Here he is a week or so after surgery.
This is a month or so post-op.
And here he is just a couple days ago! The incision is almost invisible and the infection site continues to fade.
The lighting here exaggerates the depression left from the Parotid Gland they removed (that's what causes the Frey's Syndrome - a red blotch on his cheek from the salivary nerves that are still there, but are no longer connected to the gland.) I had intended to get a picture while it was flared up, but that didn't happen.
And here's his beautiful smile! As I have said before, we are beyond thankful that the surgeon and his amazing team were able to remove the infection without damaging the facial nerve.
Every month or so, I get a comment or an email from another mom whose child has been diagnosed with this. While I am no expert, I remember wishing I knew another mom who had been through this to talk to or ask questions to. So if that's you, please don't hesitate to comment or send me an email at thoner02k @ yahoo . com. You can also read all my posts about Atypical Mycobacterium here.
Thanks for stopping by!