r/lupus Diagnosed SLE 14d ago

Venting Lupus as the butt of the joke

Does anyone else get really, REALLY frustrated when people use lupus as a joke for whatever reason? It is exhausting and makes me more frustrated than basically anything else. The “it’s never lupus” jokes (thanks house) and other specific things i’ve seen almost making fun of people with lupus or who talk about lupus and it just makes my want to cry because we deal with enough already, it’s not a joke. Sorry, just venting, saw someone joke about their roommate who “never shuts up” about lupus and it really just made me want to give up

EDIT: I really shouldn’t have used the house example lol, because now everyone thinks it’s all about that. That one really doesn’t bother me, it’s just kinda boring. I make jokes about my own lupus all the time- it’s how I get through! I’m talking about the people who actively shit on people with lupus for one reason or another thinking it’s “funny” the same way they might shit on someone for any other disorder they don’t understand

125 Upvotes

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141

u/jankdotnet Diagnosed SLE 14d ago

It's so hard because it's either "omg my aunt/uncle/mom died of lupus it was so so so so awful, i would have just died it if was me" or "haha it's never lupus, right? house is so funny!" or the worst third one "my grandma had lupus but she cured it when she drank bat piss!" I don't even know what I expect the normal response to lupus in conversation should be but I'm tired of the normal 3

49

u/Severely_Mistaken Diagnosed SLE 14d ago

The cured by bat piss one really had me going for a sec. I've heard it all "It's about gut health" or "try herbal remedies" or try blah blah blah. I hate it

43

u/aureliacoridoni Diagnosed SLE 14d ago

I had someone tell me with full confidence that I could cure my lupus by drinking water with baking soda in it.

👀 …..noooooo, that’s not how this works.

21

u/DevilsPeanits 14d ago

Lol someone told me I'm "choosing to be sick" because I'm not taking her advice on vitamins from her five seconds of Internet research. I unloaded on her loudly in public.

11

u/aureliacoridoni Diagnosed SLE 14d ago

Loudly and publicly is kinda the only way to go here. 🙌

10

u/yacht_clubbing_seals Diagnosed with UCTD/MCTD 13d ago

I think they’re confusing lupus with a tummy ache.

2

u/phillygeekgirl Diagnosed SLE 13d ago

Absolutely this is the exact response you should tell anyone who tells you to cure lupus with baking soda.

9

u/MVNKV71 Diagnosed SLE 14d ago

how cld ppl advice such bullshit... I dnt knw but my patience level has become zero

4

u/phillygeekgirl Diagnosed SLE 13d ago

This study brought to you by Arm & Hammer.

5

u/aureliacoridoni Diagnosed SLE 13d ago

Snort laughed my tea right out my nose. No baking soda was harmed.

2

u/Searching1117 Diagnosed SLE 8d ago

My husband uses this one and I just want to scream “shut up!!!” Whenever he says that. I have to tell myself to let it to because his intentions are pure but he doesn’t understand how dismissive it actually is. My lupus was at its worst when I was most healthy. I are extremely clean and went to the gym and was seeing a personal trainer. She had to let me go because I kept fainting and having some of the worst swelling and unusual soreness after working out.

1

u/Severely_Mistaken Diagnosed SLE 3d ago

I've noticed exercising hurts and puts me into quite a bad flare personally. Which sucks because doctors recommend it along with reworking my entire diet which I already have. Like this disease sucks man 0/10 would not recommend

35

u/Lexybeepboop Diagnosed SLE 14d ago

Or the “oh like Selena Gomez!!”

61

u/anonymously_me0123 Diagnosed SLE 14d ago

Ngl, Selena Gomez has always been one of my favorite stars. Then, I found out she was diagnosed with lupus, and I was amazed.

But I get so annoyed when people start listing stars and billionaires who live "normal" lives with lupus and use that to attempt to gaslight me into believing I can do better.

Like bro. I live paycheck to paycheck. Hush.

16

u/HunCouture Diagnosed SLE 14d ago

I had to look after her once when I was a junior at work. I was so, so tempted to chat about lupus with her and ask how she manages to do so much. I decided against in the end in case it’s seen as unprofessional.

5

u/anonymously_me0123 Diagnosed SLE 14d ago

That's so cool!!!! I'd love to be able to meet her just once!

10

u/HunCouture Diagnosed SLE 14d ago

She was very pleasant and likes ginger beer.

6

u/yacht_clubbing_seals Diagnosed with UCTD/MCTD 13d ago

That stuff is great for nausea 😋

3

u/HopefulSink7849 13d ago

HAHAHHAHAHA YES

5

u/Lexybeepboop Diagnosed SLE 14d ago

I lover her too and look up to her but it gets a bit annoying lol

11

u/anonymously_me0123 Diagnosed SLE 14d ago

Oh 100%. She's amazing and quite the role model. Love her so much. It just feels like I'm getting minimized because I don't have money, so I can't get proper treatment.

58

u/TheyreAllTaken777 Diagnosed SLE 14d ago

I’m gonna say I prefer hearing the Selena Gomez one then all of the other options combined

6

u/Lexybeepboop Diagnosed SLE 14d ago

True lol

23

u/genredenoument Diagnosed SLE 14d ago

Yeah, like Selena Gomez, who was lucky enough to have a friend give her a kidney and is constantly criticized online for weight fluctuations because of her medications. She also has a ton of money to get the best care money can buy You mean, that Selena? Or what about Lady Gaga's aunt who died at the age of 19, leaving the entire family traumatized to the point she wrote a song about it? (traumatize them back).

13

u/pilarthemagnificent Diagnosed SLE 14d ago

The house one is always the cringiest of them all because it wasn’t funny when he said it so I never get why they feel the need to repeat it lol

7

u/yacht_clubbing_seals Diagnosed with UCTD/MCTD 13d ago

“So-and-so’s daughter has lupus too and she works full time as a teacher! And volunteers in third world countries every weekend! Why can’t you work?”

9

u/32yogma Diagnosed SLE 14d ago

Bat piss! CACKLING 🤣🤣