Okay, so I have some more updates with specifics on Chavalah!
We will be meeting with two specialists at the Phoenix Childrens' Hospital within the next four weeks. The first will be on July 28, ON her first birthday, oh well, with a Neurologist. Her appointment is at 10 in the morning Arizona time, so if you could be praying for us that morning, that would be great. It will be our "initial" appointment discussing our concerns and seeing what the doctor wants to do with testing, and her future. The reason for our visit with the Neurologist is quite simple. Several things have shown up the older she's gotten. She has a very weak left side! Everything on her left side is very limited, the latest thing they've noticed is when she "cruises" (she really doesn't cruise but they try and get her to do it while they are here), she drags her left toe/leg/foot. She doesn't "pick it up" like a normal step. She also has stiffness in her shoulder area like her brother, and although she looks perfectly normal, Chavalah has learned to pretty much do everything or compensate for her left side, looking perfectly normal. The last thing of concern is that Chavalah is STILL sleeping nearly 20 hours a day! Yes, A DAY! And at 1 year old, she should be awake MOST of the day with maybe a short nap in the morning and a longer nap in the afternoon! And when she wakes, she doesn't make a noise, she'll just lay there. I'm constantly checking to make sure she's still there, awake and breathing! And if I don't, she'd lay there without a peep for eternity! So, these are the things we're going to be discussing. More than likely, we'll be referred and scheduled for an MRI to make sure there hadn't been a stroke in utero, and to rule out Cerebral Palsy as we did with Ezra at about this time in his life!
Our second appointment will be with an Orthopedic Specialist at PCH on August 10! Also in the 10 o'clock hour range. If you could be praying for us then also. They will be doing x-rays of her left leg to look for anything abnormal bone growth wise there. When she stands and pulls herself up to things, her left foot literally twists and her toes point AWAY from her body in an "L" shape and she stands on the arch of her foot, not on the flat of her foot. When you keep her standing and physically move her toes so they are facing straight out in front of her as they are supposed to be, her knee looks all deformed from twisting to make it "forward" as normal.
These are all very minor things in light of what COULD be happening, but all things that are still very "abnormal" and just need to be checked. Once we have been to these appointments and "diagnosed" what they actually are, they will be documented and HOPEFULLY by the end of August, beginning of September, we'll be able to hand in ALL our paperwork to our adoption specialist and she will then be able to submit everything to finalize her adoption. THEN we can contact our attorney! I'm guessing Octoberish before we have a court date with the judge! We'll see! Might be a tad sooner, or a tad later. Still I believe it will be THIS year.
Thanks again for praying!