Using Google Maps to Map Communities with Disabilities


Map of paralysis community
An interactive map of the Americas, Europe and North Africa captured on 01.05.09. It shows different coloured flags representing people within the different groups of the ‘paralysis community’. Hundreds of flags are shown, the majority are orange, depicting people who have, or have had paralysis. Another very substantial group of flags are green, showing friends and family members. Flags of yellow, blue and red also punctuate the map, representing supporters, researchers and carers. The flags swarm across the eastern portion of the United States, with substantial numbers also running up the west coast and scattered in-between. Flags also speckle the rest of the world, indicating that this may be a North American campaign spreading slowly outwards. Over time the map will change as and when more people add themselves to the chart. Above the map are the Reeve Foundation logos and a banner reading 'Be Counted: Living with Paralysis? Care about the cause? Add you voice. Show the world the strength of our community!'.'

Yesterday I received an email about a new project that the Reeve Foundation have undertaken.

In short, the Foundation are creating a Google Map that (literally) maps what the Foundation calls the Paralysis Community. This project invites people who have, or have had this condition, friends and family, professional carers, supporters and researchers to map themselves into a global community. This looks to be getting a positive response, and, like today’s Blogging Against Disablism Day, it is a strong example of the ways in which Web 2.0 technologies can be harnessed to influence our understandings of disability.

In creating visibility and connections between people, this map raises the profile of a distributed community; as well as allowing people to literally put themselves on the map and create a reflection of their shared experience as a node within a collaborative network. Due to the visual nature of Google Maps, it is difficult to create an effective alternative format for this kind of project, a reminder of the contrary nature of some media. Furthermore, I think it would be difficult for an organisation that was not a trusted charity to engineer a mass disclosure of data of this kind. But, that said, this appears to be a bold project – embracing the affordances of mapping tools and pushing them to create new and positive self-determinations.

If you’d like to take part in the Reeve Foundation’s efforts to highlight this community, visit their website here: http://campaigntocureparalysis.org/

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