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Want to help raise funds for our charity and awareness of Addison's and adrenal insufficiency? Fantastic! Find out more and get involved. Read more
Our charity is at the forefront of medical research into Addison's Disease. Help us fund medical researchers working in this important field of endocrine research. Read more
I'm raising money for the Addison's Disease Self-Help Group so that they can continue to support people with Addison's and adrenal insufficiency. Addison’s is a rare endocrine condition where the adrenal glands do not produce enough steroid hormones and can be life threatening. It affects approximately 1 in 10,000 people, meaning an estimated 300 - 350 new cases are diagnosed each year across the UK, this makes it roughly 300 times rarer than diabetes.
I'm raising money for the Addison's Disease Self-Help Group so that they can continue to support people with Addison's and adrenal insufficiency. I have Addison's as does my sister, my daughter-in-law and her father too. Talk about coincidence!
I'm raising money for the Addison's Disease Self-Help Group so that they can continue to support people like myself with Addison's and adrenal insufficiency. Addison’s is a rare endocrine condition where the adrenal glands do not produce enough steroid hormones and can be life threatening. It affects approximately 1 in 10,000 people, meaning an estimated 300 - 350 new cases are diagnosed each year across the UK, this makes it roughly 300 times rarer than diabetes.
I'm raising money for the Addison's Disease Self Help Group so that they can continue to support people with Addison's and adrenal insufficiency. Addison’s is a rare endocrine condition where the adrenal glands do not produce enough steroid hormones and can be life threatening. It affects approximately 1 in 10,000 people, meaning an estimated 300 - 350 new cases are diagnosed each year across the UK, this makes it roughly 300 times rarer than diabetes.
I was diagnosed with Addison's disease in 2017. I am passionate about raising money to both raise awareness and help support research into the treatment and management of the condition.
It's been 2 years since Zoe was diagnosed with Addison's Disease and we would like to mark the occasion by raising money for the charity who have been such a huge support to us over the past year; Addison's Disease Self Help Group (ADSHG)
I'm raising money for the Addison's Disease Self-Help Group so that they can continue to support people with Addison's and adrenal insufficiency. Addison’s is a rare endocrine condition where the adrenal glands do not produce enough steroid hormones and can be life-threatening. It affects approximately 1 in 10,000 people, meaning an estimated 300 - 350 new cases are diagnosed each year across the UK, this makes it roughly 300 times rarer than diabetes.
The Addison's Disease Self-Help Group is a charity close to my heart. I hope to spread awareness and help towards the ongoing support the charity has given to those with the disease and their families.
To support those who, like Ram, struggled with Addison's
To help find a cure for Addison's Disease
A group of us are raising money for the Addison's Disease Self Help Group so that they can continue to support people with Addison's and adrenal insufficiency. We'll be running the Cambridge Half Marathon on the 6th of March this year. Any donations are greatly appreciated!
In memory of my amazing mum Margaret Evans, I'm raising money for the Addison's Disease Self Help Group so that they can continue to support people with Addison's & adrenal insufficiency. Addison’s is a rare endocrine condition where the adrenal glands do not produce enough steroid hormones and can be life threatening. It affects approximately 1 in 10,000 people, meaning an estimated 300 - 350 new cases are diagnosed each year across the UK, this makes it roughly 300 times rarer than diabetes.
Megan's 20,000 steps per day challenge, raising vital funds & awareness for Addison's disease
I'm running 10km a day for 50 days to raise money for vital research and devlolment of a adrenal crisis epipen for people that have a steroid insufficiency.
My amazing wife, Helen, has addison's disease and I would love to raise awareness in the medical community.
In memory of Douglas McEwan, our much-missed colleague and friend.
A well loved, good friend of mine sadly died of Addison’s Disease last year and he owned Revival Clothes shop in Banbury and the new owners wanted to do a fundraiser in his memory that was unfortunately cancelled due to Covid 19.
A dear friend passed away from Addison’s disease, All of her symptoms went un-noticed and were mis diagnosed so we are raising awareness of this disease in the hope that it doesn’t happen again.