About Our Organization
AMPS Awareness Association
The first organization that is dedicated to improving the lives of kids with AMPS. We aim to raise awareness, improve livelihoods, and grow the AMPS community!
- Meet people with shared experiences
- Learn about AMPS
- Raise awareness to foster quicker diagnoses
- Find the silver lining of your condition
Hospitals with an AMPS Program
Rheumatology Patients diagnosed with AMPS
AMPS Patients Recover
Meet the Founder
Eleanor
Hi! I’m Eleanor, the founder of the AMPS Awareness Association. I was diagnosed with AMPS in 2020 after years of intense headaches and earaches. Living with such a rare condition was isolating, and finding support was a challenge. I started this organization to change that. My goal is to create a supportive community where kids and teens with AMPS can connect, share, and find hope. Together, we can face the challenges of AMPS with strength and resilience.
Helping each other can make the world better
Join us in supporting and furthering the AMPS Community. Explore the forum, resources, and the donations tab! Let us here your thoughts!
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