Jesse_da_silva

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JellyWobbles

JellyWobbles

Thoughts?

Caused controversy past few days posting about how they think fibromyalgia and chronic illnesses are make believe and used by people as an excuse to be lazy and claim pip. A few clap back videos are calling her out for being ableist.
She’s now deleted the original video, and made an apology video, however her comments to people doesn’t align with her apology aka she’s full of tit.

Seen that Bobby O has commented saying he is no longer friends with her for a reason. 👀.
 
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spring.day

Always found her really funny and love her accent but her tik toks and liking some awful comments was just a bit ignorant. It wasn’t just fibro too, she was laughing about BPD and walking aids.
Nothing prompted any of it she just wanted to laugh at people, it’s put me off her tbh
 
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JellyWobbles

JellyWobbles

spring.day said:
Always found her really funny and love her accent but her tik toks and liking some awful comments was just a bit ignorant. It wasn’t just fibro too, she was laughing about BPD and walking aids.
Nothing prompted any of it she just wanted to laugh at people, it’s put me off her tbh
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Have to agree, it’s one thing to take the piss about the whole self label warrior in profile names that she was on about but the rest of her comments (as in replies to comments - that she’s now deleted) were so bigoted and mean girl, seen her in a different light altogether.
 
L

loolabelle

I was quite shocked!! I honestly didn’t think she would think like that nor post about it on tiktok! Fibro is so misunderstood yeah there probably is a few pisstakers but having lived with someone with it, I wouldn’t wish it on anyone, because between medical professionals and people like Jess. You end up feeling shut down and unseen, like you’re going mad.
 
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bsn23

I really like her videos and I’ve always found her really funny, but I’m so gutted that she thinks it’s okay to talk like that. Fibromyalgia has completely changed my life and the past year has been horrendous because of it, it’s a lot more than just a “back ache” or “your hands hurt sometimes”. It’s debilitating and I hope she never has to experience it. I can see where she’s coming from when she says there’s no tests like blood tests etc to actually show fibromyalgia, but that doesn’t mean it’s not real. I am so conscious of telling people I have fibro because of people like her and I don’t want to be judged
 
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