The latest epilepsy news

PIP safe for current claimants after government welfare bill concession
Kami Kountcheva | The government has made a concession on its welfare bill, which means current PIP claimants won’t be affected by the changes to…
The latest epilepsy news

Government confirms PIP cuts plans in published welfare bill
Kami Kountcheva | The government welfare bill published this week confirms cuts to personal independence payments and is met with opposition by Labour MPs and…
The latest epilepsy news

‘If I told you…’ campaign launched to kickstart epilepsy conversations
Kami Kountcheva | Epilepsy Action’s new awareness campaign, focusing on friendships, relationships and work, aims to foster better understanding and empathy for people with epilepsy.
The latest epilepsy news

PIP reforms could cost 800,000 people thousands a year
Kami Kountcheva | DWP estimates 800,000 current and future PIP claimants stand to lose around £4,500 a year by 2029/30 due to the reforms, including…
Epilepsy campaigning

Epilepsy Action demands U-turn on welfare cuts
Kami Kountcheva| The ‘Don’t take the PIP’ campaign launched today is urging the government to rethink disability benefits cuts and asking for people’s support
Features

Welfare reforms – our position on PIP and what you can do
Giada Origlia | Following the Government announcement on welfare reform, here is our response, and how you can get involved.
The latest epilepsy news

Benefit cuts to PIP “damaging” for people with disabilities
Kami Kountcheva | People will need to score at least four points in a category to qualify for personal independence payments (PIP), Work and Pensions…
The latest epilepsy news

45 MPs call for urgent action on medication shortages
Kami Kountcheva | Forty-five MPs have signed a letter calling on Health Secretary Wes Streeting to review and address the cause of medication shortages and…
The latest epilepsy news

Valproate: Families “can’t wait any longer” for redress
Kami Kountcheva | Families harmed by exposure to valproate during pregnancy “can’t wait any longer”, says Epilepsy Action on the one-year anniversary of The Hughes…
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