Challenges with Breathing
In April, I visited my general practitioner due to struggles with my breathing. It seemed like my lungs weren’t completely inflating with each breath. The GP measured my blood pressure, which turned out to be exceedingly high, prompting a referral to the emergency department. This was unusual for me, as I have never previously experienced blood pressure issues. Upon arrival at A&E, I was released within three hours, with the doctors attributing my symptoms to stress from examinations. They performed blood tests, an X-ray, and an ECG, all of which returned normal results. However, my breathing concerns persisted, and now that it's been four months since the exams, it’s clear that stress isn’t the culprit. I returned to my GP, who fitted me with a 24-hour blood pressure monitor. Although my readings were lower, he informed me that they remained elevated for someone my age, 24. Consequently, he referred me to a specialist, who conducted breathing tests today, all of which were normal as well. After the evaluation, the consultant diagnosed me with "Breathing Pattern Disorder." I can’t shake the feeling that I’ve been given this label prematurely, and based on my research, it doesn’t align with the symptoms I've been experiencing. Has anyone else had a similar experience? Both my GP and I initially suspected asthma, but the consultant dismissed that possibility based on the test results.
Answers (1)

8/27/2025, 8:11:00 PM
OpenHealth AI
It sounds like you've been through quite a journey with your breathing challenges and the investigation surrounding them. Given the tests you've undergone, it's understandable you are feeling uncertain about the diagnosis of "Breathing Pattern Disorder," especially since your symptoms persist.
Summary: Breathing Pattern Disorder can involve abnormal patterns of breathing that might not always correlate with traditional lung issues. While your tests came back normal, let's focus on managing your symptoms and addressing any underlying concerns.
Explanation
Breathing Pattern Disorder often arises from a variety of factors, including anxiety, stress, or even habits developed over time in how one breathes. It can lead to feelings like breathlessness, but it doesn't always reflect a physical lung issue. Since serious lung diseases such as asthma have been ruled out based on testing, it might be beneficial to explore techniques to help regulate your breathing.
Next Steps
-
Breathing Techniques: Practice diaphragmatic or abdominal breathing exercises. This can help improve the function of your lungs and may alleviate some of the breathlessness. Aim to set aside a few minutes each day for this.
-
Relaxation Practices: Consider incorporating mindfulness, yoga, or other relaxation methods into your routine. These can address any anxiety components that may contribute to your breathing issues.
-
Physical Activity: Gradually increase your level of physical activity. Gentle exercises like walking can help improve lung capacity and overall fitness. Listen to your body and progress at your own pace.
-
Keep a Symptom Diary: Track your symptoms, including what exacerbates or alleviates them. This may help in identifying patterns or triggers you can manage.
-
Follow-up with Your GP: If you continue to experience discomfort, it’s essential to communicate openly with your GP about your concerns or seek a second opinion from another specialist if you feel your symptoms aren’t being fully addressed.
Remember that you are not alone in feeling uncertain about your diagnosis. It's important to be your own advocate, seeking clarity on how to move forward. If you have further questions or need more specific exercises, feel free to reach out.
Related Questions
Experiencing Unusual Neurological Symptoms: Should I Be Worried?
I am an 18-year-old male and I've been facing some unusual neurological symptoms lately. Is this a cause for concern? There are moments when I perform a sequence of actions in quick succession, and I feel as though my brain skips a beat, leading to unexpected outcomes. These occurrences primarily manifest when I attempt to execute actions that I have mentally outlined in advance and do so rapidly. For instance, when I engage in conversation, I often have a general idea of what I want to express, yet I don’t articulate every word precisely. While speaking quickly, I experience a peculiar sensation about halfway through my thoughts, as if I momentarily lose consciousness. This feeling leaves me as a spectator in my own body, resulting in a nonsensical noise escaping my mouth instead of my intended statement. It’s remarkably disorienting, yet strangely, it doesn’t disrupt my ongoing thought process. By the time I realize what has happened, I’ve usually continued speaking, leaving little time to react. Oddly enough, those around me do not seem to notice this anomaly. This isn’t merely a stumble or a stutter. I understand the difference; stuttering involves misjudging muscle movements in speech. While I do tend to stutter when speaking rapidly, this experience feels fundamentally different. I’ve also noticed this phenomenon when I type quickly. When attempting to input longer words, I encounter a similar moment of disconnect. Instead of hitting the intended keys, my hands carry out erratic movements than those I had envisioned. It’s essential to clarify that this disconnection doesn’t leave me feeling blank. My vision remains completely clear, and I remain mentally aware throughout the experience. Yet, it feels as if I am merely an observer, not actively processing what unfolds; I am present but not engaged. In my interpretation, it seems as though I’ve mentally prepared for an action, but when the moment comes to execute it too rapidly, my brain becomes overwhelmed. This results in a chaotic mishmash of outputs rather than the clear message I had originally planned. This issue does not appear to hinder any other aspects of my daily life apart from being somewhat inconvenient. The incidents occur roughly once every month or two and are triggered by the described patterns of movement rather than a specific schedule. Could there be a logical explanation for this? Should I be worried about these experiences?
Understanding Femoral Neck Stress Fractures: A Patient's Experience
I’m a 31-year-old woman, weighing 125 pounds and standing 5'7" tall. As an avid runner, I began experiencing intermittent pain in my right groin around mid-June. Despite my efforts to rehabilitate through strength training and continuing to run, the discomfort persisted. A month ago, my X-rays came back clear, but after an MRI three weeks ago, the radiologist's findings revealed: "There exists an incomplete stress fracture along the medial cortex of the right proximal femoral metadiaphysis." "Periosteal edema is present at the right proximal femoral metaphysis, extending to the region of the lesser trochanter. Beneath this area, edema can be observed within the medullary bone. Additionally, there is thickening localized to the medial cortex of the proximal femoral metaphysis. A linear hyperintensity on T2-weighted images appears in the thickened cortex, along with focal cortical irregularities noted in the coronal sequence." My family doctor expressed concerns that I might require surgical intervention and referred me to a fracture clinic. During my visit today, I waited for three hours to consult with an orthopedic specialist for a mere five minutes. The doctor reviewed my MRI images but concluded that nothing significant was apparent and has since recommended a bone scan. Although she advised that I am free to walk without crutches, she prohibited me from running, weightlifting, or cycling. Is it common to observe such a variance between the radiologist's conclusions and that of the orthopedic examination? My research indicates that managing this type of injury typically necessitates extended periods of non-weight bearing activity. While I am relieved to think that my condition may not be as serious as initially feared, I am anxious about the brevity of the appointment and the lack of thorough explanations regarding the shift back to full weight bearing. I’ve attached some slices of my MRI for anyone who might offer additional insight. Any thoughts would be greatly appreciated!
Experiencing Blood Clot in Stool and Chest Discomfort
I hope this post adheres to the guidelines, although I realize emergency situations are typically not accepted. However, I’m unsure if my current situation qualifies as an emergency since I feel generally well. I am a 25-year-old woman diagnosed with polycystic kidney disease (PKD) and polycystic ovarian syndrome (PCOS). My medication regimen includes oral contraceptives, metoprolol (50 mg), trazodone (100 mg), spironolactone (25 mg), Prozac (20 mg), and Jynarque (30/15 mg), in addition to promethazine for nausea as needed. I have regular consultations with a nephrologist for my PKD, which is currently in its early stages, and my glomerular filtration rate (GFR) is stable. Due to my PKD, I have experienced frequent nausea and vomiting for the past decade. Recently, I have begun to face difficulties with swallowing, alongside a sensation of a lump in my throat and chest discomfort. After discussing these symptoms with my primary care physician, she suspected a potential stricture or ulcer stemming from my extensive vomiting history and recommended an endoscopy. I’m currently waiting for scheduling details for that procedure. Earlier today, the chest and upper abdominal discomfort intensified, and during a bowel movement about an hour ago, I noticed a significant blood clot in my stool—about the size of my thumb. While it was not during my menstrual period, the clot resembled those typically seen at that time. Additionally, there was some mucus-like material, but the stool itself wasn't black, and the blood was localized to that single clot. Does this seem consistent with what my primary care doctor has indicated? Is it reasonable to hold off on the endoscopy for now? I’m not seeking specific medical guidance here; I would absolutely head to the emergency room if my pain escalates to an unbearable level. Currently, it's not severe enough for me to feel justified in using emergency services for what might be a routine aspect of my ongoing health situation. Thank you for any advice, and I apologize again if this inquiry falls outside of the accepted topics!
Post-Surgery IV Site Concerns: Is This Normal?
Age: 34, Gender: Female, Height: 5'3", Weight: 190lbs, Location: USA. I underwent a minor surgical procedure on the 12th of this month, during which an IV was placed in my hand. Three days post-operation, I noticed a faint red streak extending from the IV insertion point down to the inner area of my elbow. Although it wasn't vibrant red, my husband and I opted not to seek medical advice immediately that evening. The following day, there was notable improvement; the redness faded significantly, and by the time evening arrived, the line was nearly invisible. Now, two weeks later, I'm experiencing some concerning symptoms. The vein on the back of my hand has become raised and quite rigid, with soreness that feels akin to bruising extending down to my wrist. Applying lotion there is extremely painful, and even simple hand-washing has turned into a challenge. Should I be worried about this? Is such discomfort typical at this stage of recovery? Are there effective methods to facilitate quicker healing? It's surprising how often the back of my hand makes contact with objects during daily activities, especially now that it's so tender.
Understanding Dent Disease
At 26 years old, I recently received a diagnosis that has eluded doctors for nearly three years. After countless visits and discussions, a professor finally identified the issue, which brought me immense relief. He mentioned that throughout his extensive career, he’s encountered this condition only once—during a lecture two decades ago. While I understand it’s not life-threatening, especially since I’m on ramipril to support my kidney function, I find myself overwhelmed by the scarcity of information available on this rare disease. Given that only around 300 individuals are affected, I feel somewhat isolated in my situation and unsure of where to seek help or connect with others who understand what I'm experiencing. There is a foundation dedicated to this disease, but I found it lacking in practical resources. Furthermore, there seems to be no equivalent support in the UK. I’m sharing this in hopes that I might connect with others, be they doctors or individuals with similar experiences, who can provide insight or share their journeys with Dent disease.