They are Due in July (same time we would have welcomed our baby to the world) and his daughter has been diagnosed with the most severe kind of Spina Bifida there is.
there is a procedure that can be done but his insurance does not cover it. Here is a link read about his family and what they are going through.
http://meetmeintheapricottree.blogspot.com/
here is a link if you feel that you can give to his cause.
http://www.giveforward.com/thelittleallredgirlspinabifidafund
It would be a life changer if we could rally around this family and show our love by donating what we can.
Every penny counts.
