Keegan is up in Omaha at UNMC where he was sent due to signs of hydrocephalus aka "Water on the Brain". They did an MRI and the results showed something else which they need to do further genetic tests for. Problem is those tests will take a couple weeks to a month to come back... the Genetic Dr told me they are doing 10 different tests but he is leaning towards muscular dystrophy. There are 8 different kinds of MD ranging from not too disabling to severe so even if this is what he has, we really don't know what to expect until the tests come back. There isn't a cure yet for MD just treatment, so fingers crossed that isn't what he has, but of course we will love him the same no matter what it is.
BTTT
I prayed and thought often of this little precious child during the holidays and now. More prayers for him today. More prayers for the parents... I have no idea what they must be going through but I can only assume they are scared. The next “couple of weeks” must probably feel like a lifetime.
Continuing in prayer ...
Prayers for this little precious one of God’s.
Prayers up.