@dr_inna: Could some people be “not for real” disabled? Sure, but I don’t care if there are a few who aren’t really sick. I care that this insistence on invalidating ME/CFS from a place of ignorance causes real problems. @Fay and others like Fay deserve better from us. #creatorsearchinsights #chronicfatiguesyndrome

Inna Kanevsky, Ph. D.
Inna Kanevsky, Ph. D.
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Region: US
Tuesday 29 September 2026 00:50:13 GMT
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quinoarat
quinoarat :
ME/CFS has gotten less rare recently because it can be caused by COVID. It's not because it's trendy. I'm so sorry about your child.
2026-09-29 02:54:11
2370
genevieveauge
Genevieve Auge :
Damn didn’t realised my scoliosis was a social contagion.
2026-09-29 03:34:03
2559
bangbangbetti
BangBangBetty :
I'm butchering it but theres an analogy thats like 'there isn't more stars in the sky because the telescope was invented, we can just see them better now'
2026-09-29 05:51:30
311
roko_cos
Ray/Cove 🇬🇧🏳️‍🌈 :
Could there maybe be seemingly more left leaning people with mobility aids due to being less likely to have major internalised ableism? Or at least enough to admit they need some form of aid/accommodation rather than just pushing through.
2026-09-29 07:45:11
398
vampyre.cannibal
nico robins #1 fan :
be blocked me when I asked what degree he has
2026-09-29 03:32:36
874
septjoy
Katy🇦🇺 :
The original video is harmful. Yours is healing. I don't know if I'm expressing that correctly but thank you.
2026-09-29 05:29:11
160
backoftheballpit
Back of the Ballpit :
I am so so sick of this cane/walker point. Even if people don't need a cane/walker, who are they hurting? There's no shortage in the cane industry, they're not stealing walkers from little old ladies; who is hurt by people using an aid? Are they tripping children?
2026-09-29 16:51:11
833
saraharrison25
saraharrison25 :
I started into the medical profession in the 70's. I first heard about CFS and Fibromyalgia in the 80's. No one I have ever met was getting any social traction out of it.
2026-09-29 02:11:07
606
igavemycatfleas
Anna🫀🦕 :
There’s a lot of people in his comment section who think MECFS is just feeling tired
2026-09-29 01:27:26
1059
daisyunicorn1111
DaisyUnicorn :
Not to mention Comorbidities and struggling with symptoms that are similar to other diagnoses. Incredibly difficult to diagnose but it can be diagnosed.
2026-09-29 02:49:58
346
testosterone.cypionate
ezra 👽🐾 :
I’m still stuck on him saying it “can’t be diagnosed”. does he think nobody has been diagnosed with it ever? I’m familiar with these kind of people thinking that conditions are ~super rare~ and that “most people are faking” but is he just flat out trying to say that it’s an illness that nobody in the world has been diagnosed with
2026-09-29 03:54:28
401
curt12858
curt12858 :
You see more people using canes now because the people who need them feel less ashamed to use them. Do you think eyeglasses were just accepted by everyone when they were first a thing?
2026-09-29 16:16:51
193
b.j.o.r.k..f.a.n
b.J.o.r.k..f.a.n :
He is an investment banker. lol
2026-10-01 11:16:48
0
wrymoss2
wrymoss :
Ah, we love the ableism, sexism AND transphobia triple threat from this guy. 🫩
2026-09-29 13:05:14
26
teena123455
Tina :
i think it is clear why are you defending certain topics. why do you think people are affraid of your opinion? that is a bit presumptuous. chronic fatigue syndrome happens to people who need to isolate themselves from normal life. question is why?
2026-09-29 18:08:47
0
snowyhound
SnowyPanda :
As an ME sufferer, that video is insane. Insanely moronic. Thank you so much for combating harmful & malevolent misinformation like this. 💙💙
2026-10-01 15:13:37
0
ephyropod
. ݁₊☏⊹ .⎚࿔marmalade⋆𐙚 ̊.°❀.ೃ࿔ :
why are people hounding ME so much
2026-10-01 14:58:12
0
birdgirl411
birdgirl411 :
I have nerve damage 🤦‍♀️
2026-09-30 16:20:15
0
annatt8989
AnnaTt8989 :
Thank you. ME has destroyed my life. 11 years mostly bedbound. My only dream is that a cure is finally found
2026-09-29 04:04:01
99
valentzia.designs
valentzia.designs :
Get him Doc
2026-09-29 06:27:01
17
aisha253748
aisha253748 :
“Could some people be not for real disabled? Sure” honestly I don’t even see the need to concede that in a world without universal healthcare. When everyone is taken care of then we have a conversation about potential fakers but you can’t tell me about fakers in a world where healthcare, social support and disability benefits are scarce and insufficient.
2026-09-29 03:30:11
212
greatgraythings
Shift 🇨🇦🏳️‍🌈 :
I have CFS because I have multiple organ disease. I use a cane or wheelchair because I need a double hip replacement, and dying from multi organ disease is kinda tiring. But yeah, it's because I'm left leaning 🤣🤣
2026-09-29 05:13:29
33
disabled.ghoul
Mel :
By his reasoning my spinal cord injury was psychosomatic
2026-09-29 14:38:27
26
songsaboutjayne
Айла :
The Guardian released an urgent article on ME/CFS just a few days ago. Read it: https://www.theguardian.com/commentisfree/2026/sep/24/abandoned-dismissed-and-gaslighted-me-sufferers-betrayed
2026-09-29 03:12:32
298
alicestarlightf
Alice ♿ 🏳️‍⚧️ :
him saying neurological is psychosomatic means he is saying that the visible neurofibroma I had is psychosomatic. does he not know what those terms mean or does he not know what i.e. means?
2026-09-29 07:22:30
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