Today, I got to see a followup patient, who is still sick, but who is also much better. Elizah came into the hospital and developed acute flaccid paralysis, where all his muscles below his neck went weak. He couldn't raise his arms, move his legs, couldn't sit up by himself. Thankfully, he never had difficulty breathing, which is a bad complication of this disease which often is triggered by a viral infection. I didn't see Elizah every day in the hospital, but saw him on the weekends when I got to round our on pediatric ward. The first time I saw him, he was quite talkative, despite never meeting me before. I was asking him how he was doing, and as his mom was supporting him with her body, he told me he was well. I asked if he could move his toes - nope he said, his hands - nope, his mouth - nope again he said, which brought a laugh from his parents. There really isn't a lot we can do for him, but wait for the strength to come back. Sometimes the strength comes back fully and sometimes it doesn't. Thankfully, he has gotten some physical therapy from a volunteer PT who is here. Emma has been working with him and his family to increase his muscle strength and it seems to be working.
So when I got to see Elizah today in followup, I was happy, as he brought a smile to my face with his smile. And seeing the small, but noticeable improvement in his arms and legs from last time I saw him, was also a blessing to see. I don't have time to see all the followup patients, but I will take kids like Elizah anyday.