If you’ve ever been dismissed by doctors or felt like your body was screaming while no one listened, you’re not alone. This blog is about raising awareness for people living with invisible illness.

I didn’t start this blog because I had all the answers. I started it because I was desperate for them. I needed to understand what was happening to my body—and I knew I couldn’t be the only one.

For years, doctors dismissed my symptoms. I was told I was just “sensitive” or “anxious.” I kept switching providers, searching for someone who would actually listen. Eventually, I found trauma-informed doctors who understood how PTSD and chronic stress impact physical health. That changed everything.

That’s when I learned the name for it: Multiple Chemical Sensitivity (MCS), Fibromyalgia, and a nervous system in survival mode. I wasn’t imagining it. My body was screaming for help.

I’ve walked out of churches, stores, and salons mid-visit. I’ve slept on the floor because a mattress made me sick. I’ve spent hours decoding ingredient labels just to avoid a reaction.

Now, I read every label and trust my instincts—especially when doctors don’t understand.

This blog is my way of sharing what I wish someone had told me:
You’re not broken. You’re not crazy. You’re not alone. Healing is possible.

No filters. No fluff. Just honest conversations about natural healing, chemical sensitivity, and the fight to reclaim your life from invisible illness.