Showing posts with label People. Show all posts
Showing posts with label People. Show all posts

Thursday, 1 June 2017

REMINDING PEOPLE OF THEIR RELIGIOUS BELIEF SYSTEM REDUCES HOSTILITY



Few topics can prove more divisive than religion, with some insisting it promotes compassion, selflessness and generosity, and others arguing that it leads to intolerance, isolation and even violence.
New research conducted at York University, published in the Journal of Personality and Social Psychology, may shed some light on religion's actual influence on believers -- and the news is positive.
"Based on our premise that most people's religious beliefs are non-hostile and magnanimous, we hypothesized that being reminded of religious beliefs would normally promote less hostile reactions to the kinds of threats in everyday life that usually heighten hostility," says researcher Karina Schumann, the article's lead author, now a postdoctoral fellow at Stanford University.
To test this hypothesis, participants either received a simple reminder of their religious belief system ("which religious beliefs system do you identify with?") or not. They were then exposed to either threatening experiences (such as thinking about their own death or failing at an academic assignment) or not. They were then given a chance to judge and assign punishments for transgressors, criminals and worldview critics.
Across nine different experiments with 910 participants, the results consistently supported the hypothesis for Christians, Jews, Muslims and Hindus alike. The religiously reminded were significantly less hostile and punitive in the threatening circumstances than the non-reminded participants were (there were no effects of the religious reminders among the non-threatened participants).
"Our research suggests that people generally associate their religious beliefs with Golden Rule ideals of forgiveness and forbearance, and that they turn to them when the chips are down, in threatening circumstances," says York U psychology professor Ian McGregor, the article's second author. "This research contributes to the current dialogue on religion by demonstrating that even brief religious belief reminders not accompanied by any explicit beliefs or injunctions tend to promote more magnanimous, less hostile choices in threatening circumstances."
Though the researchers say the link between religion and magnanimity may seem surprising given that news headlines so often focus on terrorist attacks and other atrocities committed in the name of religion, their results suggest that for most people, the influence of religion may be more positive than what is often portrayed in the media.
"Part of the reason for our magnanimity finding could be that in our research we focused on religious ideals, whereas extremist groups may often be more focused on intergroup rivalries and coalitions than the core religious ideals of love and forgiveness," says Schumann. "Future research is needed to determine whether reminders of religious belief can also foster magnanimity in non-Western countries, among less educated individuals, and in the context of high-stakes conflicts in which transgressions are committed by others with competing religious convictions."



Sunday, 16 April 2017

Can Poor Sleep Patterns Cause Chronic Pain In Older People


Today's article from sciencedaily.com (see link below) looks at the link between restless and disturbed sleep patterns and chronic pain, especially amongst older people. I think almost everybody living with chronic pain can identify with that. A bad night's sleep almost always results in more pain in the morning. Whether it's the pain that causes the poor sleep, or the other way around, is the question.
 
Could Restless Sleep Cause Widespread Pain in Older People? 
Date:
February 13, 2014
Source:
Wiley

 
Summary:
Researchers in the U.K. report that non-restorative sleep is the strongest, independent predictor of widespread pain onset among adults over the age of 50. According to the study anxiety, memory impairment, and poor physical health among older adults may also increase the risk of developing widespread pain. Muscle, bone and nerve (musculoskeletal) pain is more prevalent as people age, with up to 80% of people 65 years of age and older experiencing daily pain. Widespread pain that affects multiple areas of the body —- the hallmark feature of fibromyalgia —- affects 15% of women and 10% of men over age 50 according to previous studies.

Researchers in the U.K. report that non-restorative sleep is the strongest, independent predictor of widespread pain onset among adults over the age of 50. According to the study published in Arthritis & Rheumatology (formerly Arthritis & Rheumatism), a journal of the American College of Rheumatology (ACR), anxiety, memory impairment, and poor physical health among older adults may also increase the risk of developing widespread pain.

Muscle, bone and nerve (musculoskeletal) pain is more prevalent as people age, with up to 80% of people 65 years of age and older experiencing daily pain. Widespread pain that affects multiple areas of the body -- the hallmark feature of fibromyalgia -- affects 15% of women and 10% of men over age 50 according to previous studies.

Led by Dr. John McBeth from the Arthritis Research UK Primary Care Centre, Keele University in Staffordshire, this newly published population-based prospective study identified factors that increase the risk of the development of widespread pain in older adults. The team collected data on pain, psychological and physical health, lifestyle and demographic information from 4326 adults over the age of 50 who were free of widespread pain at the start of the study (1562 subjects reported no pain and 2764 had some pain). These participants were followed up three years later for the development of widespread pain.

Results show that at follow-up, 800 (19%) reported new widespread pain. The development of new widespread pain was greater in those with some pain at the start of the study; 679 (25%) of those with some pain and 121 (8%) of those with no pain at the start developed new widespread pain at three year follow-up.

Analyses determined that pain status, anxiety, physical health-related quality of life, cognitive complaint and non-restorative sleep were associated with increased risk of widespread pain development, after adjusting for osteoarthritis (OA). Increasing age was associated with a decreased likelihood of the development of widespread pain.

"While OA is linked to new onset of widespread pain, our findings also found that poor sleep, cognition, and physical and psychological health may increase pain risk," concludes Dr. McBeth. "Combined interventions that treat both site-specific and widespread pain are needed for older adults."

Story Source:

The above story is based on materials provided by Wiley. Note: Materials may be edited for content and length.

Journal Reference:
John McBeth, Rosie J Lacey, Ross Wilkie. Predictors of new onset widespread pain in older adults Results from the prospective population-based NorStOP study. Arthritis & Rheumatology, 2013; DOI: 10.1002/art.38284

http://www.sciencedaily.com/releases/2014/02/140213083711.htm

Wednesday, 5 April 2017

SOME RICE BASED FOOD FOR PEOPLE WITH CELIAC DISEASE CONTAIN RELEVANT AMOUNT OF ARSENIC


Rice is one of the few cereal grains consumed by people with celiac disease, as it does not contain gluten. However, it can have high concentrations of a toxic substance -- arsenic -- as revealed by the analyses of flour, cakes, bread, pasta and other foods made with rice, conducted by researchers from the Miguel Hernández University of Elche, Spain. The European Union is working to establish the maximum quantities of arsenic in these products.
Celiac disease affects almost 1% of the population of the western world, a group which cannot tolerate gluten and is thus obliged to consume products without it, such as rice. But this grain, depending on its origin, can also contain worrying levels of arsenic, a toxic and carcinogenic substance.
For the majority of consumers this does not pose any problem because they do not eat much rice every day, but this is not the case for celiac disease sufferers. Researchers from the Miguel Hernández University of Elche (UMH) have analysed the presence of arsenic in flour, bread, sweets, pastas, beers and milk made with rice and intended for this particular group of the population.
The results of the analyses, presented in the journal 'Food Additives & Contaminants', warn that some of these products contain "important contents" of total arsenic (As-t, up to 120 µg/kg) and inorganic arsenic (As-i, up to 85.8 µg/kg). Total arsenic is the sum of the organic arsenic, which is combined with carbon, and inorganic arsenic, which reacts with other elements such as oxygen, chlorine and sulphur, and is more harmful.
With these figures the As-t and As-i contents only of rice used as a main ingredient -- leaving aside the other components of the food products -- were estimated and were found to be as high as 235 and 198 µg/kg, respectively..
Moreover, the daily intake of inorganic arsenic by celiac disease sufferers -- a consequence of their consumption of rice products -- was calculated as between 0.45 and 0.46 µg/kg (micrograms per kilogram of body weight) for women and men weighing 58 and 75 kg respectively. And, in the case of children (up to the age of five), these figures are even higher, ranging between 0.61 and 0.78 µg/kg, according to another study published in the 'Journal of Food Science'.
A panel of experts from the European Food Safety Authority (EFSA) of the EU established in 2009 that there is evidence to suggest that an intake range of 0.3 -- 8.0 µg/kg of body weight per day entails a risk of developing lung, skin or bladder cancer. The estimated intakes in the two studies therefore vary within this range.
As Ángel Carbonell, co-author of the studies, explains: "These figures show that we cannot exclude a risk to the health of people who consume these kinds of products," although he recognises an important point: "The European Union has not yet established legal limits for the maximum content of arsenic in rice and rice-based foods, though it is currently working on this."
Lack of legislation
The researchers' recommendation is clear: "What is needed is for health agencies to legislate to limit the levels of arsenic that cannot be exceeded in rice-based foods intended for consumers who suffer from celiac disease." Until now, celiac disease was diagnosed predominantly in children, but in recent years the profile has changed and one in every five people with the disease is over 65 years old.
Currently, every EU country is taking samples of these products, analysing them and conveying the results to the EFSA to draw up a database broad enough to be able to make decisions. The Spanish Agency for Consumer Affairs, Food Safety and Nutrition (AECOSAN) has recently sent the Spanish report, put together in collaboration with the researchers responsible for this study..
Another important recommendation they make is to include quality information on labels: "The inorganic arsenic content in every food product should be indicated, and the variety of rice used and its provenance should be identified clearly, because some are more recommended than others," affirms Sandra Munera, one of the authors.
Arsenic is naturally present in Earth's crust, but in some regions its abundance is greater than in others, and its concentration also increases with the use of pesticides. The substance then spreads through water to rice, one of the few plants that is cultivated when flooded.
One of the 'cleanest' types of rice is from the Doñana National Park, as the use of pesticides has not been permitted here and arsenic is not naturally present in large quantities. On the other hand, in countries like India and Bangladesh, where waters are contaminated with inorganic arsenic and rice constitutes a staple food for the population, the result is currently one of the largest mass poisonings in history.


Monday, 27 March 2017

Do People Really Understand Their Neuropathic Pain


Today's post from healthskills.wordpress.com (see link below) asks the question as to whether people really understand the nature of their neuropathic pain. It's a very interesting study which concludes that people do much better with their problem if they receive a cogent explanation of what's happening to them. Unfortunately, with neuropathy that's rarely the case, as doctors assume that the medical science is often too complex for their patients to understand. It is pretty much a given that patients can cope much better with symptoms if they know why they are happening and what's going on inside their bodies. After that, an explanation of any treatment is also useful.


How well do people understand their neuropathic pain? 
 Martin, S., Daniel, C. Williams,  (2014)

When coming to terms with a chronic pain problem, one of the important steps involves obtaining a diagnosis that fits with both the individual’s personal experience of their pain, and also their knowledge (drawn from what is available in the general population). If the label doesn’t square with their experience, people continue searching until they find something that does.

There has been an enormous wave of excitement about giving people good “pain education”. I’ve always been a bit anxious about the term “education”, because it can so often mean giving an information dump, leaving the person being “educated” with little or no relevant knowledge about their personal concerns – and it’s the individual and unique concerns that influence how a person interprets what is happening, and how they respond. As a result, I prefer “helping people to develop a personal pain formulation” or “reconceptualising” their pain. Putting the pedantics aside, it seems really important for health professionals to not only understand what people with pain already know about their health condition, but also to understand how people interpret what they’re told – if they’re told anything.

In this study, 75 people with neuropathic pain were asked to sort a series of statements about neuropathic pain according to their level of agreement with them. This is known as Q-methodology. The sorted statements are then analysed to identify common features amongst them.


 Four factors were identified:
Neuropathic pain is a nervous system problem, psychology influences the pain experience and acceptance, and being open to psychological interventions – this group of respondents had tried psychological treatments, their pain was on average about 6 – 7 years.


Neuropathic pain is nerve damage, psychology is irrelevant in pain experience, neutral about psychological treatments – this group of people had not tried psychological treatments, but had tried surgery and medications.


Neuropathic pain is irreparable nerve damage, symptom management is needed, psychological factors play a part in pain perception but psychological treatment is not OK – this group of individuals had pain for an average of 10 years, and they had used breathing, positive thoughts, medications and physical treatments.


Neuropathic pain cause should be identified, psychological influences may play a part, and treatment can include both medical and psychological – this group had pain for an average of 1 -2 years, and they had tried a range of medications, physical methods, yoga, meditation and complementary therapies.

The authors point out several limitations of this study – people were not recruited on the basis of an particular characteristics, there could be a number of recruitment biases, and they were all identified via online recruitment processes, therefore it’s hard to generalise. What it does indicate is that there is no coherent biopsychosocial explanation put forward by participants, they appeared to have received very little explanation about their problem, and this affected their readiness for psychological or self management interventions.

Another interesting point is how many of these participants, across all the four factor groups, described experiencing being given psychosomatic explanations of their pain. The authors write :”Across all accounts, participants’ comments indicated that they had received psychosomatic explanations of their pain and had been distressed and offended, consistent with other studies which use open-ended methods to sample patients’ experiences. (p. 353).” The influence of psychological factors was found to be associated more with adjusting to chronic pain, rather than to developing an integrated model of pain. Factor 1 were the only group to endorse the notion of acceptance, or learning to live with pain – and the groups in Factors 3 and 4 were strongly against the idea that pain could be lived with.

I find this study interesting, not so much in what it has discovered, but rather more in terms of the discussion about psychological factors and medical factors – but nothing on social factors. I find myself wondering again whether we have a biopsychological model of pain, rather than a more complex biopsychosocial model.

That being said, I agree with a point made in the conclusion: people with chronic pain value a coherent explanation for their pain, it helps resolve their worry and enables them to approach their pain differently. The problem facing people with chronic pain is how to access evidence-based and accessible information about neuropathic (or indeed any type of) pain. Often people find out about neuropathic via biomedical models, and they rarely get exposed to the complexity of a biopsychological model, let alone a biopsychosocial one.

We desperately need to understand the best ways to personalise an explanation for an individual with chronic pain. I think a case formulation approach is the most useful, but I’ve found that many clinicians think this takes “too long” and is “too complex”. I wonder about this. A formulation might take a couple of sessions, but it’s a lot less expensive and has lower risk than surgery.

In light of the very limited range of interventions for people with neuropathic pain, perhaps taking the time to respond to the person’s unique questions about their pain would be time and money well spent.

People who have chronic pain are often very reluctant to consider the influence of psychological factors on their pain, reflecting their fear that by accepting this, their pain is being dismissed as “not real”, or not legitimate. This means people may not accept (or indeed be referred for) psychological interventions. Treatment approaches based on a cognitive behavioural approach have good evidence to support them, but they don’t do much good if people are not ready for them, or even referred for them.

Martin, S., Daniel, C., & Williams, A. (2014). How do people understand their neuropathic pain? A Q-study PAIN®, 155 (2), 349-355 DOI: 10.1016/j.pain.2013.10.021

http://healthskills.wordpress.com/2014/03/11/how-well-do-people-understand-their-neuropathic-pain/

Thursday, 3 November 2016

People With Neuropathy Are Charlie Too


 This may be a simple blog about neuropathy but today's post is about the freedom to speak out against evil - nothing more, nothing less - something we have to defend as a basic human right. The attack in Paris was an attack on our freedom to tell the truth, when the truth needs to be told. 
It's too important to ignore so forgive me if you're missing your daily neuropathy article - I'm sure you'll understand.

Dutch cartoonist Joep Bertrams

This cartoon depicts a murdered cartoonist sticking his tongue out to his killer. The text in Dutch says "immortal", referring to freedom of speech. 



Tuesday, 16 August 2016

Why People With Neuropathy Need to Get Off Our Backsides!


Today's post from thebody.com (see link below) looks at the importance of exercise for people living with neuropathy. It's understandably not something people want to hear because the discomfort of neuropathy can make the idea of exercising a mountain to climb. However, if only to maintain circulation and prevent muscle wastage, it has to be done in one form or another. The benefits of exercise for neuropathy patients are also much more wide ranging than just circulation and muscular definition and in the end, it's all a matter of scale and doing what you can do but never doing nothing. Even 5 minutes a day is better than nothing but hopefully everyone can manage more than that. There are all sorts of possibilities mentioned here without having to leave the door and certainly expensive gym fees aren't necessary (unless you want to go to the gym).


Attack of the Killer Couches, or Why People With HIV and Neuropathy Need to Get Off Our Backsides! 

By Dave R. March 29, 2012

Internet links shown in these posts are designed to provide more detailed information if required.

Nobody with neuropathic pain, or tingling, or numbness wants to hear it. Neither do those people with HIV who are exhausted from the pressures, both physical and psychological, of living with HIV and its medications. These are people who on some days are so tired they can't move one foot in front of another and they just don't want to be told to go forth and exercise. Yet they have to; we must! It's a question of how much longer we want to live.

I've always resisted this sort of fire and brimstone rhetoric; whether it came from the pulpit, or politicians, or medical authorities, or from well meaning friends. Tell me to go one way and I'll go the other and with that sort of bloody-minded stubbornness driving my philosophy on life, it took me until seven years ago to give up smoking. The fact that my lung capacity improved dramatically after that particular lifestyle change certainly made me more open to logical advice but I'd still smoked like a chimney for thirty five years!

All that said I've had to summon up the courage to be arrogant and preach to people about exercise here. Please forgive the bullying tone; it's not my job to tell you what to do with your lives and I am allergic to evangelists of any sort but I do feel it's important to pass the following information on to other people who might be in the same situation.

Actually, until neuropathy put a stop to several of my physical activities, I never considered that I needed any extra physical training. Then within a couple of years of the symptoms beginning; my stomach ballooned, my muscles began to lose their tone and my fat and cholesterol levels began to rise alarmingly. I became a TOFI (thin on the outside, unhealthy fat on the inside and on the stomach). This was almost certainly thanks to my enforced lifestyle change. I've never been a narcissist but looking objectively in the mirror really shocked me! Many people with HIV will recognise the feeling that their attractiveness and self-worth can evaporate before they know it yet even with that in mind, I still didn't seriously consider doing anything about it. Neuropathic pain, sleepless nights and physical weakness were just too dominant and quickly destroyed any good intentions. I began to accept a sedentary lifestyle as being unavoidable.

My mindset all changed after watching a BBC Horizon programme about the new science of exercise (see link below). Then, for the first time I began to realise what would happen inside my body if I sat in front of the TV for the rest of my life. I confess, I haven't yet done much about it but at least I've realised what I have to do. I suddenly realised that if HIV plus neuropathy doesn't kill me then eventually, inactivity most certainly will.

More Information: Horizon: The Truth About Exercise (BBC, 2012)

So what's new about exercise?

So what sort of dramatic information provided me with a wake-up call to change my outlook and given my neuropathy problem is there anything I can do about it? First of all, the idea of hours in the gym for someone with neuropathy is pretty much a non-starter. Foot and leg issues; muscle weakness, lack of feeling in some places and pain in others; don't get me started! So when this TV programme backed by new U.S. Canadian and British research began by stating that hours in the gym and running or jogging could be unnecessary, my ears pricked up.

The second premise that all exercise regimes should be tailored to your own situation was even more attractive. The video still virtually excludes most people with neuropathy or other HIV-related problems but the mental barrier caused by the thought of months on end in an expensive gym, with no guarantee of success, is removed. Although we still won't be able to do intensive short bursts, we can see the value of doing something. Anything is so much better than nothing.

More Information: Exercises for Neuropathy

The fact that 80% of fit and healthy people don't exercise and spend up to twelve hours of the day in a chair, made scientists want to explore other options based on good science. They looked at how a sedentary lifestyle changes how the body behaves and concluded that traditional views of how to lose weight may be flawed.

Most people think they'll lose weight if they burn off the calories with lots of exercise but very few people like doing the hours of activity required. Furthermore, to burn off the calories after eating a banana, a muffin and a cappuccino, you need to run for 55 minutes! You can imagine the effort needed to burn off a McDonald's diet! In the long term, most people just won't put in the effort and these are people without illnesses to slow them down even further. Some people even 'compensate' for a couple of hours in the gym by eating more; either as a reward, or as a misguided 'energy-replacement'. So finding a shorter 'cure' would encourage more people to exercise in such a way that they will lose weight and increase the health of a nation in the process. People with neuropathy and HIV will still be reading this and muttering that walking to the gym alone would be too much, never mind doing anything when you get there, but bear with me.

When you eat fat-rich foods, the fat goes into the gut and then into the bloodstream. Unless you can keep it moving, or convert it to energy, this causes changes to your metabolism, which in turn cause a build up of fatty deposits on the walls of the blood vessels. It's a no-brainer then, to realise that you need to reduce the levels of fat in your blood.

There are different sorts of fat and it is thought that fat below the waist may not be too harmful and may even be protective in nature. Similarly, subcutaneous fat is not as dangerous as the fat stored around the organs deeper under the skin. This is called visceral fat and when it builds up around the liver and pancreas, you're heading for trouble. On an MRI scan, you'll be able to see this fat as white areas surrounding the organs deep under the skin surface. You may well be a relatively thin person but can still have dangerous levels of visceral fat. These fats are the ones that lead to Type 2 Diabetes, which if you already have neuropathy, you definitely do not want added to the list, as it is a prime cause of neuropathy itself! Diabetes is caused when insulin stops working in your system and insulin normally removes sugar from the blood.

We've got to get rid of visceral fat and that brings us back to exercise and fitness training. Scientists have found that a long walk (brisk is better but any walk will do) before, or directly after a meal, triggers the release of an enzyme which changes how the body processes fat. Nothing new there then; we've always been advised to take a walk after a heavy meal. However, the difference between walking and not walking is substantially less fat in the bloodstream. Exercise causes the fat that's trying to make its way through your blood vessels to be dumped into the muscles, where it's converted to energy, or 'burned off'. The walking also switches on genes that make a protein called lipoprotein lipase and this protein reduces fat deposits in the blood. The catch is that the exercise needs to be strenuous in order to achieve the necessary effect. I know, I agree with neuropathy patients shouting, 'Hello, we're still here!' and I also sympathise with other, fitter people with HIV, who are asking what's actually new here.

A study referenced in the BBC programme was done on the results of a thousand people, exercising four hours a week for twenty weeks. The results were startlingly different for different people. Many people just don't respond to 'normal' fitness centre regimes, which is why so many people just give up after achieving little difference in their shape. Strangely enough, it's just been established that it's also genetic and you may be a responder or a non-responder but hours of exercise won't do anything to change what is predetermined. In the future a simple DNA test will be able to determine whether you'll gain any benefit from consistent strenuous exercise but for now, you need to tailor your exercise to your own condition and the results you achieve. All exercise is good but the results will still be different for different people. This brings us a little closer to the neuropathy patient, who may be one of the most limited regarding exercise potential.

The BBC programme looked at the possibility of doing a few minutes of really intensive exercise a week (speed cycling on a home machine) and found the results to be astonishingly just as good as if you'd spent hours in the gym. It doesn't sound much but it works. Are you now beginning to hope that there may be something you can do?

More Information: Exercise to Help Ease Neuropathy Symptoms

Apart from trying to stop fat deposits building up in stores in your body, the other major benefit of exercise is of course, for your heart and lungs. They don't really know why but how good your lungs are in getting oxygen into your body is called the VO2 max and it's an important marker for future health. Improving your VO2 level will also improve your insulin sensitivity and enable sugar to be removed from your blood. Aerobic exercise also helps your physical functions, maintain body weight, fight depression and increase pain tolerance. The reward is living longer. What the scientists still don't completely understand is why short bursts of high intensity exercise will change your metabolism so positively. Glycogen stored in the muscle is apparently quickly broken down by intensive exercise and this gives a signal to your bloodstream that it must provide more glucose for energy. This in turn causes more glucose/fat to be sucked out of the blood thus not allowing it to eventually build up dangerously around your organs. It goes right against the fitness industry maxims and is definitely not in its commercial interest, but who's important here!

All this is big news for those (healthy or unhealthy) who sit a lot. We need to increase our NEAT levels. This is Non-Exercise Activity Thermogenesis and means nothing more than increasing the number of calories we can burn off during every-day living but sometimes a catchy acronym can help you remember. Being active switches on the genes that control fat levels and movement of any sort increases your metabolic rate (again the burning of calories). If 80% of people are really not taking regular exercise and have an unhealthy diet, the results are filling up the hospital wards of western societies. As neuropathy sufferers we can't feel in any way smug. The reason for all this information is to alert people with HIV to the fact that, however difficult, inactivity is a terrible option. Your body goes to standby when you sit too long and all sorts of junk builds up in your system.

Okay, all that information probably leaves you feeling somewhat frustrated if your movement is already limited by pain and disability. So what can we do for ourselves?

We've been pushed reluctantly into our chairs by neuropathy and have learned that activity can be painful but there must surely be things we can do. Unfortunately, immobility is a huge problem for neuropathy patients. It can shrink your muscles even further and cause them to lose flexibility. Your metabolism will decrease, which means again, less energy and more fat gain.

There's a huge range of physical abilities amongst neuropathy patients, according to what the disease has done to you. Many people with just numbness or tingling in a few toes may be able to carry out a great many 'normal' exercise activities. On the other hand, many people for whom every step is painful will need to search hard for things they can do. Remember, the message is, we're trying to maintain our lung and heart health with some sort of aerobic movement and we're trying to reduce the dangerous fat build-up in the blood stream and around our organs by burning off calories.

More Information: Exercise Rx for Nerve Pain

There's no way around it, whatever exercise we find to do, needs to be backed up with a healthy diet. That's obvious and doesn't need further explanation here; there are thousands of advice sources for healthy eating.

Low impact exercise rather than inactivity is the answer. In the past, people with neurological problems were often told not to exercise at all. Hopefully the information in this article has convinced you that it's pretty much essential. Sitting for hours on the couch is only going to put a stop to efficient metabolism and slow up every part of your system. It may be painful or tiring, or both but you should try never to be sitting still for more than an hour. Even if it's just five minutes exercise while you're walking around the house, try to make a habit of breaking up the pattern of sitting or lying down and try to exercise as many parts of your body as you can think of. The four links from eHow.com at the end of this article, give some excellent, easy to understand advice for people with neuropathy, who are wondering how to go about improving their fitness and general health.

It's important to reassure people who are still depressed at the thought; not because they're lazy but because exercise is just so difficult. Whatever you can manage to do is better than nothing at all. You will feel so much better if you can achieve even small steps on the road to getting fitter. See it as a daily challenge and a break from the routine of being in pain, or being exhausted. Try to give yourself a reason to be so tired.

Music is a good motivator. Put on your favourite music and let your body decide how you want to respond to it. It's a silly example but even lying on the couch, you can flex the muscles in your buttocks to the rhythm. Lying on the couch or bed, you can do all sorts of exercises: moving your legs; making letters of the alphabet with your feet. Wave your arms in circles; push your palms together, or clasp them and try to pull them apart. Flex your stomach muscles to the music; breathe deeply, squeeze a tennis ball, push full Cola bottles into the air and use them as weights, whatever; do whatever you can; invent stuff! There are so many possibilities without expensive equipment or fashionable sports gear and you know you always wanted to find a legitimate reason to listen to Abba!

More Information: Exercise (From the Foundation for Peripheral Neuropathy)

It is important to warm up before doing anything and that warming up will be relative to what you can eventually achieve. It's vitally important that you don't pull muscles, or inflame joints; that will only destroy your will to push on. Start gently and build up until you can beat your own record at whatever you're doing. It sounds childish but for the person who's disabled in some way by neuropathy or HIV-related exhaustion, literally every little bit helps and if you can make it just a little bit fun, you'll want to do more.

It's a question of building up a series of good habits; just like it is with healthy eating. Even getting up and cleaning something will give you satisfaction because it's an excellent physical exercise involving more than one group of muscles. Ideally you want to be able to build up a sweat and then you know the calories will be burned off but not everybody can do that, or come even close. This is why it's even more important that you do something, no matter how small. At the same time, you need to listen to your body. Only you will know when you've really had enough, or have done too much. Equally, only you will know if you could have done just that little bit more!

To sum up, the person struggling with neuropathy, or HIV-related fatigue, or other disabling health problems should bear in mind the four sorts of activities we need to aim towards:

Aerobic Exercise: Aerobic activities increase your heart rate, get your muscles working and raise your breathing rate.
Flexibility Exercise: Flexibility exercises mainly done during warm-ups help keep your joints flexible and reduce your chances of injury.
Strength Training Exercise: Strength training helps increase strength in bones and muscles and makes daily tasks like shopping and lifting easier for your body.
Balance Exercise: Keeping your balance system as normal as possible is especially important for neuropathy patients who have loss of feeling in their feet, or numbness, or pain. Stumbling happens far too often but there are ways of practising walking and standing in the correct manner.

For us it's all a matter of scale but hopefully you now have a good idea of why you should develop your own exercise regime based on those exercise types.

Now I understand all too well, how this will still appear as a mountain to climb for significant numbers of people. The whole message of this article is to tailor your activities to your own situation. If five, or ten minutes a day is all you can do, then it's all you can do but it's still so much better than doing nothing. Think of it as prolonging your life maybe just by minutes, or hours, or days and maybe for years!

For many others, whose physical abilities have not been so compromised by the effects of HIV, this will just appear common sense but regular exercise is also important for the person with HIV who has no health problems at all. It's logical; keeping fat down, building up muscle strength and improving your heart and lung capacity is money in the bank for the future. Michelle Obama says 'Let's move' to families but let's pretend she's also directly talking to us; hey, if it works ...!

I admit I hate exercise: most of the time I just don't have the energy; or the pain in my feet is too much, or I feel too weak. I just want to lie down in front of the TV with some comfort food at hand and take the pressure off. However, one TV programme shocked me enough to realise what's probably happening inside my body. I need to train myself to do something every day and the following day or week, do a bit more. I also need to be conscious of what I'm eating and not reward the pain and discomfort by feeding it treats!

It'll take time; as I say, I'm naturally resistant but I now realise how important it is. I want to reduce the mass of visceral fat that's both visible and having an effect on my breathing and other bodily functions. So I'm going to try to exercise my way back. I won't be turning into a gym-bunny and certainly won't be joining the ranks of muscle Mary's but the alternative of living more and more slowly and grinding to a halt on the killer couch is not an option!

Further information:
How to Walk With Neuropathy in Feet
Benefits of Exercise for People with Peripheral Neuropathy
Exercises for Idiopathic Peripheral Neuropathy
Exercises for Peripheral Neuropathy

This and other posts are based on my opinions and impressions of living with both neuropathy and HIV. Although I do my best to ensure that facts are accurate and evidence-based, that is no substitute for discussing your own treatment with your HIV specialist or neurologist. All comments are welcome.

http://www.thebody.com/content/66453/attack-of-the-killer-couches-or-why-people-with-hi.html

Wednesday, 15 June 2016

PEOPLE WITH MULTIPLE SCLEROSIS MAY BE AT INCREASED RISK OF DEVELOPING CANCER



Individuals with multiple sclerosis may have an increased risk of developing any type of cancer, with an especially high risk of developing breast cancer. That is the conclusion of a recent study published inEuropean Journal of Neurology. Because the findings contradict earlier studies, additional research is needed to determine whether a true link exists between multiple sclerosis and cancer

Previous research suggests that some individuals with autoimmune diseases may have an increased risk of developing cancer, but most studies have found no link between cancer and multiple sclerosis, an autoimmune disease that involves the central nervous system.

To investigate further, Li-Min Sun, MD, of the Zuoying Branch of Kaohsiung Armed Forces General Hospital in Kaohsiung, Taiwan, and his colleagues assessed data from the National Health Insurance System of Taiwan, including information on 1292 patients who were diagnosed with multiple sclerosis between 1997 and 2010. Each patient was matched with four participants without the condition.
"Our study was a nationwide population-based cohort study, and it revealed unexpected findings," said Dr. Sun. Specifically, the team found that individuals with multiple sclerosis were 85% more likely to develop cancer than the controls. Their risk of developing breast cancer was especially high, with more than a 2-fold increased risk over controls.

The findings suggest that patients with multiple sclerosis patients may need to be monitored closely to ensure early detection of cancer. Dr. Sun notes that it is unclear why his team's results are not consistent with most other studies. "The underlying genetic and environmental factors in Taiwan, which differ from those of western countries, might play an undetermined role. Additional large-scale studies will help improve our understanding," he said.