sent LOI (Letter of Intent)
9/2/11 LOI uploaded in china
9/7/11 Got fingerprinted
9/29/11 800A
10/14/11 DTC (Dossier to China)
10/18/2011 LID (Logged in Date)
12/14/2011 LOA!
02/03/2012 Article 5 Pickup
02/16/2012Travel Approval
03/13/2012 Travel to CHINA!!!!!
03/29/2012 Homecoming


Monday, July 26, 2010

Good results from EEG

We successfully deprived Madalyn of sleep for her EEG and she fell asleep during the test (optimal). Being sleep deprived and falling asleep maximize the chances of the EEG picking up any abnormal activity. And even with that, the test showed NO ABNORMAL SPIKING! This is great news, and means she won't go on any seizure medication for now!

We keep emergency Diastat close by in case she has another seizure. If we don't have the medicine with us, we should call head to an emergency room if the seizure lasts longer than 5 minutes.

This is the best news we could hope for, so I am very relieved.

Update:  September, 2011., 2 years later, Madalyn had a second long seizure that was stopped after 8 minutes with Diastat.  An EEG following it did show spiking this time.  A 24 hour Video EEG was ordered to help us decide if it is time for medication.  The 24 hour EEG showed frequent spiking, in several regions, sometimes crossing over to the other hemisphere.  This was not the news I had hoped for.  After much thought and research, I agreed to start the medication her neurologist recommended....Lamictal.  I trust her neurologist, but with all the side affects of seizure medications, it was hard to accept that she needs the medicine.  However, we are hoping that by controlling the spiking, her concentration and hyperactivity may improve.  We've been working our way to a therapeutic dose for 3 months, and still have a few more weeks.  Because of the risk of side affects that can be very serious (i.e. life threatening rash), the dose has to be increased very gradually.  I feel like we have already seen a great improvement in her behaviors.  Mainly her fears that were increasing, and this "look" that would come over her, especially in new places, or places with a lot of activity.   "The look" usually led to irrational tantrums that no amount of consequences or positive rewards could contain.  We have not seen this type of behavior since starting the medicine.  I had always felt like it was related to seizure activity, and since it has improved with seizure medication, I feel like I have some validation...but no one really knows...but for now, we are good.

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