Autoimmune Unfiltered
Region: US
Thursday 02 October 2025 02:00:47 GMT
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Rizzo :
Yup that’s what they did to me. Oh you’re a mom you’re tired. That’s all.
2025-10-02 15:47:02
28
123abc123abc123abc :
wow they never gave her mri
2025-10-04 11:23:56
14
itsmeegan11❌7️⃣ :
MS owner here for 19 years.
2025-12-18 09:03:31
2
🧡MS Queen Gee🦥🧡 :
Ouch … 🥺
2025-10-04 08:49:55
1
Onefabknitter :
she also has ehlers danlos syndrome
2025-12-28 03:56:13
1
Live Laugh Love :
wow that's sad.
2025-10-02 13:43:15
6
crokat1919 :
I know it’s hard
2025-12-10 08:53:48
1
kcolonna62 :
🧡🧡🧡
2025-11-06 21:38:47
1
Mo (auDHDer💙 MS warrior) :
🧡🧡🧡
2025-10-07 22:52:16
1
Sandy 💞 :
❤❤❤
2025-10-04 23:07:55
0
🤍💚Mel🧡 Ms 🧡Warrior🇿🇦💚🤍 :
🧡💪🎗️💪🧡
2025-10-06 10:16:47
1
🫧 Princess Peach 🫧 :
💔💔💔💔💔💔💔💔💔
2025-10-20 22:16:54
0
Jude :
😁
2026-01-11 16:45:08
0
Claire Goodwin :
I’m two months into my Kesimpta. The fatigue and pins & needles and involuntary jerks are getting me down. I just want to have the energy to play with my 3 years old son 🧡🧡🧡
2025-10-06 10:28:18
5
HowieG :
I have MS 45 years That’s 16629 Days MS is like having a really old stale box of chocolate you don’t know what you’re gonna get but you know it’s gonna suck and that is how each day goes 😎😎 I have great family and friends everybody’s understanding but not being able to walk without holding onto something for the last seven years and the total exhaustion and heat is the worst and missing out on doing things
2025-10-02 15:14:52
10
Pale Princess :
She had mild ms. Ms finds you. It was her card to get back in screen. Oh and she’s had stem cell.
2025-10-04 12:26:26
2
user3201871305576 :
The fatigue people aren’t able to understand how crippling it is. I compare it to bear hibernation. Your body takes over you have no choice but to close your 👀. I have slept for 2 days. My family waking me up to eat. Thank you for sharing 🧡
2025-10-19 15:14:29
1
Jill Mabey72 :
I was having neck pain for a long time.. but prior to this I’ve always felt blah, tingling, crazy headaches, insomnia, heat intolerence.. and many more symptoms. My dr always brushed me off. So now I have neck pain. Went to physio and it wasn’t getting better. Still is not better. That was about 16 months ago. So physio asked my dr for imaging and it was caught on the CT scan.. then mri follow up. I was diagnosed Nov 2024 with MS. You have to advocate for yourself and keep fighting. You know when something is wrong and you have to do everything you can do. Needless to say my dr was a little shocked at the results.
2025-10-22 11:34:15
2
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