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Dan tells us about his experiences of living with two rare diseases.
The Rare Disease Day theme this year is Research so we thought we'd share with you some our research findings from a recent survey.
An 8 year old's account of his experience with DI and his reasons for wanting to fundraise.
An extremely positive story from a family who have experienced pituitary conditions for years.
Young Isabella Andrews was born with a non-functioning pituitary gland. Here mum Kelly tells us her story.
Ten years ago I was diagnosed with a tumour on my pituitary gland that was causing a disease called acromegaly.
Lawrie's journey before and after his pituitary tumour diagnosis.
Martin's story of his Craniopharyngioma.
A normal life disrupted by acromegaly, but managed effectively. Michael’s story.