OpenHealth Q&A

Get answered by medical professionals

Seeking Guidance on ANA Test Results and Associated Health Concerns

7/28/2025, 3:40:39 PMMale25-34

I’m a 29-year-old woman seeking insights regarding some recent medical findings. After undergoing a biopsy, I received diagnoses of lichen simplex and early-stage lichen sclerosus. Unfortunately, I won’t be able to consult with my new primary physician until November. In the meantime, I am investigating whether my previous health issues could indicate an autoimmune condition, largely due to my mother's history with rheumatoid arthritis, as well as her experiences with oxalate troubles, hypothyroidism, osteoporosis, and debilitating migraines. My ANA titer results showed a reading of 1:40H with a nuclear, speckled pattern. While I am trying to remain calm and avoid jumping to any conclusions, I would appreciate guidance on how to discuss these findings with my healthcare provider. The impetus for these lab tests was a persistently low white blood cell (WBC) count over the last eight months. Interestingly, my most recent WBC levels returned to normal, though the absolute eosinophils were notably low at 8L, which I understand may not be a red flag. Additionally, my C-reactive protein (CRP) level was reported at less than 3.0. I’ve committed to repeating these lab tests in about a month as I’m currently on day seven of the Autoimmune Protocol diet. For context, I am a white female, standing 5'5" tall and weighing 137 pounds. I maintain an active lifestyle and am in the process of finding an effective stimulant for ADHD, with plans to start on 5mg of Focalin tomorrow. My daily supplements include collagen powder, Vitamin C, Omega-3, and Vitamin D3+K2. Occasionally, I apply mupirocin for MRSA flare-ups. Recently, I underwent a bilateral salpingectomy during which a small amount of endometriosis was excised. A recent bone scan revealed normal results, and earlier this year, hormone tests yielded typical values, apart from the aforementioned WBC concerns. I have previously battled Lyme disease and still contend with Epstein-Barr. Over the past few years, I've been experiencing various symptoms, including IBS-D, fatigue, swelling in my hands, newfound allergies to pets and adhesives, worsened seasonal allergies, headaches, upper abdominal pain, signs of hypoglycemia, acid reflux, and a general itchiness. This past year, I’ve noticed an increase in illnesses and longer-lasting symptoms, including a sinus infection at the start of this month that is only now beginning to resolve. My IBS symptoms have persisted for about seven years and seem to run in my family, as my mother, aunt, and maternal grandparents have similarly struggled. The MRSA infection in my nasal passages emerged years ago and tends to recur, particularly when allergies flare up and excessive tissue use leads to dryness and minor cuts. I would greatly appreciate any insights on whether these symptoms could indicate a specific condition. I expect additional tests may be required but would like to have some initial thoughts to guide my conversation with my doctor.

LupusCOPDRheumatology

Answers (1)

Cony

7/28/2025, 3:41:05 PM

OpenHealth AI

It sounds like you are navigating a complex health situation, and it's understandable to seek clarity regarding your symptoms and test results. Your ANA titer of 1:40H with a speckled pattern can suggest the possibility of an autoimmune condition, though it is not definitive. Here are some key points and next steps that may help you prepare for your upcoming discussion with your primary physician.

Key Points

  1. ANA Test and Autoimmune Conditions: An ANA (antinuclear antibody) test is often a preliminary screening tool for autoimmune disorders. While your elevated titer is noteworthy, many healthy individuals can have a positive ANA without having an autoimmune disease. Conditions such as lupus, rheumatoid arthritis, and others can cause elevated ANA levels, but further testing is needed for diagnosis.

  2. Related Symptoms and Family History: Your symptoms (fatigue, joint swelling, allergies, IBS, etc.) could potentially relate to an autoimmune disorder, especially given the family history you noted. It's essential to discuss how these symptoms have developed in order to help your physician assess your condition better.

  3. Blood Cell Count and CRP Levels: Your previous low WBC count could have various causes, including infections or bone marrow issues, but considering it is now normal is reassuring. A CRP level less than 3.0 typically indicates low inflammation, which is a good sign.

Next Steps

  1. Prepare for Your Appointment: Since your appointment is not until November, it may be helpful to compile a list of all your symptoms, how long they have lasted, and any noticeable triggers. Documenting this will help your doctor understand your medical history more clearly.

  2. Discuss Symptoms in Detail: When you meet with your physician, address your family history of autoimmune conditions and your specific symptoms, especially the ones that are most concerning you (e.g., joint swelling, IBS symptoms, fatigue). This context can guide your physician toward specific tests or examinations.

  3. Consider Further Tests: Given your symptoms and family history, ask your doctor if further autoantibody tests or specific assessments for autoimmune conditions might be warranted. For instance, rheumatoid factor (RF) or anti-CCP for rheumatoid arthritis could be evaluated.

  4. Monitor Your Diet and Symptoms: Since you're following the Autoimmune Protocol diet, keep track of any changes in symptoms, as this may provide insight into triggers or improvements in your condition.

  5. Stay Proactive with Your Health: Continue your current supplements, maintain an active lifestyle, and keep up-to-date with your blood tests as planned. If any symptoms worsen or new symptoms arise before your appointment, it may be worth reaching out to a healthcare provider sooner.

Lastly, remember that it's okay to feel anxious about your health concerns. Staying informed and prepared can help ease some of that anxiety and make your appointment more productive. You are doing a great job in advocating for your health.

Related Questions

Seeking Answers for My Ongoing Health Crisis

Age: 44 | Weight: 174lbs | Height: 5'11 | Ethnicity: Caucasian | Duration of Issues: 6.5 Years | Current Medications: None | Lifestyle: Non-smoker, non-drinker. During the spring of 2019, I experienced a sudden illness that has perplexed my healthcare providers. After numerous consultations and conversations with various medical professionals, I turn to the Reddit community in hope of finding some clarity or insight. My range of symptoms includes persistent rhinitis, cognitive difficulties such as brain fog and memory issues, heightened anxiety and depression correlated with dietary intake, chronic fatigue, early awakenings around 3 or 4 a.m., diminished libido, erectile dysfunction, blurriness in vision, dizziness, relentless tendonitis and joint pain, and symptoms of Raynaud's phenomenon more prominently affecting my right hand. I also face tingling sensations in my extremities and experience itchy, burning skin. In the initial stages of this condition, I struggled significantly with nausea, frequent vomiting, gastrointestinal disruptions, and severe muscle tightness particularly throughout my arms, legs, hips, neck, pelvic area, and jaw. Over the past year, I have lost between 41 to 43 pounds, dropping from 215 pounds to 174. I’ve undergone a multitude of tests, including MRIs, hip X-rays, an extensive array of blood tests, a colonoscopy, an endoscopy, and consultations with specialists like a rheumatologist, gastroenterologist, sports physiotherapist, and allergist. All results have come back normal. My testosterone levels were on the lower side but remained within acceptable limits, and I was found to be deficient in Vitamin D. While I have seen some modest improvements over these six years, primarily through applying a methodical approach to identify foods that exacerbate my symptoms, I still maintain a chronic level of discomfort even when avoiding these triggers. My current diet largely revolves around eating mashed potatoes and chicken daily, as they seem to keep my symptoms manageable, allowing me to think more clearly while avoiding severe tendonitis and joint pain. I underwent an elimination diet and suspect that fructans could be at the root of my problems. However, I find it hard to believe that these and Small Intestinal Bacterial Overgrowth (SIBO) treated with rifaximin could explain the broad spectrum of my symptoms, particularly the painful joints and ongoing tendonitis that arise from certain foods. This seems excessive and quite unreasonable. I apologize for any lack of coherence; summarizing six and a half years of illness is no small feat. I was previously an avid runner with immense energy, and now I feel like a shadow of my former self. I’m open to any questions and will provide further details if it would help clarify my situation. Thank you for your support in this matter.

ArthritisLupusCrohn's Disease
Male25-34
13 seconds ago

Concerns About Our Son's Health

We are the parents of a delightful four-year-old who weighs approximately 33 pounds. He was diagnosed with Immune Thrombocytopenic Purpura (ITP) around the age of two, and this condition has persisted since then. Initially, following his diagnosis, he received intravenous immunoglobulin (IVIG) in the hospital, resulting in a remarkable improvement — his platelet count surged from 12,000 to 53,000 within just 36 hours. He has been prescribed various medications, and he is currently taking Sirilimus at a dosage of 1.6 ml, along with 10 mg of Nexium. The Nexium was originally prescribed due to a different medication related to his ITP, and attempts to reduce the Nexium dosage have consistently led to significant declines in his platelet levels. The medical team at the hospital is baffled by this correlation, having stated that there is no scientific evidence to explain why the reduction in Nexium correlates with the drop in his platelet count. They suspect that there may be minor bleeding occurring in his intestines. In recent weeks, he has been experiencing intermittent fevers resembling viral infections. Approximately every three to four weeks, he develops a fever lasting one to two days. During these episodes, his temperature rises to between 101°F and 103°F, accompanied by headaches and pain in his knees. His latest fever began on a Saturday, peaking at 104.4°F. We took him to see his pediatrician, who tested for strep, influenza, and COVID-19, all of which returned negative results. The pediatrician suspected a viral cause. Over the past 48 hours, we have been administering Motrin every six hours to manage his fever; however, it only provides temporary relief. The past two days have involved vigilantly tending to him, using damp cloths to cool his forehead and back. As the cloths warm from his skin, I rinse them in cold water and reapply them to provide him with some comfort. My wife has a rheumatology appointment scheduled for tomorrow. Watching him suffer is heartbreaking, and we are increasingly concerned as the intensity of the fever spikes seems to be worsening, not just in the moment but progressing with each episode, leaving us feeling helpless. Additionally, I want to mention an incident that may or may not be connected. He has had several iron transfusions in the past, all of which were uneventful. However, during his most recent transfusion, which was administered with sucrose after the insurance denied the usual formula, he exhibited symptoms resembling anaphylaxis shortly after the infusion concluded. He became limp in my wife's arms, and there were signs of respiratory distress. A rapid response was activated, and multiple doses of epinephrine were required to stabilize him. Interestingly, subsequent blood tests conducted about half an hour after this reaction did not reflect the expected markers for anaphylaxis. At this moment, he is one hour post-administration of 5 ml of Motrin but is still experiencing a fever of 101.3°F, and he is crying from a headache. I am seriously considering taking him to the children's hospital rather than waiting for the appointment in the morning. I would appreciate any insights on what might be occurring with his health.

Multiple SclerosisLupusCrohn's Disease
Male25-34
38 minutes ago

Seeking Guidance on Persistent Back Pain and Numbness in Arms

Hello, medical professionals. I have been grappling with persistent lower back pain for over a month now, particularly around my tailbone, and I am in need of some guidance. This discomfort emerged quite suddenly during a flight around June 20, and it’s a completely new experience for me. About three weeks ago, I began to experience numbness and a tingling sensation in my arms, specifically below the elbows, occurring unpredictably. Additionally, I have been suffering from daily headaches for approximately a month, and I face challenges when I feel the urgency to urinate; I struggle to hold it in completely. I am a 27-year-old female with a medical history that includes antiphospholipid syndrome, Lyme disease, and asthma. My current psychotropic medications have been a part of my regimen for periods ranging from 2 to 7 years, so I doubt they are contributing factors. I visited urgent care, but the doctor seemed perplexed and only prescribed a muscle relaxant, ibuprofen, and lidocaine patches, none of which provided relief. Has anyone encountered similar issues or have any suggestions on potential next steps? I appreciate any insights you may have!

AsthmaMultiple SclerosisCOPD
Male25-34
38 minutes ago

Seeking a Second Opinion on Foot Health

Greetings everyone, I hope I'm in the right forum for this. I'm looking for some guidance regarding my significant other's foot issues. She is a 35-year-old woman, standing at 5'11" and weighing 250 pounds. She is Caucasian, utilizes Zyn products for nicotine but does not smoke, enjoys an occasional drink, and is currently on medication for depression. To delve into her foot problems, she experiences plantar fasciitis, overpronation, congenital fusion of her cuboidal bones, and numbness, which is not related to diabetes. Recently, she consulted a podiatrist who primarily suggested managing the pain without offering any proactive solutions for improvement. They provided her with a topical cream and hinted at the possibility of steroid injections. I'm wondering if anyone has any insights on her condition despite not having access to X-rays. Additionally, if there's another subreddit better suited for this discussion, I'd appreciate the guidance. We're hoping to find some positive news and options that might genuinely help her feet feel better. Thank you for any assistance or advice you can provide.

ArthritisInternal MedicineRheumatology
Male25-34
50 minutes ago

Seeking Answers for Unexplained Symptoms

I worry that one day I might wake up unable to move my limbs because the cause of my symptoms remains unidentified. I am in need of advice on the possible underlying issues I could be dealing with. What inquiries should I make? Whom should I approach for a referral, and which diagnostics should I ask for, just to ensure that it isn't simply attributed to anxiety? Currently, I am experiencing persistent sensations of tingling, pins and needles, and even burning across various areas of my body, and these feelings seem to intensify over time. ### Background Information: Approximately a decade ago, I began to notice intermittent tingling on the right side of my face that lasted from thirty seconds to a minute for several months. After undergoing comprehensive blood tests, a CT scan, and an MRI, nothing conclusive was found. I was reassured it was likely anxiety, with advice to disregard it unless it worsened. Ever since then, I have dealt with occasional facial tingling. Roughly five years back, the sensations extended to the right side of my head and not just my face, prompting me to revisit my doctor. I underwent more blood tests and an MRI focused on multiple sclerosis, which yielded normal results without any lesions. During a consultation with a neurologist, I was met with a nonchalant attitude and was told it was likely just my anxiety, with a suggestion to return if the symptoms escalated. Notably, these tingling episodes do not occur during times of anxiety; they seem to manifest in moments of calm. Recently, the tingling sensations have resurfaced, but now they affect both sides of my face, alongside my arms, legs, hands, feet, and even my hips and chest. These sensations have become longer-lasting and increasingly painful, accompanied by my right arm feeling as if it’s about to “fall asleep.” Additionally, I’ve been experiencing forgetfulness and difficulty concentrating. Upon another visit to my doctor, the tests returned normal results yet again: - **Normal Findings:** Blood tests including CBC, HIV, Lyme disease, a comprehensive metabolic panel (checking glucose, potassium, sodium, etc.), along with levels of B12, B1, and folate were all within range. I have the celiac gene (HLA-DQ2) but without symptoms, and my IgA and tissue transglutaminase IgA values remain normal. - **Abnormal Findings:** My vitamin B6 is elevated at 27.2 (normal range is 2.1-21.7), though my doctor dismissed this as a possible cause. My ANA was positive at 1:80 initially, later dropping to 1:40, showing a pattern of both "Mitotic, Intercellular Bridge" and "Nuclear, Speckled," which my doctor also claimed does not imply an autoimmune issue. ### Personal Context: I am a 35-year-old female, weighing 135 pounds, with a history of cyclical vomiting syndrome and vasovagal syncope (fainting during vomiting), alongside an anxiety disorder. My current medications include nortriptyline at 50 mg, buspirone at 20 mg, and I am on a birth control pill. Interestingly, these tingling sensations started while I was previously on Prozac. I have another appointment scheduled tomorrow, and I anticipate hearing the phrase "it's purely anxiety" once more, but I am not convinced that this is the case. 1. What specific questions should I pose to help clarify my situation? Would it be reasonable to request a full body CT scan? How assertive should I be in pursuing this? Normally, I accept the doctor's recommendations, but after ten years, I would like to find a definitive answer. 2. Would it be prudent to request referrals to a neurologist, rheumatologist, spine specialist, or a dermatologist? 3. If we exclude the typical explanations, what might be the potential causes of my symptoms? Is there a chance I could have a slow-developing cancer concealed along my spine? Am I at risk of awakening one day completely paralyzed due to numbness? My doctors have dismissed the more common explanations, so what unusual possibilities should I be considering?

Multiple SclerosisLupusCOPD
Male25-34
1 hour ago