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This website is about Sickle Cell Disease, or as I love to call it “Black People Disease”. I want to educate people out there about SCD, and since we are in this technology era, what best way to do it?

I am not a big fan of social media, but I am not doing this for me, this cause is bigger than me, so it’s time we start this conversation because if we, as sicklers, do not start this long overdue conversation , no one will do it for us, and I believe that when you want something done right, you have to do it yourself…

So here we go, let’s get into it!!! Enjoy the ride!!!

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