OpenHealth Q&A

Get answered by medical professionals

Understanding My Test Results: A Journey Through GI Investigations

6/18/2025, 7:00:34 PMMale25-34

I’ve previously shared my experience, but to recap, I am 29 years old, weigh 218 pounds, and I’m Black. My initial visit to a gastroenterologist was prompted by my struggles with IBS-C, which occasionally led to bright red blood appearing in my stool, along with severe acid reflux. During this consultation, the doctor reviewed my medical history and diagnosed me with iron deficiency anemia (IDA), specifically identifying it as microcytic anemia. My lab results indicated the following: - Iron: 29 mcg/dL - Transferrin Saturation: 11% - Ferritin: 14 ng/mL - Total Iron Binding Capacity (TIBC): 273 mcg/dL - B12: 390 pg Subsequently, I underwent both a colonoscopy and an endoscopy. The findings from these procedures included bile reflux and inactive gastritis, and during the surgeries, a benign polyp was also excised. Tests ruled out h. Pylori and celiac disease, and tissue samples were taken. After examining the results, the doctor concluded there was no active bleeding or any condition that could explain my anemia. Following that, I received five sessions of iron sucrose infusions, with lab tests scheduled for the first week of July to assess their effectiveness. The doctor then suggested a capsule endoscopy to investigate my small intestine, which revealed no signs of active bleeding. A few small blood vessels were noted, but they were not currently bleeding. Towards the end of the small intestine, some nodularity was observed, which the doctor mentioned was also present in the colonoscopy and is relatively common among younger individuals. Curious about the potential implications of the nodularity, I inquired whether it was a cause for concern. The recommendation was to get a CT scan of my abdomen and pelvis. With all these tests and imaging conducted, I'm left wondering what exactly the medical team is seeking. Is the nodularity a potential indicator of cancer, or could it point to something else entirely?

Crohn's DiseaseThyroid DisordersInternal Medicine

Answers (1)

Cony

6/18/2025, 7:01:09 PM

OpenHealth AI

It's understandable to feel uncertain after going through a series of tests and evaluations, especially with concerns related to nodularity and your iron deficiency anemia. Let’s break down your situation and address your key questions.

Summary of Your Situation

You are dealing with iron deficiency anemia, intermittent gastrointestinal issues, and recent findings of nodularity during your endoscopic and imaging studies. The nodularity seen can often be benign and isn’t automatically an indication of cancer, especially considering your age and medical evaluations so far.

Understanding Your Findings

  • Iron Deficiency Anemia (IDA): Your lab results indicate low iron levels and low ferritin, confirming the IDA. It’s important to address this as it can lead to fatigue and other health complications.
  • Nodularity: Nodules in the gastrointestinal tract can be associated with various conditions, including inflammatory bowel disease (like Crohn's), benign growths, and other benign variations in tissue structure. Given that the nodularity was noted in both your colon and small intestine and considering your age, it is likely that the findings are benign; however, the CT scan can provide more clarity.

Next Steps

Here’s what to focus on next as you await further results and assessments:

  1. Complete Your CT Scan: This will help your doctors better assess the nodularity and rule out any underlying conditions. Make sure to discuss any specific concerns you have before the scan.

  2. Monitor Symptoms: Keep a detailed record of any gastrointestinal symptoms you experience. Note if there are fluctuations in your acid reflux, bowel habits, or any new symptoms such as abdominal pain or changes in weight.

  3. Stay Engaged with Your Healthcare Team: Continue to communicate openly with your gastroenterologist. If you have further questions about the tests or findings, don’t hesitate to ask. Understanding the follow-up steps will help you feel more in control.

  4. Manage Iron Deficiency Anemia: Follow the treatment plan prescribed to you, including dietary adjustments. Increase your intake of iron-rich foods (like red meat, beans, and spinach) and vitamin C (which helps with iron absorption). Your doctor will likely monitor your ferritin levels closely.

  5. Consider Lifestyle Changes: If you haven’t already, adopting a diet low in irritating foods can help manage acid reflux and overall gastrointestinal health. Avoiding highly spicy, fatty, or fried foods may provide relief.

Reassurance

It's perfectly normal to feel anxious when navigating potential health issues. Remember, many findings in gastrointestinal studies are common and not necessarily alarming. The next steps will help to clarify the situation further. Focus on your health management plan, and take each step one at a time. If you have more inquiries or need further clarification, feel free to ask.

Related Questions

Micronodules Detected in Lung

Hello, I recently underwent a coronary artery calcium (CAC) scan to assess arterial plaque, and I was pleased to receive a favorable score of 7.75. However, the report highlighted the presence of several clustered micronodules located in the right upper lung, accompanied by adjacent ground-glass opacities. I am a 60-year-old male, 6 feet tall and weigh 190 pounds. I do not currently take any medications and generally enjoy excellent health. There is a family history of heart disease on my father's side. Additionally, I am a non-smoker, apart from occasional use of cannabis, and consume alcohol very infrequently. Thank you in advance for any insights you can provide!

AsthmaCOPDInternal Medicine
Male25-34
8 minutes ago

Experiencing Widespread Muscle Weakness

I’m a 36-year-old male and have recently been facing a troubling situation where the muscles throughout my body seem to be losing function—including my eyelids. The trouble began in May 2021 when I lifted a heavy garbage can with my right arm in a shrugging action. Following that, I felt a combination of pain and weakness concentrated in my right shoulder blade, as well as my shoulder and collarbone. Soon after, I noticed my shoulder began to pop and click. Afterward, I consulted with an orthopedic specialist who conducted x-rays on both of my shoulders. He informed me that everything appeared normal and dismissed the popping sounds as inconsequential. I also mentioned experiencing neck pain, but he indicated that addressing neck issues wasn’t his area of expertise. He diagnosed me with bilateral shoulder and neck discomfort and recommended physical therapy. The day after my appointment, I attempted to adjust my position in my desk chair by leaning on the left armrest, putting my forearm under the weight of my body. Suddenly, my shoulder jolted, and I felt a sharp weakness in my arm, accompanied by popping and clicking noises, similar to what happened with my right arm. I reached out to the orthopedic office to inform them about this incident, but the physician assistant who responded said the doctor would not see me again simply due to how I was sitting, and suggested I attend physical therapy first. She mentioned that if I continued to experience weakness, a neurologist might be necessary. Feeling concerned, I returned to my primary care physician for a follow-up appointment and recounted my experience. He didn’t appear worried, and my blood tests returned normal results. During the summer of 2021, I began physical therapy where the therapist diagnosed me with strains in my trapezius and rhomboid muscles. The subsequent therapy sessions consisted of painful exercises and stretches, yet I observed little to no improvement in terms of strength or stability. Activities like using the arm bike and weight machine were excruciating, and I frequently inquired whether my symptoms could be attributed to a tear or nerve damage, but the therapist insisted that was not the case and dismissed my concerns. After my tenth session, I decided it was best not to return. In April 2022, I visited a neurologist. I struggled to lift myself onto the examination table and needed assistance from a step stool. He didn't suspect any neurological issues when I asked him about an EMG or other assessments, he declined to proceed with those tests. Disheartened by these experiences, I chose not to pursue further medical consultations. Fast forward to April 9, 2025, I misstepped while descending some stairs, causing my right heel to catch, and I landed hard with my toes pointed. I had no visible signs of injury such as swelling or bruising, but soon after, I began to experience persistent pain and weakness, especially in my toes and the arch of my foot. By April 13, I instinctively elevated the toes on my left foot, and to my dismay, the same pain and weakness emerged, again without any visible signs like bruising. Since then, both feet have lacked strength, and my big toes feel unusually floppy. In July 2025, I had a troubling experience after having my hair washed at a salon. I held my neck in an awkward position for the duration, which resulted in a burning sensation. Regrettably, I didn’t express my discomfort, fearing a scene. Following this, I noticed significant weakness in the muscles at the front of my neck, under my chin, which gave the appearance of a receding chin. Additionally, my facial muscles, particularly in my cheeks, felt weak and could easily be pressed in with minimal resistance. In January 2026, I bought a new game controller for my laptop, having not played video games for a long time. Initially, it was manageable, but soon after, my hands and forearms began to feel uncomfortable and painful. This discomfort escalated significantly to where I had to discontinue use completely; my hands felt drained of energy and experienced achiness, tingling, and numbness. Then, on February 3, 2026, while seated and using my laptop, I noticed a peculiar sensation when moving my eyes. My eyelid muscles felt weak, and one of my eyelids began twitching. I found it increasingly difficult to open my eyes as widely as I used to. I plan to see a primary care physician once more, but I’m uncertain how to communicate all of this effectively to receive proper care. My circumstances have reached a point where my parents must assist me with everyday tasks, including driving, opening doors, and even lifting light objects. My ability to raise my arms above my head has become severely limited as well.

Multiple SclerosisFibromyalgiaCrohn's Disease
Male25-34
17 minutes ago

Liver Mass Assessment

Patient Profile: - Age: 61 years - Height: 5'9" - Weight: 240 lbs - Gender: Female - Lifestyle: Non-drinker, non-smoker, no illicit drugs Current Medications: - Atenolol 10mg (morning and evening) - Rosuvastatin 40mg (evening) - Duloxetine 60mg (evening) - Spironolactone 25mg (recently added) - Jardiance 10mg (recently added) Medical History: The patient has a notable history of multiple pheochromocytomas and paragangliomas, having undergone surgery on eight occasions. According to scans performed three years ago, two subcentimeter retroperitoneal masses were identified, suggestive of potential paraganglioma. Additionally, she suffers from secondary polycythemia and possesses the PHD1 gene mutation. Previously, she received treatment at a prominent research institution in the United States. However, her endocrinologist has since retired and returned to their home country. Current Condition: At present, she is mostly asymptomatic. However, in January 2026, she experienced a concerning event requiring an ambulance transport to a local emergency room, where her oxygen levels registered at 88-89%. This incident was unsettling, given her extensive medical history. The emergency physician initially diagnosed her with congestive heart failure (CHF), but upon discharge, her family medicine doctor suggested pneumonia. During her hospital stay, a cardiologist—who has never managed a pheochromocytoma patient—recommended a chemical stress test. A CT scan performed on her chest revealed a 3.2 x 2.5 cm mass located in the left lobe of her liver. Her blood tests typically show elevated levels related to pheochromocytomas; however, the laboratory does not conduct resting catecholamine testing, which leads to unreliable results, despite them being consistent over time. Furthermore, she has received care at major hospitals in Minnesota and both leading hospitals in Cleveland, Ohio. Unfortunately, when she required her last surgery, the tumor board declined her case, citing an unfavorable risk-benefit ratio. This leaves her without a specialist in pheochromocytomas. Request for Guidance: The patient is seeking advice or recommendations for her current health situation and management of her conditions.

Crohn's DiseaseThyroid DisordersEndocrinology
Male25-34
37 minutes ago

Concerns About My Daughter's Morning Health Issues

My 17-year-old daughter experiences troubling symptoms each morning, particularly on days when she needs to rise early for school or work. She often wakes up feeling dizzy and nauseated, accompanied by a rapid heartbeat exceeding 100 beats per minute. This situation prevents her from being able to eat and may persist for several hours, or in some cases, throughout the entire day. Standing at 5 feet 8 inches tall (172 cm) and weighing 121 pounds (55 kg), her physical health otherwise seems fine. I have a personal history of inappropriate sinus tachycardia (IST), which is why I take beta-blockers for management. A few years ago, she consulted a cardiologist regarding her frequent episodes of near-fainting, who recommended increasing her water intake and adding more salt to her meals. Given the persistent nature of her symptoms, I am contemplating whether a follow-up appointment with the cardiologist is warranted, especially since all previous tests, including ECG and ultrasound, came back normal. This situation significantly affects her daily life, restricting her ability to engage fully in school and work. Any suggestions would be greatly appreciated!

Crohn's DiseaseThyroid DisordersCOPD
Male25-34
1 hour ago

Concerns Regarding Neurological Health

Hello! I received an epilepsy diagnosis back in 2008, and throughout this time, various MRI and CT imaging studies have indicated issues related to cerebral function and encephalopathy. Despite consulting multiple neurologists over the years, I’ve found that none of them appear worried about the encephalopathy aspect. Shouldn’t this be something to take more seriously? My cognitive abilities, including memory and vision, have noticeably deteriorated as time has passed. I’m feeling lost since my previous neurologists have not acknowledged my concerns adequately. If anyone could offer guidance or suggest resources, I would greatly appreciate it. In addition to epilepsy, my other medical conditions include Narcolepsy, Lynch Syndrome, Migraines, a mutation associated with HLA-B27, and Hashimoto's disease, along with others that escape me for the moment. Currently, I’m on a medication regimen that includes Lamictal, Xcopri, Hydroxyzine, Solifenacin, Zoloft, Wellbutrin, Sunosi, Aimovig, and Famotidine.

Multiple SclerosisLupusThyroid Disorders
Male25-34
1 hour ago