@xaaliburidallahhu:

Xaaliburidallah Huseen
Xaaliburidallah Huseen
Open In TikTok:
Region: ET
Tuesday 18 November 2025 16:03:07 GMT
232123
44212
2541
37223

Music

Download

Comments

nasirko01
Nasir :
Ustaaz jaalatamaa keenyaa umurii keessaan rabbiin nuuf haa dheeressuu rabbiin
2025-11-18 22:48:23
51
user7988882904713
Naneee kab :
sheka janajo sumana arage salata ke wajina salami
2025-11-22 07:54:32
2
ahme69527
Ahmad :
ustaaz dura sirriitti addaabaafadhaa. yoo mana barumsaatti barattoonni shaashii uffatanii hindhufne jedhame dhiisuun dirqama. seera mana barumsaa kabajuun dirqama ta,a. waan hundumaafuu tasgabbii barbaachisa. miira keessaa baya.
2025-11-18 17:15:03
26
milkeessoo
Allah is one :
dhugaa keessan ustaaz wly
2026-05-26 01:48:56
1
nasrii131
nasrii oro :
dhugaa rabii baayee tokko isin jaaladha rabiin isin haajaalatu🤲🤲🤲🤲🤲🤲🤲🤲
2026-04-01 03:16:47
1
kalidmustefa345
k_l_i_d_o_m_u_s_x :
jiradha woga 1000
2026-04-29 12:05:01
1
nimonaa.arsii5
Nimonaa Arsii :
inshaalaa
2026-02-12 20:54:56
1
abdulkarimislamic
Abdul karim Islamic☪️🇨🇦🇨🇦 :
mee naamn ustaaz jalaatan
2025-11-19 10:52:54
11
user3827611996173
bashir xahiro :
wolyii dhugaa issnii wojii jiraa
2025-11-18 20:52:47
6
abduljelil448
@abduljaiilibrahim :
mashaa alaah mashaa alaah mashaa alaah mashaa alaah
2026-01-20 07:13:01
1
ustaazwallagga13
Ustaaz Wallaggaa :
maasha allaaha ustaaz Barri sun kuteera amantii keenya niwaregamna
2025-11-18 16:38:39
6
user6363620014959
aslan :
ammalle irra deeb'aa dhagayaa jedhanii ustaza kenna jaalatamaa
2025-11-19 13:01:24
6
ekramjamal661gmail.com
JAMAL :
mashaalaha
2025-11-18 16:39:43
5
ogetoedeo
Ogeto Edeo :
Leenca keenya kan RABBIIN nuuf gumaache baayyee sijaalanna
2025-11-18 21:22:23
8
abdulaziz.gurro
LīJ̌ wāłłø cīřŕō :
@50
2026-01-21 09:21:43
1
hamdusalman
hamdusalman :
birhaanu naggaan ergamaa faannooti jibba muslima akka qabu ni bekkamaa,mirga kenya kara nagaanis ta'e karaa biraatin gaafannaa islamumman lubbu keenya
2025-11-18 16:38:03
10
saalih_umar
Salih صالح :
itti himaa akkanatti xaalibuu🙏
2025-11-19 01:49:32
6
saadiqookingman
nimoonaa oro :
maasha allah ustaaz keenya
2026-01-17 17:47:45
1
kaliildammaa
kaliildammaa :
lnshallah Islamummaa kenaaf ni woregamna
2026-01-13 23:35:42
1
user8540748247394
yaallah :
maasha alla dhugadha
2026-01-24 22:07:06
1
sabirinaam
Hallalu Doogo Islammumate :
yaaa rajaala keenya nuuf jabaadhaa rabbi umrii isin haa kaayu
2026-01-14 07:09:08
1
abdisultan17
✅️ABDIl90🇸🇦 :
dhugaa jettaan ustazi keenyaa
2026-01-25 16:42:58
1
oromo.may.king0588216809
Hamza mahammed H/gudata :
ustaza kena isin bira jira nujabadha lubu ken fida isilamuma hayatuu🥰🥰
2025-11-22 19:59:34
1
abdiljalil
success :
ustaazii umriin keessan nuuf haa turuu 🥰🥰🥰🥰🥰
2025-11-27 05:12:15
1
r619117
Rehima sultan :
mashaallah itti nuuf hima ustaz kenyaa🥰🥰
2025-11-27 18:13:13
1
To see more videos from user @xaaliburidallahhu, please go to the Tikwm homepage.

Other Videos

If you have an invisible illness, then you probably have an album full of pictures like this… Pictures you take for your doctor so you can document what your body looks like with the rashes, the sores, the hair-loss, and the fevers. I have an entire album on my phone filled with pictures like these. After a 6 year journey of symptoms and searching for answers, I was finally diagnosed with lupus. And these photos are a small glimpse into what living with it can actually look like. Butterfly rashes… Hair loss… Rashes that appear without warning and anytime i’m in the sun too long… Mouth ulcers that make it hard to eat or talk… Fevers and body aches… A level of fatigue that sleep doesn’t fix… Weight loss putting me under 100lbs…  And then there’s everything you can’t see. Lupus is called an invisible disease for a reason. I can look completely fine on the outside while my body is fighting something I can’t always explain. That’s why I’m sharing these pictures now. Because someone else might be looking at their own pictures and wondering if anyone understands. If you’re still searching for answers, don’t lose hope. My journey to a diagnosis took 6 years. Sometimes it takes time, but you know your body better than anyone. I’ve been working with LupusOrg to volunteer, and use our platform to bring more awareness to lupus and autoimmune diseases. And this year, I’m taking that a step further by leading the Walk to End Lupus Now. 💜🦋 I’ll be walking in: 📍 DALLAS September 26 at 9:00 AM Klyde Warren Park 📍 NEW YORK CITY October 3 Check-in: 8:30 AM Seaport Square, 89 South Street If you’re in Dallas or NYC, I would love to see you there. Come walk with me, bring your family or friends, wear purple, and help me make an invisible disease a little more visible. 💜 For everyone living with lupus. For everyone still searching for answers. For everyone who has an album on their phone full of pictures they never thought they’d have to take. I see you. 🦋💜 #kayandtayofficial #couples #relationships
If you have an invisible illness, then you probably have an album full of pictures like this… Pictures you take for your doctor so you can document what your body looks like with the rashes, the sores, the hair-loss, and the fevers. I have an entire album on my phone filled with pictures like these. After a 6 year journey of symptoms and searching for answers, I was finally diagnosed with lupus. And these photos are a small glimpse into what living with it can actually look like. Butterfly rashes… Hair loss… Rashes that appear without warning and anytime i’m in the sun too long… Mouth ulcers that make it hard to eat or talk… Fevers and body aches… A level of fatigue that sleep doesn’t fix… Weight loss putting me under 100lbs… And then there’s everything you can’t see. Lupus is called an invisible disease for a reason. I can look completely fine on the outside while my body is fighting something I can’t always explain. That’s why I’m sharing these pictures now. Because someone else might be looking at their own pictures and wondering if anyone understands. If you’re still searching for answers, don’t lose hope. My journey to a diagnosis took 6 years. Sometimes it takes time, but you know your body better than anyone. I’ve been working with LupusOrg to volunteer, and use our platform to bring more awareness to lupus and autoimmune diseases. And this year, I’m taking that a step further by leading the Walk to End Lupus Now. 💜🦋 I’ll be walking in: 📍 DALLAS September 26 at 9:00 AM Klyde Warren Park 📍 NEW YORK CITY October 3 Check-in: 8:30 AM Seaport Square, 89 South Street If you’re in Dallas or NYC, I would love to see you there. Come walk with me, bring your family or friends, wear purple, and help me make an invisible disease a little more visible. 💜 For everyone living with lupus. For everyone still searching for answers. For everyone who has an album on their phone full of pictures they never thought they’d have to take. I see you. 🦋💜 #kayandtayofficial #couples #relationships

About