News and updates - Pituitary Foundation

Our patient panel explores ‘Living well with a pituitary condition’

Research Opportunity: Improving the diagnosis and referral of people with visual problems caused by brain or pituitary tumours

The Bristol support group is relaunching!

‘I have become a zebra with too many stripes’ – Tilly Rose’s story for Rare Disease Day 2026

Important supply update: Pfizer Genotropin (somatropin) reusable pen device

Francesca’s story: A three-year undiagnosed rollercoaster

Acromegaly and nutrition survey

Exciting changes to our Endocrine Nurse Helpline

Queen’s Square Pituitary Patient Research Open Day 6th December 2025 – a patient blog

The desmopressin nasal spray is back!

North Wiltshire support group launch

Stay well with Winter vaccines!

Emergency care staff – we need to hear from you!

Resilience, self-advocacy and hope: Liv’s story

Going for your first colonoscopy? Here’s what you need to know.

Being cortisol dependant – Benedict’s story

A pituitary diagnosis while pregnant

How to deal with difficult life events if you have a chronic condition

Desmopressin shortage: October update

Learnings from WAPO’s Global Summit

Managing mental health difficulties and a pituitary diagnosis

Cushing’s symptoms survey opportunity

What life looks like now that I’ve stopped working

Launching a new LGBTQIA+ support group

September 2025 Desmopressin Shortage Update