T minus 15 days.
Here.
We.
Go.
Again.
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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
Labels
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
Feedjit
Followers
Blog Archive
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2011
(142)
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December
(15)
- A brief but delightful look back
- Merry Christmas!
- A sick kid plus not swallowing...
- A rough 24 hours...
- It's still complicated.
- It's complicated.
- The trip down...
- More Traveling Awareness Bears
- Micah meets MaKenzie... and Luke and Leia
- Really unlike me...
- About that time...
- Christmas fun
- A PG-13 Post, parents.
- The hotel rooms are booked.
- Next surgery...
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▼
December
(15)
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