Susan Phillips, 21 years old
People who sickle cell disease and dating sickle cell disease have abnormal hemoglobin, called hemoglobin S or sickle hemoglobin, in their red blood cells. Hemoglobin is a protein in red blood cells that carries oxygen throughout the body. When a person has two hemoglobin S genes hemoglobin SSthe disease is called sickle cell anemia. This is the most common and often most severe type of sickle cell disease. Hemoglobin SD and hemoglobin SE are much less common.
But in Nigeria, the first date conversation is more likely to be about your DNA than if you watch 'Grey's Anatomy' or where you like to vacation. Chat with us in Facebook Messenger. Find out what's happening in the world as it sickle cell disease and dating. More Videos Graphic by Abdulwahab Oshomah Abubakar
Do you share the fact that you have SCD with your new partner? If so, how and when do you do it? In this post, inspired by a recent question on Twitter, we'll give you a few rules to follow that can help make dating with SCD a bit smoother.
Sickle cell disease and dating
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To respond to this question, you have to remember that people with sickle cell are people first. We are not abnormal creatures, we are people, just like you. We have emotions, feelings, dreams, hopes and desires. We want to be in a a good relationship with someone sickle cell disease and dating loves us and treats us well. This applies to every human, and just because we have sickle cell does not exclude one from this paradigm. I will acknowledge that dating and being in a relationship with someone that has a complex medical condition can be challenging, but it is DOABLE.
SCD is a group of inherited red blood cell disorders. Healthy red blood cells are sickle cell disease and dating, and they move through small blood vessels to carry oxygen to all parts of the body. The sickle cells die early, which causes a constant shortage of red blood cells. Also, when they travel through small blood vessels, they get stuck and clog the blood flow. This can cause pain and other serious problems such infection, acute chest syndrome and stroke. This is commonly called sickle cell anemia and is usually the most severe form of the disease. Hemoglobin is a protein that allows red blood cells to carry oxygen to all parts of the body. This is usually a milder form of SCD. Did you know SCD affects people from many parts of the world? The severity of these rarer types of SCD varies.
Visit the HCP website. Your stories are leading the Generation S movement. Together, we're raising awareness and showing the world what living with sickle cell disease SCD is really like. Generation S is encouraging those who live with sickle cell disease to share their experiences.