Intense Coccyx Pain While Sitting and Standing, Bowel Movement Modifications, and Tingling Sensations in Legs
I am a 24-year-old woman who occasionally uses an albuterol inhaler for my asthma, and I don't have any other medical issues. I have not experienced any injuries or falls. Approximately 8 to 9 months ago, I began to notice significant pain in my tailbone, which has progressively worsened to the extent that sitting has become impossible. Additionally, standing has also become increasingly uncomfortable. Lying flat on my back is quite painful, as is leaning forward when seated. Along with the tailbone discomfort, I'm feeling a tingling sensation in both of my legs and have observed alterations in my bowel habits. I previously had no problems with diarrhea, but for the last three months, I have been facing diarrhea about 90% of the time. Despite trying various remedies, the coccyx pain remains unaffected by adjustments to my posture, applying a heating pad, taking 800mg of ibuprofen, and experimenting with numerous types of cushions. None of these interventions provide any relief. I have scheduled an appointment with a healthcare provider, but the earliest slot available is next month. Therefore, I am seeking advice in this forum. I am contemplating requesting an MRI as a precautionary measure to exclude any serious underlying conditions.
Answers (1)

8/16/2025, 5:21:06 PM
OpenHealth AI
It sounds like you're experiencing significant discomfort and distress due to your coccyx pain and other associated symptoms. Your concerns, particularly around the worsening pain and changes in your bowel habits, are very valid, and I appreciate your proactive approach in seeking relief.
Main Points:
- Persistent coccyx pain can result from various causes, including inflammation, muscle tightness, or referred pain from other areas.
- The tingling in your legs and bowel changes, especially diarrhea, require careful attention as they may indicate a related condition.
- An MRI may be a reasonable request to investigate further given your symptoms, but there are also immediate strategies you can try for relief.
Explanation:
Coccyx (tailbone) pain, known as coccydynia, can become exacerbated by prolonged sitting or positions that put stress on the tailbone. The fact that you're also experiencing tingling in your legs and changes in bowel habits can be concerning, as these could suggest issues involving nerve compression or other underlying conditions.
Next Steps:
-
Pain Management:
- While you mentioned that ibuprofen hasn’t helped much, consider alternating with acetaminophen as it might provide different effects.
- Look for a cushion designed specifically for coccyx pain, such as a “donut” or a wedge-shaped cushion that can relieve pressure on the tailbone.
- Continue using a heating pad; applying heat can sometimes reduce muscle tension and ease pain.
-
Physical Position Adjustments:
- While waiting for your appointment, try to adjust your sitting posture. When sitting, lean forward slightly to alleviate pressure on the tailbone.
- If possible, practice standing or lying in positions that minimize discomfort until you find relief.
-
Gentle Stretching and Mobility:
- Engage in gentle stretching exercises targeting the lower back and pelvic area to alleviate tightness that may contribute to discomfort.
- Pelvic floor exercises or yoga (specifically gentle poses) can also be beneficial and can help reduce tension in muscles surrounding the coccyx.
-
Track Your Symptoms:
- Keep a detailed diary of your symptoms, including when pain occurs, bowel patterns, and any activities that exacerbate or relieve your symptoms. This record will be useful for your healthcare provider when you do have your appointment.
-
Consider MRI Discussion:
- Prepare to discuss the possibility of an MRI with your healthcare provider, especially considering the leg tingling and bowel changes. While it’s good to be proactive, your provider will assess the necessity based on clinical evaluation.
Conclusion:
Your situation deserves attention, and while you wait for an appointment, focus on both immediate pain management and documenting your symptoms. Don't hesitate to reach out for help if your symptoms worsen or if new troubling symptoms arise, such as numbness, severe weakness, or changes in bladder function. Wishing you relief and hoping for answers soon!
Related Questions
Struggling with Persistent Postnasal Drip for Over Four Years – Seeking Answers
For more than four years, I have been tormented by relentless postnasal drip, and it has truly exhausted me. This ordeal began a few weeks prior to my initial experience with Covid (at least, the one I’m aware of), and it has lingered ever since. The sensation is perpetually the same: mucus accumulates consistently in the back of my throat and nose, necessitating constant swallowing and snorting. It’s a persistent issue that I endure throughout the day. While it’s annoying during waking hours, nighttime transforms it into a distressing situation. I find it challenging to fall asleep as I can feel mucus collecting, and occasionally, I wake up gasping, as though my airways are obstructed. There are moments when it takes me several seconds to recover my breath, during which my heart races so intensely that I fear I might collapse. On numerous occasions, I have experienced panic attacks during the night as a direct result. I genuinely cannot recall the last time I experienced restful sleep. I suspect sleep apnea as a possibility, but primarily due to the postnasal drip; on nights when the issue is less severe, I manage to sleep reasonably well. I’ve consulted countless medical professionals, including several ENT specialists, allergists, and head and neck experts. I’ve attempted various treatments: medications for reflux, allergy drugs, immunotherapy (even undergoing Odactra for almost a year), steroid nasal rinses, inhalers, antibiotics, septoplasty with turbinate reduction, and the RhinAer procedure among others. I’ve undergone scans, scopes, and allergy evaluations (dust mites were identified, yet I don’t exhibit any allergy symptoms apart from the postnasal drip). Unfortunately, nothing has proven effective. Having visited esteemed specialists in my area, my most recent doctor was candid with me, stating, “I’m at a loss as to how to assist you.” After years of experimenting with different therapies, medical interventions, and adjustments to my daily habits, I find myself no closer to a solution. The nighttime episodes, in particular, are increasingly concerning, leading me to believe that the situation could become perilous. I am yearning for any kind of insight. Since this began, I have lived in two distinct apartment buildings in New York City, which suggests that my immediate surroundings may not be the culprit. Could this condition be related to emerging issues that medical professionals have yet to identify? Might it be tied to lingering effects of Covid? Has anyone faced a similar struggle? If so, was there an effective solution for you?
Ongoing Symptoms Post-Stroke Despite Normal Imaging Results
A 68-year-old male, standing at 6'3" and weighing 180 pounds, presents a complex medical history. He has a history of atrial fibrillation for which he underwent ablation therapy. He also has benign prostatic hyperplasia and is scheduled for surgery soon. His history includes five transient ischemic attacks (TIAs) and two strokes, yet all imaging, including CT angiography of the carotids, appeared normal, aside from a previous mention of a lacunar infarct that has not been referenced in subsequent evaluations. Currently, he is on medications including Apixaban, Rosuvastatin, and Tamsulosin. A significant event occurred a few months back when he experienced sepsis following a prostate biopsy. The patient has noted instability upon standing from a seated position, often veering to the right. Despite this, he maintains an active lifestyle, playing golf three times weekly, adheres to a healthy diet, abstains from alcohol, and is averse to smoking, although he uses a vape. My husband continues to face challenges following his latest TIA/stroke. He frequently experiences persistent symptoms including weakness on the left side, slowness in speech, and difficulty retrieving words—although he describes being able to visualize them mentally, verbalizing them proves challenging. This TIA occurred merely weeks after he recovered from the sepsis episode. While he is capable of walking and communicating and seems generally well, he struggles with significant left arm weakness and discomfort when lifting. Additionally, there are signs of muscle wasting, particularly in the upper arm. Fatigue is a constant issue, and unless he takes a nap, his speech difficulties tend to resurface; however, he feels better after resting. Yesterday, we spent considerable time in the emergency department where blood tests, an ECG, and a CT scan were conducted, all returning normal results. An MRI of the head and neck was performed too, but the outcomes will be available on Monday. Depending on those results, a referral might be necessary to a stroke clinic or further to neurology. We would greatly appreciate any insights or recommendations regarding potential inquiries we should make or additional tests that might be needed. Thank you for your time and consideration!
Is This Multiple Sclerosis?
At 41 years old and female, I've been facing a range of neurological issues for nearly a decade, particularly after suffering a severe bout with mono. Initially, my symptoms were manageable fatigue, soon followed by episodes of dizziness. As time progressed, I noticed persistent discomfort in my joints accompanied by stiffness that would fluctuate, lasting anywhere from several days to weeks. After consulting a rheumatologist multiple times, the results came back normal, with no apparent problems in my joints or any signs of autoimmune disorders. It wasn’t until I stumbled upon gabapentin that I discovered it alleviated the peculiar pain I was experiencing — a shooting sensation that seemed to travel among various joints in my body. Moreover, since the onset of COVID, I have been intermittently grappling with a discomfort I associate with my gallbladder; however, this pain does not align with the traditional symptoms of gallstones nor is it related to my diet. Interestingly, despite having a gallstone, gabapentin has also managed to relieve that pain, even when it escalated to a level so intense I believed it was constricting my rib cage. More recently, I've started experiencing tingling sensations in my right arm, coupled with a burning feeling on the surface of my hands. I underwent an MRI recently and noticed some lesions present. While I'm not necessarily convinced they indicate multiple sclerosis, I am curious about others' thoughts on this matter.
Need Advice on Shin Hematoma
I am a 21-year-old female who experienced a blow to my shin while playing football last Sunday, resulting in a hematoma due to not wearing shin guards. The very next day, I consulted my doctor, who recommended following R.I.C.E. (Rest, Ice, Compression, Elevation) alongside a course of medications: 1. Enzoflam 2. Phlogam 3. Pantodac 4. Limcee 5. Cissqplus I was instructed to take the first three medications over five days, while the other two supplements were to be taken for a fortnight. This consultation took place on Monday. By Thursday, I noticed some new redness and bruising that had not appeared initially, necessitating a follow-up visit. During this appointment, my doctor prescribed: 1. Ceftum 500mg 2. Oflin 200mg 3. Vizylac Initially, my foot had swollen significantly due to the injury, but thankfully, the swelling has reduced, and my ankles have returned to their normal state—though a few bruises remain. The concern now is that as the swelling has diminished, the hematoma has become much more noticeable, resembling the size of a tennis ball, which is quite alarming. I cannot meet with my doctor until tomorrow, but the anxiety this situation brings is overwhelming. Is there a cause for concern, or should I allow time for healing? Importantly, I have not observed any signs of infection, as there have been no new areas of redness, and the hematoma does not exhibit warmth.
Seeking Support for My Toddler's Ongoing Health Challenges
Hello everyone, I'm reaching out for advice regarding my two-year-old daughter (born in August 2021). We have been navigating a complex health journey, and I am in search of recommendations for the next steps we can take. ### Key Concerns: - She has experienced itchiness since she was an infant. - At the age of one, we were advised to eliminate dairy from her diet; this made a significant improvement in her itching, yet other issues persist. - She continues to use a specialized formula for Cow's Milk Protein Allergy (CMPA) to ensure she receives adequate vitamins. - Her diet remains rather simple, consisting mainly of boiled chicken, eggs, rice, oats, zucchini, carrots, salmon, blueberries, and bananas. - She is very small, weighing under 20 pounds at two years old and has to wear clothing sized for 6-12 month olds. - I also have twin six-month-old babies who are exhibiting similar growth concerns; they each weigh only 12 pounds and are exclusively breastfed. I am on a diet free of soy and dairy. - I feel desperate, as I'm struggling to find a doctor who is committed to solving this complicated situation. ### Observed Food Reactions: - She seems to be allergic or intolerant to several foods, including strawberries, mangoes, coconut, cashew, pistachio, and dairy (both casein and whey), even reacting to things like salami. - She is sensitive to gas-inducing foods like beans, which leads to severe bloating and discomfort. - Recently, after we flavored chicken by boiling it with onion, she had a severe reaction that included gas, restlessness, and diarrhea that night. - We have also noted reactions to mushrooms and sweet potatoes, leading to gas and undigested food in her stools. ### Current Symptoms: - She experiences frequent diarrhea, which can be watery and odorous, often containing undigested food. In her lifetime, I do not believe she has gone two consecutive days without diarrhea. - Her stomach discomfort—bloating and gas—can interrupt her sleep, especially after eating anything outside her core diet. - We are noticing ongoing reactions to foods with unpredictable triggers; introducing something new often results in diarrhea, gas, and sleepless nights. - Historically, she has been a very happy baby, and this change has been concerning as she has never exhibited colic-like symptoms. ### Testing Completed to Date: - We've conducted blood work, urine tests, and stool analyses, which have all come back mostly normal. - Stool tests indicated positive reducing sugars, which may suggest carbohydrate malabsorption. - A pancreatic elastase level of over 800 ruled out pancreatic insufficiency. - Calprotectin levels were below 50, indicating no inflammatory bowel disease. - Her thyroid, kidney, and liver functions were normal, and her IgE levels are within the standard range. - The neonatal metabolic screening at birth did not reveal any major metabolic disorders. - Five stool samples for parasitology returned negative results. - She has seen specialists, including a cardiologist, nephrologist, and endocrinologist, all of whom have reported normal findings. - A consistently high BUN/Creatinine ratio and slightly low globulin with a high A-G ratio have been noted, as well as moderately elevated Vitamin E levels. ### Current Situation: - We have already consulted two gastroenterologists, but both have dismissed her issues as merely a milk allergy. - We are contemplating asking for a biopsy to rule out eosinophilic gastrointestinal disease, as it appears there is an immune response at play—why does her body react negatively to virtually every new food introduced? ### Questions: - Given the combination of chronic diarrhea, numerous food reactions, and ongoing itchiness, should we consider this to be more aligned with allergies/immune issues, or might it indicate genetic/metabolic problems? - Is seeking a GI biopsy the next logical step? - Should we advocate for a broader allergy panel, and what would that entail? - If it were your child, what actions would you take next? I feel incredibly dismissed and aimless in this process. My main desire is to identify her condition accurately to alleviate her suffering and determine the right dietary solutions. We are currently focusing heavily on improving her gut health with a low FODMAP diet, probiotics, and various supplements.