@justembaswrld: honestly, it hurt my heart to read this. one because it felt like a personal attack, like my story, my life was as disposable and unimportant as a dirty paper towel. in fact, causing more harm, than it could ever good. and two because how sad for someone to feel they have the privilege to single handedly discredit a huge number of individuals based on an opinion, publicly, and proud to publish it. you don’t ask to be sick. but if you are so brutally handed the title, it takes years to accept after dreaming of it your whole life. it takes years to learn how to be proud, to learn to navigate, to learn to exist with it. and yes poppy, sharing these things create awareness. levels we’ve never been exposed to before, but how incredible. because now people can solve their problems, people can feel seen and heard and understood. it’s not an identity, or a token we collect. it’s our lives you are talking about. #fyp #recovery #chronicillness #livertransplant #foryou

emma
emma
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Region: US
Thursday 10 September 2026 04:18:08 GMT
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rileycumminss
riley cummins :
where’s poppy i just wanna chat
2026-09-10 04:51:29
55
livinggforthehopeofitall
elle ☮︎︎ :
the disgustinggg implication that disabled people sharing their lives like everyone else does dubs them a “sickfluencer” is simply saying disabled people shouldn’t be seen by the public. it’s 2026 poppy♿️
2026-09-10 05:37:27
46
bookwoem6
bookwoem :
As a chronically sick mama to a chronically sick teenager I am so incredibly comforted to see content creators who are chronically sick; it makes us feel not so alone.
2026-09-11 01:10:55
9
chloemarikag
IT’S CLO XO ◡̈ :
Literally been debating speaking on this. Thank you for giving me the bravery
2026-09-12 10:50:20
4
mollayyyyee
molls :
poppy has made a few new enemies
2026-09-10 14:46:11
1
katynestvibes
Katy | SAHM :
I had Hodgkin’s lymphoma and I was so scared I would never have a normal life again. I didn’t let that define me any longer. Now I’m a mother to my beautiful baby boy and so blessed to be in remission for almost 3 years!
2026-09-10 15:05:50
21
markmessingham
Mark :
This is just part of a bigger picture. Here in the UK, it started with politicians and the press discrediting autism and ADHD and now they are making it more widespread, attacking other disabled people too. They are literally causing hatred towards anyone who isn't what they consider as normally functioning.
2026-09-10 05:27:16
2
days2721
Days :
I am currently struggling with auto immune Hepatitis and everything that comes with it and have been for 8 years , also dealt with breast cancer and never have I let my diagnosis define who I am. I am a mom of 3 and still work full time. Some people just don’t understand
2026-09-10 20:04:20
1
sydniestrycula
sydniestrycula :
You’re the coolest girl I know
2026-09-10 14:22:46
2
bellawalsertv
bellawalsertv :
!!!! And you can say that again
2026-09-10 11:36:44
2
caitmendy
CAIT MENDY :
Who wakes up and wants to be sick the rest of their life?? “Economic inactivity”???? OMG I am mad
2026-09-10 17:45:21
4
emma_bur00
˚₊‧꒰ა emma catherine ໒꒱ ‧₊˚ :
you are so strong 🩷
2026-09-10 04:21:40
4
ashmarie619
ash :
you are quite literally spreading awareness and educating people on such a serious thing too? so i don't understand why people think that way about chronically ill people.
2026-09-10 05:52:12
3
silly.lily.foundation
Silly Lily Foundation :
Reposted so fast
2026-09-10 20:23:29
1
kathrynbusbyyy
kathryn :
Clock it
2026-09-10 16:38:48
1
llamaluvrr
Kate :
I know that’s right
2026-09-10 05:06:33
1
mollayyyyee
molls :
i love you & i love seeing how much stronger than you’re diagnosis you are
2026-09-10 14:46:01
2
chloemarikag
IT’S CLO XO ◡̈ :
This. This. This. 👏🏼
2026-09-12 10:49:40
1
livinggforthehopeofitall
elle ☮︎︎ :
talk about it 🗣️🗣️🗣️
2026-09-10 05:33:05
1
kennedy827318774_
𝓚𝓮𝓷𝓷𝓮𝓭𝔂𝔂🎃🥥 :
My mom had the same diagnosis as you for 4 years and she passed on new years I hope you get better
2026-09-10 22:52:20
1
amandabennett814
amanda b 🌪 :
PROUD of you, thank you for sharing your story, you’ve helped me get through mine. 💕
2026-09-10 05:40:22
1
mistercharmer
Mr.Charmer :
will always be a fan of yours. one of the toughest human beings alive
2026-09-11 03:24:11
0
brutus.beefcake48
Brutus Beefcake :
Well said, Queen! 💖💖
2026-09-11 16:22:55
0
kwest150
Kwest1 :
Emma, your comments are so much appreciated. I struggle with certain people who like to laugh and comment about what I call my “liver belly”. I had end-stage cirrhosis and received a transplant a few years ago. Even with that my belly still sticks out. I still have the autoimmune disease, PBC, that caused the cirrhosis. It’s like waiting for the other shoe to drop. I’m proud I made it through the transplant so well, especially with the judgements from others. I’m so happy you are here to educate the public. You do a great service for us and Im always so happy when I see you and how well you’ve recovered. I know it’s an ongoing battle for us.
2026-09-13 01:18:39
0
abeachbum
A Beach Bum 😎🏝️🤙🏼 :
The hardest part is getting people to understand that we may WANT to but sometimes we just CAN’T. It gets me down because I feel like I’m missing out while others think I’m just dipping out. 😎🏝️🤙🏼
2026-09-30 13:05:21
0
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