In this episode of the Lupus Foundation of America's The Expert Series podcast, we focus on managing lupus when access to a rheumatologist is limited, including regular testing, medication management, telehealth, and self-advocacy. Our guest, Dr. Candace Feldman, shares how people living with lupus can document symptoms, prepare for appointments, communicate medication concerns, and use healthcare resources effectively while staying engaged in their ongoing care.
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This episode will help you understand:
Diagnosis delays and access issues in lupus care
How to prioritize symptom monitoring and documentation
The importance of medication adherence and management
The role of telehealth in ongoing lupus management
Self-advocacy and patient-provider communication
Related Resources:
Ask a Lupus Health Educator (LFA): https://www.lupus.org/care-support/ask-a-health-educator
Find Support Near You (LFA): https://www.lupus.org/resources/find-support-near-you
National Resource Center on Lupus (LFA): https://www.lupus.org/resources
The Expert Series (LFA): https://www.lupus.org/resources/lupus-the-expert-series
American College of Rheumatology: https://rheumatology.org/
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