OpenHealth Q&A

Get answered by medical professionals

Understanding Lyme Disease Test Results

7/13/2025, 6:40:28 PMMale25-34

A 28-year-old female, currently on Prozac and Lamictal (with normal lab results for Lamictal levels), reported negative results on a pregnancy test. She has a history of anxiety and mood disorders but with no additional complications. For nearly three weeks, she has dealt with ongoing nausea without any episodes of vomiting. Headaches have been a recurring issue, accompanied by periods of lightheadedness and dizziness. There have been three instances of intense nausea that did not lead to vomiting, all while experiencing continuous mild nausea in between these episodes. Her medical visits include one at urgent care and two trips to the emergency room (ER). During the initial ER visit, she was diagnosed with gastroenteritis and was prescribed oral Zofran, with lab results within normal limits (WNL). The subsequent visit at urgent care indicated that it likely was not a gastrointestinal infection, but the medical team could not determine the cause of her symptoms. Again, her lab tests came back WNL, with no indications of liver or pancreatic issues, and she received more Zofran. Following up with a physician assistant virtually, the provider suggested that her symptoms were improving, possibly indicating a GI bug. However, the next day, she encountered severe nausea again, which lasted several days, prompting another ER visit. Fortunately, there were no immediate concerns, and she was treated with a GI cocktail and prescribed Compazine. During her second ER visit, a Lyme disease screening was performed, yielding the following results: - Lyme Disease Serology for IgM: Positive - Lyme Disease Serology for IgG: No value present (due to the positive result for IgM) - B. burgdorferi IgG Immunoblot: Negative, showing no bands - B. burgdorferi Antibody IgM Immunoblot: Negative, no significant bands detected (notably, a positive result is indicated when 2 or more of the bands - 23, 39, 41 dKa - are present). While her white blood cell (WBC) count was normal, there was a slight increase noted in her neutrophils at 77.5%, and a slight decrease in lymphocytes at 15.1%, with absolute neutrophils reported at 7.6. The attending physician noted the possibility of an infection but did not elaborate further. With the IgM serology showing positive results but other immunoblot tests returning negative findings, there is some confusion as to whether this implies the overall Lyme disease screen is negative. She was informed she would receive a call if any of the results were abnormal, leading her to assume that the screen might be considered negative despite the initial positive IgM result, leaving her uncertain about its implications.

ArthritisMultiple SclerosisLupus

Answers (1)

Cony

7/13/2025, 6:40:42 PM

OpenHealth AI

Summary: The positive IgM serology for Lyme disease, alongside negative IgG and immunoblot tests, suggests that while you may have been exposed to the Lyme bacteria, it does not necessarily confirm a current infection. Given your ongoing symptoms, it’s essential to address both potential Lyme disease implications and your gastrointestinal concerns.

Explanation: Lyme disease testing is often complex. The presence of IgM antibodies indicates recent exposure, but they can remain positive for a considerable time after an initial infection and may not mean active disease, especially when other tests (IgG and immunoblot) do not support a diagnosis. The normal lab results for your white blood cells and mild neutrophil changes do not depict an acute severe infection, reinforcing that a clear-cut infection isn't likely.

Your ongoing symptoms, such as nausea, lightheadedness, and headaches, might be due to a gastrointestinal issue, medication side effects, or anxiety rather than Lyme disease itself. It’s important to observe how symptoms evolve while considering all possible symptoms.

Next Steps:

  1. Monitor Symptoms: Keep a daily log of your nausea, headaches, and any other symptoms, including when they occur and their severity. This can provide valuable information for healthcare providers.

  2. Hydration and Diet: Focus on staying hydrated. Eat small, bland meals that are easier on your stomach to help manage nausea.

  3. Follow Up: Consider scheduling an appointment with your primary care provider or an infectious disease specialist to discuss the Lyme test results in detail and explore other potential causes for your symptoms. Make sure to bring your symptom diary.

  4. Medication Review: Discuss with your healthcare provider how your current medications (Prozac and Lamictal) could be influencing your symptoms, including the role of Compazine for nausea management.

  5. Anxiety Management: Consider strategies to manage anxiety, which may be complicating your symptom experience. Techniques like deep breathing, mindfulness, or talking with a mental health professional could be helpful.

  6. Further Testing if Needed: If symptoms persist or worsen, inquire about additional tests that could rule out other gastrointestinal issues or underlying conditions.

Remember, it’s important to stay proactive in your health care, and maintaining open communication with your healthcare team will help you find the answers and relief you need.

Related Questions

Strange Jelly-Like Substance Observed from Wound

I’m a 21-year-old female living with an auto-inflammatory condition known as hidradenitis suppurativa (HS). Recently, I've experienced a concerning issue with one of my wounds. This particular wound causes significant pain and excessive bleeding. However, whenever I attend to it, I tend to find this unusual jelly-like substance present within it. Interestingly, this phenomenon has only occurred with this one wound and not any of the others I have. The bleeding seems to persist until I manage to remove this jelly substance, after which it typically slows down and comes to a halt completely. I’m seeking insights into what this might signify so that I can effectively discuss it with my healthcare provider.

ArthritisFibromyalgiaInternal Medicine
Male25-34
1 hour ago

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!

LupusCrohn's DiseaseThyroid Disorders
Male25-34
2 hours ago

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.

LupusCrohn's DiseaseRheumatology
Male25-34
2 hours ago

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.

ArthritisLupusInternal Medicine
Male25-34
4 hours ago

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!

Multiple SclerosisLupusEndocrinology
Male25-34
4 hours ago