Your heart is a vital organ, tirelessly pumping blood throughout your body whether you are resting, carrying out your daily activities, or exercising strenuously. It is the muscular powerhouse at the center of your circulatory system, and its healthy function keeps you alive, deliver-
ing nourishing blood to every cell of every tissue in your body.
The heart and the circulatory system together make up your cardio- vascular system, which accomplishes the complex function of distribut- ing oxygen and other nutrients to body cells, as well as carrying away carbon dioxide and other waste products of cellular function for elimi- nation. Your heart provides the pumping action and force to push your blood ?rst through the lungs to take on oxygen, and then out into the circulatory system. Your circulatory system ferries the blood out to body tissues via arteries, then back to the heart through veins. More than 60,000 miles of blood vessels are involved in this vast network.
The heart itself is about the size of a ?st and weighs less than a pound. To “put your hand over your heart,” you place it just to the left of your sternum, or breast bone, which is located in the center of your chest. You can usually feel your heart’s regular beat, because the right side of the roughly cone-shaped organ tilts closest to your chest wall at this point. Behind the heart are the lungs. These organs are well pro- tected within the bony structure of your chest cavity, with the spinal column and ribs behind them.
Month: July 2009
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Your Heart and Circulatory System
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Problems with urination and bowels
Urinary and bowel function problems probably cause the most inconvenience to a person with MS. They can be embarrassing to cope with and may be the ones most difficult to discuss with your doctor. As such symptoms in MS are likely to result from damage to the spinal cord, they may also be associated with sexual dysfunction as well as other symptoms such as weakness and spasticity.
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Costs involved
Many complementary therapies (acupuncture and osteopathy to name only two) are increasingly recognized as having significant benefits and can, in certain circumstances and limited geographic areas, be made available through the NHS. Many GPs are now more willing to accept and recommend alternatives. However, at present in many cases you will have to pay for your own treatment. The appropriate registration bodies can provide details of registered practitioners in your local area and provide guidance on how much you might expect to pay. You may find
the addresses of these registration bodies through the British Complementary Medicine Association or the Institute of Complementary Medicine. -
Finding a practitioner
Finding a competent practitioner for a complementary therapy is not always easy. There is little statutory regulation for qualifications or practice for most of the therapies and therapists. However, the best ways of finding a practitioner are through:
• an MS resource or therapy centre, where often other people with MS and staff in the centre will have experience of particular therapists;
• a recommendation or referral from a neurologist, GP or other healthcare professional;
• registers set up by the professional bodies of whichever therapy you are interested in;
• referral for homeopathy to one of the NHS hospitals providing this service;
• contacting the British Complementary Medicine Association, or the Institute of Complementary Medicine (see Appendix 1).Ask whether practitioners are trained and licensed; whether they are insured for malpractice, negligence or accident; and how complaints are handled. One of the key things is to try and ensure that whichever therapist you go to has a good understanding of MS. Both of you should be able to evaluate its benefits.
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Safety of complementary therapies
Few complementary therapies have been fully scientifically evaluated, especially in relation to MS. Almost any therapy, scientifically evaluated or not, that has the power to produce very good and positive results, has the potential to do harm. Although complementary therapies are considered as ‘natural’ and, almost by association, to be intrinsically safe, this is not always the case. For example, some herbal medicines have to be very carefully targeted to symptoms and very sensitively administered, otherwise they may be harmful. So it is important both to ask about side effects, i.e. those other than the wanted effects, of
complementary therapies, and to be alert in case they occur. Note that practitioners may expect initial ‘reactions’ or ‘aggravations’ or symptoms as part of the effective working of the therapy. A competent therapist should both warn you about these and what to do, if and when they occur. -
Assessing the value of complementary therapies
There is still a great deal of scepticism amongst many doctors and health professionals about CAM in relation to MS. This is because many CAM therapies have not been fully evaluated using controlled clinical trials – the main way through which conventional medicine is assessed (see Chapter 18). In this situation positive information about CAM is often
from CAM practitioners themselves who have a vested interest in their success. Thus people with MS may feel they are caught in the middle, with outright medical scepticism on the one hand, and very partial and enthusiastic support from CAM practitioners on the other hand. Another issue is that many doctors, compared with people with Multiple Sclerosis, may have very different views and interpretations about the value of CAM therapies in a situation where there is no cure for MS. The way forward, pending more formal assessments of CAM therapies, is to provide as accurate and unbiased information as possible for those who are considering their use.
There are certain key questions that you should ask yourself in relation to any CAM therapy, particularly a new one about which substantial claims are being made:• What detailed evidence is there that the CAM therapy might help my MS?
• Who has endorsed the therapy? Have leading MS Research Centres or the MS Society supported the use of the therapy?
• What are the possible side effects?
• How expensive is it in relation to the assumed benefits?
• How easy is it to access and undergo?
• Are its practitioners well trained, professionally recognized and insured?
• Would it involve you giving up, or not taking, professional medical advice or treatments?One of the difficulties for people with MS in relation to many CAM therapies is that, for the most part, they are focused on treating ‘the whole person’ and on general health, rather than specifically focused on the MS. Thus there is little precise information about any effects on the MS itself. However, as a broad principle, even if the course of your MS is not changed but your general health is improved, this can be helpful in managing your life with MS.
Of course there are many stories about individual cases where a CAM therapy is argued to have dramatically changed the course of Multiple Sclerosis. Although such stories are very attractive and enticing to people with a condition such as MS, you would be right to be sceptical yourself about whether the CAM therapy itself had caused this change, and even more so about the general effects of such a therapy on all people with MS. You should be very wary about claims of ‘miraculous’ or ‘amazing’ results from a CAM therapy. If the claims sound too good to be true, they are just that. Also be concerned about the main evidence for a CAM being given in the form of individual testimonials, rather than through more
systematic research. MS is notoriously unpredictable and thus it requires a very careful and controlled study to eliminate any other reasons for a change in the MS.
As a broad guide, the issue for people with MS considering using a CAM therapy is balancing what you consider to be the personal benefits against any side effects and the costs incurred. Realistically it is unlikely that a cure will be found for MS from amongst CAM therapies. However, by feeling better through using them, you may consider that your symptoms have been eased and you feel a lot better about day-to-day living – not least because, unlike many professional staff in the hard- pressed NHS, many complementary therapists have the time to discuss your concerns at length.
A book called Therapeutic Claims in Multiple Sclerosis (see Appendix 2) evaluates many therapies proposed for MS. It covers over a hundred different therapies. It has to be said that the evaluation is from a very robust scientific point of view, the evaluations are decisive and usually dismissive on the grounds of lack of scientific evidence for effectiveness. Nevertheless, descriptions of the main aspects of the therapy are helpfully given. A book more sympathetic to the possibilities of CAM therapies in MS, but which is still based on rigorous evaluations, has been written by A. C. Bowling (Alternative Medicine and Multiple Sclerosis), and there is an associated website that may be helpful to people with MS.
For another sympathetic view of the possible benefits of complementary medicine, you might try the Institute of Complementary Medicine (see Appendix 1), which adopts a very rigorous approach to the evaluation of such therapies, or the individual professional associations of the therapy concerned. This would also enable you to check the qualifications, experience and regulation of their members. -
Complementary therapies and Multiple Sclerosis
When there is no current scientifically accepted cure for a disease, people understandably want to try other means of management. Many people over the last 30 or 40 years have claimed that they have the answer to MS, but the difficult problem for all such potential therapies is to find out whether there really is a connection between the treatment and a remission.
A distinguishing characteristic of complementary therapies is their focus on the ‘whole person’, using the body’s own healing powers. Many of these therapies are only now being scientifically studied. Some complementary therapies fall outside what is considered conventional scientific medicine, but may be used alongside it, such as acupuncture. Other therapies are generally considered much more unorthodox by the medical profession (described as ‘alternative’), e.g. naturopathy, herbalism or crystal healing. However, complementary and alternative treatments are often considered as a group under the heading of CAM (complementary and alternative medicines).
Research suggests that up to 60% of people with Multiple Sclerosis are using some form of CAM – people with MS visit CAM practitioners nearly 50% more often than others without MS. Whilst some people use CAM alone, by far the majority use both CAM and conventional medicine together. -
Other support
Many people with MS will need professional support services and assistance at some time, to manage the changes in their lifestyles, and to monitor effects of any new drugs. Depending on the precise nature of your MS and its effects, such services may include nursing, physiotherapy, occupational therapy, speech therapy, psychological assessment and support, counselling and advice on housing, employment, financial and other similar issues (see later chapters). Such professional support services for all the many consequences of MS have not previously been adequate, in fact often woefully inadequate and ill coordinated. Despite serious financial constraints, there are now many attempts underway locally to provide better coordinated services and support.
Rehabilitation
‘Rehabilitation’ is perhaps the new watchword of longer term care in MS. Broadly it means professional care targeted to achieve your maximum potential. Regional Rehabilitation Units have been created in recent years for the support of people with many conditions, but there are also an increasing number of more specialist MS rehabilitation units or programmes. At present there are only a limited number of places available on these rehabilitation programmes, and there is a selection process involved, usually on the basis of who might be expected medically to get the most benefit.
During inpatient rehabilitation you would normally be in a hospital or rehabilitation centre as a patient for some weeks, depending on the programme, your MS and how you progress. In this time you might be offered:• regular assessment and monitoring of your condition
• carefully targeted drug therapies as appropriate
• intensive physiotherapy and occupational therapy
• nursing care
• possibly speech therapy, and
• psychological and counselling support.Within a structured programme the aim will be to tailor aspects of this programme to your individual situation and needs. Following the time spent as a patient, you would probably have periodic further assessments to determine how you are progressing. Increasingly MS clinics are being opened in major centres providing support for more people with MS than is available on a lengthy inpatient basis. The aim is to undertake systematic rehabilitation here on an outpatient basis. There is a concern that outpatient care may not be sufficiently intensive to produce major change in functioning.
How useful is rehabilitation?
There is increasing evidence that rehabilitation programmes provide some benefits for people with MS. Studies of rehabilitation programmes are very difficult to undertake in MS for various reasons:
• People have very different types of MS, and it is still unclear as to who would most benefit from the programmes.
• There is no completely standardized programme of rehabilitation.Studies that have been undertaken so far appear to suggest that a range of benefits arise for many people in the short to medium term but,
after 1 year or more from the end of an inpatient programme, there is decreasing difference between those who have been through the programme and those who have not. Almost as soon as people with MS are discharged from rehabilitation programmes, they begin gradually to lose the gains that they had from the programme. This is not really surprising because, back home, they do not for the most part have the intensive care available in the programme, and all sorts of other issues intervene to complicate people’s lives. This is why there is an increasing emphasis on outpatient care through MS clinics and MS ‘drop-in’ centres to provide ways of continuing to offer ongoing treatment.
Further studies in this area are being undertaken to see whether there are particular symptoms or abilities that benefit over the longer term more than others from rehabilitation programmes, and which people with MS might benefit most from them.Going into hospital
Given the range and increasing complexity of tests and treatments, a stay in hospital – even as a day patient –is not uncommon and, if such a stay can be organized over a period of 2 or 3 days, it may be easier for both your neurologist and you to have these undertaken in hospital rather than on an outpatient basis, although outpatient visits will subsequently be necessary. Some treatments are given in hospital. However, neurologists do not agree on how long that hospital stay should be; some feel that the drugs can be administered with very short stays (a matter of hours), while others feel that a day or two to a week, depending on the therapy, may be necessary. Some people with MS may need to go to hospital for investigation of particular symptoms (e.g. urinary problems).
In general, there is very substantial financial pressure, among other issues, to reduce both the number and length of stays in hospital. So, where possible, your hospital stays will be shorter except when you go in for inpatient rehabilitation (see above) and more and more people are given self-injection teaching where necessary. -
Visiting your GP/neurologist/MS Specialist Nurse
Getting the most out of your visit
• Ask for an explanation of any words that you don’t understand –
including illnesses, medicines, symptoms or treatments.
• Ask what results you can expect from any drugs, therapies or medications given to you. Should you expect only a little or a more significant change in your condition? When should these changes occur?
• Ask about any other options that you might have and their advantages or disadvantages.
• Ask about side effects that you might have from any drugs or therapies prescribed for you.
• Ask about any follow-up procedures. When and on what basis will you be seen next time?
• Before a visit to your doctor, write anything down that you need to ask, noting important points that you don’t want to forget to discuss.
• Note down important points arising from your discussions with your doctor as soon as possible. Increasingly, some doctors are
now happy to allow you to tape record your discussions to jog your memory of what he or she said. Research has shown that having such a recording is a great help to yourself, and your family, in following a doctor’s observations or advice.
• Keep a diary of important events or issues between visits to the doctor, so that you can discuss these at your next visit.Seeing your GP notes
Under recent legislation all patients have the right to see their complete medical notes, and to request corrections to, or deletions of, any inaccurate material – particularly regarding comments on a patient’s attitude or state of mind. The doctor is fully entitled to either sit with you whilst you examine the notes or recover reasonable costs of providing copies (including administration costs). However, you can be refused access to notes when there is a reasonable concern that the contents may have an adverse effect on your welfare. Most doctors are very willing to comply graciously with such a request.
Having a check-up
The purpose of the traditional neurological check-up, for which people with Multiple Sclerosis are asked to return every 6 months or year, is gradually changing. Previously, because there was no real therapy to slow down the course of the disease, the check-up was used to monitor the speed of its progression, and to offer symptomatic and appropriate advice. Many people found this a frustrating system, for often their symptoms were as well controlled as they were likely to be, given the modest resources available, and the consultations following a routine examination frequently appeared cursory, focusing on further decline (or any newly acquired neurological problems) since the last check-up.
However, this approach is changing, as neurologists now turn their attention far more towards assisting people to manage MS medically over the longer term, rather than largely focusing on getting the diagnosis right and seeking confirmation of that through monitoring the disease.
Neurologists now focus far more on what is described as the ‘rehabilitative’ approach to MS, the battery of newer drugs that might affect the course of MS, and the increasing recognition of the contribution of other professions to your care. All this is changing the
‘check-up’ process, making it more likely to be of value to you. Often you will be seen by other specialists – perhaps specially trained nurses – as well as the neurologist; thus the increasing use of MS clinics of the drop- in variety is beginning to make the problematic ‘check-up’ experience of old a matter of the past. However, there are still areas of the country where the old system prevails, and in this case it is very important that you ensure that your questions and concerns are addressed in the consultation with your neurologist – after all it is a two-way discussion.
It is important anyway that some periodic monitoring of your Multiple Sclerosis is undertaken, to give you further information about likely developments in the disease, and to assess your eligibility for newer drugs, or possibly trials of experimental drugs, that is if you wish to participate. In this case a neurological examination will determine, over the course of time, how many episodes of MS have occurred, how many individual areas of the nervous system have been affected, and the rate at which new areas are being affected. You may also have an MRI scan, which records similar information about changes in plaques, plaque location and severity, but which may, from your point of view, be little related to your symptoms. Your clinical history is also vital when your neurologist is dealing with any new episode of MS that occurs.