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Support for the loss of Graysen Wickham

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I am starting this GoFundMe for my best friend who lost her 2 year old son tonight. 


Graysen Wickham was born October 11th, 2018 with a rare chromosomal defect called RYR1 Myopathy. His future was very uncertain as this defect can cause musculoskeletal disfunction which leads to breathing, feeding, and growth problems.

Graysen spent time in the St. Clous NICU as well as Children's Hospital before he as finally able to go home to his family.

Of course though, Graysen amazedus all by meeting developmental milestones quickly, which were originally a fear that he may never accomplish. 


Shortly after birth, Graysen was put on a trach tube and feeding tube. A few short months ago, in August, the doctors removed his trach as he had made amazing progress and could breathe on his own.


The evening of November 3rd brought great sorrow to the Wickham family home as Graysen suddenly stopped breathing and resuscitation did not prevail and he was called home to Jesus.


Graysen was a lively, vibrant, typical boy who loved vacuums, Elmo, and playing with his siblings.


Offical cause is unknown at this time. Graysen leaves behind his mom (Renee), dad (Kevin), brother (Brayden), and sister (Evelyn). 


This family has had more than their fair share of hardship in 2020 and this GoFundMe is to assist with costs of funeral arrangements and living expenses as time will be needed off from work.
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Donations 

  • Dean Hendrickson
    • $100
    • 4 yrs
  • Lindsey Stach
    • $50
    • 4 yrs
  • Anonymous
    • $200
    • 4 yrs
  • Courtney Givens
    • $25
    • 4 yrs
  • Josh Atencio
    • $50
    • 4 yrs
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Organizer and beneficiary

Christine Williams
Organizer
Big Lake, MN
Kevin Wickham
Beneficiary

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