A Long Update
The neurologist called today, which immediately made my heart drop. Typically, good news means a call from the nurse. Bad news means a call from the doctor. The doctor called to let me know a couple things. First off, she let me know that Solomon had no seizure activity in his EEG. This is great news! Praise God. All the markers for Infantile Spasms were gone. There was one questionable area in the EEG, however, where there was some slowing of the brain activity (yeah, I didn't really understand it either). I probed and probed, trying to understand what she meant (is this good, bad, neither, both?). But from the doctor who speaks "doctor-ese" and asks, "did Solomon have any clinical episodes?" (translated: "did he have any seizures"), the most I could get from her was that the slowing could be nothing or it could be significant. So, I called the pediatrician.
We are so, so thankful for our pediatrician (and if you're in the area and looking for a good doctor, I'd highly recommend him!). He is patient and speaks at a normal, human level (i.e. a level at which I can comprehend what he's saying). The pediatrician said that the slowing in the EEG could indicate an area where Solomon is prone to having seizures. He said, however, that he thinks it's more likely that it's a portion of Solomon's brain that is still developing and because it is not fully developed, it is not firing and connecting at as fast a rate as the rest of his brain; a very normal thing in infants. All this to say, we just have to wait and see. But I'm thankful that the pediatrician seemed to think it was likely the "nothing" on the scale of "nothing to significant" given by the neurologist.
We still covet your prayers. Solomon is definitely doing so much better than he was a few months ago. He is starting to try to get around (scooting on his butt Asher style). He's getting on his knees occasionally and very vocal with his likes and dislikes. He's delayed for sure, but the doctor seems hopeful he'll be able to catch up. We are working towards getting him into an OTPT in the next few weeks to start working towards that end.
The neurologist said we can bump his EEG's out to every 3-4 weeks now, instead of every 2-3 weeks, so that is encouraging. She said she would like to keep him on his current anti-seizure medication for another 1-2 months, and then begin the process of switching his medication in order to avoid the side effects of his current medication (vision loss). Like I said, we still covet your prayers. We have a long road ahead of us. Please pray for me, as I seem to spiral emotionally around the weeks of his doctors appointments. Pray for joy for me, as well as rest in a Sovereign God. We are thankful that God continues to heal our son and believe He is doing this good work in Solomon. May He alone be glorified!









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