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@kiahspurle: the way she thought it was the cat😭🖐🏻#fyp #Coming2America #OurHouse2021 #prank #scare #mcyt

kiah
kiah
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Region: GB
Saturday 06 March 2021 14:54:37 GMT
19430658
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Comments

__bobby.x
Bobby Duran :
I’m crying so much💀💀
2021-03-17 18:11:14
102601
ashwrldd._
swag :
U SCREAMED SO AGGRESSIVELY PLS
2021-03-08 20:20:46
61647
imyoan
Yoan :
DADÆ
2021-03-31 18:53:20
9519
jiinsrj
Dm me please 😻 :
PLEASE SHE SAID DEMON MODE-
2021-03-20 00:05:14
57271
.jkaurbasra
🤍🧸 𝐉𝐚𝐬𝐦𝐞𝐞𝐧 🧸🤍 :
"Oreo" 👹
2021-03-17 20:01:07
75021
lucyerinx
lucy <3 :
i cant even 💀
2021-03-18 20:11:48
47167
potchary
Potchary :
10 Jahre ✨Therapie✨
2021-03-07 02:11:43
31836
opttiiss
optis :
that scream dawg
2021-03-21 22:16:20
8665
tiide1
Tilde :
Dad ey
2021-03-07 15:24:38
11149
mchl.mnke
user5109758021018 :
Der schrei straight out of hell
2021-03-07 20:34:13
28799
allebasi.rosa
isabellarosa :
con che coraggio ha guardato sotto il letto.
2021-03-08 13:20:44
6876
kinkh7789j5hhjj755tck
bklligv nl :
5 jahre haft 8 jahre schaden
2021-03-10 19:49:14
5553
marvel_g1rl1
new acc: marvel_g1rl1_2 :
ich hätte mich nie getraut unter das Bett zu schauen
2021-03-11 14:34:44
4439
vampyul.x3
ᥫ᭡ :
DIE ARMEE AHAHAHAHA
2021-03-07 15:25:10
5231
ebruslifestyleecke
EbrusLifestyleEcke :
Du wärst nicht mehr meine Schwester 😅
2021-03-23 20:11:36
2803
tushkanapushke
Katya :
Я представляю как она теперь будет всю жизнь боятся под крвать смотреть
2021-03-15 14:33:23
4484
flafel_zohar
flafel_zohar :
✨DAD? DadAaY?!✨
2021-03-08 18:55:29
40720
anomarwauzi
△⃒⃘ Schnützel ⚯͛ :
Die Schwester ist kurz gestorben🪦
2021-03-11 18:35:43
3544
nisefuimaono
nisefuimaono :
SHE’S BOLD! #1 rule: never look under your bed 😂
2021-03-07 01:50:16
77049
tx1cr_
mariehelene :
It's the ✨daddaay✨ for me 😂
2021-03-15 16:34:29
39881
eu_betarice
Massu 🦆 :
DADEIH!!!!!!!
2021-03-07 03:15:08
6399
mattandomar
Matt & Omar :
the scream 😭
2021-03-07 01:17:16
7101
_khaby.lamely_
ig:Leon.z17 :
PLEASE WHEN YOU SCREAMED-
2021-03-09 18:33:50
14711
To see more videos from user @kiahspurle, please go to the Tikwm homepage.

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What we wish you knew about Ehlers Danlos Syndrome & Hypermobility Spectrum Disorder this EDS & HSD awareness month A little reminder that this series is community led. I asked people with EDS & HSD in my stories what they wished others understood about these conditions, then brought those responses together into this “What We Wish You Knew” video. 1. It’s not just being ‘bendy’ EDS and HSD are connective tissue disorders. Connective tissue is basically the glue that holds everything in your body together meaning that EDS & HSD can affect the whole body. Joints, skin, organs, digestion, cardiovascular system and more. They are multisystemic conditions. 2. It looks different for everyone Some people need mobility aids, some don’t, and both are valid. Some people are in constant pain, others experience different symptoms. There are 13 subtypes of EDS, and even within the same diagnosis, no two people are the same. 3. HSD is not ‘less than’ hEDS Hypermobility Spectrum Disorder isn’t a milder or less important version of hEDS. It can be just as painful, just as complex, and just as disabling. The label doesn’t define the impact. 4. Getting diagnosed and supported is difficult and takes a long time. On average, it can take around 10 to 12 years to get a diagnosis. Many people are dismissed, gaslit, or told nothing is wrong. Even after diagnosis, specialist support is limited, and many healthcare professionals still aren’t properly trained on the conditions. 5. It’s painful and exhausting There’s no cure, limited treatment options, and not enough research. It’s often misunderstood, downplayed, or underestimated. And trying to function in a body that feels like it’s constantly struggling to hold itself together is exhausting. What would you add to the list let me know in the comments. And what have you learnt about EDS & HSD this awareness month. Please share this video to continue to help raise awareness. #EhlersDanlosSyndrome #EDS #HSD #EDSAwarenessMonth
What we wish you knew about Ehlers Danlos Syndrome & Hypermobility Spectrum Disorder this EDS & HSD awareness month A little reminder that this series is community led. I asked people with EDS & HSD in my stories what they wished others understood about these conditions, then brought those responses together into this “What We Wish You Knew” video. 1. It’s not just being ‘bendy’ EDS and HSD are connective tissue disorders. Connective tissue is basically the glue that holds everything in your body together meaning that EDS & HSD can affect the whole body. Joints, skin, organs, digestion, cardiovascular system and more. They are multisystemic conditions. 2. It looks different for everyone Some people need mobility aids, some don’t, and both are valid. Some people are in constant pain, others experience different symptoms. There are 13 subtypes of EDS, and even within the same diagnosis, no two people are the same. 3. HSD is not ‘less than’ hEDS Hypermobility Spectrum Disorder isn’t a milder or less important version of hEDS. It can be just as painful, just as complex, and just as disabling. The label doesn’t define the impact. 4. Getting diagnosed and supported is difficult and takes a long time. On average, it can take around 10 to 12 years to get a diagnosis. Many people are dismissed, gaslit, or told nothing is wrong. Even after diagnosis, specialist support is limited, and many healthcare professionals still aren’t properly trained on the conditions. 5. It’s painful and exhausting There’s no cure, limited treatment options, and not enough research. It’s often misunderstood, downplayed, or underestimated. And trying to function in a body that feels like it’s constantly struggling to hold itself together is exhausting. What would you add to the list let me know in the comments. And what have you learnt about EDS & HSD this awareness month. Please share this video to continue to help raise awareness. #EhlersDanlosSyndrome #EDS #HSD #EDSAwarenessMonth
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