If you are experiencing an emotional crisis during coronavirus we are here to support you! Please see our Covid-19 section for ways we can do this!

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Factor 8 interviews Christina Burgess, HBDCA founder

Jason Evans, founder of independent haemophilia support group Factor 8 speaks to our founder and director Christina Burgess about support available for the victims and families of the contaminated blood scandal. Christina talks about the services that HBDCA offers and the potential routes of access that are available to ex-beneficiaries of the Macfarlane Trust, including […]

Reflections on COVID-19 film now available

Members of the bleeding disorders community speak about the impact of Covid-19, and share their tips on coping well during the global pandemic. For those within the bleeding disorders community who may already be vulnerable, the challenges of Covid-19 can activate myriad feelings and concerns.  We spoke to some members within the community to understand […]

HBDCA launches Liberty, providing psychological support to the Infected Blood community

HBDCA is pleased to announce the launch of LIBERTY, a dedicated provision under the HBDCA banner servicing the needs of the Infected Blood community. HBDCA Liberty supports people infected and affected by Contaminated Blood through partnering with funding schemes to provide ongoing psychological support. HBDCA, with its unique understanding of the complex issues faced, provides […]

The Haemophilia Society endorse HBDCA

The UK Haemophilia Society have referred members for the first time to HBDCA services, acknowledging the challenging times in which we find ourselves with Covid-19. HBDCA CEO, Christina Burgess, said: “I am delighted that The Haemophilia Society has shared, with its members, our HBDCA initiative to offer free crisis support during the Covid-19 pandemic. It […]

HBDCA appoint Ros Cooper as Ambassador

We’re thrilled to announce today Ros Cooper as HBDCA’s Ambassador. We are delighted to have Ros’ passion and voice as we strive to provide crucial access to psychological support for the UK’s bleeding disorder community.  Ros was just a baby when she was diagnosed with severe von Willebrands disorder, and during her university years discovered […]

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