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This blog is about the journey of our son Micah and his battle with lymphatic malformation (sometimes called cystic hygroma). He is the light of our lives!
About Me
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AAC
baby girl
birthday
blended diet
fetal care center
fun trips
funny
holidays
hospital
Kyleigh
lymphatic malformation
Micahs Medical Miracle Story
Micahs surgical history
milestone
PECS
pneumatosis
rapamycin
school system
sirolimus
SMO
surgery
thankful thursdays
trach
Traveling Awareness Bears
tube feeding
Great pictures and a great video! Thanks for sharing with those of us who can't be there. It is great to see our little miracle boy growing so fast and being so active. It was so good to see all of your family and Sarah's, too. I haven't seen little Abram yet, either. What a great thanksgiving for all of you. Prayers continue to be answered. Thanking the Lord, Miriam
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