Morgan and Logan sliding
Kroy and Logan sliding
Well, we travelled up to Columbus to see Logan's favorite eye doctor, Dr. Dave Rogers...He asked how the patching was going ...and we were honest...it has never gone too well...and the older he gets , the more creative he becomes in taking or "rubbing" the patch off... and to be quite honest...I have never really noticed a difference...I had been doing research on atropine drops and Dr. Dave said we could give it a try...SO...he hates the drops...we put a drop of the atropine in his good eye and it dilates that eye...in turn, forcing him to use his bad eye..I know it sound like I am
torturing this poor baby...but before we do surgery, he wants that right eye to be as strong as possible.
He is still thinking Logan has ocular albinism..but we wont have a definite diagnosis til he is about 3..He is thinking Logan's vision is 20/400...
which is considered legally blind...I am just not quite sure I believe him...He did say this could be one of the reason's for the delay in walking...but Logan certainly has great motor skills..he is the FASTEST crawler.We go back in 8 weeks and hopefully we
will get new glasses...this will be his 3rd pair and he is only 15 months old!!!
A few weeks ago I thought about turning the blog "private" however, whenever someone "googles" ocular albinism, our blog pops up...I have gotten about 5-10 email from moms whose child has been diagnosed with this condition and I enjoy telling them about my experience and different ways of keeping glasses on and different eye exercises we use...That same week a mom e-mailed me and I knew that was a sign to not go private...Hope yall all have a great week.