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The visual impact of pituitary tumours

One of the key effects of a pituitary tumour which can lead to diagnosis is where it is interfering with eyesight. Dr Denize Atan discusses the visual impact of pituitary tumours. 

Lauren - Why I'm campaigning for The Pituitary Foundation

Acromegaly patient Lauren tells us why she's inspired to raise awareness for The Pituitary Foundation.

Living with Acromegaly - Steve & Lauren

Two patients share their personal experiences of living with Acromegaly.

My pituitary tumour history - Barry's story

Dr Barry Culpin tells us about his very long journey to diagnosis almost 20 years ago.

Living with Acromegaly - Rachel & Carolyn

Two patients share their personal experiences of living with Acromegaly.

"What if I'm not cured?"

Dr Niki Karavitaki and Dr John Ayuk discuss the options for further treatment if pituitary removal through surgery is not successful.

Scottish review of Pegvisomant - patient responses needed

The Pituitary Foundation is participating in The Scottish Medicines Consortium review of Pegvisomant, representing the patient/carer perspective and we would very much appreciate your important input. 

What to expect when you have pituitary surgery

Mr Shaz Ahmed tells us what to expect with pituitary surgery.

Summer campaign launch - Think Adrenal Insufficiency

Think Adrenal Insufficiency 

Nurse Appeal: Why is this helpline so important?

Psychologist, Dr Sue Jackson, tells us why our nurse helpline is such a valuable service for pituitary patients.