Just Another Statistic
Battling Invisible Autoimmune Illness and Visible Medical Failure
After 18 months of misdiagnosis, Axel Reid nearly died from the disease he actually had: Systemic Lupus.
Imagine trusting doctors with your life, only to discover they ignored critical blood tests, dismissed clear symptoms, and covered up their mistakes. This is the true story of a 28-year-old London trader whose mysterious illness baffled doctors, triggered life-threatening reactions to the wrong medications, and exposed shocking failures in private healthcare.
What you'll discover:
- Blood test results that clearly showed lupus—ignored for 18 months
- Specialist recommendations that were never followed
- Medical records that mysteriously disappeared
- A legal battle that exposed how the system protects its own
- The devastating reality of living with undiagnosed autoimmune disease
Was negligence involved? YOU be the judge.
After reading, cast your vote on whether justice was served. See what thousands of other readers think at the link provided in the book.
For autoimmune patients, medical professionals, and anyone who's ever felt dismissed by the healthcare system.
Available on Amazon Worldwide:
Literary Titan Silver Book Award Winner
Recognised for excellence in memoir writing
View All ReviewsFeatured in Literary Titan
"Just Another Statistic follows Axel Reid's long, confusing, and often frightening medical journey as he battles invisible autoimmune disease while navigating a healthcare system that keeps misreading the clues."
"I found myself drawn into the rawness of the author's voice. There's no polish, no tidy narrative arcs, and that's what makes it hit harder. The repetition and spiraling thoughts, especially in the sections where the illness affects his cognition, gave me a weird cocktail of sympathy and discomfort."
"The author writes the way someone thinks when they're scared and exhausted... It's messy in a way that feels honest. Some chapters had me sitting back, just letting the weight of it settle, especially when he describes moments where his mind simply stops working. These parts aren't dramatic. They're just unsettling, and that simplicity made them powerful."
"I'd recommend this memoir to anyone who wants to understand autoimmune disease beyond medical definitions, and to readers who appreciate raw, unfiltered life narratives. It's especially powerful for anyone who's been dismissed by doctors or felt lost in a system that values test results over lived experience."
Read the full review →"I felt cheated by the system. The doctors colluded despite overwhelming evidence... Writing this book became essential because the story needed to be told, but not just mine. Thousands of patients go through this same pattern of dismissal and misdiagnosis."
"Writing about it now has been harder than I expected. Reliving the experience and the frustration - knowing the doctors involved faced no accountability - still makes me furious... However, I never agreed not to write about it. They probably didn't worry about that anyway - my life expectancy was supposed to be short."
Read the full interview →Join the Movement
After 18 months of misdiagnosis IN HOSPITAL with textbook lupus symptoms, I realised something:
We're teaching patients to recognise lupus.
But patients already KNOW something's wrong.
We need to teach DOCTORS to recognise it earlier.
Lupus Diagnostic Education
A Facebook group where patients share diagnostic delay case studies and medical professionals learn what textbooks miss.
This is NOT a support group - it's an educational space to create systemic change
Help improve medical education and reduce the 6-year average diagnostic delay