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RT @robmcd85: If you are looking for a pain diary please feel free to use this. If you'd like it in another format just let me know. Can be…

Patient Booklet

What Is Fibromyalgia?

Fibromyalgia is a chronic condition of widespread pain and profound fatigue. The pain tends to be felt as diffuse aching or burning, often described as head to toe. It may be worse at some times than at others. It may also change location, usually becoming more severe in parts of the body that are used most.

The fatigue ranges from feeling tired, to the exhaustion of a flu-like illness. It may come and go and people can suddenly feel drained of all energy – as if someone just “pulled the plug”.

Fibromyalgia is a common illness. In fact, it is more common than rheumatoid arthritis and can even be more painful. Prevalence of Fibromyalgia: A Survey in Five European Countries (see www.fmauk.org/prevalence for details) put the prevalence of FM at between 2.9 and 4.7%. People with mild to moderate cases of fibromyalgia are usually able to live a normal life, given the appropriate treatment.

If symptoms are severe, however, people may not be able to hold down a paying job or enjoy much of a social life. The name fibromyalgia is made up from “fibro” for fibrous tissues such as tendons and ligaments; “my” indicating muscles; and “algia” meaning pain.

Symptoms

Besides pain and fatigue fibromyalgia symptoms often include:

  • unrefreshing sleep – waking up tired and stiff
  • headaches – ranging from ordinary types to migraine
  • irritable bowel – alternating diarrhoea and constipation, sometimes accompanied by gas in the abdomen or nausea
  • cognitive disturbances including lack of concentration, temporary memory impairment and word mix up
  • clumsiness and dizziness
  • sensitivity to changes in the weather and to noise, bright lights, smoke and other environmental factors
  • allergies

Diagnosis

Fibromyalgia is not new, but for most of the last century it was difficult to diagnose. Part of the problem has been that the condition could not be identified in the standard laboratory tests or x-rays. Moreover, many of its signs and symptoms are found in other conditions as well – especially in chronic fatigue syndrome (CFS).

Two Canadian doctors developed a way of diagnosing fibromyalgia in the 1970s and in 1990 an international committee published requirements for diagnosis that are now widely accepted. Once other medical conditions have been ruled out through tests and the patient’s history, diagnosis depends on two main symptoms:

  • pain in all four quadrants of the body for at least three months together with
  • pain in at least 11 out of 18 tender point sites when they are pressed. The “tender points”, or spots of extreme tenderness, are rarely noticed by the patient until they are pressed.

What Causes Fibromyalgia?

Fibromyalgia often develops after some sort of trauma that seems to act as a trigger, such as a fall or car accident, a viral infection, childbirth, an operation or an emotional event. Sometimes the condition begins without any obvious trigger. The actual cause of fibromyalgia has not yet been found. Over the past several years, however, research has produced some insights into this puzzling condition. For instance, it has been known that most people with fibromyalgia are deprived of deep restorative sleep.

Current studies may find out how to improve the quality of sleep and some of the prescribed medicine is specifically aimed at addressing the lack of restorative sleep.

Research has identified a deficiency in Serotonin in the central nervous system coupled with a threefold increase in the neurotransmiter substance P, found in spinal fluid and which transmits pain signals.

The effect is disordered sensory processing. The brain registers pain when others might experience a slight ache or stiffness. It is hoped that more research will discover the cause and result in more effective treatment.

Current Treatment

At the present time treatment for fibromyalgia aims at reducing pain and improving sleep. In other words, some of the symptoms are being treated, rather than the condition itself.

Pharmacological management

Over-the-counter medications may help relieve the pain of fibromyalgia but severe pain may require the expertise of a pain clinic. It is best to discuss any form of pain relief with your specialist or GP. It is most important to note that

medications work for some people and not others. Pharmacological management of FM in the UK often involves 'off-label' medications focused on the relief of discrete symptoms rather than treatment of the condition. A number of drug therapies have shown effectiveness in randomised clinical trials, leading to approval by the Food and Drug Administration in America of pregabalin, duloxetine and milnacipran for the treatment of fibromyalgia.

Medications most often prescribed for fibromyalgia are tricyclic drugs also used to treat depression although doses for fibromyalgia are much lower than for depression. In some cases these drugs will help both sleep and pain.

However, many people find available medications either insufficient to control their symptoms or difficult to tolerate due to a high incidence of adverse effects. Thus, all medications should be reviewed at regular intervals to monitor their efficacy.

Support from family, friends and other people who have fibromyalgia is extremely valuable to those who have fibromyalgia. Professional counselling may help some people to cope with this illness and to take an active part in their own treatment. For more information on medications please visit www.fmauk.org/medications

Learning to manage the condition seems, so far, to be the most successful way of dealing with fibromyalgia.

A combination of heat, rest, exercise and reducing stress can enable some people with fibromyalgia to maintain a productive life.

Managing Fibromyalgia

The best way to cope with fibromyalgia is to use a number of techniques that ease the symptoms as much as possible.

Relaxation is one technique that works really well for almost everybody with fibromyalgia. It reduces tension in the mind and body right away. The results are calming for all the symptoms, especially for the pain. Relaxation can be learned from books, tapes, videos or special courses.

Heat is important. A hot water bottle and hot baths or showers will help reduce pain and banish morning stiffness. Soaking hands and feet in hot water for a few minutes can ease their aching. Exercise is the most common prescription for fibromyalgia and Dr Pellegrino’s section on this has invaluable advice about the form this should take.

Although no particular diet has been shown to help fibromyalgia, a healthy, balanced diet is important to provide protein, vitamins and minerals. It is best to avoid or at least cut down on coffee, tea and alcohol. Some sufferers have a tendency to gain weight and this can be distressing in itself. If you follow a healthy diet this should in turn help with your weight control.

People with fibromyalgia can have good days and bad days. On a good day it is important to pace yourself; overdoing it may simply make matters worse. Rest is also important. Listen to your body when it tells you to slow down.

 


 

Exercise
by M J Pellegrino MD

Individuals with fibromyalgia are faced with an exercise dilemma. Because the muscles are so tight and painful in fibromyalgia, they are often aggravated by any attempt to exercise. If the muscles aren’t used enough, they can more easily flare up with any attempt to do activity. Often, the person with fibromyalgia will experience increased pain or full-blown flare up when attempting to increase activity.

Although it is difficult for individuals with fibromyalgia to exercise, it is not an impossible task. My experience in seeing and treating thousands of fibromyalgia patients over the years is that most are able to develop a successful individualised exercise programme. Some people are able to be more active than others, but I believe that everyone with fibromyalgia has the potential to improve their activity to decrease pain and improve function.

Telling a patient with fibromyalgia to exercise is part of the often used cliché, “easier said than done.” I emphasise to patients that any exercise is better than no exercise and that each individual has to find a proper balance of exercise that works best for him or her.

A prescription for exercise in someone with fibromyalgia needs to be flexible. There is no one type of exercise that works best for everyone, and what works for one may not work for someone else. The key goals of an exercise programme are to find what works, develop a successful home programme and maintain a stable balance or baseline.

I have found that there are two components of exercise that, in combination, seem to work best for fibromyalgia patients. They are stretching and a light conditioning programme. I consider stretching a form of exercise that is readily available wherever we are. Because fibromyalgia muscles are so tight, they are more vulnerable to sprains and strains, so it is especially important that this tightness be counteracted by stretching. Stretching can de done in bed, in the shower, at work, at home and just about anywhere and anytime. It is a vital part of the fibromyalgia person’s home programme and if I had to choose one thing to recommend, it would be stretching.

Stretching should be done regularly and consistently. An initial approach is to train the individual in self-passive stretching techniques. These do not require any specific equipment and can be done on different body parts including head, neck, trunk, shoulders, upper body, low back, hips and legs.

Dozens of stretching exercises are possible and all of them can be beneficial for given individuals when properly instructed. With stretching, one should achieve increased flexibility, decrease pain and, ultimately, decrease vulnerability to muscle sprains and flare-ups.

One should move slowly and gently when stretching without jerking or bouncing the soft tissues. We teach patients to find a feeling of stretch within their comfort zone, and they practise deep breathing exercises as part of the stretching. Exercises using elastic bands can combine dynamic stretching with strengthening of the muscles.

Stretches can be demonstrated by a knowledgeable health professional but the individual needs to develop a home programme on a regular and consistent basis. When beginning stretching, one should only do a few stretches a day. No more than three seconds hold at a time, but gradually work over several weeks to where one is able to perform up to ten repetitions per stretch, two or three times a day as needed.

A light conditioning programme means enough exercise to stimulate the cardiovascular system and strengthen the muscles without overworking or exhausting them and increasing pain. A light conditioning programme should not be started until an individual is comfortable with a regular daily stretching programme. Light conditioning does not mean intensive aerobic activity. Usually the activity involves periods of stretching, strengthening, relaxation and conditioning of muscles. This alternating strategy usually works best for fibromyalgia muscles. A proper warm up, good breathing techniques, proper postures, awareness of the body’s response to the exercise programme and cool down period are all necessary components of a light conditioning programme.

Examples of light conditioning exercises could include walking, cycling, aquatics, dancing and low impact aerobics. As a rule, one should try to perform light conditioning exercises at least three times a week for 20-30 minutes. Also, I recommend that one take off every other day with a light conditioning programme to allow the body a chance to rest and recuperate, although different individuals can perform a daily exercise programme depending on the body’s abilities and needs. When starting out, it is best to perform about 10 minutes per session for the first week until at least 30 minutes three times a week is reached.

The exercising individual needs to have realistic goals. I tell patients not to put pressure on themselves to exercise longer and harder in order to feel better. The amount of time spent exercising is not as important as the actual effort to exercise.

People with more severe forms of fibromyalgia usually do not tolerate exercises that involve weight lifting (free weights or machines), or exercise equipment that involve using arm pulleys. These exercises provide a continuous resistance on the muscles and over stimulate them, causing increased pain. Certain exercise equipment can be helpful in fibromyalgia and I always advise people to try the equipment first to determine if it is tolerated and it is helpful before actually purchasing it. Many people with fibromyalgia have nearly-new exercise equipment sitting unused in the basement.

Once a successful exercise programme is under way, the individual with fibromyalgia usually feels better. Even patients who find it too painful to do any light conditioning exercise can usually benefit from a stretching programme. I believe that fibromyalgia flare-ups are rarely caused by the actual exercise programme. Rather the flare-ups are due to some other cause.

During a flare-up, I recommend that the exercise programme be reduced and emphasise the importance of continuing the exercise programme in spite of a flare-up and not stopping the whole programme altogether. If one stops exercising muscles that are flared-up, these muscles will get tighter and will quickly become de-conditioned and thus will become even harder to reactivate when resuming the exercise programme.

Many people with fibromyalgia have had negative experiences with exercising. The goal is to make exercise a positive experience for someone with fibromyalgia.

Mark Pellegrino M.D. is uniquely qualified to help patients with fibromyalgia. Not only is he a physician whose area of special interest is treating this condition, he has it himself. Elected to Phi Beta Kappa as an undergraduate at The Ohio State University, Dr Pellegrino was also an honours graduate from Ohio State’s College of Medicine. At the same institution he served as the chief resident in the Physical Medicine Residency programme.

Dr Pellegrino is Board Certified in Physical medicine and Rehabilitation and he is a member of the American Academy of Physical medicine and Rehabilitation and the American Congress of Rehabilitation medicine. He serves as Medical Director for Rehabilitation at a local hospital in Canton, Ohio where he also practices and lives with his wife and children.

 


 

Welfare Benefits

If you are unable to get help from your CAB, Welfare Rights or a disability agency such as DIAL please contact the Benefits Helpline.

Employment and Support Allowance

If you come under ESA we would advise that you go to your CAB or Welfare Rights for help with this as it is quite complex. More information will be found on our website as it becomes available.

Neither fibromyalgia nor any other illness is an open door to any benefit. What matters is how the illness affects you. It may be that you suffer from another problem as well as fibromyalgia; this should not matter as any judgement should be based on the amount of help required. What the illness is, may however, have a bearing on deciding for how long you should be awarded a benefit.

In recent times it has become far more difficult to get DLA or for it to be accepted that you cannot work. You may know of people who do not seem to be as disabled as you are, who have been awarded one of these benefits whilst you are struggling to get anything. This unfortunately is not uncommon.

DLA

There are two components to DLA – mobility and care. Even if you only fill in details for one component the other will be looked at also. Therefore it is advisable to fill in both parts. The mobility component has a low and high rate. You cannot apply for one rate in particular, as it is up to the decision maker to decide which, if any, you qualify for. If you re-apply for DLA (either components) you could lose what you already have.

Mobility component

The main criterion here is whether you are unable or virtually unable to walk without severe discomfort. The problem for people with fibromyalgia is convincing someone of that severe discomfort and that it can prevent us walking very far. When assessing this for yourself, measure what is an average distance to walk for you and how long it takes to walk that distance (along the flat, not uphill or upstairs). This must be a very short distance and has been stated as being no more than 50 metres and probably less even on one of your better days. However any additional information that you give is very important.

Care component

One of the criteria for this part is whether or not you can cook a meal from raw meat and two raw vegetables for yourself on a regular basis, using a normal oven.

Other criteria concern your personal hands-on care requirements e.g. having a bath, washing your hair, getting out of a chair etc.. Housework needs and shopping are not considered for this benefit. It is the amount of care you need that determines the rate at which you will qualify for the care component. Thus it is essential that you put down the amount of time that you need help for, even if it is only sometimes two minutes; the minutes add up!

If having read this you think you qualify for DLA, please do the following:

  1. Keep a diary.
  2. Contact your local Department for Works and Pension (formerly Benefits Agency) and ask for a claim pack.
  3. Study the pack carefully, take measurements and make notes on a separate piece of paper.
  4. Write down everything you suffer from e.g. Irritable Bowel, Raynaud’s Disease. Do not assume that the decision maker or even the doctor knows that they can be part of the fibromyalgia syndrome.
  5. Go to or contact your local Citizen’s Advice Bureau, Welfare Rights office or disability agency such as DIAL and get help filling in the forms. This is essential.
  6. Keep a copy.
  7. If you are not successful you should ask for a review and failing that you can go to appeal. You have only one month in which to appeal.
  8. Get help from the CAB or Welfare Rights for a review or appeal. Ask if someone from one of these organisations can represent you – if they can you have a considerably higher chance of winning your appeal (probably 30% higher). Please note it is now necessary to ask for an oral hearing if you wish to attend the hearing yourself.
  9. If your appeal fails:
    1. You can apply again after 1 month. Prior to this they will look at your previous form.
    2. You will be told that you can appeal to the Commissioners. N.B. This can only be done on a point of law, not on the basis that you do not agree with the decision.

Incapacity benefit

For those still on IB the major concern with this benefit is the “All Work” test. The aim of this questionnaire is to discover whether you are fit to do ANY work at all, not just the job you were doing. To pass it you must score 15 points. The questions deal with how far you can walk, how long you can sit down or stand up, climbing stairs, picking up objects, bowel and bladder control and mental problems. If you receive one of these forms, please do not panic but follow these steps:

  1. Go through the form carefully and make notes on all the areas you have problems with. Remember that if you say, for example, that you could walk 200 metres, this means for 5 consecutive days. Then ask yourself if this is actually the truth. If not make a note as to why not.
  2. Go to or contact your local CAB or Welfare Rights office and get help in filling in the form. This is essential.

It is also very helpful if your doctor supports you, because if you are turned down, particularly for Incapacity Benefit, their support whilst you go to review or appeal will be important to you.

If you are already in the process with either of these benefits please firstly go to your local CAB or Welfare Rights for help. If you are then still having problems we will talk these through with you, but the Association cannot write letters to support your case, because each person is affected differently.

One of the most frequent comments we hear from people with fibromyalgia is, “The government does not recognise fibromyalgia.” This is not true. We have in writing that the government does recognise fibromyalgia and if you need this evidence please contact us. Fibromyalgia is also listed in a book that the Department for Works and Pensions doctors use for Incapacity Benefit and possibly for DLA. The description is correct but in our opinion inadequate.

It is often individual doctors’ lack of awareness of fibromyalgia that cause difficulties. A medical pack for professionals is available and will be posted directly to them on receipt of their details. www.fmauk.org/benefits

 


 

For Those Who Care

It can be difficult to live with and care for a person suffering from a chronic painful condition like fibromyalgia – but you need not cope alone. Fibromyalgia Association UK not only cares about those diagnosed with fibromyalgia, but also cares about you, the people who live with and look after us.

This section has been written to allay some of your fears and help you gain a better understanding of some of the problems we face. Fibromyalgia affects people in different degrees. Those with mild to moderate symptoms can lead a relatively normal life, with a few adjustments.

If symptoms are severe our lives are changed drastically, but fibromyalgia is not life threatening.

Symptoms

Now that your friend, partner or relation has been diagnosed with fibromyalgia you will be asking “What is it and what does it mean?”

The word fibromyalgia means pain in the muscles and fibres, fibro (fibres) my (muscles) algia (pain). The many ways it can affect the various systems of the body are explained in the section “What is fibromyalgia?”

We Look so Well

In view of the constantly changing levels and sites of pain you may have thought that the person troubled with

fibromyalgia was going mad or simply being idle. Don’t feel guilty if you have, for many of us have had the same thoughts about ourselves. How can we look so well and feel so bad?

Fibromyalgia is often referred to as the invisible condition or the irritable everything because there are no visible signs, but inside we are hurting and our self esteem can be very low. We may feel that we are letting everyone down.

Try to talk about these feelings and learn to recognise mood swings and down days. Work together to reduce daily levels of stress: everyone will benefit.

The two main symptoms of fibromyalgia are pain and fatigue, but muscle stiffness is also a very troublesome symptom. This usually occurs after sleeping or lying in one position. Once we get moving the stiffness will normally ease after an hour or two, but in some people it can last all day. Stiffness and pain can also occur if we sit in one position for too long. This needs to be considered when planning journeys.

We Have Our Bad Days

Flare ups of pain are another problem that can make us feel low. We may be doing all the right things and suddenly the pain will increase. Often there will be no obvious reason, but at other times we will be able to identify the cause, usually overdoing some physical activity such as household chores, DIY or gardening.

Short bouts of depression may occur from time to time, but this should not last more than a day or two: if it does the doctor should be consulted. Sometimes counselling may be recommended. This is not because fibromyalgia “is all in the mind” but because the syndrome, especially the constant pain, affects the whole person including the mental outlook. It is normal to feel afraid, angry, and anxious when dealing with a chronic condition and talking to a trained counsellor allows these feelings to be brought into the open and dealt with.

No one medication will alleviate all the symptoms of fibromyalgia but a combination of medicines may help to relieve pain and promote sleep. At the moment there is no cure for fibromyalgia, and the best that a doctor can do is to give guidance in ways of coping and treating some of the symptoms. The treatments and medications that work vary from one person to another and the person with fibromyalgia is the only one who can tell what is working. It may take a long time and many appointments to discover the right mix for any individual.

Making the Most of a Good Day

We may not be able to do all the things we used to do, but it is important to have fun and mingle with the outside

world. List ideas for short outings to places with room to move around; keep up with visits to and from friends and family; visit parks and gardens where a walk can be enjoyed and then a rest on a bench (or more comfortable seat). There are lots of places to go. Just getting out for half an hour can make all the difference.

It is important that you do not become isolated. You may not be as caring and understanding if you feel trapped and resentful; make sure you keep up with your own social life.

Team Work

Fibromyalgia is a very individual illness. It affects people in many different ways and learning to cope is better for all the family and friends. Discuss what action to take to make life better for everybody.

Many people with fibromyalgia have very mild symptoms; they can lead a relatively normal life and can carry on in their employment, but they will need an understanding caring partner, family and/or friends. They will still have bad days.

You may have noticed that a person with fibromyalgia becomes easily confused and has short term memory blanks, perhaps forgetting a birthday or anniversary, getting words mixed up or missing them out altogether, sometimes stopping in the middle of a sentence completely forgetting what was being said. These symptoms are often more distressing than the pain and fatigue.

  • Writing can sometimes be difficult; the use of a computer can assist.
  • Art and crafts can ease tension.
  • Crosswords and games can keep the mind working.
  • Keep a good supply of books and anything else that will entertain.
  • Encourage the learning of new skills. Change can be very rewarding.

What are the tasks that people with fibromyalgia find most difficult? Even carrying a shopping bag can cause us difficulties. Think about the jobs that you can do together with you supplying the muscle. Working together can be fun. If you can see that fibromyalgia is taking over, suggest a rest or a hot bath and have a cosy meal on a tray to continue the relaxation.

It will unwind you as well. You can also help by making small changes around the home or at work. Simple things like storing items on more accessible shelves will avoid excessive reaching and bending; keeping the floor area clear will avoid nearly tripping or falling which can jar the muscles. Look around the home or workplace together and you will probably be able to identify several ways of making life easier and safer. Remember safety at home and work is important for everyone.

As we have already said, rest plays a vital part in coping with fibromyalgia. Always plan day-to day activities to include rest periods; do a little and rest a little. Gradual exercise also plays an important role in the management of fibromyalgia. Why not exercise together. Make it part of your weekly routine. In order to cope we need to find out what suits us best by trial and error. Nobody else can do this for us but we do need your help and understanding.

The Future

Family and friends can help a great deal in the management of fibromyalgia by learning as much as possible about the

condition. Not only does the person diagnosed with fibromyalgia have frustrations, so do people who are trying to understand the problems we face. Discussing problems and working together can make such a difference to our lives and the lives of those that give us their love and care.

It can be difficult to keep cheerful when your life style changes and relationships can become strained. We all have stress at some time in our lives and it is often difficult to complain when a member of the family, friend or work colleague is unwell. Have you got another family member or friend you can talk to?

It’s good to talk.

It can also be difficult to remember that we are not just a collection of symptoms but a whole person with ambitions and dreams just like everybody else. We don’t like having fibromyalgia but we have found that by taking positive steps, people are learning to cope and manage the condition. There is an area on our forums that is specifically for carers and family that you might benefit from participating in. Research is now taking place all over the world; the future is brighter and the only way is forward.

The goal is to live life in spite of fibromyalgia rather than having no life because of it. Take each day as it comes and make the most of it together.

 


 

 

Pregnancy and Newborns

Pregnancy and coping with a newborn baby can seem a daunting task when you live with the pain and fatigue of fibromyalgia. You may find yourself asking: how will pregnancy affect my symptoms? And, how will I manage to cope with the demands of a newborn baby? There are currently very few research studies published on this topic, so the following information has mainly been gathered from women who have experienced pregnancy while having fibromyalgia and is designed to offer encouragement, advice and coping skills for this exciting time in your life.

All the women we have spoken to agree that although the experience of childbirth may bring additional discomfort it is so worthwhile and positively encourage other women with fibromyalgia to go for it. They emphasise that the key is forward planning, knowing your limitations and being prepared to ask for help.

Conceiving

Before conceiving it is important to discuss the safety of your current medications with your GP. The majority of drugs prescribed for fibromyalgia are not safe during pregnancy and you will need to discontinue them gradually to allow them to clear your system before you try to conceive. Be sure to also check any over the counter medications you are taking, as some herbs can contribute to a miscarriage.

There is no evidence that fibromyalgia affects conception. It is natural to take up to a year to conceive, but if you are having problems consult your GP who will be able to advise you.

Pregnancy - The early stages

The first three months can be difficult, especially as you have come off your pain and sleep medications. Your hormones are changing dramatically and you may experience morning sickness, fatigue, mood swings and increased sensitivity to smell.

Try heat and cold packs, warm baths, gentle massage and stretching to ease pain and stiffness. Paracetamol is generally considered safe during pregnancy, so ask your GP if you need additional pain relief. On the plus side, your happiness and anticipation of your new baby can lead to the release of endorphins, your body's natural painkillers.

The middle months

In general, women with fibromyalgia report feeling better than ever during this time, with reduced pain and increased energy. The powerful hormone effects taking place in your body can mask your fibromyalgia symptoms making these months of pregnancy more comfortable. The hormone relaxin, for example, allows your pelvic girdle to expand by modifying the connective tissue and the fibres in your muscles and ligaments. This means that your ligaments relax offering welcomed pain relief.

This stage of pregnancy is an ideal time to start planning for your baby's arrival. It is a good idea to ask your GP for a referral to an occupational therapist who will be able to advise you on suitable equipment to purchase, methods of lifting your baby and comfortable positions for breast-feeding. This is also the time to decide what help you will need and to ask friends and family members to be prepared to take on certain roles. Here is a list of practical tips from mothers with fibromyalgia:

  • Treat the coming of your baby as a new project and prepare for it accordingly.
  • Choose a cot with a height adjustable base to avoid bending over when lifting your baby in and out of the cot.
  • Choose a buggy that is lightweight, easy to fold with one hand and has a handle that adjusts to the proper height for you.
  • Buy a grab stick for picking things up off the floor without bending.
  • Use a bath unit that allows you to bathe your baby at standing height to avoid bending. These units often come with a changing mat facility.
  • Buy baby clothes with zips rather than poppers or consider substituting poppers with Velcro.
  • Baby proof your house while you have more time and energy.

The final months

Increasing physical discomfort in the late stages of pregnancy is typical for all women. As your shape continues to change and the frontal weight increases you may experience lower back pain, limited mobility, and find it hard to find a comfortable position to sleep in. The weight pushing upwards can lead to heartburn and you will need to rest more due to increasing fatigue. This is the time to take it easy, employ your relaxation techniques and take one day at a time.

Giving Birth

Labour is difficult for all women and each labour experience is different and individual, therefore it is difficult to judge to what extent fibromyalgia contributes to the pain of giving birth. Women with fibromyalgia have reported experiencing one easy birth and one difficult one and say that additional pregnancies do not seem to aggravate fibromyalgia symptoms further. Listen to your own body and do what you think is right for you. Decide in advance how you wish to give birth and whether you want to have an epidural, use a TENS machine or have other forms of pain relief.

The powerful hormone effects together with the delight of your new baby can mask any pain and exhaustion for the first 24 hours. However, expect to feel exhausted, your body has just undergone a huge ordeal and your hormones are beginning to crash. Your fibromyalgia symptoms may return with a vengeance, which can be quite a shock if you have enjoyed relief during your pregnancy. This period can be tough and you will need help and understanding from your partner and family.

Practical Tips for Caring for Your Newborn

  • Find a method of breast-feeding that is comfortable for you. Use pillows to position the baby so you do not have to take the weight or consider breast-feeding lying down.
  • Consider bottle-feeding if the constant sleep disturbance of night­time feeds is causing you unbearable pain. Bottle-feeding means that Dad can take a turn and you can restart your medications.
  • Sleep when your baby sleeps. Get as much rest as possible.
  • Deal with any symptoms of postnatal depression promptly.
  • Ask for help when you need it.

Further help:

Disabled Parents Network (DPN) - provides information, advice and peer-support to anyone with a disability or long-term illness who is, or wants to be a parent. There is also a discussion forum with a section specifically for parents with fibromyalgia.

www.disabledparentsnetwork.org.uk
This email address is being protected from spambots. You need JavaScript enabled to view it.

Helpline: 0300 3300 639
10am – 4pm Mon – Fri and
7pm – 9 pm Weds

The Baby Challenge:

A Handbook on Pregnancy for Women with Physical Disability, by MJ Campion
If you are worried and would like to email a professional midwife with experience of fibromyalgia you could contact Denyse at: This email address is being protected from spambots. You need JavaScript enabled to view it.

Children and Young People

Young people have been diagnosed with fibromyalgia and we have a specific booklet designed for them with information for parents/carers and teaching staff. Please request this from the office, details of which are on the back cover. You can also download Children and Young Persons Booklet


 

How To Be A Fibromyalgia Survivor

Educate Yourself / Learn about the condition / Accept that you have fibromyalgia and it is not life threatening, not deforming, not paralysing/ Understand that at this present time there is no cure for fibromyalgia, but you can do a lot to help yourself / Make contact with a Local Support Group.

FM_survivor_diagram2

With the help of medical professionals develop your own home exercise programme. Consider stretching as a form of exercise. Expect some discomfort when beginning exercise, start at a very low level and make sure you build up very, very slowly. Consider varying your exercise programme. Consider undertaking your exercise programme with a friend.

If you are a medical professional and would like some copies of this booklet for your patients please get in touch using the details below and we will be pleased to send some out to you.

 


 

 

Where To Get More Information

Fibromyalgia Association UK offers a range of support and information including:

  • National Helpline
  • Benefits Helpline
  • Complimentary information booklets for doctors and other professionals
  • Books and videos
  • Monthly magazine
  • Website
  • Contacts with legal specialists
  • Conferences
  • Local support group and helpline contacts

The association is run largely by volunteers, most of whom have fibromyalgia. Our main aims are:

  • To make people aware of fibromyalgia and its affects: to the public at large and to the health professionals that are responsible for diagnosing and treating people with the condition.
  • To support people with fibromyalgia through contact with support groups and others with the condition.
  • To lobby for more effective, available treatment.

If you are a medical professional and would like some copies of this booklet for your patients please get in touch using the details below and we will be pleased to send some out to you. 

  FMA UK, Training and Enterprise Centre, Applewood Grove, Cradley Heath, B64 6EW.  
  National Helpline: 0300 999 3333
10am – 4pm weekdays

Benefits Helpline: 0300 999 0055
Monday and Friday 10am – 12 noon
 
 
  Email This email address is being protected from spambots. You need JavaScript enabled to view it.
Website www.fmauk.org

Support Group Information: www.fmauk.org/groups
 
 
Registered charity number 1042582

This leaflet is sponsored by Pernaton UK, in support of
Fibromyalgia Association UK.
Contact Pernaton UK - Tel: 0121 444 6585
 
 

Published 06/09 Review Date 11/10
 






 

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