@miimarix3: поздравления еще принимаются ) ахахахаха 😈

MIMARIX
MIMARIX
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Region: CZ
Tuesday 03 June 2025 21:41:26 GMT
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favvmarix0
Kinder.so🍫 :
а ведь сейчас ей 17
2026-07-20 06:29:12
4
elmopiooo
𐙚ʍᴀɯуᴧя ᴧᴇᴩиᴋ давидик𐙚 :
красотка 💓💓❣️
2025-06-03 21:50:34
2
name342071
)) :
МАШУНЬ С ПРОШЕДШИМ!!💋
2025-06-12 20:24:55
2
lesyaleis
vik_rrs1 :
с днём рождения💗💗💗
2025-06-03 21:45:41
1
elmopiooo
𐙚ʍᴀɯуᴧя ᴧᴇᴩиᴋ давидик𐙚 :
с днём рождения🥺
2025-06-03 21:50:51
1
elmopiooo
𐙚ʍᴀɯуᴧя ᴧᴇᴩиᴋ давидик𐙚 :
Машечка прости что вчера не было видео просто не было времени, сегодня видео будут а завтра наверное нет прости💋💋💋💓💓💓❣️❣️❤️❤️💗
2025-06-05 09:43:27
0
xqvryw
eva :
🥰
2025-07-03 11:33:03
0
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Thank you so much for all of the love and support we’ve received since I shared the video about Esmae’s journey and her SMA diagnosis. ✨ We are so incredibly grateful for every donation towards her equipment and physiotherapy, as well as all of the lovely comments, messages, shares and encouragement. There really are kind people in this world, and I hope you know just how much you’re helping Esmae. 🫶🏽  A few people have let me know that the GoFundMe link isn’t working on TikTok. Unfortunately, TikTok still isn’t allowing me to add a clickable link to my profile at the moment. If you’d like to support Esmae, please go to the GoFundMe website and search “Esmae’s SMA Journey” and it should come straight up. 🤍 Thank you all so much for your support - it honestly means the world to us. ✨ A huge thank you to @EDP24 for reaching out and wanting to share Esmae’s story in the paper. Not only does this help spread awareness of SMA, but it also gives more people the chance to hear about Esmae’s journey. 🗞️ It’s also amazing news that SMA is now being added to newborn screening across the UK. It brings so much hope knowing that future babies born with SMA can be diagnosed and start treatment from birth, before symptoms appear and before the condition has the chance to progress. No child or parent should have to experience the uncertainty, fear and heartbreak that so many current SMA families have faced. Knowing that future families will have the opportunity for early diagnosis and treatment from day one is truly life-changing, and that in itself feels like a miracle. 🤍 It’s a bittersweet moment. 🥹 #sma #spinalmuscularatrophy #gofundme #edp24 #ourstory
Thank you so much for all of the love and support we’ve received since I shared the video about Esmae’s journey and her SMA diagnosis. ✨ We are so incredibly grateful for every donation towards her equipment and physiotherapy, as well as all of the lovely comments, messages, shares and encouragement. There really are kind people in this world, and I hope you know just how much you’re helping Esmae. 🫶🏽 A few people have let me know that the GoFundMe link isn’t working on TikTok. Unfortunately, TikTok still isn’t allowing me to add a clickable link to my profile at the moment. If you’d like to support Esmae, please go to the GoFundMe website and search “Esmae’s SMA Journey” and it should come straight up. 🤍 Thank you all so much for your support - it honestly means the world to us. ✨ A huge thank you to @EDP24 for reaching out and wanting to share Esmae’s story in the paper. Not only does this help spread awareness of SMA, but it also gives more people the chance to hear about Esmae’s journey. 🗞️ It’s also amazing news that SMA is now being added to newborn screening across the UK. It brings so much hope knowing that future babies born with SMA can be diagnosed and start treatment from birth, before symptoms appear and before the condition has the chance to progress. No child or parent should have to experience the uncertainty, fear and heartbreak that so many current SMA families have faced. Knowing that future families will have the opportunity for early diagnosis and treatment from day one is truly life-changing, and that in itself feels like a miracle. 🤍 It’s a bittersweet moment. 🥹 #sma #spinalmuscularatrophy #gofundme #edp24 #ourstory

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