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#Rarebutreal Reel by @one.raregirl - 10 years. No answers. Then came FOP-a one-in-a-million diagnosis. Rare, but real. Watch, share, and help raise awareness. Every share makes a diffe
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@one.raregirl
10 years. No answers. Then came FOP—a one-in-a-million diagnosis. Rare, but real. Watch, share, and help raise awareness. Every share makes a difference. Because every rare story matters and our voices deserve to be heard. #FOPawareness #RareButReal #rarediseases #fibrodysplasiaossificansprogressiva #advocate #awarenesscampaign #awarenessiskey
#Rarebutreal Reel by @theex_ploreworld - ### What's actually happening in the video? It's a real (but rare) atmospheric phenomenon: a rotating vortex cloud (mesocyclone-like structure) formed
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@theex_ploreworld
### What’s actually happening in the video? It’s a real (but rare) atmospheric phenomenon: a rotating vortex cloud (mesocyclone-like structure) formed by strong updrafts spinning moisture into a dramatic swirling shape. The intense, colorful glow comes from the city’s bright lights reflecting off the dense, moisture-laden cloud layers—no CGI, no aliens, no holograms. Similar events have occurred in urban areas with heavy light pollution and specific weather conditions (strong convection + low-level moisture). A previous Grok response in the thread (from late Feb/early March 2026 context) described it exactly that way: “That’s a rare rotating vortex cloud (mesocyclone-like) over Hong Kong’s skyline from late Feb 2026. Strong updrafts spun the moisture into that swirling vortex shape, while the city’s lights reflected off it to create the glowing pink/purple/green colors. Purely natural—no edits or anomalies!” ## Public reactions (from replies/quotes) The thread exploded with a classic mix of speculation: - Many called it Project Blue Beam (conspiracy theory about holographic fake skies/aliens for control). - Others said AI-generated or fake ("“t'’ fuckin AI, people, come the fuck on"”. - Some went full mystical/religious (Quran references, "“仙到元婴期渡劫” i.e., cultivation tribulation lightning in xianxia terms). - A few asked Grok directly for explanations. - Skeptics mocked believers, and vice versa—very polarized, as usual for viral weird-sky videos.
#Rarebutreal Reel by @outshinelabels - "July 26th is National Disability Independence Day, which serves as a reminder of the ongoing struggle for accessibility, inclusion, and empowerment f
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@outshinelabels
“July 26th is National Disability Independence Day, which serves as a reminder of the ongoing struggle for accessibility, inclusion, and empowerment for individuals with disabilities. As the Director of Joy @innersenseorganicbeauty, Morgan brings the internal team together during meetings, connects with salon partners and Pro Stylists, establishes exciting dialogue with customers and posts uplifting content to social — ensuring our brand values of individuality and authenticity are reflected in all that we do. Today, she shares with us best practices for washing our hair. Don’t forget to awaken your Innersense products!” — @innersenseorganicbeauty Morgan was recently the Ambassador for the 2024 National Williams Syndrome convention in Phoenix, AZ too! Make sure you watch the last clip of her throwing the 1st Pitch at the Diamondback’s game, on 7-11-24. #NationalDisabilityIndependenceDay #DisabilityMonth #inclusión #inclusion #DisabilityintheWorkplace #inclusaosocial #WilliamsSyndrome #WSAwareness #RareButReal #RareDisease
#Rarebutreal Reel by @realwomensrelief - He didn't sleep for nights. Not because of the kids. Because a piece of paper told him they weren't his. And for a moment-he believed it ⬇️ There was
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@realwomensrelief
He didn’t sleep for nights. Not because of the kids. Because a piece of paper told him they weren’t his. And for a moment—he believed it ⬇️ There was no affair. No mistake. Just a rare genetic twist most people never hear about: *chimerism*. It happens when two embryos merge early in the womb—one absorbs the other, and the surviving body carries two sets of DNA. In his case? His blood and saliva carried one genetic identity. But the DNA in his reproductive cells—was completely different. That’s why the paternity test said “zero match.” Even though he’s always been their father 😅 It almost broke him. The stress. The doubt. The feeling that his own body had betrayed him. But we got answers—and he started to rebuild. More rest. Cleaner meals. Emotional support. And NAD+ therapy—for energy, clarity, and recovery after the biggest emotional shock of our lives. We’re okay now. The kids are healthy. And the truth? It brought us closer than ever ❤️ Want to support your own recovery—whether it’s stress, burnout, or a full identity crisis? Check the link in bio. Use code *NADA51* for a discount on everything that helped us heal. #chimera #chimerism #DNAshock #ChimerismExplained #PaternityMystery #FamilyHealing #ModernGenetics #HealthAfterStress #NADplus #ParenthoodJourney #RareButReal #EmotionalRecovery #PostTraumaSupport #TruthInYourCells #usa #pregnancy #healing #health #family #momlife #newbeginnings #over40 #baby #womenshealth #chicagomom #oregonmom #newyorker #arizona #washington #losangeles
#Rarebutreal Reel by @holly.hamilton.17 (verified account) - Now being a dad is his greatest joy. ❤️ Life with CEP didn't stop him. It just made him stronger. #Porphyria #CEPAwareness #RareButReal #FamilyOverE
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@holly.hamilton.17
Now being a dad is his greatest joy. ❤️ Life with CEP didn’t stop him. It just made him stronger. #Porphyria #CEPAwareness #RareButReal #FamilyOverEverything
#Rarebutreal Reel by @friedreichsataxianews - Let us know in the comments if you've experienced this-and what happened. #FriedreichsAtaxiaNews #Bionews #RareDisease #FALife #BioNews #Neuromuscular
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@friedreichsataxianews
Let us know in the comments if you’ve experienced this—and what happened. #FriedreichsAtaxiaNews #Bionews #RareDisease #FALife #BioNews #NeuromuscularDisorder #DisabilityAwareness #ChronicIllnessCommunity #RareButReal #FANews
#Rarebutreal Reel by @simplyhumanaustralia - She was diagnosed with Stage 4 Rhabdomyosarcoma - a rare and aggressive pediatric soft tissue cancer, seen in fewer than 250 adults each year. 💔 July
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@simplyhumanaustralia
She was diagnosed with Stage 4 Rhabdomyosarcoma — a rare and aggressive pediatric soft tissue cancer, seen in fewer than 250 adults each year. 💔 July is Sarcoma Awareness Month — a reminder that rare doesn’t mean impossible. Early awareness can save lives. #SarcomaAwarenessMonth #Rhabdomyosarcoma #RareButReal #ChildhoodCancerAwareness #SarcomaStrong #FightSarcoma #SoftTissueCancer #CancerAwareness #RareCancerSupport #SarcomaWarrior video credit: tianasymone_
#Rarebutreal Reel by @headlines24h (verified account) - In Canada, a man filmed an extremely rare white moose in the forest - not AI, but a real animal affected by leucism. Leucism is a rare genetic mutati
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@headlines24h
In Canada, a man filmed an extremely rare white moose in the forest — not AI, but a real animal affected by leucism. Leucism is a rare genetic mutation that makes the animal’s fur appear pale while the eyes remain their natural color — unlike albinism. Only a few hundred white moose are believed to exist worldwide. Found in Canada, the United States, and Scandinavia, seeing one in the wild is an extraordinary and unforgettable moment. #WhiteMoose #RareWildlife #Leucism #NatureDiscovery #WildlifePhotography
#Rarebutreal Reel by @emergencyresilience (verified account) - I added a clip from the beginning of the video to the end of this Reel that demonstrates the most obvious signs of life in their pulseless patient***
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@emergencyresilience
I added a clip from the beginning of the video to the end of this Reel that demonstrates the most obvious signs of life in their pulseless patient*** A lack of awareness of CPRIC causes delays in treatment and can be potentially traumatic for both the patient and providers. I applaud this crew for taking the initiative to submit this video for publication in a resuscitation journal so that we can further our awareness and learn from their experience. We need more awareness, education, and most importantly, some protocols to guide our medics and EMT’s on what to do when they encounter this. Ignoring it and deciding it’s too infrequent to warrant formal direction will not make it go away and is not taking into consideration the moral injury this put our providers at risk of experiencing. The publication can be found in the following link with an additional link to the video located at the bottom of the first page under Appendix A: https://www.resuscitationjournal.com/action/showPdf?pii=S0300-9572%2820%2930280-X #cpric #cpr #cprinducedconsciousness #zombiecodes #rarebutreal
#Rarebutreal Reel by @littlelightbigfight_ourfamily - On #RareDiseaseDay2026, we wanted to share a little piece of our journey… a journey filled with challenges we never expected, strength we never knew w
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@littlelightbigfight_ourfamily
On #RareDiseaseDay2026, we wanted to share a little piece of our journey… a journey filled with challenges we never expected, strength we never knew we had, and a love that somehow grows deeper with every hurdle. When we look back at how far we’ve come, the hospital nights, the countless appointments, the fears we don’t always say out loud, we also see something else… ✨ the courage of a little girl who fights every single day, ✨ the resilience of a family who just keeps going, ✨ the moments of joy we’ve learnt to treasure like gold. We are so unbelievably proud of Liwsi. Proud of her bravery, her determination, her spark. Proud of the way she lights up even the hardest days. Proud of how she shows us what truly matters. And we’re proud of our family, for finding hope in the chaos, laughter in the heaviness, and love in the middle of all the unknowns. It’s challenging, every single day, but we do it with full hearts, with purpose, and with a love that carries us through everything. To every family walking a similar path… we see you, we stand with you, and today we honour your strength too. 💙💜💚 #RareDiseaseDay2026 #LittleLightBigFight #TeamLiwsi #RareButReal ProudFamily
#Rarebutreal Reel by @decodingwrlds - 🚫🔎 Things You Should NEVER Google 😨💀 Curiosity is powerful. But sometimes… it's a trap. Some searches don't just shock you - they stay in your
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@decodingwrlds
🚫🔎 Things You Should NEVER Google 😨💀 Curiosity is powerful. But sometimes… it’s a trap. Some searches don’t just shock you — they stay in your head. 🦠 Rare Medical Images: Real conditions are far more graphic than you imagine 🕳 Deep-Sea Creatures Up Close: The ocean’s abyss looks disturbingly alien 🐍 Parasitic Infections: Some organisms live inside the human body — and the photos are real 🧠 Extreme Phobias Visualized: Once you see it, your brain won’t forget it 🩸 Unfiltered Crime Scene Terms: The internet doesn’t censor reality The worst part? You can’t “unsee” what you find. The internet has no warning label. One search can ruin your night. 💬 What’s something you regret Googling? 👉 Follow @decodingwrlds as we decode the darker side of curiosity. 🎥 Video Credit: DM for credits/removal to the real owner. . . . #dontgoogle #darkinternet #curiosity #decodingwrlds #reels
#Rarebutreal Reel by @mckenziejaynedesign - Let's take a moment to talk about the unsung heroes in our homes - the siblings of children with special needs. 💛 They grow up learning a kind of lo
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@mckenziejaynedesign
Let’s take a moment to talk about the unsung heroes in our homes — the siblings of children with special needs. 💛 They grow up learning a kind of love most people don’t understand. They wait patiently while therapy runs late. They give up front seats, quiet moments, and sometimes attention — without ever asking why. They cheer for milestones that others might overlook. And they do it all with hearts full of understanding and compassion beyond their years. These are the quiet warriors. The protectors. The encouragers. The ones who remind us what unconditional love really looks like. To the siblings — we see you. You’re changing the world in your own beautiful way. 🫶 #SiblingsAreHeroes #SpecialNeedsFamily #UnconditionalLove #SiblingLove #InclusionMatters #RareButReal #DisabilityAwareness #TheHeartOfOurFamily #SpecialNeedsSiblings #WarriorSiblings #EmpathyInAction #PatienceAndLove #RealLifeHeroes #SCN2A #AutismSiblings #RareDiseaseFamily #AdvocacyStartsYoung #FamilyFirst #DifferentNotLess #NeurodiversityCelebration

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