I want to begin this post by confessing that it becomes impossible to update a blog when you forget your username. Now that I've successfully logged in, an update is in order.
S went in for his annual neurology check up at the end of June. We were told that he looks wonderful and that this visit could have been the last. However, our neurologist wanted to see him one more time. We will go back next July for our final checkup. Provided that S stays seizure free between now and next July (which he should), he will not need to have any more EEGs.
S is still being seen twice a month by a physical and cognitive therapist. We recently added an occupational therapist to the mix. S has choked several times on crunchy foods, so he got assessed for a feeding delay. The occupational therapist agreed to take him on as a client for a few months, but she thinks he'll learn quickly enough to be finished with OT by October. Our cognitive therapist has told us that S will definitely not qualify for CT at his annual evaluation in October since he's doing so well. The physical therapist is the only one we might continue to see on a regular basis. S is still having some balance issues that cause him to fall. Our neurologist believes S' balance may be the only thing that was affected by the seizures. It's much better than what it could have been, so we won't complain. We recently took him to get a hip x ray done to rule out misalignment of the hips. All results came back normal, so we're waiting to see where to go next to help his balance.
S is saying more words than I can count and repeats everything we say. He has even begun stringing words into simple sentences. S has also surprised us by taking an interest in letters. He can now recognize 13 letters when asked to find random letters in a puzzle. S has also learned to climb stairs, so he's keeping mommy and daddy on their toes!
We are also very excited to announce that S will officially be one year seizure free on July 30th! This is a huge milestone for S, and we are so excited to celebrate with him. Be on the lookout for celebration pictures later this month. Don't forget to send him a congratulations that day if you think of it!
Wednesday, July 15, 2015
Thursday, January 29, 2015
Checking In
It has been a while since I last posted on S's progress. Let me preface this post by saying that this is strictly an update. No reason to worry!
S went for a neurology check up today. There was no EEG today as his last visit had shown a clear EEG. S' neurologist let us know that he was developing normally for a child his age, and that the reason for this is solely due to the fact that we caught his spasms so early.
S will not return for another neurology appointment until July. After that, we will be seen in January. If nothing happens between now and his second birthday, then S will no longer be a patient with neurology. As silly as it sounds, I feel like that last check up will be very bittersweet for the Hill family. I feel as though a part of us will always be attached to this neurologist because she has been with us from the very beginning of this incredibly difficult road.
I wanted to give an update today to celebrate an upcoming milestone. As of January 31st, 2015, S will have been six months seizure free! We are so thankful to have this celebration be a reality. Six months ago, it seemed impossible that we would ever reach this milestone.
We got an informal assessment done on S' cognitive and physical development yesterday. He is now considered to be within the 18 - 24 month age group in physical development. He is right on track or ahead for his age in every other area. The only deficit he currently has is with receptive communication. There is a 7% delay in that area. However, the cognitive therapist is not concerned and feels he will catch up quickly. Both the cognitive and physical therapists feel the spasms didn't affect his development at all.
We are so grateful to be able to share such positive news with everyone, and we hope the goods news only continues as time goes on!
S went for a neurology check up today. There was no EEG today as his last visit had shown a clear EEG. S' neurologist let us know that he was developing normally for a child his age, and that the reason for this is solely due to the fact that we caught his spasms so early.
S will not return for another neurology appointment until July. After that, we will be seen in January. If nothing happens between now and his second birthday, then S will no longer be a patient with neurology. As silly as it sounds, I feel like that last check up will be very bittersweet for the Hill family. I feel as though a part of us will always be attached to this neurologist because she has been with us from the very beginning of this incredibly difficult road.
I wanted to give an update today to celebrate an upcoming milestone. As of January 31st, 2015, S will have been six months seizure free! We are so thankful to have this celebration be a reality. Six months ago, it seemed impossible that we would ever reach this milestone.
We got an informal assessment done on S' cognitive and physical development yesterday. He is now considered to be within the 18 - 24 month age group in physical development. He is right on track or ahead for his age in every other area. The only deficit he currently has is with receptive communication. There is a 7% delay in that area. However, the cognitive therapist is not concerned and feels he will catch up quickly. Both the cognitive and physical therapists feel the spasms didn't affect his development at all.
We are so grateful to be able to share such positive news with everyone, and we hope the goods news only continues as time goes on!
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