Rare Disease Day takes place on 28th February, raising awareness and generating change for the 300 million people worldwide living with a rare disease.
If you would like us to share your story of living with lupus on Rare Disease Day, email chanpreet@lupusuk.org.uk with a 500-word article and accompanying photos by 23rd February.
Your stories will be shared on LUPUS UK's website and social media accounts :).
Osteonecrosis and other rare bone diseases
Is there anyone on long term steroid therapy? Could you share your stories. The pros in specific. 
