As bleeding disorders are rare, many people will never encounter The Haemophilia Society; we are largely invisible beyond the communities we serve. So we have to work doubly hard to raise both awareness and understanding of bleeding disorders and vital funds needed to give those affected the services they deserve and need to live the best life they can.
HOW DO WE DO THIS?
We use various ways to get our messages out there:
We run regular awareness campaigns, such as Talking Red
We tell stories from our members in the public domain
We share our research and reports with key decision makers
REACHING OUT INTO THE LOCAL COMMUNITY
We will build our relationships with members via our local groups and new youth ambassador
programme, enabling members to articulate their voice more effectively and establish an
inclusive and mutually supportive community. This includes recruiting and training community
advocates, campaigners and fundraisers.
HOW YOU CAN HELP
Have you got ideas for fundraisers or for an awareness campaign? We would love to support you since together we can amplify the message and ensure people have greater awareness about bleeding disorders.
If you’re a member you can sign up and get involved. Why not:
Share our posts on social media
Attend our events or run your own
Tell us your story
SHARING IS CARING
Sign up for more information on news, events and fundraising