@felicia.berg02: Hahhahahah @Elin0404

Felicia.bergg

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Region: SE

Tuesday 15 September 2026 11:53:24 GMT

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Meja Karlsson :

AHAHAAHAHAH HELT UTAN ATT TÄNKA

2026-09-15 19:03:08

1031

bamb1baee :

O dem sa att shakespeare var död

2026-09-16 17:00:21

307

noni :

bästa reflexen!!

2026-09-15 21:16:55

218

𝓁ℴ𝓀𝒶 𝒽𝒶̈𝓁𝓁𝑔𝓇ℯ𝓃 :

2026-09-15 15:18:21

231

Soso :

Poesi

2026-09-15 20:16:30

89

Elin0404 :

Hahahah orkar inte😂

2026-09-15 11:54:54

63

Bibbi :

Freudian slip 😭

2026-09-17 18:32:39

25

🪽 :

Hahahahaha helt rätt

2026-09-15 18:54:03

28

Alexandra.Akbari :

Love her

2026-09-16 18:08:53

19

Lenita.stromstedt_ :

HAHHAA

2026-09-15 14:28:06

45

HonDenDär 🤍 :

JA FKN DÖR

2026-09-17 08:59:57

6

🐞🐾 :

Wait fattar inte ..

2026-09-17 16:54:43

3

? :

Varför fattar jag ej..

2026-09-21 22:53:36

1

Lalaa🐈‍⬛ :

2026-09-15 19:58:46

13

sassa :

HAHAHAHAH

2026-09-15 12:17:28

12

Sara Omvri :

Hahahahahahhaa

2026-09-15 18:31:00

2

𝓢𝓮𝓵𝓶𝓪♛ :

HAHAHAHAHAHAHAH

2026-09-15 22:01:57

1

Melinda :

2026-09-16 13:13:14

1

Milo :

HAHAHGAG

2026-09-15 20:20:33

1

Kajbalaj :

2026-09-15 19:25:01

1

SLEJ 🗯️ :

HAHAH

2026-09-15 18:32:40

1

veraA :

gag

2026-09-25 12:27:26

0

hilma✮ :

2026-09-22 15:40:16

0

Marre🌺 :

2026-09-16 07:15:47

1

user88babyy :

Hahahah Queen lowkey

2026-09-20 12:10:02

0

To see more videos from user @felicia.berg02, please go to the Tikwm homepage.

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I saw a comment today that honestly stopped me in my tracks. A mother was sharing the life of her daughter, a little girl with significant disabilities who relies on medical equipment. Someone decided to declare that this child has a “miserable life,” referred to her as a “meat puppet,” and accused her mother of keeping her alive and using her daughter merely for content. Let that sink in. As a mother of a child with Down syndrome, I can tell you how incredibly wrong that perspective can be. Parents of children with disabilities don't share our lives online because we think our children are content. We share because visibility matters. We share because there are people who have never spent time with someone who has a disability. People who have never seen the appointments, the therapies, the victories, the frustrations, the belly laughs, the stubbornness, the personality, the milestones that may look different but are celebrated just as fiercely sometimes even more so because the journey to achieve that milestone was much longer. We share so you can SEE the child instead of seeing a diagnosis. We share so you can learn that a child who communicates differently still has something to say. That a child who moves differently still wants to play. That a child who learns differently is still learning. That a child who needs medical equipment is still a CHILD. And yes, sometimes we share the hard stuff, too. Because disability isn't a carefully edited highlight reel. There are difficult days. There are scary moments. There are things our children have to work harder to accomplish than other children. But difficult does not automatically mean miserable. Different does not mean less. Needing medical support does not mean a life isn't worth living. And a parent choosing to share their child's journey does not mean they are exploiting their child. For many of us, we're trying to change the world our children are growing up in. We're trying to replace fear with understanding. Pity with acceptance. Ignorance with education. And stereotypes with an actual human face. My son has Down syndrome. He is not a diagnosis walking around in a little body. He's a little boy with a personality, preferences, opinions, humor, frustrations, joys and an entire life ahead of him. And I want people to know him. I want people to see him. I want people to understand that children with disabilities aren't here merely to be cared for. They are here to live, learn, love, laugh, experience, grow and participate in this world right alongside everyone else. That's why we share. Not because our children are content. Because our children deserve to be seen. #downsyndromeawareness #Declan #fypシ

I saw a comment today that honestly stopped me in my tracks. A mother was sharing the life of her daughter, a little girl with significant disabilities who relies on medical equipment. Someone decided to declare that this child has a “miserable life,” referred to her as a “meat puppet,” and accused her mother of keeping her alive and using her daughter merely for content. Let that sink in. As a mother of a child with Down syndrome, I can tell you how incredibly wrong that perspective can be. Parents of children with disabilities don't share our lives online because we think our children are content. We share because visibility matters. We share because there are people who have never spent time with someone who has a disability. People who have never seen the appointments, the therapies, the victories, the frustrations, the belly laughs, the stubbornness, the personality, the milestones that may look different but are celebrated just as fiercely sometimes even more so because the journey to achieve that milestone was much longer. We share so you can SEE the child instead of seeing a diagnosis. We share so you can learn that a child who communicates differently still has something to say. That a child who moves differently still wants to play. That a child who learns differently is still learning. That a child who needs medical equipment is still a CHILD. And yes, sometimes we share the hard stuff, too. Because disability isn't a carefully edited highlight reel. There are difficult days. There are scary moments. There are things our children have to work harder to accomplish than other children. But difficult does not automatically mean miserable. Different does not mean less. Needing medical support does not mean a life isn't worth living. And a parent choosing to share their child's journey does not mean they are exploiting their child. For many of us, we're trying to change the world our children are growing up in. We're trying to replace fear with understanding. Pity with acceptance. Ignorance with education. And stereotypes with an actual human face. My son has Down syndrome. He is not a diagnosis walking around in a little body. He's a little boy with a personality, preferences, opinions, humor, frustrations, joys and an entire life ahead of him. And I want people to know him. I want people to see him. I want people to understand that children with disabilities aren't here merely to be cared for. They are here to live, learn, love, laugh, experience, grow and participate in this world right alongside everyone else. That's why we share. Not because our children are content. Because our children deserve to be seen. #downsyndromeawareness #Declan #fypシ

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