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, May 7, 2012

Getting ready to meet mommy's work today!

I overheard Madalyn telling her about my work and that she was "going to love walking around in mommy's classroom".

Sunday, May 6, 2012

missing Lamictal, and MRI update

Josephine- Is doing great!  She is so sweet, and I'm  not sure if I've expressed enough to my friends and family just how happy I am that I took the leap of faith and brought her home.  She is a perfect fit for us.  She LOVES her grandparents already!  She can't get enough of going up to Pap for a little rough play time.  She started saying her Aunt "Na Na's" name, and giving her hugs.  She loves water, and says "water".  And her sister is the funniest and greatest person in her world...which, I just love for Madalyn:)

She is walking everywhere.  Everyday she gets more balanced and stronger. 

The MRI...I received the report and look forward to talking to the neurologist at the next appointment, or before.  Most was exactly as I was prepared for..."extensive damage" of left hemisphere.  However, there is one part I need more information on.  It says she has severe MCA stenosis and even mentions another test "if it would alter clinical management".   Thanks to my friend Nancy (Thanks!!) I talked to her brother that is a physician that could give me the "non-googled" definitions of what I was reading.  It seems she has narrowing of the main artery to the damaged hemisphere.  That could have been what caused the stroke, or it could have been as a result of the stroke.  More than likely all of her activity is being successfully taken care of by her right hemisphere....so, hopefully even if means that more damage could happen in the damaged hemisphere it would not affect her.  But, I want to talk to her doctor about it as soon as possible.  She is perfect just the way she is....she is one of the lucky children that survived a stroke (20-40% of childhood strokes are fatal)...we can't afford another stroke though! I don't think that is a true risk...but as a non medical person, that's what it sounded like...so I need to be sure it's a normal part of her type of stroke...with no additional risks of future strokes.

Madalyn's rash is almost gone.  Getting abruptly off the Lamictal has made it clear just how much it was helping her.  I hope we can find another seizure medicine that works for her.  Please pray for no seizures as her body goes through the last days of getting all the Lamictal out of her body and that the rash goes away so we can get back to the happy place we were before last week's allergic reaction!

Saturday, May 5, 2012

Friday, May 4, 2012

Better

The rash is somewhat better.  The new places it had appeared have grown lighter/smaller.  It is still pretty bad on the original places.  I'm happy that it is not getting worse, and actually looks better!

Thursday, May 3, 2012

MRI Results and rash update

The nurse gave read me parts from the MRI report on the phone today.   I vaguely remember hearing "extensive damage" and I think I was processing that, so maybe I missed the other details.  I do remember asking if it was localized, and she said no, it sounds large.   So, tomorrow I'll call and ask her to mail me the report....then I'll be ready to ask more questions at our appointment with Dr. Parker in June. I'll continue to remind myself that she is doing great, and an MRI doesn't place limits on these awesome kids.

Madalyn's rash is worse.  It has now spread to her feet, hands, and upper thigh.  It is still on her back (and extends all the way down), chest, around her knees, and over her right shoulder.  The instructions remain the same.  Watch closely for any signs of issues in the mouth, eyes, or mucus membranes.  Unless it improves, I'll keep her home from school again tomorrow. 


Madalyn's chest
Madalyn's back

Wednesday, May 2, 2012

Best news first

The MRI went well, and we should have results in a few days.  Although Josephine was quite agitated upon waking from the anesthesia, she recovered within the hour and was happy all day.  I met a really neat and inspiring person while waiting.  I enjoyed talking to her, and it helped the wait go more quickly.

Now for the bummer news.  Madalyn had a small rash yesterday. I sent a note to school, reminding them of the risk of "Steven Johnson's Syndrome" from her seizure medicine....figuring I was overreacting, but nervous anyway.  Today, the rash was worse.  I dropped her off at school, and made an appointment for her to see our pediatrician this afternoon.  I talked to Michelle (school nurse and much more!:)) during the day and told her we were going to the doctor.  She looked up our medicine and the side affects to be familiar with the situation.  Did I mention she is awesome?

I picked her up early for the appointment.  At that time the rash was significantly worse.  Dr. Denney looked at it and because it did not fit into any "normal" rash, he felt we needed to call Dr. Parker and probably stop the seizure medicine.  I don't suggest googling Steven Johnson's Syndrome, but if you do you will see why they don't take chances.  Basically, he said that the rash doesn't have to look any particular way for it to become Steven Johnsons, so we have to stop the medicine.  Dr. Parker called him back immediately and agreed.  She reminded me to keep the Diastat on hand in case she has a seizure since we are having to quit without tapering and can't start another medicine until the rash is gone. 

So, the bummer is that we finally got to the therapeutic dose, and now we have to stop.  The blessing is the rash is responding to the Benadryl and has not gotten any worse tonight.  This is good, because if it had gotten significantly worse, or showed up on any mucous membrane, it would have meant going to the ER.  The other good news is that we were able to see Dr. Denney today.  He was able to talk to our neurologist immediately, and we know what to do.  The other huge blessing is that she started with a rash in China that looked similar to yesterday's.  While in China, I emailed it to Dr. Denney and he thought it looked like a viral rash.  And it went away on it's own. I'm so thankful the need to stop her medicine waited until we were back home, with any medical support we may need!

MRI is today

The MRI is today.  Right now my biggest concern is not being able to feed Josephine prior to the test.    I'll distract her, and not let her see Madalyn eat breakfast, but I hate this part of sedation! However, I am so glad that UMC has changed the way they sedate for MRIs.  Madalyn had to drink an alcohol based drink for the MRI that we had to force down her throat.  It made her gag, throw up, and then literally suffer from a hangover for hours.  Now, they use anesthesia, and I'm told it's much easier and safer for the children.  Thank goodness!!!!

The purpose of the MRI is to determine location and extent of her brain damage.   It will likely confirm that her hemiplegia was caused by an inutero stroke.  Her China report said she had "left brain atrophy".  I believe this is comparable to the "volume loss", that is seen in Madalyn's report.

As a comparison, Madalyn's MRI report says the following:
There is noted enlargement of the body of the right lateral ventricle with loss of periventricular white matter.  A tiny amount of residual hemosiderin situated within this parenchymca defect on the right.   Impression:  Evidence of old parenchyma insult with volume loss within the right lateral fontral lobe and ex vacuo dilation of the underlying body of the right ventricle.  This is most likely due to prior grade IV germinal matrix hemorrhage. 

As Madalyn has proven, the best indicator of how well a child will do is how well they are doing....and Josephine is doing great.

Still, I'd really like an optimistic MRI today!

Last month....


 On our way home...with two children that had finally fallen asleep on the long plane ride. 

4 week report due to China

Our first post placement report is due to China since we have been home 4 weeks!  Kenisha, our social worker, came to visit to make sure all is going well.  This will be the first of many reports due to China over the next few years.  Along with each of these reports, all adoptive families  are requird to send 10 current photos.  The pictures go to the government officials in China, therefore, they must be culturally sensitive, as well as place an emphasis on "family life".  Some examples include no food on mouth (birthday party/spagetti pictures), child should not show too much bare skin, child should look happy, and pets should not be pictured too close to child.  Notice in our "backyard baseball" picture, two dogs are watching us; we kept nudging them away from us to get the picture:)






Tuesday, May 1, 2012

She is walking!!

She is walking!