Loss of Taste and Smell: Is it Covid-Related or a Tumor?
Greetings. Back in 2020, I contracted Covid and experienced a complete loss of taste and smell. Fast forward to 2021, I was identified with a Pituitary adenoma. Surprisingly, after this diagnosis, no specialist bothered to review my MRI results. Since then, I've encountered significant health issues, including nearly 100 pounds of weight gain, the onset of acne, a condition I typically don’t experience, and noticeable hair thinning. I find myself at a loss, having experienced a drastic decline in my well-being. It’s been five years without any sense of taste or smell. I’m desperate for guidance on what steps to take next. I haven’t observed any improvements regarding my situation.
Answers (1)
12/13/2025, 10:40:33 PM
OpenHealth AI
I understand how challenging your situation has been, especially with the loss of taste and smell for such an extended period, along with the other health issues you've described. It's important to address these concerns systematically, as they could be interlinked.
Summary of Main Points:
- Loss of taste and smell persisting for years needs careful evaluation.
- Your weight gain, acne, and hair thinning may relate to hormonal changes from the pituitary adenoma.
- Further investigation is crucial for tailored treatment and management.
Explanation:
The loss of taste and smell you experienced after COVID-19, while common for many, can persist in some individuals. Additionally, the pituitary adenoma may disrupt hormone levels, potentially causing symptoms like weight gain, acne, and hair thinning due to hormonal imbalances (such as changes in cortisol, insulin, and sex hormones).
It’s concerning that your MRI results haven’t been reviewed by a specialist, as this may provide insights into treatment options or monitor the adenoma's status.
Prioritized Next Steps:
-
Document Symptoms: Keep a detailed diary of your symptoms. Note the onset, duration, severity, and any factors that seem to affect them. This information can be invaluable during consultations.
-
Seek Medical Attention: Arrange a consultation with an endocrinologist. They can help evaluate how the pituitary adenoma is affecting your overall health, particularly hormone levels. Make sure to request a thorough review of your MRI results and discuss your current symptoms.
-
Request Comprehensive Testing: Ask for blood tests to check hormone levels, including thyroid function, cortisol, and sex hormones. This will help identify any imbalances that may be causing your symptoms.
-
Consider a Taste and Smell Evaluation: An otolaryngologist (ENT specialist) can assess your persistent loss of taste and smell, potentially providing a diagnosis or management plan.
-
Maintain a Healthy Lifestyle: Focus on a balanced diet, regular physical activity (as tolerated), and sufficient hydration. This can help manage weight and improve overall well-being, even while you seek medical advice.
Your health concerns are valid, and taking these steps can provide clarity and direction toward improving your quality of life. Please feel free to reach out for any further questions or support during this process.
Related Questions
Hernia Diagnosis Without Follow-Up: A Conflicting Situation
A 22-year-old male recently visited the emergency room due to discomfort in his lower abdomen. Upon examination, the medical team was indecisive about whether he was experiencing an oblique muscle problem or a hernia. Surprisingly, they opted against performing a CT scan or ultrasound and did not schedule any follow-up appointments. To the best of my knowledge, hernias typically do not resolve themselves with merely the use of ace bandages or over-the-counter pain medication; surgical intervention is usually necessary for proper treatment. Is there a specific rationale behind their reluctance to pursue further diagnostic testing or surgery?
Unexplained Episodes of Abdominal Discomfort
Age: 28 Gender: Female Weight: 194 lbs Height: 5’7" Current Medications: Vitamin D, Fish Oil, B Complex Vitamins, Birth Control Pills, Vyvanse 30 mg Health Background: Asthma, Eczema, Gastroesophageal Reflux Disease (GERD) Since August 2025, I've experienced three occurrences of intense abdominal discomfort that necessitated visits to the emergency room for pain management. These episodes usually strike at night, escalating to unbearable levels within around 30 minutes. None of the sitting positions seem to provide relief, and gastrointestinal medications have proven largely ineffective. Only strong pain relievers seem to alleviate the suffering. After the peak of the pain subsides, my abdomen remains sensitive for more than three days. I can accurately identify the location of the discomfort, which appears to be between the midepigastric area and near the gallbladder. The pain is difficult to articulate, yet it presents as a severe burning and aching sensation. Interestingly, there does not seem to be any specific food intake related to these pain episodes. I underwent an H. Pylori breath test that returned negative results. Additionally, I had an esophagogastroduodenoscopy (EGD). Although the biopsies were also negative for H. Pylori, they did reveal residual liquid in my stomach and a small section of intestinal metaplasia. My complete blood count (CBC) and comprehensive metabolic panel (CMP) results were normal, except for elevated LDL levels, which I’m already aware of. My gastroenterologist has recommended a gastric emptying study (GES) to evaluate the functionality of my stomach. If results indicate no issues, we will then investigate the gallbladder. Are there alternative explanations for my symptoms? Should I be worried about autoimmune metaplastic atrophic gastritis (AMAG)? While I have been diagnosed with GERD, this pain feels distinctly different from the GERD-related discomfort. I am not entirely sure it is gastroparesis, even though I occasionally regurgitate if I eat too quickly; I do not experience nausea or malnutrition. I have researched extensively, and my symptoms align with biliary colic. However, I am anxious about the possibility of gallstones not appearing in the ultrasound. My gastroenterologist is not particularly concerned about the intestinal metaplasia, but being only 28 years old, I find this worrying. As a medical student, these painful episodes significantly hinder my studies and academic progress.
Understanding My Symptoms: A Personal Account
I’m sharing my experiences here, as I haven’t received much feedback elsewhere. I am a 15-year-old female, measuring about 5 feet tall (152 cm) and weighing between 105 and 110 pounds (47-50 kg). I identify as Hispanic and Cuban, and legally fall under the white classification. I reside in Palm Beach County, Florida, and I am a U.S. citizen. I have a diagnosis of Autism and previously had ADD, although that diagnosis has been dropped, which leaves me unsure about my current condition—whether ADHD applies or not. Additionally, I have a past history of anemia, although it is currently not diagnosed. For the past year, I've experienced a range of symptoms that appear intermittently and are often present almost daily. While these symptoms vary, they haven’t subsided. I’ve noticed that both physical activity and caffeine can either trigger or exacerbate these issues. Now, I’d like to detail the symptoms I've been facing. One of my major concerns is my balance; when I stand, I often feel unsteady, and sometimes I even limp. This particular symptom is quite troubling as it occurs frequently. I also experience occasional dizziness and fatigue, which leaves me feeling too weak to move, causing me to remain still for prolonged periods. During episodes of significant fatigue or balance issues, I find myself starting to stutter and I suspect my speech may slur at times. Additionally, my hands sometimes shake, especially when I struggle to walk. There could be other symptoms I haven’t recalled yet, but this is what I remember for now. I will provide updates if I think of anything else, and I welcome any engagement. Furthermore, I’ve noticed irregularities with my heart rate. Initially, when these symptoms began, my resting heart rate dropped from the 80s and 90s to the 50s and 60s; this lower rate has persisted. Lately, however, even simple tasks such as standing, walking short distances, or rocking back and forth (which I do as a self-soothing mechanism) have caused my heart rate to spike to the 100s. These changes are new, while the other symptoms have been consistent for about a year. I genuinely seek guidance or support, as I feel uneasy relying on AI for self-assessment. Unfortunately, I can't afford doctor visits at this time, and my caretaker has shown little concern for my well-being. Therefore, please refrain from suggesting medical consultations. Thank you for taking the time to read my story. I’m open to any questions.
Understanding Lymph Node Sensitivity
A 32-year-old female with a BMI of 28 poses a concern about potential lymph node activity. Over the past three months, she has noticed tender areas coinciding with her menstrual cycle. She has detected slight lumps, but is careful not to press deeply into the tissue to avoid further discomfort. Initially, in December, the sensitivity was localized to the left side of her breast. In January, she observed similar tenderness in her inner left thigh, and by February, both areas and the region above her armpit were affected. Additionally, she has been experiencing fluctuations in her hormonal balance lately. The discomfort in her left breast has persisted for most of this time since December. She wonders whether this is a typical response from lymph nodes due to hormonal changes or if it would be advisable to consult her general practitioner for further evaluation.
Seeking Guidance on Recurring Pilonidal Sinus Issues
I'm a 17-year-old male of Indian descent, standing at 5'8" and weighing 103 kilograms, and I'm dealing with pilonidal sinus problems. My issues began when I noticed blood on the toilet seat; I initially dismissed it as perhaps an anal fissure. However, after four months, I visited a doctor who diagnosed me with a pilonidal sinus. My symptoms included an unpleasant odor and bloody discharge that often stained my clothing. Subsequently, I was placed on a surgical waiting list. By the time my surgery arrived, the situation had worsened significantly, making the procedure even more traumatic and painful than anticipated. The surgeon ended up removing more tissue than originally planned. During my recovery, I inspected the surgical site and discovered a noticeable indentation at the top with various irregular bumps extending down. The doctor assured me that these would eventually fade, but instead, they collected lint and hair over time. Fast forward a year, and I began to notice the same familiar odor again, filling me with anxiety about a potential recurrence. Now, as an 11th grader, I am under pressure to maintain good grades and cannot afford to miss school. Presently, my symptoms include the telltale smell, although I haven’t observed any discharge or developed any additional openings aside from the dimple left from my previous surgery. Before the operation, the infected sinuses extended close to the rectum, which is why I am concerned that a new pilonidal sinus may have formed in the same area. At this moment, I am free from pain but cannot shake the anxiety surrounding the reappearance of the odor associated with this uncomfortable condition.