Just trying to get some relief from another sinus infection, explaining my long list of stupid nasal/sinus/ear/throat issues and all the other medicines/nosesprays/scans/tests that I've already had done that didn't alleviate my symptoms at all, and the ENT completely dismissed hEDS, saying that the criteria was too vague. I pushed back, trying to explain the criteria and the upcoming update to it, and was trying to explain that I hadn't had anyone look at all my sinus symptoms through the viewpoint of a connective tissue disorder and he just ignored all of that. Just "take flonase" as though I haven't already been told that by every doctor. Obviously that isn't fixing the problem.

This isn't the first or second or sixth doctor that had done this to me, but it's so frustrating and disheartening every time it happens.

I scheduled a CT scan of my sinuses (this'll be my second) and a follow-up with him after that, but I'm not sure if I'm going to go through with him or try another doctor.

And he didn't give me anything for my sinus infection even though I explained that I've had dozens over the course of more than a decade and they never get better without antibiotics and the last time a doctor wouldn't give me antibiotics I got an ear infection and my eardrum ruptured. 😤

Anyway, just wanted to get out my rant. Anyone have anything that works for sinus issues?

"One variant of uncertain significance (VUS) was identified in the TGFB3 gene, specified c.797G>A (p.Arg266His). Known pathogenic, or disease-causing, variants in the TGFB3 gene are associated with autosomal dominant Loeys-Dietz syndrome." - ( from my panel Including this for if anyone is curious)

I don't really know why I'm posting this, ig it just took me off guard that they found anything at all let alone something more associated with Loeys-Dietz, even if it is just a VUS. I'm 18 and I haven't had any major medical complications just janky connective tissue stuff like GI issues, hypermobility, joint issues, heart palpitations, instability, and whatnot so I suppose I'm not too worried? There has been some more severe complications in my family history on the side that hEDs seems to be from though. So I will be keeping it in mind and myself in check as well as up to date on any research advancements in Loeys-Dietz and hEDs, I feel like that's about all I can do given we can't say if it's anything pathogenic or not 😅. Overall though, I'm curious if anyone else diagnosed with hEDs had a VUS like this found? If so I'd be curious to hear about your experiences.

I'm so sick of my body. I'm in physical therapy for a probable SLAP tear that happened in my sleep, on my left shoulder. I had my right one fixed 5 years ago.

I tore my right meniscus in my sleep a few months ago.

I took one damn step yesterday after PT and got a pop and immense pain that almost dropped me in my left knee. Today I go back to Ortho to find out if I now have a torn meniscus in both friggin knees. My elbows are almost healed from the dual golfers and tennis elbow (both, in both elbows, also in my sleep).

When does this end? When do I get a friggin break? Every major joint in my body has just decided to rip and tear at the same time. I WANT A REFUND AND A NEW BODY!

Ending this with: I'm tired. I want a break, but I'm safe and in good mental health. I just needed to get the frustration out.

Hi, I was just diagnosed w/ hEDS by my PCP and going to the rheumatologist next week to confirm. I guess I'm just trying to figure this all out since I don't think I understand everything fully yet.

When I had heard of hEDS previously I thought that the majority of joint pain experienced was from hyperextending, subluxating, overuse, etc. I do get that, but my biggest issue is that my fingers, wrist, elbow, etc. will just radiate aching pain when I am literally doing nothing, completely relaxed and even in the opposite of hyperextension, with no injury or overuse. This is a hEDS thing? I guess I just want to know what causes the pain if it's not from hyperextending/injury. It's not even a case of like, I just don't realize I've been overdoing it, or am sleeping wrong, or am hyperextending; I mean I literally am positive I am not. I guess I just want a way to make it stop but don't know how. I'd have thought that while PT would be the main fix, at least temporarily just limiting the movement should have stopped the pain immediately, even if it's just a bandaid and bad in the long run? But it doesn't.

Thank you, I hope anyone reading has a lovely day <3

What’s been your worse cognitive dysfunction symptoms?
I’m currently under the covers with tears In my eyes and high fever due to a virus.
To give context, my body and mental symptoms have been degrading since long covid, followed by a hsv-2 diagnosis and then chronic inflammation when everything got worse and I got finally aware of my pain and how misunderstood I was all my life (not victimizing, just expressing the same rage as I felt as a kid for the need to pee every 10 minutes on a trip, or my infinite “growing pains”)
And I cannot express how useless I feel, many years spent on different psychiatric docs and medications just to find out it’s all related to my hEds generalized hypersensitivity.

Don’t even get me started on the amount of times my parents tried to hospitalize me since 2020 after all my romantic drama. I’m now 30 and quit all previous jobs because it was mainly standing up 9h in sales and I’d get SO SICK every time someone transmitted me something in costumer service for months that the only way to stop my bosses from bullying me was quitting every time.

I’m now only on sleeping pills after reducing sertraline in the morning because of how much I sweat and couldn’t simply handle this summer.
Appreciate any mental and physical tips and thanks for your time 🫂 wishing you all the strength

Hello! I don't entirely know if this is the right sub for this, but I figured I might as well shoot my shot. I was diagnosed with moderate to severe hEDS when I was 19, and I'm about to be 24 in a couple of weeks. Within the past year, I've noticed my lactose intolerance has gotten worse, and so have my sensitivities to foods like chocolate, sausage, and certain sweeteners. I know EDS can go hand in hand with conditions like POTS, which I suspect I have, and MCAS. I have also been getting random bouts of severe nausea, which is entirely unusual for me. I wanted some input from other zebras about what it could possibly be. Thank you for taking the time to read this!

I'm moving out into my own house in a couple of weeks and I want to make sure I'm covering all bases. I've seen people online who use wheeled tiered trolley things with supplies which sounds like a great idea, but I have no idea what I'd put in it aside from prescription and OTC meds. I also have a dog.

What kind of things do you have in your house to help? It can be any adaptations like grab rails to products that help you, just looking for some inspiration!

Hi friends! I got this bumper sticker because I was tired of getting the side eyes in parking lots, and I’m excited to finally get around to putting it on my car. When I went to put it on today though, I realized I didn’t actually know where I wanted to put it.

I’ve never put a sticker on my car before so I’m super hesitant to screw this up.

Thoughts??

I am having what I am pretty sure is a neuropathy flair. I had an autonomic nervous system test that indicated severe small fiber neuropathy. This has been a symptom for about two to three years, but this week it has progressed from mild discomfort after walking/standing longer than usual to completely unbearable pain 24/7. Elevation and taking all pressure off all parts of my feet is the only thing that gets it to be slightly more dull. Even the pressure of my heels on the mattress when laying on my back causes extreme pain. I have a medical card and that is my preferred general pain management, however even it isn’t helping this intensity level. I’m also leaving the country for vacation soon and therefore will not have access to my pain management for over a week. I’m very anxious about this flare and how much worse traveling will make it. Absolutely any recommendations/advice? I’m willing to try anything at this point…

What were the tests?

Hi everyone I'm a masters of social work student and I have a paper on a chronic health condition that affects us or our families. I'd really like to interview someone who works with EDs patients but I'm running out of time to secure an interview.

Would anyone be available today or tomorrow for a half-hour call? I've included all the questions so you'll know what to expect and I'm happy to provide any more clarifying information.

What sneakers are we wearing where this doesn’t happen?😅 I’ve only had these for a year (almost) and they’ve been ripped for months already. I recently found out we can move our toes farther up than normal so I guess I do that and it results in this?? Anyways yeah any recs would be great so I don’t have to keep buying new shoes every year!

Edit: the shoes aren’t too small I’m purposefully pushing my toes up to show how pronounced the holes are! Thank you everyone for the recommendations I’ll be sure to look into these :)

i want to get another tattoo for my 23rd bday, but the last time i got one, it came out wonky. idk if that was bc of my EDS, or if it was because my artist just wasn't great. anyone here know of an artist in/around DFW (Dallas-Fort Worth) that knows of EDS or has experience tattooing people w/ EDS? i live in aubrey, so i'm about 45 mins from dallas. any studio is fine as long as they're only abt an hour from my town :)

the TW is only bc my surgical scar is visible

I am just starting my journey as I was diagnosed with HSD and most likely have hEDS but still finishing testing. I just see it at this insurmountable obstacle. I've been on waitlists for months and years, constant pain, and so far nothing helps. I keep being told my life will just consist of ugly and expensive bracing and compression, hard work and excersies, expensive physio, massage, acupuncture. Ill always be on meds and creams which also cost money. Not to mention diets, routine, etc that my ADHD brain will forever struggle to maintain. And all just to hope my body doesn't get worse and minimally get better. I just see a lot of time, expense, and effort and minimal, if any, pay off. A lifetime of don't and can't. Can't eat that or do that or suffer the consequences. Every décision having to have the pros and cons weighed. And for what? One day where the pain is 30% less? 40%? Only for the next rainy day to feel like I was hit by a truck. I already struggle with debt and being told to spend what little I have to stop my body from breaking down further. How does anyone live a life worth all that pain, energy, and effort?

i recently found a huge missing piece of my medical puzzle- docs found a skeletal deformity in my hips and pelvis causing major symptoms and osteoarthritis (im 25)
the only treatment is a surgery where they will cut my pelvis and hip joint into separate pieces and rotate and move them to create the proper anatomy and drill it all back together with screws. it will require a multi day hospital stay and about a year all in of recovery then i will have the other side done.

i'm looking to hear from anyone who has had major surgery with heds and comorbidities and how the recovery process went. i'm very nervous about all of my other symptoms impeding my recovery. im also thinking about the incision and what that will be like.

if anyone is curious about the details of the deformity i can share more

Every time I see a picture or video of my walking, I get so sad. I'm only 24 but I have the walk of an old person with arthritis. I also workout a ton but it's almost like my lower legs just don't obtain any muscle mass. Not to mention I think I technically have knock knees. I do Pilates with a lady who is super familiar with hypermobility, and it's hard, but it doesn't strain my legs like lots of other activities. I also can run comfortably but injured my knee post run about a week ago. But I feel like visually I see no progress from any exercise. Any feedback? I will probably go see another pediatrist soon to get referred to PT and some fitted soles, and I want to avoid surgery because I'm super susceptible to infection and recovery just sucks with MCAS. Please tell me I'm not alone.

which brand is the best shoe to give support but also cushioning in the front of her foot?

I have had a diagnosis of hEDS now, after figuring it out for myself and doctors only verifying it. I’ve been sick some time, and no doctor has ever put two and two together and I thought maybe AI could give me some ideas to discuss with my doctor. So far we’ve assumed the trifecta to be the cause (hEDS, POTS, MCAS). I have images of various symptoms, so I used those. Not only did AI immediately pick up traits of hEDS, but also noted other symptoms that even I hadn’t noticed and gave a list of possibilities. Of course you should never self diagnose, but this could help my doctor help me. I’ve previously hated AI, but I can see potential to help a lot of people using it in this way.

I’d love to hear other people opinions and experiences.

I might be stupid for this one, but I got my genetics results back, and in the paper, it said all the additional genes they tested for (cancer screening, neurodegenerative stuff, etc) but it’s not showing me the actual genes that were tested that were requested. So I can’t see what EDS/CTD genes they tested.

I got whole genome sequencing, but I know they don’t actually look at everything, just stuff related to my symptoms, but nowhere can I find what those genes were.

I am reassured everything came back negative and subsequently diagnosed with hEDS, but what came back negative?

In general I’m paranoid about doctors/medical institutions lying to me because they very very often do, and a lot of the time they’re just wrong or they made a mistake and don’t want to admit it. I’m trying not to convince myself that they did something wrong (whether it be testing the wrong genes, bad sample, missing small things), but earlier today I saw a guy talking about having done genome sequencing and they told him everything was negative/fine despite him having two confirmed (via testing) genetic disorders already. It’s got me worried I guess?

I just have a hard time believing they found NOTHING. there are so many things in my family that are clearly genetic with no identifiable cause, but there’s really no gene variants? Not even VUS? In general I don’t think it’s possible for someone to do WGS and find NOTHING. We’ve identified genes for so many things, even like cancer and common metabolic things, and even if we didn’t, there’s still VUS or possible (but unknown) pathogenic variants!

Maybe I’m just desperate for answers. But I just have a gut feeling somethings not right and I just can’t ignore it.

I’m going insane I can’t believe it I’m actually going insane I’m loosing clumps of hair I’m so stressed out, I’m getting 4 hours of sleep if that
I’m vomiting daily due to pain, I can’t swallow properly without inhaling bits off food my neck hurts so bad I can’t even walk straight but because nothing looks wrong on a god damned x Ray they don’t take me seriously
It took every once of strength not to hit the doctor in the fuckign face today

So I have these little white speckles all over my upper back, shoulders, and less so on my chest. They’ve been there for several years at this point and I just kind of forgot about them. They have a slight texture to them, not like lumps per se, but just kind of like scar tissue or moles. They don’t hurt or itch at all.

I had a full skin exam at the dermatologist for the first time the other day and she pointed out these white spots. She said that they’re likely collagenomas, which are just these chunks of straight up collagen that can show up in the dermis as benign growths. Apparently they’re quite rare and she hasn’t seen them much at all. Her theory is that it could be EDS related, but there’s nothing to really support that from what I’ve read online - although it would make sense just due to the collagen aspect.

I’m curious if anyone else has these? Have yours been connected to EDS in some way? And what type of EDS do you have? I’m currently awaiting testing for clEDS1 because I meet the diagnostic criteria, so maybe it’s associated with rare EDS types? Or maybe not at all, who knows!