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@prince_rafi_520: #foryou #foryoupage #videoviral

R A F I ⚡️
R A F I ⚡️
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Sunday 19 July 2026 11:27:34 GMT
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Comments

orx_demon_
𝐃𝐄𝐌𝐎𝐍🕸️ :
right 😮‍💨🤌
2026-07-22 12:26:03
0
_robin_688
Ro Bin🧃 :
bhai doraichi 🙏
2026-07-19 14:18:50
37
tiktok.6302
B2K ✓1 :
টিক টকে সবাই নেতা ☹️😕
2026-07-21 15:08:11
25
.sr.roman8
S..🚩🌿 :
2026-07-20 10:29:27
11
mohammadmiraz693
🌹🍁_MIRAZ+Sonia 🫶🥺 :
আমার বন্ধু হবেন
2026-07-20 16:42:19
4
sg_bijoy_2
😺 লাল বিলাই 🕊️ :
@💥 S h a h a d 💥:যে মেসির জন্য ফুটবলকে ভালোবাসা শুরু করলাম সে মেসি আজ ফুটবল বিদায় জানালো-/😅💔, তাই আমিও তোমাদের বিদায় জানিয়ে দিলাম, যদি মেসি ফিরে আসে তাহলে আমিও ফিরে আসবো...🙂🫶
2026-07-21 12:30:18
2
mdnazmul3214
ƝᎯz҉ɱµℓ Ꭰꫝɴɢᴇʀ メ :
2026-07-20 07:39:12
2
habibsumaa5
ব্যর্থ প্রেমিক 😅😅🚭 :
কিশোরগঞ্জের পোলাপান আমরা🤟🤟
2026-07-20 16:31:27
2
bikeloverboy03
❤️‍🩹💯❤️‍🔥ＭARUF💯🚩🇦🇷😅 :
😎😎
2026-07-21 11:59:43
0
muhammad.mizan356
Muhammad Mizan :
hom ✌️✌️✌️
2026-07-22 13:24:53
0
mahadihassam..........99
Mahadi 99 :
হুম নেতা হয়ে গেছে😁😁😁
2026-07-22 14:00:11
0
samir.chy555
Samir🚬$ :
tikkk
2026-07-22 13:50:28
0
kosto.jibon06
🆁🅴🅳🅾🆈 ꔪＯＰ ᭄ ☯࿐ :
[Sticker]
2026-07-22 14:26:03
0
To see more videos from user @prince_rafi_520, 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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iu nhao khi còn tay trắng 😚#xuhuong
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