Hello everyone! Sorry I’ve been such a slacker with this blog lately, but things have been really busy!!! The jet lag is long gone and we have definitely settled into our routine. I had no idea how much of an adjustment it would be going from a one child family to a two child family. Abby is on the move….ALL THE TIME! :) :) I think I forgot how energetic toddlers are! But things have been great! Emily’s been such a great sister and the sibling jealousy episodes have been few and far between. Emily loves to help with everything and one day pronounced to me “I am sooooo happy. I LOVE having a baby sister in the house!”
As for Abby, she is making incredible gains each day. As you all know, we adopted her through a special needs program, and we went into this adoption expecting her to potentially have some degree of cerebral palsy, which would most likely affect her motor skills and coordination.
Since we've been back, we've had her evaluated by several doctors and specialists. As it turns out, she does not have CP at all, but has what they call an "orphanage delay". When we first met her, Abby was VERY weak (but many kids are “low tone” coming from the orphanage, as they haven’t had a chance to practice their physical skills)....so our pediatric neurologist suggested that we contact early intervention to set up evaluations and get her whatever therapies Abby might need to catch up. She also said that she expected Abby to catch up quickly to her peers.
Then we scheduled an MRI to look closely at the brain, and an EEG to check for seizure activity (as she has had one known seizure). So I called early intervention right away, and about 1 ½ weeks later, our service coordinator came to the house. Then yesterday, Abby was evaluated by both a speech therapist and an EI teacher (to get an overall developmental assessment). This afternoon, the physical therapist comes to do his evaluation.
On Tuesday, Abby had her MRI- which went smoothly. She had to be put under general anesthesia, which wasn’t fun (as Abby HATED the I.V. and fought with everything she had), but we made it through. Last night, we got the results back (the neurologist called), and it turns out that her brain looks NORMAL!!!!! The only thing they saw is called benign external hydrocephalus. Basically, there is a little bit of extra fluid in her skull. Sometimes kids with larger than average size heads have this extra fluid to fill the space between the brain and the skull. It could be caused by an injury or can just happen if large heads run in the family. The neurologist said that this usually resolves on its own by about 2-3 years of age....and that this is no cause for concern/ is fairly common. No intervention necessary. They will just do check ups on her, from time to time. Whew!!! Sometimes kids with this are prone to seizure, but it could be that once this fluid goes away, she will never have another seizure again. Well, I guess we'll have a better idea after the EEG.
As for her progress, I have to laugh…because since requesting her early intervention evaluations 3 weeks ago, Abby has met many of her developmental milestones on fast-forward. By the time the therapy is set up, she might not need it anymore. LOL! Let’s see….we’ve had her home for less than a month and here is her before and after:
Before (when we first adopted her at 20 months), Abby:
-Could not move from lying down to sitting
-Could sit unsupported, but could be thrown off balance VERY easily
-Could not move from sitting to standing
-Could only walk while holding on to someone’s hands
-Could not catch herself when she fell from sitting or standing positions (would fall over in “one piece” and would whack her head)
-Could not crawl (would “inchworm” or move forward on belly “army style”)
-Could not pick up small objects with her hands- i.e. feed self Cheerios
-Could not drink
-Could barely support her own head
Today Abby (at 21 months):
-Crawls by herself
-Independently moves from lying down to sitting AND sitting to standing
-Has good sitting balance
-Walks by herself (no support), forwards, backwards , side to side, in circles, etc
-multitasks (walks while doing something else…i.e. playing with toy, clapping hands, etc)
-Can bend over (from standing position) to pick up object from floor without losing balance
-Can drink from cup, bottle, straw, sippy cup etc.
-Can feed self finger foods
-Is trying to climb onto furniture
-And when she does fall (which is becoming rarer all the time), she knows how to fall on butt or knees (appropriately), and can usually even catch herself and regain balance
-pushes rolling objects while standing (doll strollers or play shopping carts, etc)
-Is trying to walk up stairs
It is AMAZING. She has done met YEAR’S worth of milestones in the past few weeks. I am so excited to see what a few more weeks will bring…..maybe cartwheels or headstands? Heehee.