Friday, April 17, 2009

New pics!!
















I took Hannah and Blitzen to Portrait Innovations to have their pictures taken together. It was a wonderful photo shoot. Danielle did a fantastic job with both of them. She went above and beyond to make it a great experience!!
The duo continues to do fantastic. He is alerting to her seizures at home and at school. We continue to be amazed at how accurate he is!!! Their bond continues to grow every day. It is so sweet to see how he checks on her through out the day. So sweet!!!
We are now weaning Hannah off of her medication. By the first or second week of May, she will be off meds completely. We will stay at home until her seizures are coming fast and furious then they will admit her to the monitoring unit that day. They have assured us they will have a room for us. That remains to be seen!!! We will be staying in the hospital as long as it takes to get these seizures on EEG. Hopefully then we will know if she will be a surgical candidate.....

3 comments:

Anonymous said...

I had a blast taking your pictures! Thank you for your kind words! I really hope to see you again and I hope all goes well for Hannah in these next few weeks!

The Kurjian Family said...

What a blessing Blitzen will be to Hannah & your family! We will be praying for you & for Gary while he is deployed.

The Kurjian Family said...

May I link your blog to mine?

Beautiful Hannah...

How this journey started....

Hannah was born prematurely at 34 weeks gestation. She was a relatively healthy preemie; initially having difficulty maintaining body temperature and needing to grow. She weighed 4 pounds 9 ounces at birth. When she was four months old she began to drool, non stop. We were told the first year she was "teething." At 18 months old, we really started searching for reasons of why her shirt was always soaking wet. We saw various specialists who always sent us to another specialist, saying "everything looks okay." She spent years in oral motor/feeding therapy to help her not to drool. It wasn't until she was four years old and in preschool that we started to get some answers. Her preschool teacher commented one day that she wasn't reponding when her name was called. I took this information to her pediatrician who then orderd an EEG, "just to rule it out." Much to our shock and amazement, the results showed, she was having seizures. That is the day our journey REALLY began. Once she began taking seizure medication the drooling almost stopped completely. (She will still drool to this day when she is having seizure activity). Since then, it has been a roller coaster; countless medications and medication changes. She has never really reponded well to any medication.

About two years after she was diagnosed with epilepsy, the doctors noticed that her blood pressure was running high. After many tests, she was diagnosed with hypertension. We still are not sure why, but her cardiologist feels her blood vessels are thicker than normal.

About this same time, we also began looking into why Hannah was such a horrible sleeper. She would thrash, talk, move every which way, during her sleep. The sleep studies revealed that she has alveolar hypoventilation sydrome, which means she has too much carbon dioxide in her system when she sleeps. To help this, she wears a BI-PAP at night. This has been monumental in giving her more effective and quality of sleep.

Every day is a challenge for Hannah and our family as a whole. Blitzen has been an absolutely wonderful addition. She calms herself sometimes just by petting and loving on him. He has been trained in behavior disruptions and will sometimes be able to stop a meltdown from getting out of control.
It has been extra hard on the whole family since daddy is deployed to Iraq. He has been gone since January 09 and will gone until Jan 2010. We get to talk with him by phone and on the web cam; which is nice, but not the same!! Blitzen has helped to make his absence go just a little smoother....