
Help baby Liam fight lifelong medical issues!
Liam is a 6-month-old twin fighting cystic fibrosis. His fund covers his daily care, a safe home setup, and the medical travel his mom can't manage alone.


Jace lives with profound disabilities and has just been diagnosed with a Chiari malformation. His mum Mara is raising funds for the therapies and treatments that keep changing his life.
Mara Givenrod for JaceContributes toward a therapy intensive on Jace's treatment plan, including the travel and accommodation his care away from home requires.
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Newest update: Jace has been diagnosed with a Chiari malformation in his brain and we are awaiting a neurosurgery consult. The wait lists in Ontario are extremely long, plus the symptoms he's been having, so I have decided to pursue an opinion from at least one other children's hospital with a Chiari expert sooner, but there is a fee required.
Hi everyone! I wanted to start a fresh campaign for 2026 so everyone can clearly see what the plans are for this year and how the funds will be used.
If you're new here / just finding our story — my name is Mara and I am raising funds for the ongoing treatments and therapies that have changed my child with profound disabilities' life.

If you feel led to donate to help us continue to see what can only be described as miracles, thank you so much.
2026 treatment/therapy breakdown: OT/PT intensive — completed; turbinate reduction, tonsil and adenoid removal — completed; travel and place to stay for MUSE cell treatment; Melillo method intensive; low level laser for home.
(This will continue to be updated as we know more. This also does not include January 2026 as this fundraiser was started in February.)
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