For example, I know in the future when I plan to have children, even know with person that I date, my status some how always comes up because I sometimes get sick and I really really get sick and I just give them a heads up on why that happens to me so badly. So they wanna know well how I got it, and if they have children with me would their kids get it and so on. I'm just very proud that I can share this information with more people and so that would understand its affects on those who have it and what it can do to those who have the trait when their immune system goes to work when they have something as small as a cold can hospitalize them as it did me numerous of times before.
I think I would have liked to expand on the treatment section of my webtext more. Because the disease affects the blood which has to be circulated throughout the body, this disease can affect the entire body and your functions. So I did mention it but I was so caught up in talking about what it is and how to prevent it in your children, I had limited information on that aspect. I did enjoy googling the information though. It was interesting to actually see some websites that showed like a picture in motion demonstrating what the sickle cells actually does when it blocks the vessels from their circulating. A lot of websites were geared towards parents and how to deal with their children that had the disease. My recommended readings and the stories of the many different people who lived with the disease was another better example of how some may deal with it. I loved the story about the little girl that had to get her leg amputated because of the disease but overcame and studied and practiced dance. That alone can show that the disease is not crippling but it motivates so to speak.
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