Myaware is the name for the Myasthenia Gravis Association. MGA has been around since May 1976. We support people with myasthenia and their families, increase public and medical awareness of the condition and raise funds for research and support staff.

If you’ve just been diagnosed with myasthenia, you’ve come to the right place. Our aim is to make your life easier. We provide information, advice and support. Call us now or join myaware, our online community. You will have free access to our resource centre which includes advice on everything from the latest medical developments and treatments to how to negotiate the benefits system. You can also get in touch with other members who understand what you are going through.


It’s bad enough getting to grips with a rare medical condition, you don’t have to struggle through the benefits system too. My name is Steve Bradshaw and I am your dedicated benefits advisor.

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You’ll find fact sheets with the latest news and changes to the benefits system here.

If in doubt, get in touch and I’ll give you advice on how to ensure information specifically relevant to someone with myasthenia is included in the application.

There are a number of ways that we are trying to assist you and we hope to develop and build on this as we go forward.

The Department of Work and Pensions has produced an on-line Personal Independence Payments (PIPs) toolkit. This includes general information about claiming for PIPs. However for members of Myaware a free of charge, personal benefits service is available to ensure that information specifically relevant to someone with myasthenia is included in any application. Myaware has prepared an leaflet giving an explanation of the purpose, working and impact of the new Employment and Support Allowance. Please also find a link to useful government help lines and addresses.

The Employment Support Allowance - What is it? - Impact and Claiming

Government help lines and addresses


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