Let’s talk. In a brief, no-pressure chat, we’ll discuss your situation, goals, and whether this service is the right fit. You’ll get to ask questions, share your story, and see if we’re on the same page.
We don’t replace doctors. We enhance your ability to work with them. Our role is to shine a light on what’s been missed in the past, forensically go through your medical history, map out possible next steps, and help you become a stronger advocate for your own health.
We offer expert case navigation, research-backed insight, and personalised support for patients facing rare, overlapping, or misunderstood symptoms. Whether you’ve had ten different labels, no label at all, or doctors who’ve told you “it’s all in your head,” we’re here to help you move forward with confidence.
When you’re living with a complex or undiagnosed health condition, the hardest part isn’t always the illness itself — it’s the constant dead-ends, dismissals, and diagnoses that never seem to fit. At Investigative Diagnostics, we exist to help people caught in this medical no-man’s-land.
We offer expert case navigation, research-backed insight, and personalised support for patients facing rare, overlapping, or misunderstood symptoms. Whether you’ve had ten different labels, no label at all, or doctors who’ve told you “it’s all in your head,” we’re here to help you move forward with confidence.
Too often, rare or multisystem illnesses are misinterpreted or mislabelled as anxiety, psychosomatic, or simply “inconclusive.” We take a fresh look at your case from the outside, combining your medical data with a sharp, research-driven lens to uncover what might have been missed. This isn’t about proving doctors wrong — it’s about giving you the best shot at the right diagnosis.
Our process involves going through your history with precision — lab results, scans, consultant letters, symptom logs — to look for patterns, inconsistencies, and signs of under-investigated conditions. Whether it’s a mitochondrial issue, connective tissue disorder, autoimmune overlap, or neuroendocrine dysfunction, we help bring overlooked pieces into view.
Medical professionals are overwhelmed, and long histories often get skimmed or misunderstood. That’s why one of our core services is crafting clear, concise, and structured case summaries — documents you can hand to your next consultant that tell your story logically, with all the right clinical markers highlighted.
This makes a huge difference. A well-constructed summary saves time, builds credibility, and increases the chances that your doctor will truly listen. We also provide tailored lists of questions to ask, suggested testing paths, and if relevant, summaries of published case studies that align with your situation.
With access to up-to-date medical literature, case reports, and clinical guidelines, we explore possible diagnoses and help you understand what might be contributing to your symptoms. This isn’t DIY medicine — it’s informed support, designed to complement the care you receive from licensed professionals.
We don’t guess. We research. We help you understand the relevance of things like mitochondrial genetics, autoimmune patterns, autonomic dysfunction, endocrine disruption, or obscure rare diseases that often get overlooked. And we explain it in a way that makes sense — no medical degree required.
We know what it feels like to sit across from a doctor and not be believed. At Investigative Diagnostics, empathy isn’t an add-on — it’s the foundation. This service was born from personal experience with years of misdiagnosis, near-crises, and a relentless fight for clarity. That’s why our approach is rooted in validation, understanding, and strategy.
You don’t have to face this alone, and you don’t have to keep guessing. With our support, you’ll walk into your next appointment with a structured plan, the right language, and the confidence that comes from finally feeling heard. You may not have the answers yet — but together, we’ll get you closer.
