1. Thank you all for your prayers and words of encouragement. It is easy to feel alone as a "special needs" mom. It means so much to me to know that so many people care about and love my girls so much.
2. Annabelle's behavior and patience through the morning was amazing! After a long car ride, late dinner, early morning, unfamiliar meals, and being away from home, we were prepared for the worst. But she gave us her best. We were in appointments from 8:30-11:30. Not once did she whine or complain. In fact, she was very curious, and excited to see Hazel's x-rays. Maybe we have a future x-ray technician on our hands?
3. I cannot say enough about the Ronald McDonald House! There was a moment when we thought they wouldn't have a room available for us, but they offered a room voucher for a nearby hotel since we had booked our room ahead of time. (Because they never know for sure how long a family will need a room, they cannot guarantee room availability). However, they called us back a few hours later, and reconfirmed that we would indeed have a room in the House. While there, the girls were able to enjoy the play rooms, and we were able to enjoy having hot meals provided for us.
4. Hazel's doctors are very happy with what they saw. Hazel's spine looks wonderful, and she is showing no signs of hydrocephalus or other complications related to her Achondroplasia. Yay! They want to see her again in 6 months for another followup.
5. She slept enough during her sleep study to get sufficient data. After screaming, and pulling at the nasal cannula (used for monitoring oxygen flow) for a full 2 hours, she finally exhausted herself, and slept until 5am, only waking 2 or 3 times when she lost her pacifier. This time around, I personally slept better than her last sleep study, as I knew more of what to expect.
All that being said, we had a very wonderful trip to Delaware. We even got to meet with another LP family for a playground play-date.
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| Used with permission from http://www.aisforadelaide.com |
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