Only One Address
Sjögren's UK now only has one postal address.
Please ensure all mail is sent to our current address, as post sent elsewhere may not reach us.
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.
HOW WRITING BECAME MY THERAPY –
JILL RUTHERFORD’S STORY
“It has changed my life totally. I now live a restricted life dictated by my levels of fatigue and general feeling of unwellness. I have to pace myself..."
RESILIENCE AND MENTAL HEALTH - OVERCOMING ADVERSITY THROUGH PHYSICAL AND MENTAL CHALLENGES
“ Mental health is increasingly recognised as a cornerstone of overall wellbeing, especially in the face of adversity. The story of a former Royal Marine Commando..."
HOW WRITING BECAME MY THERAPY –
JILL RUTHERFORD’S STORY
“It has changed my life totally. I now live a restricted life dictated by my levels of fatigue and general feeling of unwellness. I have to pace myself..."
