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Most people think Sjögren's means dry eyes and dry mouth — an inconvenience, not a crisis. Content creator Melissa Taylor spent four years and countless doctors chasing an answer, while her real symptoms — crushing fatigue, brain fog, dizziness, digestive issues — got scattered across separate diagnoses. Here's what she wishes she'd known, and why the "dryness only" story is costing patients their careers, relationships, and years of their lives.
Why does it take so long to get diagnosed with myositis and what happens next? Getting diagnosed with myositis can take months, even years. A rheumatologist explains why the symptoms are so easy to miss, and two patients share what their own diagnosis journeys really looked like.
New research shows most people with myositis live with real pain — even though medical textbooks have long called it a "painless" disease. Here's what's actually going on, and how to talk to your doctor about it.
Some days, "Autoimmune Warrior" says she feels like she could take on the world. Other days, she can't lift her head off the pillow. After more than a decade with polymyositis, she's still fighting — and still looking forward.
If you live with a chronic condition like myositis, tracking your symptoms can be one of the most powerful things you do for your health. Learn why keeping track of symptoms between appointments can help you manage your condition.
The latest health headlines to help you stay informed, take control of your care, and advocate for better health.
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