A recent article published online by WYZA (a clever website name targetted at - and for - older Australians) has drawn attention to CBS in their health section. It features testimonies of two Australians living with CBS. To read the full article, click here.
The Foundation welcomes any personal accounts of one's CBS experiences. The sharing of stories can help break the stigma and silence associated with this syndrome. As people living with CBS begin to learn that their experiences are quite common, it can encourage them to discuss their own CBS journey. In turn, this can assist to open up the public discussion of CBS.
It is only through people speaking up - and this includes carers, medical and allied health care professionals - that the syndrome can emerge from its slumber and take its rightful place in public awareness.
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The Charles Bonnet Syndrome Foundation is dedicated to raising awareness of CBS, what signs to look out for and how to better manage this condition.
As a charitable organisation, we rely principally upon memberships and donations to continue our work.
Please help us to support more people affected by CBS.
