We finally made it home on Monday and had our appointment with our pediatrician on Tuesday. Her routine newborn check up was great, but he did tell us that there was definitely something wrong with her eye and he wanted us to be seen by an ophthalmologist.
We were able to get an appointment as a work-in today with a pediatric ocular plastic surgeon in Birmingham. We knew we needed to be seen by an actual pediatric ophthalmologist, but he had a two month waiting list! We wanted to be seen sooner than that, so we took the appointment with the plastic surgeon, hoping to at least get an answer or a referral to someone else.
We headed to Birmingham today and made it to our 2:00 appointment at about 1:30, expecting to be there for several hours since we were being worked in . Thankfully, we were only in the waiting room about 10 minutes before we were called back to see they doctor. He was wonderful! He looked at her eye and told us she had what is called microphthalmia, which is a developmental eye disorder that basically means a "small eye". For some reason her left eye did not develop properly. There is no known cause, it is not necessarily genetic and is not linked to anything that might have happened during pregnancy. He told us that her eye would never grow normally and that she would never be able to see from that eye. He then told us he would really like for us to see a pediatric ophthalmologist, Fred. (the same doctor that had a two month waiting period) and sent us over to his office. We were put in a room to be seen--all before our scheduled 2:00 appointment! The Lord totally went before us and opened the doors for us to be seen by exactly who we needed to see. In less than an hour we were seen by two specialists! The pediatric ophthalmologist did a more thorough exam using a tool to open her eyes and confirmed what Dr. Long had told us about the microphthalmia. We were concerned about her vision in her right eye, but he said she has a completely healthy right eye--Praise the Lord!
Where we go from here: in 3 months we will go to the Alabama Eye Foundation to be educated on and hopefully fitted for what is known as conformers that we will put in her left eye. The goal with these will be to help her eye socket and lid grow as her face grows so she doesn't have any asymmetry in her features. Eventually she will be given a prosthetic eye that she will use. Both doctors said that the prosthetics are great and you often may not even notice when people have them.
It's never easy when your child is "sick" in any way, but as Dr. Long told us today, this is a bump in the road, not a catastrophe. We went expecting similar news to what we received and we were glad to get clear answers and know that we are on the best path for Isla. Even when we were suspect of there being a problem, Brittany and I reminded ourselves (Zack writing now) that the masterful Creator formed Isla in the womb and knew exactly what He was doing. As far as we know, Isla will live a healthy, happy life, just like our other children. She is beautiful, and we can't wait to watch her grow with her brother and sister. The Psalmist says,
Behold, children are a heritage from the LORD,
the fruit of the womb a reward.
Like arrows in the hand of a warrior
are the children of one's youth.
Blessed is the man
who fills his quiver with them!
He shall not be put to shame
when he speaks with his enemies in the gate.
(Psalm 127:3-5 ESV)
Our quiver is filling up! We will covet your prayers as we continue this journey with Isla. There are obvious challenges that will come along the way, but as we've already seen today, the Lord is faithful and is going before us preparing the way.....not surprising though is it!?














































