Dan tells us about his 2017 as Volunteer Ambassador for The Pituitary Foundation and as a patient representative at events.
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Diurnal authorised to produce adrenal insufficiency treatment for paediatric patients
"I’m not sure where to begin, so I’ll cover the highlights leading up to the loss of my pituitary gland....."
DHEA in the news
Nick's pituitary journey began in 1997 and here he describes how the diagnosis effected both his work and personal life, and how he has learnt to manage his condition.
More than 1,000 people took part in our 2016 Patient Survey and we are very grateful to each and every one of you as this survey has led to The Foundation gaining some vital statistics, some of which we will tell you about here.
The Foundation takes part in regular policy work, and we campaign on key issues facing pituitary patients to improve care and services. Here is a quick update on a few of our most recent activities.
It's been incredible awareness for us to see Amy's Cushing's story featured in the Daily Mail. Read more here.
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.
See our opening hours for our various helplines over the Christmas period, and what extra support we will be offering on Christmas Day.