I would like to know why it took 26 doctors 11 years to correctly diagnose me with late-stage neuro-lyme disease when I had a history of camping, a bulls-eye rash, and symptom s list which read like a lyme brochure. The only symptom missing was death... Why? Why did it take so long, and btw, now correctly diagnosed, more than $1,500,000 (not a typo) spent on my treatment the last 5 years. Why have I had to travel out of state to see a doctor willing to treat long-term, and why when so many of us show improvement with long-term treatment is it so often denied? Why is this epidemic being ignored by the medical profession?