@callie.meese: 🫠🫠🫠 #chronicillness #invisibledisability #dynamicdisability #chronicillnessawareness #chronicallyill

callie
callie
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Thursday 03 September 2026 20:05:40 GMT
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jillkottmeier
Jill Kottmeier :
Chronic illness does not get you casseroles.
2026-09-03 21:41:08
795
lidlidlihehe
💜 :
People do more for pregnant women than for chronically ill people. We didn’t chose this
2026-09-04 09:08:54
172
simplysammyk
Samantha Dell :
My own family stopped inviting me to things. No one asks me how I’m doing. Not even my friends. It’s so isolating.
2026-09-03 22:42:14
441
827hannah
Hannah 💕⚾️ :
I dealt with this not long ago. People started dropping like flies not understanding that in a flare I can’t do things. It’s so isolating.
2026-09-07 12:43:18
0
user6166718606115
user6166718606115 :
It's the worst when it's your own family too
2026-09-03 22:38:39
91
itsme.tonyp
ItsMe.TonyP :
TV and social media makes it look like the community will rally around you. Everyone gets together and donates time and materials to help you fix this, modify that to your needs, raise funds, blah blah blah. The truth? You never hear from anyone ever again.
2026-09-03 21:26:11
210
briellej
BrielleJ :
my mom has lupus and she still shames me for "not feeling well". like WHAT?!
2026-09-06 15:29:17
1
dannytheedancedoula
dannytheedancedoula :
Mind you casserole would be perfect and so helpful during a flare up
2026-09-04 13:06:03
122
chasinghappiness.ca
Crystal Steers :
Chronic illness gets you judged and a lot of “you were fine last time I saw you”
2026-09-07 16:50:10
0
lovesherfurbabies2
Jackie1999 :
So true sadly
2026-09-07 06:35:59
0
3bigmisssteak
glizzy🌭mcguire :
friends and family asking when i’m getting better. i’m not. that’s why it’s called chronic 🙄
2026-09-04 12:08:27
16
evanescents8
Opossum :
I’ve had so much surgery because of my EDS, I’m talking every couple of months, and no one cares anymore. No one checks in or spends time with me during recovery. I don’t even get like, a good luck text. It makes me so sad. It feels like everyone’s annoyed like “how annoying he’s having another surgery” even my mom acts incredibly inconvenienced to have to help take care of me during every recovery.
2026-09-06 17:07:07
0
eclipsed_by_eds
Amy :
“How is it always something?” Mhmm yep, bye Felicia 👋
2026-09-03 21:17:59
12
ameliaspeakshermind
AmeliaTalks :
Yup. I’m grown to accept my disease and how it impacts me. Anytime I struggle with this acceptance, it’s because someone else is struggling with it.
2026-09-04 18:23:08
30
amalie_magnusson
Amalie :
Mind you, they only see us on our BEST of days. They don't see us stuck in bed the other 80% of the time.
2026-09-05 11:34:49
9
thatkaleygering
Kaley :
I just stay home and I don’t make new friends. It’s so much easier.
2026-09-04 00:35:23
15
jay_ekeh
jay_ekeh :
They run, like RUN! And they try not to talk about it but thank God for the friends I have
2026-09-07 23:29:29
0
anniesmacandpees
annie :
I’ve never had less support in my life than when I haven’t gotten better in three years
2026-09-03 22:31:48
99
leotiehayes98
Lilly🪶🖤 :
My sister got diagnosed with epilepsy around 2019-2020, and I make it my life mission to make damn sure that my baby sister never feels like a burden, or like she can’t tell me what’s wrong. She will always have me to depend on.
2026-09-03 23:06:28
40
viannasausages11
viannasausages11 :
People like it when there’s hope to get better. Everyone always gets so rude when I say there is no cure, I’m going to be sick for the rest of my life
2026-09-04 20:05:16
7
leahmxrie2
leah :
So true like people will ask you how you are, but don’t really want to know especially if you’re struggling as it’s chronic
2026-09-03 20:11:35
50
krixnn
Krixnn🫧 :
I keep getting told I’m young and to shake it all off and just do my best. Even by my doctors, how disheartening it is to be young and chronically ill. Then you have people say “oh you’re just lazy”. It actually hurts to hear so much, if only those people could see how I can’t live my life normally anymore.
2026-09-04 22:34:58
9
shebeauty40
shebeauty :
My cousin told me she went quiet on me because she feels bad about me not getting better and she doesn't know what to do with me...
2026-09-04 16:26:16
5
ritualroses
Erin :
My perspective is that illnesses like fibro, chronic fatigue , pots , lyme, etc … they expose doctors lack of knowledge. The medical industry doesn’t like negative publicityso they don’t give us the same concern or public attention other illnesses get. This creates a vacuum around our healthcare and support systems.
2026-09-04 00:46:03
39
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