Edward's Journey

About the Foundation

How It All Started

Edward F. Hardy, who was diagnosed with the disease at 6 months, has been hospitalized several times with near-death experiences. Despite his challenges caused by sickle cell, he continues to power through his everyday life as a business owner. He lives with his wife and 2 children in Cleveland, Ohio.

Edward’s journey and experiences have motivated him to help those who are going through the difficulties of the sickle cell disease – carriers, caregivers, as well as their family and friends.

Through the Edward F. Hardy Sickle Cell Foundation, he would like to continue providing assistance and resources to instil hope to the members of the sickle cell community.

The Foundation's Mission

The mission of the Edward F. Hardy Sickle Cell Foundation is to break the cycle of mistreatment toward Sickle Cell patients, raise awareness of Sickle Cell disease to the world, and deliver support to the Sickle Cell population and their caregivers, aiding in a longer life span.

The Foundation's Goals

Academic Scholarships

Summer Camps

Transportation

Podcasts

Financial Assistance

Counseling Services

Can we help you further?

If you have any questions or require assistance linked to sickle cell,
please don’t hesitate to keep in touch.

Resources

Videos

Living With Sickle Cell disease: Personal Stories

Those living with sickle cell battle it out every single day. Watch and listen to the stories of these warriors. 

Mechanism of Sickle Cell Disease

Here is a thorough overview of the sickle cell disease explained to the young ones. 

How can we help sickle cell warriors?

There are many ways to help out sickle cell patients. Here’s one way to extend that much needed help. 

Infographics

How to Stay Healthy

Edward shared his tips on how to find systems that work to keep the crises at bay. 

How to Give Support

Not everyone has a good support system. If you know someone who has sickle cell, how can you help?

Seeking Support Systems

Going through the sickle cell condition is very challenging.
No one should go through it alone.

Support Our Work

Your support in the form of information,
referrals, and resources is greatly appreciated.