Understanding Unusual Paresthesia During Rest
Summary: Why do I experience sensations of pins and needles while feeling relaxed and warm instead of in cold or anxious states? I am a 42-year-old woman, weighing 180 pounds and standing 5 feet 8 inches tall, and I frequently experience sensations of pins and needles. Generally, it is believed that these sensations occur when nerves receive insufficient blood flow, often due to cold temperatures, anxiety, or physical constriction of blood vessels. However, my situation seems to be the exact opposite, as I tend to experience this phenomenon primarily when I am warm and completely at ease. Typically, these sensations manifest in my thighs when I am resting in bed, whether sitting up or lying down. These pins and needles often rush in and out rather than being a steady feeling, distinguishing them from the typical sensation of a leg ‘falling asleep.’ Additionally, when I take Adderall and then choose to relax rather than engage in work, I sometimes feel tingling sensations in my vulva, which is more uncomfortable than enjoyable. When I get particularly warm, I also notice these sensations occurring in my face, affecting both sides, as well as in my scalp, where they often feel more diffuse and mobile. Intriguingly, these scalp tingles typically arise during an exhalation, contrasting with the significant pain in my ears and head that I experience when I breathe in cool air. While I do tend to have paresthesia caused by overuse of my arms and hands, often linked to conditions like carpal tunnel syndrome, the sensations I describe here are noticeably distinct and not linked to physical exertion or inflamed tendons. Most notably, the thigh and scalp sensations feel more transient and fluid, whereas those in the face and vulva are generally steadier but still mild, differing significantly from the annoying ‘tickle’ sensation when a limb falls asleep. Medical Evaluations: - I have consulted with my primary care physician several times regarding these sensations. - I have undergone two blood tests, both of which returned normal results apart from consistently elevated ANA levels. These tests ruled out conditions such as diabetes, inflammation markers, rheumatoid arthritis, thyroid issues, and anemia. - A CT scan conducted a few years ago to investigate facial tingling was normal. - I also had a nerve conduction study on my arms due to complaints at that time, which was likely related to carpal tunnel syndrome and has since resolved on its own; the results were normal. - An ultrasound of my left calf was performed after I experienced sudden swelling in that area last summer, along with a menthol-like sensation as the swelling subsided. The ultrasound results were normal, ruling out blood clots. - A recent CT scan of my sinuses was ordered due to a severe headache coupled with chronic post-nasal drip. The findings showed no signs of sinus disease or structural obstructions. Medications: I have been prescribed sertraline for depression, Adderall XR for ADHD, and Nikki birth control for premenstrual dysphoric disorder, all of which I have been taking for about 4 or 5 years. Recently, I was prescribed propranolol for headaches by an ENT specialist, but I haven’t noticed significant improvements—only increased tiredness and dizziness. Additional Information that May Be Relevant: I identify as a highly sensitive person and experience a phenomenon known as “frisson,” where I feel a similar tingling sensation, triggered by strong emotional responses to music or beauty, often in the same areas as the aforementioned paresthesias (legs, scalp). My limited experiences with marijuana have consistently resulted in full-body tingles, a sensation I’ve learned is not common. I have cold sensitivity characterized by Raynaud's phenomenon affecting my feet, but I usually feel just coldness or numbness without paresthesia. This condition runs in my family; my three brothers and son also experience similar symptoms. My sensitivity also extends to the nose and nipples. My hands, once severely affected, now show less sensitivity. I suffer from progressive sensorineural hearing loss since childhood, with no family history of early onset. Furthermore, chronic fatigue has been a long-standing issue that seems to worsen with age—I've often joked that sleeping is my hidden talent, as I tend to need significantly more sleep than my peers. While Adderall has helped manage this fatigue, I wonder if it contributes to the more frequent paresthesias I’ve experienced in recent years. Although I feel these sensations even when not medicated, their prevalence raises questions regarding prolonged use side effects. Lastly, I have dealt with Achenbach syndrome over the last couple of years, experiencing random vessel pops in my left hand and foot. I also have a history of chronic pubic symphysis pain and other joint instability issues related to hypermobility in my pelvis, though I've been evaluated for hypermobility traits without findings indicative of broader syndromes. I don’t have any significant flexibility elsewhere, and I’m not pregnant. I commonly experience various forms of dizziness, particularly when sitting down to dinner, which seems inconsistent and perplexing. The onset of dizziness often occurs when transitioning from a task to relaxation, but it frequently does not correlate with food intake, suggesting possible connections with my medication or daily rhythm instead. This unique combination of symptoms presents a complex picture worthy of further exploration.
Answers (1)
12/16/2025, 8:11:03 PM
OpenHealth AI
It sounds like you're experiencing a range of sensations that can be quite perplexing and frustrating. Paresthesia (the pins and needles feeling) can have multiple causes, even when the sensations occur during periods of relaxation and warmth. Let's break down your concerns and explore next steps.
Main Points:
- Paresthesia During Relaxation: You are experiencing unusual sensations of tingling in various parts of your body, primarily when you are relaxed and warm, which is atypical compared to common triggers.
- Complex Medical History: Your background includes several medical evaluations, some with results showing elevated ANA levels but otherwise normal findings across various tests.
- Medication Considerations: You are on several medications that could impact sensation and should be carefully assessed.
Explanation:
Paresthesia can occur due to:
- Nerve Sensitivity: Conditions like heightened sensitivity or dysregulation of the nervous system can lead to sensations that don't have a clear trigger.
- Medication Effects: Some medications, like Adderall, can contribute to heightened sensations or anxiety, which may exacerbate the feeling of pins and needles.
- Circulation Issues: Although you've ruled out significant circulatory problems, you mentioned coping with Raynaud's phenomenon, which involves blood flow sensitivity.
- Psychological Factors: Anxiety and stress can also create or amplify these sensations, sometimes especially pronounced in highly sensitive individuals.
Next Steps:
- Symptom Journal: Keep a detailed log of your paresthesia episodes, noting the context (time of day, activity prior, feelings before onset) and how long they last. This may help identify triggers.
- Medication Review: Discuss with your healthcare provider the possibility of side effects from your medications, including Adderall and sertraline, and evaluate if adjustments are necessary.
- Nerve Assessment: While previous tests showed normal results, consider revisiting assessments or referring to a neurologist for deeper evaluation of potential nerve entrapment or sensory neuropathy.
- Mind-Body Approaches: Practicing relaxation techniques, such as mindfulness meditation or gentle yoga, could help manage sensations and improve overall anxiety or stress levels.
- Further Testing: Discuss with your healthcare provider about the need for any further testing, given your elevated ANA levels and complex symptomatology. This might include autoimmune screening if deemed necessary.
Ongoing Support:
Your symptoms are complex, and it’s important to maintain open communication with your healthcare team. Exploring your feelings and experiences with a support group or therapist might also provide additional coping strategies. Remember, you're not alone in navigating these challenges.
Related Questions
Battling Chronic Nausea and Vomiting for Over Two Years
For the past two years, I (age 26, female) have been enduring an incredibly challenging health situation. I experience intense nausea daily and find myself vomiting numerous times, with almost nothing providing relief. To provide some background, I’m from West Texas and I currently weigh around 190 pounds, standing at 5’7”. Initially, my weight was about 211 pounds when these symptoms began, and it fluctuates frequently between 190 and 225 pounds. I engage in vaping and consume THC. Previously diagnosed with hypothyroidism, my condition seemingly resolved, according to my healthcare providers. Additionally, I have polycystic ovarian syndrome (PCOS). I have consistently faced irregular bowel movements, with stools that are loose and sometimes appear to have mucus. Compounding my struggles, I've also suffered from migraines. I have had an IUD for over five years, experiencing two insertions of the Kyleena device. In December 2022, my battle with health took a severe turn when I was diagnosed with stage 4 Hodgkin’s Lymphoma, requiring chemotherapy treatment, specifically AVBD (Apologies for not recalling the exact medication names). By July 2023, I had fortunately achieved remission. However, after reaching remission, my vomiting worsened, transforming from primarily white foam to a mixture of 80% bile, any food I attempt to consume, and still white foam. This intense vomiting, accompanied by significant pain in my upper back, escalated to more than eight episodes daily by November 2023. At that time, THC seemed to be the only avenue for me to retain any food. During this tumultuous period, I consulted various doctors who, after confirming I wasn’t pregnant, attributed my symptoms to Cannabinoid Hyperemesis Syndrome (CHS). Immediately, I ceased THC consumption for over six months, yet the vomiting continued unabated. Each time, doctors would prescribe ondansetron, regardless of my claims that it provided no relief. I experimented with various diets recommended by medical professionals, but there were no improvements in my condition. Eventually, I obtained a referral to a gastroenterologist who intended to perform an endoscopy. However, the procedure was prohibitively expensive even with insurance, and thus was never conducted. This doctor also ordered blood tests to rule out several gastrointestinal disorders, such as Crohn's disease, Irritable Bowel Syndrome (IBS), and gluten sensitivity, but all results came back normal. Afterward, I had another appointment with a different gastroenterologist, but the doctor failed to meet with me. Instead, a nurse informed me that the doctor had merely recommended promethazine without conducting any tests or scheduling further visits. When I mentioned the possibility of gallbladder issues, the doctor laughed dismissively at my suggestion. Discussing my situation with my oncologist, he suggested that my heightened sensitivity to food odors stemmed from my chemotherapy experiences while I was working in fast food. While food smells indeed affect me, I'm primarily triggered by medical scents such as rubbing alcohol and cleaning agents. This ongoing ordeal has been overwhelmingly distressing. I now experience episodes of vomiting accompanied by bright red blood, presumably due to a throat tear. When I first encountered this troubling symptom, I consulted a doctor who appeared unfazed and prescribed a promethazine suppository, which does help but makes me extremely drowsy. My nausea persists nearly around the clock, often feeling as if there’s a heaviness in the upper part of my abdomen. I frequent urgent care facilities when my symptoms intensify, only to be met with minimal assistance since this is a chronic issue. Currently, I lack a primary care physician. Whenever I sought one, I encountered skepticism regarding my condition, with some healthcare professionals implying that I was exaggerating my symptoms. Though many physicians who do take my situation seriously seem baffled, I've lost count of the diverse medical experts I've consulted about these ongoing issues. If anyone has insight or suggestions, I would genuinely appreciate it. I can share my latest bloodwork results if that would be helpful—just let me know!
Strange Stomach Sensation Leading to Waking Up
Greetings. I'm a 36-year-old male, standing at 172 centimeters and weighing 90 kilograms. I don't take any medications, nor do I smoke. I've been living with diastasis recti for several years now, and I may also have irritable bowel syndrome (IBS). Additionally, I deal with fatty liver and kidney stones, though I assume these last two conditions are not related to my current concern. Occasionally, I experience a peculiar sensation that jolts me awake; it feels like a quick pulsing in my stomach. I’ve noticed it tends to affect the left side when I’m lying on my left side and the right side when on my right. Remarkably, it can occur even when I’m on my back. This strange feeling often escalates into a surge that fully rouses me. Alongside this, I sometimes feel prickling sensations throughout my body and fleeting lightheadedness. When this sensation disturbs my sleep while I’m turned to my side, shifting onto my back or the opposite side might alleviate it, but not always. In instances where I awaken while lying on my back, I discovered that gently pressing my hands on either side of my stomach can help, as can rising to a sitting or standing position. However, during my last two episodes—one a couple of weeks ago and another tonight—those techniques weren’t effective right away, which made me feel a bit anxious, prompting me to seek advice. Does anyone have insight into what might be going on? By the way, I’ve undergone routine ultrasound examinations of my abdomen by two different physicians during check-ups, both of whom assured me that everything appears normal, including my abdominal aorta and internal organs. They didn’t identify any issues at that time.
Swelling Beneath My Chin Near the Jawline
18-Year-Old Male: I'm reaching out to any medical professionals who might provide insights into my situation. I've been using marijuana since I was 14, but now, at 17, I'm making an effort to stop and have been clean for 18 days. Recently, I've discovered an unusual swelling located just beneath my chin, behind my jaw. It causes some discomfort when I move, yet it doesn’t feel painful continuously. I'm somewhat anxious that this could be indicative of a more serious issue, especially considering it's positioned near my chin's lymph nodes. Any advice or information would be greatly appreciated as it might help alleviate my worry.
Seeking Insights: My Journey with Undiagnosed Neurological Symptoms
Hello everyone, I'm a 34-year-old female grappling with neurological symptoms that first appeared in October, and I’m eager to hear from anyone who might have faced similar challenges. My journey began with unexpected migraines, blurred vision, and an ongoing sensation of being off-balance or intoxicated. Gradually, I began experiencing mainly sensory-related symptoms, such as tingling and burning sensations, feelings of extreme heat and cold, sharp pains radiating in my arms and back, as well as discomfort in my hands and toes, alongside intermittent numbness. I also endure varying degrees of weakness and heaviness in my right side, specifically my arm and leg, although I haven’t suffered complete functional loss. The nature of my symptoms is erratic; they fluctuate rather than consistently deteriorate. An MRI revealed mild, scattered lesions in the white matter, which were deemed nonspecific. Further tests from a lumbar puncture returned normal results, showing no markers of inflammation, and the oligoclonal bands were not present. A thorough range of lab tests yielded no significant findings. After evaluating my case, the neurology team suggested a possible diagnosis of MS and administered a three-day course of intravenous steroids. While I noticed a slight improvement in some sensory pain, my symptoms persist and continue to vary day by day. I still experience headaches and pressure in my head along with episodes of blurred vision, but there have been no new deficits since treatment. I am reaching out to connect with others who have had similar experiences. I would like to learn about the insights or diagnoses you encountered and what treatments proved beneficial (such as those related to migraine disorders, dysautonomia, or sensory neuropathy, for example). If you have navigated a similar path, I would greatly appreciate your sharing your story. Thank you!
Should I Seek Medical Attention for Left Ear Pulsatile Tinnitus?
A 31-year-old woman reports an ongoing issue with pulsatile tinnitus, which she is currently experiencing solely in her left ear. Although she's noticed this condition intermittently before, she hadn’t paid it much mind due to the absence of pain. Recently, however, her curiosity piqued her interest in researching the condition, where she stumbled upon information suggesting it could be serious. Usually, she avoids searching online for health worries, but now she is contemplating whether a visit to the doctor might be warranted. Can anyone advise on the need for a medical evaluation in this case?