OpenHealth Q&A

Get answered by medical professionals

Persistent Discomfort: My Ongoing Hyoid Bone Issues

2/5/2026, 5:20:40 AMMale25-34

Summary: As a 32-year-old female, I've been struggling with an abnormal hyoid bone that pops during swallowing and neck movements, leading to persistent discomfort and disruption in my daily life. Despite exploring various treatment options, I find myself at a loss and am seeking advice. In 2019, I awoke to a troubling issue: my hyoid bone started to act erratically. Each time I swallow or move my head, a popping sound emerges, occurring on both sides of my neck. It feels as if the hyoid is colliding with surrounding structures, and at times, this leads to excruciating pain, particularly when it's pinched. For instance, such a pinch can generate sharp, intense sensations radiating through my face, neck, and chest, lasting for days. Choking episodes while eating or even swallowing saliva are frequent, especially when my head is in motion. Additionally, the muscles around my hyoid are consistently swollen and tender, while my neck remains stiff and sore. Even during sleep, I experience choking that wakes me up coughing and gasping for breath. The discomfort makes resting difficult because the pressure from lying down exacerbates the misalignment of my hyoid. The only position that somewhat alleviates the popping is looking upwards and tilting my chin back, though it still happens occasionally. Others can feel the popping sensation by gently pressing on my throat as I swallow, yet I cannot reposition it or alleviate the issue, even temporarily. I have consulted numerous specialists, including ENT doctors, orthopedic professionals, physical therapists, and massage therapists. Thankfully, we ruled out various injuries and conditions, including Eagle’s syndrome, and all blood tests have come back normal. One ENT suggested that the problem would resolve itself naturally, but it hasn’t; the popping is incessant. Another physician advised that I would need to learn to cope with it. While that might be true, managing the unrelenting pain and choking episodes is daunting. Unfortunately, many health professionals appear unsure about addressing this concern. I’ve found some temporary relief through methods like massages, ibuprofen, lidocaine patches, and muscle relaxants, yet none eliminate the popping itself. Eventually, I was referred to an ENT with expertise in this area. He indicated that my problem might stem from injury, weight changes, or age, and noted that my hyoid bone is slightly longer than average, although he doubted this was a primary factor. He mentioned the possibility of shaving it down, but raised concerns about it potentially worsening my swallowing issues, so I declined that route. He attempted steroid injections into the hyoid muscles to reduce inflammation and pain, claiming some patients experience lasting relief. Unfortunately, I did not find success, as the negative side effects outweighed any benefits. Although he recommended physical therapy, which I have been pursuing, the relief achieved has only been fleeting. One physical therapist even told me I have a low threshold for discomfort, suggesting that everyone feels some pain as they age, which is frustrating to hear. I feel as though I’ve exhausted all options, and the situation is driving me to the brink. With every year that passes, my quality of life and financial situation seem to deteriorate due to this ailment. I’m reaching out to see if anyone on Reddit has faced similar experiences and what has worked for them. The posts I’ve encountered often link to conditions like hypermobility, Ehlers-Danlos syndrome (EDS), or TMJ disorders, which is why I’m seeking input from these communities. Has anyone experienced similar popping? Were you able to find relief? I appreciate any advice or recommendations. Additional Information: I have several friends diagnosed with EDS, prompting discussions with my primary care doctor. After performing the Brighton test, I received a score of 2, leading us to believe that EDS is not the underlying issue. While I can effortlessly bend my thumbs to my forearm, my joints generally do not hyperextend, and I have never been able to touch my toes, even during my childhood or while participating in competitive sports. Stiffness and a lack of flexibility have always characterized my physicality. However, I can partially dislocate my wrists and ankles, and although my left side is more affected, I can do this at will depending on how pressure is applied. A few years back, I sought medical attention due to frequent tripping, and I remember a training PA exclaiming how loose my joints felt, much to the dismay of his supervisor. I can also pop my wrists and elbows, similar to cracking knuckles, and there is slight laxity in my elbows, noticeable mostly when I shake my arms. In childhood, I could move my kneecap freely, but as I matured, the discomfort made me stop, and it seems some of that earlier laxity has diminished, though I can still pop my kneecap. I had a cousin with EDS, but I understand the significance of genetics is not absolute. Additionally, I grapple with idiopathic hypersomnia, diagnosed in 2012, which I likely had for much longer. Initially labeled as borderline narcolepsy type 2, it’s now more accurately diagnosed as idiopathic hypersomnia. I tend to react oddly to medications, experiencing various side effects. Stimulants, whether from coffee, tea, or prescribed medications, fail to have any effect, only causing headaches and dizziness. I also have a history of waking during routine medical procedures that required anesthesia. Sleep-related issues also include grinding my teeth, a habit I've had since childhood. While the popping does not seem linked directly to this habit, there are flare-ups of both conditions independent of each other. Yet, when my jaw is particularly tight from grinding, the pops are noticeably more painful. This connection has been addressed with all my ENTs and sleep specialists, yet none show concern about its contribution to my current issues.

LupusFibromyalgiaEndocrinology

Answers (1)

Cony

2/5/2026, 5:21:06 AM

OpenHealth AI

The discomfort you're experiencing with your hyoid bone, including symptoms like popping, pain, and choking, sounds very challenging and understandably affects your quality of life. It's commendable that you've sought various specialists and treatments. Since you're seeking advice, let's focus on manageable steps to alleviate some of your discomfort while considering your diagnosed issues and overall health.

Main Points

  1. Manage Muscle Tension: Address the muscle strain around the hyoid.
  2. Explore Physical Therapy Techniques: Specific exercises or therapies may further help.
  3. Consider Sleep Positioning: Improve sleep hygiene to minimize choking and discomfort.

Explanation

The popping and discomfort around the hyoid bone can be related to muscle tension, structural irregularities, or issues like TMJ, which you've already touched on. The popping sound itself can stem from interactions with nearby muscular and connective structures. Your chronic pain and hypersomnia complicate the situation but also guide your self-care approach.

Given your symptoms, it’s crucial to focus on relieving muscle tension, which can exacerbate the popping and pain. Additionally, considering adaptations in your daily routine and sleep environment can help mitigate choking and pain episodes.

Next Steps

  1. Muscle Relaxation:

    • Heat Therapy: Apply a warm compress to the neck region before bed to relax muscles.
    • Gentle Stretching: Incorporate gentle neck stretches into your routine (e.g., tilting your head slowly side to side) to enhance flexibility without causing pain.
  2. Targeted Physical Therapy:

    • Discuss specific modalities with your physical therapist, such as myofascial release or dry needling. These techniques might provide deeper relief.
    • Investigate techniques like craniosacral therapy, which some individuals find helpful for resolving chronic tension.
  3. Sleep Hygiene Adjustments:

    • Repositioning: Experiment with sleep positions to minimize pressure on your neck (consider using a specialized neck pillow).
    • Stay Elevated: Keep your upper body elevated with pillows to alleviate choking during sleep.
  4. Jaw and Neck Care:

    • If you notice more pain correlating with teeth grinding, consult with a dentist about a nighttime bite guard. It can help reduce tension in your jaw that may lead to increased discomfort.
  5. Mindfulness and Relaxation Techniques:

    • Explore practices like deep breathing, meditation, or gentle yoga to manage pain perception and reduce stress-related muscle tension.

While you've encountered many challenges, adjusting your overall approach to managing symptoms could yield some relief. It's essential to keep an ongoing dialogue with your healthcare team about any new techniques you are trying and how they impact your overall situation. Please let me know if you would like further details on any of these suggestions.

Related Questions

Concerns About Oily Urine

Hello, I’m a 17-year-old female, standing at 4'11". I maintain a healthy lifestyle—no smoking or alcohol consumption, and I don’t take any medications. I’ve recently noticed that my urine appears oily when viewed in the toilet. To investigate, I collected a sample in a cup, and it didn’t have that same appearance. I feel completely fine otherwise, exhibiting no pain, fever, or unusual symptoms. My health anxiety is heightening my concerns over this issue. This oily appearance has persisted for about six weeks, and my anxious thoughts keep leading me to believe it could signify something serious. Some people have suggested conditions like diabetes, a urinary tract infection, or issues related to kidney function, but I have generally enjoyed good health throughout my life and my family has no history of kidney problems or diabetes. In October 2022, I experienced a urinary tract infection, which I treated with a week-long course of antibiotics, along with IV fluids and increased water intake. Recently, I sought emergency care because I developed an itchy rash on my chest that resembled hives. Medical professionals conducted a urine analysis and comprehensive blood tests, all of which yielded normal results. However, it was noted that there were traces of blood in my urine, leading them to suspect a recurrent UTI, and I was prescribed another seven-day course of antibiotics, which I completed. Coincidentally, I began my menstrual cycle the following day, so it’s uncertain whether the symptoms were related to the UTI or simply my period. Additionally, they ruled out sepsis during the tests, yet the cause of the rash remains undiscovered. If you have any insights or explanations for my oily urine, I would greatly appreciate your input. For more detailed information, you can find it linked below.

DiabetesHypertensionEndocrinology
Male25-34
18 minutes ago

Chronic Neck Pain in My 9-Month-Old Son

Hello, I’m reaching out about my son who turns nine months old in April and has been experiencing ongoing neck discomfort. He weighs 43 kg and measures 1.1 m in height. For quite some time now, he's been voicing concerns about pain in his neck. I consulted with a physician, and they inquired about whether his vision seemed affected or if he could identify a specific painful area, both of which he could not. The doctor suggested that his neck issues might stem from poor sleeping posture. Additionally, I've noticed that he tends to sweat excessively; he has been a heavy sweater since infancy. I'm curious if this sweating could be connected to his neck pain. Another observation is that he is somewhat overweight for his age.

ArthritisLupusCrohn's Disease
Male25-34
38 minutes ago

Seeking Guidance for My Ongoing Chronic Pain Condition

I'm reaching out for some advice on how to approach my new physician regarding a long-standing pain issue that's been challenging to manage. Here's what I'm hoping to gain: 1. Improved communication strategies to better articulate my symptoms and health concerns to my new doctor. 2. Recommendations on specific tests to request, along with potential diagnoses that may align with my experiences. **Background Information:** I’m a 23-year-old woman who has battled this condition since I was 13. The onset occurred during my middle school years when I dedicated extensive time to piano practice for my exams. Unfortunately, this led to persistent pain that diminished my ability to use my hands effectively; I vividly remember months when gripping a pencil was impossible. For approximately six years, this pattern dominated my life—I would initially practice vigorously and then suffer from debilitating hand pain. Whenever I consulted a physician, their advice was primarily about resting more, which provided minimal relief. Furthermore, my experience with healthcare providers has been frustrating; it appears that they frequently leave practice shortly after beginning to treat me, leaving my condition inadequately monitored. Over time, my situation has deteriorated, even though it has now been six years since I’ve played the piano. Initially, I experienced pain localized in both wrists, but it has since extended to my fingers, hands, elbows, and shoulders. **Core Symptoms:** - The pain is not constant. I've learned to navigate my daily activities carefully to minimize discomfort. This includes adjusting how I hold objects and alternating between my right and left hands to prevent strain. - Unexpected contact can trigger severe pain, reducing me to tears and, on bad days, confining me to bed due to the intensity of the sensation, rendering even minor movements unbearable. - To describe the pain, I liken it to a migraine in my arms or hands, as if there’s a solid piece of metal trying to wrench its way out of my arm. **Additional Symptoms Include:** - An aversion to having my back touched, a sensitivity that predates my wrist issues. It feels akin to an emotional disturbance rather than physical pain. - My skin doesn’t stretch properly; pinching it is nearly impossible. - Significant swelling often prevents me from comfortably wearing wrist braces, which I usually rely on. - While I can’t pop my back or crack my knuckles, my ankles click without issue. - Writing with a pencil is particularly painful whereas using whiteboards is more manageable. **Tests Conducted:** - X-rays revealed no abnormalities. - Nerve tests indicated no issues. - An ultrasound also showed nothing wrong. - I'm currently on a waiting list for an MRI, which may take 1-2 years. Given the timeline, I’m uncertain about remaining in this city, which complicates matters. - Recent blood tests (results are available in a comment) highlighted past liver enzyme concerns due to regular Tylenol use for pain relief. **Treatments Attempted:** - Acupuncture proved painful and ineffective. - Massage therapy was intolerable after just a few minutes. - Physiotherapy yielded no results and was excruciating. - Ultrasonic therapy produced no notable benefits but was painless. - Lidocaine injections provided remarkable relief for several months but are currently unavailable until I can access a new clinic, which might take a year. **Medications Tried:** - Gabapentin provided brief relief but lost effectiveness after a week. - Naproxen did not help and caused nausea. - Tylenol remains the most effective option but the maximum recommended dose no longer suffices to manage pain. - Voltaren’s effectiveness is limited, requiring excessive application to feel any effect. - Other medications, including Celecoxib and Nortriptyline, did not yield positive results and caused side effects like nausea and sadness. Currently, I rely solely on Tylenol, taking around 2 to 4 daily to help with inflammation. **Bonus Question:** Any suggestions on how to avoid appearing as though I'm seeking narcotics? I frequently find myself needing to explain my past treatments to new doctors, and it often leads to skepticism about my intentions. I appreciate any insights or advice you may be able to provide. It's disheartening when people warn me about the potential for my condition becoming permanent if I don't take action, yet I often feel unsupported in finding a resolution.

ArthritisFibromyalgiaInternal Medicine
Male25-34
58 minutes ago

Increasing Facial Numbness After Consuming Alcohol

Hello everyone, this is my first time contributing to this community, so I apologize if my post isn’t perfectly formatted. Whenever I consume alcohol, I (18, female) notice that my face begins to tingle, and eventually, it becomes completely numb. This troubling issue has only arisen in the past year, and I find it becoming more severe with each drink. I consider myself a lightweight when it comes to drinking, as I rarely indulge and don’t spend much on alcohol; I’ve only ever had a maximum of two shots of tequila at one time, usually during special occasions about once or twice every three months. In terms of my health, I’m generally well, aside from experiencing migraines occasionally, for which I take almotriptan. These headaches are triggered by straining my eyes, and I have prescribed glasses that I seldom wear, mostly because my migraines aren’t frequent enough to warrant it. However, when they do occur, they are quite severe. The reason I’m reaching out is that I’m uncertain whether I should be concerned enough to contact my general practitioner. I don’t want to waste anyone’s time over something that might seem trivial, but I’m seeking advice from those who might have more knowledge or expertise. I’m usually skeptical about the information I find on the internet. If anyone could offer reassurance or insight about whether this is a rare occurrence or a potential symptom, I would greatly appreciate it. Thank you for your help! 😭

Multiple SclerosisLupusCrohn's Disease
Male25-34
2 hours ago

Hand Bumps Concern?

At 16 years old, standing about 5 feet 6 inches tall and weighing approximately 80 kg, I’ve encountered a troubling issue: two nights ago, I noticed an unusual series of red bumps on my right hand. They feel exceptionally dry and tend to burn. Recently, I’ve observed a minor amount of similar bumps appearing on my left hand within the last 12 hours. The discomfort in my right hand has been intermittent; it seemed to improve, but then suddenly flared up again. I’ve been taking Epuris since November to manage hormonal acne, yet I’ve never experienced anything like this before. Although I have PCOS, I’m unsure how it ties into this situation. Initially, I suspected it could be an allergic reaction, but my diet and daily habits have remained unchanged. My parents did change laundry detergents, which made me consider that as a possible cause. However, the rash seems to be confined to my hands and doesn’t affect areas that are consistently in contact with clothing, leaving me puzzled about the source. My next appointment with the doctor is set for three weeks from now, but I’m worried this might be a serious condition. What should my next steps be?

LupusCrohn's DiseaseEndocrinology
Male25-34
2 hours ago