Tuesday, May 18, 2010

Children's Rare Disease Network...

RAREblog

2 comments:

kyna said...

this is awesome Karen! What an amazing vision! So proud of who you are, and proud to call you friend! :o)

Heidi said...

Wonderful!! Sadly, this is so true about not having available resources because we're so busy ourselves. I always love your energy and what you continue to do for other special families needing support through such difficult times. Hugs to your sweet girl-
Heidi & Jack.