How It Feels to Have SCD

Last updated: June 2021

One of the most difficult stages of my life was accepting life as a sickle cell patient. You can imagine how society will treat you. My eyes are yellow and I don't go out because of that. I am always in the house. This is my experience having SCD.

Can you relate? Leave a comment below.

By providing your email address, you are agreeing to our privacy policy.

 

More on this topic

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The Sickle-Cell.com team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

Join the conversation

Please read our rules before commenting.

Community Poll

Have you taken our In America Survey yet?