OpenHealth Q&A

Get answered by medical professionals

Seeking Guidance on Symptoms: What Should I Discuss with My Doctor?

7/15/2025, 5:01:26 PMMale25-34

Hello everyone, today has been particularly overwhelming for me, so I’m hoping to gather some insights from you all. A bit about my situation: I’m a 28-year-old female living with a diagnosis of depression, generalized anxiety disorder (GAD), and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Currently, I’m struggling with these conditions and find myself largely confined to my home or bed. My current medications include 10mg of Escitalopram and 25mg of Quetiapine, but I feel like they are losing their effectiveness. Additionally, I take various supplements including calcium, magnesium, multivitamins, omega-3 fatty acids, and zinc. Alongside my mental health challenges, I’ve been experiencing several troubling symptoms: • A persistent dryness in my mouth and throat, despite a sensation of fullness as if my stomach has enough water. At times, it feels like my whole body is dehydrated. • A vague but constant feeling of depletion throughout my body—this is not just fatigue; it feels as though my cells and muscles are not receiving the nourishment they require, and even what does get through doesn’t seem to sustain. • Previously, I often desired sugary, carbohydrate-rich, and fatty foods while disregarding protein. Recently, however, I suddenly find myself averse to sugary and overly carb-filled items, though it doesn't feel like a mental or restrictive choice. • I’ve experimented with electrolyte drinks, but their taste and sweetness leave a strange aftertaste that exacerbates my dry mouth. • I have a hunger that does not translate into an appetite, leading to further weakness and discomfort. • Consuming food has become a challenge—nothing too sweet or heavy can sit well, but eating large portions seems to overwhelm me. • The process of having a bowel movement feels exhausting; it feels like it drains my energy entirely, increases my heart rate, leaves me breathless, and makes me extremely thirsty. • I’m struggling with temperature regulation and experience sudden hot flashes where I feel overheated. • My blood pressure tends to be low, but my heart rate is often elevated. • I frequently notice my toes feeling cold, even in warm conditions, yet I don’t experience a chilling sensation in my feet. It’s challenging to discern which of these symptoms stem from psychological factors or the nervous system, the effects of ME/CFS, the medication I’m on, or perhaps other underlying physical issues such as adrenal or electrolyte imbalances. Any suggestions on what I should consider discussing with my healthcare provider would be immensely helpful (though I’m unsure how I would actually manage to get to my GP!). Thank you for your support! 🙏🏻

Multiple SclerosisLupusFibromyalgia

Answers (1)

Cony

7/15/2025, 5:02:04 PM

OpenHealth AI

Thank you for sharing your situation; it sounds very challenging and overwhelming. Your symptoms and experiences merit careful consideration and discussion with your healthcare provider. Here’s a structured approach to help you identify key areas to discuss.

Main Points

  1. Medication Effectiveness: You’re feeling as though your current medications may not be working well anymore.
  2. Symptom Identification: Several troubling symptoms need evaluation to determine their origin and appropriate treatment.
  3. General Health Concerns: You’re facing issues related to hydration, energy, appetite, digestion, temperature regulation, and more.

Explanation

Your complex health background, including depression, GAD, and ME/CFS, can intertwine with physical symptoms, making it hard to pinpoint the causes. Having a conversation with your doctor about these concerns is essential for adjusting your treatment plan effectively. A thorough evaluation can help identify whether your symptoms stem from medication side effects, your chronic conditions, or other health issues such as adrenal insufficiency or electrolyte imbalances.

Next Steps

  1. Make a List of Symptoms: Draft a list of your symptoms, noting their frequency, triggers, and any changes over time. This will help your doctor understand your condition better during the consultation.

  2. Discuss Medication Concerns:

    • Effectiveness of Current Medications: Share your feelings about the effectiveness of Escitalopram and Quetiapine. Ask if an adjustment or alternative options might be beneficial.
    • Possible Side Effects: Discuss the possibility that some of your symptoms may be side effects of your current medications.
  3. Hydration and Nutrition:

    • Talk about your experience with dry mouth and unusual hunger. Express your concerns regarding selective food aversions and how this changes your eating habits.
    • Consider discussing hydration strategies that might be easier for you, such as focusing on less sweet options or discussing specific electrolyte balance tests.
  4. Energy and Fatigue Management:

    • Address the constant feeling of depletion, energy drain from bowel movements, and changes in appetite. Explore whether therapies or dietary changes could assist in managing your ME/CFS symptoms more effectively.
  5. Temperature Regulation and Blood Pressure:

    • Mention your issues with temperature regulation and changes in heart rate and blood pressure. These physical symptoms need attention to rule out any potential underlying conditions.
  6. Utilize Virtual Consultations:

    • If getting to your GP is difficult, consider virtual appointments. Many healthcare providers offer telehealth services, which can be more convenient and help facilitate easier communication about your symptoms.

Final Thoughts

I encourage you to take your time with this process. Communicating openly with your healthcare provider using your symptom list can guide your discussions and lead to better treatment options. Remember, you’re not alone in this, and seeking medical guidance is a strong step toward improving your health and well-being. If you need further assistance or information about these topics, feel free to reach out!

Related Questions

Battling Chronic Nausea and Vomiting for Over Two Years

For the past two years, I (age 26, female) have been enduring an incredibly challenging health situation. I experience intense nausea daily and find myself vomiting numerous times, with almost nothing providing relief. To provide some background, I’m from West Texas and I currently weigh around 190 pounds, standing at 5’7”. Initially, my weight was about 211 pounds when these symptoms began, and it fluctuates frequently between 190 and 225 pounds. I engage in vaping and consume THC. Previously diagnosed with hypothyroidism, my condition seemingly resolved, according to my healthcare providers. Additionally, I have polycystic ovarian syndrome (PCOS). I have consistently faced irregular bowel movements, with stools that are loose and sometimes appear to have mucus. Compounding my struggles, I've also suffered from migraines. I have had an IUD for over five years, experiencing two insertions of the Kyleena device. In December 2022, my battle with health took a severe turn when I was diagnosed with stage 4 Hodgkin’s Lymphoma, requiring chemotherapy treatment, specifically AVBD (Apologies for not recalling the exact medication names). By July 2023, I had fortunately achieved remission. However, after reaching remission, my vomiting worsened, transforming from primarily white foam to a mixture of 80% bile, any food I attempt to consume, and still white foam. This intense vomiting, accompanied by significant pain in my upper back, escalated to more than eight episodes daily by November 2023. At that time, THC seemed to be the only avenue for me to retain any food. During this tumultuous period, I consulted various doctors who, after confirming I wasn’t pregnant, attributed my symptoms to Cannabinoid Hyperemesis Syndrome (CHS). Immediately, I ceased THC consumption for over six months, yet the vomiting continued unabated. Each time, doctors would prescribe ondansetron, regardless of my claims that it provided no relief. I experimented with various diets recommended by medical professionals, but there were no improvements in my condition. Eventually, I obtained a referral to a gastroenterologist who intended to perform an endoscopy. However, the procedure was prohibitively expensive even with insurance, and thus was never conducted. This doctor also ordered blood tests to rule out several gastrointestinal disorders, such as Crohn's disease, Irritable Bowel Syndrome (IBS), and gluten sensitivity, but all results came back normal. Afterward, I had another appointment with a different gastroenterologist, but the doctor failed to meet with me. Instead, a nurse informed me that the doctor had merely recommended promethazine without conducting any tests or scheduling further visits. When I mentioned the possibility of gallbladder issues, the doctor laughed dismissively at my suggestion. Discussing my situation with my oncologist, he suggested that my heightened sensitivity to food odors stemmed from my chemotherapy experiences while I was working in fast food. While food smells indeed affect me, I'm primarily triggered by medical scents such as rubbing alcohol and cleaning agents. This ongoing ordeal has been overwhelmingly distressing. I now experience episodes of vomiting accompanied by bright red blood, presumably due to a throat tear. When I first encountered this troubling symptom, I consulted a doctor who appeared unfazed and prescribed a promethazine suppository, which does help but makes me extremely drowsy. My nausea persists nearly around the clock, often feeling as if there’s a heaviness in the upper part of my abdomen. I frequent urgent care facilities when my symptoms intensify, only to be met with minimal assistance since this is a chronic issue. Currently, I lack a primary care physician. Whenever I sought one, I encountered skepticism regarding my condition, with some healthcare professionals implying that I was exaggerating my symptoms. Though many physicians who do take my situation seriously seem baffled, I've lost count of the diverse medical experts I've consulted about these ongoing issues. If anyone has insight or suggestions, I would genuinely appreciate it. I can share my latest bloodwork results if that would be helpful—just let me know!

LupusCrohn's DiseaseThyroid Disorders
Male25-34
13 minutes ago

Strange Stomach Sensation Leading to Waking Up

Greetings. I'm a 36-year-old male, standing at 172 centimeters and weighing 90 kilograms. I don't take any medications, nor do I smoke. I've been living with diastasis recti for several years now, and I may also have irritable bowel syndrome (IBS). Additionally, I deal with fatty liver and kidney stones, though I assume these last two conditions are not related to my current concern. Occasionally, I experience a peculiar sensation that jolts me awake; it feels like a quick pulsing in my stomach. I’ve noticed it tends to affect the left side when I’m lying on my left side and the right side when on my right. Remarkably, it can occur even when I’m on my back. This strange feeling often escalates into a surge that fully rouses me. Alongside this, I sometimes feel prickling sensations throughout my body and fleeting lightheadedness. When this sensation disturbs my sleep while I’m turned to my side, shifting onto my back or the opposite side might alleviate it, but not always. In instances where I awaken while lying on my back, I discovered that gently pressing my hands on either side of my stomach can help, as can rising to a sitting or standing position. However, during my last two episodes—one a couple of weeks ago and another tonight—those techniques weren’t effective right away, which made me feel a bit anxious, prompting me to seek advice. Does anyone have insight into what might be going on? By the way, I’ve undergone routine ultrasound examinations of my abdomen by two different physicians during check-ups, both of whom assured me that everything appears normal, including my abdominal aorta and internal organs. They didn’t identify any issues at that time.

LupusCrohn's DiseaseRheumatology
Male25-34
1 hour ago

Healing Progress Post-GBS: Toe Concerns

I am a 28-year-old male, measuring 5 feet 10 inches and weighing 131 pounds. My current medications include Fomadatine and Zyrtec, prescribed due to my ongoing battle with Chronic Gastritis and SIBO. I maintain a healthy lifestyle, abstaining from both smoking and alcohol. My health concern revolves around the toe adjacent to my pinky toe on my left foot, as well as my pinky toe on the right foot. Since August of last year, I have been on the mend from Guillain Barre Syndrome. Recently, I've noticed that at night, the skin on my feet tends to turn a reddish pink, although this usually improves after I walk around. However, two of my toes have remained red, with one appearing slightly swollen. Generally, my pinky toes are quite thick, but the condition of my left foot's toe is worrisome for me. It seems that I'm unable to upload an image to illustrate my issue.

FibromyalgiaCrohn's DiseaseCOPD
Male25-34
2 hours ago

Swelling Beneath My Chin Near the Jawline

18-Year-Old Male: I'm reaching out to any medical professionals who might provide insights into my situation. I've been using marijuana since I was 14, but now, at 17, I'm making an effort to stop and have been clean for 18 days. Recently, I've discovered an unusual swelling located just beneath my chin, behind my jaw. It causes some discomfort when I move, yet it doesn’t feel painful continuously. I'm somewhat anxious that this could be indicative of a more serious issue, especially considering it's positioned near my chin's lymph nodes. Any advice or information would be greatly appreciated as it might help alleviate my worry.

ArthritisLupusInternal Medicine
Male25-34
2 hours ago

Seeking Insights: My Journey with Undiagnosed Neurological Symptoms

Hello everyone, I'm a 34-year-old female grappling with neurological symptoms that first appeared in October, and I’m eager to hear from anyone who might have faced similar challenges. My journey began with unexpected migraines, blurred vision, and an ongoing sensation of being off-balance or intoxicated. Gradually, I began experiencing mainly sensory-related symptoms, such as tingling and burning sensations, feelings of extreme heat and cold, sharp pains radiating in my arms and back, as well as discomfort in my hands and toes, alongside intermittent numbness. I also endure varying degrees of weakness and heaviness in my right side, specifically my arm and leg, although I haven’t suffered complete functional loss. The nature of my symptoms is erratic; they fluctuate rather than consistently deteriorate. An MRI revealed mild, scattered lesions in the white matter, which were deemed nonspecific. Further tests from a lumbar puncture returned normal results, showing no markers of inflammation, and the oligoclonal bands were not present. A thorough range of lab tests yielded no significant findings. After evaluating my case, the neurology team suggested a possible diagnosis of MS and administered a three-day course of intravenous steroids. While I noticed a slight improvement in some sensory pain, my symptoms persist and continue to vary day by day. I still experience headaches and pressure in my head along with episodes of blurred vision, but there have been no new deficits since treatment. I am reaching out to connect with others who have had similar experiences. I would like to learn about the insights or diagnoses you encountered and what treatments proved beneficial (such as those related to migraine disorders, dysautonomia, or sensory neuropathy, for example). If you have navigated a similar path, I would greatly appreciate your sharing your story. Thank you!

Multiple SclerosisLupusEndocrinology
Male25-34
3 hours ago