Not Your Typical Mom

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Review: Rosanna in Autumn Sunrise 🌅 Falling in love with Rosanna by @Rene of Paris Wigs (Alexander Couture Collection) from @Tia Maria Wigs Boutique This wavy bob is the ultimate "cool girl" vibe. The soft bangs are perfectly wispy, and the beachy waves give it that effortless, ready-to-wear texture I’m obsessed with. The Autumn Sunrise color is a total dream—it's a rich, dimensional blend featuring a neutral medium-brown root that transitions into shimmering golden copper-red and light ash blonde highlights. It literally looks like a morning glow! Plus, this wig is heat-friendly, so you can switch up the style whenever you want. If you're looking for a chic, low-maintenance update, this is the one! #wigtok #syntheticwig #wigreview #lacefrontwigs #hairtransformation

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Tried @EllaOla Brands multivitamin for my son who has autism and ARFID. He drank his juice no issue and I’ve tried everything!! I’ll update on how it’s helped him after he’s been on it a few weeks!!! I am not affiliated with this brand at all. I have just been overcome with ads and I will try anything to get my kid getting some vitamins in his system. #arfidawareness #ellaola #autismawareness #autismfamily

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Dysautonomia didn’t kill me. It just quietly took my life apart piece by piece while I was expected to smile and pretend I was okay. People know how to rally around a medical condition with a clear label, a treatment plan, and a beginning, middle, and end. They struggle to understand a condition like Dysautonomia that is chronic, relentless, disruptive, poorly understood, and easy for outsiders to dismiss because you don’t “look sick.” That mismatch is brutal and unfair. There is a real grief in watching other people receive compassion, accommodations, and credibility while you get doubt, eye rolls, or psychiatric labels. Dysautonomia is especially cruel because it chips away at the ordinary things people take for granted. Going to work. Social plans. Grocery shopping. Travel. Standing in a freaking line. Even getting through a day without calculating fluids, salt, medications, and energy. It’s not one big battle. It’s thousands of tiny ones, every single day. That loss is real. And it deserves recognition. Just because something doesn’t kill you doesn’t mean it doesn’t take your life. Thankfully, I am one of the lucky ones. I found a cardiologist who took me seriously, and I have not had a hospital admission in almost a year. I am so happy that he helped me take my life back. #Dysautonomia #POTS