@wheredidbecsgo: Invisible disease, invisible symptoms does not equal no disease #chronicillness #chronicpain #invisibleillness #stigma #suffering

wheredidbecsgo
wheredidbecsgo
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Region: CA
Tuesday 03 February 2026 20:59:43 GMT
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jananthemothercluckers
Jana & The Mothercluckers :
I don’t have the shaky voice but I am very halted which I’ve never had bfr
2026-02-03 21:49:14
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rose_nielsen1
rose_nielsen1 :
I have fibromyalgia & arthritis and my doctor still has a hard time believing how much pain I have.
2026-02-04 04:14:55
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naomification
Nome 🇬🇧 :
absolutely! I'm 34 with mild Elhers-Danlos and moderate osteoarthritis in my knee. It took me so long to get help and every Dr that sees my scans ALWAYS say "you're too young" yeah thanks I wish that was the case! I have learnt to be more understanding. followed you for a while and have massive admiration for you and your amazing spirit.
2026-02-03 21:45:58
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cornflakes121
cornflakes1$ :
I was left with pain after sit. Don’t care what anyone thinks. It’s my body.🤷‍♀️
2026-02-05 01:36:47
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love_lga
Love_LGA 🇨🇦 :
I worked in dementia care for 9 years before developing ME/CFS. The neuro inflammation I experience is similar to the cognitive struggles experienced in dementia and Alzheimer disease. It’s so frustrating and incredibly hard to get any kind of help or support. A lot of what you have described I am experiencing. 💔Thank you for advocating ❤️
2026-02-04 16:26:05
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tracey.amos1
Tracey Amos :
So very true!!! Invisible but happening in real time. Symptoms are what someone tells you not just what presents visually…thank you for your phenomenal determination in getting this out in the open and normalizing discussion & support!!! You are magnificent!!! 😁💪❤️✌️🙏
2026-02-03 21:54:26
8
lilyofthevalley95
Lily Ofthevalley957 :
Your bangs are cool today ❤️
2026-02-04 05:53:21
1
shellisart_79
shellsart🤍✨️ :
Apathy is literally the worst 😕 I hate those moments in my life when I go through seasons of Apathy because I'm a big feeler also . So I can imagine how awful that amongst all your other symptoms would be 🥺🤍
2026-02-05 13:16:17
2
gmaine66
user4322395942982 :
Exactly I have had chronic migraines since I was a child and never was heard or listened to!!! Just in the last 5 years I’ve finally been to see a neurologist about them who let me unload 55 years of frustration!! And has been trying to help me but still haven’t been able to get them under control!!! So very frustrating to say the least!
2026-02-04 20:39:44
3
kimberlyuryszvalade
KImberly Urysz-Valade :
and the doctors saying "its your anxiety"...which is so lame and a cop out i think
2026-02-04 02:57:54
8
annleboubon
🇨🇦~ Ann~ 🇨🇦 :
sitting here in tears watching this , Cause I've experienced alot that your mentioning . its scary and bery lonely as i no longer even go out , easier to just stay home 😢
2026-02-05 22:02:34
2
eringill4
Erin Gill :
Thank you for sharing. All of these symptoms are small issues individually, but you put them all together and it's a nightmare. No wonder you're so exhausted.
2026-02-07 23:09:40
1
joceline.muise.co
Joceline Muise-Comeau :
So very true. 🩷 I have MS and people don’t understand.
2026-02-04 15:31:19
1
newzealandcat
Catzyme🇳🇿🐶🐈 :
Preach
2026-04-03 03:12:33
1
kimmie5455
Kimmie :
my husband's voice got shaky and yes he was easily off of balance
2026-02-04 03:26:06
2
kimberlyuryszvalade
KImberly Urysz-Valade :
Hugs Rebecca 🫂
2026-02-04 03:05:52
3
jananthemothercluckers
Jana & The Mothercluckers :
Thank you for sharing. I exp most of these too. I am posting a very similar message right now.
2026-02-03 21:47:21
3
canadiansmutlover
Sara🖤 :
Reminds me of shopping online when sleeping. Instead of sleep walking or talking I sleep shop. The sh*t that’s come in the mail! Weird haha I now need to keep my phone in a different room
2026-02-04 18:35:16
1
sherryrp78
Sherry P :
Yes you look at my sister w sjogrens and she looks normal but has severe flares or body aches so bad
2026-02-04 00:00:20
3
anita.bodde
Anita Bodde :
Amen to that. That makes you feel invisible 🫥
2026-02-04 02:29:21
2
betsy7805
BettyBoop78 :
The federal government discriminates too by denying the majority of DTBC applications made by people with non visible but disabling illnesses like rheumatoid, celiac, hashimoros, cfs, me, long covid etc - even with a family doctor advocating it seems like they have a very hard time believing
2026-02-12 03:51:28
2
evamacinnis775
Eva Mac Innis775🇨🇦 :
So very true !
2026-02-04 11:57:53
1
horsegirltaken
Tara Powell840 :
These videos are going to reach so many people , I’m so glad u chose to post ur journey , thank you ❤️
2026-02-19 04:49:37
0
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