Jill
Region: US
Sunday 13 July 2025 17:08:02 GMT
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mikaylarusso_ :
also it’s so hard to have empathy whenever someone complains about something so small. and im like bruh i wish those were my biggest problems
2025-07-14 02:11:48
181
Heaps of Creeps :
It’s the “drink more water” or “maybe you should try a different diet” as if I haven’t tried every last think possible. I have a chronic illness I’m not dehydrated or lazy or malnourished 🤡
2025-07-14 22:29:25
52
Amanda - Colouring AUS 🇦🇺 :
Yes! And having them complain about some minor inconvenience with their health or being tired when it will last a day or two and they can just sleep it off! They truly have no idea what we carry silently every hour of every day.
2025-07-30 07:08:09
1
Bex_leigh :
THIS 🗣️🗣️🗣️
2025-07-22 19:30:17
0
❄️✨Emmy✨🌨 :
This plus like my friends are lovely and always say like “I’m sorry your dealing with that” or “oh that’s aweful” which like I appreciate the support but it makes me feel like I’m fishing for sympathy which I’m not I’m just sharing my experiences and explaining why I do things certain wyd but there’s still that anxiety voice in my head that tells me they are sick of hearing about my issues and to stop making them feel sorry for me and it’s just 🫠
2025-07-13 20:06:44
56
🌸 El 🌸 :
Not to mention trying to keep up with them whilst they are speed walking and they don't even notice 😭
2025-07-14 04:53:18
40
Tee 🤍🇨🇦 :
Still trying to grow that community for myself .. it’s exhausting & everytime I feel like I’m getting a little traction something else pops up.. start MCAS meds next week with the goal being IVIG in November.. just a never ending cycle of things always popping up & needing to be strong yet again ❤️🩹
2025-07-27 05:36:57
0
user1685379327712 :
Yes! And they want to ARGUE with you about it. Like the audacity for them to act like they know more about me than me and my doctors
2025-07-16 03:38:10
7
Tanjadella :
Being jealous about my friends everyday problems and realtionship dramas cause these are all still a life while my own body makes me feel less alive most of times. I miss those small feeling problems which I could still have control while with my illness I don't.
2025-07-18 19:28:25
2
Mapachi :
This is why I had to start isolating
2025-07-30 17:35:47
0
Juno :
REAL
2025-07-23 14:19:37
0
anna :
We get you 🩷
2025-07-19 21:57:51
0
Ashton Valenzuela :
the most relatable thing i’ve ever seen 😭
2025-07-15 17:36:43
1
juliecanete_karate :
It’s hurt when they say “I get it” because they don’t, and I’m happy they don’t, I wouldn’t want them to; but don’t say u understand if u haven’t a clue :(
2025-07-14 03:05:08
71
Hazel <🐳☂️3 :
that's so true😭
2025-07-21 09:40:11
0
Hannah :
I feel like such a bad friend anymore because I don’t want to go out and I don’t even feel like seeing people. I love all my friends dearly but its so hard to explain how I feel with a chronic illness. It takes everything just to get out bed. I hate feeling like this 😞 its so exhausting
2025-07-14 01:03:58
11
EternitysChild :
My needs for psych meds being questioned because I am young... jesus... or need to sit down more often. Wish they could live 1 week in my body and see how it is like when you stand in one place for hours or bend too much.
2025-07-19 01:39:44
0
Ally Kat 🇦🇺 :
I’m a type one diabetic. I didn’t show up for a housewarming party today… still haven’t heard from that group of friends. While I’m trying to balance the right amount of insulin so I don’t end up in hospital. I’m fucking tired
2025-07-19 10:48:27
0
B 🍒 :
I hate seeing people move their body’s all crazy .. I’m like you can really get hurt 😭😞 I have a spinal injury from a car accident so I’m like overboard on safety now. & anything anyone tells me I always find a way to think of myself and my pain and what I’m going through of course I don’t say anything, but I’m just in my mind a lot. ( like for example my sister-in-law telling me she’s gonna have to be off for two weeks when I’ve been off of work since November last year😭)
2025-07-26 23:39:48
0
Azizah 🍉 :
I couldn't remember much of my 20s because of all the traumatic events that happened to me due to my Lupus SLE hospitalisation from Seizures, Pneumonia, having almost lost my eyesight all together got to much for me that I had to isolate myself for months just so I dont have to explain to people anymore. it saddens me till this day that I was robbed of my youth and not being able to experience what I had lost. my youth, relationships, major events etc. 💔
2025-07-29 04:28:17
0
Jaylee :
It’s torture living every day like that idk how I can keep going the rest of my life like this
2025-07-13 23:04:01
7
stillsoftinside | Lisa :
Omg this 🥲❤️🩹
2025-07-21 09:15:09
0
maryanne3110🪴🦥 :
...and most of them have no awareness of what you have to go through just to meet up for an hour or so and how much you'll pay for it afterwards 😔💜
2025-07-21 10:23:05
3
✨DOMINIKA✨ :
True 100%
2025-07-21 06:11:09
0
Zoeee 🧜🏼♀️🦋🌙 :
Yeah it really is…
2025-07-18 22:10:38
0
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