In 2016, I was diagnosed with Acromegaly, a rare disorder where the body produces too much growth hormone due to a pituitary adenoma. I’ve had surgery, medication, and finally radiotherapy in 2022.

The worst is behind me now, and I’m doing well. In fact, I'm doing great! But there are some lasting effects. Four years on, chronic fatigue and frequent migraines mean I can't do as much as I used to.

And while I’m lucky to have received brilliant care, there are times when I need the kind of personal support that medical professionals managing my treatment just can't provide.

The Pituitary Foundation

The Pituitary Foundation runs a free helpline, so I've been able to talk to someone who understands what it’s like to live with my condition. It’s good to get the full picture, and to know I’m not alone.

They also host regular free online events, where leading experts share their knowledge, discuss the latest research and developments in treatment, and answer questions.

The Challenge

Not everyone with a pituitary condition can manage a 5K run, or climb a mountain, 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