CAPS (Cryopyrin-Associated Periodic Syndrome)–Helpful Links
Resources
There are support groups and organizations online that offer additional information about CAPS (cryopyrin-associated periodic syndrome). The main goal of these groups is to help people understand these diseases and help improve the lives of people with CAPS (cryopyrin-associated periodic syndrome).
Ongoing Updates for New Users
Complete the Screener and print to discuss with your physician. Also, register to receive ongoing updates about CAPS (cryopyrin-associated periodic syndrome).
Support Groups and Organizations
Visit any of the sites below to learn more:
- Genetics Home Reference Guide
- National Organization for Rare Disorders (NORD)
- National Institutes of Health Office of Rare Diseases Research
CAPS Connect USA
Join CAPS Connect USA to share your experiences:
- This site helps people living with CAPS (cryopyrin-associated periodic syndrome) and healthcare professionals get connected
Patients and their caregivers can:
- Locate other CAPS (cryopyrin-associated periodic syndrome) patients and caregivers across the United States with similar interests
- Share inspirational stories about their disease
- Communicate with others
- Identify physicians familiar with CAPS (cryopyrin-associated periodic syndrome)
Healthcare professionals can:
- Identify themselves as a healthcare professional familiar with CAPS (cryopyrin-associated periodic syndrome)
- Communicate with other healthcare professionals
Patient Brochure
Download an educational patient brochure on CAPS (cryopyrin-associated periodic syndrome) brought to you by Novartis Pharmaceuticals Corporation.
By browsing the Internet, you may come across other Web sites that support CAPS (cryopyrin-associated periodic syndrome) and allow people with CAPS (cryopyrin-associated periodic syndrome) to share their experiences. However, your doctor's advice is the best advice to follow.
