5.9K views · 366 reactions | Eliza, who is 3 next week, has a rare...
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5.9K views · 366 reactions | Eliza, who is 3 next week, has a rare...
6K views5 days ago
FacebookThe Pride of Britain Awards
Figures and data in Stxbp1/Munc18-1 haploinsufficiency impairs inhibition and mediates key neurological features of STXBP1 encephalopathy
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Feb 19, 2020
elifesciences.org
What is the STXBP1 syndrome?
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What is the STXBP1 syndrome?
6.5K viewsDec 4, 2018
YouTubeAlbert R
Will she ever walk? ❤️‍🩹 Mila has a rare neurological disorder called STXBP1, which affects how her brain communicates with her body. Walking doesn’t come naturally to her — every step has to be taught through therapy, repetition, and patience. There are no guarantees. But there is effort. And there is hope. A new year means new hope, new goals, and new chances to grow. Thank you for being part of Mila’s journey — for the love, encouragement, and kindness you show her every day. Let’s see what
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Will she ever walk? ❤️‍🩹 Mila has a rare neurological disorder called S…
101.2K views1 month ago
FacebookMila Johnson
If you’ve never heard of STXBP1… this is your sign to learn 🧬 STXBP1 is a rare genetic neurological disorder that affects how the brain communicates with the body. It often impacts movement, development, and can cause seizures. For kids like Mila, nothing comes automatically. Every movement takes effort. Every milestone takes time, repetition, and a lot of therapy. But STXBP1 doesn’t define who she is. She feels joy. She recognizes love. She tries every single day. This is about awareness. This
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If you’ve never heard of STXBP1… this is your sign to learn 🧬 STXBP1 …
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FacebookMila Johnson
¿Qué es el síndrome STXBP1?
2:35
¿Qué es el síndrome STXBP1?
1.6K viewsNov 6, 2018
YouTubealbert regatero garcia
Mila lives with a rare gene mutation called STXBP1, but her story is about strength, joy, and love—not a diagnosis. If you’ve been here from the beginning or just found us… what’s something you love about Mila? 🤍 #reels #shorts #viral | Mila Johnson
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Mila lives with a rare gene mutation called STXBP1, but her story is ab…
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FacebookMila Johnson
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STXBP1 Summit 2021: Welcome & Clinical Update
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VimeoSTXBP1 Foundation
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stxbp1disorders.org
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STXBP1 European Summit 2023: Session I: Part 1
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VimeoSTXBP1 Foundation
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What It’s Like Living With STXBP1 🙏🏻#viral #shorts #reels #youtube #…
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This is our story - STXBP1
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22K views · 5K reactions | Walking with STXBP1 looks different. It tak…
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Watch this! She Melts Like a Candle! 🥹 #youtube #reels #shorts #therapy …
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Elle (2018)
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YouTubeFilmakademie Baden-Württemberg
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