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I’m not sensitive, you’re an A%$hole.

I hate Facebook.  Since 2008 when I joined, I’ve always hated it—Twitter was my first “super” social site and is currently my favorite.  I say “super” social sites because we won’t count AOL Voices, Black Planet, and Myspace (may they rest in peace), but these “super” social sites have IPO’s—yes, I have stock in Twitter since it is my favorite social site.  But I didn’t come on here to talk about social site preferences, but rather the content. In the last few days, Facebook has erupted with adorable (and not so adorable) photos of Daughter/Son appreciation.  Those who are childless have had the luxury of looking at the photos shared, whereas some (like me) scroll right past all the photos only stopping at what incites us.  So, the asshole part, okay, I’m getting to it.  Let me put this out there for those who may have sensitivities to my delivery, approach, or candor. This isn't a blog to negate parenting or complain about a post, but instead, the son/dau...
Recent posts

Life with Sickle Cell: Conclusion, but it ain't over

It's a wrap, Sickle Cell Awareness Month comes to an end!    I am so proud of those who donated to Sickle Cell, reposted my blogs and joined me in the conversation of Sickle Cell—this is all part of awareness.   Please, let my experience be the conversation you have for years to come as you make others aware of Sickle Cell!    In conclusion to my Sickle Cell journey, I will wrap up with my last, horrific hospitalization.   For many of you, you read the, “Won’t he do it” blog from 2015 when I spoke on the experience of the hospitalization, but if you did not read it, here is the link to get caught up, look you get 2 blogs in 1!  https://maliseaqueen.blogspot.com/2015/12/wont-he-do-it-on-christmas-eve.html In short, in 2014 I started to have breathing issues and it all started after I participated in the Sickle Cell walk (ironically).   It felt as though a gorilla was holding an elephant and they’re sitting on my chest, and th...

Life with Sickle Cell: Sickle Support

Wow, thank you all for reading, commenting, and DONATING!   OMG, ya’ll exceed the goal of $200 in donations to the Seattle Sickle Cell Task Force.   I have the BEST followers of my blog, thank you!   If you have not donated, it's not too late you still have time, the link is on my FB page or just reach out to your local Sickle Cell Chapter.  While we appreciate the money that jingles, we appreciate the money that folds!   Also, if you cannot donate do not feel bad, please share my story or share a Sickle Cell post.  Awareness is the MOST IMPORTANT thing!   You can share this on your social media page, it's that simple!  It shouldn't be on the shoulders of people who have the disease to mobilize the message, it should be a community effort to promote awareness, education and  encourage GENETIC TESTING!  EVERYONE , PLEASE GET GENETIC TESTING EVERYONE , PLEASE GET GENETIC TESTING EVERYONE , PLEAS...