SJOGREN'S ADVOCATE

The official name change to Sjogren's disease can be used to encourage clinicians to address the serious, systemic nature of Sjogren's.

Sjogren's patients deserve the same level of knowledge, compassion, and coordinated care that breast cancer patients are offered.

Sjogren's diagnosis is often long delayed. Learn how to use the Sjogren's Foundation Diagnosis Handout to advocate for diagnosis.

Most people with Sjogren's remain undiagnosed due to lack of clinician training and awareness.

Learn how self-advocacy helped me get diagnosed and treated for POTS, an autonomic disorder.

Many people with Sjogren's are told they have functional disorders, when their symptoms are direct, physical Sjogren's manifestations.

Clinicians who believe the" nuisance sicca disease" myth are being led astray by outdated assumptions about the disease.

The most important thing for clinicians to know about Sjogren's is that it is a serious systemic disease.

Learn how to choose handouts that work well for clinician education, and why you can trust the information on Sjogren's Advocate.

Patients often a hard time finding doctors who understand Sjogren's and take it seriously.

The new ICD-10 codes for Sjogren's offer an easy, low-key want to educate clinicians about the systemic nature of the disease.

Rheumatologists have few opportunities to stay abreast of Sjogren’s knowledge. Sjogren’s is neglected at every level of medical education....