@hannas.health.journey: A day in my life with Multiple Sclerosis #multiplesclerosis #chronicillness #autoimmunedisease #neurologicaldisorder #mswarrior

hannas.health.journey
hannas.health.journey
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Region: US
Tuesday 09 September 2025 01:11:05 GMT
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chronicallyemm4
Emma | MS diaries :
sometimes i think i’ll never be a mom cause how could i when i have bad days, but then i watch ms creators like u that are moms and still managing on ur flare days and it gives me hope
2025-09-09 01:56:13
82
jenniferparlegreco88
Jennifer Parlegreco :
This is exactly how I walk too in the morning. MS takes over everything from us 🙄🧡
2025-09-09 04:44:47
37
brocknroll19
Erin :
May I ask what type of MS you have? I’m newly diagnosed and everything online is so scary
2025-09-10 23:22:21
9
alewithms
AlewithMS 👩🏻‍🦼‍➡️ :
Thank you for being so vulnerable 🥺🧡 some need to physically see that MS is not easy for us and this truly showed! 🫂
2025-09-09 02:26:11
10
lokifan07
George Washington :
hey, that is how I walk sometimes. 😂 I see a neuro in a couple of weeks.
2025-11-18 02:11:30
0
tina306354
Tina :
I feel like I have it also. is mri necessary to diagnose?
2025-09-16 10:00:36
1
charlotte_rae96
The Charlotte Rae :
How do you manage to film when you're struggling? I think it's so valuable to show the reality of living with chronic illness but I can't organise myself on good days let alone bad! Much love you are awesome xx
2025-09-14 18:23:11
3
jep8989
Caffeinecookie :
Do you get muscle twitches (fasciculations?)
2025-09-09 19:11:29
3
nackhole
nicole :
it's been a big ginger ale week for me too😅 stay strong, we got this mama🧡
2025-09-10 01:45:07
2
txzoo__
Tazoo 🍉 :
Please use a cane indoors to keep you safe 😩
2025-09-09 16:06:29
2
adamryan_esports
Adam Ryan :
You’re doing amazing thanks for spreading awareness and being so open🧡
2025-09-09 10:26:57
3
iamjonny1
Iamjonny :
It’s hard but we’ll get through this. God bless 🙏
2025-09-09 03:57:13
1
tinysavage4ft7
Tiny Savage4FT7 :
I give you props cause of my MS I had to stop homeschooling:( but they’re my ride or die they keep me alive
2025-09-09 11:49:20
2
dj_linchi
It’s me DJ. Linchi :
My kiddos do online too. Ms warrior isn’t crazy how as soon as we wake up we know the limitations we have. I hate the shaking hands and numbness on hands and feet.
2025-09-09 07:22:47
1
nunziata10404
nunziata10404 :
same kind of day 🥺🥺🥺❤️❤️❤️I'm so sorry ❤️❤️❤️
2025-09-09 01:19:28
2
rachel_b1222
Rachel🦇 :
Were your lesions found after you already started having symptoms? Kinda wondering about MS but my brain MRI from last year was clean
2025-09-10 22:29:26
0
dalaimama_peace
Rebecca ⭕️ 💜 :
gentle hugs for you 💕
2025-09-09 01:29:18
1
deeohgeetherescue
Deeohgee the rescue ❌ :
Yea I understand and can emphasize.
2025-10-13 06:24:20
1
jeriberry93
Jeriberry93 🍓🧸🫧 :
You are soooooo strong❤️
2025-09-09 10:50:32
2
jaymofisher
🧡jamie fisher🧡 :
100% i was diagnosed 10 weeks ago
2025-09-09 11:07:06
2
lexi.sage2
Lexi 🩷 :
I was diagnosed at 25. I am turning 30 next month. I'm a mom of 3 and currently working in bed because I'm just too exhausted to get up. thank you for being vulnerable and bringing awareness to our condition 🧡🧡
2025-09-09 17:20:32
2
kurkisandra
sandra kurki | IG @kurkisandra :
Oh my gosh I have never seen some other MS-fighter walk just like I do on my bad days😩😭❤️greetings from Finland❤
2025-09-10 18:38:12
1
denij619
denij :
22 years here I know exactly how you feel🙏
2025-09-09 20:56:56
1
salted.cherries
𝒮𝒽𝒶𝓎 :
And here I was thinking I was unique with my ginger ale lol.
2026-08-15 03:07:21
0
lucieking73
Lucie King :
This has been my weekend :( x
2025-09-09 12:14:08
0
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