Difference between revisions of "Electrical Eggs"

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  We now operate as an Advice & Advocacy service, particularly for fans who feel they have been treated unfairly at a convention. Advice on access rights & service provision are always available to event organisers: there are no fees or charges.
 
  We now operate as an Advice & Advocacy service, particularly for fans who feel they have been treated unfairly at a convention. Advice on access rights & service provision are always available to event organisers: there are no fees or charges.
  
{{group | website=http://www.electrical-eggs.org.uk | start=1995 | end=2005}}
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{{group | website=https://www.electrical-eggs.org.uk | start=1995 | end=2005}}
 
[[Category:UK]]
 
[[Category:UK]]

Latest revision as of 14:24, 28 November 2022

Electrical Eggs is at least two organizations (located in the US and UK) with the US organization established in 1986 by Samanda b Jeude and Esther Breslau. Jeude wrote:

“And about that time I met Esther Breslau. And Esther is also a polio survivor, but at this point she doesn’t have the syndrome. And we both were really ticked off that Baltimore [[[Constellation]], the 1983 Worldcon] was trying their best and it was impossible to get around. So we started thinking about it [services for the handicapped at conventions] in ’84…. In ’85 …we did up some guidelines and Esther tried out the guidelines at Chilicon, which was the NASFIC. [[[LoneStarCon]]]… We tested it at Confederation [Worldcon 1986]… and they gave us money to start up Electrical Eggs. And the name came because I was trying to tell somebody about my new electric legs, and I had the hiccups. Don said, ‘Great.’ Eggs are one of the strongest structures in nature, and yet it is very fragile. Perfect name for the organization.”

Ten years later, a similar organization was set up in Britain. As their website says:

UK is a fan-run, non-profit making organisation, established in 1995, with permission from Electrical Eggs Ltd in the United States (now non-operational). The original aim was to help SF event organisers to run an accessible convention in compliance with new legislation(the Disability Discrimination Act, now known as the Equalities Act) for anyone affected by physical disabilities, either permanent or temporary disabilities.

This includes people affected by illness, injury, surgery or age and special consideration for fans with mental health issues or learning disabilities.

We have not operated directly at conventions since 2005. We believe that event organisers should now be quite familiar with their legal obligations and have a sound working knowledge of reasonable adjustments to make their event accessible for everyone!

We now operate as an Advice & Advocacy service, particularly for fans who feel they have been treated unfairly at a convention. Advice on access rights & service provision are always available to event organisers: there are no fees or charges.

Group Website 19952005
This is a group page. Please extend it by adding information about when and where the group formed, its members, how long it was active, notable accomplishments, external links to the group's website, etc.

When there's a floreat (Fl.), this indicates the time or times for which we have found evidence that the group existed. This is probably not going to represent the group's full lifetime, so please update it if you can!