Waves
Liam's favorite pool while we were on vacation in the Dell's was the wave pool. He loved everything about it - getting splashed, the waves pushing him up and down, riding in the tube, jumping the waves in the shallow section... and especially laughing at me when I got splashed!
This picture reminds me of the progress and results we're seeing in him since the stroke. Some days are very good days - he seems to find his words more easily, his confidence seems high, things almost seem normal. Other days aren't so good - he struggles most of the day to find his words, he realizes he can't find them, things are clearly not normal.
Yesterday, however, was a very good day. In the morning hours before speech therapy his words were coming easily. His confidence was high, which sometimes meant he'd say the wrong word, but would be able to fix it when asked if that's what he really wanted to say. He went to speech and his therapist said he did a great job with all the activities that morning.
After speech we ate lunch in the car and headed over to see the neurologist. The day just got better.
His angiogram showed no abnormalities in the vessels of his neck. The EEG we had done showed normal activity in his brain. Most importantly for this test, the activity around the section of brain that was damaged was not slowed at all - the doctor was very glad to report this. (Just a side note - the area of the brain that did not get blood/oxygen is dead and cannot be repaired. So, the neurologist is interested in the area surrounding that section.)
I brought up our concern about the daily aspirin Liam has been taking. Aspirin is a blood thinner and is often prescribed to stroke patients to prevent any further clotting. Since he's been on this Liam has been bruising more easily (and he really doesn't need help with that) and of course when he falls and scrapes a knee we need to be sure that the blood will clot. The doctor would like us to continue with the aspirin until six months post-stroke. After listening to my concerns he figured the dosage of a baby aspirin could be split in half and still be enough for my 40 pound Liam - so we will continue with the drug, but only give him a half a pill a day. Hopefully this will help with the bruises we've been seeing.
The doctor reminded me of what he told us in the hospital - that all of the children he's seen with this type and location of stroke have no long term deficits. I was thankful to hear this again after six weeks of recovery. He said everything will just take time and nobody knows how long. I voiced my concern about his speech/language and he encouraged us to continue with the therapy and be patient.
We left the appointment and scheduled our next one for December. December! Until then all we've got on Liam's schedule is therapy. No more tests. No more specialists. Just therapy!
Labels: angiogram, aphasia, childhood stroke, doctors, EEG, hopeful, ischemic stroke, liam, neurology, parenting after a stroke, recovery
0 Comments:
Post a Comment
Subscribe to Post Comments [Atom]
<< Home