Scotland: getting the right treatment and care
Would would you like to find out about today?
Epilepsy services in Scotland might be very different depending on whether you live near a city like Glasgow or Edinburgh, or if you live in a very rural area. Your diagnosis and treatment will follow SIGN (Scottish Intercollegiate Guidelines Network) guidelines.
On this page we explain the treatment journey that you might go on, and the standards you can expect from your healthcare team. If these standards fall short, we have more information about your rights if you live in Scotland.
We have more information about getting an epilepsy diagnosis. This includes information about seeing a neurologist, what happens at your first appointment and what tests you may have.
At the bottom of the page, we also list some organisations that can help if you need support to get the right treatment and care.
How should my epilepsy be treated?
-
Care plans
If the specialist diagnoses you with epilepsy, they will tell you about possible treatment options. They should also agree an epilepsy care plan with you. This should cover your treatment, what to do if you have a seizure, and any preferences or lifestyle issues you have discussed. A care plan is especially useful for people who have long seizures or status epilepticus.
See our information about care plans to download.
-
Epilepsy medicines
The main way to control your seizures is with epilepsy medicine. The decision about starting epilepsy medicine should be a joint one between you and your epilepsy specialist. The specialist will choose epilepsy medicines that match your seizure type. Sometimes taking more than one epilepsy medicine at once can offer you better seizure control than a single medicine. The recommendation is, wherever possible, to limit the number of epilepsy medicines you take to 2 or at the most 3.
The SIGN guidelines have more information about medicines they recommend for treating epilepsy.
When a new epilepsy medicine comes on the market, the Scottish Medicines Consortium has to accept it before the NHS Boards in Scotland can prescribe it.
Epilepsy medicine is available in different versions made by different companies. The SIGN guidelines say that while you are taking an epilepsy medicine, you should be able to stay on the same manufacturer’s version of it. The Medicines and Healthcare products Regulatory Agency (MHRA) guidance on switching epilepsy medicines also applies to Scotland.
For more information see switching between different versions of epilepsy medicine.
Who will I see about my epilepsy treatment and epilepsy care in Scotland?
Your epilepsy will be treated by your neurologist, GP, and your epilepsy specialist nurse if there is one in your area. These are nurses with training and expertise in epilepsy.
They can help with:
- Answering questions about your treatment and living with epilepsy
- Offering you an information and care-planning session that includes looking at your emotional wellbeing and ways to manage your epilepsy
- Supporting you to reach your goals, achieve independence and improve confidence
- Helping you to become an expert in your own epilepsy
- Guiding you through shared decision-making
- Being a link between you and your neurologist
- In some areas, epilepsy specialist nurses have extra training so that they can prescribe epilepsy medicines
How often should I have a review of my treatment?
The SIGN guidelines say you should have a review of your epilepsy treatment at least once a year. If your seizures are controlled, you should still have an annual review with your GP. For those who continue to have seizures, this is usually with a specialist. You may also need to see a specialist for your review:
- If you have side effects from your epilepsy medicines
- If you are planning on becoming pregnant
- If you want to stop taking epilepsy medicine
- If you are able to get pregnant and are taking sodium valproate
Children and young people should have their review with a specialist at least once a year. This can be more often if needed.
What if my seizures are difficult to control?
If you have had a few different epilepsy medicines and they haven’t been able to give you seizure control, you may need to have your diagnosis reviewed. The epilepsy specialist is also likely to check that you are taking your epilepsy medicine as prescribed. If you continue to have seizures, the epilepsy specialist may consider reviewing some of your epilepsy medicines.
If you’re struggling with side effects of your epilepsy medicines, you may want to talk to your epilepsy specialist about a reduction of your epilepsy medicines. This could mean you have a few more seizures but that the side effects from the epilepsy medicines are more bearable. But it’s important only to do this with the advice and guidance of a specialist.
If your epilepsy is difficult to control, your specialist might refer you to a more specialised epilepsy consultant or specialist epilepsy centre such as the William Quarriers Epilepsy Centre in Glasgow. They may want to do this:
- If you are still having seizures (especially tonic-clonic ones) and
- If you have tried two different epilepsy medicines at the right dose
Your specialist might refer you to a neurosurgeon to see if surgery is an option for you. If you are not suitable for surgery, your specialist may suggest another treatment option, such as VNS (vagus nerve stimulation) or ketogenic diet therapy.
People with epilepsy and learning disabilities
The SIGN guidelines say that all NHS Boards should make sure that people with learning disabilities who have complex epilepsy have access to specialist neurological services. This should include access to learning disabilities epilepsy specialist nurses and learning disabilities psychiatrists if needed.
I have more questions. Who can I ask?
Ideally your epilepsy specialist can answer questions you may have, including those on safety and lifestyle. They may arrange for you to see an epilepsy specialist nurse if there is one at your hospital who can help to answer your questions. Your epilepsy nurse may not be available on the same day. Sometimes you may be able to contact the nurse by phone. See Questions to ask your doctor for some suggestions of things to ask.
You can also contact the freephone The Epilepsy Action helpline or the Epilepsy Scotland helpline.
What can I do if I’m not happy with my treatment or care in Scotland?
If you are unhappy with any part of your epilepsy care, you could:
-
Talk to the people involved
Talking to the people involved can sometimes be the easiest way to resolve any problems. You could talk to your GP, the GP practice manager, your epilepsy specialist or epilepsy nurse. They may be able to reassure you, or make sure that the problem doesn’t happen again. Your specialist should be able to explain why they have made their diagnosis, or why they think the treatment they are recommending is right for you.
-
See a different healthcare professional
If you’re not happy with your treatment from a GP, you could book an appointment with a different GP at the same surgery. If you don’t feel happy seeing any of the GPs at your current surgery, you have the right to leave and register with a different surgery.
If you want to see a different specialist, see the section below.
-
Make a complaint
You have the right to complain about any aspect of NHS care or treatment, and to have your complaint dealt with properly. The Patient Advice & Support Service (PASS) can help you with making a complaint.
PASS is a free, confidential information, advice and support organisation for anyone wanting to give feedback, make comments, raise concerns or make a complaint about treatment and care provided by the NHS in Scotland. You access this service through Citizens Advice Scotland.
Citizens Advice also has information about your rights as an NHS patient.
Can I get access to my health records?
Healthcare professionals are legally required to show you your health records if you ask for them. This should be done for free. There are a few different records. It may take a little while for you to be able to see them.
The NHS website gives more information about accessing your health records.
Can I get a second opinion from a different specialist?
If you’re not happy with the diagnosis or treatment recommended by your current specialist, you might consider asking for a second opinion. You don’t have a legal right to a second opinion, but if you ask for one your GP or specialist should consider your request.
There are 2 ways you can ask for a second opinion:
- Ask your current specialist to arrange for you to see someone else or
- Ask your GP to refer you to a different specialist
Getting a second opinion from a different specialist doesn’t automatically mean they’ll take over your care. If you want to be treated by the new specialist you’ll need to arrange this with the hospital.
The Patient Advice & Support Service (PASS) may be able to help you with this.
What if I need extra care and support?
If your epilepsy means that you need extra care and support, you may qualify for help from your local council. You have the right to ask them for a needs assessment to see if this is the case. A carer, friend, family member or your GP can also ask for a needs assessment for you.
During a needs assessment, your local council care team will look at how you cope with day-to-day living, and identify if you might need support from social care services. The type of support you get will depend on your individual needs, but can include things like:
- Getting you a seizure alarm
- Making adaptations to your home to make it safer for you
- Getting you some help with household tasks, such as cooking and cleaning
- Moving you to more suitable accommodation
Carers Scotland has more information about needs assessments.
Local councils are legally obliged to carry out a needs assessment for anyone who might need extra care and support. If they decide you are eligible to get help, they also have a duty to provide this help to you. How much of this help they pay for and how much you have to pay towards it is based on your circumstances.
If you need extra care and support, you may also be entitled to some benefits. To find out what benefits you and your family are entitled to, you can contact a specialist benefits advice service such as Citizens Advice.
How can I complain about my local council?
If you’re not happy with your needs assessment, you can complain to your local council. They have a duty to investigate your complaint. If they can’t resolve your complaint, you can ask the Scottish Public Services Ombudsman to investigate.
Useful websites and organisations
Epilepsy Scotland provides information, support and services in Scotland.
Helpline: 0808 800 2200
Scottish Intercollegiate Guidelines Network (SIGN)
SIGN develops evidence-based clinical practice guidelines for the National Health Service (NHS) in Scotland.
The Patients Rights Act 2011 lists your basic rights as a patient.
NHS Boards
NHS Boards are responsible for the protection and the improvement of healthcare services. Find your local NHS Board
Health Improvement Scotland – Community Engagement
(Previously known as the Scottish Health Council).
Health Improvement Scotland aims to engage with individuals and communities to shape local services and influence national policy.
NHS Inform offers a range of health information.
This is an organisation aiming to improve and protect the health and wellbeing of all of Scotland’s people.
NHS 24 – call 111
You can call 111 for urgent health advice when your GP practice or dentist is closed.
Citizens Advice
Citizens Advice provides advice to everyone on their rights and responsibilities. They have information about your rights as an NHS patient.
Patient Advice & Support Service (PASS)
Patient Advice & Support Service is a free, confidential information, advice and support for anyone wanting to give feedback, make comments, raise concerns or make a complaint about treatment and care provided by the NHS in Scotland. You access this service through Citizens Advice.
Advocacy services
An advocate is someone who can speak up for you if you find it difficult to do so yourself. This could involve them talking to the healthcare professionals involved in your care, attending meetings and appointments with you, or helping you to make a complaint.
Advocate services are free and independent of the NHS and social services.
Sign up for the latest updates from Epilepsy Action
"*" indicates required fields