L & K Update...better late than never.
It has been too long since my last blog. I enjoy it and it is such an outlet for me. Today's tidbits will entail the details of our journey with Lydia and Knox who are visually impaired. Many of you know this journey well but right now we are in the thick of things again it just does my heart well to write. So here goes... Each year we see our Indy ophthalmologist twice per year for regular vision checks to ensure that neither of them have lost any vision. On that front, so far so good. In February and March we took both Lydia and Knox to see Dr. H at the University of Michigan Kellogg Eye Center. He is a brilliant physician and retinal specialist. His bedside manner is not always the best but he is a world-renown specialist. For Lydia's visit, Dr. H still seemed a bit puzzled by the results of her testing and was hopeful that by seeing Knox, we could move in some direction toward genetic testing. So far, she still presents with some sort of albinism, a cone dystr