Top Ten Reason Why Sickle Cell Sucks Balls

As I am laying here waiting for my drugs to kick in I can’t help but to think about just how much I hate having Sickle Cell Anemia. I know, I should be grateful that it’s not something worse. I should be thankful that I have a full head of hair and not have cancer that would cause it to all fall out due to treatment. And yes, I am thankful I don’t have any STD, because the thought of carrying that kind of luggage and not being able to have sex, well. . . I would just recommend to everyone to start buying stock in the sex toy industry because I would blow their sells through the roof.

Yes, I am thankful that things are not worse, but that doesn’t stop me from getting pissed off at what I do have to face. So, here are my top ten reasons why Sickle Cell Disease sucks balls:

10. Because stupid people keep calling it a ‘black’ disease when it affects people of ALL colors and races. (Diseases don’t racial profile, only people do!)

9. Because doctors always assume I’m a drug addict because of how much I know about pain killers. I only know about them because I need them to survive!

8. Because a Sickle Cell crisis always happens at the worst time- like two days before graduation or the night before my wedding.

7. Because once you say the word ‘disease’, even the cute guy’s flunky ugly friend doesn’t want to date you.

6. Because no body likes the ‘sick kid’ on their team.

5. Because even though Sickle Cell is one of the oldest diseases known to men it is also the most ignored. No Awareness + No Funding= No Cure

4. Because I will never be able to  see Paris due to the fact that my body can’t handle the flight without going into a crisis.

3. Because IV’s and blood transfusion bags never look good on anyone.

2. Because I hate the look of frustration and anger on my Boy Toy’s face because he knows there is nothing he can do to take my pain away.

1. Because I can’t knit when I’m in this much pain!!!!

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8 thoughts on “Top Ten Reason Why Sickle Cell Sucks Balls

  1. Hi,
    It’s so easy for people to say “hang tough” but unless you have been there no knows what you go through. Don’t have sickle cell but do have conditions that bring chronic pain on a daily basis. You re right – the flair comes at the worst possible time. I hope that you can find some relief. My thoughts and prayers are with you.
    Pat aka westies

  2. I have sickle cell also and yes it does sucks. I hate having sicke cell and is currently, as I type, lying in a hospital bed now and have been in the hospital for 10 days and in pain for 10 days. It is 3 days away until 2014 and my 6yo baby girl still have not opened her presents from Christmas. I hate having sickle cell, the doctors think your just an addict, you have to miss days of work, which means limited funds, which means you have to worry about are you still gonna have a job when you get it the hospital and how you’re gonna pay bills if you don’t have enough pto hours.

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