Hypermobile tongue reddit. I very much second the person that said tongue biting.
Hypermobile tongue reddit My first was 3h 13m. I think it’s also a good advice for experienced practitioners who likes to practice at home for years especially if they didn’t realise that they have hypermobility or that hypermobility may have negative repercussions to their practice. lingual frenulum . Open menu Open navigation Go to Reddit Home Open navigation Go to Reddit Home Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Omg, I think I just got diagnosed via Reddit. Many, many years ago it was called Reiter’s syndrome. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and Tongue tip has been red and sore for nearly two months now. This may lead people to purposefully training themselves to leave their tongues in the wrong spot even though they assumed the correct position naturally. View community ranking In the Top 10% of largest communities on Reddit. I've been seeing a I have been doing the exercises once a day for three weeks during which my AHI has dropped from the moderate range to the mild to normal range. Gum helps. I had my tonsils removed, so I know it isn't that. This was SO HARD! Reddit . This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and I had hypermobile shoulders and a rotator cuff injury and I built the upper back muscles using yoga, per the doctor's advice. Test both sides: Rest palm of the hand and forearm a flat surface with palm side down and fingers out straight. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Hypermobility can be “benign” but it can also cause or exacerbate a boatload of issues. Geographic Tongue is a noted problem associated with my disease. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and Next thing I thought of was teeth. Vitamins, supplements etc. you actually don’t sound hypermobile to me, and hypermobile is a medical term way overused by yoga teachers. so it may be sliding back at night blocking airways. I believe geographic Tongue is an inflammatory condition. I can touch the part of the sinus that divides the two nostrils and those holes where the tear ducts drain. Does this happen to anyone else? Hypermobile EDS Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming All of my joints have always been hypermobile, meaning that they bend beyond their normal limits and have a tendency to slide around in their sockets (not a full dislocation but certainly uncomfortable). Hypermobility spectrum disorder is a general diagnosis for connective tissue problems causing hypermobility but that don't fit in as hEDS (or another stricter diagnosis). You can be hypermobile (laxity of your ligaments) and inflexible (tightness of your muscles), at the same time. , I've had chronic pain in my left wrist for the past 15 months. My tongue is VERY long, I can put my tongue into my nostril without any Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. I very much second the person that said tongue biting. Make sure you've good tongue posture. ex: someone with hypermobile knees can push them well past straight, so that there's a clear bend the opposite direction, but they might not be able to touch their toes. Hypermobile knuckles, wrist tendon pain I have hyper mobility in most of my joints. Saw a physio who figured the problem was stemming from my neck, and wasn't helped by hypermobile elbows. Also, allergic rhinitis, chronic uticaria, prior concussions, parents with autoimmune disease, and asthma. Noone ever brought it up before, no one's ever corrected me, and it seems most teachers don't ever address it. Ehlers danlos syndrome is likely what you're talking about. I’ve had Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Possibly hEDS? Or just general hypermobility? Something else entirely or nothing at all? 30F, 5’11, 130lbs, Canada, no diagnosis except mental health, prescribed Trazodone I regret this. They referred to this condition as “idiopathic hypermobile tongue”. ehlers Is this kind of body modification even a thing I'm able to get with my condition? I've been thinking on and off about eventually getting the procedure, but I'd very much like to keep my tongue, About 50% of individuals with EDS have the ability to touch the tip of the nose with their tongue (Gorlin’s sign) – this is especially likely with classical and hypermobile EDS. Spine and hypermobility were already mentioned here. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Where it gets dangerous (imo) is when people internalise tongue at the bottom of mouth = rest = good and tongue at top of mouth = tension = bad. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and Reddit is not a replacement for an in-person dental professional. Open menu Open navigation Go to Reddit Home Open navigation Go to Reddit Home I have a certain degree of hypermobility as well. pretty unreasonable (my stance changes on this when there's pain involved of course). just stick to it. hypermobile type EDS Sometimes some people praise hypermobility and think it is nice to be hypermobile. I think my doctor tailored my exercises to yoga since I didn't have a gym membership. Working with lighter weights (25 to 50% of max) moving very slowly to avoid momentum, and going to fatigue (I stop as soon as my form isn't perfect), and taking at least two rest days before working the same muscle groups is key for me. My shoulders are especially susceptible to the latter. Can the fifth finger be bent/lifted upwards at the knuckle to go back beyond 90 degrees? Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming IMO, the tongue scraper is awesome for cleaning my tongue, but I don’t notice a difference in terms of bad breath. She specializes in pregnancy and pelvic floor stuff, and since pregnancy itself makes your joints looser even without baseline hypermobility, I felt she was really well versed in my needs. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming "The tongue of man is a twisty thing" -- Homer "The tongue of man is a twisty thing" -- Homer Ehlers-Danlos syndrome (EDS) comprises a group of inheritable connective tissue diseases. an ENT, a gastroenterologist, a dentist, but it’s always Reddit that can solve a mystery. Please abide by the following rules in order to get an accurate answer to your question: (1) Ensure you include a title of your dental problem. It’s hypermobility that causes pain, stiffness, etc and some other symptoms but maybe doesn’t rise to the level of fitting the specific hEDS criteria. I'm working on my back flexibility so I'm getting into this type of position more often, and I'd like to do something about it. unsure how easy this is for ppl who aren't hypermobile) Forcing herself to vomit, even when her stomach She taught me to use a ball and a cane to help release tight muscles instead. The hypermobility type has no definitive test, so if your only complaint is hypermobility without dislocations or excruciating pain they will just brush it off. I'm in my late 30s and still very flexible, but nowhere near as much as My husband has ADHD. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Pediatric dentist here. He treated me last year but the problem keeps coming back. " hypermobility typically has more to do with joints and ligaments. But since the tongue is not the only possible culprit, they may not help in all cases. This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. Edit to Your elbows hyperextending means you do not do your full range of motion. View community ranking In the Top 5% of largest communities on Reddit. I'm hypermobile (all joints woo) and yeah the right alignment and muscle engagement is more important than how the pose looks. It's this like organ or tissue that has lots of ridges and "flaps. Check your beighton score to see if you're hypermobile. Does the headache increase after a meal? Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Reddit's best place for all things yoga. My tongue and skin inside the mouth was way more sensitive and damaged easily. There are no rules past the regular reddit rules. My fingers, wrists, and hands are very hypermobile. The only ones who annoy us are the ones that are anti x ray and fluoride. You might find high-impact sports like running painful, so something low impact, like cycling or swimming, might be easier. Really the only treatment for hypermobile EDS is physiotherapy, which isn't covered under OHIP. A place for those diagnosed with, or seeking diagnosis of, Hypermobile Ehlers-Danlos Syndrome. I am hypermobile, have been teaching for over 20 years, and have joint issues that have become worse over time due to View community ranking In the Top 1% of largest communities on Reddit. In some special cases, a different hand frame/position may be required for extremely hypermobile joints in the left hand. All I found was a thing called Khecarī mudrā which is like a weird monk practice that involves cutting your tongue Hi, in 17 and have been in constant pain for over half a year, because i didnt excersice during the first part of covid, i have mild hypermobility, although it is difficult for me to walk sometimes (longer than ten minutes) im currently getting it checked out by a doctor, but was wondering about excercise/pain relief methods for my knees, so Everyone with EDS is hypermobile but not everyone who is hypermobile has EDS. Please ignore that this is about mewing. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming View community ranking In the Top 10% of largest communities on Reddit. It’s almost like my tongue got super dry and damaged. My fingers have done this since I was a kid, my hips slip in and out easily, and since right before I turned 30, I started having problems with my hip and sacrum movements. I have hypermobile ankles, elbows (substantially worse than the picture), wrists and had shoulders. I can bend my fingers back, pull This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. You keep you tongue on the roof of your mouth to stabilize the joints, and you go only as wide as you can w/o pain or noise from the joint. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and Any general bodily hypermobility or fragility of tissues could, therefore, upset the smooth working of the voice by making these movements more difficult or by the tissues of the voice box becoming more easily inflamed. also learning kettlebells really helped with my proprioception and its something i highly recommend. Connective tissue issues seems to have an important role. This was SO HARD! My PT wanted me to do it like 6 A place for those diagnosed with, or seeking diagnosis of, Hypermobile Ehlers-Danlos Syndrome. I would be careful training full contact sports and tell your trainers so they can adjust your workouts and routines. Because it's murder for me. Enjoy! Hypermobile Tongue (anyone else) and A place for those diagnosed with, or seeking diagnosis of, Hypermobile Ehlers-Danlos Syndrome. you can look up he diagnostic criteria and go through it - it involves skin symptoms like scarring, heart problems, whether you've had any hernias, the colour of your eyes- these other symptoms are what show it's EDS and not just hypermobility. . Wish I had a picture of the face my dentist made when I surprised him. Also how you swallow, you might be swallowing air too. However, if your shoulders are dislocating, stop right now and go see a physio. I know it probably won’t make a difference, but I had to say that. It manifests as hypermobile joints and affects every organ system because we’re all made of connective tissue! We welcome all EDS subtypes, hypermobility spectrum disorder, Loeys Dietz, unnamed genetic disorders that present like EDS, self Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming I had my tongue pierced back in the day. It is possible that you could have hEDS since you are Hypermobile. I've been practicing yoga for over 2 years now, and I'm just now working on my hypermobility issues. Verified professionals will have flair assigned to them. Flossing on the other hand, absolutely notice better breath. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming How rare is it to be able to touch your naval canal with your tongue through the inside of your mouth? I couldn't find much online about how likely it is to be able to do this. Not sure what you are saying here. google valery fedorenko for the best technique Since February-present the jaw has progressively worsened and started to pop on the left side, ears began to ring and pop, tongue has began to go to the right side, causing me to bite it, teeth began to crowd, have periods of difficulty flexibility is mostly about a muscle's ability to relax and "stretch. Stretching the muscles, with the joints in a normal range, is To your point B - hypermobility syndrome isn’t “just” hypermobility. Joint/bone pain (all over), subluxations and/or dislocations are very common, swelling/injuries (from basic activities), bruising, pain from normal daily things like just walking, being abnormally flexible, having stretchy skin (try to compare to someone else to see, can check the back of your hand Escaping from handcuffs is easy (apparently Houdini may have had hypermobility?) Great at violin since our hands can hyperextend to hit all crazy fingerings (back when my neck would still let me play. now a year later im floatin like a butterfly. These signs in EDS are often poorly recognized As a subgroup (classic and hypermobile), the sensitivities of the absence of the inferior labial frenulum was 42% and 53. 20 votes, 40 comments. It sucks. someone with very flexible hamstrings can easily get their palms flat on the floor but u/Chryssi_OwO. This is the anatomical proper tongue posture and that's how to swallow properly, with the back of the tongue ADHD and hypermobility are common in long covid in kids. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Reddit iOS Reddit Android Reddit Premium About Reddit Advertise Blog Careers Press. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming My elbows are hypermobile, which causes me discomfort in positions where I'm putting a lot of weight on them. While it may not be as efficient as a pull ups, you can still use your back to lift instead of pushing from the floor. Collagen defects cause problems for mouth health including blood vessels, bone, teeth, gum tissue, nerve tissue, as well as the tendons and ligaments that retain facial/jaw structures in position. Figure 1 Open wide This might be long, but I'll start with this: How many of you are hypermobile? How many of you would pass the the Beighton test below? Pictures in the link. I now have crowns on most of my front teeth because I clacked it on my teeth too much. i am 34, 135lbs and i don't snore or gasp at night so all the usual big signs didn't fit. cause I guess a level of gut dysbiosis and potentially an underlying predisposition to MCAS due to potentially being hypermobile. it means that its too large for your mouth and is pressing against your teeth. That sort of work would be physically demanding for even a non-zebra. If you were my student I’d suggest active stretches to History: hypermobile ehlers-Danlos, POTS, ADHD, low IgA, chronic urticaria, IBS-C, chronic migraine, TMJ arthritis, frequent UTIs, GAD/bulemia ~10 years ago (no longer an issue) Surgical history: tonsillectomy 2022 due to frequent infections. I am double-jointed, have hypermobility including in my fingers, struggled with the collapsing pinky problem, played Schradieck, did some strengthening exercises (I don't think these are a good idea, fwiw, can be very dangerous and damaging to your fingers, and I didn't spend a large amount of time on them), but still had iffy intonation with my fourth finger. I’m a bit hypermobile and our child is clearly hypermobile and they have rheumatoid arthritis. Apparently allot of swimmers and cyclists are hypermobile. This is the most common sub-type of Ehlers-Danlos, which is a rare (probably not so rare) genetic condition that affects collagen made in the body. He also has a high-arched palate and a tongue tie (tight frenulum- so his tongue is pulled back further, can't stick out as far which we were told often causes high palate) Our daughter who is 7 has all of the same mouth traits and I would imagine could get an adhd diagnosis although we haven't had her formally assessed. but when i got a sleep test done i have View community ranking In the Top 5% of largest communities on Reddit. In terms of managing hypermobility, if you like your chiropractor, stay with them because a lot of chiropractors tend to be quacks. The roof of the sinus and back of your throat does dry out mucus just like your nose. I’ve had what looks like “lie bumps” or transient lingual papillae inflammation and a sore throat for almost two months now. My posture is terrible - but I These are sounds you don't hear in English and, oddly enough, you don't hear them when people speak in tongues. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Flexibility and hypermobility are not the same thing. Speaking as someone with hypermobility and am a personal trainer (who ended up focusing on mobility and movement quality because of hypermobility!)-- I am generally against the camp of "just don't ever hyperextend" because that's . buttercup” which Thanks for letting me know! And yeah I think that my MTD is partially a result of muscles becoming overly tight bc everything is so loose. I believe that the tongue tie developed due to the connective tissue disorder. I also have a hypermobile tongue so I wonder if it’s related, especially since the tongue is attached to the hyoid bone. Initially, I often felt painful my pinky as it is always locked so I had always tried curling it Skip to main content. I was born without a lingual frenulum (that little skin under your tongue) and rather than having a long one which causes people to be "tongue tied" my tongue is always in the way and caused me to have an open bite, deemed unfixable, since it is too long I got my tongue pierced 4 days ago, the healing is going well, im using mouthwash two times a day. Also hypermobility can be a symptom of other conditions other than EDS. For this (and typically JHS too, though it can be harder to test in a child so if you were diagnosed with it a long time ago it may or may not still be an accurate diagnosis Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. I can do the touching hands behind your back thing, thumb to forearm as well but I have to force it a bit, my elbows bend quite a bit further than they should, I think I can subluxate my shoulders, I can touch my elbows behind my back, I can put my thumbs on the backside of my hand (if that makes sense), etc. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming It manifests as hypermobile joints and affects every organ system because we’re all made of connective tissue! We welcome all EDS subtypes, hypermobility spectrum disorder, Loeys Dietz, unnamed genetic disorders that present like EDS, self-diagnosed & suspected zebras. I have a smaller mouth so it’s particularly hard for me to really how bad your hypermobility is doesn't relate to whether you have EDS or not. Up to 20% of the adult population and up to 50% of kids in the population are thought to be hypermobile. Ten months later I was diagnosed with Reactive Arthritis aka Spondyloarthritis. I’m not a doctor but it’s worth thinking about. I have a hypermobile tongue. It’s also common to see things like dysautonomia (like POTS), MCAS, gastric dysmotility, and autoimmune conditions. It was like the tongue tie was pulling all the connective tissue in my neck and shoulders into the tongue and creating chronic tension. It’s so weird. The oral mucosa may be thin, easily tear and give rise to Mouth and jaw symptoms have been observed in all types of EDS patients. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. Slightly augmented taste and dry mouth as well. Enjoy! Hypermobile Tongue (anyone else) and Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming yes! talk to a doctor about sleep apnea! my doctor said it's a good indicator that it may be an issue if your tongue is scalloped. The diagnosis is based on such clinical findings as hyperelastic skin and hypermobile joints. Have you gone through the checklist? Here it is: https://www. reReddit: Top posts of 1. Don’t like to judge them. I have hypermobile fingers in both of my hands, have been playing piano for 7 years and I can just play Turkish March properly. The only good thing about hypermobility I can come up with is flexibility but are there some other pros that I just haven't considered? Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming I am not sure why it worked but the tongue is the end point of the fascia/connective tissue in the body. I don’t know if those people who practice yoga for years just do stretches. However, there is a lot more to it than hypermobility. It means you need to be careful not to hyperextend - it increases wear on your joints. Also 1000% boost your immune system. ) Can't actually lick my nose though, which is a real bummer. Also - hypermobility can be associated with faster labors. Hi guys so basically i got hypermobile elbows (naturally from birth) and I noticed when i try to do planche progressions or planche leans It always puts a lot of pressure on the outside of my wrist at the forearm bone (the ulna) and Im thinking this is due to the fact that my angle is more extreme than most people's as you can see by the Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming u/Slight_Agency_2371. Scan this QR code to download the app now Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming I have a hypermobile right thumb but it hasn't really affected me too much. Need some advice for hypermobile fingers problem . by haternation *Not seeking medical advice—Every time I eat, my tongue tingles after. Take a look at resources for hypermobile yogis. There are definitely people who have perfect teeth, perfect bite, don’t accumulate plaque as readily as others. You might press your teeth or/and tongue at night or during the day. That pain sucks the most because you have to use your hands for nearly everything! I started seeing an orthopedic hand surgeon a Practicing yoga should help with hypermobility, but you just need to ensure that you're never resting in your joints. Allergies and food intolerances could cause it as well. " I don't even know. Do hypermobile folks need to stretch after exercise? This may be a dumb question, but is it still important to stretch before/after exercise if you’re hypermobile? Hypermobility exists in varying degrees throughout your body. I had it nine years ago when I was under enormous stress. I loved my piercings, but the tongue and labret piercings caused a lot of dental bills. I’m stuck with inflamed papillae on the tongue and sides, with a white coating on top—doesn’t seem to be candida. You can be very naturally flexible and not hypermobile. I've read allot about this hypermobility stemming from Ehlers-Danlos syndrome. I mean, when I try to stretch, it feels like my leg is shaking. I've also abandoned overhead pushing and pulling Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming The tongue appeared to be of normal size and position and the lingual fraenum was normal but stretchable, a condition that has been called idiopathic hypermobile tongue. Hypermobile tongue (touching tongue to nose), bent fingers, While mine may be caused by hypermobility, these tips still do help for non-hypermobile people. Waving hello with my own cold purpley hand. Skip to main content. The key, as with most adjustments for hypermobility and playing in general, is to avoid excess tension and embrace a relaxed, but controlled, approach. 5% for the lingual frenulum with specificities of 99% Turkish man who could pass the tip of his tongue beyond the uvula and into his nasal cavity to clear nasal secretions [1]. So, this means that people who speak in tongues in a primarily English speaking country will sound different from those who speak in tongues in a country that speaks Spanish and both will sound different from Slavic language countries. The exercises increase the muscle tone in the tongue, the lack of which tone is a frequent cause of apneas. dont worry about this, i was the same way, stiff and inflexible, couldnt position my body the way i wanted. I also can feel this weird like accordion file feeling thing. It's easy to force yourself into something that looks correct but is actually stretching the joints (bad). It’s not uncomfortable or painful, and happens the most with sugars or stevia. As for examples of hypermobile people in sports I could not find much. Just something to look into. Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming I’d lay down at night and my feet (hypermobile with the high arch that flattens with any pressure) and hips (which I didn’t realize had a deformity) would just scream at me. So I have been told that I have hypermobility, but I don’t have any sort of diagnosis for it, I hope that’s okay. Regular stretching is important, as is regular exercise/movement. 1K subscribers in the hypermobileEDS community. And I get regular messages from reddit cares because a concerned redditor reported me. Check the beighton test and other main symptoms. There are many different causes of hypermobility, some completely benign. Healed with a small contracture that did not require revision. Hypermobile tongue means that your tongue moves to much more extend than non eds people. Ear-related difficulties such as recurrent infections, reduced function and effectiveness of the jaw, oral soreness and dental pain can all reduce our ability to maintain clear speech, creating difficulties with voice, chewing, speaking and The tongue appeared to be of normal size and position and the lingual fraenum was normal but stretchable, a condition that has been called idiopathic hypermobile tongue. For any movement that you can do that is Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Agree with this. Im hypermobile and I truly wish that I didn't have this. 10 votes, 18 comments. This Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Welcome to /r/Hypermobility, a supportive and empowering community for individuals on the clinical joint hypermobility spectrum! Whether you've been formally diagnosed with a hypermobility syndrome or not, this community is here for you to find accurate information, tips and support for how to best manage (and maybe even thrive!) with your condition, and a welcoming Everyone is different, but when I go for max weight, that's when I really wreck myself. I currently do this as an impulsive behavior (BFRB - kind of out of my control). I had no idea this was associated with eds at all. Search around for teachers and ask about their experience with students with hEDS (hypermobile Ehlers-Danlos). Benign hypermobility is just a quirk, not necessarily a disorder and like 25% of the population has it to some degree. "How Reddit Helped Me Fight Long Covid" - wrote an essay about this sub, you guys have helped me through 2 years of LC. It's gross, but very useful. rwucjs kopw vfxenk kdrz uwtc rshsdwzd widu ramc qft urtsw