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.
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.
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