OpenHealth Q&A

Get answered by medical professionals

Navigating Chronic Headaches: A Frustrating Journey

7/27/2025, 5:40:34 PMMale25-34

I am a 38-year-old male, weighing 280 pounds and standing 6 feet tall. My health records indicate that I manage high cholesterol and major depressive disorder effectively, for which I am prescribed 40 mg of Vilazodone and 40 mg of Rosuvastatin daily. Please bear with me as I outline my situation in detail; it has been a lengthy and challenging ordeal. Over the past five years, I have undergone routine blood tests. While it revealed a few issues with my cholesterol levels (specifically low HDL) and somewhat reduced testosterone levels (around 300), there have been no significant findings. For more than five years, I have been plagued by persistent headaches. They began gradually, without any clear trigger. The pain typically hovers around a level of 3, occasionally spiking to 6, but rarely dropping below 2. These headaches are frequently accompanied by sensations of dizziness, a feeling of being faint, brain fog, struggles with word retrieval, difficulties in concentration, and very mild tinnitus. I do not experience any sensitivity to lights, sounds, or smells. Interestingly, I find slight relief when lying down. In addition, I have suffered three isolated episodes of vertigo over the past five years, each lasting from mere seconds to a few days. Around the same period my headaches started, I experienced a pinched nerve in my neck, likely due to an awkward sleeping position. The associated arm tingling improved with physical therapy. I consulted with a neurologist regarding the pinched nerve, who ordered MRIs of my brain and spine. Those results did not reveal anything alarming, except for a mildly slipped disc in my neck. Subsequently, I sought help from another neurologist who attempted various treatments for my headaches, trialing medications such as topiramate, NSAIDs, Sumatriptan, CGRP inhibitors, and Botox. Unfortunately, none provided any lasting relief. The neurologist speculated that my symptoms might be linked to the two antidepressants I was taking: Effexor and Wellbutrin. After tapering off these medications under psychiatric supervision, I saw no improvement over a six-month period. This prompted me to switch back to a different antidepressant due to a significant exacerbation of depressive symptoms. I was then referred to a cardiologist to investigate potential conditions like POTS (Postural Orthostatic Tachycardia Syndrome). A cardiac ultrasound appeared normal, and the stress test revealed vasovagal syncope but ruled out POTS. My psychiatrist later suggested that my symptoms could be anxiety-related, leading me to enroll in an outpatient anxiety support program. While I could relate to some aspects of the symptoms discussed, my own anxiety levels were quite mild. To manage my attention difficulties, the psychiatrist prescribed Adderall, which turned out to be the most effective treatment for improving my symptoms. However, the side effects, such as insomnia and irritability, became challenging to handle. Eventually, I was referred to a prominent academic medical institution where I consulted with five different neurologists specializing in various fields and was directed to a headache clinic. At the headache clinic, I was advised to limit my caffeine intake from three cups to two or fewer daily, but this change did not alleviate my symptoms. They also scheduled a sleep study, which revealed mild sleep apnea. I received a CPAP machine and adhered to its use for over a year, yet this did not lead to any improvement. The headache clinic subsequently connected me with a doctor involved in research on spontaneous cerebrospinal fluid (CSF) leaks. Following a series of at-home self-assessments, this physician recommended advanced imaging techniques (a CT myelogram with contrast) and suggested an epidural blood patch. The imaging results were negative, but the specialist estimated there remained a 30% possibility of a CSF leak undetected in the scans and noted areas that appeared "suspicious." I underwent four separate blood patch procedures aimed at addressing these areas. While recovery sometimes brought temporary relief, the benefits were fleeting. Furthermore, the neurologist team referred me to an Otolaryngology specialist for vestibular testing, which included various assessments. These tests indicated slight issues with vestibular function, leading to referrals for physical therapy. Six months of vestibular rehabilitation passed without noticeable improvement, and conditions like BPPV and vestibular migraines were ruled out. Lately, I have taken a six-month break from treatment, mainly due to fatigue from the endless cycle of appointments and the absence of definitive answers. However, I am now eager to resume seeking solutions that could enhance my quality of life despite my ongoing symptoms or perhaps lead to a real understanding and resolution of my condition. Thus, I find myself asking: Where do I go from here? Should I revisit the headache clinic at the academic center? Is it worthwhile to consult with a neurologist again? Or am I better off exploring alternative resources?

HypertensionInternal MedicineEndocrinology

Answers (1)

Cony

7/27/2025, 5:40:51 PM

OpenHealth AI

It's completely understandable to feel overwhelmed after a long journey with chronic headaches. Your situation appears complex, and your commitment to seeking a solution is commendable. It sounds like you've already taken extensive steps to identify and manage your symptoms, so let’s focus on actionable next steps that could potentially lead you to an improved quality of life.

Summary of Key Points

  1. Multiple causes of headaches have been considered, but a clear solution has not been found.
  2. Previous treatments and evaluations, including neurological assessments and vestibular testing, have not yielded lasting relief.
  3. There may still be unexplored options, especially regarding management strategies or alternative therapies.

Explanation

Chronic headaches can often be multifactorial, meaning they can be influenced by a combination of neurological, vascular, musculoskeletal, and even psychological factors. Given your history of depression and the medications involved, it’s important to take a holistic view of your health. The symptoms you're experiencing, such as dizziness and cognitive difficulties, may link back to your primary headache type, which could be tension-type headaches, migraines, or even cervicogenic headaches (originating from the neck).

While you've made great strides with evaluations and treatments, it’s clear that a consistent course of management has been elusive. Continuing to explore different angles can be beneficial.

Next Steps

  1. Return to the Headache Clinic: Since this facility specializes in headache management, revisiting them might provide new insights. They may have suggestions for monitoring your symptoms over time or adjusting treatment goals. Highlight any changes in your symptoms since your last visit.

  2. Comprehensive Re-evaluation: Consider asking for a thorough re-assessment that includes:

    • Referral to a physical therapist who specializes in headache management, focusing on both cervical and vestibular rehabilitation.
    • Testing for other potential chronic conditions that could underpin your symptoms, like autoimmune disorders or connective tissue diseases.
  3. Explore Integrative Approaches:

    • Look into cognitive-behavioral therapy (CBT) or mindfulness techniques to manage anxiety and stress, which may play a role in your headaches.
    • Gentle activities like yoga or tai chi may also help with relaxation and potentially reduce headache frequency and severity.
  4. Maintain and Optimize Headache Diary: Keep a detailed journal of headache occurrences, triggers, and relief methods, including activities, food intake, and stress levels. This record may offer valuable insights to your healthcare providers.

  5. Lifestyle Considerations:

    • Evaluate your sleep hygiene. Improving sleep quality may significantly impact headache management.
    • Continue limiting caffeine and consider potential food triggers (e.g., aged cheese, processed meats) that might exacerbate symptoms.
  6. Discuss Medication Adjustments: Given your experiences with various medications, consider discussing with your neurologist any potential new or combination therapies that haven't been tried or might suit your symptoms better.

Remember, progress in complex cases can be gradual, and it’s important to remain patient and positive while you work through this process. Your ability to articulate your symptoms and advocate for yourself is a powerful tool in seeking relief. Don't hesitate to ask your healthcare providers about different avenues that might be available to you.

Related Questions

Concerns About My Toes

Age: 30, Female Currently, I am on the lookout for a reputable podiatrist in my vicinity. However, I've encountered a perplexing issue with my foot. Just last night, I noticed a growth on the side of my toe, something entirely new to me. I maintain a nutritious diet and have a demanding job that requires me to be on my feet quite often. My footwear includes brands such as Brooks Ghost Runners, Hoka Bondi 9’s, and Nike Motiva’s, and I don’t opt for restrictive socks. I also apply Vick’s Vaporub to my feet, a practice handed down from my family, and stick with simple, non-fragrant lotions like Vanicream and CeraVe SA Cream for my skin. In addition, I am curious about the my big toenail's change in color. What might be the underlying reasons for this? Also, I have these persistent dark spots on my toes that I've struggled with since my days on the runway. Despite my efforts, nothing has succeeded in lightening or diminishing their appearance. I'm just looking to determine if there might have been a factor from the past that could have contributed to these issues. I’m not sure what else to include, but I’m open to answering any questions you might have. Thank you for your attention! Best wishes from a worried soul!

ArthritisFibromyalgiaInternal Medicine
Male25-34
3 minutes ago

7-Month-Old Child with Abernethy Malformation - Exploring Treatment Options

# 7-Month-Old Child with Abernethy Malformation - Exploring Treatment Options ## [7-Month-Old] Identified with Abernethy Malformation (Congenital Portosystemic Shunt) - Treatment Methods? **Age:** 7 months **Gender:** Female **Height:** Age-appropriate **Weight:** Currently 9 kg, was 2.8 kg at birth **Ethnicity:** Asian **Duration of Symptoms:** Present since birth **Location:** Uzbekistan **Pre-existing Health Issues:** Abernethy malformation (congenital portosystemic shunt), liver hemangiomas, chronic jaundice, anemia **Current Treatments:** Supportive management --- ## INITIAL PRESENTATION (June 2025 - July 2025) Our daughter arrived on **June 27, 2025**, presenting with: - Birth weight: **2.8 kg** - Marked jaundice (yellowing of skin and sclera) - Pale or clay-colored stools - **Bilirubin level: 245 μmol/L** (typically <20) An immediate ultrasound indicated multiple liver anomalies, initially thought to be hemangiomas. --- ## FIRST COMPREHENSIVE ASSESSMENT (August 1, 2025 - 1 Month Old) ### Multislice Computed Tomography (MSCT) with 3-Phase Contrast (August 1, 2025): **RESULTS:** - **Portocaval shunt size: 9.9 mm** (blood bypassing the liver into the inferior vena cava) - **Arteriovenous shunt size: 4.4 mm** - **Portal vein size: 6.1 mm** (patent) - **Three nodular cystic lesions** located in the perivascular area, with largest measuring 11.6×20.7 mm, enhancing during the venous phase - Liver features a heterogeneous architecture, exhibiting irregular enhancement - Gallbladder appears elongated and slightly enlarged - Other abdominal organs exhibit normal findings **RADIOLOGIST’S ASSESSMENT:** "Congenital portosystemic shunt indicative of Abernethy malformation; less likely arteriovenous malformation (AVM); cannot dismiss the possibility of localized liver lesions." **ADVICE:** Seek consultations with an abdominal and vascular surgeon. ### Blood Tests (August 1, 2025): **Complete Blood Count:** - WBC: 10.44 × 10⁹/L (normal range) - **RBC: 2.1 × 10¹²/L** (LOW - indicating severe anemia) - **Hemoglobin: 69 g/L** (CRITICALLY LOW; normal is 117-166) - Platelets: 403 × 10⁹/L (elevated) **Biochemistry Analysis:** - Urea: 1.80 mmol/L (normal) - Creatinine: 33.4 μmol/L (normal) - **ALT: >1000 IU/mL** (EXTREMELY HIGH - severe liver dysfunction) --- ## FOLLOW-UP IMAGING (December 16, 2025 - 5.5 Months Old) ### Liver Ultrasound: **RESULTS:** - Right lobe: 64 mm, left lobe: 43 mm - Liver capsule appears irregular and vague - **Parenchyma: heterogeneous, showing 7 hypo-isoechoic nodules** (sizes range from 11.5×10.7 mm to 17.6×15.4 mm) - Capsule features uneven contours - Blood flow noted during Doppler examination - No dilation in intrahepatic bile ducts - **Portal vein: 3.9 mm** (decreased from 6.1 mm - indicating improvement) - Common bile duct: 1.4 mm - Gallbladder: measures 43.7×9.2 mm (pear-shaped, wall thickness 2.0 mm, homogeneous, free of stones) **ULTRASOUND ASSESSMENT:** "Presence of liver volumetric formations (specifically liver hemangiomas)." --- ## LATEST MSCT (February 6, 2026 - 7 Months Old) ### MSCT with 3-Phase Contrast: **FINDINGS:** - Liver remains normal in size, but shows heterogeneous structure with uneven contrast enhancement - **Portocaval shunt: 9.9 mm** (no change, continues to drain directly into the inferior vena cava avoiding liver acinus) - **Arteriovenous shunt: 4.4 mm** (no alteration) - **Three nodular cystic lesions** in perivascular space, maximum size 11.6×20.7 mm, enhancing in the venous phase - **Portal vein: 6.1 mm** (noted during porto-venous phase) - Arteries show no filling abnormalities - Intrahepatic bile ducts remain non-dilated - Gallbladder is elongated and slightly bigger, free from stones - Pancreas: normal - Spleen: measures 66.9×38.5 mm (not enlarged), splenic vein is 3.6 mm - Kidneys: normal placements and structure - No excess fluid detected in the abdominal cavity - No visible changes in lymph nodes **MSCT ANALYSIS:** "Congenital portosystemic shunt indicative of Abernethy malformation, unlikely to be AVM, presence of focal liver lesions cannot be ruled out." **RECOMMENDATION:** Engage with an abdominal and vascular surgeon. --- ## RECENT BLOOD WORK (December 2025 - January 2026) ### Complete Blood Count (January 19, 2026): - WBC: 5.8 × 10⁹/L (SHOWS IMPROVEMENT) - **RBC: 2.93 × 10¹²/L** (IMPROVED but still low) - **Hemoglobin: 72 g/L** (SHOWS IMPROVEMENT but still low) - Platelets: 223 × 10⁹/L (BACK TO NORMAL) - Neutrophils: 30.0% - Lymphocytes: 64.8% - Monocytes: 4.6% ### Biochemistry (January 28, 2026): - Total protein level: 67 g/L (slightly deficient) - Creatinine: 20.7 μmol/L - **Total Bilirubin: 242 μmol/L** (STILL HIGH - unchanged) - **Direct Bilirubin: 142 μmol/L** (VERY HIGH) - **ALT: 50 IU/mL** (DRASTICALLY LOWER from >1000!) --- ## OVERVIEW OF PROGRESS OVER 6 MONTHS | Parameter | August 2025 | January 2026 | Change | |------------------|-------------|---------------|--------------------------| | **Hemoglobin** | 69 g/L | 72 g/L | ↗ Slight improvement | | **RBC** | 2.1 | 2.93 | ↗ Improved | | **ALT** | >1000 | 50 | ✓✓ MAJOR IMPROVEMENT | | **Bilirubin** | 245 | 242 | → Unchanged (still elevated) | | **Portal vein** | 6.1 mm | 3.9 mm (US) | ↗ Decreased | | **Platelets** | 403 | 223 | ↘ Normalized | | **Shunt size** | 9.9 mm | 9.9 mm | → No Change | --- ## CURRENT SITUATION (February 2026 - 7 Months Old) - **Weight:** 9 kg (good growth rate in spite of condition) - **Jaundice:** Continues to be present (yellow skin) - **Stools:** Remain pale/clay-colored - **Development:** Achieving appropriate milestones - **Energy:** Appears to have a good energy level - **Feeding:** Normal appetite --- ## QUESTIONS FOR r/AskDocs We have been informed this is **Type 2 Abernethy malformation** (portal vein present). **Three treatment avenues have been proposed:** ### Option 1: **Endovascular Coil Embolization** (minimally invasive approach) - A catheter is inserted via the leg vein to access the shunt and deploy coils/plugs to close the abnormal vessels - Pros: No surgical incision, minimal discomfort, short hospital stay (2-4 days), no scars, enhanced safety - Duration: 1-2 hours - Recovery: 2-4 weeks for jaundice to show improvement ### Option 2: **Open Surgical Intervention** - An incision in the abdomen to ligate abnormal vessels and redirect blood to the liver - Pros: Direct visualization, effective results - Cons: Surgical scar, longer recovery time (7-14 days in hospital) - Duration: 2-4 hours ### Option 3: **Liver Transplantation** - We have been advised this is not necessary as the portal vein is functional and liver health is improving. --- ## SPECIFIC QUESTIONS TO CONSIDER: 1. **With a functional portal vein (6.1 mm) and improving liver function (ALT normalized), is it advisable to pursue endovascular closure as the preferred treatment?** 2. **Despite ALT levels improving, the bilirubin remains consistently high (242). Should this be a cause for concern? Is there a prospect for it to normalize post shunt closure?** 3. **Are the hemangiomas/nodules (11.6×20.7 mm) linked to the shunt? Will they likely resolve following shunt repair?** 4. **How urgent is the proposed intervention? Is immediate action required, or is there flexibility to wait a few months?** 5. **What complications should we be vigilant for during the waiting period?** 6. **Regarding endovascular closure - what is the average success rate for infants aged 7 months? Are there concerns regarding the shunt size (9.9 mm)?** 7. **The measurement of the portal vein has shown improvement from 6.1 mm to 3.9 mm; should this be perceived as a positive sign or a reason for concern?** 8. **Are there special directives (diet modifications, medications) we should consider while awaiting the procedure?** 9. **Post-procedure, how long should we expect it might take for:** - Normalization of bilirubin levels? - Return of stool color to normal? - Resolution of jaundice? - Regression of hemangiomas? 10. **Can you recommend any specialized centers for pediatric Abernethy malformation treatments? We are located in Uzbekistan but are prepared to travel (to Turkey, Russia, South Korea, etc.)** --- ## ADDITIONAL INFORMATION - No family history of hepatic diseases - Pregnancy and delivery were normal - No additional congenital defects identified - Immunizations up to date - No history of bleeding disorders - No signs indicative of encephalopathy - Child is alert and engaged --- **I can supply actual MSCT images and comprehensive lab reports if they would be of assistance.** We sincerely appreciate any insights you can provide. We are striving to make the most informed decision regarding our daughter’s care and highly value expert medical opinions. **TL;DR:** 7-month-old diagnosed with Abernethy Type 2 malformation (9.9 mm portocaval shunt, patent portal vein). Liver functionality is improving (normalized ALT) while bilirubin remains elevated (242). Evaluating options between endovascular coil embolization and open surgery. Seeking expert advice on optimal treatment strategy and timing.

Thyroid DisordersInternal MedicineEndocrinology
Male25-34
22 minutes ago

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

Understanding Tuberculosis Exposure Risk

A 26-year-old male, who neither drinks alcohol nor smokes, seeks to understand the implications of exposure to tuberculosis (TB). As an anesthesia technician, I became concerned after I encountered a TB-positive patient about a month ago. I had to enter the patient’s room several times to perform blood gas tests. On my first entry, I mistakenly wore my N95 mask incorrectly due to the hectic nature of attending to multiple rooms. From my research, it appears that TB is quite transmissible; direct exposure can pose a serious risk of infection. Transmission usually requires prolonged contact with an infected individual, particularly in a close or face-to-face setting. In this case, the patient was lying face down and appeared to be sleeping when I entered. I have already undergone testing for TB, but I am eager to deepen my understanding of the risks involved in these situations.

COPDInternal MedicineEndocrinology
Male25-34
3 hours ago

24M | Unexplained Fainting Incident

**Note:** I previously shared this story, but it was inexplicably removed. I’m a 24-year-old male without any medical diagnosis or prescription medications. While I do consume alcohol occasionally, I hadn’t been drinking before this happened. Around 3 a.m., I got up from bed to use the restroom. As soon as I began to urinate, I suddenly felt a wave of dizziness. The next moment I was aware of was regaining consciousness in the bathtub, startled awake by the sensation of something dripping on me—only to discover it was my own blood. This was my first experience with fainting. When I came to, confusion set in. I was disoriented and couldn’t comprehend why I was being dripped on while in what I thought was my “bed.” Strangely, I also imagined that I was lying on a collection of marbles (which I actually don’t own)—this turned out to be the shattered glass of my shower door lying around me. I’m uncertain whether I lost consciousness first and then fell, or if the fall caused my brief blackout. It took me a few moments to understand why I was in the bathroom at all. I’m not sure how long I was out; I only remember it was around 3 in the morning when I initially got up, and about the same time when I regained consciousness. I dialed 911, and the ambulance arrived promptly. They checked my vitals, performed an EKG and measured my blood sugar, finding nothing unusual. At the emergency room, they repeated the vital checks, conducted a CT scan, drew blood, and took x-rays—yet still no abnormalities were detected. I had several cuts on my face and left arm (curiously, this is the arm that would have been turned away from the door), along with bruising around my ribs. Since the incident, I’ve been suffering from headaches and pain in my ribs. I received stitches on both my face and arm. The nurse suggested I could have stronger pain relief, but I opted for just Toradol. They eventually discharged me, stating, "We’re unsure what caused this, but return if it happens again." What might have triggered such an incident? How can I safeguard against it reoccurring if they remain uncertain about the cause?

Thyroid DisordersCOPDInternal Medicine
Male25-34
3 hours ago