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Sian's story - Cushing's

Cushing's patient, Sian, tells us her diagnosis story and also shares the link to her blog, which is documenting her second round of surgery. 

Christmas telephone & office opening hours

See our opening hours for our various helplines over the Christmas period, and what extra support we will be offering on Christmas Day.

Welcoming our new Medical Committee members

We are delighted that we’ve recently had some new additions to the Committee, meaning we currently have a team of 26, and we’d like to introduce them to you here.

A mum's story of her 4 year old - pituitary awareness

It's been incredible awareness for us to see the story of Emily feature in the Mirror, the Sun and the Mail.

Research Study - Understanding the Needs of Children with Pituitary Conditions

Calling young people - your chance to take part in a research study!

Year in Review

2017 has been another busy year for The Pituitary Foundation, campaigning to raise awareness of key issues facing patients, and providing support to our patient community. 

Pegvisomant is now available in Scotland and Wales

The Pituitary Foundation is delighted to hear that this vital medication will now be made available on the NHS to patients with uncontrolled Acromegaly in Scotland. 

Why I wanted to write ‘Living with Hypopituitarism and other things that happened to come along’

Patient and author, Marilyn Harvey, tells us why she decided to write her book, 'Living with Hypopituitarism and other things that happened to come along’.

Jim’s story - diagnosed by my optician

Jim tells us how a routine eye examination identified a pituitary macro adenoma. He also encourages everyone to attend these examinations even if they think there is no need.

Salford Royal NHS Foundation Trust - Patient Seminar Day

Salford Royal NHS Foundation Trust is holding a Pituitary patient seminar event on 10th November 2017 at Britannia Hotel on Portland Street, Manchester.