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Survey for adults in England with neurological conditions

The Neurological Alliance is currently carrying out a major survey of adults with neurological conditions in England. The findings will be crucial in helping us to understand what progress is being made in improving neurological services, and what still needs to happen.

It is particularly important that people with rare conditions like A-T make their voices heard. Often their needs tend to be overlooked for those of the more common conditions. Please click on the picture above to find a link to the survey.

Calendar 2015

The first A-T Society Calendar goes on sale in September for delivery October onwards.

It was created with the help of 20 Sqn. Royal Logistics Corps and the amazing children and families who live with A-T.

All proceeds of the Calendar will go to medical research into treatments and a cure for Ataxia-Telangiectasia.

We love it and we hope you will too!

Shop online Research into AT

Image of William's blog

  A-T the front line

In a new approach to talking about our work, our chief executive William has started a blog. This is a page where from time to time he posts informal articles about some of the things he has been doing, issues he has been thinking about or other items that have caught his eye. Click on the image above to visit the blog.

The idea is to give an idea of some of the things which are going on in the background but aren't ready to become full website items and also to allow a more personal view. It's an experiment, so let us know what you think.

New diagnosis