OpenHealth Q&A

Get answered by medical professionals

Should I Drain This Blister from My Burn?

8/17/2025, 8:01:00 PMMale25-34

I am a 35-year-old male, standing at 5 feet 7 inches tall and weighing 195 pounds. I take no daily medications except for omeprazole and have no known allergies, overall I’d say my health is pretty stable. Recently, I suffered a burn on my leg, which occurred more than two days ago. I sought treatment at an urgent care facility, where I was diagnosed with first and second-degree burns. Currently, I’m applying a silver-infused cream in the morning and mupirocin ointment before bedtime on the one blister that has already burst on its own. Fortunately, I’m not experiencing any discomfort and there are no signs of infection that I can detect. To be honest, my main concern at this point is how it looks. The blister itself is rather sizeable, roughly the diameter of a half dollar and about half an inch thick at its most swollen part. While I understand that it will eventually reabsorb over time, I'm wondering whether it would speed up the healing process if I carefully sterilize a small needle to drain it and continue my routine with the silver cream and mupirocin. I have a lingering worry that the blister might rupture on its own, which leads me to think that taking control of the situation now might result in a cleaner outcome in the long run.

Multiple SclerosisFibromyalgiaInternal Medicine

Answers (1)

Cony

8/17/2025, 8:01:46 PM

OpenHealth AI

It’s great that you’re seeking advice on managing your burn and concern for its appearance. Here's the key takeaway: Avoid draining the blister yourself. Instead, focus on proper care to promote healing without increasing the risk of infection.

Explanation:

Blisters form as a natural protective mechanism for skin that has been burned. They help shield the underlying tissue from infection and further injury. Since you’ve already had a blister that burst, allowing your body to heal naturally is generally the best approach. Draining a blister might seem like it could speed up healing, but it can introduce bacteria and complicate the healing process if not done in a sterile manner.

Next Steps:

  1. Leave the Blister Intact: If you have a larger blister that hasn’t burst yet, try to keep it that way. Protect it with a clean, non-stick bandage. This will help it heal better and reduce the risk of infection.

  2. Keep it Clean: Continue applying the silver-infused cream and mupirocin as directed. These will help prevent infection and promote healing.

  3. Monitor for Signs of Infection: Watch for any signs of infection, such as increased redness, swelling, warmth, pus, or increased pain. If you notice any of these symptoms, take action immediately to address them.

  4. Patience with Healing: Understand that healing can take time. Scarring will gradually improve, and keeping the area moisturized can help in the long run.

  5. Comfort Measures: If you’re concerned about how it looks and want to discuss options for scar management once healing is complete, consider researching silicone gel sheets or consulting with a dermatologist in the future for aesthetic concerns.

By being patient and careful, you're supporting your body's healing process while minimizing risks. Let me know if you have further questions!

Related Questions

Understanding Perforated Eardrums

Hello everyone. I'm a 29-year-old female, and recently I've discovered that both of my eardrums have perforations. For the past month, I've been struggling with a severe inner ear infection affecting both ears. Initially, I was prescribed Amoxicillin and Prednisone at an urgent care facility. However, after noticing no improvement, I was switched to Cefdinir just last week. Today, I took a look at my ears using a small wax removal tool, and to my shock, I found holes in both eardrums. I understand that ear infections can lead to this condition, which likely explains the ongoing discomfort I’m experiencing. My concern now is whether I should seek emergency care or if a visit to my family doctor will suffice. It’s nearly midnight where I am, but I can reach out to my doctor in the morning. I just want to ensure that this isn't a situation that requires immediate attention. Additionally, I’ve realized that the idea of a bug entering through my perforated eardrums is quite frightening! Thank you all for your support ❤️

AsthmaLupusInternal Medicine
Male25-34
24 minutes ago

Could This Have Been a Seizure?

A while back, I had an experience that continues to trouble me. Let me start by clarifying that I am not against vaccinations; I'm simply sharing my personal encounter. After receiving my initial meningitis vaccine, which I believe was administered alongside another one—possibly HPV—I suddenly felt faint. My vision went dark, and I collapsed. Medical staff transported me to another area in the clinic, where they administered smelling salts to revive me. I attributed this incident to not having eaten that day and didn’t experience any further symptoms at that time. However, years later, when I went for my second meningitis vaccine, I informed the clinic personnel about my previous reaction. They dismissed my concerns and assured me that everything would be fine. After a short wait following the vaccination, they deemed me ready to leave. Once I got into the car—thankfully, my guardian was driving—I began to see swirling, kaleidoscopic patterns on the road that wouldn’t leave my sight. Breathing became a struggle, and again, my vision faded to black. I have no memory of what transpired next. When I regained consciousness, I was soaked in sweat and my body was aching. Though it felt like just a few moments had passed, my guardian recounted that I had convulsed and mumbled for approximately 10 to 15 minutes. This incident occurred years ago, but it has left me feeling traumatized, leading to a fear of needles. I find myself wondering whether this could have been a seizure, as I’ve faced skepticism regarding my experience. I'm eager to know if what I experienced was indeed possible. For context, I am 19 years old, assigned female at birth, do not smoke or drink, weigh around 100 pounds, and I am not on any medication.

Multiple SclerosisCrohn's DiseaseCOPD
Male25-34
35 minutes ago

Understanding Long-Term CMV Issues: A Patient's Journey

Hello, I’m reaching out to share my health journey and seek insights regarding a perplexing aspect of my condition. At 26 years old, standing 5’6” and weighing 200 lbs, I do not smoke or engage in illicit drugs. My ongoing health struggles include fibromyalgia and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Currently, my treatment regimen consists of medications like Allegra, Claritin, and Tylenol. When I was a child, I encountered a significant medical incident that has lingered into my adult years. Unfortunately, it appears that I have exhausted available treatment alternatives, leaving me primarily confined to my home. I spend most of my time in bed to prevent exacerbating my condition, which leads to immobility. I am not seeking specific treatment advice, but I do have some questions regarding a mysterious aspect of my medical history that has puzzled my doctors. For two years, I experienced elevated IgM titers for cytomegalovirus (CMV), yet my IgG results always came back negative. Last year, I was retested, and both IgM and IgG were negative. I had previously noted some alleviation of my symptoms after the two-year mark, indicating the infection had likely resolved. However, it struck me as strange that I have never developed IgG antibodies. What could this imply? Is there a possibility of reactivation? If I were to fall ill again, could I face the same prolonged symptoms? While I tend not to be overly anxious, I wonder whether I should take precautions, such as wearing a mask during medical visits. Here is a summary of my medical timeline: - August 2013: I suffered a concussion resulting in a loss of consciousness, memory loss, and episodes of disorientation lasting about two hours. After brain scans in the hospital, I returned home, but continued to experience headaches for the following weeks. - January 2014: I began to encounter significant fatigue and excessive sleepiness, which hindered my ability to engage in physical activity. - February 2014: I visited the emergency room due to an intense, full-body rash. Despite consultations with multiple doctors and a series of tests revealing no clear abnormalities in my blood work, my symptoms remained debilitating. The rash persisted alongside my excessive sleeping, resembling the fatigue associated with mononucleosis. I was forced to withdraw from school and focus solely on rest. - August 2014: A test for CMV was conducted, yielding results of IgG < 0.90 (negative) and IgM 2.8 (high). The medical team suggested that this indicated a recent infection; however, I had been suffering from these symptoms for months. Illness continued, prompting a cycle of doctor visits and tests that produced no conclusions. My inability to attend school—offline or online—alongside cognitive difficulties, left me in a constant state of lethargy. - January 2016: Another test for CMV revealed IgG at 0.2 (negative) and IgM at 3.6 (high). By 2017, I noticed I could stay awake longer and engage my mind despite the challenges. This was perceived as a sign that, if CMV was the cause of my illness, it was subsiding. I began attempting to move around, but the experience was often very painful. From 2017 onward, I gradually regained some functionality, although pain and post-activity fatigue remained significant challenges. Leaving the house briefly would often result in several days of recovery in bed. I was advised to maintain a fitness routine for better recovery, so I attempted hikes when possible. Despite this, I experienced a recurrence of my rash and intensified symptoms for extended periods. Nevertheless, I managed to incorporate some daily activity, including walks lasting 30 minutes or more, mindful of the risk of deconditioning linked to back issues and plantar fasciitis, which exacerbated with inactivity. - 2024: A recent CMV test yielded negative results for both IgG and IgM. - 2025: I find myself largely housebound again, as any increase in activity leads to muscle stiffness and feelings of paralysis. My current activity level is lower than in previous years, which helps mitigate some symptoms, though it comes with its own set of complications. Reduced mobility means less pain overall, provided I limit my activities to brief bursts. I recently received a diagnosis of ME/CFS, but the suggestions provided were already part of my current approach. This realization has led me to accept that I may be disabled for life, prompting me to pursue disability benefits—a long and arduous process. In conducting research for supporting documentation, I have reflected on that one test which appeared to hold a potential explanation for my condition. My concerns about the CMV antibody results linger, as they seemingly defy expectations; IgG should have surfaced following the initial illness. Shouldn't I have developed it by now? I’m left to wonder if I experienced any false positives or negatives in testing or if my immune response was impaired. Alternatively, could it be that CMV is not the root cause of my illness, despite exhibiting similar symptoms? While there may be no definitive answers, I would appreciate hearing from professionals who might shed light on these shared experiences. Although I have consulted numerous specialists over the years, none have been able to clarify this specific scenario. My general practitioner is supportive, yet she, along with my new ME/CFS specialist, hasn’t provided insight on these nuances. Thank you for taking the time to read my story. I would love to hear your thoughts.

Multiple SclerosisFibromyalgiaCrohn's Disease
Male25-34
1 hour ago

Unusual Symptoms Following a Viral Infection

Hello, I'm a 22-year-old female and I've been dealing with some unusual symptoms since I fell ill a few weeks back. To give you some context, I tend to catch colds every few months. It typically begins with a scratchy throat, and by the next day, I’m usually feeling quite miserable. I experience high fevers, along with severe pain in my back and legs, which can be nearly intolerable, as well as headaches. This time, after about a week, I started to feel somewhat normal again. Since recovering, however, I've noticed my eyes have become red and are somewhat painful. Additionally, I have developed small red spots on my lips and around my mouth, along with what seems to resemble angular cheilitis. It's all a bit peculiar. I would greatly appreciate any guidance or insights regarding these symptoms!

ArthritisLupusFibromyalgia
Male25-34
1 hour ago

What Should I Do After Taking 40mg of Abilify Instead of My Prescribed Dose?

As a 22-year-old female, I was meant to take 20mg of Abilify, but I've accidentally been using 40mg daily for the last month. This confusion likely arose from my medications being mixed together; I have two bottles of Abilify, each containing 30 tablets, which I didn’t separate properly. They ended up mixed in with my other nighttime medications, all of which are simpler since they are just single pills except for Lamictal, which comes in a distinctive bottle. I only became aware of this error about half an hour ago. After running out of the higher dosage, I contacted my psychiatrist’s office but didn't receive a prompt response. Fortunately, I managed to secure an emergency supply of 20mg pills from the pharmacy that I’ve been taking for the last three evenings. I've also made an appointment with my primary care physician, who has sent over a new prescription, but the pharmacy indicated that I shouldn’t have run out yet. Just last night, I took my final emergency dose, and while searching for the second bottle, I came across two empty Abilify containers in my medication bag. Now I find myself in a dilemma: having adjusted to 40mg for the entire month, I'm now out of pills completely. I’m feeling anxious about how I will cope tomorrow, especially given my bipolar II condition, as I am experiencing unusual sensations without my Abilify. Who should I reach out to for help? Should I get in touch with the pharmacy, or is it better to speak with my psychiatrist or primary care physician? I need guidance on how to resolve this issue effectively. Additionally, my current medication regimen includes 500mg of Metformin, 40mg of Pantoprazole taken twice daily, 200mg of Lamictal, 50mg of Trazodone, 2mg of extended-release Guanfacine, 60mg of Duloxetine, and an unspecified dosage of Metoprolol.

Thyroid DisordersInternal MedicineEndocrinology
Male25-34
1 hour ago