As a patient, healthcare provider, family member, friend or visitor, we hope you will get connected with the Sjögren's Syndrome Foundation.
We have many opportunities for you to learn more about Sjögren's, volunteer your time, or help us raise awareness for this common, yet little known disease.
Here are some of the ways you can Get Connected:
By joining the Foundation you will not only receive our 10 newsletter a year, The Moisture Seekers, packed with vital information from medical experts and fellow patients, but you will also become connected with other Sjögren's patients through our member community. In this community you will find archived articles from the The Moisture Seekers, access to member-only information, and the ability to talk with other members.
Visiting a local support group or attending a patient seminar offer great opportunities to meet other Sjögren's patients while also expanding your knowledge of the disease. Support Groups are held in over 80 cities throughout the United States and Canada. The Foundation also hosts one 2-day patient seminar each year, which include expert presentations by healthcare professionals.
Through SSF Events
From Sjögren's Walkabouts to Sip for Sjögren's Fine Water Tastings, there are events for everyone. These projects all help to raise crucial funds for the fight against Sjögren's while also helping to raise awareness within our communities. If you don’t see an event in your area, consider contacting the Foundation to learn more about how you can host one. Also — consider joining Team Sjögren's, our marathon training program.
Donate your time to one of our events, seminars, or by becoming a support group leader. Contact us today to add your voice to our advocacy efforts or to receive future information about programs and services available in your area.