News and Updates - Pituitary Foundation

We’re launching a support group in Edinburgh!

Desmopressin shortage survey

‘Alone we are rare; together we are strong’ – Why Sara is setting up a new support group

Weight Gain – Is it my pituitary?

Prescription frequency – Tell us about your experience!

Why community matters for pituitary patients and their families

Factors influencing self-management of adrenal crises in patients with adrenal insufficiency: A qualitative study

We’re pushing for action on the desmo nasal spray shortage

Watch our new Cushing’s awareness video!

Understanding the cause of hypotonic polyuria: What does the future of diagnosis look like?

Cortisol and Cushing’s: Exploring health, disease and the current research landscape

Research opportunity: Using advanced imaging to detect pituitary adenomas

Pituitary adenoma surgery: What are the research priorities?

Adrenal insufficiency and the importance of self-advocacy

The team attends the BES conference!

AVP deficiency survey: Call out for clinician input

Update on supply issue with desmopressin nasal spray

School, netball and a pituitary tumour – Tessa’s story of a childhood craniopharyngioma

Pushing for a diagnosis – Sophie’s rare disease story

Understanding Sick Day Rules

Life as an endocrine specialist nurse

Fasting with adrenal insufficiency: What you need to know

Kent support group relaunches

How a thunderclap headache changed my life – Emily’s story

Running for rare disease awareness: Jerome’s story