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.

We understand that Addison’s disease is a rare disease and we want to raise awareness as one of our company employees has been affected with Addison’s disease and has been subjected to the issues it can have on daily life. We would like to raise money for the Addison's Disease Self-Help Group so that they can continue to support people with Addison's and adrenal insufficiency and raise awareness for the disease as a whole.

Addison's disease and the Addison's Disease Self-Help Group (ADSHG)

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.

Life-long treatment with replacement steroid hormones is required. Medication is usually taken several times daily at carefully timed intervals and individuals must also know how to administer an emergency hydrocortisone injection to prevent a potentially fatal adrenal crisis.

At the ADSHG, we are here to support the Addison’s and adrenal insufficiency community and their healthcare providers to promote better medical understanding of this rare condition, campaign for and support everyone affected by adrenal failure, and fund vital research.

Do grab a cuppa and have a read about what the condition is, what we do, and how you can support people you know who have the condition if they become unwell.

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Another big thank you from everyone at the ADSHG.

Liam Hughes