Found 75 results. Showing Page 5 of 8

Pat’s Story – a carer’s review 12 years on

"Looking back over the last 12 years, since Tony had his diagnosis, (pituitary apoplexy from a macro prolactinoma) we have at times had quite a roller coaster of a ride!"

Mike's story - 25 years on

One of our Volunteers, Mike, talks about his experience of diagnosis 25 years ago and how his life has changed since.

Jackie's story - Cyber knife

In January, I experienced Cyber Knife and wanted to tell my story not for negatives but to help others.

A rugby player’s pituitary journey

A rugby player's story of trying to get back to his normal life after diagnosis.

Hydrocortisone regime – Gail’s story

Gail tells us about her new hydrocortisone regime and the reasons behind this.

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.

"There is an acromegaly community out there" - the success of the first UK Acromegaly Meetup

"The meet up bought home to me that I am not fighting this alone" - read more about the first UK Acromegaly Meetup here.