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What if my sexuality is a secret third option
#queer community#and they were gay#love is love#lgbtq community#sexuality#sexuality crisis#am i a man or am I a muppet#queer pride#queer#nonbinary#lesbian???#asexual#lgbt pride#imposter syndrome
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Hello dears ! I am asking you to support my campaign to help me to reach my goal. I am now in bad need to your support to help me stay alive and safe. Gaza is a very dangerous place either on the level of livelihood or on the level of souls. I need your monetary support to ensble me to get the basic needs for my family till Rafah crossing point reopens to move my family to safety and peace.Pleasd help a family be alive through your small donations or througn your shares to others.Thank you so much for your stand beside people in need .
Signal boosting, please help donate to this family if you guys can 🩵
#from the river to the sea palestine will be free#gaza genocide#donations#viralpost#mutual aid#signal boost#no pride in genocide
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Hello, 👋
I hope you are well. 🌷
I am Ahmed From Gaza City 🇵🇸
My family is in urgent need of assistance due to the war. Any donation or sharing of my campaign can make a huge difference.
Please help us if you can. 🙏❤️🙏Thank you from the bottom of my heart for any support. ❤️
"My children need your donations."🙏🙏🙏
🚨IF YOU IGNORE THIS, YOU ARE DOOMING MY FAMILY TO DEATH.
Hi everyone, let’s try and boost this family’s fundraiser and help them raise some funds! If you can’t donate to them, share and repost for visibility!
https://gofund.me/35c30c67
#viralpost#i stand with gaza#from the river to the sea palestine will be free#viral news#mutual aid#gofundme#go fund them#financial assistance
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art by the.gauntlets
Dr. Huda Abu Khater's Instagram
gofundme to help them
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Help A Teenage Girl Evacuate Gaza!
Hi everyone, I'm reposting this one from Instagram, illustration is by myself and depicts Amal. She reached out to me to share her story and her evacuation fund.
Amal's situation is exceedingly dire. She has faced extreme difficulty accessing food and medicine she desperately needs. Airstrikes and famine conditions have forced Amal to navigate an increasingly dangerous Gaza, in which she is already internally displaced. Amal is only 18 years old, and has been forced to give up her high school and college dreams in order to survive this genocide. Please join me in making sure this teenage girl has something to eat and a future to look forward to.
Remember, the minimum donation is only $5! Even a small donation will help tremendously, so don't be afraid to give what you can! Don't forget to share if you can't donate!
(Disclaimer: I am not Palestinian, I was just asked to share this fundraiser.)
#free palestine#gaza#free gaza#palestine#from the river to the sea palestine will be free#gaza genocide#gaza strip#all eyes on rafah#viralpost#viral#gofundme#i stand with palestine#i stand with gaza
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Being loaded into an ambulance: Sorry am I ruining the vibe?
#rare disease#dysautonomia#inappropriate sinus tachycardia#orthostatic hypotension#ehlers danlos awareness#gastroparesis#pots#ist#ambulance#ambulatory wheelchair user#things that may or may not have happened#funny memes#severe disability#disability pride
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Hypokalemia, hypokalemia when I catch you hypokalemia.. Having to get potassium chloride replacement should be considered cruel and unusual istg
#gastroparesis#intestinal failure#intestinal paralysis#hot girl stomach problems#ehlers danlos awareness#scleroderma#diffuse scleroderma#hypokalemia#malabsorption#malnutrition#malnourishment#organ failure#organ dysfunction#rare disease#cutie with a tubi#feeding tube
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Bitches with EDS be like: the braces stay on during sex!
#ehlers danlos awareness#rare disease#dysautonomia#inappropriate sinus tachycardia#orthostatic hypotension#pots#ist#funny#funny memes#my memes#viralpost#gastroparesis#acespec#asexual#are we all just in a silly goofy mood?
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I saw your dysautonomia post. I've been diagnosed for over a year and known for longer but my doctor keeps refusing to prescribe me a wheelchair despite the fact I can't walk further than down the hall without one. They keep trying to send me to physical therapy (only for one body part at a time due to insurance despite also having chronic pain evenly in my whole body and experiencing post-exertional malaise even from light physical therapy). Other than just finding a new doc, which I've been working on, do you have any advice for how to get a doc to actually prescribe the mobility aids you need?
(I am lucky enough to have a decently fitted one that I cannot self propel but can be pushed in, but my partner also has POTS so that's rarely an option and only for short trips (which only because in her own words hers is "better managed" than mine currently). But I really do need probably a motorized one at this point and I know other disabled people often know how exactly to get through to a doc so even if I can't convince my current doc I can hopefully use any tips when I find a new one.)
I wish I had better advice, but I would definitely look for educated physicians who are familiar with dysautonomia and fiddle around with medications (Corlanor/Ivabravine and infusions are the only things that has even helped remotely with mine). I had the same issue with a lot of doctors and was gaslit about not having EDS until my neurologist, shortly after diagnosing me with 3 types of dysautonomia, also diagnosed me with EDS (it was glaringly obvious apparently. I’m extremely hypermobile, can dislocate things on command and experience daily dislocations/subluxations, history of heart issues that he now escalated to four regurgitating valves, stretchy, velvety skin, strophic scarring, gastroparesis, at the time pending MCAS diagnosis, etc). If you can, there are organizations that will loan out wheelchairs for relatively cheap or free for people who need them, the difficulty is just finding one that’s near you or will ship to you! Also, I would definitely recommend a lightweight, motorized wheelchair or a regular wheelchair with motorized attachments like a smart drive or motorized wheels. The weight is going to be a big factor, especially if your partner is also disabled/chronically ill and you guys need to be able to transfer it into the car. I’m kinda in the same boat right now where even in a normal lightweight wheelchair (without motorization), my heart rate will get up to 200 and I can’t push myself for more than a minute really. I’ve been stuck using my forearm crutches to get around everywhere, but since that doesn’t do anything for my heart rate or blood pressure, I’m limited to doing anything (albeit not very much) to extremely good days. I’ll link some cheaper models below, and please feel free to dm me for more advice, I’m always happy to help other people out 🩵
#dysautonomia#inappropriate sinus tachycardia#orthostatic hypotension#rare disease#pots#postural orthostatic tachycardia syndrome#ist#disabilties#severe disability#rare disability#ehlers danlos awareness#disabled#important#viralpost#information#advice
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Happy gay month queers, and remember our queer siblings in Palestine! !!
#queer pride#queer#sapphic#nblw#nonbinary#genderqueer#transgender#transmasc#asexual#panromantic#gay#gay love#chappell roan#taste the rainbow#girls kissing girls#hayley kiyoko#free palestine#from the river to the sea palestine will be free#no pride in genocide
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Idk how else to cope with the fact that my dysautonomia is so severe and nothing seems to work. Corlanor was helping for a few weeks and now it’s just not anymore. I could definitely increase the dose, as well as my midodrine but how many meds do I have to be on to even have some semblance of normal. I’m literally on LDN, Corlanor, Midodrine, and get IV fluids for prescription management and have salt pills I take daily/regularly! I can’t tolerate the abdominal compression thing my old cardiologist recommended due to my gastrointestinal paralysis (especially now with my GJ tube) and high quality compression socks are impossible to find/afford. Ik I need to get my AAG (autoimmune autonomic ganglionopathy) and PAF (pure autonomic failure) testing done but I’ve legit been in and out of the hospital for months where they also found I have a fucking hole in my heart?? 🫠 screams. I wish I wasn’t broke and so sick bc I would benefit so much from having a SD
#dysautonomia#inappropriate sinus tachycardia#orthostatic hypotension#rare disease#pots#ehlers danlos awareness#gastroparesis#ist#syncope#chronic illness#chronically ill#heart disease#structural heart disease#there’s a literal hole in my heart#central line#severe disability#head injury#mcas#feeding tube#Spotify
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The fact that I passed out while working, had a low blood sugar episode, got a 72 hour video EEG placed, and then reached close to a HR of 200bpm from CRAWLING up the stairs and just walking to the bathroom? Foul.
#seizures#dysautonomia#pots#rare disease#rare disability#ist#orthostatic hypotension#low blood pressure#low blood sugar#gastroparesis#EDS#ehlers danlos awareness#inappropriate sinus tachycardia#seizure disorder#tic disorder#syncope
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‘Sodozo&&3’’ekmkeodoxkzjznz !!!!!!
I’m so normal about them (I’m going feral)
(Alt text on image)
“I’m so lucky I get to come home to you”
A little midwest emo RainDrop for today. I pictured this as Dew and Rain coming home tipsy and giggly from a late game night at Mountain and Swiss’ place, kissing and stumbling back onto the bed as they try to lose their shoes~
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I don’t think Ghost is given hardly enough credit for what they do. Tobias has found a way to masterfully merge his love for music, distrust in organized religion, and just the quintessential one essence of self love (and a lot of horniness).
Also every single one of their members are just GOOFY, okay? This band doesn’t take themselves seriously, like at all, and they manage to make everyone in their fan base smile. Their fans are the sweetest, and honestly, probably one of the least toxic of the fandoms you could be in.
The band Ghost is so fucking funny to me. Their frontman currently looks like this:
Or some version of a horny goth clown, but the guy underneath it has got the wettest saddest eyes I've ever seen. Just look at him:
This man admits to being very sensitive and cries at the drop of a hat.
He has a wife and kids.
He wears the costume because he doesn't like the way he looks on stage as a rockstar.
He treats the audience like his children. They're officially called the children of Ghost for that and also because of the play on "children of god."
The band literally fucks around on stage while riffing this badass music. They go through physical comedy skits every concert like the three stooges. For example:
Two demons throw guitar picks at each other when they get angy.
One guy grinds and licks the stage like a cat in heat.
One of them shakes their tits at goth clown man and scares him shitless.
One of them twirls goth clown man like a ballerina as he dances by them.
Several of them slap goth clown's ass when he waddles by.
He created the band to make people happy, to celebrate being a fucking weirdo because he always felt left out, and to make fun of Christianity because it makes people feel bad. He lost his older brother, and it tore him up so bad that the music he made as a result launched him into a worldwide music career.
This man ends every concert "ritual" with three things:
1. Be nice to each other
2. Help each other
3. Go fuck yourself
(Literally and figuratively)
Their music is 70% "fuck me I'm so horny", 10% "I love you so much" and 20% "ethereal badass metal".
Look at how much fun he's having, dude.
It's literally just a rock band filled with the nicest people on earth wearing costumes like a Shakespearean play. And all they do is make up funny little lore stories and serve cunt.
#the band ghost#ghost#tobias forge#papa iv#papa emeritus iv#dewdrop ghoul#hard rock#rock music#metal music#nameless ghouls#ghoul squad#deconstructing religion
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