Over the next few weeks, we will be looking at the different types of seizures. In this first part, our Helpline and Information Officer, Stuart Macgee looks at seizures which only affect one part of the brain. These are known as focal seizures, also known as partial seizures.
Ryan was diagnosed with epilepsy 20 years ago aged just 12. Here he shares his experiences of growing up with epilepsy, challenges he has faced and what advice he would give to someone newly diagnosed.
For the sixth Scottish Parliament election, we decided to make six asks of the next Scottish Government and group of MSPs elected. Our Policy Assistant, Anna Telfer, provides information on our second election ask, which is to ensure there is at least one adult and one paediatric Epilepsy Specialist Nurse in each health board.
Our Chief Executive, Lesslie Young, looks at how the lessons learned from the COVID-19 pandemic must be used to address the inequalities faced by people with learning disabilities.
For the sixth Scottish Parliament election, we decided to make six asks of the next Scottish Government and group of MSPs elected. Our Interim Policy and Communications Manager, Rona Johnson, provides information on our third election ask, which is to ask new disability benefits assessors to be specifically trained to understand fluctuating conditions like epilepsy.
Our Helpline and Information Officer, Uschi Stickroth provides information on when you can consider to come off your anti-epileptic drugs (AEDs) and things to consider when coming off your AEDs.
For the sixth Scottish Parliament election, we decided to make six asks of the next Scottish Government and group of MSPs elected. Our Policy Assistant, Anna Telfer, provides information on our fourth election ask, which is encourage employment in people with neurological conditions.
It is well known there is a correlation between epilepsy and learning disability. Around one in three people with mild to moderate learning disability also have epilepsy.
Our Policy Assistant, Anna Telfer, provides information on published guidance on COVID-19 vaccines and neurological conditions from The Association of British Neurologists (ABN).
Our Wellbeing Manager, Vicki Burns talks about the importance of being self-compassionate and caring for ourselves during this challenging time.
As this is the sixth Scottish Parliament election, we decided to make six asks of the next Scottish Government and group of MSPs elected. Our Interim Policy and Communications Manager, Rona Johnson provides information on our fifth election ask, which is support neurophysiology in Scotland.
Elle began having seizures during her childhood. Here she shares her experiences and how she wants to encourage people to not feel ashamed of having epilepsy.
Our Chief Executive, Lesslie Young looks at how the impact of the pandemic on children and young adults who live with disadvantage and disability every day may be irreparable.
On Children’s Mental Health Week, our Helpline and Information Officer, Stuart Macgee looks at identifying depression in children and young people and the possible causes.
It is normal to feel anxious, sad or depressed during these difficult times. However, there is support out there to help you get through it. Our Wellbeing Manager, Vicki Burns provides information on how we can support you.
Last week, we were delighted to launch our 2021 Scottish Parliament Manifesto. As this is the sixth Scottish Parliament election, we decided to make six asks of the next Scottish Government and group of MSPs elected. Our Policy Assistant, Anna Telfer provides information on our sixth election ask, which is funded PhDs in epilepsy.
Our Helpline and Information Officer, Uschi Stickroth provides some information and helpful pointers for people who have been recently diagnosed with epilepsy.
Our 100 Mile Challenge is off to a great start with lots of our supporters signing up. We had a chat with Rihannon who explained what this challenge means to her.
We are excited to launch our 2021 Scottish Parliament manifesto. This year, people in Scotland will cast their vote in the Scottish Parliament elections, Thursday 6 May 2021.
Our Chief Executive, Lesslie Young, looks at the importance of seeking support when experiencing loneliness during and beyond COVID-19 lockdown.
Our Youth Development Worker, Kirstyn Cameron looks at ways you can help look after your child’s mental health especially during this difficult time.
The Scottish Government are holding a series of online events regarding important aspects of new disability benefits. Our Welfare Rights Officer, Tracey Millar explains.
Our Helpline and Information Officer, Stuart Macgee, discusses some coping strategies to keep well in the days and weeks ahead during lockdown.
A new UK wide study is seeking women with epilepsy to participate in research to develop a preconception care pathway for women with epilepsy in the UK.
Our fantastic supporter Tammy tells us why she has signed up to the Winter Ben Nevis Trek in March 2021 and her experiences of being diagnosed with epilepsy as a teenager.
As we head towards the end of 2020, our Chief Executive, Lesslie Young, looks at how the year has been a stark reminder of how we have treated and continue to the treat the vulnerable in our society and the experience it has given us to shape the future of social care.
The Joint Committee on Vaccination and Immunisation (JCVI) have announced advice on how COVID-19 vaccines should be distributed across the UK.
Our Helpline and Information Officer, Uschi Stickroth, looks at the trials and tribulations, and sometimes funny side, of providing a helpline and information service working from home.
According to a new study in the British Medical Journal (BMJ), there is a slight increased risk of hospital admission and death from COVID-19 in people with epilepsy.
Nyaka Mwanza is a freelance writer for MyEpilepsyTeam. Here she shares her story of being diagnosed with epilepsy and what it is like to live with the condition.
Our Interim Policy and External Affairs Manager, Rona Johnson looks at the new Scottish Child Payment benefit, which was developed to help some families meet the costs of raising a family.
Chief Executive Lesslie Young looks at the move to digital, the importance of remaining flexible, innovative, and accepting meaningful communication is more than looking at and touching a cold screen.
Our Director of Operations, Pauline Stansfield looks at how Epilepsy Scotland continue to support staff and communities throughout the pandemic.
Our Helpline & Information Officer, Stuart Macgee provides information on the Equality Act and how it helps people with epilepsy have a fairer and better chance to be interviewed and offered a job.
Jonathan developed epilepsy when he was seven years old. Here he shares his story and how after having brain surgery, which stopped his seizures, also led him to lose weight and lead a healthier lifestyle.
Chloe was diagnosed with epilepsy eight years ago while she was at high school. Here she describes how epilepsy has affected her and what she would say to someone who has been recently diagnosed.
Our Chief Executive, Lesslie Young looks at how providing support to others during a crisis can be good for everyone.
Megan has been living with epilepsy for three years and was diagnosed whilst studying at university. Here Megan shares the challenges she has faced and how epilepsy has affected her.
Epilepsy is predominantly an invisible condition. This can bring additional challenges to those living with it. Our Chief Executive, Lesslie Young, explains why awareness weeks like Invisible Disabilities Week are needed more than ever.
Murray is climbing Ben Nevis in March 2021 to help raise vital funds for Epilepsy Scotland. This extreme challenge is set over an entire weekend. Murray explains what this challenge means to him.
Our Chief Executive, Lesslie Young looks at research conducted by the Scottish Learning Disability Observatory (SLDO) which focussed on research into deaths of children with learning disabilities living in Scotland.
Our Helpline & Information Officer, Stuart Macgee provides information on ways to help deal with and reduce anxiety, especially during this uncertain time.
Our Policy and Campaigns Officer, Rona Johnson, provides an update on our impact of COVID-19 and Epilepsy report and the results of our most recent survey.
Our Helpline and Information officer, Uschi Stickroth, talks about mental health and emotional wellbeing.
Our Chief Executive, Lesslie Young looks at the restrictions affecting university students and how people with learning disabilities have been living through this for the last six months and more.
Leanne was diagnosed with epilepsy when she was 18 years old. Here Leanne shares her story of living with epilepsy and how cycling has helped her have some independence.
Simone has been living with epilepsy for 33 years. Here she shares her experiences, challenges faced and how she has overcome them.
Our Chief Executive, Lesslie Young, looks at the importance of person-centred learning and the role voluntary organisations play to provide holistic learning support.
Our Youth Development Worker, Kirstyn Cameron looks at the important role teachers play in helping each child with epilepsy lead as fulfilling life as possible.
Vice-chair of Epilepsy Scotland’s board of directors, Kirsty Lynch, explains why she joined Epilepsy Scotland as a trustee and the challenges faced during the COVID-19 pandemic.
