38-Year-Old Male – Persistent Left-Sided Chest, Neck, and Head Pain with Internal Discomfort Following Cannabis Use Five Years Ago
**Demographics:** 38 years old, Male **Symptom Duration:** 5 years (constant, day and night) **Affected Areas:** Left side of the chest (precordial region), clavicle, shoulder, posterior neck, and left hemisphere of the head. **Current Medications:** Quetiapine 25–50 mg nightly. **Previous Medications Attempted:** Pregabalin, duloxetine, mecobalamin (Vitamin B12), eperisone, magnesium. **Medical History:** No formal diagnoses offered so far. Non-smoker; does not currently consume alcohol or drugs. --- 🔍 **Main Concern:** For the past five years, I have been enduring a persistent dull ache along with a profound sensation of internal swelling that affects my left chest, collarbone, shoulder, back of the neck, and the left side of my head. This distress initiated after a significant episode during a depressive period when I was excessively using cannabis. The incident involved severe, piercing chest pain alongside palpitations, and an uncomfortable burning sensation, which then radiated to the left shoulder, neck, and head, resulting in a feeling of impending catastrophe. Since this frightening episode, the discomfort and sense of swelling have remained constant without any change. 🧪 **Diagnostic Assessments and Treatments Undertaken:** **1. Cardiology:** - A 24-hour Holter monitor revealed a first-degree AV block and a second-degree Mobitz I AV block during sleep episodes (lowest heart rate recorded 30 bpm). - The cardiologist attributed these findings to benign vagal hyperactivity. - Other cardiological evaluations, including echocardiograms and lab tests, yielded normal results. **2. Neurology and Imaging:** - Comprehensive MRI and CT scans of the brain and spinal regions (cervical, thoracic, and lumbar) indicated no notable abnormalities. - Attempted mecobalamin (B12) for treatment; while it provided slight pain alleviation initially, it later resulted in additional pain points and twitching, leading to its discontinuation. - Pregabalin and duloxetine offered minimal relief, with symptoms re-emerging post-treatment. - Eperisone, a muscle relaxant, reduced pain by approximately 30%, yet the swelling persisted, and I experienced a pulling sensation in affected areas when treatment stopped. - Magnesium (350mg elemental): Helped somewhat with mood stabilization but induced tightness in the chest, dizziness, and fatigue, and significantly lowered my heart rate compared to my baseline (approximately 80 bpm). Additionally, it triggered a sensation of nervous hyperactivity from my chest radiating to the left side of my brain, necessitating its cessation. **3. Sleep Disturbances:** - Natural sleep eludes me due to ongoing nervous inhibition in the precordial area. I am currently dependent on quetiapine (25–50 mg) to help induce sleep. **4. Conventional Therapy:** - I have attempted a “small-needle knife” fascia release technique (from Traditional Chinese Medicine) which provided slight superficial relief; however, deeper pain points in the chest and cranial regions could not be treated safely. - The practitioner noted the tissue in these areas is extremely tight and firm. 📉 **Symptom Characteristics:** - Continuous dull ache and a sensation of internal swelling. - Triggers include: - Nervous system stimulants (caffeine, green tea, chocolate, levofloxacin). - Physical activity or pressure on affected areas. - Low-frequency sounds or music with heavy bass. - Slight improvement with: - Resting, applying warm compresses, and gentle, non-invasive manipulation (though benefits are temporary). ❓ **Inquiries:** 1. Could my condition be linked to central sensitization, autonomic dysfunction, or a potential undiagnosed nerve entrapment or fascia issue? 2. Are there safe imaging techniques or treatment options available for deep fascial nerve swelling or irritation, particularly in areas difficult to access through standard dry needling? 3. Would pursuing advanced imaging methods such as MR neurography, functional MRI, or ultrasound-guided fascia assessment be beneficial? 4. Are there non-invasive methodologies available for addressing nerve hypersensitivity that may be kinder to fragile or overly responsive nerves? Thank you for taking the time to read this. This condition has profoundly impacted my daily existence and mental well-being, and I am eager to receive any medical insights or suggestions for further exploration.
Answers (1)

7/6/2025, 1:31:00 PM
OpenHealth AI
Your persistent left-sided pain, discomfort, and sense of internal swelling indicate a complex and prolonged condition, likely influenced by various factors, including possible stress responses following the initial episode. Given your extensive evaluations and treatments so far, let’s focus on your concerns about potential underlying mechanisms and management strategies.
Main Points:
- Your symptoms may be associated with central sensitization or increased nerve sensitivity.
- Exploration of advanced imaging could be useful, but practical treatments should be prioritized.
- There are non-invasive approaches to help manage nerve hypersensitivity.
Explanation:
Your history suggests a possible link between your symptoms and central sensitization, which occurs when the nervous system becomes overly responsive to stimuli. This can happen after stress or trauma, like your experience with cannabis and the subsequent panic-like symptoms. Given that conventional treatments have provided limited relief, it's essential to evaluate alternative strategies to ease your discomfort.
Next Steps:
-
Consider Non-Pharmacological Approaches:
- Physical Therapy: A therapist familiar with myofascial release techniques may aid in manipulating tight tissue and relearning movement patterns to reduce discomfort. Combining gentle stretching, stabilization exercises, and relaxation techniques may enhance results.
- Cognitive Behavioral Therapy (CBT): Working with a mental health professional can address anxiety related to your symptoms, promoting coping mechanisms that help mitigate stress-induced exacerbations.
-
Evaluate for Nerve Sensitivity Management:
- Transcutaneous Electrical Nerve Stimulation (TENS): This technique uses low-voltage electrical currents to relieve pain and may work by disrupting pain signals.
- Mindfulness and Relaxation Techniques: Practices like yoga, meditation, or guided imagery can help improve pain management and stress resilience.
-
Consider Advanced Imaging Techniques:
- While MR neurography or ultrasound can potentially provide insights into nerve entrapments or fascial issues, they may not always yield actionable treatment pathways. Discuss these options specifically with a healthcare provider to assess their necessity based on your situation.
-
Track Your Symptoms: Keep a symptom diary noting triggers, pain intensity, and associated activities or foods. This can help identify patterns that may guide temporal management.
-
Social and Support Networks: Engaging in support groups or forums where you can connect with others experiencing similar issues can offer emotional support and practical coping strategies.
While your symptoms have been debilitating, continued exploration of treatment options and support systems aimed at managing both physical and psychological components can lead to improved quality of life. If you need further clarification or have any more questions regarding specific treatments, feel free to ask.
Related Questions
Experiences with Emergency Departments: A Deeply Troubling Journey
In my previous post, I described some difficult encounters at two different emergency departments. To provide context, I am currently a 33-year-old female identifying as AFAB and pursuing a Master's in Psychology, intending to specialize in neuro-imaging. I have been diagnosed with ASD and ADHD and I take medications including sertraline, adderall, and occasionally propranolol. On June 10th, my urogynaecologist referred me for an MRI; however, I received no follow-up care afterward. A peer review of the initial findings by the radiologist is ongoing, and the patient relations department is involved. I have been experiencing significant pain, unusual bleeding, discharge with an odor, lower back discomfort, and incontinence, which has unfortunately forced me to leave a job I cherished. My blood tests have indicated infection and irregular liver function. During my last visit to the ED, the doctor kept me for over ten hours without providing food or water. He dismissed my concerns regarding Caudal Duplication Syndrome and the possibility of uterine cancer, failing to recognize my endometriosis and omitting critical information about the size of my uterus from the CT scan in his report. He spoke only a couple of sentences to me and refused my requests for a second opinion or transfer to another facility. Discontented with this experience, I sought help at a different emergency department the following day. Here, the attending physician diagnosed me with "Delusional Disorder" and labeled me as "Gravely Disabled," which resulted in being placed in a barren room with urine on the floor. I was manhandled and administered sedatives, enduring a 24-hour hold with my phone confiscated. My abnormal imaging results and bloodwork were ignored entirely. My psychiatrist is aware of the mistreatment I've faced at these facilities, and he has diligently documented various aspects of my mental health, including my autism, which I believe contributes considerably to this ongoing mistreatment. I am struggling emotionally with these distressing experiences, and I have recorded instances of elevated blood pressure without any plan for follow-up care. At home, my partner's perception of my situation as being irrational only heightens my anxiety and distress.
Feeling Overwhelmed by Health Concerns
At 37 years of age and having never smoked, I've found myself grappling with a slew of health issues. Following a bout of pneumonia last fall, I've had three respiratory infections, and I'm still experiencing troubling shortness of breath, accompanied by episodes of fever and night sweats. Fatigue has become a constant companion in my life. Recently, I underwent a benign breast biopsy, yet I suspect my health has been compromised by something I've encountered, as I'm now facing moments of choking while eating, reminiscent of my earlier pneumonia experience. In January, I had a thyroid ultrasound along with some additional tests. However, I’m uncertain how to share my blood test results effectively since the format is a bit confusing. Here are the details from the thyroid ultrasound: **Ultrasound Report** **History:** Difficulty swallowing **Comparison:** There are no previous studies available for comparison. **Technique:** An ultrasound scan of the thyroid and surrounding soft tissues was conducted. **Findings:** - **Thyroid size:** The isthmus measures 0.4 cm. - Right thyroid lobe dimensions are 4.7 x 1.1 x 1.4 cm, while the left measures 4.1 x 1.2 x 1.1 cm. - **Texture:** Uniform - **Nodules:** No nodules ≥ 1 cm detected. - No spongiform or mixed nodules seen. - Scattered lymph nodes are noted bilaterally in the neck, with the largest on the right measuring 2.6 x 0.7 x 1.9 cm at level 2. Various nodes on the left side were also identified. **Summary of Comments:** The regional lymph nodes appear unremarkable. **Impressions:** 1. No thyroid nodules present. 2. Lymph nodes are prominent, more so on the right side, but within normal limits. The ACR TI-RADS recommendations state that if any nodules are found, follow-up actions will depend on their size. Additionally, I often feel pressure in my neck when I move my head, and I occasionally find it difficult to swallow water. It seems that during episodes of illness, this difficulty intensifies. My blood work suggests that I could be experiencing anemia, although I’m not certain if anything notable stands out among the results: - **WBC**: 7.5 (normal range: 3.4 - 10.8) - **RBC**: 4.47 (normal range: 3.77 - 5.28) - **Hemoglobin**: 12.6 (normal range: 11.1 - 15.9) - **Hematocrit**: 40.2 (normal range: 34.0 - 46.6) - **MCV**: 90 (normal range: 79 - 97) - **MCH**: 28.2 (normal range: 26.6 - 33.0) - **MCHC**: 31.3 (normal range: 31.5 - 35.7, slightly low) - **Platelets**: 378 (normal range: 150 - 450) - **Neutrophils**: 52% - **Lymphocytes**: 39% - **Monocytes**: 8% - **Eosinophils**: 1% - **Basophils**: 0% For the next steps, I am scheduled for a chest X-ray, although I have been recovering from the breast biopsy and am taking it slow. Thank you for your understanding as I navigate these challenges.
Feeling Ignored by Healthcare Providers on POTS/CFS Symptoms
It seems like I'm not being heard by any of the doctors I've consulted. I'm an 18-year-old female, weighing 44 kg and standing at 167 cm tall. Despite my efforts to gain weight, I find it incredibly difficult no matter how much I consume. My current medications include omeprazole, birth control, duloxetine, docustate, and melatonin. I also struggle with IBS-C, functional nausea, and scoliosis. My resting heart rate is consistently above 105 bpm, even when I'm just sitting or lying still. However, as soon as I stand or descend even a few stairs, my heart rate skyrockets to between 125 and 150 bpm, often accompanied by tunnel vision or temporary vision loss. Other symptoms I experience include: - My nails turn purple when I stand, and I become short of breath very quickly. - I suffer from chest pains while at rest. - I experience random episodes of shakiness, extreme sensitivity to heat, and frequent palpitations throughout the day. - My digestive system is a constant source of distress, leading to significant nausea; I rely on cyclizine every morning to manage it. - I deal with joint pain, severe fatigue, hypermobility, headaches, cognitive fog, hot flashes, low blood pressure, and probably more symptoms that I might have overlooked. Taking a shower is a particularly difficult task for me, as my feet also turn purple, and I often end up with a headache along with nausea or stomach discomfort. The entire process takes an extended period due to my arms tiring out quickly, compounded by my overall exhaustion. I try to take at least one nap daily because it’s often the only way I can manage some level of function. Despite taking 8 mg of melatonin, I still struggle with insomnia, a problem I've battled for years. My symptoms tend to be at their worst in the mornings, which can sometimes prevent me from leaving my home due to their severity. Regardless of how I advocate for my health, doctors often dismiss my concerns, labeling conditions like POTS and fibromyalgia as trendy diagnoses, while my test results come back normal. I feel completely drained. I am reaching out for guidance—what can I do or say to ensure that medical professionals take my situation seriously? I've attempted increasing my fiber intake, trying to gain weight, and staying hydrated, plus I've had two hospital visits in the last four months related to these issues.
Navigating Symptoms and Tests Without an Autoimmune Diagnosis
Hello everyone! I'm reaching out to seek advice on additional testing I might consider and strategies for managing my growing array of symptoms. I'll gladly respond to any inquiries and would deeply appreciate your insights! Also, if this seems somewhat familiar, I previously shared a more detailed post but opted to streamline it for clarity. **Overview:** I'm a 26-year-old Caucasian woman of Eastern European descent, standing at 5'7" and weighing 125 pounds, currently residing in the Northeast region of the United States. **Symptoms I'm Experiencing:** *(onset since February 2024)* - Fluctuating between constipation and diarrhea related to IBS (longest diarrheal episode lasted over two months with a weight loss of 15 pounds) - Bloating and abdominal distension - Escalated acid reflux (a lifelong issue; medications have been ineffective) - Increased vocal hoarseness (diagnosed at age 19 with vocal nodules and tension dysphonia) - Severe itching on the scalp (no visible redness or skin flakes) - Notable hair shedding (more prominent during intense itching episodes, with no scratching) - Deteriorated skin lesions (suspected psoriasis) - Reduced appetite, accompanied by heartburn and stomach discomfort, particularly in the mornings - Experiencing six consecutive respiratory infections from September to December 2024, including another COVID case; I've only had a few mild colds in the last six months - Hormonal imbalances (notable for increased facial and upper lip hair, jaw and cheek acne, mid-cycle discomfort, significant pre-menstrual swelling, bloating, breast tenderness, and fluctuating mood) - Recurring yeast infections - Intensified migraines - Diagnosed with low bone density that resulted in a tibia fracture - Disturbed sleep patterns (characterized by waking too early, difficulty staying asleep, and trouble falling asleep) - Worsening temporomandibular joint issues and teeth grinding - Severe night sweats - Occasional fatigue **Medical History and Tests Conducted:** - Diagnosed with **IgA deficiency** in childhood following several strep infections - Diagnosed with **Celiac disease** at 19 (the only autoimmune condition identified so far; my mother has the same condition, while my father has Vitiligo) - Gynecology exam revealed **polycystic ovaries** in my teenage years; I was prescribed Inofolic and primarily symptom-free from hormonal issues until recently - My neurologist explored treatment options for **migraines**, including Nortriptyline and beta blockers, and although I did not respond to these, I found success with Ajovy - A dermatologist suspects psoriasis and suggested a treatment with Skyrizi, which raises concerns for me due to my history of yeast infections - My rheumatologist ruled out Lupus and Sjogren’s, noting normal CRP levels. The only noteworthy test results are a **positive ANA (1:320, speckled)** and levels of **RNP antibodies, IgG (1.5)** that are above standard - Gastroenterologist dismissed Crohn’s disease and ulcerative colitis possibilities, and while SIBO was suspected, breath tests yielded negative results. I have undergone extensive testing, including stool tests, X-rays, CAT scans (showing a high stool burden despite laxative usage), and both colonoscopy and endoscopy with biopsies (the latter indicating chronic low-grade gastritis, but otherwise normal) - An endocrinologist has documented **low bone density** through a DEXA scan - Allergy testing revealed sensitivities to grass, formaldehyde, cobalt, and nickel - ENT evaluation confirmed **vocal nodules**, **muscle tension dysphonia**, a deviated septum, and chronic, non-allergic rhinitis - I was screened for POTS/dysautonomia, but results were normal **Current Priorities:** 1. Are there any rare autoimmune disorders that might warrant testing? 2. What additional assessments would you recommend? 3. Should I see other specialists, such as an immunologist or seek a second opinion from another rheumatologist? 4. Any suggestions for managing this range of symptoms without resorting to an extensive medication regimen? I would greatly value any thoughts or similar experiences you might share. Thank you immensely for your help!
Possible Illness Evaluation
A 26-year-old male weighing 200 pounds, who does not smoke and has no history of chronic health issues, is experiencing a set of concerning symptoms. He does not currently have a fever. His symptoms include trouble swallowing, persistent fatigue, pain in the jaw, and a notably painful and swollen lymph node region, particularly on one side of the neck. Despite these signs of illness, he is not exhibiting any fever. Could it be possible that he is suffering from an infection even in the absence of fever?