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.
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See our opening hours for our various helplines over the Christmas period, and what extra support we will be offering on Christmas Day.
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.
It's been incredible awareness for us to see the story of Emily feature in the Mirror, the Sun and the Mail.
Calling young people - your chance to take part in a research study!
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.
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.
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 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 is holding a Pituitary patient seminar event on 10th November 2017 at Britannia Hotel on Portland Street, Manchester.