Category: sjogrens
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7 Advocacy Phrases Every Sjogren’s Patient Should Know
For my Sjogren’s patients, medical appointments can feel like a battleground where you have to hold the line and get strategic. It took me four years and four rheumatologists to get diagnosed. It can be rough out there! If you’ve ever heard frustrating comments like: “A diagnosis doesn’t really matter.” “Your labs are normal, so…
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Affordable Sjogren’s Mini Courses for Every Step of your Autoimmune Journey
When Dr. Sarah Schafer of Sjogren’s Advocate and I created the masterclass Streamlining Sjogren’s: How to Navigate a Path to Diagnosis and Treatment, our goal was simple: give patients a clear roadmap to understanding Sjogren’s disease, which is far too often misunderstood and dismissed. We poured months into building a five-hour video masterclass with downloadable…
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Sneaky Sjogren’s: Commonly Overlooked Symptoms That Delay Diagnosis and Treatment
Sjogren’s is a master of disguise—it doesn’t walk into the doctor’s office wearing a big flashing “CALL ME SJOGREN’S” sign. It tiptoes around and spreads its symptoms across different body systems. Forcing specialists to play medical hide-and-seek (and many providers aren’t good at that game). Most people know Sjogren’s for its poster children: dry eyes…
Little Engine Patient Advocacy 