Sickle Cell Disease
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Good Bye 2019
It’s been a while I have been able to sit and write something, but the hip journey had been difficult. I finally had my surgery on December 13, 2019. I spent my 47th birth in pain and about 8 hours discharged from the hospital, Thanksgiving was a lonely dinner and Christmas was spent sleeping the Continue reading
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Forced to Fly: When Discomfort Is God’s Way of Moving You
A Move That Didn’t Feel Like Home In 2023, I made a big move to Houston, Texas—hoping for a fresh start, new opportunities, and perhaps deeper connections with family. But here’s the truth: I’ve been miserable. At first, I thought it might just be the adjustment phase. Maybe it was the heat. Maybe it was Continue reading
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Sickle Cell Anemia 101
What is Sickle Cell Anemia? Sickle cell anemia, or sickle cell disease (SCD), is a genetic disease of the red blood cells (RBCs). Normally, RBCs are shaped like discs, which gives them the flexibility to travel through even the smallest blood vessels. However, with this disease, the RBCs have an abnormal crescent shape resembling a Continue reading
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Recovery Week 8: The Waiting, the Weary, and the Word
Week 8 of shoulder surgery recovery brings frustration, faith, and slow progress. Andrea reflects on healing, the reality of pain, and strength found in Scripture. Happy Sabbath / Saturday ☀️ (This one’s short—but real.) We’re at Week 8 of recovery, and let me just say…This is taking way longer than I anticipated. My doctor warned Continue reading
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“Recovery Week 7: Ready or Not, I’m Going Back to the Classroom”
At 7 weeks post shoulder surgery, Andrea shares her latest progress, pain management with natural remedies, and returning to the classroom while preparing for another surgery. Healing continues—one day, one choice, one step at a time. Recovery Week 7: Ready or Not—Here I Come! Well, ready or not, school starts Monday…And that means:Back to the Continue reading
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“How Are You Doing? The Question We Ask, But Rarely Mean”
“How are you doing?” is a question we hear daily—but do people really care? Here’s a reflection on chronic illness, invisible struggles, and what that common question truly means for those living with lifelong conditions. How Are You Doing? It’s one of the most common greetings in the world.Right after “Hello,” we say:“How are you Continue reading
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“Fascination with the Body: My Sickle Cell Journey and Discovering Avascular Necrosis”
Living with Sickle Cell Disease has shown me how remarkable the human body is—and how faith, persistence, and the right questions uncovered years of hidden damage. Here’s my AVN timeline and what I’ve learned about pain, patience, and healing. Introduction: The Body Is a Fascinating Map Part 1: The Start of the Pain – 2016–2017 Continue reading
About Me
I LIVE LOVE LAUGH LEARN – the only way I know how to survive this life! I am a free-spirited, independent, or uninhibited person. I began this blogging journey years ago for sharing my thoughts on everyday life. Since then, so much has happened including me being in a coma because of Sickle Cell with brain damage and extreme trials in life. I am still struggling, but I feel someone can be motivated through my journey, thoughts, feelings, and life.
Phoenix: Live Love Laugh 