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Patty and Robert talk about the power of knowing what you can do to monitor someone with an LFS diagnosis.
Whitney shares her thoughts on laughter as medicine.
Kanika shares how letting siblings participate in care helps.
Kanika talks about finding strength for your child after diagnosis.
John explains that knowledge is power with an LFS diagnosis.
Corbin and his family share staying close to your family and connecting with others who have LFS helps.
Mindy and Breanna talk about making each day count.
Andrea shares how she helps Kiera keep up with school.