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Emmalee Special Needs Girl Bike

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We the Campbell's are a working class family trying to provide for our little princess girl. We do not receive any government assistance because her Syndrome isn't on the pre-approved list for support so we unfortunately have to seek help from friends, family, and generous people in the community.

Emmalee Campbell was born missing part of her first chromosome. She was diagnosed at age 2 with 1p36 Deletion Syndrome. This Syndrome is still relatively new and can only be detected through microarray genetic testing. She struggled during the early years of her life, having seizures, multiple surgeries, including on her heart (Amplatzer Occluder being implanted). Emmalee cannot speak, but has learned over 100 signs (ASL), she struggles to walk so utilizes a children’s wheelchair but is the happiest little girl you ever would meet!
 
 What is 1p36 Deletion Syndrome?
 
Emmalee means the world to us as her parents and we only want to provide her health and happiness. Through this fund-raising our goal is to purchase a Custom Special Needs bike (Pink color of course ) which will allow our little Angel to be able to ride independently.

A typical child can ride most bikes purchased through big box retailers, but Emmalee needs something special because she is very special to everyone she meets. Her smiles are precious, her hugs melt your heart, and she doesn't have a mean bone in her body. She loves animals, smart device apps, and being outside.

Thank you so much from the bottom of hearts in helping us be able to provide this little girl something extra special in her life.

God bless you and keep you,

The Campbell Family

Donations 

  • Aleah Dechant
    • $30 
    • 9 yrs
  • Ladies Missionary Society Weston Church of Christ
    • $60 (Offline)
    • 9 yrs
  • Anonymous
    • $200 (Offline)
    • 9 yrs

Organizer

Tracee Campbell
Organizer
Orlando, FL

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