This is my 3rd year attempt to do this Health Activist Writer's Month Challenge and see it all the way through the month of November. Third time is a charm, right? I have a lists of prompts, I can do this. I will do this.
Each day, WEGO Health, an awesome empowerment network of over 100,000 health activists, posts a prompt and health activists around the world reflect, write and post their experiences with their health in response to these posts. If you've read this far, I thank you. You'll be reading a lot about HIV for the next 28 days. Let's start, shall we?
My quote is actually from myself...Yeah, conceited much? I'll explain...
"Knowledge may be the power, but the application of knowledge is the cure." - Kamaria Laffrey
February 2007 was my first time ever publicly sharing my story. I was at Hurst Chapel AME Church and it was their
National Black HIV/AIDS Awareness Day Town Hall.
The local paper came to my house to interview me, people were telling me how brave I was and how inspiring I was. This continued happening, to my delight because I felt like I was spreading awareness to get people tested and not fall into the same blissful ignorance I lived in when it came to HIV prevention. All was well until after a couple of years, I ended my speech and during Q&A, a woman stood to tell me that I was an inspiration and needed to get my story out to more "young people" because "knowledge is power."
Well...
True, but why limit knowledge to just young people when HIV knows no age, gender, race, religion, career, etc., and if I'm such an inspiration, which in the correct context of personal application is a verb; what exactly have I inspired one to do? Get tested? Gather these young people that need more knowledge to fuel their power? I was conflicted by this popular quote by
Francis Bacon and the context in which it was used towards me.
I responded to her with this analogy (and I'm paraphrasing because I've said this in many settings in various ways, but this is the gist):
"Knowledge may be the power, but if I KNOW that I am supposed to wear a seat belt in spite of my safe driving because there are other drivers on the road, yet I don't 'wear the seat belt...where is my power? If I KNOW that condoms and having an undetectable viral load eliminate my risk of transmitting HIV to someone else but I don't do either...where is my power? We KNOW a lot of things in our lives, but if we don't APPLY what we know, we perish - physically, emotionally, socially, spiritually, mentally, etc. The application of knowledge is the power, simply knowing is never enough. Plus, we must share what we know with others and not hoard it to ourselves, (therefore, why I speak about my personal experience of contracting HIV to anyone who will listen)."
I got a soft applause and a few nods of agreement after I said that, but no one has engaged me in dialogue that I am wrong (not that I'm trying to be right, but I am trying to prove a point) and I feel strongly about this concept that I have engraved it in the very fiber of being an HIV advocate. I apply this to more than just HIV work.
I can't just complain about change, I have to BE the change.
I can't just say I am gifted or blessed, I have to walk worthy in that by sharing my talents with others and using them to fulfill my purpose in this world.
I can't just look at a cupcake and not lick the icing off the top, I have to devour it's buttercream exquisiteness...
Ok, that last one took a weird sugar deprived turn, but you get the point. I hope.
So,there you have it. What's your favorite quote? Or what's a cliche or saying that drives you crazy because people use it out of context? I have a whole list of HIV stigma based ones...but we can talk about that another day.
Thanks for reading - please comment and share...I want to hear from you!
xoxo
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