Strange Issue with My Penis
At the age of 17 and standing 5’11", I experienced an unexpected injury to my penis while I was engaged in masturbation around mid to late 2024. During a moment of clumsiness, I inadvertently squeezed, which led to a temporary inability to achieve an erection. Thankfully, I recognized that recovery was on the horizon, and after about 20 to 30 days, I was able to regain erections comparable to those I had prior to the incident. However, I noticed a peculiar phenomenon where my flaccid state occasionally became swollen, likely due to increased blood flow; light pressure would relieve the swelling, though it would return later. This was not accompanied by any discomfort or changes in my ability to achieve an erection. I remember it being somewhat bothersome, particularly affecting my ability to urinate until the swelling subsided, which happened when I sat down and exerted a bit of pressure. Some months later, I decided to try LSD. Interestingly, it didn’t induce much in the way of hallucinations for me, but I did experience some wavy vision and a sense of lightheartedness. During this trip, I felt extreme discomfort, as if my penis was under significant pressure, and it appeared noticeably soft and shrunken. After about two days, everything returned to its usual state. Fortunately, the puffiness I had been experiencing disappeared, although it would reemerge for a few hours after I masturbated shortly after my last session (within the same two days). Beyond that, my condition seemed fairly normal. Recently, I acquired a cannabis vape, and unlike the previous one I had tried, this one triggered some puffiness while in a flaccid state. It's worth mentioning that this puffiness did not hinder my ability to achieve an erection and would dissipate once I became aroused. I observed that the higher I felt, the more pronounced the effects were; there was one instance where I experienced discomfort from being too high, but this subsided the following morning. Remarkably, I found that I no longer had to exert pressure to urinate; it flowed freely when I was in a sitting position. Just today, I consumed cannabis and engaged in masturbation, which resulted in an unusual sensation, causing my erection to last significantly longer. As I’m writing this, the puffiness I experienced post-injury has returned; however, this time it felt firm instead of filled with blood. I needed to apply similar pressure while seated to alleviate the swelling for urination. This time, I didn’t feel anything particularly unusual. I plan to take a break from cannabis to see if my body recovers. I suspect that my original injury might have led to a pulled muscle somewhere in my pelvis, as I experienced pain while walking following the incident. At present, the puffiness continues to fluctuate, appearing and disappearing every few minutes. If anyone has insights or advice on this issue, I would greatly appreciate it.
Answers (1)
8/7/2025, 8:02:09 PM
OpenHealth AI
It sounds like you’ve had quite a journey with these symptoms, and it’s important to address your concerns regarding the swelling and discomfort you’ve experienced. Your report of fluctuations in swelling, particularly related to arousal and after using substances, suggests there may be a few physiological factors at play.
Key Points:
- Injury Recovery: Your initial injury seems to have resolved, as indicated by the return of normal erectile function over time.
- Swelling Phenomena: The recurring puffiness could be related to increased blood flow during arousal, muscle tension, or even some form of mild edema.
- Substance Effects: Cannabis and possibly your experiences with LSD may be affecting your vascular response and muscle tension, which can lead to temporary changes in your state of arousal and swelling.
Explanation:
While it’s reassuring that you can achieve erections normally, the swelling and changes in your penile state may stem from:
- Hydraulic Changes: Increased blood flow during arousal can cause temporary swelling, which might feel firmer or softer based on your state of arousal and muscle tension.
- Muscular or Vascular Response: If you did sustain a minor injury that affected the surrounding muscles or vessels, postural changes and tension can also create sensations of firmness or swelling.
- Impact of Substances: Both cannabis and LSD can alter your perception of bodily sensations, which might explain the differences you felt during and after their use.
Next Steps to Consider:
- Monitor Your Symptoms: Keep a diary to track when the puffiness occurs, its severity, and any activities (like substance use or masturbation) that may correlate with its occurrence.
- Limit Substances: As planned, take a break from cannabis and other substances to assess if the puffiness improves. This could clarify if they are a contributing factor.
- Hydration and Relaxation: Ensure you’re adequately hydrated and consider techniques like stretching or relaxing pelvic muscles, as tension can exacerbate discomfort.
- Pelvic Floor Exercises: Engaging in gentle pelvic floor exercises (like Kegels) could help improve muscle tone and response without putting stress on the area.
- Consultation Consideration: Although you may feel fine otherwise, if the puffiness continues or worsens, think about consulting a healthcare provider for a thorough assessment. They can evaluate for any underlying concerns related to your injury or muscle tension.
It’s great that you’re being proactive about your health. Maintaining open communication about any changes or worries is key, and you’re taking the right steps by monitoring your body’s responses. Let me know if you have more questions or need further guidance!
Related Questions
Concerns Over My Partner's Persistent Pain and Resistance to Seek Medical Help
I’m facing a worrying situation with my partner, a 40-year-old man who stands 6 feet 1 inch tall and weighs approximately 19 stone. Here's a brief overview of his medical background: Twenty years ago, he experienced two instances of deep vein thrombosis (DVT) in his left shoulder. Following the second incident, doctors discovered an abnormal growth of a rib that was pressing against a vein, which was the cause of those DVTs. More recently, he dealt with a blood clot in his calf last year. Fortunately, that was successfully treated, and he returned to his normal health. Although he was advised to continue taking apixaban for the long term, he has, unfortunately, chosen not to follow through with this guidance. He also has a history of elevated blood pressure. For the past couple of days, he has been experiencing two concerning symptoms that emerged simultaneously: a persistent cough with no accompanying cold or flu signs, and a severe pain located on the right side of his torso. He describes this discomfort as being mostly in his stomach yet extending slightly to his back. I would pinpoint the troubled area as the lower part of his ribs along the side of his body. It's unusual for him to express discomfort or complain about his health, so his recent grievances signal to me that the pain is likely quite significant. Despite my repeated suggestions for him to visit a doctor, he insists that he may have simply pulled a muscle. To manage the pain, he's been applying an ibuprofen cream (voltarol) and taking naproxen, but neither seems to provide relief. What might be the underlying issue here? I hope that some medical professionals who see this post can offer their insights, which might persuade him to consider making a doctor’s appointment. I’m open to providing any additional information you might require for a more informed perspective. Thank you for your help!
Struggling with Bleeding and Pain Since Christmas
I'm a 27-year-old woman from the UK, and I've reached a point of exasperation. I'm reaching out because I hope someone can provide insight or guidance on what I should discuss with my doctors. Please excuse any grammar or spelling errors as I have dyslexia. I've been diagnosed with endometriosis and underwent surgery in 2022 for confirmation of that diagnosis. On December 15th, I had my birth control implant removed after nearly two years. During that period, I experienced severe menstrual cramps and PMS. My GP started me on Drospirenone 3mg and Estetrol 14.2mg COCP in October to alleviate these symptoms and suppress my periods, which provided some relief. Prior to this situation, I occasionally dealt with flare-ups that typically lasted a few days or up to a week. To help manage the discomfort, I have been prescribed Duloxetine at a dosage of 90mg. I had an ultrasound earlier this summer, and the results came back normal. Currently, I am awaiting an MRI. Last year, my smear test results were also clear. After the removal of my implant in December, I began bleeding on Christmas Eve. Initially, I could manage with just a panty liner, but over the next few weeks, the bleeding intensified, requiring the use of pads due to increased blood flow and blood clots. Given my history with endometriosis, pain isn't unfamiliar to me; my average pain level is around a 4, but it has recently escalated to 7 or 8. In the past couple of weeks, the discomfort has worsened. My job demands physical activity, and bending over now causes pain in my back and legs. Additionally, I experience discomfort when my bladder fills, and urination is painful, although it doesn't feel like a urinary tract infection. I've also been waking up at night to use the restroom. My doctor performed a urine dip test that showed no signs of infection, though there was blood in my urine, which he indicated was to be expected. Recently, my GP prescribed Tranexamic acid 500mg and Mefenamic acid 500mg, which helped with the blood clots, but I'm still experiencing bleeding and significant pain. I've been diligent about taking my medication, treating it like a strict regimen. I returned to the GP, who referred me for another ultrasound and advised me to go to A&E if the pain worsens. I've been resting as much as possible while still trying to maintain some level of activity, but it hasn't provided much relief. Any assistance or advice would be immensely appreciated! Thank you!
Experiencing Unusual Sensitivity to Paracetamol
Hello, Reddit community! I'm a newcomer here, so please bear with me as I navigate this platform as well as the rules. I appreciate your understanding regarding my writing skills. I find myself in a situation that lacks sufficient information online, and I'm reaching out for insights from others. Currently, I have reasons to believe that I might be experiencing a unique sensitivity to paracetamol, and I’d like to share my timeline regarding this matter. Throughout my life, I generally had no issues with paracetamol. I used various brands multiple times and felt fine. However, starting in the fourth grade, I began to experience difficulties with it. My initial problems were respiratory-related, but soon they also affected my gastrointestinal system. I haven't had any formal testing yet, but I can safely use other pain relievers like NSAIDs without any adverse effects. Initially, I tolerated paracetamol relatively well; my early symptoms seemed like common side effects. Unfortunately, it escalated to severe reactions, including vomiting, tightening of the throat, blood in my mucus, and shortness of breath. In my confusion, I thought limiting my dosage could help, which it did temporarily, but eventually even the reduced amounts failed to be effective. I experimented with syrup formulations that contain less paracetamol or where it isn't the primary ingredient, and found those to be more manageable. Recently, however, even those have become problematic, making it necessary for me to seek alternatives to paracetamol, as it has become increasingly intolerable. Through my research, I discovered that such reactions often stem from cross-sensitivity to other medications or from preexisting respiratory conditions. I lack a history of asthma or other respiratory issues, so I’m inclined to dismiss that possibility, although I remain uncertain. Moreover, I have no known allergies, which adds to my confusion since my reactions only occur with this one particular medication while all others seem fine. It is difficult for me to process this change, especially since I used to have no issues with paracetamol. It is widely available and generally considered safe, so I struggle to understand the source of my suffering. Many people insist that these reactions are normal side effects, leading me to question whether I am overreacting. The immediacy of my reactions intensifies my concern; I don’t even need to swallow the medication completely before I notice my throat constricting, increased mucus production, and shortly thereafter, some blood in my mucus along with persistent coughing. This pattern has become consistent, whereas it used to depend on the dosage. Now, regardless of how much I take, the same symptoms occur. I’ve tried to dismiss it, not wanting to worry my parents or seek medical attention for a dosage safety test, fearing I’ve already pushed my body too much. However, I am considering discussing my concerns with my mother since she is increasingly worried about my use of this medication. I’m not seeking a diagnosis or medical advice—I understand I should probably consult a professional. I’m just interested in knowing if anyone else has faced similar experiences, as the confusion grows. What I once assumed were normal side effects now seem to signify something more concerning.
Chronic Hypersomnia Since Adolescence: A Seeking Path for Answers
I am a 30-year-old white male, standing 5 feet 11 inches tall and weighing 160 pounds, residing in the United States. **Current Medications:** - Adderall XR 40 mg - Sunosi 150 mg - Lisinopril 40 mg - Atenolol 25 mg - Tolvaptan 60 mg **Medical Background:** - Autosomal Dominant Polycystic Kidney Disease (ADPKD) at stage 2 (eGFR 67) - Obstructive Sleep Apnea (utilizing CPAP machine since July 2024) - Complex Post-Traumatic Stress Disorder (CPTSD) **Symptoms Experienced:** - Persistent and overwhelming sleepiness—more than just fatigue—accompanied by a heavy feeling in my face and chest; I struggle to keep my eyes open and often feel as if I am burdened. - I sleep for 10 to 14 hours every night, supplemented by involuntary naps lasting 1 to 2 hours multiple times throughout the day. - None of my sleep feels restorative, leading to a groggy, hangover-like state upon waking. - Cognitive challenges including a lack of focus, forgetfulness, and trouble retrieving words, which have grown more pronounced over the last four years. - Activities as simple as showering or cooking now feel like moving through molasses. - I experience low physical endurance and lengthy recovery times, even though I previously maintained a regular exercise routine. My late father exhibited similar symptoms with the addition of seizures he associated with alcoholism, although he was never assessed medically. I, on the other hand, do not have any alcohol or addiction issues. **Specialist Consultations:** - **Sleep Specialist:** A Multiple Sleep Latency Test (MSLT) ruled out narcolepsy with no Sleep Onset REM Periods (SOREMs) and a 12-minute latency. I comply with CPAP therapy for an average of eight hours each night, but there has been no alleviation of my symptoms. Testing revealed no periodic limb movement disorders, alpha-delta intrusions, or unexplained nighttime arousals. - **Nephrologist:** Symptoms are considered unlikely to stem from my current stage of ADPKD. Tests show I’m not anemic, with standard iron levels. - **Rheumatologist:** An ANA titer of 1:320 with a speckled and nucleolar pattern appears elevated; however, all specific autoimmune tests returned negative. Monitoring was suggested without a clear diagnosis provided. - **Psychiatrist:** It was determined that my symptoms do not seem to be connected to mental health issues. My therapist has also validated in a letter that my condition is unrelated to psychological factors. - **Miscellaneous Findings:** An arachnoid cyst was detected in my brain. My white blood cell count is borderline low and my red blood cell count alternates between normal and low realms. Testosterone levels are within the normal range, though morning cortisol is slightly elevated. Normetanephrine is elevated at 2.15 nmol/L, while metanephrine remains normal at 0.27 nmol/L. Both Vitamin D and B12 levels are adequate. Tests for STIs returned negative results. **Current Situation:** I am currently on disability, unable to work even in part-time capacities and can no longer engage in exercise, finding myself nearly confined to my home. I feel as though I am being sent from one specialist to another without gaining clarity on my condition. What avenues should I explore next? Which type of medical professional might offer further insight? I'm beginning to doubt my own experiences, pondering if I am merely being lazy or overly sensitive.
Chronic Foot Pain: Seeking Insights on Possible Causes
I'm reaching out to gather thoughts on a perplexing issue I'm facing. Since my first pregnancy back in 2020, I've been dealing with intense foot pain that appears unpredictably. It all started when I was about seven months along while working long shifts in a busy kitchen, four days a week, for eight hours each day. At the time, I dismissed the discomfort as something typical for pregnancy, but it fortunately subsided about six months after giving birth to my first child. Fast forward to late 2024, when I became pregnant with my second child. By now, I had transitioned to being a stay-at-home mother, with none of the rigorous demands of my previous job. However, around three months into this new pregnancy, the foot pain reemerged and has persisted ever since. My youngest is turning two this month, which helps frame this timeline. The pain has oscillated between being severe and manageable, but the previous six months have marked a significant decline into debilitating territory. When I am at rest, I feel sharp pains in my metatarsals that radiate up to my knees. To alleviate some discomfort, I’ve been altering my walking style to shift weight more onto my heels instead of the balls of my feet. However, this adjustment has introduced a new level of discomfort in my heels. Ironically, the only relief I find is while walking. Nonetheless, excessive walking—even something as simple as taking my oldest to school for a brief ten-minute journey—leaves me nearly immobilized the following day. Currently, I’m on a regimen of 50 mg of APO-Diclofenac DR, taken twice daily, yet I’ve found no relief. Previously, I also tried 500 mg of naproxen twice a day without any positive outcomes. I've experimented with various footwear, but none have alleviated the pain. My primary care physician has arranged for bilateral x-rays and blood tests to check for conditions like gout and markers for osteoarthritis and rheumatoid arthritis, among other things. So far, all tests have returned normal. There have been occasions where I’ve had to keep my oldest child at home from school simply because I’m unable to walk even a short distance, such as the fifty steps from my bedroom to the kitchen. Standing causes distress, and even elevating my feet while resting feels unbearable. Additionally, any gentle touch to my feet triggers intense pain that shoots up my shins. The only feedback I’ve received from my doctor so far is that it likely stems from inflammation, along with a recommendation to expedite weight loss. I had a chiropractor assess my condition, and they noted that I am hypermobile, but I’m unsure how significant that could be to my situation. If you have any questions for clarification, I’d be more than willing to respond. I’m enduring considerable pain and would greatly appreciate any suggestions on possible avenues for finding relief.