Hyperbaric Oxygen Therapy for Eli

Our son Eli was born in 2015 with a very rare genetic syndrome, Börjeson-Forssman-Lehman Syndrome. Since that day, we have not stopped fighting to give him the best chance at living a fulfilling life full of good health and independence.Eli has hypotonia, an intellectual impairment, global developmental delays and impaired vision. Our promise to Eli, to never give up or accept his limitations, continues to come at a great cost. So far we have been able to manage it on our own, but it has now come to a point where we need to reach out to our community, friends and family and ask for help. We have recently begun Hyperbaric Oxygen Therapy, which is proven to help children with Eli's range of conditions. But for it to be effective, Eli needs a minimum of 50 treatments at $170 per session, 3 x a week. With a total of $8,500. Along with the ongoing cost of Eli's other weekly therapies and medications this is not sustainable for us to continue on our own. Any donation will go a long way to help towards Eli's therapy and giving him a quality of life. Thank you in adavance for your support, it is truly appreciated.

Donations ()

  • Tylah Cadden 
    • $50 
    • 29 mos
  • Jane Josefsberg 
    • $500 
    • 30 mos
  • Ben Dube 
    • $340 
    • 30 mos
  • Amy Massingham 
    • $100 
    • 30 mos
  • Anonymous 
    • $11 
    • 30 mos
See all

Organizer

Elizabeth Matthews 
Organizer
Nerang, QLD
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