Does this sped actually think that being able to see your veins through the skin on your dong or hands is something out of the ordinary? Has he never encountered another white person in his entire life??? The fuck man?I bring part 3 of wang, our male munchie.
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December 1st, back to the GERD.Thinking of switching medications.
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Again, being pretty liberal with the term “us”, Kyle.
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December 2nd, chasing that aneurysm and looking for a new excuse to plague his ER.
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Numberwang reveals that his at home genetic testing came back all clear so decides to start munching for the conditions he hadn’t been tested for. Informs somebody who has already been diagnosed that they should be looking at this too because he’s a bellend.
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December 3rd, please tell me that my pain isn’t completely benign so that I can go waste resources in the ER again.
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December 3rd, returns to r/illnessfakers to white knight Anelise and demonstrates he still has no idea what he’s talking about. Fun to remember that one post he made months and months back which claimed an eating disorder.
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Still white knighting munchies. You totally can’t cause your own heart attack!
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December 4th, admits he’s still trying to score cromolyn from his GP. Complains that it takes forever for him to get the dozens of free doctor’s appointments he’s been wasting over the past few months.
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Kyle and his degree from the Bing medical school diagnoses another individual with the munchie serving platter over reddit.
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December 7th, back in r/illnessfakers to white knight Amanda/Ren this time. A person who has admitted several times that she has not had a hEDS diagnosis. I think they would both get on.
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Still bleating on about his translucent skin.
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With an at home test but congratulations on accepting that you don’t have vEDS after months insisting you must have vEDS including getting snippy and dramatic when other people tell you that you don’t have vEDS.
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Numberwang tells us more about his lovely munchie clumps. Still claiming he has a connective tissue disease despite his at home genetic testing coming back all clear and Kyle admitting he doesn’t meet the diagnostic criteria for hEDS.
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8th December, still claiming ehlers-danlos. Digging through his old blood test results looking for any borderline result to munch over. He’s told that it means nothing and he insists he still has a connective tissue disorder.
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8th December, oh? Kyle implies he has finally been diagnosed with hyperPOTS. His body going tingly during a panic attack must be related to that.
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He returns to his post back in September to state that he is “fairly confident” he has hyperPOTS. So no diagnosis. Shocker. But the only reason it’s taking so long is because he has a severe lack of “knowledable” professionals around him.
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The erectile dysfunction shows up as well as him claiming EDS again.
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It’s still december 8th and Wang starts munching chiari “formation”. He wonders if this puts him at risk of stroke. This is a fair assumption as he has symptomatically been lacking oxygen to his brain for several months now.
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December 9th, Wang decides to hit up his doctor for some guanfacin (a non-stimulant ADHD med that somebody else told him they were on a few weeks back).
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December 10th, Numberwang chimps out at his unsuspecting mother like a fucking lunatic and attributes it to hyperPOTS.
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Yes Kyle, your post orthostatic tachycardia is occurring when you’re laying down. Stop telling people you have EDS. You do not have EDS.
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Still december 10th, looking for medication that affects his self diagnosed POTS.
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December 11th, Numberwang returns to r/illnessfakers to white knight Amanda/Ren again.
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Posts claiming translucent skin again and explaining he has never had a dissection (not even one of those invisible ones he never noticed). Explains that he spent $400 on his at home genetics test because doctors still wouldn’t order him a panel at the taxpayer’s expense for no fucking reason. The 3 weeks before he got his results (plus a week time waiting for his genetic test to arrive) takes us right up to his birthday on 10th October which strongly confirms my suspicions he used birthday money to purchase it (which is sad).
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Numberwang claims an elevated ANA but stated his doctors didn’t follow it up (likely because it was borderline or inconsequential). Says he doesn’t have a dry mouth and he doesn’t cry much. Still claiming EDS and POTS.
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Is sjogren’s lethal?
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Still talking about hyperPOTS and norepinephrine like he knows what he’s talking about. Also diagnoses somebody else with it because why the fuck not. Also starting to think gastroparesis.
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December 13th- “Can fucking about with my medications cause my made up gastroparesis”.
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Skip the diagnosis and straight on to the asspat harvesting. He doesn’t vomit yet but don’t you worry, he’s got it penciled in.
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December 14th, still no diagnosis.
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December 15th, if you forgot Kyle’s dick doesn’t work, don’t worry because he will remind you. Wanking is not the cure.His last post about his girlfriend was on November 19th so it sounds like she's still in the picture.
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One munchie claims that all their mental health issues were a misdiagnosis and it was all symptoms of… dislocations? Kyle gets excited as he realises maybe he has been unknowingly dislocating things all along.
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16th December - tells somebody else looking for an online diagnosis they probably have EDS rather than Marfan’s as though his IQ isn’t a number you can find on a clock.
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December 17th, it’s really serious guys. Sometimes his blood pressure is high and sometimes it’s low.
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December 18th, still munching for sjogrens and insisting on the hyperPOTS.
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Joint hypermobility syndrome comes into play as though the two things are interchangeable. Also still harping on about the MCAS despite his doctor refusing to even refer him.
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December 19th, his undiagnosed hyperPOTS makes him itch. Admits he never had a tilt table test despite marching around reddit informing every poor sucker he can harass that he has hyperPOTS.
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Atoms apple lmao
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20th December, Numberwang worries that his at home genetic testing isn’t suitable for medical diagnosis.
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Uses his medical diploma from Google to talk about Marfan’s. One guy refers to his post history. Kyle admits he’s rather dumb.
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December 20th, “practically begs” his doctor to prescribe clonidine but actually makes it over to the anxiety subreddit albeit to blame it on his imaginary medical conditions.
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It’s Christmas day and Kyle wants to know if his joints clicking are EDS as he discussed with the munchie who totally doesn’t have BPD.
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Kyle has thoughts on munchausens and insists you can totally prove you have EDS by demonstrating hypermobility alone.
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Still Christmas day and Kyle is still asking about other genetic tests. Admits to the health anxiety for once which may explain why he’s asking questions about loeys-dietz on reddit rather than eating christmas dinner.
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Kyle imagines he has EDS or loeys-dietz (but the ones he can’t genetically test for at home). Remember when he said he didn’t meet the diagnostic criteria for hEDS? That was fun.
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Boxing day, time to try and munch lupus or vasculitis.
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December 27th, are normal calluses on his fingers scleroderma or is it his made up EDS?
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December 28th, back to telling the MCAS subreddit he has POTS and EDS.
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December 30th, those spasms and the hiatal hernia come up again.
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December 30th, Numbnuts posts his at home genetic testing results on reddit. Confirms nothing fun was found.
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Finds out they’re useless because there’s no such thing as a crystal ball to tell you if you’re going to randomly have a heart dissection. Gets told to see an actual geneticist.
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On new years eve he talks to people in the EDS subreddit about how drunk he gets with his undiagnosed POTS.
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Ponders where blood is going because he doesn’t bleed all over the place (except when he’s having his arteries rupture without him noticing of course.) I can't imagine how his doctor must feel when he shows up to appointments and acts like he knows what he's talking about
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Tells the poor soul that explains to him what happens to the water he drinks that he is developing gastroparesis.
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And some final thoughts in 2019, he never ever feels thirsty...View attachment 1395133Kyle is ringing in the new year by asking about liquid IV and if he can get it outside of the hospital.
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January 2nd - Numberwang returns to his post on scleroderma and reckons the calluses on his fingers mean his blood vessels are doing the same. Acknowledges the anxiety.
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January 3rd- Wang is telling other people to use the at home genetic testing. He claims his veins are super visible (they’re not). Insists that it would be uncommon for somebody with his veins to not have EDS.
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January 6th- Upon hearing he may be able to genetically test for sjogrens which he’s been munching for, he asks another user about 23&me. Despite already having completed a home DNA test.
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January 7th - Still saying he has EDS.
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January 7th - Claiming EDS and POTS without a diagnosis. He claims he has a tolerance to lidocaine and tells us his electrolytes were fine when they were checked.
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More self diagnosis.
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January 8th - Looking at chiari again. Time to start munching for a standing MRI.
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Goes straight to r/chiari to find out if the neurologist appointment he scored for his POTS (still not diagnosed, still claiming) can diagnose him with it too.
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January 8th- Says he’s looking at a connective tissue disease akin to how somebody may be looking to purchase a car. Insists it’s severe. Still claims translucent skin despite being told by several people his skin is normal. Wants to know if the medication he begged his GP for will actually help his self diagnosed issues. It’s almost as if you should let your doctor diagnose and then subsequently treat you.
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Spends the rest of the 8th posting his penis on various subreddits because he thinks it has varicose veins. He opted not to post it in the pecker checker thread.
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Are these varicose veins on my penis?
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Is reassured that veiny peens are normal by a chap called dribblyboi.
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January 9th, tells reddit he has a gastric emptying scan for his alleged gastroparesis on the 10th. We never hear about this again. It’s almost as if the gastroparesis he was claiming over on the ehlers danlos subreddit was entirely self diagnosed.
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Diagnosing other people in r/dermatology with connective tissue diseases months after they've posted.
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Doctor is still rolling her eyes at him when he is still pestering her for lyme treatment despite his tests coming back clear.
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Tells somebody else he has EDS, POTS and likely MCAS. Still has none of them diagnosed.
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Telling people Marfans was ruled out by his at home genetic test.
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Back to diagnosing everybody he comes across with EDS and claiming his veins are visible. Not a doctor. Not qualified. Varicose veins are pretty common in pregnant women so his uneducated guess is shit.
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He never gets sick. He must be sick.
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January 11th, tries salt pills for his POTS for an entire day and decides they don’t work.
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Allergic to laughing.
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January 13th, still claiming EDS.
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January 16th. Somebody tells somebody else that they do not meet the diagnostic criteria for EDS and point out that the same shit Wang claims is common. Wang disagrees. Flat feet are not part of the diagnostic criteria.
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Wang reckons he has classical EDS but reckons he needs more genetics testing because his at home kit doesn’t cut it.
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Back to munching for chiari when OP just wants a fitbit recommendation.
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January 17th, wang returns to a post he made a month previously to complain that hEDS doesn’t get enough of the spotlight even though he doesn’t have an EDS diagnosis and nothing has indicated he has a vascular condition. Is looking at classical like EDS.
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Wang spends January 21st feeling up his chest.
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The medication he self prescribed from himself after nagging his GP until she caved is making him feel worse. All he knows is he has POTS. Still not diagnosed.
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HyperPOTS makes him itchy for two weeks lmao. Confirms he is travelling to Montreal for testing for POTS (so STILL not diagnosed but still claiming).
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January 22nd, claiming water causes him issues with his gastroparesis. But no word of results from GES or any treatment plans (and let’s face it, we’d have heard about it by now if he was diagnosed).
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My theory is he went back to his GP after the clonidine “didn’t work” and begged for another medication which she caved and prescribed whilst he waits to see the specialist in Montreal. Back to munching MCAS and admits the doctors don’t think he has it.
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January 23rd, munching for thoracic outlet syndrome. Never mentioned these symptoms before.
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Gluten test came back all good. Still claiming stomach issues caused by EDS. No mention of the results of his GES for gastroparesis.
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Tells reddit he had two of the positive markers for sjogrens (and now subsequently has the symptoms!) His doctor still doesn’t think he has Sjogrens. It sounds like he’s seen the results and is just running with it now.
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January 24th, back to CCI.
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Admits he’s not as hypermobile as he’s been letting on. Telling more people about his positive ANA. Hints that he’s seeing a rheumatologist. Is still telling people he has EDS/HJD.
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January 23rd, munching after scleroderma.
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Finds out about the connection between POTS and Raynaud’s. He admits his fingers are red when cold and none of them turn white.
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Determined to collect all the comorbidities, he rinses his hands under cold water for 2 minutes to demonstrate his raynaud’s. He shares some of the grossest looking toe nails I’ve seen as well as completely normal hands with ZERO indication of Raynaud’s.
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January 26th, Necroing month old threads to as about Sjogrens.
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Posts asking about tingling. Still claiming EDS and POTS. Still has neither diagnosed.View attachment 1395190View attachment 1395193
Starts necroing other old threads including one of his to see if he should buy himself a cervical collar.View attachment 1395196February 1st, Wang is allergic to hot drinks which is either due to his POTS or his MCAS.
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Continues to not know the word cough.
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Back to giving medical advice.
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Lumpy chest again.
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Still not diagnosed with POTS and EDS. Lists psychosomatic symptoms and is hoping for a CCI diagnosis. Complains his self prescribed treatment for his undiagnosed POTS isn’t working so it must be time to jump straight to surgery.
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User questions his logic and is confused as to why he has prescribed himself exercises and why he expects results in 2 weeks. It’s definitely due to a lack of specialist help where he lives.
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February 2nd, back to health anxiety. Small crack from his neck must be a rupture. His hospital (and I guess the ones in all the local towns considering his ER hopping) is shitty.
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Argues with people over in r/medical.
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Posts on a comment about seeing Henderson a month after it was made to ask why a neck brace would be needed for a flight to Montreal to see neurology.
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February 4th, replying to month old comments finding out how he can get a CSF leak diagnosed. Emails a clinic in America.
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February 5th, intermittent pulsatile tinnitus may be hardening veins.
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Has been to ER again for his “dissections” and was likely diagnosed with anxiety again.
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Is his sjogrens he isn’t diagnosed with yet causing all of his “neurological” symptoms?
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February 7th, replies to another munchie saying he is annoyed that people dismiss his undiagnosed EDS because he doesn’t have chronic pain,
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February 7th, posts asking about thoracic outlet syndrome and is advised to see a surgeon. Explains his nerve conduction test (they put electrodes on your arms, zap you and see i if it travels along your nerves came up squeaky clean. For some reason thinks they didn’t find anything because his arms were straight.
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February 7th, doesn’t have an EDS type (because he doesn't have EDS. Says he’s had auras his whole life.
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February 8th, more self diagnosis, back to TOS.
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February 8th, complaining that the ER won’t help him with his thoracic outlet syndrome which he has AS WELL as the EDS he is in the “middle” of getting diagnosed.
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February 9th - Wants an apple watch to do a god damn EKG because I guess his at home EKG isn’t good enough.
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February 10th, asking people posting in a subreddit for clot survivors about their TOS.
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February 11th, IIH, still claiming POTS and a connective tissue disease.
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More migraine shit.
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Spends a lot of time gargling white fluid.
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Devastated to find out he may be allergic to sex as though that’s not the least of his sexual worries.
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February 11th - Back to telling people about his elevated ANA and SSA.
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February 11th, Wang has tinnitus.
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February 12th, tells somebody with ordinary scarring to ask their doctor about EDS.
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February 12th - Eyes “pulsing”. Starting to wonder if Wang took the phrase “It’s all in your head” and just ran with it with all this IHH bullshit.
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Joins us over in IFGW to blog about being chronically dehydrated.
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February 12th. If your symptoms are caused by CCI is your IHH really idiopathic?
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February 13th, if you can munch one diagnosis maybe he can munch them all.
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Still looking at sjogrens.
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I love that Wang seems to think everybody around him thinks he has sjogrens rather than garden variety hayfever like Bloomsatnight’s doctors.
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His doctors are ignoring his test results! (Probably because they’re borderline and he has had countless bloods).
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“For some reason”
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Will his GP give him a lumbar puncture?
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Still not diagnosed with EDS, still claiming it. Diagnoses himself with sjogrens using an online test.
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Claims to have been evaluated for connective tissue diseases, still doesn’t have a diagnosis. Confirms rheumatologist thought nothing of his levels.
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February 14th, tells somebody else that they shouldn’t worry about vEDS without a good reason much like he spent months doing.
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Asks somebody else about another genetics test in the hopes he can order another genetic test. Sadly the website only sells the testing kits to actual doctors. Finds out his test probably isn’t as accurate as one carried out by actual doctors.
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Sounds like legit medical testing to me.
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Back to talking about vEDS in a way that almost seems fetishistic.
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February 15th, diagnosing and prescribing PT to somebody who is dying of EDS lmao
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Back to posting in r//illnessfakers to show his expertise on EDS. Continues to tell people that beighton score is all you need to be diagnosed with EDS lmao.
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February 15th, googling more medications. Hopes the POTS doctor will also diagnose him with a CSF leak or IIH.
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God dammit Kyle, you’ve already ruled our vEDS with your home test.
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February 15th, another test came up absolutely fine so Wang starts looking for new tests he can munch in order to continue wasting money and resources.
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February 16th, “probably has sjogrens”.
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February 19th, trying to diagnose thoracic outlet syndrome at home.
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Suddenly the white fluid at the back of his throat is mostly clear since being told that cerebral spinal fluid is clear. Says his POTS never makes him pass out (he will contradict himself later).
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February 21st, more TOS stuff.
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Based on him reckoning he has raynaud’s based on completely normal limbs, I’m going to hazard a guess that he has no idea what blood pooling actually looks like.
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February 22nd, Kyle posts on somebody else’s post in r/radiology and gets called out for asking for medical advice.
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February 22nd and 23rd spent discussing IIH and CSF leak with leakybrainjuice.
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February 24th, This is all stuff you should ask your doctor but you won’t because they already told you that this is all in your head.
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February 26th, prescribing himself PT again.
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Pretty much all of this is made up. Still not been diagnosed with EDS. Has not been told that his spine is hypermobile.
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February 26th, starting the autoimmune protocol.
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More guesswork on his part. Rheum doesn’t want to diagnose sjogrens. No lip biopsy was ordered. I find it rather strange that a rheumatologist would “suspect a connective tissue disease” and yet not give an inkling as to which one it may be.
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On February 29th he slept on his arm.
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And he’s concerned about stroke. Tells people he has TOS despite this being a self diagnosis.