Variable Redness Around Recent Injury
46-year-old female, weighing 140 lbs, diagnosed with EDS and POTS, experiencing perimenopause, currently on low-dose birth control, refraining from alcohol consumption, uses medical marijuana. On Friday evening, while preparing an old area rug for disposal, I accidentally scraped my ankle/shin with a utility knife. The blade was freshly changed, resulting in a clean cut approximately half an inch in length. I rinsed the cut with water, treated it with hydrogen peroxide (as it was my only option aside from scented soap), applied polysporin, and sealed it with a bandaid, then resumed my activities. By Saturday morning, my ankle felt somewhat tight, exhibited minor swelling, and exhibited an emerging red spot that progressively intensifying throughout the day. To be cautious, I planned to visit urgent care if the condition remained unchanged or worsened by morning. However, upon awakening on Sunday, I noticed noticeable improvement; most of the redness had subsided, swelling and stiffness had diminished, so I opted against a medical visit. Later that evening around 5 PM, when I went to redress the wound, I discovered that the redness had reappeared and had increased in size. The area adjacent to the cut is somewhat tender to touch, but I am not experiencing any significant pain, discharge, or unusual odor; it doesn’t feel notably warm, perhaps just slightly. I have noticed occasional itchiness but it is not persistent. Upon inspection, the cut appears to be deeper than originally assessed, potentially requiring stitches. Additionally, my air conditioning is malfunctioning, leaving my home at approximately 82 degrees, which may contribute to the situation.
Answers (1)

7/6/2025, 11:20:33 PM
OpenHealth AI
It sounds like your injury has undergone some fluctuations in healing, which can be common, especially given your medical history of EDS and POTS. Initially, the swelling and redness are likely part of the body's natural reaction to an injury, but since you're observing some variable changes, it's important to monitor the healing process closely.
Explanation
The redness around a cut can be a sign of normal healing, irritation, or potential infection, especially if it fluctuates. While it's a good sign that you noticed improvement initially, the return of redness and tenderness might warrant further attention. A few factors could be at play, including the environment (like your home's temperature) and the depth of the cut, potentially leading to delayed healing.
Next Steps
-
Continue Monitoring: Keep a close eye on the redness, swelling, and any changes in the wound area. Look for worsening symptoms like increasing tenderness, warmth, or the appearance of pus, as these can indicate an infection.
-
Wound Care:
- Keep the cut clean and covered to protect it from irritation.
- Change the dressing daily and observe for any signs of infection.
- Avoid using hydrogen peroxide repeatedly since it can irritate the tissue; consider using mild soap and water instead for cleaning.
-
Skin Soothing: If you experience itchiness, apply a hypoallergenic ointment or moisturizer around the area—not directly on the cut—if there's no broken skin. This can help reduce irritation.
-
Temperature Control: Since the temperature in your home is higher than usual, consider ways to cool down your environment if you are feeling uncomfortable. Excessive heat can exacerbate swelling and discomfort.
-
Assessment of Depth: If the wound continues to appear deeper or if you're concerned it may require stitches, consider seeking medical advice soon. It's essential to ensure the cut is healing properly to prevent complications.
If there is no noticeable improvement or if you develop new concerning symptoms, it may be prudent to consult a healthcare provider to evaluate the injury more thoroughly. Remember, it’s always better to err on the side of caution when it comes to wounds, especially if there are underlying health considerations.
Related Questions
Inquiries for Neurologists Regarding Immature Teratomas, Chemotherapy-Induced Neuropathy, and Disease Progression
2023-10-20 F30 - 165 lbs Current Medical Conditions: - UCTD/Borderline SLE (currently in remission) - Psoriasis - ADHD - Ovarian Cancer (1 year in remission) My treatment regimen included four cycles of the BEP chemotherapy regimen. Presently, my medications consist of Metoprolol (25mg administered twice daily) and Lyrica. It's been about one year since I completed my treatment for ovarian cancer. Prior to my diagnosis, there were suspicions of SLE and the possibility of an underlying neurological issue. An earlier nerve biopsy conducted by my previous rheumatologist revealed borderline results, and he also noticed that I lack mobility in my ankles while being hypermobile at my knees. Approximately six months before my cancer diagnosis, I was experiencing symptoms such as increasing weakness, occasional burning sensations in my right hand and arm, as well as episodes of shock-like sensations radiating up my back. Subsequently, I began experiencing episodes of vertigo and became highly sensitive to specific lights that would provoke these dizzy spells, significantly impacting my ability to walk without feeling faint. Following my diagnosis, I conducted some research about my cancer and encountered a case study of a patient exhibiting symptoms akin to mine, who tested positive for the Nmdar antibody and was diagnosed with a paraneoplastic syndrome related to her cancer. I requested both an MRI and an Nmdar antibody test from my oncologist; however, the antibody test returned negative, and the MRI detected an inconsequential small lesion. Notably, in the study, the woman only showed positive antibody results after a spinal tap was performed. Fast forward a year, and I am realizing the reoccurrence of vertigo symptoms, additionally noticing a worsening of my neuropathy primarily on the right side of my body. This leads me to ponder: given that I underwent chemotherapy, would it not have eradicated any antibodies potentially responsible for these symptoms? Could these present issues be indicative of a distinct neurological disorder, or is it typical for chemotherapy-induced neuropathy to evolve in this manner? I recently underwent DNA testing which indicated a high risk for celiac disease, multiple sclerosis, and other autoimmune disorders due to a correlated gene. In the past three months, I experienced several emergency room visits without yielding definitive answers. During one episode, I suffered from severe nausea and projectile vomiting, which led to my dehydration. Although I tested negative for H. pylori, I noticed some improvement by eliminating gluten and subsequently received a gastrointestinal referral. I lost around 15 lbs over the month due to the lasting nausea. Subsequent to this, I faced significant sleep disturbances, only managing 2-3 hours of sleep per night. My circadian rhythm seemed disrupted, causing numerous attempts to regulate it to prove fruitless. A troubling episode occurred while shopping, where my vertigo symptoms resurfaced. I felt sudden heaviness in my lower body as lights began triggering dizziness, complicating my focus. Upon exiting the store, I experienced acute stabbing pains in my right thigh radiating down to my knee and calf. Later that evening, the pain persisted alongside numbness in my right arm for about 15 minutes, which was accompanied by chest pains, prompting another ER visit due to concerns of a clot or other serious conditions. While assessments indicated normal results, I found myself dehydrated once more and saw a mild abnormality in my ECG readings. Just a couple of days later, I faced another alarming episode characterized by a sudden increase in heart rate to 170 bpm as I walked to my car. Despite a stabilization by the time I reached the ER, I nearly fainted during a blood draw. Throughout these visits, one nurse hypothesized iron deficiency anemia, leading me to take iron supplements which positively impacted my sleep and circadian issues. However, stabbing pains persisted, albeit with reduced intensity, and my neurologist switched my medication from Gabapentin to Lyrica, providing some relief, though not completely. My cardiologist has yet to ascertain the cause of my symptoms, and neither has my primary care provider. Currently, my symptoms predominantly affect the right side of my body, which raises questions about whether the previously deemed insignificant left-sided brain lesion might be more clinically relevant than initially thought, given the correlated symptoms. Strenuous walking causes numbness in my right leg, and there have been episodes of tingling sensations or temporary immobility in my right arm. Post-surgery, I had a concerning reaction to Benadryl that involved a dull spinal ache followed by intense thirst, burning sensations, and severe weakness in my legs and chest. The episode rendered me unable to think clearly, lasting around half an hour and resulting in wariness towards Benadryl moving forward. Similarly, morphine elicited a strong negative reaction involving burning sensations, nausea, and dizziness. I've also encountered heart palpitations and tachycardia without a clear diagnosis, and gastrointestinal symptoms linked to gluten have frequently caused fatigue and dizziness. Conditions like diabetes and blood clots have been ruled out. My previous rheumatologist suspected POTS, yet the new cardiologist has not conducted testing. Currently, I am taking Metoprolol, which has effectively managed my blood pressure, tachycardia, and palpitations. An MRI from about a year ago revealed a tiny lesion in a region associated with MS on the left side of my brain, while an EMG suggested CIDP; however, my current neurologist believes that the test was improperly conducted. This EMG coincided with my ovarian cancer diagnosis. Notably, my chemotherapy-induced neuropathy typically ends at my wrists and ankles, yet I’m experiencing different neuropathy predominantly affecting my right side. Recently, I was referred to a Neuro-Ophthalmologist due to a significant decline in my right eye's vision, accompanied by floaters, strobe-like flashes, and pain. What inquiries should I present to my neurologist? Is it plausible that the Nmdar antibody could remain present post-chemotherapy? Would a spinal tap be advisable? I suspect my neuropathy is worsening, yet it feels distinctly different from my chemotherapy-induced experience—what could this signify? I am willing to share some of my test results if necessary and would greatly value a new perspective on my situation.
Understanding Bertolotti's Syndrome
Greetings everyone, My name is Chiheb, a 25-year-old male standing at 175 cm and weighing 65 kg. I have been diagnosed with Bertolotti’s syndrome type 3b. For the past two years, I’ve been struggling with lower back pain. The discomfort tends to be most noticeable in the mornings, often subsiding as the day progresses. I experience increased pain particularly when I lean forward. I’m seeking advice on how to manage this condition effectively. Any suggestions would be greatly appreciated! Thank you!
Struggling with Mixed Incontinence: Seeking Solutions
A few years back, I received a diagnosis of mixed incontinence, and unfortunately, my condition has deteriorated significantly since then. As a 35-year-old mother of four—three of whom I delivered vaginally and one via cesarean—I find this situation particularly challenging. My struggles escalated further in 2019 when I faced a severe kidney stone, reportedly the size of a golf ball, prompting me to undergo four procedures over three months. Additionally, last year, I was diagnosed with diverticulosis, which complicates matters further. Recently, my incontinence has taken a turn for the worse, leaving me disheartened and frustrated. I've pursued physical therapy, but progress has been minimal. After bringing my worsening symptoms to my doctor's attention a couple of months ago, he referred me to a specialist. However, to my dismay, there’s a substantial wait time of about a year. Given my repeated visits for this issue, I feel frustrated by the delay in proper referral. Daily life has become increasingly cumbersome, as I rely on a pad, changing it multiple times a day. I even invested in specialized leak-proof underwear, yet I still need to use a pad along with it. This ongoing problem has plagued me for a considerable time, and it’s now becoming unmanageable. I’m eager to learn if there’s any possibility of accelerating my referral or if there are ways to navigate this waiting list effectively. Furthermore, I’m contemplating whether bladder lift surgery might be a viable option worth discussing when I finally meet with the specialist. I’m also anxious about the potential long-term implications of my condition, as it often leads to situations where I struggle to maintain control, even while walking. This constant worry has made it difficult to focus on anything else.
Understanding Chronic Back Pain: Seeking Guidance
Greetings! I am a 17-year-old female who has been enduring significant back pain for approximately six to seven years. The exact onset of this discomfort is unclear to me, but it has been a persistent issue. Until recently, I haven't focused on it much due to other pressing health matters but now feel the need to address it. The pain primarily centers around my spine and lower back, intensifying when I lie down or engage in physically demanding activities. It also aggravates after prolonged periods of standing. Fortunately, the discomfort does not extend beyond my neck. While lying down, whether on my side or back, I experience a sharp, unusual pain that only subsides if I tense my back muscles. Relaxation takes about 20 to 30 seconds. Even short breaks, like standing up for a minute to retrieve something, result in the same level of pain upon returning to a lying position. Lying on my side may alleviate the pain somewhat; however, the discomfort returns immediately if I switch back to my back. When I engage in any substantial activity for about half an hour, my right shoulder begins to hurt, with pain radiating from a specific spot that feels swollen or tense. This shoulder discomfort occurs after being seated or standing for extended periods. Additionally, I've been dealing with what appears to be sciatica symptoms in my right leg. I previously visited a chiropractor weekly or bi-weekly during my in-person schooling. Now that I am homeschooled, I have more time to focus on my discomfort. At school, I often found it unbearable to sit comfortably, prompting me to call my mother to take me home due to the pain. The chiropractor noted that I was in the early stages of scoliosis, but nothing else seemed abnormal. I’ve been informed that my growth should be complete, meaning my condition shouldn't worsen. Unfortunately, the relief from those chiropractic sessions was short-lived. About a week ago, I consulted with an orthopedic specialist who recommended starting physical therapy and prescribed pain medications to assess their effectiveness. He hinted at a possible disc issue, but I did not retain all the details. If the situation doesn't improve, he suggested further MRIs and potentially additional X-rays, which my mom and I prefer to avoid due to my previous exposure to radiation. My main concern during the appointment was the sciatica, which made it challenging to convey how troubling my ordinary back pain is. I managed to express my concerns several times but kept getting referred back to the sciatica issue. I just began a regimen of Naproxen (500mg, twice daily for five days) a couple of hours ago, which provided slight relief while lying down but not much else. Physical therapy is anticipated to start this Tuesday, and my sister will help me with some initial exercises starting tomorrow. Interestingly, the orthopedic doctor reviewed the abdominal MRI I underwent in May for a different issue and noticed a growth that appeared to resemble a cyst rather than something more concerning. I can provide those images if necessary; they were not intended for the orthopedic visit but rather for another specialist, which is why he was uncertain about the findings. This pain has significantly impacted my life, and I'm eager for insights on potential causes and solutions. I own a Belgian horse and ride regularly, which serves as my form of exercise, alongside various barn chores for 2-4 hours at least once or twice a week, depending on the weather. I sometimes volunteer nearly every day. While I hold some extra weight, much of it is muscle, and I have been actively trying to lose weight through dietary changes and increased physical activity. Could anyone shed some light on what might be causing my symptoms or suggest specific terminology I could use in discussions with my doctor?
Interpreting Rising Antibody Levels Following Antibiotic Treatment
I’m a 24-year-old female and the title might seem unclear. I've undergone two tests for tularemia, where my IgM levels were low but my IgG came back completely positive. Despite consulting several physicians who were uncertain about my diagnosis, I was prescribed a two-week course of doxycycline. Following my treatment, I retested and observed an increase in my IgM levels, prompting me to question whether this indicates that I truly have tularemia. Additionally, I found the antibiotics to have worsened my condition instead of improving it.