PATIENT STORIES
Whether you’re living with Sjögren’s or supporting someone who is, your experiences can inspire, educate, and connect others in our community. Your story could be featured on our website and social media!
Together, let’s amplify the voices of those impacted by Sjögren’s and show the world what it’s really like to live with this condition.
Fill in our form here or directly email us at office@sjogrensuk.org to share your story.
LIVING WITH MY SJOGREN'S YETI
WHAT I HAVE LEARNED SO FAR
I have decided that “gate crasher” or “interloper” are not the right words to describe my Sjogren’s. That may be because eventually, both will leave. Sjogren’s will never leave.
LIZ'S STORY – THE POWER OF MEDITATION
I was diagnosed with Sjögren’s about fifteen years ago.
I have periods of dry eyes, dry mouth, also dry nostrils, and more recently days of fatigue, more often morning fatigue, as well as sleeping problems.
DIAGNOSED BY ACCIDENT: IMOGEN’S SJÖGREN’S JOURNEY
I was diagnosed last year by accident, I had blood tests for lower back pain and they tested rheumatoid factor and mine came back at 256 when it’s supposed to be less than 20.
