@inforakyart: CAYALAH MAKCIK! BERKOBAR-KOBAR SEMANGAT MEMPERTAHANKAN KEPIMPINAN PAKATAN HARAPAN YAB PMX #prnnegerisembilan #pakatanharapan #anwaribrahim #kekalharapan #PH

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Region: MY

Monday 20 July 2026 12:08:39 GMT

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Comments

Founder Kek Pisang :

JOM RAMAI² KITA BIRU KAN NEGERI SEMBILAN 🥰🥰🥰🥰🥰🥰

2026-07-20 17:09:08

520

HAFIEDZ :

Bersama Tolak Dap dan Pakatan Harapan Di Negeri Sembilan

2026-07-20 16:12:05

716

zuqey :

bijak makcik ,tahu bersyukur berbanding ramai di luar sana 👍👍👍

2026-07-20 12:21:35

846

NORSILA KHALID :

Ramai rakyat N9 memang cerdik pandai. Bersyukurlah kita ada PMX DSAI

2026-07-20 13:32:38

467

sham :

PMX TERBAIK kerja kuat tanpa ambil gaji PM pun... Allahuakbar

2026-07-20 13:37:03

275

Afi Rex🇲🇾🇵🇸 :

Setelah menilai kenyataan mak cik sy sedar tetap tolak ph

2026-07-20 19:07:44

199

atok mas :

TERBAIK LH.... WALAU DAH BER UMUR.. BERFIKIRAN JAUH

2026-07-20 14:11:19

173

Anna Ties :

zaman Najib kami tak dapat bantuan apa apa tapi sekarang hampir semua bantuan kami dapat terima kasih PMX Anwar Ibrahim memang terbaik God bless you always 🙏

2026-07-22 02:14:57

32

maya masian :

Pmx tetap trbaik 👍👍 sokong PMx

2026-07-20 23:36:28

45

dalinamohdraus :

UMNO BN TETAP DI HATI SELAMANYA.

2026-07-21 03:05:20

42

RedJade1128 :

undi bn atau pn...bia oghang nk kato tk sodar diri...kito pakat ghamai2 tolak ph

2026-07-21 02:07:03

82

ramesh ram :

betul2 hormat mak cik. terima kasih pmx terbaik 🥰🥰

2026-07-20 13:21:50

93

Pak Ndak :

saya sokong ckp makcik...bijak nilai pmx... terbaik

2026-07-20 12:59:25

21

karimismail183 :

terbaik mk cik ni

2026-07-20 12:17:03

78

Tokman :

terbaik mak cik

2026-07-20 12:36:15

31

kanimozhi :

org N9 bijak👍

2026-07-20 14:10:07

20

tokmat@ :

terbaik akak fikiran kehadapan

2026-07-20 13:50:42

6

Fikri Mohd :

terbaiklah makcik👍👍👍

2026-07-20 12:18:00

36

mantini LP_3 :

Terima Kasih Makcik...Jelas,Padu Dan Menyakinkan KAMI Rakyat Malaysia.✍️🤲🤝

2026-07-20 13:55:06

20

بوبو :

terbaik

2026-07-20 12:33:37

22

Kartel Kentang :

Xpo lah cik. Ikut acik la. Kami tetap nk tuka gomen. Gomen skg ni byk buat hutang. Ape pon x nmpk.

2026-07-20 17:27:06

29

Jihie :

Terbaik lah makcik.

2026-07-20 13:56:25

14

chemasriahabubaka5 :

puan seorang yang bijak👍

2026-07-20 13:46:59

32

joe jambol :

aku dh menilai tetap nk tukar kerajaan

2026-07-20 16:28:30

229

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

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This video is raw, unedited (besides cutting), and deeply personal. (sorry about my fan) It is Disability Pride Month, and I want to bring awareness to myalgic encephalomyelitis. ME has completely changed my life. I used to be a 20 year old who worked an office job, would go out with friends, and be able to walk, and dance, and be a functional member of society. In 2018, that all changed. Despite this illness impairing my brain, I remember the first sign that something wasn't wrong so clearly. I had just attended a Pride festival, and the day after, my hips were so achy in a way that they had never been before. I didn't think much of it at the time as I had spent the night before dancing alot, so I ignored it. When physical activity continued to make my body ache, I decided to go to my doctor. They ran blood tests, and found I had a vitamin D deficiency, and an underacting thyroid. They perscribed me meds, and told me to see if they helped. Problem solved. Except it didn't fix the issue. So when I went back to tell them I was still experiencing my symptoms, they sent me to Rheumatology, and it was a downward spiral from there. I have been going back and forth, bounced between departments on and off for these past 8 years. A cocophany of

This video is raw, unedited (besides cutting), and deeply personal. (sorry about my fan) It is Disability Pride Month, and I want to bring awareness to myalgic encephalomyelitis. ME has completely changed my life. I used to be a 20 year old who worked an office job, would go out with friends, and be able to walk, and dance, and be a functional member of society. In 2018, that all changed. Despite this illness impairing my brain, I remember the first sign that something wasn't wrong so clearly. I had just attended a Pride festival, and the day after, my hips were so achy in a way that they had never been before. I didn't think much of it at the time as I had spent the night before dancing alot, so I ignored it. When physical activity continued to make my body ache, I decided to go to my doctor. They ran blood tests, and found I had a vitamin D deficiency, and an underacting thyroid. They perscribed me meds, and told me to see if they helped. Problem solved. Except it didn't fix the issue. So when I went back to tell them I was still experiencing my symptoms, they sent me to Rheumatology, and it was a downward spiral from there. I have been going back and forth, bounced between departments on and off for these past 8 years. A cocophany of "normal" test results, mri scan results, coping therapy, acupunture, the works. And in this time, I wasn't getting any better. The day that I first used a walking stick felt simultaneously like a blessing, and my greatest defeat. I should be able to walk normally, but I needed an aid to help with my pain. The grief kept coming from there. 8 years on, and I am effectively bed bound most of the time. I don't go outside, I can't work, and I live to survive. There are small moments of solace where I can do things I enjoy, or spend time with those I care for, but everything I do has to be calculated so I don't hurt myself. This illness is devastating, and we have to advocate for ourselves because even most doctors have so little information about this condition. It is one of the last things they tend to diagnose you with because of how life altering it is. To those of us who do have it though, having a name is everything. So please remember the name of this illness: Myalgic Encephalomyelitis. Research it, listen to those of us who are telling you how bad it is. We need your support, and understanding, and love. We deserve to live <3 #fyp #disability #disabilityawareness #myalgicencephalomyelitis #chronicillnessawareness #cfs #cfsme #vtuber

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