Tingling and Red Spots on Lower Legs
I’m a 28-year-old female, measuring 5 feet 9 inches and weighing 230 pounds. Lately, after spending an entire day on my feet, I’ve experienced a tingling and stinging sensation across the lower parts of my legs. Upon returning home and changing out of my sweatpants, I observed that my legs had developed a vivid red coloration in a blotchy distribution. The following day, this presentation shifted into numerous tiny red dots that were flat against the skin. The tingling persisted but improved significantly. Fast forward about two weeks, and I’m now encountering that familiar tingling sensation again, along with an increase in the small red spots scattered on my skin. I don’t have any known medical issues, yet I previously dealt with significantly low levels of B12 and vitamin D during a decade-long vegan diet. I try to supplement these nutrients when I can, and during my last blood test, my levels had improved (they were still on the lower end but within a healthy spectrum), though it’s been a couple of years since then.
Answers (1)

6/26/2025, 1:20:36 AM
OpenHealth AI
You’ve described tingling, stinging sensations in your lower legs and the appearance of red spots that have changed over two weeks. This could be related to peripheral neuropathy, irritation from prolonged standing, or vascular issues, but it’s important to consider your previous B12 and vitamin D deficiencies as well.
Explanation: The tingling and stinging in your legs can occur when nerves become irritated or compressed, often from standing for long periods. The red spots could be due to inflammation or changes in blood flow, especially after activity. Your history of low B12 and vitamin D might relate to nerve health, as deficiencies in these vitamins can lead to neuropathy.
Next Steps:
-
Take Breaks While Standing: If you know you will be on your feet for long periods, take breaks to sit down and elevate your legs for a few minutes. This can help reduce swelling and improve circulation.
-
Hydration: Ensure you are well-hydrated, as dehydration can exacerbate tingling sensations. Drink plenty of water throughout the day.
-
Monitor Symptoms: Keep track of when the tingling and red spots occur, noting any potential triggers such as time spent on your feet, types of shoes, or any recent activities.
-
Evaluate Vitamin Levels: Since you have a history of B12 and vitamin D deficiency, consider retesting your levels if it has been a while since your last blood test. This can help ensure you are within optimal ranges for nerve health.
-
Gentle Stretching and Exercise: Incorporate simple stretching exercises for your legs and feet. Gentle walking can also promote better blood circulation, which may alleviate some symptoms.
-
Avoid Irritants: Be mindful of any products that come into contact with your skin, as they may cause irritation leading to redness and spots.
If you experience worsening symptoms, such as persistent or severe pain, significant swelling, or changes in sensation, consider seeking further evaluation. This approach will help determine any underlying conditions and refine your management plan.
Related Questions
Old Scar Experience: Unwanted Discomfort After Years of Healing
At 23 years old, I have a burn scar on my left shin that dates back twelve years. It's fairly small, roughly the size of a two-dollar coin, originally caused by a heating pack used for gloves that slipped through my pocket, causing a burn overnight. The injury was quite severe, resembling medium-rare steak due to the extent of the burns, and resulted in a scar that is now a patch of perfectly smooth, numb skin devoid of hair growth. For over a decade, I’ve had no issues or pain from it. Recently, however, I've started to experience some discomfort that has escalated from mild itching to more pronounced sensations including aching, burning, tingling, and a prickling feeling similar to electric shocks. The discomfort seems to radiate from the scar itself. While I still don't feel any sensation directly on the scar when touched, the surrounding area quickly develops the pins and needles sensation. I’m curious if this kind of discomfort is common, especially after such a long time post-injury. Is it typical for scars to start causing pain many years later? I’m also interested in any potential remedies to ease the discomfort and whether this issue might resolve itself eventually.
Persistent Abdominal Discomfort: A Journey
This marks my initial post on Reddit, so I'd appreciate some gentle feedback. At 31 years old, I have been grappling with abdominal discomfort since my late teens. Initially, the pain resembles a mild cramp or ache in my stomach, but within about an hour, it escalates to an unbearable level. Over the years, I've noticed an increase in the severity of these episodes, which last somewhere between 6 to 8 hours. During these painful episodes, I often feel sweaty and overheated, and I find myself either curled up in a fetal position or pacing around the house. My bowel movements remain relatively unchanged; although I tend to feel the urge to use the bathroom, it rarely yields any significant relief. The sensation is distinct from constipation, even if that comparison might make sense. Typically, the discomfort begins in my lower abdomen (around the belly button area) but intensifies to involve my entire midsection—from my ribs to my hips and encompassing my back. Although I've never been pregnant, the pain feels similar to what one might imagine labor contractions would feel like, yet it's continuous. Over-the-counter medications such as Tylenol, Advil, or Aleve have proven ineffective against the pain. I have been prescribed tramadol, which doesn’t completely alleviate my discomfort; rather, I often find that it sedates me enough to eventually sleep through the episode. Afterward, I feel exhausted and somewhat lethargic, a sensation that predates my tramadol prescriptions. The frequency of these painful episodes appears completely erratic. There are times when I might experience several occurrences in a short period, only to go six months without any incidents. During my early encounters with this pain (around ages 19 or 20), I sought help at the Emergency Room. Initially, I was diagnosed with a bladder infection and prescribed antibiotics, but the pain would return a few months later. On one occasion, doctors administered Buscopan for what they believed was spasms associated with the bladder infection. Remarkably, this was before the era when we could check our lab results online, and during my ER visits, only a urine test was conducted—no blood tests. I spent a considerable amount of time believing the issues were due to bladder infections, which never fully added up in my mind. I was instructed by a doctor to practice proper hygiene after sexual activity, even though I hadn't been sexually active for over a year at that point. Eventually, I stopped visiting the ER because it became clear they weren't offering any real solutions, and I learned to endure the pain, knowing it would eventually subside on its own. Fast forward to 2019: the impact of these episodes had begun to interfere significantly with my work as a lifeguard—hard to oversee a pool while in extreme discomfort. Therefore, I sought meaningful answers from my family doctor, who ordered blood tests, stool samples, and an abdominal ultrasound. The results didn’t reveal anything alarming, aside from a diagnosis of fatty liver disease, which concerned me but didn’t explain my symptoms. At the time, I weighed 170 pounds at 5’3”, and while I wasn’t in optimal health, I wasn’t significantly overweight either. Later, I inquired about potential food allergies, specifically gluten and dairy. Testing indicated an abnormal reaction to gluten, leading me to eliminate it from my diet entirely. When I queried about undergoing a scope and biopsy for celiac disease, my doctor advised against it. Soon after, my doctor relocated, and I was assigned a new one. Despite adhering to a gluten-free regimen for nearly a year, I continued to experience these episodes. Interestingly, whenever I indulged in gluten, I didn’t seem to have any adverse reactions. My new doctor eventually referred me for a colonoscopy and endoscopy. At this point, I had abandoned the gluten-free lifestyle because it had become cumbersome without any discernible pain relief. Ironically, the day of my procedure coincided with the day after my 30th birthday. They discovered one small polyp, which was removed, but the biopsy for celiac disease returned negative. I was diagnosed with chronic gastritis, and although tested for H. pylori, the results were negative. Both my doctor and I hoped that this gastritis could explain my discomfort, and I was prescribed a PPI, which I took for about a year. Sadly, my painful episodes continued. If I ever forgot to take the medication, the gastritis would make itself known through upper abdominal pain. During this time, I also dealt with painful menstrual cramps and irregular cycles. A pelvic ultrasound revealed "Small peripheral follicles in the right ovary, indicative of a PCOS variant,” with the conclusion suggesting possible PCOS. In March 2024, I developed achy pain in my right flank and abdomen. I made an appointment with my family doctor, who suggested it was likely a kidney stone or urinary tract infection (UTI). I was placed on antibiotics, but shortly after completing the medication, I experienced one of my usual painful episodes, this time with increased discomfort on the right side. I suspected it was different from my typical stomach pain, leading me to seek ER assistance, where I was told I had a bladder infection based on leukocytes found in my urine. I requested a culture, which returned negative for bacteria. Blood test results showed some flagged values, but overall, nothing alarming. The ER doctor theorized gallstones and indicated that an ultrasound was necessary, advising me to avoid fatty foods until then. Eventually, the follow-up ultrasound revealed again a fatty liver and a "Friesian cap gallbladder," yet there were no other indications of stones or sources of my abdominal discomfort. My family doctor consulted a surgeon about the gallbladder's unusual shape, but they dismissed it as a potential cause for my pain. In due course, I was prescribed tramadol for pain management along with Accel-hyoscine, neither of which seemed to significantly relieve the extreme pain. I began to restrict my use of medications for when the discomfort became unbearable. During this time, I also made the decision to resume birth control (Depo), as I couldn’t recall whether the pain episodes reduced while I was taking it, possibly due to endometriosis. However, after a year of being on Depo, I continued experiencing episodes with no clear correlation to my menstrual cycle. In March this year, I again experienced severe abdominal pain, compounded by right-sided discomfort. This pain persisted for a few days, leaving me feeling fatigued and bedridden. My husband insisted I visit the ER on the third day, where a doctor expressed concern about possible appendicitis, but noted that being a woman meant it could also be related to reproductive health issues. I was referred for a CT scan, which I underwent that week. My blood tests revealed some high cell counts, which concerned doctors. The CT scan results indicated mild fatty infiltration of the liver but no acute issues in the abdomen. However, an unusual focus was noted in the iliopsoas muscle on the right, measuring 38 x 16.8 x 19.4 mm, warranting an MRI for further investigation. My family doctor was uncertain if this finding contributed to my pain, confessing he hadn’t encountered it before, only hearing about similar cases while practicing in Africa. Consequently, I was referred to a surgeon, who ordered an MRI and consultation with a gastroenterologist. The MRI findings revealed a benign thin-walled multiloculated cyst in the iliopsoas tendon, suggesting a long-standing condition, with differential diagnoses including iliopsoas bursitis or possible issues buttressing the labrum. Since February, however, I have been free from those painful attacks. My growing frustration mounts as I finally connected with the gastro doctor, who requested more stool and blood tests, along with yet another abdominal ultrasound despite a CT scan conducted recently. This time, the stool sample returned positive for Yersinia enterocolitica infection, an unknown factor as I had no symptoms. Still, following my insistence, I received antibiotics to treat it due to its potential to masquerade as appendicitis. My hope to resolve this experience was palpable, although the gastro doctor expressed skepticism about its relevance. While awaiting further ultrasound results, I met with the surgeon, who opined that I should not have been referred for the cyst since it likely wouldn’t cause abdominal discomfort. We reviewed the chronological issues I've encountered along with possible explanations, ultimately contemplating a HIDA scan as my next step. The week following this, my gastro doctor called with the ultrasound results revealing nothing new about my fatty liver and fixated on weight loss as a solution—something I was already aware of but took as somewhat condescending. The communication was challenging as the doctor was located six hours away and I had difficulty understanding through the heavy accent. While I tried to explain that these pains surfaced when I weighed as little as 150 pounds, the doctor demonstrated little regard for my historical context and opinions, dismissing the suggestion from the referring surgeon for a HIDA scan. Instead, he proposed another imaging test—a CT scan, despite my recent history with the same procedure. Currently, I have reached out to the surgeon's office for their input, and I'm scheduling an appointment with my family doctor to explore the possibility of seeking a different gastro doctor. As for diagnosis, my current doctor suspects irritable bowel syndrome (IBS), but I’m hesitant to accept this label. It feels too simplistic considering the complexity of my situation, and I want to ensure that all potential underlying causes are thoroughly investigated. He prescribed Librax to try as a remedy for the next time I experience an episode. At this stage, I feel uncertain about the next steps to take.
Struggling for Recognition in My Health Journey
As a 34-year-old woman, six months after my second cesarean section, I find the need to express my ongoing health challenges. I've contended with frequent illnesses since childhood, often facing ridicule and being labeled a hypochondriac, with others dismissing my symptoms as mere allergies. This perpetual belittlement has left me feeling like my genuine struggles are overlooked, contributing to a significant decline in my overall well-being. I feel lost in my pursuit for adequate support and treatment. Currently, I carry several diagnoses, including: - Long COVID - PTSD - Generalized Anxiety Disorder (GAD) - Attention Deficit Hyperactivity Disorder (ADHD, combined) - Depression - Obsessive-Compulsive Disorder (OCD) Additionally, I experienced gestational diabetes and mild preeclampsia during both of my pregnancies. Today, I reached out to my psychiatrist to discuss the possibility of reevaluating my current medication regimen, as I believe the combination I’m on may not be serving me well — though I acknowledge I'm not a medical professional. Presently, my medications include: - Lamictal 100mg - Wellbutrin 150mg - Adderall XR 30mg in the morning - Adderall IR 10mg in the afternoon - Clonazepam .5mg as needed for panic attacks - Recently added, Effexor, which I started at 75mg. However, for the first two weeks, I felt overwhelmingly intoxicated, and my OCD symptoms intensified, causing me to go several nights without sleep. After discussing my concerns with my psychiatrist, she increased my dosage to 150mg. It has now been over a month, and I fear I may be experiencing negative side effects from the Effexor. My energy levels are at an all-time low — my appetite has diminished, and it's only with the aid of clonazepam that I'm able to consume any food. Sleep eludes me for at least three nights each week, and I find myself consumed by incessant thoughts and compulsive behaviors, along with heightened anxiety that makes even stepping outside feel daunting. My symptoms frequently surface in episodes, particularly following a traumatic event in 2019 — the loss of my closest relative. My ongoing issues include: - Chronic respiratory infections - Recurrent white tongue and a swollen throat - Unexplained bruises on my body - Joint discomfort, especially in my hands - Persistent chest pressure and tightness - Difficulty taking deep breaths, at times feeling a lump in my throat - A continual urge to clear my throat - An inconsistent cough - Fluctuating heart rates that can surge from 66 to 140 within seconds - Often resting at an average heart rate of around 115 - An incessant feeling of a racing heart, which I have mentioned to various doctors, only to be attributed to "postpartum anxiety" — yet, I experience it consistently throughout my day. - Scalp flare-ups with scaly patches that sometimes bleed and itch intensely, making it one of my most distressing issues. - Dizziness and a lightheaded sensation, especially when standing - Challenges with swallowing - Pronounced fatigue and lethargy - Intense insomnia - Intolerance to both heat and cold - A persistent fogginess in my memory, frequently forgetting conversations shortly thereafter - Jaw pain and tension - Recurrent bladder discomfort. Despite multiple tests indicating normal lab results, I have identified recurring patterns and abnormal findings in my medical history. When I sought care for back pain at the ER, an X-ray was deemed normal, yet they noted fluid in my lungs without raising any concerns. Each time I seek help for respiratory illness, I receive a diagnosis of walking pneumonia and a prescription for antibiotics. I am reaching out for any advice or insights and would appreciate suggestions for specific tests or imaging I might request.
Assistance for Delayed Wound Healing
I’m a 29-year-old female weighing 222 pounds, a non-smoker currently on medications such as Plaquenil, Imuran, and Citalopram. My medical history includes a diagnosis of Sjögren's syndrome, along with anxiety and depression. For the past six months, I’ve been taking azathioprine to manage my Sjögren's symptoms. Recently, I experienced a severe breakout attributed to my menstrual cycle. Regrettably, I found myself picking at some of the blemishes, which has resulted in scabs and persistent acne on my upper back, chest, and face. It’s been three weeks since this occurred, and despite my efforts to avoid further picking, the spots show no signs of healing. The acne takes an unusually long time to resolve even when left untouched. I do my best to keep my skin moisturized and treat it gently, but I am eager to find ways to enhance the healing process. I’m feeling quite overwhelmed. I contacted my rheumatologist regarding this issue, and she advised me to consult a dermatologist if my condition doesn't improve. Unfortunately, accessing a dermatologist is a challenge for me due to insurance coverage limitations.
Navigating Life After Four Episodes of Psychosis
At 39 years old, I find myself as a Sudanese refugee residing in Egypt, grappling with the aftermath of four psychotic episodes. Since 2007, I have been dealing with obsessive-compulsive disorder, and a physician has also diagnosed me with major depressive disorder. My current medication regimen includes 30 mg of aripiprazole and 100 mg of faverin. To manage my psychotic symptoms, I receive monthly intramuscular injections of 50 mg haloperidol. I am reaching out to understand whether it is likely that I will need to continue this medication for the long term. Furthermore, I am curious about what the future holds for someone with a history of psychotic breaks; specifically, what areas should I prioritize moving forward? Presently, I am without a job and struggling with obesity, weighing in at 353 pounds. I apologize if my tone seems pessimistic, but I am sincerely seeking guidance into my situation.