Help my Kalista come home

My baby girl Kalista has been on the NICU since her birth on Aug. 7th 2020. She may still be on there for several more months. While I was pregnant with her I was diagnosed with a genetic disease called myotonic dystrophy. My form of it is less severe than her form. Her form is called congenital myotonic dystrophy. Meaning she was born with it. The doctors say she is on the more severe spectrum of it. Right now Kalistas father and I are up at the hospital so much that it is hard for us to get and keep a job. With classes for her care starting soon it will be near impossible for us to do anything other than what is needed for her to come home. So I'm asking you all to help me out just a little. Anything will help.

Donations

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  • Judy Schraeder 
    • $25 
    • 1 mo
  • Anonymous 
    • $25 
    • 1 mo
  • Anonymous 
    • $30 
    • 1 mo
  • Katelyn Pyles 
    • $25 
    • 1 mo
  • Anna Klein Fink 
    • $100 
    • 1 mo
See all

Organizer

Kaylee Mather 
Organizer
Tonganoxie, KS
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