This committee has spent two months planning, designing, and organizing efforts for this as well as a billboard, tv appearance, and school efforts to raise awareness about this wonderful community.
COMING SOON: RARE DISEASE DAY
Never a lull for us!
Team members gathered for a few hours last night to prep & wrap packages for over 95 patients to help them remember and celebrate how special being RARE really is!
COMING SOON: RARE DISEASE DAY
Team members gathered for a few hours last night to prep & wrap packages for over 95 patients to help them remember and celebrate how special being RARE really is!
#raredisease #RareDiseaseDay #nord #theavalonfoundation #kc4k #painbox

ALT COMING SOON: RARE DISEASE DAY Never a lull for us! Team members gathered for a few hours last night to prep & wrap packages for over 95 patients to help them remember and celebrate how special being RARE really is! This committee has spent two months planning, designing, and organizing efforts for this as well as a billboard, tv appearance, and school efforts to raise awareness about this wonderful community. #raredisease #RareDiseaseDay #nord #theavalonfoundation #kc4k #painbox #kc4k #YouthLeadershipDevelopment #youthleadership
On #RareDiseaseDay we will be raising awareness for the rare community. Check out rarediseases.org/rare-diseas… on February 28 to join the celebration. Learn how you can #ShowYourStripes
HONORING OUR SENIORS 2023
Kelsey Gruber, Katy Gruber, & Avalon Ayres
Original #KC4K Advisory Board members & founder are honored at their last annual event for their leadership, compassion, commitment, & contribution over the last six years.
#youthleadership #theavalonfoundation
The Avalon Foundation retweeted
Besides easing the painful journey of treatment, @kc4ktaf also seeks to empower kids and guide them to become passionate leaders.
nbc24.com/whats-going-on/rec…
We’ve just earned our 2023 Silver Seal with @CandidDotOrg! We are excited to share the work our nonprofit does through our #NonprofitProfile. Learn how you can support us and make a difference.
guidestar.org/profile/82-124…
Winter 2022 Digital Issue nonprofitquarterly.org/winte… via @npquarterly
The Avalon Foundation retweeted
Congress has some important unfinished business to complete before the end of the year for its constituents with #RareDiseases. NORD President and CEO Peter Saltonstall explains what's at stake in this new commentary in @TheWellNews bit.ly/3hrS3p1
The Avalon Foundation retweeted
Congratulations to @kc4ktaf for your #RareImpact Award! 🌟
Before you tap “Buy Now” on Amazon, consider using Amazon Smile and listing The Avalon Foundation of Toledo as your charity of choice. A portion of your purchase goes directly to us! Every cent adds up, allowing us to take on more patient families:
smile.amazon.com/ch/82-12401…
It's that time of year again: Best of Toledo 2021 Nominations! Please consider nominating The Avalon Foundation for best Charity/Nonprofit. Happy nominating and thank you for your support! ow.ly/by0O50GdlNf
We are growing -- big time -- which means we now have new positions open on our adult board (The Avalon Foundation or TAF) and our youth board (Kids Caring for Kids or KC4K). Contact us via the website or to learn more: kidscaringforkids.org/how-to…
You can now sponsor a rare family’s #PainBox program for $700 (all tax deductible)! Your donation will make a direct and meaningful impact in the life of a rare family.
kidscaringforkids.org/make-a…
We have some exciting events coming up, and we could really use some volunteer committee members to help with event planning. Contact us if you are interested via our website: kidscaringforkids.org/how-to…
We continue to see an increase in patient requests for our #PainBox program! This means we are seeking youth Shopping Mentors to help create and fill each unique #PainBox, catered to our patients and their families. Could this be you?
kidscaringforkids.org/how-to…
Our very own #KC4K volunteer Becca Tittl created this for us: a QR code! If you feel moved to donate to The Avalon Foundation, where kids help kids with rare diseases, please use this handy QR code.












