Welcome!

Hi everyone! 

My name is Eleanor, and I am the founder of AMPS Awareness Association. I was diagnosed with AMPS in 2020 and have lived with 24/7 headaches and earaches since 2019. I know how isolating the condition can be, but it is important to see the silver lining in the diagnosis. You live with pain that people without AMPS can't even imagine, and you are doing a great job! We can persevere! We can conquer all obstacles! That's our superpower. We have faced hard times, but we got through them! We not only survived, but we are and will continue to thrive. 

That's what AMPS Awareness Association is for. It is our community. We can support each other through the hard times, and the happy times. We can educate, we can collaborate, and we can raise awareness. 

Welcome to the community!

Eleanor