pain and get some new cells and feel better. So it’s really like a constant process. It’s not like something that they just sit back and have to deal with and don’t do anything about it. There’s a constant proactive fight…those are the three big takeaways from it.
You mentioned the constant transfusions that sickle cell warriors have to go through. I know you’re a blood donor yourself. Can you speak to the importance of blood donors, especially Black donors, when it comes to the sickle cell community?
I think there are simply not enough Black donors out there. We need more and it’s clear that it will directly benefit warriors. I’m sure [there are] dozens of ways that this can benefit people, but specifically all these sickle cell warriors who are out there. For patients with sickle cell disease, blood donors who are Black are almost three times more likely to be a match for the blood that’s needed and that was another eye-opener for me. We are in a better position to directly help sickle cell patients being Black. That statistic alone is huge – there’s a great chance that if you give blood, you’re gonna be able to help some of these warriors be able to live a more peaceful life and pain-free life. That’s something that – when I posted about it and put it out there to my followers and everything – that was one of the main points that I wanted to drive home is that you can directly benefit somebody today. Also, it’s so simple to sign up for [a] blood donation.
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Going back to the piece you put together for this project, can you walk me through your thought process when you were putting it together?
So the piece that I called ‘Transfusion’ there’s a couple of parts to it:
- One, I wanted people to see the struggle that a warrior goes through but also the hope and health that a transfusion can bring. I wanted to directly visualize what sickle cell disease is showing the kind of disfigured sickle-shaped cells on the left side and…the healthy cells on the right.
- Then, really giving people a way to easily understand it by just hand signs like with the C&O crossing their arms to be able to say this is literally what sickle cell is and this is the process of transfusion and this is how you can help in that process. So you see the young woman, who is a warrior, who is putting up that sign of transfusion telling people what she’s going through, but also kind of an invitation to help alleviate some of that pain that she deals with on a day-to-day basis.
That was really the whole intent of the piece and I’m just so honored that I could be able to be a part of this. I was really happy to see the reception of the piece and how people received it.
You’ve done a great job of sharing what a sickle cell warrior has to go through and creating awareness. Is there anything else you want people to know about sickle cell warriors?
Going back to the struggles that they have – part of the things that we were talking about on the call with the warriors was how many day-to-day things that a lot of us take for granted. While they’re waiting for their next transfusion, they’re dealing with life. So it’s like dealing with bosses and teachers, and even family members who may not even believe them when they say that they’re not feeling well. I feel like they have to have this extra level of patience and calmness to be able to even get to that next transfusion because there’s one young boy who when he’s dealing with this extreme pain and not able to go to class or finish his homework or whatever, he deals with teachers who literally don’t comprehend what he’s saying or maybe don’t believe him when he explains how painful it is. It’s very easy for his grades to suffer and that can be very discouraging for young students. And just all the warriors – they all receive that kind of question of ‘Well you don’t look sick, what’s wrong? Is there something really wrong?’ It’s the worst pain that you’ve ever felt in your life, so just a reminder… there’s something that we can all do to try to help them in their process of trying to get transfusions and trying to live healthier lives and get rid of this disease.
What’s next for you on your artivism journey?
Next for me and my artivism journey [is] my new picture book, which is called “The Artivist” on September 5th. I’m very excited because it’s about what I just did with the American Red Cross. It speaks on tackling global health, war, racism, inequality – all these things – and tries to show how artivism can really inspire people to make a positive change in the world related to all of these broken bones (things that aren’t working right in the world). That’s what artivism is about and it’s a picture book so it really speaks to the young creatives, but really it’s for all ages – anybody who was created. I think everybody is creative. How we can use our creativity to speak to these broken bones and try to make the world a better place? So very excited for that and excited for everybody to become an artivist in some way and call out these issues and try to bring us all together.
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If you are interested in donating blood, make an appointment now by using the Red Cross Blood Donor App, visiting RedCrossBlood.org/OurBlood or calling 1-800-RED CROSS (1-800-733-2767).