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There was a time in my life when I was still on my feet. Still moving. Still pushing through each day with a stubborn kind of determination that only makes sense in hindsight. Back then, I didn’t have my FND diagnosis. I didn’t even have answers — just a body that wasn’t behaving, a mind that felt disconnected, and symptoms that came and went like uninvited storms. I kept telling myself, “Push through it… you’re fine… you’re just tired… keep going.” And I did. Because when you don’t have a name for what’s happening, you blame yourself instead. You think you’re being dramatic. You think it’s stress. You think you’re weak. But I wasn’t weak. I was unwell — and I didn’t know it yet. Looking back, I can see all the little signs. The collapsing legs, the shaking hands, the dizziness, the exhaustion that felt like gravity had doubled overnight. But back then, I just kept going… because life doesn’t pause for symptoms you can’t explain. I was on my feet — but barely. Holding everything together with grit, stubbornness, and a whole lot of “just get through today.” When the FND diagnosis finally came, it didn’t break me. It gave me clarity. It gave me language. It gave me permission to stop blaming myself. But I’ll never forget that version of me — the one who walked miles on legs that were already failing, who hid symptoms behind a smile, and who fought battles she didn’t even have the words for yet. She survived long enough for me to understand what was happening. And for that, I honour her. 🎥 Thanks for watching. If this story resonates, don’t forget to LIKE, COMMENT, and SUBSCRIBE — and hit that bell so you don’t miss the next one. 📌 Hashtags: #FND #FunctionalNeurologicalDisorder #LifeBeforeDiagnosis #InvisibleIllness #SurvivorStory #MyStory #AustralianCreator #PetinaSpeaks #MyVillageOfPeople #GlamReimagined #ChronicIllnessAwareness #YouAreNotAlone