07/18/2026
Four years ago, our world changed forever with Cameron’s diagnosis of Neuroendocrine Cell Hyperplasia of Infancy (NEHI).
Two years ago, we chose to turn that diagnosis into something bigger than ourselves. We launched CamO Fund with one simple mission: to ensure no child or family facing childhood interstitial lung disease (chILD) has to walk this journey alone.
💙 Because of you…
✨ Over $17,000 has been raised to support childhood interstitial lung disease.
✨ We’ve provided Breath of Hope Bags to newly diagnosed families.
✨ We’ve expanded awareness of these incredibly rare diseases.
✨ We’ve begun building a community rooted in hope, advocacy, and support.
But we’re just getting started.
Every donation fuels research. Every volunteer strengthens our mission. Every share helps another family discover they’re not alone.
If Cameron’s story has ever touched your heart, we invite you to help us take the next step:
💙 Make a donation.
🤝 Volunteer at an event.
📣 Share our mission with your family, friends, and community.
🫁 Help us raise awareness for children living with chILD.
Together, we can create a future filled with more answers, more support, and more hope for every child diagnosed with childhood interstitial lung disease.
Thank you for believing in this mission and for being a part of Cameron’s story. We can’t wait to see what we’ll accomplish together next.
💙 Donate, get involved, or learn more at www.thecamofund.org
