I love this quote, because as my fellow Sickle Cell Warriors know: we don’t have a choice but to get back up and continue the fight. Hey Readers, hope you all love this quote as much as I do. Be encouraged!
Hey Readers! I’ve been sick a lot lately, so I haven’t been able to blog the way I would like. Not to worry though, I’m back on my writing now, so I’ll be updating you guys a lot. This blog is basically going to be me venting, so bare with me. Well, as you all know by now, I have Sickle Cell Disease; and it’s very true that in a lot of ways I’m not able to do what other people can. I get that – hate it – but I get it. The problem I have with this is when everybody treats me like I’m going to literally break if I try to do ANYTHING! I understand that I have to pace myself when doing things, but dang!… that doesn’t mean my life should come to a complete halt and sit around doing nothing day-in and day-out. I don’t think people really understand how demeaning that is. Don’t get me wrong, I know that when someone does this to me, it’s done out of love; but I’m a grown woman, it feels terrible to always be looked at as less than. I’m mostly seen as this sickly person that needs to be looked after, it just sucks… I try not to let stuff like this get to me – because once again – I know it’s not done in a malicious way; but I’m only human, so of course it does get to me at times. I mean really, how old do I have to get before people start seeing me as an adult?? Logically I know that my age isn’t the problem, it’s the sad but very real fact that I have a disease that is killing people daily. So, I guess all I can do is understand the reason I am treated the way I’m treated, but also continue to try getting them to understand my point of view. Writing these blogs also help, it’s my way of venting and getting things like this off my chest. I’m not mad though, more frustrated than anything. I love my family to death though, so I can’t hold this against them, when I know they’re just trying to protect me the best way they know how. Alright Readers, I’m going to keep this blog short. Later guys!
Hey Readers! I just uploaded another video for you all on my YouTube page. Check it out and let me know what you think. Don’t forget to subscribe, like, and comment!! This video wasn’t all that long; I just wanted to let y’all know what’s going on with me while it’s happening, not months later. Let’s get Sickle Cell Disease awareness out there people!