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.
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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.
The Pituitary Foundation is currently running a campaign with optometrists to raise awareness and try to decrease diagnosis times. Here we have a story from patient, Phil, who talks about being diagnosed immediately by his optician.
Christine tells us about her long diagnosis, dealing with Acromegaly, and how the lack of knowledge about adrenal insufficiency in hospital nearly lost her her life.