# data[].attributes.headline
What Long Covid Taught Me About Life TED Talk

# data[].attributes.subject
What Long Covid Taught Me About Life TED Talk

# data[].attributes.body
Giorgia Lupi presents a talk about how Long COVID symptoms have impacted her life and how she has recorded them.

# data[].attributes.headline
NEWCIS - North East Wales Carers Information Service

# data[].attributes.subject
NEWCIS - North East Wales Carers Information Service

# data[].attributes.body
Support organisation for carers in Denbighshire, Flintshire and Wrexham

# data[].attributes.attachment_link.description
NEWCIS deliver information, one to one support, training and counselling to unpaid carers in North East Wales.

# data[].attributes.headline
When Long COVID rewrites your love story

# data[].attributes.subject
When Long COVID rewrites your love story

# data[].attributes.body
An audio account of how a couple continue to negotiate life dealing with the impact of Long COVID

# data[].attributes.attachment_link.title
When Long Covid Rewrites Your Love Story

# data[].attributes.attachment_link.description
Eighteen million Americans have been diagnosed with long COVID. One couple shares their experience navigating the condition’s many symptoms and its emotional toll — together.

# data[].attributes.headline
North Wales Collaborative Carers Support

# data[].attributes.subject
North Wales Collaborative Carers Support

# data[].attributes.body
Information about resources for carers in North Wales

# data[].attributes.attachment_link.readable_text
Carers come from all walks of life, all cultures and can be any age. Many people don't recognise themselves as carers, but they look after people with an illness, disability, frailty, addiction, mental health problem or learning disability or they may be parent carers.

Carers in Wales are supported under the Social Services and Well-being (Wales) Act 2014 which ensures that carers, who provide unpaid care to family members or friends, have specific rights and access to support services.

Across North Wales, six local authorities are working in partnership with Betsi Cadwaladr University Health Board and third sector organisations to support carers. Each local authority offers a range of services and support tailored to carers where they live.

Click on the links below for carer information and advice in your area:

Anglesey
Isle of Anglesey Council Carers Outreach Service Action for Children Ynys Môn
Conwy
Conwy County Borough Council Carers Outreach Service WCD Young Carers
Denbighshire
Denbighshire County Council North East Wales Carer Information Service (NEWCIS) WCD Young Carers
Flintshire
Flintshire County Council North East Wales Carer Information Service (NEWCIS)
Gwynedd
Cyngor Gwynedd Carers Outreach Service Action for Children Gwynedd
Wrexham
Wrexham County Borough Council North East Wales Carer Information Service (NEWCIS) WCD Young Carers
Annual Carers Grant

North Wales Carers Strategy
North Wales Carers' Strategy: Summary PDF North Wales Carers Strategy PDF Appendix 1 - What matters to carers PDF Appendix 2 - Carers journeys PDF Appendix 3 - Resource mapping report PDF
Contact us

Email: northwalescollaborative@denbighshire.gov.uk
Phone: 01824 712432

# data[].attributes.attachment_link.description
Carers come from all walks of life, all cultures and can be any age. Many people don't recognise themselves as carers, but they look after people with an illness, disability, frailty, addiction, mental health problem or learning disability or they may be parent carers.

# data[].attributes.body
Advice and support resource for Carers in Wales

# data[].attributes.attachment_link.description
Registered charity number 246329 (England & Wales) and SC039307(Scotland). Company limited by guarantee registered in England and Wales number 864097

# data[].attributes.headline
Carers Outreach for Anglesey, Conwy & Gwynedd

# data[].attributes.subject
Carers Outreach for Anglesey, Conwy & Gwynedd

# data[].attributes.body
Advice and support for carers in North West Wales. Excellent resource with lots of advice and links to other resources.

# data[].attributes.attachment_link.readable_text
We are Carers Outreach Service. If you are an unpaid adult carer in North Wales then we can help and support you.
We are a registered charity and we provide support in Gwynedd, Conwy and Anglesey.

No one should have to care alone

We recognise that each caring situation is unique and carers have many different needs. Our friendly and experienced team understand what it's like to be a carer and can help you to cope with your caring role.
Whether you need information, support or just some time for yourself, we are here for you...

# data[].attributes.attachment_link.title
Carers Outreach Service North West Wales

# data[].attributes.attachment_link.description
Carers Outreach Service is a registered charity that supports adult carers in North West Wales. We cover Gwynedd, Conwy and Anglesey and have offices in Bangor, Penrhyndeudraeth, Colwyn Bay and Llangefni. We provide a fully bilingual service and carers are welcome to contact us and request a service in either Welsh or English.

# data[].attributes.headline
The Long Covid Rehabilitation Booklet from Leeds Teaching Hospitals NHS Trust

# data[].attributes.subject
The Long Covid Rehabilitation Booklet from Leeds Teaching Hospitals NHS Trust

# data[].attributes.body
Website containing a lot of information about symptoms of Long COVID and techniques to help manage those symptoms

# data[].attributes.attachment_link.readable_text
View or download this information as a PDF
The team that will be working with you are:
Leeds Long COVID Community Rehabilitation Service Tel: 0113 843 3496
What is Long COVID?

Post COVID-19 Syndrome is also called Long COVID. It describes the signs and symptoms that develop during or following an infection consistent with COVID-19, which continues for more than 12 weeks and are not explained by an alternative diagnosis.

The condition usually presents with clusters of symptoms, often overlapping, which may change over time and can affect any system within your body.

The severity of your illness after catching COVID-19 does not indicate whether you will go on to develop Long COVID. In other words, you may have a mild dose of COVID-19 and then develop Long COVID. Or, you may have been severely ill with COVID-19 and then suffer no longer term after effects.
Back to top
Commonly reported symptoms

There is a broad spectrum of symptoms that you may or may not experience with Long COVID.

Please seek advice from your GP or by calling 111 if you feel your symptoms are worsening and might need further investigation.
Back to top
Caution

There are certain medical complications that can arise while recovering from COVID-19 that need an urgent medical review. It's important to contact a healthcare professional (GP, 111 or 999 as appropriate) if you experience any 'red flag' symptoms:

You become very short of breath with minimal activity that does not improve with any of the positions for easing breathlessness.

There is a change in how breathless you are at rest that does not get better by using the breathing control techniques.

You experience chest pain, racing of the heartbeat or dizziness in certain positions or during exercise or activity.

Your confusion is getting worse or you have difficulty speaking or understanding speech.

You have new weakness in your face, arm or leg, especially on one side of the body.

Your anxiety or mood worsens, or you have thoughts of harming yourself.

(WHO - Support for rehabilitation: self-management after COVID-19-related illness, 2nd edition)
Back to top
What causes Long COVID

At time of writing there has been no definitive cause of why some people get Long COVID and others do not. Research is ongoing across the world to try to identify the cause. We believe that it is impacting on our autonomic nervous system in many people we see in Leeds causing dysautonomia.
Back to top
Understanding the nervous system

Our nervous system is made up of a network of nerves across the whole of our bodies that takes information to and from the brain and spinal cord (the central nervous system). It contains some nerves that carry sensations and instructions that we are consciously aware of and under our control.

The other part of our nervous system is the autonomic nervous system. This controls processes which we are not consciously in control of such as how fast our heart should beat, what blood pressure we should have and when to initiate digestion of food.

The autonomic nervous system has two branches - the sympathetic branch and the parasympathetic branch. The sympathetic nervous system response is also known as the 'fight or flight response'. The parasympathetic response is also known as the 'rest and digest' response. Usually these branches are balanced, with one counteracting the other to bring the body into a state of balance.
Back to top
Dysautonomia

Dysautonomia refers to these two responses not being in a healthy balance with each other. The fight or flight response is useful for getting us out of short-lived periods of danger. For instance, if you cross a road and a car comes hurtling towards you, your heart rate increases, your reaction time improves and you get out of the way. However, what seems to happen in Long COVID is the 'fight or flight' response goes into overdrive. Our bodies are not used to being in this response for a long period of time. This can contribute to many symptoms of Long COVID including fast heart rate, dizziness and dry mouth. Importantly, it is very draining on the body's energy resources to be in this state for a long time and it can contribute to fatigue.
Back to top
How is dysautonomia diagnosed and treated?

One way of us knowing if dysautonomia is contributing to your symptoms is by doing a test called the 'Lean test'. This will be carried out when you have your initial assessment. It is a test of your heart rate and blood pressure when lying for 2-3 minutes and then on standing whilst leaning against a wall for 10 minutes. Certain changes in your heart rate and blood pressure during this test are suggestive of dysautonomia. If you have dysautonomia this will be discussed with you along with management strategies. Any activity that relaxes you will be helpful for stimulating the 'rest and digest' response and drawing you out of the 'fight or flight' response to help bring the body back into balance. This may include mindfulness, meditation, being in nature etc and your rehab team will help you find what works for you.
Back to top
The emotional impact of Long COVID

The experience of having COVID-19 can be very frightening. It is understandable that the experience of contracting the virus and then suffering from ongoing symptoms for months afterwards can have a huge emotional impact.

Having ongoing symptoms can cause common problems:
Back to top
What can help?

Speaking to family and friends.

Trying to do activities that you find enjoyable and relaxing.

Not being too hard on yourself if there are things that you are finding harder to do, and remind yourself that recovery takes time.

Focusing on what you can control.

Worries about finances and/or getting back to work.

Worries about family or friends becoming ill and suffering.

Health experts not always being able to answer all your questions or give explanations.

Unpleasant images from when you were first unwell, that might seem to come 'out of the blue'.

Nightmares.

Feelings of panic with any hospital reminders/medical appointments.

Back to top
Menopause and Long COVID

Long COVID seems to affect more women than men and particularly in the age group 40-60. This has lead researchers to question if there is a link between Long COVID and menopause. So far it has been felt likely that covid infection could impact the ovaries, reducing hormone production and potentially this could exacerbate the symptoms of menopause. Further research into this area is ongoing.

There are many overlapping symptoms between Long COVID and menopause. Some of these include; 'brain fog', poor sleep, headaches, fatigue, joint pains, anxiety and low mood. Menopause in addition can present with hot flushes and disruption to periods. The average age in the UK is 51 but women can have menopausal symptoms prior to this as hormone levels fluctuate (perimenopause).

If you feel that any of your symptoms could be menopausal rather than related to Long COVID alone then please discuss this with your GP. Treatments for menopausal symptoms include lifestyle changes, hormone replacement therapy and there are other medication options too. These can, in some women, have huge benefits to quality of life.
Back to top
Relaxation

Relaxation is an important part of energy conservation. It can help you to control your anxiety, improve the quality of your sleep, reduce pain and help manage the symptoms of dysautonomia. Below is a technique you can use to manage anxiety and help you relax.

Grounding technique

Take slow gentle breaths and ask yourself:

1. What are five things I can see?

2. What are four things I can feel?

3. What are three things I can hear?

4. What are two things I can smell?

5. What is one thing I can taste?

Think of the answers slowly to yourself, one sense at a time and spend at least ten seconds focusing on each one.

There are a number of different relaxation techniques you can try, different people prefer different techniques. You can search on the internet to explore different strategies.

Progressive muscle relaxation

Mediation

Mindfulness

Guided imagery or visualisation

Alexander technique

Aromatherapy

Tai Chi

Yoga nidra

Music.

Back to top
Thinking patterns and symptoms

It is important to remember that your symptoms are a normal part of your recovery following COVID-19.

Worrying and thinking about your symptoms can often make them worse. This is partly due to paying attention to something will magnify or increase it.

If you focus on your breathing or heart rate for a couple of minutes you will feel the sensations more. This is the same with all Long COVID symptoms. For example, if you focus on headaches, you will likely get more headaches, if you focus on poor sleep you will likely struggle to sleep and if you focus on struggling to concentrate, concentration will become increasingly difficult.

Before you experienced COVID-19 you may have had some of these symptoms, therefore treat them in the same way you would have done before. We do not mean for you to ignore your symptoms, and you should still discuss any ongoing symptoms with your medical team as they may be able to offer treatment to help.

Often symptoms are linked; meaning an increase in one symptom leads to an increase in another symptom. If you are fatigued your concentration will be affected, this in turn will affect your memory. These lapses of memory can increase your anxiety, which increases your fatigue. As you can see this goes round in a cycle. Therefore, an improvement in one area should lead to an improvement in another.

During your recovery you will have good days and bad days, and periods of ups and downs. This is normal and it is important not to dwell on the negative. Throughout your rehabilitation try to be kind to yourself, and not too critical. Consider what advice you might give to a friend and treat yourself in the same way.

At the back of this booklet, you will find a list useful online links. These are a fantastic resource to support your wellbeing.
Back to top
Breathlessness and Long COVID

Breathlessness is a very common symptom in people with Long COVID. Your lungs can become inflamed with your initial infection and the effort of breathing can increase.

You may be breathing more quickly and shallower than normal, however, it is important to try and stay calm.

As your lungs recover and time passes into the 12 week mark following infection, there can be other reasons for your breathlessness to continue. These can be due to:

(Please note that this is not an exhaustive list as research is ongoing into this area).

Other areas of our body can become more tense or work harder when our breathing pattern has changed, or we are breathless. For example, we may start to breathe more from our upper chest, or we may become more tense in our shoulders. This uses much more energy, and the muscles can become tired and sore.

We encourage breathing control to help manage your breathlessness, improve your breathing pattern, help manage anxiety, help regulate your autonomic nervous system, reduce fatigue, and improve posture.

Practice at rest to begin with then use during activity.
Back to top
Breathing control - something to help you relax

1. Get in a comfortable position (preferably in lying or in sitting) and allow your body to relax.

2. Close your eyes and bring your attention to your breathing.

3. Breathe in and out through your nose (or mouth if you are unable to do this - but work towards trying to breathe through your nose in time).

4. Put a hand on your stomach and recognise how it rises and falls when you breathe in and out.

5. As you breath in through your nose, let the air come low into your lungs, pushing your tummy out against your hands, and then breathing out, let your tummy sink back in.

6. Try to breathe in for the count of one, PAUSE and then out for count of two, working towards a longer breath out than in. This will slow your breathing rate down.

7. Notice areas of tension in your body and try to release this with each breath out.

8. Gradually try to make your breaths slower.

Back to top
Rectangular breathing

This is a useful exercise to try when feeling breathless on activity but is beneficial to practice several times of day when relaxed to start, and build on from the breathing control.

Look at your surroundings for something rectangular - perhaps a window or television for example. Breath in on the short edge and out on the long edge, ensuring that the breath out is completely passive and greater in length than the breath in. Aim to breath in and out through the nose slowly.

You are aiming towards breathing in for a count of four and breathing out for a count of six, however the main thing to achieve is a longer out breath than in breath. Early indications from research suggest that this helps with many symptoms of dysautonomia, when performed for 10 minutes (minimum of 5 minutes), 2-3 times a day gets the best results, especially if the last session if done before or in bed.

This may also be a useful technique for you to do when you are preparing to do something that you deem likely to be stressful, such as a work meeting, and then also to do this afterwards as a way of supporting recovery. Routine is key, try to build this into your everyday for optimum results.

Back to top
Positions of ease:

These positions may help reduce your breathlessness and effort of breathing. Practice your breathing control in these positions.

High side lying:

Lie on your side.

Use multiple pillows under your head and shoulders.

Bend your knees a little.

Supported forward sitting:

Sitting upright, lean forward on to a table.

Add as many pillows as required.

Forward sitting:

Sit leaning forward.

Rest your forearms on your knees.

Relax your chest and shoulders.

Supported standing:

Stand leaning forward and use a chair, bench or wall for support.

Relax your chest and shoulders.

Prone lying:

Lie on your tummy (prone) resting your forehead on the backs of your hands.

If you usually have difficulty lying on your tummy, or you have shoulder problems, you may wish to use the other positions shown.

Back to top
Pursed lip breathing

Pursed lip breathing can be used at any time to help you control your breathing. This helps to empty all the air out of your lungs in a slow and controlled manner.

1. Breathe in gently through your nose.

2. Then purse your lips as though you're going to blow out a candle.

3. Blow out with your lips in this pursed position. Imagine gently blowing out a candle when you breathe out. Blow out only for as long as is comfortable - don't force your lungs to empty.

Back to top
Blow as you go

This is useful during activities that make you breathless e.g. lifting an object (can be used with pursed lip breathing):

1. Breathe in before you make the effort.

2. Breathe out whilst making the effort (e.g. as you lift the object).

3. Always breathe out on the hardest part of the action.

Back to top
Cough and Long COVID

How can I manage my cough?

You may be experiencing a persistent, dry cough. This can be irritating, exhausting and can lead to inflammation in your upper airways.

There are techniques that you can use to help to reduce the amount you cough. By supressing your cough, you can break the cycle of coughing and help reduce your symptoms.

Supress the urge to cough

1. Breathing in and out through your nose instead of your mouth.

2. Sucking on boiled sweets or lollipops.

3. Having regular drinks/sips of fluids.

Stop cough exercise

As soon as you feel the urge to cough, close your mouth and cover it with your hand (SMOTHER the cough). At the same time, make yourself SWALLOW. STOP breathing - take a pause. When you start to breathe again, breathe in and out through your nose SOFTLY.
Smother - Swallow - Stop - Soft is a good way to remember this exercise.
If you cough at night, try lying in a different position and / or use pillows to prop yourself up.
Back to top
Fatigue management

Fatigue is the most common debilitating symptom that is experienced in Long COVID. It is often described as an overwhelming sense of tiredness which can be physical, emotional, cognitive, social and spiritual.

Fatigue can impact on all activities of daily living for example, returning to work, cooking / planning a meal, holding and understanding a conversation, caring responsibilities and playing with your children.

Understanding how to get the most out your limited energy envelope is a puzzle which is individual to you. Understand all the pieces of your personal puzzle so you can piece back a life which uses your limited energy to maximise your quality of life.

Physical Fatigue

Some people find that when they are fatigued their body feels overwhelmingly heavy and that moving takes an enormous amount of energy. When increasing your levels of activity, you may experience an increase in physical symptoms, e.g. muscular aches and pains. This can be a normal process and may require careful monitoring.

Mental and Cognitive Fatigue

Many people find that when they are fatigued it becomes difficult to think, concentrate or take in new information and that memory and learning is affected. Some people find even basic word finding and thinking difficult.

The fatigue people are experiencing with Long COVID leaves them exhausted after completing the most basic of tasks, and some people wake up feeling as tired as they did when they went to sleep.

Fatigue affects people in different ways, and it may change from week to week, day to day or hour to hour. It may also mean people have reduced motivation to do anything because they are so fatigued and know that undertaking the smallest task will leave them exhausted. This can be difficult to explain to family/friends/colleagues.

Informing and helping others to understand your fatigue and how it impacts on you can make a big difference to how you cope with and manage your fatigue (see A.D.A.P.T.E.R.S further on for recommendations on how to do this).
Back to top
Sleep

A lack of sleep or poor sleep quality can make fatigue worse.

Sleep can be adversely affected by a number of things:

Pain

Needing the toilet

Screen time too near to trying to sleep

Spending more time than usual inside

Too much caffeine

Alcohol

Noise

Temperature (too warm or too cold)

Mood (anxiety/depression)

PTSD and flashbacks.

When thinking about your sleep and the effect it is likely to be having on your fatigue, it is important to consider each of these issues and make any necessary changes to minimise the impact.

There is a 'Sleep Well' online session provided by Leeds Mental Health and Wellbeing Service. This is a valuable free resource, see links at the end of this booklet.

ADAPTERS

Applying these principles may help you in managing your levels of fatigue:
Back to top
The 3 Ps = Pace, Prioritise and Plan

When recovering from any serious illness most people will experience ups and downs with their symptoms for a variety of reasons.

People tend to use these symptoms to decide how much they do. So on 'good days' they may try to do more, often trying to 'catch up' and very often then overdo it. This can then result in experiencing a bad day and some people describe this as a 'relapse' when they might experience more symptoms, feel low and are able to do very little.

It is important to remember that all activity takes energy, whether it is physical, mental or emotional.

You might have noticed that when you 'overdo' things, your symptoms are worse, and you need to rest more. Resting decreases the symptoms and you are tempted to be active again. This is called the 'boom and bust pattern' and is detrimental to your recovery.

By keeping your energy exertion within the upper and lower lines you prevent the 'busting' which unfortunately can lead to PESE (post exertion symptom exacerbation) sometimes referred to as PEM (post exertional malaise).

Pacing

Pacing is a strategy that helps you to get out of this boom and bust cycle and helps you to manage your activities without aggravating your symptoms.

You should develop an activity plan which allows you to stay within your current 'energy envelope' and therefore avoid 'overdoing things'. Your levels of activity can then be increased in a controlled way over time as your stamina increases.

By pacing your activities, you are ensuring that:

You are controlling the demands you place on yourself.

These demands are in line with your current capabilities.

You are exposing your body and mind to these demands in a regular controlled way.

By aiming not to 'overdo' activity on good days, it is possible to avoid the severity of symptoms on bad days, therefore making it easier to predict the level of activity you will be able to achieve on any given day.

The first step is to think about how much activity you are able to carry out at the moment, even on a 'not so good' day. It is important not to compare yourself to others or to how much you could do before.

From this, you will be able to set a baseline of activity. This is the amount of activity you will carry out every day.

It can be tempting to use your energy on days you feel good. How you use your energy can have an impact on your levels of fatigue.

Prioritise

When energy supplies are limited, you may need to make sure that the energy you use is spent on activities that are the most important to you. It may also be useful to identify what activities in your day are necessary, i.e., which tasks 'need' to be done and which do you 'want' to do, what activities could be carried out at a different time or day, and which activities somebody else could assist with.

Prioritising activities is very individual and what may be a priority for some may not be for others. For example, it may be important for someone to use their energy to have a shower each morning and for someone else, they may limit this to three times a week to ensure they save their energy to carry out a leisure task that is important to them.

Tip: It may be useful to write down the activities that you both want and need to do throughout the day. You could then score these activities to help you to prioritise them. This will also help you in planning your day.

Plan

When planning your day or week, spread your activities out rather than trying to fit them all in one day. Think about when your energy levels may be at their best and try to complete high energy tasks at this time.

Can an activity be graded so that it doesn't have to be completed all at once? E.g. cleaning one room as opposed to the whole of the house.

Before starting an activity, it is useful to think about what you are required to complete in that particular activity. It is helpful to have an organised working space and ensure that you have all items to hand to avoid you having to use more energy going back and forth.

Can you conserve energy by sitting down to complete some of the tasks? E.g. preparing vegetables for cooking.

As well as planning your activities, it is equally as important to plan your rest and relaxation times to allow you to 'recharge.'

Creating an activity diary or a daily plan will help you to pace yourself and prioritise what you want and need to do.

It may take a few attempts to get right, but once you feel you have found your baseline it is important to ensure a period of consistency before this is increased again.

Fatigue scoring

When you are ready, you can gradually increase the amount of activity you are doing but be careful not to build up too quickly. As a general rule it is suggested an increase of no more than 10%.

Once you have made an increase, you will need to keep the levels stable before increasing again.
Back to top
Activity and Fatigue Diary

You can download this diary from the link at the top of the page.
Back to top
Cognition

Cognition means someone's 'thinking skills'. People can experience a range of difficulties with their thinking skills post-COVID-19 affecting memory, attention, information processing, planning and organisation.

A common symptom experienced is Brain Fog. Brain Fog is a term used to explain a number of symptoms that affect someone's ability to think. This involves feeling confused, disorganised, having memory problems, finding it hard to focus and having slower processing of information.

Brain Fog is often made worse by fatigue, meaning the more tired a person is, the more they notice increased difficulty with their thinking skills.

To support your thinking skills, consider the following:

Please refer to /request the Long COVID Rehabilitation service 'Brain fog' booklet for further information and advice.
Back to top
Communication

Sometimes people experience difficulties with their ability to communicate; this can affect the way that they communicate with other people.

You may experience one or more of the following difficulties:

Understanding what people are saying to you

Reading

Putting your thoughts and feelings into words

Having a conversation

Finding the correct word

Having slurred speech.

These symptoms can be worse when you are fatigued or feeling stressed. If you are having difficulty with your communication, speak to your GP or your therapist.
Back to top
Nutrition and hydration

Good nutrition and hydration help to support your body in recovery from COVID-19 and Long COVID as well as helping to rebuild your muscle strength and function as part of your rehabilitation. Even though you may not feel hungry or thirsty, it is important to eat and drink well.

If you have specific dietary requirements, please check with a healthcare professional that the information is safe for you to follow.

Hydration

Being well hydrated helps your body to function and aids mobilisation and recovery.

Drink regularly throughout the day - aim to have eight cups of fluid each day (2 litres).

Take small, frequent sips of liquids every few minutes if you are not able to drink large amounts at one time.

Aim to drink enough fluid to keep your urine a pale straw colour.

All fluids (except alcohol) count, try to have a variety including ne milk-based drink and once fresh fruit juice each day.

A varied and nourishing diet

You may require more nutrition than usual to support your body during and after illness.

Dieting with the aim of reducing body weight is not recommended during acute illness or recovery, due to the risk of reducing your muscle mass, strength and exacerbating fatigue.

Eat regularly and avoid missing meals. A well-balanced diet contains foods from all the food groups.

The Eatwell Guide shows how much of what we eat overall should come from each food group to achieve a healthy, balanced diet.

You do not need to achieve this balance with every meal but try to get the balance right over a day or even a week.

For more information visit:
https://www.nhs.uk/live-well/eat-well/the-eatwell-guide

The low glycaemic index diet

Carbohydrate containing foods can be classed according to their glycaemic index (GI). This is how quickly the sugar from these foods is absorbed into the body. Eating foods which have a low GI can help manage energy levels. The sugar from these foods is absorbed more slowly giving us a slower and more sustained release of energy.

If you are struggling with fatigue try and have a low GI food at each meal.

Bread

Multigrain, granary, rye, seeded, wholegrain, oat, sourdough

Potatoes

New potatoes in skins, sweet potato, yam

Pasta

Brown, all pasta if cooked to al dente

Rice

Basmati, long grain, brown

Other grains

Bulgar wheat, barley, couscous, quinoa

Breakfast cereals

Porridge, muesli, most oat or bran-based cereals

For more information:
https://www.bda.uk.com/resource/glycaemic-index.html Back to top
Unwanted weight changes

Long COVID can affect peoples' appetite and weight in different ways. Some people find they gain unwanted weight and others suffer with a reduced appetite and consequently lose weight.

Practical tips to help you eat and drink well

Gut symptoms such as bloating, stomach pains and changes to bowel habits

Probiotics

The gut is filled with trillions of microbes which can be known as either 'good' or 'bad' bacteria, depending on how they impact our bodies. Research has found that an imbalance of gut microflora, therefore lower levels of 'good' bacteria, is common after being infected with Covid-19. This can lead to adverse gastrointestinal (gut) and non-gastrointestinal symptoms. Having reduced levels of healthy bacteria in the gut can increase inflammation, increasing instances of loose stools, bloating and gas, as well as impacting respiratory function, worsening fatigue and can also affect the immune system.

Although Covid-19 can upset the balance of microflora, other contributing factors may include sedentary lifestyles, smoking and antibiotic, antacid or steroid use. Dietary factors include a low intake of fibre-rich food including fruit and vegetables and a high intake of processed meat and refined sugar.

We can aim to improve gut microflora by focusing on probiotic and prebiotic intake.

Probiotics = are live bacteria with proven health benefits. Probiotic supplements can be bought in the form of capsules, sachets and yogurts. Different probiotics play different roles in the body, therefore if you do not notice improvements in symptoms after 4-6 weeks of taking a regular probiotic, consider trialling another bacteria strain or brand. Probiotics can also be found in fermented milk drinks such as kefir.

Prebiotics = what that the bacteria feeds on and increases their growth, this can be found in foods such as fruits, vegetables, beans, legumes, nuts and grains.

Other fermented foods can also improve gut microbiome diversity. These include foods such as kombucha, kimchi, sauerkraut and other fermented vegetables.

Research has identified the benefit of a diverse diet, containing both prebiotics and probiotics on improving Long COVID symptoms, their severity and persistence including cough, fatigue and overall wellbeing, likely due to positive changes to gut microflora.

Please see the Eatwell Guide and website link in this booklet for more information on how to achieve a nutritionally balanced and varied diet.

For more information:
https://www.bda.uk.com/resource/long-covid-and-diet.html
If you have any concerns about your eating and drinking speak to your GP or therapist within the Long COVID team.
Back to top
How could COVID-19 affect my swallowing?

COVID can affect your breathing. This can interrupt the breathe-swallow pattern as you need to hold your breath momentarily while you swallow. Due to this you may find that you become breathless while eating and drinking, or that it is hard to hold your breath to swallow, or you may cough when you swallow.

You may have had a stay in Intensive Care (ICU). This can result in weakening of the muscles used for swallowing as they haven't been used while you were unwell or asleep. Over time, the muscles will rebuild strength as you build up your intake.

If you had a breathing tube this can sometimes cause some bruising and swelling to your throat and voice box. Sometimes this can result in one or both of the vocal folds not moving properly, which can cause changes to your voice and reduced protection for your airway when you swallow. Usually, these affects are temporary and will resolve over time.

Some descriptions of swallowing difficulties:

Coughing or choking when eating and drinking

Throat clearing when eating and drinking

Gurgly / wet voice

Recurrent chest infections

Poor appetite

Weight loss

Feeling as though food is getting stuck.

Back to top
How could COVID-19 affect my voice, throat and upper airways?

COVID-19 can cause a sore throat, laryngitis and a cough, and some people may have needed a ventilator with a breathing tube through the voice-box which can cause an injury. Your voice may be weak and breathy or hoarse and you may have difficulties with voice projection.

Laryngeal hypersensitivity: irritation of the vocal folds leading to long-term or chronic coughing, throat clearing, changes to the voice, how the voice sounds or feels or a feeling of a lump in the throat.

Upper airway difficulties: difficulties with breathing which can also include chronic coughing.

Other influences may be dehydration of your voice box, acid reflux, fatigue and stress.

Will my voice return to normal?

The experience of being ill can be emotionally draining and for some people deeply upsetting. Our emotions and voice are closely linked so be aware that emotional recovery and vocal recovery often progress hand in hand.

In most people the inflammation and damage to your voice box should get better over time without treatment. However, if it doesn't, please seek a referral to the Ear, Nose and Throat (ENT) department or Speech and Language Therapy via your GP.
Back to top
Social life and hobbies

When you have been ill, you may feel different, and you might not want to do the things you used to enjoy.

You may not feel like seeing lots of people at the same time, and you might find it hard to concentrate to read or watch television. As you recover, your concentration will get better, and your memory will improve.

Try to find activities that you enjoy doing while you recover; this might include starting a new hobby or finding different ways to continue with old hobbies.

It is important that you have a balance of 'work, rest and play'. Try to make sure that each day you can do a good balance of 'work, rest and play' allowing yourself time to do things you enjoy, as well as the things you have to do.
Back to top
Returning to work with Long COVID

If you have a job to return to and wish to return to that job, early discussions with your workplace manager and occupational health department are often a good idea. This will help your employer to develop a better understanding of your ongoing symptoms and manageable daily activity.

To support a successful return to work it is often helpful to have a flexible and phased return. This might include altered hours or altered duties. These adjustments to your work will aim to help you to manage your symptoms during your recovery.

Before returning to work it is important to think about the physical and cognitive demands. 'Cognitive demands' means the thinking skills required for your job. Examples might include attention, problem solving or organisation.

These skills should be compared to how much you can manage at home. Ideally the amount you can do at home should start to match the amount you need to do at work.

It can be helpful to get some 'feedback' on your current abilities. This is beneficial as you may have been out of work for some time and may not be aware of how tired or unfit you are.

Through doing some normal day to day activities at home, you can begin to understand your current abilities.

Examples of activities to try (providing this is safe):

Many of these activities need similar skills and abilities that you will need to have for returning to work. For example, using your home computer for emails and social media can help you to build up your typing skills and concentration.

Now consider:

How are you managing with these tasks?

What went well?

Did you struggle with anything?

Is there anything that you need to practice?

The more information that you have about how you find different activities at home will help to inform you when you will be ready to return to work. This information can also help you to structure your return to work and understand any changes that you might need when you are at work. This will ensure a successful return to your job.

Your GP can discuss any changes that you may need to return to work, as well as your local COVID Rehabilitation Team. Please request/refer to the Long COVID Rehabilitation 'Return to work' booklet for further support.
Back to top
Physical activity advice in Long COVID

Being ill at home, or in hospital with COVID-19, and struggling with Long COVID over a long period of time can result in a significant reduction in your muscle strength and endurance.

Exercise is very important for regaining your muscle strength and endurance, but this needs to be managed alongside any other Long COVID symptoms.

Activities around the house and gentle short walks whilst pacing are considered suitable whilst you are recovering before returning to exercise.

Using the BORG scale will help you regulate your exertion and develop a good understanding of the level of activity or exercise that you should be working towards. It is a good tool to help you understand any symptoms of breathlessness you might have.

Staying active during your recovery has many benefits such as:

Maintaining your energy levels.

Good for anxiety and depression.

However, in Long COVID how we maintain our activity levels is key. We must avoid increasing activity levels in such a way that makes our Long COVID symptoms worse and this is very personal to you and must be paced.

How to use the BORG scale during activity and exercise

Below is the BORG scale; you can use it to understand how hard you are working whilst undertaking any physical activity and/or during exercise.

Using this scale during activity and exercise will really give you guidance and a greater understanding about the safe level to challenge yourself and help you to increase your activity/exercise in safe phases.

(WHO - Support for rehabilitation: self-management after COVID-19-related illness, 2nd edition)
Back to top
Exercise and fatigue

If you are suffering from on-going fatigue, please seek advice from a healthcare professional before getting back to general exercise.

Fatigue and exercise need to be carefully considered and phased to prevent Post Exertional Malaise (PEM) also known as Post exertional symptom exacerbation (PESE) and a 'relapse' of your symptoms.

PESE symptoms include a marked physical and/or mental fatigue in response to increased activity/exercise. This can be debilitating and cause a relapse.

The exhaustion felt may be immediately after the activity/exercise or may be delayed by hours or days. Recovery normally takes 24 hours or longer affecting your fatigue levels, concentration, sleep, memory and can cause muscle/joint pains and flu' like symptoms.

To avoid PESE, follow the advice in the fatigue management section on pacing of activities.

When increasing activity or introducing exercise it is important that we work through phases gradually. Ideas of what to include in each phase are coming up.

If you experience PESE symptoms after exercise, then we recommend you try the following to see if this helps:

Monitor your heart rate as you exercise and introduce new exercises. Keep your heart rate at less than 60% of your maximal heart rate.

Monitor your rate of perceived exertion using the Borg Rating of Perceived Exertion Scale (0-10) and drop back a phase if required.

Trial recumbent exercises, i.e. where you are laying down or sat with back supported like on a recumbent bike.

If this does not help and you continue to experience PESE then please stop and speak to your therapist. Do not try to push through to the next phase of activity.

To calculate your maximal heart rate you subtract your age from 220 then multiply the answer by 0.6

(220 - age) x 0.6 = 60% of your maximal heart rate

E.g. if you are 40 years old then 220-40 = 180, 180 x 0.6 = 108.
During exercise you aim to keep your pulse at less than 108 beats per minute.

You can monitor your heart rate by taking your pulse or you may have a phone or smart watch that can do this for you. If you find you're unable to keep your heart rate at this level, please seek advice from a healthcare professional.
Back to top
Exercise and chest pain and/or a racing heartbeat

If you are suffering from chest pain, palpitations, severe breathlessness or feel faint then please seek advice from a health care professional before starting any exercise programme, they will ensure that you have had the necessary investigations prior to starting exercise.

If you have a diagnosis of any cardiac problems or autonomic nervous system problems such as Postural Orthostatic Tachycardia Syndrome, you may need a more individualised exercise programme than the suggestions below.
Back to top
Phases of exercise

We suggest you consider your return to exercise in five phases; the following sections describe these phases and give suggestions (see BORG and phases table on page 43).

You are aiming to return to your normal baseline, i.e. your pre covid level of fitness. For example, if the activity/exercise ideas listed in phase two are what you would usually do, then this is your phase five as it represents being back to normal. If you have previous injuries or specific illnesses, weakness then please discuss this with your healthcare professional before starting any new activity or exercise.

No exercise should be painful. If you experience pain, chest pain, feel faint or dizzy during exercise you should stop immediately. If symptoms persist, contact your GP, 111 or 999 to seek medical advice. Do not restart your exercise programme until you have been seen by your healthcare professional.

Phase 1 - Preparation for return to exercise

Types of exercise: Gentle walking, breathing exercises, flexibility and stretching, yoga nidra.
Working at a BORG score of 0-1.

Relaxed breathing

Breathing control exercise - see 'Breathlessness and Long COVID' section.

Stretching ideas

The following are examples of simple stretches and flexibility exercises that can be used alongside your progression through the five phases. You may wish to use positions and movements you are already familiar with; the key is to work at a level which feels manageable and helpful. If you are unsure where to start, speak to your healthcare professional.

Stretches should always feel like a stretch, never pain. Take the movement to where you feel the stretch start and take time to notice how you feel. Over time you may find you can stretch further into your range of movement and there are less feelings of stiffness or tension. This is positive and can help your return to activity or exercise.

Knee rolls:

Lie on your back with your knees bent, feet flat on the floor/bed. Gently roll your knees towards the right side, allowing a gentle twist through your spine. Return to the middle, and then repeat going to the left side.

Knee to chest:

Lie on your back if able, with your knees bent and feet flat. One at a time, gently hug your knee to your chest, holding for a couple of seconds before lowering.

Head turning:

Gently turn your head to the right until there is a gentle stretch through your neck. You can place your fingers on your chin to help guide the movement. Repeat in both directions if you are able.

Neck side bends:

Take your head over to the side with your ear lowering towards your shoulder. Place your hand gently on your head to help guide the movement, and allow your shoulder to stay relaxed. You should feel the stretch on the opposite side of your neck. Repeat in both directions if you are able.

Shoulder rolls:

Sit comfortably and gently roll your shoulders backwards in circles. If it feels ok, try rolling them forwards too.

Side bending:

Sit on a chair, then gently bend over to one side, preferably with your arm over your head as shown. Steady yourself by resting the other hand on the edge of the chair.

Spine twist:

Start by sitting comfortably, then turn to your right side allowing a gentle twist through your spine. You can use the back of the chair to help you hold the stretch. Return to the start, then repeat in the opposite direction.

Phase 2 - Low intensity activity

Phase 3 - Moderate intensity aerobic and strength exercises

Phase 4 - Moderate intensity aerobic and strength exercises with co-ordination and functioning skills

Phase 5 - Return to your baseline exercises

Be able to complete your regular activity/exercise programme without exacerbating your symptoms.

For example, to be able to carry out your daily routine such as shopping, cleaning or work. Or, it could be returning to your usual exercise routine. This is very individual and depends on your pre-COVID activity and fitness levels.
BORG score - working up to 10, depending on your usual exercise or activity regime.
Speak to your healthcare professional for further advice on returning to usual exercise or activity. You can build a tailored exercise programme specific to your needs by speaking to a physiotherapist.
Back to top
Research opportunities

The Leeds Long COVID Rehabilitation Service has a Patient, Carer and Public Involvement (PCPI) group. This enables people with experience of the condition, carers and interested members of the public to work collaboratively with the clinical and research team on service improvements, evaluations, research design and delivery. There are also national studies which you may wish to volunteer to participate in and these can be found below:
www.fundingawards.nihr.ac.uk/search/programme/Long%20COVID Back to top
Useful resources
Back to top
Authors:

R. Tarrant (COVID-19 pathway Co-ordinator and Physiotherapist, Leeds Community Healthcare NHS Trust), J. Davison (COVID-19 Rehabilitaion Pathway Co-ordinator and Physiotherapist, Leeds Community Healthcare NHS Trust), S. France (Occupational Therapist, Leeds Community Healthcare NHS Trust), J. Sharda (Occupational Therapist, Leeds Community Healthcare NHS Trust), S. Witton (Occupational Therapist, Leeds Community Healthcare NHS Trust), H. Diskin (Dietician, Leeds Community Healthcare NHS Trust), R. Jasper (Dietician, Leeds Community Healthcare NHS Trust), C. Bland (Physiotherapist, Leeds Community Healthcare NHS Trust), B. Godfrey (Physiotherapist, Leeds Community Healthcare NHS Trust), K. Patel (Physiotherapist, Leeds Community Healthcare NHS Trust), K. McEwan (Physiotherapist, Leeds Community Healthcare NHS Trust), Z. Fox (Physiotherapist, Leeds Community Healthcare NHS Trust), C. Turner (Physiotherapist), M. Parker (Therapy Assistant, Leeds Community Healthcare NHS Trust), F. Cicognini (Speech and Language Therapist, Leeds Teaching Hospitals NHS Trust), Dr Manoj Sivan (Associate Clinical Professor and Consultant in Rehabilitation Medicine University of Leeds, Leeds Teaching Hospitals NHS Trust and Leeds Community Healthcare NHS Trust), Dr J. Corrado (Specialist Registrar in Rehabilitation Medicine, Leeds Community Healthcare NHS Trust), D. Ross (Physiotherapist, Leeds Teaching Hospitals NHS Trust and Leeds Community Healthcare NHS Trust).

Corresponding author:

Rachel Tarrant (COVID-19 Rehabilitation Pathway Co-ordinator, Specialist Respiratory Physiotherapist)

Acknowledgements

With grateful thanks to the Liverpool Heart and Chest Hospital, for permission to use and adapt their leaflet for Leeds patients. Artwork kindly provided by Leeds Teaching Hospitals NHS Trust Medical Illustration Services.

# data[].attributes.attachment_link.title
Long Covid rehabilitation booklet - Leeds Teaching Hospitals NHS Trust

# data[].attributes.attachment_link.description
Information on Long COVID signs and symptoms that develop during or following an infection consistent with COVID-19, which continue for more than 12 weeks and are not explained by an alternative diagnosis.

# data[].attributes.body
Website with information about symptoms of Long Covid.

# data[].attributes.attachment_link.readable_text
Illustrations by Tom Bailey

(also known as post-COVID-19 condition and post-COVID-19 syndrome) is the experience of still being unwell in the weeks, months or even years following a COVID-19 infection.

Long Covid symptoms can have a range of effects on people, and people with Long Covid can find it hard to put symptoms into words so others know what it is really like.

This website has been informed by the findings of the STIMULATE-ICP active case finding and studies which seek to understand experiences of Long Covid in order to support people's help seeking. It has also been co- developed with people living with Long Covid and professionals who work with people living with Long Covid. It can be used as a tool to help people living with Long Covid talk about their symptoms so they can get care and support.

Topics covered within this tool:

Throughout each section we have included example experiences from others with Long Covid symptoms to show that you are not alone!

Please navigate to the relevant section for more information.

A printer friendly PDF version of this website can be found here

# data[].attributes.attachment_link.description
Illustrations by Tom Bailey (also known as post-COVID-19 condition and post-COVID-19 syndrome ) is the experience of still being unwell in the weeks, months or even years following a COVID-19 infection. Long Covid symptoms can have a range of effects on people, and people with Long Covid can find it hard to put symptoms into words so others know what it is really like.

# data[].attributes.body
Strategies and tips on managing fatigue

# data[].attributes.body
Online Long Covid support group. Lots of advice, support and resources

# data[].attributes.attachment_link.description
Long Covid Support is a registered charity in England and Wales. Our focus is to campaign and advocate in the UK for recognition, rehabilitation and research into treatments and to facilitate international peer support.

# data[].attributes.body
Signposting resource for social care and community organisations

# data[].attributes.body
Signposting resource for social care and community organisations