OpenHealth Q&A

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Mental Health Questions

Three Months of Irregular Periods: Is This PCOS or Something More Serious?

I'm a 27-year-old woman, standing 6 feet tall and weighing approximately 200 pounds. I’ve previously experimented with medications like tranexamic acid and norethisterone, but they haven’t helped. I don’t smoke, and I only consume alcohol on a few occasions throughout the year. Now, let me explain my situation more clearly: I’ve always dealt with an unpredictable menstrual cycle, but things took a turn in November when I experienced excruciating cramps (it felt as if my insides were being constricted) followed by an exceptionally heavy menstrual flow. After that, the bleeding didn’t stop; it's been going on for three months now, occasionally fluctuating between light spotting and heavy flow. I’ve made several visits to my healthcare provider, and they've attempted to manage the bleeding with various treatments while an ultrasound has been scheduled. While I await further evaluation, I find my energy completely drained. I’ve suffered from persistent headaches for over a week, and despite my effort to stay hydrated by drinking plenty before bed, I wake up feeling parched. Recently, I’ve started taking iron supplements, yet I still experience bouts of lightheadedness, and my chest aches almost constantly. I realize these symptoms could stem from blood loss or hormonal imbalances, but as I search for temporary relief for my discomfort, I’m constantly confronted with alarming possibilities during my research, which heightens my anxiety as I wait for answers. It feels like I haven't been at ease for months. Additionally, being autistic complicates my experience further due to sensory sensitivities during my menstrual cycle, contributing to a feeling of impending dread about the situation, which I believe others would relate to. My family has also begun expressing concern over my persistent headaches and fatigue; I’m hoping to find comfort knowing that these experiences are not unusual. I suspect that polycystic ovary syndrome (PCOS) may play a role in what I’m experiencing, but the accumulation of these additional symptoms leads me to wonder if there are other conditions I should be vigilant about. Furthermore, I suffer from chronic inflammation, though the cause remains unidentified, and I endure episodes of back pain that can last for days. Occasionally, I feel sharp, shooting pains primarily in my thighs, but sometimes in my chest as well, typically lasting about a minute. I also have moments of tingling in my extremities, reminiscent of that pins-and-needles sensation. Although I don't believe these issues are connected, the combination of everything makes me increasingly anxious.

ADHDAnxietyDepression
Male25-34
34 minutes ago

How Can I Ensure My Healthcare Provider Listens to My Concerns?

As a 17-year-old female, I am grappling with several vitamin deficiencies, notably in Iron, Vitamin D, and Magnesium, among others. My health challenges extend beyond these deficiencies to include pre-diabetes, insulin resistance, polycystic ovary syndrome (PCOS), anemia, and significant struggles with severe depression and anxiety. The focus of this message is primarily on my Vitamin D deficiency, which is the most debilitating for me. A couple of months back, my doctor prescribed Drisdol to help elevate my vitamin levels. Based on my gynecologist’s recommendation, I opted for a six-week course instead of the twelve-week regimen. After completing the Drisdol treatment, I returned a few weeks later for blood tests, only to find out that my levels had risen by a mere six points. While an increase might appear substantial, my initial Vitamin D level was alarmingly low at 13 ng/ml, and it reached only 20 ng/ml post-treatment. The hospital’s standard range is 30-100 ng/ml, indicating I remain well below what is considered healthy. This testing took place in November, and I am uncertain if there have been any improvements since. I am curious about potential reasons for my low levels besides limited outdoor activity. My doctors seem inclined to prescribe medications or recommend solutions that have failed to yield results in the past, such as multivitamins. This situation is parallel with my iron levels; I've undergone multiple IV iron treatments just to bring those back to a barely acceptable range. I have another appointment with my primary care physician in two weeks, and my primary concern is how to communicate that I feel my concerns are not being taken seriously. My doctor has misdiagnosed me previously and has overlooked some of my symptoms. I genuinely want guidance on how to ensure that my struggles, which significantly disrupt my daily life and contribute to my mental health deterioration, are acknowledged and addressed.

PsychiatryAnxietyDepression
Male25-34
2 hours ago

Understanding Sepsis: A Personal Experience

I have been hospitalized twice due to urosepsis, resulting in kidney infections each time. During both incidents, the medical opinions regarding my diagnosis varied significantly. **First Incident:** During my initial hospitalization, I arrived at the emergency department with a fever exceeding 40 degrees Celsius that lasted for two days, accompanied by chills, low blood pressure, and a rapid heart rate. I was promptly administered IV antibiotics. The attending ED physician described my condition as serious, stating that I was experiencing 'septic blood' and told me I was fortunate to be receiving treatment. After spending approximately three to four days in the hospital, I later discussed my condition with my general practitioner. When I mentioned having sepsis, she chuckled and remarked, "You did not have sepsis; you were simply quite ill." **Second Incident, 18 Months Later:** In my second encounter, I returned to the emergency department with a moderate fever of 38 degrees Celsius for one day, along with chills, low blood pressure, and a fast heart rate. This time, a different physician informed me that there was a significant level of infection in my blood. I later learned that my white blood cell count was 22. When I inquired if this indicated that I had sepsis, he confirmed that it did. I was subsequently admitted for treatment. Today, during a follow-up with the discharge doctor, I sought clarification about my sepsis diagnosis once more. Unfortunately, he provided unclear responses, suggesting that a specific threshold must be met for the diagnosis. This inconsistency has left me perplexed. I would greatly appreciate any insights or explanations on this matter. Thank you!

PsychiatryPsychologyDepression
Male25-34
2 hours ago

Seeking Insights on My Distressing Symptoms

Hello, I’m a 22-year-old female grappling with some puzzling health issues. For the past several years, I’ve experienced a series of unusual symptoms, particularly whenever I rise early in the morning. While this wasn't a major concern during my school years, transitioning into the workforce has amplified the challenge significantly. The core issue emerges when I wake up between 5 a.m. and 9 a.m.; I find myself unable to engage in any activities that involve standing or moving around. The symptoms I encounter include: • Severe nausea that often leads to vomiting, alongside a relentless queasiness. • A pervasive sense of weakness. • Episodes of dizziness. • Occasional shaking. • Fluctuations in body temperature, feeling uncomfortably cold or hot. • There are moments when I feel faint, where my vision starts to fade. Fortunately, I’ve learned to drop into a squat when this occurs, which helps maintain my consciousness. These issues make fulfilling my job responsibilities exceedingly difficult, particularly since I have been limited to morning shifts lately. I have attempted various remedies to alleviate these symptoms, including adjusting my sleep patterns, experimenting with my diet (both increasing and decreasing food intake), trying nausea medication, and being more mindful of my overall nutrition. Regrettably, none of these strategies have yielded any significant improvement. It's important to mention that I do have some underlying health concerns; however, my physician has indicated that they are not serious enough to necessitate any urgent interventions. My medical history includes a bicuspid aortic valve, mild prolapse, orthostatic hypotension, and gastroesophageal reflux disease (GERD). The only medication I currently take is omeprazole for my GERD. At this juncture, I am open to any advice or suggestions, as my current state is quite debilitating. Any insights from those who may have experienced similar symptoms would be greatly appreciated.

InsomniaDepressionStress
Male25-34
4 hours ago

Suspecting an EBV Relapse? Need Insights!

Greetings everyone, I’m a 24-year-old female, and I realize that browsing Reddit for health issues might not be the wisest choice. Still, I find myself questioning whether I could possibly have Epstein-Barr Virus (EBV). Back in December, I experienced an unusual illness, characterized by a swollen lymph node on my right side and localized pain in the upper right part of my throat. The fever wasn’t extreme, peaking around 100°F, but I definitely dealt with chills and an overwhelming sense of fatigue, making even simple tasks feel like monumental challenges. There were a couple of nights when I felt nauseous enough to vomit a little, and diarrhea added to my discomfort. Before experiencing the vomiting and diarrhea, I consulted a doctor who attributed my symptoms to post-nasal drip, causing fluid to block my Eustachian tube. I was tested for both influenza strains and COVID-19, all returning negative results. The doctor concluded it was simply a cold. Fortunately, I recovered within a week. I know that some individuals have prolonged recoveries from mono, so I hesitated to get tested for EBV antibodies. Also, many of my coworkers were ill that same week, so I assumed I caught whatever bug was circulating. However, yesterday I woke up feeling congested, achy, and utterly exhausted, and I ended up vomiting once last night. Today has been spent mostly in bed, and although I feel slightly better now, I'm still quite fatigued. The reason I’m sharing this is that I can’t shake the feeling that my previous illness was more serious than just a common cold. The experience significantly impacted my mental well-being, heightening my anxiety surrounding my health, which I strive to protect against illness. Since that episode, I’ve felt quite off balance. I would appreciate any thoughts or insights on this! Thank you!

AnxietyDepressionStress
Male25-34
4 hours ago

Feeling Lost in My Health Journey: Seeking Understanding and Support

Age 29, weighing 268 lbs, and standing at 5'8", plus a history as a smoker. I've managed to eliminate alcohol, drugs, and fast food from my life in the past year. I have been diagnosed with Hashimoto's disease, resistant hypertension, and metabolic syndrome (MASH). Eighteen months ago, I encountered a significant health crisis that necessitated a five-day hospitalization. I underwent numerous tests including MRIs and CT scans, but all results returned as unremarkable, with no signs of tumors on the adrenal glands. My heart echo test was also clear. Following this, I was prescribed four medications for blood pressure and 150 mcg of levothyroxine, after which I felt stable for about six months. For half a year, I experienced no major issues, and my lab results showed a gradual return to normal ranges. Ten months back, I began experiencing symptoms associated with hyperthyroidism, including heart palpitations, heightened anxiety, and feelings of impending doom. Despite normal lab results—save for elevated ALT and AST levels—I was told my symptoms could be attributed to stress. An adjustment in my thyroid medication to 175 mcg ensued, and I felt stable for another five to six months. However, five months ago, the heart palpitations returned, with my heart rate spiking to 150 beats per minute while simply resting on the couch. My body was signaling a need for help, prompting immense fear and the sensation of shallow breathing. A trip to the emergency room led to lab tests showing a TSH of 0.03 and normal levels of T4 and T3. There were elevated white blood cell counts, specifically neutrophils, which my doctors attributed to a recent tattoo. They reviewed my previous scans, confirming that serious conditions had been ruled out, and I chose to return home rather than undergo further interventions. I was told I might be overmedicated for my thyroid condition and was given propranolol before being discharged. At my follow-up with my primary care provider, I was prescribed hydroxyzine for anxiety and underwent a ten-day washout period off levothyroxine. I resumed at 137 mcg for a week and, unfortunately, the hyper symptoms reappeared. After a three-day washout, I restarted at 75 mcg. Four weeks later, I found myself hypo, with a TSH jumping to 18. I sought ER care due to tingling in half of my body and a heart rate elevating into the 140s, suspecting I might be having a stroke. Thankfully, the doctors concluded it was anxiety. After adjusting to 88 mcg of levothyroxine, I hoped to stabilize my thyroid function further. In the last three months, I've experienced sporadic adrenaline rushes accompanied by mild palpitations; however, no significant additional symptoms arose. I've used propranolol occasionally, which helps, yet I strive to manage without it as much as possible. Hydroxyzine hasn't provided substantial benefits, so I began adding fish oil, myo-inositol, NAC, and collagen peptides to my regimen. Six weeks ago, I noticed a marked improvement in how I felt, which led to a growing sense of safety within my body again. Two weeks back, I contracted a minor illness and felt fatigued without respiratory symptoms, purportedly affecting my overall stamina. Last week, as I started to recuperate, I had recent blood tests that showed a decline in white blood cell counts, although they remained elevated. All other parameters, including ALT and AST, were normal, with TSH at 4.45 and T4 at 1.3. Today, I awoke with a sense of imbalance. After taking my usual medications, my heart rate soared to 130 during a meeting, prompting me to take 20 mg of propranolol, which helped reduce it to the 90s. I decided to visit an urgent care center as a precaution; their examination revealed mostly normal results with the exception of a white blood cell count of 12.1 and a urine pH of 9. I'm someone who generally faces challenges with resilience. My mental health is stable, yet I find myself increasingly fatigued, anxious, and frightened as I navigate this troubling situation. Despite my lifestyle improvements over the past year, I now feel uneasy in my own skin. I've even developed anxiety about sleeping some nights. To cope with these emotions, I am seeking professional help. I'm sharing my experience in hopes that perhaps someone else has faced similar challenges and can relate to what I'm going through. Thank you for reading.

InsomniaAnxietyDepression
Male25-34
4 hours ago

Understanding the Causes of Diffuse Burning Sensation: Neuropathic, Autoimmune or Stress-Related?

**Age:** 35 **Gender:** Female **Duration:** Experiencing symptoms for approximately three months; had similar issues last year which eventually subsided. **Medications:** Occasionally take Vitamin D. **Lifestyle Factors:** No smoking or drug use. **Medical History:** Struggles with significant anxiety and depression. Hello, I'm seeking advice as I await the results of my ongoing tests. I’ve been dealing with a **burning sensation** akin to the feeling of being too close to a flame. This discomfort predominantly affects my **thighs and abdomen**, but I have also felt it in my **lower back, arms, and calves**. - The level of pain varies, ranging from **mild discomfort to severe agony**. - The sensation is not localized and tends to shift locations. - Sometimes, standing up or stretching provides relief. - There is no identifiable trigger for these symptoms. **Additional Information:** - I experience **high levels of anxiety**, and my neurologist has noted similar sensations linked to anxiety-based conditions. - However, I’ve never encountered burning sensations related to my anxiety previously, which makes me question how valid this explanation is. **Diagnostic Journey Thus Far:** - Consulted with a **neurologist**; symptoms do not align with MS. - Recent blood tests indicated slightly elevated cholesterol and a **high ANA level**, though I’ve been informed this could be nonspecific. - **MRI** is currently pending. - I have an upcoming appointment with **rheumatology**. **Inquiries:** 1. Is it possible for anxiety to induce **widespread burning sensations** like this, despite having no prior similar experiences? 2. Does the **intermittent nature** of these sensations point more towards neuropathic or autoimmune origins? 3. If the investigations yield no answers, which medical specialty should I consider consulting next? Thank you for taking the time to assist me.

AnxietyDepressionStress
Male25-34
4 hours ago

Concerned About Symptoms, But Snow Keeps My Doctor's Office Closed: Is It Safe to Wait?

Hi there! I’d like to share a little background about myself before diving into my current situation. I'm a 19-year-old female, weighing in at 112 pounds and standing 5 feet 2 inches tall. My current medications include clindamycin four times daily, amoxicillin twice daily, a daily dose of 30 mg Vyvanse, a multivitamin, and a women’s health probiotic (the specific name is a little tricky for me). Recently, I’ve been battling treatment-resistant strep throat, which prompted my doctor to prescribe both antibiotics four days ago. Prior to this, I was on keflex for a span of 10 days, and before that, I had amoxicillin once a day for 10 days, but it failed to eradicate the strep bacteria. I’ve essentially had strep for about 24 days now, maybe even longer. I initially mistook my symptoms for a cold after recovering from Influenza A, which I had just before this issue. When I visited the doctor for the last time, I was not experiencing the symptoms I have now. In fact, I thought I was past the worst of the strep ordeal and only had sinus infection symptoms, which have since dissipated thanks to the new antibiotics. However, my doctor checked me for strep again due to my recent history with it, and much to my surprise, the test came back positive. He warned me to be vigilant for signs of "scarlet fever" or "rheumatic fever" and sent me home with my current medications. A throat culture was taken, but results are pending, expected by Wednesday—if the weather cooperates. Unfortunately, a heavy snowfall occurred right after my doctor’s visit, and it has since snowed again. The office was closed today, which heightened my anxiety. Here are the symptoms I’m currently dealing with: **Symptoms Began With:** - A low-grade fever (between 99 and 100 degrees), persisting even with ibuprofen and antibiotics. - A mild, nagging headache—unusual for me, as I rarely get headaches. - Significant muscle discomfort in my lower back area, similar to pre-menstrual cramps, but more intense (my period isn’t due). - Pain in the middle of my back, particularly when I bend or arch my back, which is atypical for me due to my active job. Initial discomfort was concerning, but I wondered if it was a reaction to the antibiotics. However, two days ago, I noticed additional, more alarming symptoms: **New Symptoms Include:** - An odd feeling of tightness in my chest, which I can sometimes ignore (possibly just anxiety?). - A rapid heart rate, fluctuating between 100 and 115 BPM while lying down. Initially, I overlooked this, attributing it to the Vyvanse, but it occurs even after the medication’s effects have worn off at night. - A rash identical to the ring-like pattern associated with rheumatic fever, which appears and disappears, worsening in the shower and when bending over—it’s localized to my arms. - Facial twitching that includes scowling and blinking, coupled with an unexpected clumsiness. While my grip remains strong, it’s unsettling. - Difficulty in verbal expression, subtle but noticeable if my boyfriend points it out. He described me as stuttering as if I’m struggling to articulate my thoughts. I initially dismissed this constructively, but I’ve read it can happen. - The most troubling symptom: my fingers are curling involuntarily. My left hand’s pinky and ring finger seem to bend as if I’m trying to make a fist; they curl at all joints, and while I can consciously straighten them briefly, they naturally revert. Interestingly, they seem more bent today than yesterday, though there’s no pain involved—just an unsettling mild concern. I finally summoned the courage to discuss my symptoms with my family, who urged me to see the doctor, but due to the snow, my grandpa could only take me in his sturdier vehicle after confirming an appointment. Despite his willingness, I’m hesitant because I don’t want to be ridiculed, and I’d prefer to avoid the hospital altogether, fearing secondary infections. So, to get to my main query: is it safe for me to hold off until Wednesday for a consultation with my doctor concerning the possibility of rheumatic fever? It feels unlikely, making my apprehension seem exaggerated, but the symptom overlap is uncanny. Thank you for taking the time to read my lengthy post, and I apologize for any scattered thoughts—I aimed to include all relevant details!

ADHDAnxietyDepression
Male25-34
5 hours ago

Seeking Answers for My Health Struggles

While the title might sound overly dramatic, I genuinely feel like I'm unraveling here. 🤦🏼‍♀️ I’m a 29-year-old woman residing in the UK. My health issues began in November 2024, which is when I first consulted a physician. At that time, I had taken up running in an effort to lose weight. Approximately ten minutes into my runs, I started experiencing tingling sensations in my feet. This eventually escalated to a prickly feeling, followed by complete numbness that left me awkwardly limping back to my vehicle. My physician advised me to cease running and focus on losing weight, then sent me on my way. Shortly thereafter, I began to experience numbness and tingling in my right thigh whenever I lay on my back to sleep. I mentioned it to my mother, who dismissed it—she had experienced something similar due to a slipped disc in her youth. So, I carried on with my life. In March 2025, I started using Mounjaro to assist in my weight loss efforts, having struggled significantly before that and also facing a PCOS diagnosis a couple of years prior. By the time my next major symptom appeared, I had shed 2 stone. In June 2025, I began facing alarming issues with vertigo; every time I stood up, I would feel as though my head were spinning, and my vision would fade to black. This was an entirely new sensation for me. I informed my doctors about my use of Mounjaro, but they did not attribute my symptoms to it. Blood tests were conducted, most results coming back normal except for an elevated C-reactive protein (CRP) level of 18. Subsequent blood tests showed a consistent elevation in CRP, with levels ranging from 13 to 22 over several months. I was then referred to a cardiologist, who performed an echocardiogram and a 24-hour ECG, both yielding normal results. My heart rate varied between 43 and 137 beats per minute. Throughout the duration of the ECG, I experienced severe numbness in my legs, which continued to be an issue. Since I struggled to comfortably sleep on my side due to the ECG, I had frequently to revert to sleeping on my back, often waking around 4 AM from intense, shooting pain in my right thigh, accompanied by numbness across both legs. Following the ECG, my previously manageable lower back pain escalated, and the numbness in my legs worsened in frequency. Consequently, I was referred for MRI imaging of my lumbar and cervical spine. The doctors suggested that there might be compression on my lumbar nerves causing the leg numbness and possibly something in my cervical spine contributing to the dizziness. In the timeframe between my MRI referral and the actual procedure, I encountered a month where I struggled to eat properly as each meal resulted in debilitating bloating and discomfort. Additional bloodwork confirmed my elevated CRP levels, alongside a stool test. Fortunately, the bloating eventually subsided, but its cause remains unclear to me and whether it connects to my other symptoms. I underwent an MRI, which showed a clear cervical spine but revealed minor bulging discs at L4/L5/S1. According to the GP, these findings were unlikely responsible for my various issues. Now, I’m being referred to neurology for further evaluation, with the MRI results provided to me on January 22, 2026. From November 2024 to January 2026, I have mainly experienced increasing numbness in my legs (predominantly in my right thigh), intensifying lower back pain, and worsening dizziness upon standing. The dizziness has become particularly concerning; in the past week, I nearly fainted on three separate occasions. Where it was previously merely an annoyance, the sensation has escalated to the point where I feel I might collapse. Additionally, I've recently started to endure severe headaches and migraines. Although I’ve dealt with headaches before, these recent episodes are excruciating and can linger for hours. Do these symptoms correlate with one another? Could anyone offer potential insights into what’s happening? Thus far, doctors have casually mentioned conditions such as PoTS and MS, albeit in passing. Interestingly, I should note that I am now 4.5 stone lighter than when these symptoms first emerged.

AnxietyDepressionStress
Male25-34
5 hours ago

Strange Symptoms: Alcohol Intolerance Emerges

Age: 21, Height: 5’2", Weight: 97 lbs Medical Background: History of premature ventricular contractions (PVCs) and supraventricular tachycardia (SVT), mitral valve prolapse, polycystic kidney disease (Mayo class 1A, eGFR 88), dysglycemia, and von Willebrand's disease. Current Medications: Cardizem as needed (last used a while ago) and a Mirena IUD. About four weeks ago, I discovered a swollen lymph node in my groin area. It was quite firm, didn't move much, and was not painful. I experienced no other symptoms, and there have been no recent vaccinations, STDs, or urinary tract infections. Two weeks prior, I visited my doctor, who suggested an ultrasound. The findings indicated a lymph node measuring 2.3 x 1.6 x 2.7 cm with signs of hypervascularity and a heterogeneous cortex but with a preserved fatty hilum. The radiologist indicated a likelihood of benign conditions while still advising correlation with possible malignancy due to the observed cortex and vascularity. I'm aware of the low cancer risk associated with this, so I'm not overly concerned, although I thought it might be useful information. I completed a short course of doxycycline antibiotics, but it had no effect. I've communicated this to my doctor, but I haven't received a response yet. Additionally, two weeks ago, I began to feel increasingly fatigued. Despite getting 8-12 hours of sleep and needing daytime naps, I still felt tired. Without naps, I find myself asleep by 8 PM. Additionally, I've been experiencing itchy skin, which I attribute to the recent winter weather since I've had flare-ups resembling eczema in the past, although this time I'm noticing it in some unusual areas, such as my chest, where I've never had issues before. I've been on a higher protein diet for several weeks as I’m hitting the gym occasionally, engaging in mild resistance exercises three times a week. Although I am not extremely active otherwise, my weight has dropped; I was 104 lbs a few weeks back. Concerning alcohol: Last night, I had just under two drinks. Typically, I can handle around four drinks without any issues. However, as I began my second drink, I experienced sudden discomfort and severe nausea. I felt excessively warm, flushed, and my heart raced. I had eaten normally throughout the day and stayed hydrated, drinking water continuously while enjoying my drinks. Once I returned home, I quickly fell asleep due to feeling nauseous and unwell. I had some leftover zofran from a prior kidney infection in October, but even that didn't alleviate my discomfort. At midnight, I awoke with severe stomach pain, alternating temperature sensations, excessive sweating, goosebumps, and PVCs. I struggled with dry heaving and felt dizzy every time I tried to move. I managed to get to the couch and slept for another few hours, only for the cycle to repeat. Once I fell asleep again, I felt somewhat improved afterward, though still weak and foggy. I took more electrolytes and stayed hydrated, managing to eat without issue thereafter. What’s concerning is that I normally can drink several drinks and feel fine. This reaction is entirely unprecedented for me. There were no changes in my diet, activities, or exposure to illness, and I don’t have Asian heritage, which can sometimes be associated with alcohol intolerance. A few weeks before this incident, I did have three drinks and felt a weird throbbing pain in my lymph node, but I attributed that to something unrelated. Could anyone shed light on why I might suddenly be unable to tolerate alcohol? What actions should I take moving forward? Should I bring up all these symptoms, or would it come off as overwhelming or unfocused? 🤔

AddictionAnxietyDepression
Male25-34
5 hours ago