Posts

Showing posts from February, 2025

🌞 Learning to Live with Lupus & the Sun ☀️

  🌞 Learning to Live with Lupus & the Sun ☀️ When I first got sick, just 15 minutes in the mid-day sun would leave me with a fever and a lupus flare-up for days. I’ll never forget the day I was told I was basically allergic to the sun . This was one of the hardest adjustments for me. Like…how does that even make sense?! The very thing that gives life, warmth, and energy—my body was rejecting it. It felt unfair and confusing, and then it quickly turned terrifying… I’ll never forget the day I was out helping my husband stain the fence. I was in the hot sun for maybe 10 minutes , then tried to hold a post steady for him, and suddenly, my body shut down. I immediately became extremely weak and thought I might pass out. Debilitating fatigue , fever, and joint pain hit me like a truck. I was bedbound for 4-5 days after that… That moment changed everything. I used to LOVE the sun —always at the lake, out on the boat, soaking it all in.I avoided direct sunlight, convince...

It’s Time to Heal: Choosing Healing Over Survival

Image
It’s Time to Heal: Choosing Healing Over Survival For so long, I thought I just had to deal with it—the joint pain, the fatigue, the endless flare-ups that controlled my life. I thought healing was out of my hands, that my body was simply working against me. But what I didn’t realize was that my body wasn’t attacking me for no reason… it was crying out for my help. So, I made a choice. To stop just surviving and start truly healing. ✨ I stopped ignoring the symptoms and started listening to what my body needs. ✨ I stopped fueling inflammation and started nourishing my cells. ✨ I stopped living in fear of my diagnosis and started believing in my ability to heal. ✨ I stopped waiting for change and started making small, intentional shifts every single day. And slowly… things changed. My pain lessened. My energy returned. My mind became clearer. My body felt alive again. Healing isn’t a one-time event. It’s not a magic pill or a quick fix. It’s a daily commitment to giving your body what...

The Power of Food as Medicine

How Over-Nourishing My Body Helped Me Heal I used to think food was just food—something to fill my stomach and keep me going. But when lupus took over my body, I realized that everything I ate was either fueling my healing or feeding my inflammation. At my worst, I was barely eating enough— skipping meals, running on whatever was convenient, and unknowingly starving my body of what it truly needed. I was in survival mode— exhausted, inflamed, and breaking down. The joint pain was unbearable, my energy was nonexistent, my hair was falling out, I had fevers left and right, and flare-ups felt like they controlled my life. Something had to change. That’s when I shifted my focus from just eating to truly nourishing my body. Instead of restricting, I started flooding my system with nutrients —greens, fresh fruits, anti-inflammatory foods, and healing herbs. I stopped just surviving and started thriving. 🥬 I prioritized whole, plant-based foods —fueling my cells with what they needed to ...

Diagnosis ~ Healing

The Road to Diagnosis: When My Body Began to Fail Me I didn’t wake up one day knowing I had lupus. It crept in, slowly, quietly—until it consumed me. At first, it was just exhaustion, the kind that sleep never seemed to fix. Then came the joint pain, stiffness so intense that simple movements felt impossible. My body ached in ways I couldn’t explain.My hair started falling out in clumps. My face swelled. My skin burned in the sun like it had turned against me. And then, the worst days came—the ones where my husband had to carry me out of bed because my body refused to move. My legs felt like they no longer belonged to me. The pain was unbearable, but the fear was worse. Doctor after doctor, test after test, and still… no answers. I started to wonder if I was imagining it. If it was all in my head. But deep down, I knew— something was wrong. And then, I heard the words: "You have lupus." I finally had a name for my pain, but I also had a choice—accept this as my fore...