About The Organisation

About Evans Syndrome UK

Bert’s awareness was founded in Abergele , North Wales November 2011 by his wife Amanda Wirth and son, Callum Wirth. Together they have managed to build a team of people willing to help them in their fight for against Evans Syndrome. Evans Syndrome needs to be noticed by the government and health authorities that there needs to be more research into this disease without doubt. At the moment there is very little research in the UK.
Our aims for Bert’s awareness:
1. To raise awareness of Evans syndrome
2. To get more research into Evans Syndrome
3. To find has many people with Evans Syndrome in the UK
4. To help families with Evans Syndrome  with support, advice, guidance and help.
5. Bert’s awareness to achieve charitable status

Meet the Team

Evans Syndrome UK Bert's Awareness is an organisation that was created to help raise awareness of Evans Syndrome but it couldn't been done by magic! over the past few Months Amanda Wirth has pushed as hard as she can to get the name out in the public eye.
With a few newspaper appearances all ready to her name who is to stay how far she can take it!
But their are a few more people to mention, Callum Wirth (Bert's and Amanda's son) , Arrow Park hospital, in fact their are to many to mention as the support has been overwhelming for the couple and we hope to see this continues.

Events organisation

There are a lot of events being organised at the moment for Evans Syndrome UK Bert's Awareness those events will include, charity nights, coach trips, sponsored walks and more. but the majority of these aren't being organised by Amanda (She deserves a break) they are being organised by the Evans Syndrome UK Bert's Awareness so expect to see more of us soon!

Get in tocuh

Contact us via email: amanda@evanssyndromeuk.org.uk or callumw44@outlook.com