In 2016, after years of unexplained headaches, I was diagnosed with Acromegaly, a rare disorder where the body produces too much growth hormone due to a benign tumour on the pituitary gland. I've had surgery, medication and finally radiotherapy in 2022.

Fortunately, the worst is behind me now and I'm doing well, but it's not been plain sailing. Four years on, chronic fatigue and migraines affect me every day and, try as I might, I just can't do as much as I used to. It's fair to say life has changed quite a bit.

And while I’m lucky to have received brilliant care, and to know that my Endocrinology team will always look after me, there are times when I need the kind of support that doctors managing my treatment can't provide.

The Pituitary Foundation

The Pituitary Foundation runs a free helpline, which means I've been able to talk to someone who knows what it's like to live with my condition.

They also host regular free online events, where leading experts share their knowledge and answer questions.

I honestly can't imagine how I would have made sense of it all without their help.

The Challenge

Not everyone with a pituitary condition can run 5K or manage a long hike or climb, and with this in mind, the foundation has launched Move Your Way, inviting fundraisers to set their own achievable targets.

I've decided to complete a 30-minute walk every day for the month of April!

How Can You Help?

If you would like to support me, and help raise money for this fantastic charity, please consider donating. Any amount, no matter how small, is appreciated.

All money raised goes directly to fund specialist help, psychological support, vital services, and reliable information for people affected by pituitary conditions across the UK.

Thank you!

Amy