"Winning the War Against Rheumatoid Arthritis"

RA is a condition that forces half of patients to become disabled from the work force within five to ten years? and reduces life expectancy by as much as 18 years. RA affects about one per cent of the world?s adult population, most commonly women between the ages of 30 and 50.

The good news is that a tremendous amount of progress has been made within the last ten years in identifying patients earlier and treating the disease more aggressively. Patients with RA, if treated appropriately, can lead a relatively normal life. This is in stark contrast to the wheel-chair bound existence common as recently as 20 years ago!

Experts in the field consider early rheumatoid arthritis to be a medical emergency with mortality and morbidity equal to that for diabetes, asthma, heart disease, and other life-threatening conditions.

Rheumatoid arthritis attacks the joints in a symmetric fashion (both sides of the body affected equally) with the most common areas being the hands, wrists, ankles, knees, and feet. In addition to the swelling and pain, patients with RA often have profound fatigue and stiffness.

Rheumatoid arthritis is an autoimmune disease that attacks not only joints, but internal organs such as the blood vessels, lungs, heart, and eyes. Patients with RA are at increased risk for heart attack, stroke, and lymphoma.

Since many other types of arthritis such as gout, lupus, and osteoarthritis can look like RA a careful diagnostic approach is needed.

Laboratory testing has its pitfalls. The rheumatoid factor, a blood test found to be positive in about 80 per cent of individuals with RA, may also be positive in other disease conditions. Couple that with the fact that 20 per cent of patients with RA will be rheumatoid factor negative, then it becomes clear a diagnosis should not hinge on the results of blood tests alone.

Imaging procedures can also be misleading. Conventional x-rays often miss the erosions found with early disease. Newer imaging technologies such as magnetic resonance imaging (MRI) and ultrasound are much more sensitive.

After the diagnosis is made, there is even more hope for a patient today. In the past, non steroidal anti-inflammatory drugs (NSAIDS) used to be considered a cornerstone of therapy. That is no longer true.

Disease-modifying anti-rheumatic drugs (DMARDS) are being used earlier. Among the DMARDS currently being used are methotrexate, leflunomide (Arava), azathioprine (Imuran), sulfasalazine (Azulfidine), cyclosporine, and hydroxychloroquine (Plaquenil). These drugs attack the immune cells responsible for chronic inflammation. While DMARDS alone in combination are effective, they are relatively non-specific. Often, combinations of DMARDS are required.

Biologic Response Modifiers (BRMS) can target the disease more specifically than DMARDS. RA is a disease that is dependent on the signaling that occurs between immune cells. The signaling takes place through the use of special chemical messengers called cytokines. BRMS act at both the cytokine (chemical messenger) as well as the cellular level allowing the disease to be better controlled and in some instances put into remission.

Biologic response modifiers, which include drugs that suppress tumor necrosis factor (TNF), appear to be particularly effective.

Tumor necrosis factor is a protein that is produced by the immune cells. TNF is the major culprit responsible for inflammation-inducing damage. By block the effects of TNF, better control of RA can be achieved.

Three anti-TNF drugs are currently available: etanercept (Enbrel), adalimumab (Humira), and infliximab (Remicade). Another biologic drug, anakinra (Kineret) blocks interleukin, a different cytokine.

These drugs allow patients to have their disease controlled to such an extent that most are able to enjoy a normal work and leisure existence.

On the horizon are other biologic drugs that work at different points in the immune system- on different cytokines and on different pathways- to allow even greater as well as more specific control of disease. Since rheumatoid arthritis is a disease with many different cytokine and cellular mechanisms responsible for damage, attacking the disease at different points makes sense. In the future it may be possible to identify patients through specific tissue signals (called ?biomarkers?). These biomarkers will allow physicians to type patients and give patients the specific therapy that will work best for them. Once that is achieved, the possibility of a cure becomes a reality.

Everything, though, starts with early accurate diagnosis. If damage is allowed to occur the chances for remission drop dramatically!

Dr. Wei (pronounced ?way?) is a board-certified rheumatologist and Clinical Director of the nationally respected Arthritis and Osteoporosis Center of Maryland. He is a Clinical Assistant Professor of Medicine at the University of Maryland School of Medicine and has served as a consultant to the Arthritis Branch of the National Institutes of Health. He is a Fellow of the American College of Rheumatology and the American College of Physicians. For more information on arthritis and related conditions, go to: http://www.arthritis-treatment-and-relief.com

Preventing Headaches and Reducing Their Impact

Whether speaking of migraines, tension-type headaches or other recurring head pains, it's safe to say that the best headache attack is the one you don't have. Even if you have found an effective treatment for resolving a headache that is already underway, there is nothing about today's as-needed treatment that will keep next week's attack from occurring.

Headache treatments come in two forms?abortive and preventive. The abortive form is familiar to most people. It means something you do to get rid of a headache that has already started. Usually it consists of an over-the-counter or prescription medication, but in some cases, a non-drug approach works. By contrast, a preventive treatment is something you do every day with the goal of keeping some future attacks from even starting. These, too, can involve drug and non-drug strategies.

Billions of dollars are spent each year on abortive remedies. For the most part, they are dollars well spent. And for people who have infrequent headaches that are rapidly and reliably resolved by an abortive treatment, a preventive treatment might be needless.

But if attacks are frequent, hard to resolve, interfere with usual activities?or side-effects from the abortive treatment interfere with usual activities?then a preventive treatment should be considered. Employing a preventive remedy does not preclude also using an abortive measure: each can be part of an integrated plan.

Before discussing specific treatments for specific headache types, let's consider the impacts of recurring headaches. The more obvious impact is the sheer unpleasantness and suffering involved in an attack. However, another impact?though less obvious?is in its own way just as important. And that is the associated disability or loss of function that comes with an attack.

If a headache attack is severe, then whatever else was planned for that day goes out the window?it's just not going to happen. If an attack is moderate in intensity, then usual activities might be possible, but occur more slowly, less efficiently, or require more effort to produce. This, too, represents headache-associated disability.

An increasing trend in the field of headache management is for practitioners to address their patients' loss of function as well as their pain and suffering. Drs. Richard Lipton and Walter Stewart designed a questionnaire to estimate headache-associated disability, called the MIDAS (Migraine Disability Assessment) scale which can also be used for non-migraine headaches.

Measuring and then re-measuring MIDAS is one method for judging if a preventive treatment is effective. But to accurately detect the effectiveness (or lack of effectiveness) of a preventive headache treatment there should also be some sort of day-by-day recording system.

It might be as minimal as a check-mark on the calendar for each day with any symptoms. Another system is to summarize at the end of each day that one day's headache-impact by selecting one of the following four descriptions?none, mild, moderate or severe. Numerically inclined people can assign scores of 0-3 to these choices and then run averages and other statistics for each calendar month.

For people with recurring or continuous pain there is a tendency to live moment-to-moment without a view of the longer-term pattern. A recording system helps capture the big picture. It would be a mistake to judge the effectiveness of any treatment by what happened with symptoms in just the last few days. Generally, a month or longer is required to judge fairly and accurately.

So now that we have decided to consider a preventive treatment for our headaches and have put in place a system for measuring the treatment's outcome, what specific remedies are available?

It depends, of course, on the kind of headaches being treated. Let's discuss two of the most common types?migraine and tension-type headaches.

For prevention of migraine, the best-studied and most effective drug treatments are available by prescription only in the U.S. These include propranolol (brand name Inderal), amitriptyline (Elavil), divalproex (Depakote) and topirimate (Topamax).

Riboflavin (vitamin B2) at 400 milligrams per day was shown in one controlled study to have migraine-preventing actions. (At this dose?far higher than what is needed to treat vitamin deficiency?riboflavin should be considered a drug rather than a vitamin.) The herb feverfew has also shown benefit in controlled trials, but it is important to remember that this, too, is a drug and can have side-effects. As is the case with other drugs, it should not be used during pregnancy.

Non-drug strategies of proven effectiveness in migraine prevention include therapist-supervised programs of stress management, relaxation, biofeedback and cognitive-behavioral therapy. Studies of acupuncture have shown mixed results. Avoiding individually determined triggers for attacks carries no risk and can reduce the attack rate.

For tension-type headaches amitripyline is the best-studied drug for prevention of attacks. Note that this drug is also a leading treatment for migraine, so people unlucky enough to have both kinds of headaches can obtain benefit from just one drug. Unfortunately, even at the low doses used for headache prevention, amitriptyline can cause daytime drowsiness (even when administered at bedtime) or annoying oral dryness. Because of this, substitution of a better-tolerated, though less-studied drug in amitriptyline's family (tricyclic antidepressants) is sometimes required. Tizanidine (Zanaflex) has also shown benefit in controlled trials.

Non-drug strategies for tension-type headache have also been proved effective. These include similar behavioral interventions to those mentioned for migraine?stress management, relaxation, biofeedback and cognitive-behavioral therapy.

It would be wonderful if preventive treatments stopped headaches entirely. If they did, a measurement system would not be necessary. But a more realistic goal for preventive treatment is to reduce overall headache symptoms by at least half, or to an extent that an individual patient finds meaningful. When this occurs, a preventive approach can be a valuable addition to a program of headache management.

(C) 2005 by Gary Cordingley

Gary Cordingley, MD, PhD, is a clinical neurologist, teacher and researcher. For more health-related articles, see his website at: http://www.cordingleyneurology.com

A Healthy Way to be Sick

A person who deals with a physical condition that is beyond their control has to accept an inner depth, which is uncommon in society. If all we do is try to fit into society, we ignore the unique opportunity our illness offers. Our illness forces us beyond the socially accepted depth and allows us an inner exploration most people ignore.

I am partially blind, so it is hard for me to see my outer world. This forces me to look within and explore parts of myself that are not a normal part of society. I am legally blind looking outside of myself, but most people are legally blind looking within. If I had to choose which was worst, inner blindness would be my choice. I believe it is the cause of most of our suffering.

I have had multiple sclerosis since 1981 and I have tried every possible cure that came my way. I am on a weekly shot medication today, but I have tried several diets. I do acupuncture and massage treatments regularly and I have done several alternative treatments including Bee venom and purification methods. I benefited from these treatments; but I am still legally blind with several other symptoms of multiple sclerosis.

Looking Within

Over the decades of making serious efforts to heal myself using everything that held promise, I learned a beautiful lesson. No matter who you are or what condition you are in, the silence beyond our thinking mind is an amazing resource for fulfillment. Becoming aware of that resource is what I call a healthy way to be sick.

That silence is free from disturbing thoughts and fears, giving you a shelter where you are free from your illness and the struggle you are in. It is at that depth the Wisdom of your Body responds to your medication without the distractions from your thinking mind. Even when you are dealing with a chronic illness, like multiple sclerosis, there is an inner peace at that depth. In my condition, if I was to limit my focus to my superficial thinking mind, I would easily become depressed. I am forced to go deeper.

Once I was asked how do we create the ideal state of mind? My answer was: Take away everything that isn't the Ideal State of Mind. When imperfection is removed, we have what existed before we were messed up. In other words, deep within all of us is a wisdom that may not be perfect, but is free to change and evolve. The real task we all face is to learn how can we return to that ideal state of mind.

When we rely on the wisdom of the body, we learn to accept the beauty of life. Our illness or disability may limit us as we adapt to society, but that same situation has the power to force us into a wonderful self-acceptance and that is what I think is a healthy way to be sick. From that state of mind you create an inner healing environment, where you become an active partner with your doctor.

Use your thinking mind to uplift your spirits and work with your doctor and medical team. Your thoughts were not created to depress you or limit you in any way. Thinking, like the clothes you wear can be put on or taken off. Dress up to meet the incredible challenge where you consciously participate in healing. Don't go shabby to an event that is so significant.

Copyright ? 2005 Marc A. Lerner

Marc Lerner is the President of Life Skills Inc. and the author of The Life Skills Approach. He lectures frequently to patients in a health crisis and those undergoing emotional trauma, to help them harness inner resources to overcome these obstacles. For more information and a free e-book, please visit http://www.lifeskillsinc.com

Expert Patient: A New Approach to Chronic Disease Management for the 21st Century

PART 1: INTRODUCTION TO CHRONIC DISEASE SELF-MANAGEMENT

Are You an Expert Patient? Can your Doctor(s) say the following about you?

My Patient knows more about the disease than I do; as much about the disease as I do, and enough about his/her symptoms that it is easy to communicate with him/her.

Why is becoming an Expert Patient so important? There is plenty of emerging research about the needs of 21st century patients. Most of that research centers around the concept of Illness Self-Management, for what is called chronic illness.

What, you ask, is a chronic illness. Health concerns are usually classified as either acute or chronic. Acute illnesses usually begin abruptly and last only a short time. Most people with an acute illness can expect to return to normal health. A strep throat is an example of an acute illness: it is easy to diagnose with a lab test and is cured with antibiotics.

Chronic diseases are different. They usually develop slowly, last long periods of time, and often are never cured. In most cases, there is no cure. The long-term effects may be difficult to predict. Some conditions cause few problems. Others cause only episodic problems or symptoms that can be controlled with medication. However, in some cases, a chronic disease may severely limit a person's ability to work, go to school or take care of routine needs. Examples of chronic diseases include, but are in no way limited to: diabetes, congestive heart failure, asthma, hypertension, chronic kidney disease, depression, irritable bowel syndrome, arthritis, emphysema, fibromyalgia, parkinsons symdrom, and multiple sclerosis - just to mention a few.

Why is Chronic Disease Self-Management so important a concept for those with a chronic condition? For the person with a chronic condition, there is no way not to self-manage the disease/illness. If one retires from life and stays at home as a depressed person this is a type of self-management. On the other hand, many people learn to deal with their conditions and remain active, happy participants in life.

Chronic Disease Self-Management covers the following areas:

1) knowing how to recognize and respond to changes in a chronic disease
2) dealing with problems and emergencies
3) using medicines and treatments effectively
4) finding and using community resources
5) getting enough exercise
6) coping with fatigue, pain and sleep problems
7) maintaining good nutrition
8) making decisions about when to seek medical help
9) working with your doctor(s) and other care providers
10) talking about your illness with family and friends
11) managing work, family and social activities

It is the learning of the skills necessary for this later type of proactive disease/illness self-management that is the subject of this document. The information about developing the skills is fascinating; and, they (the skills) really are the key to DECIDING, and remaining active, happy participants with a quality of life as full as you can make it.

Research and practical experience in North America and Britain are showing that today?s patients with chronic diseases need not be mere recipients of care. They can become key decision-makers in the treatment process. By ensuring that knowledge of their condition is developed to a point where they are empowered to take some responsibility for its management and work in partnership with their health and social care providers, patients can be given greater control over their lives. (Note: Once again, this process of acquiring the knowledge of your condition so that you can reach the self-management level with your Doctor(s) is one of the primary purposes behind the www.disabilitykey.com website.)

Self-management programs can be specifically designed (between you and your Doctor(s)) to reduce the severity of symptoms and improve confidence, resourcefulness and self-efficacy (a big word that basically means self reliance).

PART 2: WHY BECOME A CHRONIC DISEASE SELF-MANAGER?

For those of you who have had an opportunity to read about my professional career , you will see that I started out as a Federal Auditor of Human Resources practices, policies and procedures (which is why I was able to create the Disabilitykey Workbook in the first place). As an Auditor, I always wanted to know what is the ROI (Return on Investment) as they say in the business world, for anything I worked on, or for any initiative I tackled. Why would people with chronic illnesses want to learn how to manage their disease symptoms? Why would their Doctors want them to learn and do these things? What is in it for both patients and Doctors?

First of all, it was a fascinating subject for me to research! And, imagine my surprise to learn that, even though the original Chronic Disease Self-Management study was conducted here in the United States at Stanford University, it appears that, at this point in time, (mid-2005), England, Scotland, and Australia appear to be further along in actually implementing programs than we are here in the US! And, imagine my chagrin to find out that to be able to take the great online training program to become certified in chronic disease management, you have to live in England!

In the United Kingdom, their Department of Health came to the following conclsion:

Little has been done to prepare patients for long-term management of their diseases. They face many challenges in coping with discomfort and disability and carrying out treatment programs on a regular basis. They need to modify behavior to minimize undesirable outcomes, adjusting their social and work lives to accommodate their symptoms and functional limitations and deal with the emotional consequences. For their care to be effective, they must become adept at interpreting and reporting symptoms, judging the trends and tempo of their illness and participating with health professionals in management decisions. (Note: language has been Americanized for greater ease of understanding here in America on, what they [the United Kingdom call, the other side of the Pond.)

It was the chief medical officer for the United Kingdom, who first introduced the name ?expert patient. He said that expert patients are people who have the confidence, skills, information and knowledge to play a central role in the management of life with chronic diseases. Doesn't this sound logical?

Here are some Chronic Illness statistics here in the US.

?In the US for example, LESS than ONE PERCENT of the people who stand to benefit from self managing their chronic arthritis - do so.

?Chronic disease has become pandemic in the United States, and estimates are that it will affect 148 million people by the year 2030.

?Patients with chronic illnesses cost the health care system over three times more than individuals without chronic conditions.

?The Population of U.S. adults over 65 is expected to double between 2000 and 2030.

?Over 80% of adults over 65 years of age have one or more chronic conditions -- over 60% have two or more chronic conditions.

?Consumers with five or more chronic conditions account for two-thirds of all Medicare spending.

?People with chronic conditions are responsible for 78% of all health care spending, 95% of all Medicare spending, and 77% of all Medicaid spending for community-dwelling adults.

?The U.S. has by far the most expensive health care system in the world -- but lags most other developed countries in key quality and consumer outcomes.

However, it is the following statistic about how much ACTUAL TIME, on average, that a patient here in the United States spends with their Doctor(s) that really got my attention. On average, we with a Chronic Dieseae spend around three hours per year with a health professional. This means that the patient is left to manage his/her own condition for the other 8757 hours of the year. If you, or someone you know has a chronic illness, wouldn't you be more comfortable knowing what to do during those other 8,757 hours that you are not in a health professional's presence? I sure did, and I didn't even know that such a thing as chronic disease management as a concept existed when I did the work depicted in the Disabilitykey Workbook. I only knew that I needed a way to live the best possible life IN SPITE of my chronic disease; I wanted to control it; I did NOT want it controlling me!

OK, chronic disease management just seems to make sense. But, the Auditor in me asks, are there measurable, objective results that this concept is worthwhile? And, according to the Agency for Healthcare Research and Quality (AHRQ), there are.

AHRQ-funded research at the Stanford University Patient Education Research Center led to development of the Chronic Disease Symptom Management Program (CDSMP). Standford's CDSMP is a 17-hour course taught by trained lay people that teaches patients with chronic disease how to 1) better manage their symptoms, 2) adhere to medication regimens, and 3) maintain functional ability.

Over a period of 2 years, AHRQ-funded investigators compared health behaviors, health status, and health services use in patients age 40 to 90 years (average age, 65) who had completed the CDSMP. When compared to baseline measures taken for the 6 months prior to the CDSMP, researchers found the following.

1.After 6 months, CDSMP participants had:

Increased exercise.
Better coping strategies and symptom management.
Better communication with their physicians.
Improvement in their self-rated health, disability, social and role activities, and health distress.
More energy and less fatigue.
Decreased disability.
Fewer physician visits and hospitalizations.

2.After 1 year, CDSMP participants had:

Significant improvements in energy, health status, social and role activities, and self-efficacy.
Less fatigue or health distress.
Fewer visits to the emergency room.
No decline in activity or role functions, even though there was a slight increase in disability after 1 year.

3.After 2 years, CDSMP participants had:

No further increase in disability.
Reduced health distress.
Fewer visits to physicians and emergency rooms.
Increased self-efficacy.

Another source of actual results from people who have made the decision to become Chronic Disease Self-Managers comes from The United Kingdom. The United Kingdom has a website describing the recent results of their Expert Patient Programme (EPP). The website provides periodic ?eUpdates? to inform people about new developments within the Expert Patients Programme such as new publications, forthcoming events and news from the national team.

The EPP is a National Health Service (NHS) lay led self-management programme for people living with any long-term health condition(s). Groups of 8-16 participants, with a mix of different conditions, meet over six weekly sessions and are led through a structured course by trained tutors who are also living with a long-term condition. Each session (lasting two and a half hours) looks at ways to better manage the effects of their long-term condition. For more information about the EPP please visit the EPP website at www.expertpatients.nhs.uk

EPP PILOT INTERNAL EVALUATION

Internal evaluation data from approximately 1000 EPP participants who completed the course between Jan 2003 and Jan 2005 indicates that the programme is achieving its aims in:

1) Providing significant numbers of people with long term conditions with the confidence and skills to better manage their condition on a daily basis.

- 45% said they felt more confident that they would not let common symptoms (pain, tiredness, depression and breathlessness) interfere with their lives.

- 38% felt that such symptoms were less severe 4 - 6 months after completing the course.

- 33% felt better prepared for consultations with health professionals.

2) Providing significant reductions in service usage by people with long term conditions completing the EPP course.

- 7% reductions in GP consultations

- 10% reductions in Outpatient visits

- 16% reductions in A&E attendances (US note: note sure what this is.)

- 9% reductions in Physiotherapy use

Over 94% of those who took part felt supported and satisfied with the course.

If you want to sign up to receive periodic updated information about what the Brits are doing, you too can sign up to receive an eUpdate as they call them. It is FREE, and you can sign up by going to: www.expertpatients.nhs.uk.

WHAT IS CHRONIC DISEASE SELF-MANAGEMENT

Chronic Disease Self-Management; Self-Efficacy; great terms, but what do they really mean, and how does one start to become a Chronic Disease Self-Manager?

Consider the following quotations associated with these concepts.

1) Row Your Own Boat - Chronic Disease Self-Management.
2) ?Every bird flies with its own wings. Swahili proverb

What do the two quotations have in common? First of all, the desire, then the knowledge, then the action to take back control over your health, and your life.

Here are questions ? a ?mini quizz? that you can use to ask yourself about your readiness to adopt the concept of Chronic Disease Self-Management (or, to assist someone else in their journey toward this objective).

CHRONIC DISEASE SELF-MANAGEMENT READINESS TEST

Created By Stanford University?s Patient Education Research Center, this test is called: Self-Efficacy for Managing Chonic Diseases 6-Item Scale. The test measures how confident you are that you can keep ?your situation? (i.e., the situation addressed in each of the following 6 questions) caused by your disease from interfering with the things you want to do?

For each of the following questions, please choose the number (between 1 and 10) that corresponds to how confident you are that you can keep the symptoms caused by your disease from interfering with the things you want to do? #1 represents Not at all confident; #10 represents Totally confident.

1) How confident are you that you can keep the fatigue caused by your disease from interfering with the things you want to do?

2) How confident are you that you can keep the physical discomfort or pain of your disease from interfering with the things you want to do?

3) How confident are you that you can keep the emotional distress caused by your disease from interfering with the things you want to do?

4) How confident are you that you can keep any other symptoms or

health problems you have from interfering with the things you want to do?

5) How confident are you that you can do the different tasks and activities needed to manage your health condition so as to reduce your need to see a doctor?

6) How confident are you that you can do things other than just taking medication to reduce how much you illness affects your everyday life?

The higher you score toward 10 on each question, the more self-efficacy you have. (Reminder: self-efficacy is the belief in one's capabilities to organize and execute the sources of action required to manage situations.) As you can probably figure out, I score either 9 or 10 on each question. My Disabilitykey Workbook (see www.disabilitykey.com) and the confidence that I received by first, executing the processes contined there-in for myself, and then in developing the Workbook to assist others, has allowed my self-efficacy to be high.

OK, you have rated yourself, and you want to know more about the WHAT of this topic. First, we will discuss the definition of Chronic Disease Self-Management; next, the stages of a chronic disease self-help behavioral change; and, finally, something called social learning theory.

Definition of Chronic Disease Self-Management

Based on a comprehensive literature review of over 400 articles, Researchers have proposed the following definition.

Chronic disease self-management involves [the person with the chronic disease engaging in activities that protect and promote health, monitoring and managing of symptoms and signs of illness, managing the impacts of illness on functioning, emotions and interpersonal relationships and adhering to treatment regimes. There are a number of key elements to this definition that will enable us to develop a practical concept of self-management. It is important to note that these elements are about the behaviors of the patient, rather than models of self-management for health care systems, service providers or health professionals. These elements suggest that self-management:

? Entails engaging in activities that promote health;

? Involves managing a chronic condition by monitoring signs and symptoms;

? Entails dealing with the effect of a chronic condition on personal well being and interpersonal relationships; and

? Involves following a treatment plan prescribed to you by your Doctor(s).

The definition of self-management encompasses a range of behaviors, as well as knowledge and attitudes and is an important starting point towards the development of a concept of chronic disease self-management.

HELP

Getting from where you are to Becoming a Chronic Disease Self-Manager: Stages of Behavioral Change

A model of behavior change that has been applied to chronic disease self-management is based on research on how people change behavior, either on their own or within an intervention program (i.e., some sort of action to assist in the change). The theory is that the ceasing of risk behaviors (eg. smoking) and acquisition of health promoting behaviors (eg. physical activity, relaxation) involves the progression through the stages of change. They are:

? Pre-contemplation [not thinking of change
? Contemplation [thinking of change
? Determination [ taking preliminary steps to change
? Action [ actively engaging behavior change
? Maintenance [ sustained behavioral change
? Relapse [ can occur at any point.

Behavioral change is facilitated by a personal sense of control. If people believe that they can take action to solve a problem, they become more inclined to do so and feel more committed to this decision. This can do attitude mirrors a sense of control over one's environment. It reflects the belief of being able to master challenging demands by means of adaptive action. It can also be regarded as an optimistic view of one's capacity to deal with stress. (Not to sound redundant, but this really is about the glass being half-full and NOT half-empty.)

Social Learning

OK; now we understand the behavioral change steps; now, on to the social learning stage. The theoretical underpinning of effective chronic disease self-management programs should be based on social learning and behavioral theories. The key principles of these theories as applied to chronic disease self-management are:

? Disease management skills are learned and behavior is self-directed;

? Motivation and confidence (including self-efficacy) in managing one's condition dictate an individual's success;

? The social environment (ie. family, workplace & health care system) support or impede self-management; and

? Monitoring and responding to changes in disease state, symptoms, emotions and functioning improve adaptation to the chronic condition.

PART 3: BECOMING TRAINED IN CHRONIC DISEASE SELF-MANAGEMENT

How do you become trained in Chronic Disease Self-Management? Here are the primary resources available.

1) Start with your own health insurance company. Call up the Customer Service folks in Plan, and ask if they offer Chronic Disease Self Management Program classes. My Internet searches indicate that many of the larger companies are offering such classes for their enrolees. And, in some cases, self-management is becoming a requirement of retaining insurance coverage!

2) Go to your State's Home Website, and look up the Department of Health, and of Aging. In some cases they might be the same, in others, different. Call each and see if/when they will be offering classes in your city/county for Chronic Disease Self Management Program.

3) Use one of the many Internet search engines to locate this statement: (your state) Chronic Disease Self-Management Program (CDSMP). This should help you locate classes in your state. In my state, they located classes by county and city. Some of the bigger states even offer classes derived from the original Standford research program.

4) Use one of the many Internet search engines to ask locate this statement: Chronic Disease Self-Management Program (CDSMP). This should provide you with additional options.

5) Finally, and probably the best source, from the original Stanford site where the concept was created, there is a link to each state?s CDSMP sites: http://patienteducation.stanford.edu/programs/cdsites.html If you go to this site, you can click onto your state and see which organizations in your state are licensed to offer the Chronic Disease Self-Management program.

PART 4: CONCLUSION

The National Center for Quality Assurance (NCQA) in their 2004 Health Care Quality Report comments that the U.S. healthcare system as a whole remains plagued by deadly quality gaps that contribute to 42,000 to 79,000 avoidable deaths every year and $1.8 Billion in excess medical costs due to the system's routine failure to provide needed care.

According to Catherine Hoffman of the Henry J. Kaiser Family Foundation, nearly half the people in the U.S. are living with chronic conditions, at a cost of $234 billion in lost productivity and $425 billion in medical spending per year. These figures are rising. Moreover, they do not include billions of dollars in lost productivity of employees who miss work to care for family members who have chronic conditions.

Many people with chronic conditions, as well as family members who care for them, also suffer needlessly from the physical and emotional effects of their illness. By helping people change their behaviors and adapt to their conditions, self-management programs often increase people's adherence to medical treatments, strengthen their control of pain and symptoms, and improve their overall emotional well-being.

About Disabilitykey.com & Carolyn Magura:

Disabilitykey.com is a website designed to assist each person in his/her own unique quest to navigate through the difficult and often conflicting and misleading information about coping with disabilities.

Carolyn Magura, noted disability / ADA expert, has written an e-Book documenting the process that allowed her to:

a) continue to work and receive her ?full salary? while on Long Term Disability; and

b) become the first person in her State to qualify for Social Security Disability the FIRST TIME, in UNDER 30 DAYS.

Click here to receive Carolyn 's easy-to-read, easy-to-follow direct guide through this difficult, trying process. If you are disabled, don't let this disabiling process disable you. Read Carolyn's Disability Key Blog.

Attention Deficit Disorder: What is it?

Attention Deficit Disorder is a complex condition that is not well understood at the present time by many clinicians and the general public. New information is being discovered rapidly however. Dr. Amen is one of the pioneers in this field and this article is meant to summarize his work. Attention Deficit Disorder (ADD) and Attention Deficit Disorder with Hyperactivity (ADHD) occur as a result of neurological dysfunction in the prefrontal cortex of the brain. This is the newest part of our tri-brain system in evolutionary terms. It is the part of our brain that performs executive functions. The functions of this brain deal with 1) attention span, 2) perseverance, 3) judgment, 4) organization, 5) impulse control, 6) self-monitoring and supervision, 7) problem solving, 8) critical thinking, 9) forward thinking, 10) learning from experience, 11) ability to feel and express emotions, 12) interaction with the limbic system, and 13) empathy.

Whenever there is a problem with this part of the brain, a number of skills that many human beings take for granted would not be available in any optimal way. The following are problems that develop when the prefrontal cortex is affected. 1) Short attention span, 2) distractibility, 3) lack of perseverance, 4) impulse control problems, 5) hyperactivity, 6) chronic lateness and poor time management, 7) disorganization, 8) procrastination, 9) unavailability of emotions, 10) misperceptions, 11) poor judgment, 12) trouble learning from experience, 13) short-term memory loss, and 14) social and test anxiety.

The exact neurological problem with ADD is unknown at this time. However SPECT scans, single photon emission computed tomography, which measures cerebral blood flow and metabolic activity patterns, has noted that when someone with ADD concentrates, their prefrontal lobe activity decreases significantly. This essentially means that under stress and concentration someone with these disorders cannot bring to bear their full cognitive capacity.

It is theorized that our usual ability to screen out and attend to stimuli of our choice is impaired with these individuals. I like to think of it as going to the mall during the summer. It is too bright and there are too many people around, but it is not overwhelming. However, at Christmas time after a couple of hours at the mall people are so over-stimulated that it is hard to find the car. People with ADD feel this way almost all the time.

There are five recommended courses of treatment for someone with ADD or ADHD. Physicians often give an antidepressant such as Wellbutrin and Strattera, which tends to calm the limbic system and increase dopamine, a neurotransmitter. In my experience as a therapist, this can be helpful but stimulants, the second course, seem to do a better job. Stimulants given in small doses, so the mood alteration is minimal, act in a paradoxical manner. This means that instead of accelerating a person they help to focus and calm them while still allowing the prefrontal lobe to remain active. They also seem to increase dopamine. This neurotransmitter is negatively affected with people suffering from ADD. The third regimen, a combination of an anti-depressant and a stimulant, seems to work best for most people suffering from most forms of ADD. The fourth treatment consists of teaching relaxation, stress-management, organizational, and socializing skills. This should always be included as part of treatment whether or not medication is used.

Another form of treatment is the naturopathic approach. Due to my background I cannot adequately discuss this method, and as yet am not sufficiently familiar with the treatment to be able to measure its efficacy. At the present time, supplements, vitamins and chiropractic care seem to be effective as an adjunct to stimulants.

There are numerous misconceptions about Attention Deficit Disorder and a lot of emotional fervor about the diagnosis. It reminds me of the debate over Prozac several years ago or whether or not Alcoholism is a disease or a moral defect. It is understandable that people worry about giving young children a mood-altering drug. However, any time medication is considered as an approach, the physician needs to carefully assess both the costs the benefits and the severity of the problem. Most medication difficulties with ADD result from mismanagement. When the appropriate amount of medication is used with ADD the benefits are immense and the cost is minimal. A person?s life changes dramatically for the better. It is as if for the first time a person can think clearly and their self-esteem soars.

There is still a tendency in this country to feel that people need to pull themselves up by the bootstraps regardless of the severity of the problem. They are often blamed for their own illness. This happens a lot with ADD.

True ADHD with hyperactivity is rather easy to diagnose. However, only in the last ten years was ADD inattentive type recognized. This diagnosis is hard to spot and often is characterized by a general spacyness and inability to track conversations. It also used to be common knowledge that children were the only ones to suffer from this disorder and that once they became 14 they grew out of it. What is more common is that in the normal course of experimentation with drugs and alcohol a person with this disorder finds amphetamines and becomes addicted to them. Almost the right drug, wrong dose! Most people do not grow out of the disease. Interestingly enough, even with hard-core Methadrine addicts, if they are put on a small dose of Adderall, 20- 30 mg. of sustained release 1-2 times a day, they thrive and it does not reactivate the addictive process.

Dr. Daniel G. Amen is one of the acknowledged leaders in the field for the study of Attention Deficit Disorder. He has expanded the classifications of this condition within the last two years from the standard two types of Hyperactive and Inattentive by adding four more distinct types of ADD. He has done this by exhaustive research and has been aided by the SPECT scan, which is a sophisticated brain scanning tool that measures and clearly shows what part of the brain is most active. What is most impressive about his work is that he stresses the need for a multi-treatment approach. This includes attention to diet, exercise, vitamins, supplements, traditional psychotropic drugs, and behavioral techniques.

In ?Healing ADD? Dr. Amen lists the six types of ADD as 1) Classic hyperactive, 2) Inattentive, 3) Over focused, 4) Temporal, 5) Limbic, and 6) Ring of Fire. Each of these types has much in common, but also differences in symptoms and treatment.

All of the types of ADD have as their primary feature periodic impairment of the prefrontal cortex of the brain and dopamine involvement. Classic ADD is characterized by both hyperactivity and inattentiveness. It is usually quite easy to treat by a combination of a high protein diet, aerobic exercise, a stimulant such as Adderall or Ritalin, and possibly the supplement of L-Tyrosine. Often an anti-depressant is used as well.

Inattentive ADD lacks the hyperactivity, but people who suffer from it have a difficult time focusing and are often very scattered. As with the classic type the prefrontal cortex is involved. The treatment for inattentive ADD is usually exactly the same as the classic type.

Overfocused ADD exhibits the same problems and symptoms of prefrontal cortex as with classic and inattentive ADD, but the difference is that the sufferer of over focused often cannot break away from a thought or behavior. This is because the cingulate system of the brain is overactive and often locks a person into self-destructive, negative, or repetitive behavior. Often a stimulant will cause temper problems if used alone. Therefore, it is usually helpful to have the person take an anti-depressant first and only later to add the stimulant. Another possible treatment is to use St. Johns Wort, a natural herbal anti-depressant, but it is important not to use both a traditional and an herbal anti-depressant at the same time. The other forms of treatment such as diet and exercise is the same as the first two types of ADD.

Temporal ADD is still characterized by problems with the prefrontal cortex, but the temporal area of the brain is often affected. This could be from a previous head injury, but not necessarily. All the symptoms remain the same, but often extreme bouts of anger are also included. The treatment for this type is usually a stimulant and an anti-convulsant such as Depecote. All other treatment is the same except the following supplements can be used: GABA, Ginkgo Biloba, or Vitamin E.

Limbic ADD is when the limbic area of the brain is also affected in addition to the prefrontal cortex. This type of ADD has the symptoms of inattentive ADD, but a significant amount of depression is also present. A stimulant and an anti-depressant are indicated. Aerobic exercise is needed, but often a complex carbohydrate and protein mixed diet is indicated. The following supplements are used: SAMe or L-tyrosine.

Ring of Fire ADD is a very disorganized and severe form of ADD that is a combination of all the other types. The entire brain is lit up on a SPECT scan. In addition to the standard treatment of a stimulant and an anti-depressant, an anti-psychotic like Respiridal is often called for. Dietary and exercise treatment is the same as in inattentive type. The following supplements are possibly needed: GABA or Omega-3. Other supplements that have been found helpful with ADD in general are Zinc, Flax seed oil, and Serephos.

Attention Deficit Disorder is a neurological dysfunction that has no known cure at the present time. However, the good news is that effective treatment is available and following the protocol can improve how a person feels and functions more dramatically than many psychiatric conditions. What I find so attractive about the work of Dr. Amen is that he treats the whole person. He stresses the need for appropriate psychotropic medication, but also believes that a clinician needs to pay attention to diet, exercise, and behavioral strategies to fully address ADD.

? 2003 Jef Gazley, M.S., LMFT www.asktheinternettherapist.com

www.hypnosistapes4health.com

JEF GAZLEY, M.S., LMFT, DCC has practiced psychotherapy for over thirty years and is the owner operator of http://www.asktheinternettherapist.com since 1998 and http://www.hypnosistapes4health.com. He is the author of eight mental health educational videos and DVDs and is currently writing a book on distance counseling. Jef is State Licensed in General Counseling, Marriage/Family, and Substance Abuse in Arizona and is a certified hypnotherapist. He is dedicated to guiding individuals to achieving a life long commitment to mental health and relationship mastery. In his private practice in Scottsdale, Arizona, Jef specializes in ADD, love addiction, hypnotherapy, dysfunctional families, codependency, trauma, and gay and lesbian issues. He is a trained counselor in EMDR, NET?, TFT, hypnotist, and Applied Kinesiology. Jef received his B.A. in Psychology, History, and Teaching from the University of Washington and his Masters in Counseling from the University of Oregon.

Stroke: The First 24 Hours After A Brain Attack

Although stroke is the third-leading cause of death in the U.S. and the number one cause of disability, this condition doesn't get the respect and attention it deserves. When people have sudden chest pain, they know they might have a heart attack. They call 9-1-1 and seek help immediately. But people who suddenly become weak or numb on one side of their body, or experience sudden problems with speech or vision, often act unhurried in seeking help.

Why is this? One possibility is that heart attacks are usually painful. Strokes are not necessarily painful, and even when pain is present, it can be mild. Pain is a powerful motivator, and some people have the mistaken belief that all serious medical conditions hurt, and the seriousness of the problem is proportionate to the intensity of pain. Also, because the brain is a more complicated organ than the heart, symptoms of strokes can also be more complex, making them harder to identify.

In both strokes and heart attacks a portion of a body-organ has experienced a sudden disruption of its circulation. Increasingly, strokes are called brain attacks to emphasize the parallel with heart attacks. As a neurologist, I sometimes describe a stroke as a heart attack of the brain. Reflecting my bias as a brain specialist, I also describe a heart attack as a stroke of the heart, but--what can I say?--this terminology hasn't caught on.

If you suspect stroke in another person, the American Stroke Association recommends a quick, 3-step, screening test to identify cases:

  • Ask the person to raise their arms and keep them up. In many stroke victims one arm doesn't go up or, once up, sags.
  • Ask the person to smile. A lopsided or one-sided smile can indicate trouble.
  • Ask the person to repeat a simple sentence. If it comes out garbled or unclear--or not at all--a stroke is likely.
  • While it's better to have some system of detection than no system, this screen misses strokes affecting the parts of the brain involved in sensation or vision which are just as serious as strokes causing paralysis or loss of speech.

    So now that emergency help has been summoned, what happens next?

    The emergency squad, upon arrival, sizes up the situation and measures vital signs, including rate and adequacy of breathing, pulse rate and blood pressure. They insert an IV line, check the blood-sugar level via a finger-stick method, apply pads to the chest to monitor heartbeats, and often administer oxygen as well. Then they transport the patient to the nearest emergency department.

    Upon the patient's arrival, the medical team obtains more history and examines the patient more thoroughly. They draw blood to measure blood-sugar, blood-counts and blood-clotting function, as well as other blood-chemicals, including those showing the presence or absence of a concurrent heart attack. They perform an electrocardiogram (EKG) and continue the process of monitoring vital signs and heart-rhythms initiated by the squad.

    A computed tomographic (CT) scan of the head is usually done soon after the patient's arrival. CT scans can detect the 1-in-6 kind of stroke involving bleeding within the brain, but often fail to detect the more usual kind of stroke, called an infarction, caused by a blocked blood-vessel. This is because, in the first 24 hours, damaged brain-tissue can look just like healthy tissue to the scanner's x-ray beam. The CT scan also screens for other brain diseases, like brain tumors or infections, that might mimic a stroke, but call for completely different treatments.

    So far, the discussion has been all about testing. What about treatment? What can be done to improve outcome, reduce the severity of the impairment and prevent death?

    A useful way to think of a brain infarction is as a central core of forever-lost brain cells that no treatment can revive, surrounded by a larger zone of sick brain-tissue that may or may not recover. Early treatments focus on this surrounding tissue that is on the bubble, trying to influence it to survive rather than die.

    One dramatic but controversial treatment is to use an intravenous clot-busting drug called t-PA (tissue plasminogen activator). The potential benefit of using this drug is to reduce the eventual impairment of the patient caused by the stroke. However, the drug also increases the likelihood of brain-hemorrhage, and physicians are not unanimous in believing that the benefits of this treatment outweigh its risks. However, one point of agreement is that if t-PA is going to be used, it has to be administered within 3 hours of the stroke's onset. Arriving at the emergency room after 2 hours and 59 minutes isn't good enough because a clinical evaluation, CT scan and blood tests all need to be completed before the drug is infused.

    Less dramatic treatments are every bit as important--and quite possibly more important--than use of a clot-busting drug. It's the simple things that often matter most, but because they're so simple, sometimes they are unappreciated or even forgotten.

    One such treatment is to manage the body-temperature. Fever increases the size of the stroke, so when an elevated temperature is present, it needs to be decreased right away. Another little detail is to manage the blood-sugar. Oddly, an elevated blood-sugar is toxic to the oxygen-deprived but still-surviving brain cells. So the emergency team should aggressively treat elevated blood-sugars by administering insulin.

    Yet another issue of crucial importance is to urgently treat severe anemia (decreased red blood cells) by transfusing blood. Oxygen molecules are transported to the brain attached to molecules of hemoglobin within red blood cells. So if there are fewer red blood-cells, less oxygen is delivered to the sick brain-tissue. Providing more red blood-cells increases oxygen-delivery.

    Of course, if the patient's blood-pressure is severely elevated, it needs to be decreased, but mildly-to-moderately elevated blood-pressures might actually improve blood-flow to the damaged tissue. If the patient's blood-pressure is excessively low, this is bad, too, and is treated by infusing salt-water or administering medication. Dangerous heart-rhythms also need to be treated, as does a concurrent heart attack, when present.

    The principal value of being in a hospital with a fresh stroke is to achieve clinical stability in a monitored environment where rapid interventions can be made when called for. The hospital also provides a setting in which more extensive tests can also be performed, though not necessarily in the first 24 hours, that seek to understand why the stroke occurred and what can be done to prevent another brain attack.

    (C) 2005 by Gary Cordingley

    Gary Cordingley, MD, PhD, is a clinical neurologist, teacher and researcher who works in Athens, Ohio. For more health-related articles see his website at: http://www.cordingleyneurology.com

    Autism Is Now Believed To Affect 1 In Every 166 People

    What is Autism

    Autism is a developmental disability that affects, often severely, a person's ability to communicate and socially interact with others. It is four times more prevalent in males than females.

    Currently, autism is believed to affect 1 in every 166 people. The rate of people being diagnosed with autism has increased substantially over the past two decades.

    Although this may be in part due to improved diagnostic techniques and to changes in the criteria for autism spectrum disorders, the majority of experts agree these changes are not enough to explain the epidemic rates at which autism is being diagnosed.

    Autism Spectrum Disorders is an umbrella term that includes classic autism (also known as Kanner's autism or Kanner's syndrome), Asperger's syndrome, and pervasive developmental disorder (PDD).

    Autism is considered a spectrum disorder because the number and intensity of the symptoms people with autism display may vary widely. However, all people with autism demonstrate impairments in the following three areas: communication, social relationships and restricted patterns of behavior.

    The spectrum ranges from those who are severely affected, less able, and dependent on others to those who are of above-average intelligence and independent, yet lacking in social skills.

    What Causes Autism?

    Unfortunately, no one knows the answer. This is one of the primary missions of Cure Autism Now to fund the crucial and necessary research to discover the cause of autism, in order to design effective treatments and, eventually, find a cure.

    Here is what is known so far:

    There is a genetic predisposition for autism spectrum disorders.

    Some brain circuits are different in a person with autism.

    Serotonin, a neurotransmitter important for normal brain functioning and behavior, has been found to be elevated in a subgroup of people with autism.

    Some children with autism and related disorders have biochemical and immunological problems.

    Many experts in the field of autism - for example Dr. Edward Ritvo of the University of California Los Angeles - theorize that there exists a genetic predisposition to autism spectrum disorders.

    This predisposition, perhaps encoded within a certain gene, interacts with an as-yet-unknown environmental factor or factors and causes alterations to the immune system, the sensory nervous system, the brain and often the gastrointestinal tract as well. These changes then cause the affected person to exhibit the symptoms of autism.

    Autism Does Not Discriminate

    Last year I went on a 5K walk at Dodger Stadium in Los Angeles benefiting Cure Autism Now. I saw thousands of children, their families and friends that are affected in one way or another by autism.

    There were people from all walks of life, professional people like athletes, lawyers, doctors and people you see everyday in your own community. People with children that have autism, all getting together to raise money to help find a cure.

    Before the walk, I received a letter from a mother whose 4 year old son Danny has autism. She was asking for donations and letting people know about the Cure Autism Now second annual Walk-A-Thon.

    After reading her letter, I had a better understanding of not only what autism was, but what parents and the children with autism go through on a daily basis. Below is part of that letter. I think after reading it, you will be more understanding as I was.

    Start of letter

    It's Walk-a-Thon time! A year has passed so quickly. I want to share with you the progress that Danny has made.

    He is amazing. A year ago he couldn't even tell me he loved me. Now, when I say I love you Danny he yells back I love you more!!! I waited so long to hear those words. But what is so difficult is the fact that he doesn't know what the words mean. He says them from memory. It's like a recording. Every time I say I love you... he automatically responds with the same answer, which is very common with most autistic children.

    I ask him what he did in school each day and he can tell me bits and pieces, but he also repeats the same thing everyday or tells me what they did a month ago.

    Autistic children have amazing memories. He can take a brand new puzzle, dump all the pieces off the board, pick up any piece without hesitation and put it in it's proper place without even thinking. His mind is incredible.

    I wake up in the mornings wondering what kind of day Danny is going to have, and I pray that it's a good one. He is extremely sensitive to his surroundings. If things don't go in the same pattern that he is used to, he flips out...screaming and kicking.

    I still find myself in denial sometimes. When we are out in public, I try to do everything in my power to make sure Danny gets his way, as to not cause a scene.

    I remember one Friday, I wanted to take a special day and make it all about Danny, I was going to take him to an indoor playground. It was pouring rain that Friday, but we trampled through the parking lot and into the playground and took off our shoes.

    Danny wanted to play the video game and another little boy also wanted to play. Danny doesn't do well when other people are in his space, so he started screaming at the top of his lungs, threw himself on the floor kicking me and anything else that got in his way.

    I tried to pick him up but he was kicking so hard I could barely lift him. Every mother and child in the place was staring at me. I tried to calm him, but his screams got louder, as they always do when you try to reason with him.

    As I carried Danny to the bathroom to get him away from everyone else, I heard one of the moms say to her friend...I wish she would shut that kid up!!! I couldn't help but break into tears.

    We didn't even last five minutes in public. I grabbed our shoes in one hand, Danny in the other and ran to the car in my socks in the pouring rain. I just sat in my car and cried.

    I wish that woman could spend just ONE day in the life of Danny. I sometimes want to wear a sign around my neck that say My child is autistic, please excuse the excessive noise.

    Despite Danny's outbursts...he has made incredible progress. He is talking so much. Almost too much. (just kidding) He can write his name all on his own and is starting to sing songs(which he would never do before) He is a very expressive little boy...

    End of letter.

    After reading that letter, now when I see a child screaming and kicking in a store or someplace, and we all have, I think that the child may be autistic. It made me realize that it's not the child's or the parents fault and I should be more understanding.

    The number of autistic cases is rising faster than we can count, but progress is being made. At Cure Autism Now, they are currently funding more than 15 research projects examining the causes of autism. You can go to Danny's page at Cure Autism Now and you will see a picture of Danny, who is 5 years old now and his father at last years Walk-A-Thon. You can donate what you can, learn more about autism and find out where there might be a Walk-A-Thon in your area. Danny's page

    Thank you,

    About The Author

    Paul Bittle is the owner of http://www.bitsnwits.com an information web site with free articles and free courses. Also, for Danny's page you can go to Bits N Wits home page and look for Special Announcement.

    Ten Alternate Energy Sources To Live Well With Global Warming

    Feeling hot under the collar?

    Glaciers and polar ice are melting, ocean levels are rising, hot, dry weather, huge forest fires, water restrictions, crop failures?

    You name it, if these don?t feature in your life yet, they soon will. Global warming and climate change are facts of life now, according to the International Panel on Climate Change, and many scientists.

    Huge problems beyond our control!

    But are you hot under the collar?

    If you?re not, you probably live in a city where half of the Earth?s citizens live now and take much for granted. Because in city living we are far removed from natural processes that deliver our food, clothing and energy.

    Does your child even know that milk comes from a cow - or a soya bean if you?re that way inclined - and not from a milk carton?

    Even in the city you cannot stick your head in the sand (or under the asphalt?) and you are not immune from climate change. Witnesses are the 15,000 mostly elderly people that died in Paris alone in the sizzling hot European summer of 2003. Or the many killed in New Orleans at the ?hands? of cyclone Katrina.

    And if you are hot under the collar, do you think perhaps that there will be some miraculous scientific break-through so they ever-responsible ?They? will fix the Earth? The ultimate stem cell technology maybe that can clone a new home for us!

    Seriously, for many of us it is all too hard.

    All we want is to live a life where we may raise our children to have a future.

    A future of some predictability: of schooling, a job, a family, community, of achievements and an enjoyable life - on a healthy planet Earth.

    Is this a fading dream, once a reasonable expectation?

    Maybe, maybe not.

    Our world is changing. There are great challenges ahead and it is too late to stop global warming. The Earth has changed and the processes it uses to regulate itself are adjusting themselves. And these changes will not suit human life as it is.

    But you are not powerless.

    Each person alone can change the world, one by one. Let me explain.

    Do I say that these problems are under our control then?

    Well, yes and no.

    We are talking about a severely disabled world really.

    And from the experience of disability we can learn how to survive and thrive!

    ?Come on, get real?, you say? Do I hear: ?Just show me the right alternate energy sources and we?ll get out of this mess.?

    Yes, we desperately do need to switch to renewable energy sources that do not make a greenhouse out of our home, the Earth. But all the technology in the world will never be enough to survive and flourish>.

    Renewable energy sources alone will not teach us to accept limits, unpredictability and what it is to lead a rewarding life.

    How we have lived collectively, in our billions, for the last few hundred years, has got us to this point. And by changing what we do we can live through climate change as best as we might.

    Even now.

    It?s simple and it?s hard work. No way out of that.

    Many people with severe disabilities know this. And they report the same or better life satisfaction as anyone else?under highly challenging, vulnerable circumstances.

    So, we can learn to live well in a disabled world.

    Regardless of what is to come you and I will be well served by the beliefs and strategies that people with disabilities use to - not just to survive - but to live well.

    These are true alternate energy sources.

    Those that guide us how to use what we have sustainably.

    These 'disabled people' believe this:

    * Accept that all of us are fragile and vulnerable
    * The world is full of limits. We need some of these to live well.
    * Vulnerability and dependence are an inevitable part of a whole life
    * No-one is independent, but interdependent
    * Connection with others is our lifeline and our wellbeing

    And they do this:

    * Engage with others to build positive relationship, where you live, work and play
    * Pay attention to other?s needs and that of the environment
    * Take responsibility for the situation you?re in
    * Care for others and the environment competently
    * Be assertive and use your humour and creativity

    Not all people with disabilities act in this way of course. And I?d be the last to portray people with disabilities as heroes. We?re just people - trying to get on.

    You try that!

    Talk to that elderly woman in your street. Offer a hand when someone needs it.

    Doing such small things will connect you with others and your environment.

    And do also use the ?regular? renewable alternate energy sources, and recycle too.

    You can change your local world by acting in these ways.

    And if all fails - regardless?

    Well, it?s the only way to go!

    Perhaps your world might be just as hot but it?ll be cooler under your collar!

    Dr Erik Leipoldt has long been concerned about the effects of global warming. In particular he uses his own experience of severe disability in practical approaches towards alternate energy sources to survive and thrive in our environmentally disabled world. See http://www.alternate-energy-sources.com/

    The Challenge Of Living with Different Disabilities

    If you are affected with any one of a number of disabilities you know how hard it can make your life. In this article we are going to discuss a couple of basic disabilities and ways to help live with them.

    First off let us state that disabilities can come naturally or unnaturally. You can be born with them or have them pop up at an older age. This means you should be prepared for them no matter how good you think your health is.

    Being blind affects many people throughout the world. This disability is when you cannot see out of your eyes. It is possible to be legally blind and still be able to see a little. Usually, however, it is so little as to make little difference.

    By being blind will limit a lot with your life. You won?t be able to see or do many of the things you love. However, using brail you can still read and enjoy a good book. Also, a lot of blind people learn to use their hearing to a very effective level.

    Being deaf is a very bad disability. However, this one has fewer consequences than some of the others. While you may not be able to hear you can still communicate with people via sign language or some speech if you can learn to read lips. There are lots of deaf people who do very well for themselves in life.

    The next big disability is being mute. This is where you cannot talk and can?t make speaking sounds. This is one of the easier disabilities to overcome because you don?t need to speak to communicate.

    Disabilities can also include amputated or lack of limbs, genetic disorders, and many other things which cause a person not to be able to lead a normal life.

    When everything is said and done there is no easy way to live with a disability. There are plenty of ways to make it easier on a person with a disability but sadly, there is no real solution.

    Learn more by visiting our Disability Awareness site: http://disabilityawareness.typepad.com/

    Preparing to See a Social Security Doctor

    I have recently been asked about preparing to see a Social Security Doctor who will conduct an examination to determine the applicant's eligibility for SSDI. This can be a scary proposition; also, if you do not take control of the situation upfront, your chances of success GREATLY DECREASE!!!

    Here are some tips to increase your chances of using this situation in your favor of attaining your SSDI eligibility.

    When they tell you that they want you to see their Dr. it means that, for whatever reason, the information from your own personal Doctor was not sufficient for them to determine whether the SYMPTOMS of your illnesses impact your daily living activities to such a degree that you cannot perform work in some capacity, given your education, training, work history and age that will pay you more than the monthy qualifying amount ($860/month currently).

    It also means that you probably did not follow the process outlined in the DisabilityKey Workbook, acquired at the www.disabilitykey.com website. So, let's see if we can help you play catch-up.

    Here are the links to the Social Security form called Residual Functional Capacity. The first is an explanation of how it is to be filled out. The second is to a copy of the actual form.

    http://policy.ssa.gov/poms.NSF/lnx/0424510050

    http://policy.ssa.gov/poms.NSF/lnx/0424510055

    In a nutshell, the Social Security Administration needs to have evidence - preferably your Doctor(s)' chart notes and the results of any and all objective tests completed on you - that will allow them to complete this form about you. If they don't have it, they will send you to their Dr to get it.

    In a perfect world, you would have taken this form into your own personal Doctor AHEAD OF TIME and completed it with him/her, and provided it to SSA with your application (that's what I did, and what I advise folks to do).

    To see an actual example of a type of this form completed, check out the articles portions of the www.disabilitykey.com website.

    BUT, the best situation is to gollow the process in the DisabilityKey Workbook up front, and present the completed package to the Social Security Administration!

    Best of Luck.

    About DisabilityKey.com

    The Disability Key Website ( http://www.disabilitykey.com ) is designed to assist each person in his/her own unique quest to navigate through the difficult and often conflicting and misleading information about coping with a disability.

    Carolyn Magura, noted disability expert, has written an e-Book documenting the process that allowed her to:

    a) continue to work and receive her ?full salary? while on Long Term Disability; and

    b) become the first person in her State to qualify for Social Security Disability the FIRST TIME, in UNDER 30 DAYS.

    To download Carolyn's e-book, click on the following link: http://www.disabilitykey.com/products.htm

    Top Health Tips for the Elderly to Start You Off in the Right Direction

    1. Don?t begrudge spending money on your own comfort, health and quality of life. You deserve it!

    AND FOR THE OVER-60?S -

    The government?s annual fuel allowance of ?200 is meant to be used for our warmth and comfort, and to ease the worry of the increased heating bill.

    The Winter Fuel Payments Help line is 0845 9 151515 If you are receiving a disability or income-related benefit, you may be able to claim a grant of up to ?2,500 for insulation and heating improvements. Call Home Energy Efficiency Scheme 0800 952 0600. If you receive disability and income-related benefits you can claim Cold Weather Payments if the temperature falls below 00 C for 7 consecutive days.

    There is also the Staywarm scheme. For a fixed charge you can use as much gas or electricity as you need. 0800 1 694 694 Finally, if you are unable to pay your winter fuel bill, in the first instance contact your supplier explaining your problem and informing them that you are a pensioner. Good news worth remembering, is that electricity companies and British Gas have a policy of not disconnecting pensioners between 1 October and 31 March ? so keep warm and don?t panic.

    AND DO YOU NEED REMINDING - DON?T WASTE YOUR MONEY AND HEALTH ON CIGARETTES. RESEARCHERS TELL US THAT THE AVERAGE BRITISH SMOKER WILL SPEND ?91,832.43 ON CIGARETTES IN A LIFETIME. (Now, I?ve never smoked so I wonder what happened to my ?91,OOO?)

    2. Keep your mind active, crosswords, sudoka, hobbies, etc. NEVER STOP LEARNING. If you have an interested mind, people are more likely to enjoy your company and be interested in you.

    3. Keep your body active. As the saying goes, if you don?t use it, you?ll lose it Walk in the fresh air if possible. If you enjoy company while you are walking then join a rambling group. (Often ?rambling clubs? for the retired are more socially inclined ?ambling clubs?). Gardening combines the benefits of fresh air, exercise and the results can give you immeasurable pleasure. Dancing; particularly formation or line dancing exercises the memory also. Swimming, is a particularly good exercise for all parts of the body with the added advantage that the water is supporting you and therefore there is no weight on the joints.

    4. Feed your body with the correct foods. You wouldn?t expect your car to work efficiently if you fed it the incorrect fuel. So feed your body with nutritious foods that contain the necessary vitamins and minerals in order for it to return optimum performance. With winter approaching we need to build up our immune system, so in addition to a well balanced diet of fresh fruit, fresh vegetables and nourishing protein (laced with the benefits of virgin olive oil and garlic), we should add a few supplements to help us on our way. In addition to a good multi-vitamin tablet, you?ll probably benefit from extra Vitamin C, Echinacea, EPA fish oils, selenium, ginko biloba to aid circulation, particularly to the extremities, and glucosomine to help with those aching joints.

    Don?t forget your flu jab and the jab against pneumonia for the over 70?s. There is also really excellent news on the common cold front. At long last there appears to be something that stops a cold developing. Vicks First Defence is a spray that you use at the first sign of a cold and it stops the cold virus in its tracks. This miracle goes on sale during October 05.

    5. Socialise. Possibly I don?t have to remind you about this as the majority of retired folk I meet complain that they are busier now than ever they were, that there are not enough hours in the day, and they wonder how they ever found time to go to work. There are so many clubs and groups to join. To name a few popular ones, U3A (University of the Third Age) for both sexes and with interesting speakers, and offering numerous sub sections for specific group interests and hobbies, Women?s Institute, (has gained a new image after the film Calendar Girls), Townswomen?s Guild, Gardening Clubs, Art Clubs, etc., and many clubs aimed specifically at the retired.

    If transport is a problem, remember most local authorities offer free or reduced bus fares for senior citizens and travel tokens for the disabled. There is a Senior Railcard for reduced train fares for the over 60?s. National Express have a Routesixty Scheme which enables over 60?s to travel nationwide very cheaply (Tel 08705 808080). Also, occasionally, National Express offer their ?go anywhere for ?5 scheme?.

    If you have difficulty in getting around the town, then there is Shopmobility where you can hire mobility scooters (various models and sizes available) and electric and manual wheelchairs. Shopmobility is usually manned by helpers who will be only too pleased to instruct and allow you to practice before you are let loose on the town. Also there is the added advantage that there is usually a free car park attached to Shopmobility for clients? convenience. If you have difficulty in using public transport, often local authorities provide a ?dial-a-ride? service from your home to the shopping centre.

    Well, whatever you do ? ENJOY IT! We were always told that laughter is the best medicine and now we know it to be true ? it raises the serotonin levels in the brain and gives you that ?feel good? factor.

    Visit Mabels?Maintaining Bygone Times, containing numerous articles thoughtfully researched mainly for the older person. You may access these articles by visiting http://www.mabels.org.uk/ - You will learn about the best tips, latest news & advice to improve your health, fitness, finances & retirement as well as information on nostalgic topics, places to visit, leisure & lifestyle, mobility & helpful organisations to make the most out of life and much, much more to benefit Your Quality of Life.

    How To Identify Your Own Depression

    Depression. What is it? Why would a normally healthy, optomistic person get depressed? If things go wrong, don't you just talk yourself out of feeling sorry for yourself? So what if your 23 year marriage ends, and your soon-to-be ex-husband moves in with your best friend; you are left to cope with 2 devestated teenagers; you loose your father and father-in-law to cancer; you have extreme job challenges; and, your new condo, purchased without REALLY knowing what to look for (just don't buy a home with a laundry room upstairs over the living room!) and you develop a roof leak, and a laundry leak into the living room. AND, you are the primary care giver for a very needy Mother.

    You can handle all of this, right? And, when, the next year, you loose your Mother and Grandmother to cancer too, it doesn't send you over the edge, does it? Particularly when you also have Multiple Sclerosis, which has been misdiagnosed for over 35 years, and the worst thing for MS is stress and anxiety. You can handle everything, right?

    Well, I found that I couldn't. Consider the following list of symptoms that one should review if you think that you might be suffering from depression. OR, if you, like me, are convinced that you CAN HANDLE IT, if the rain would just stop; or, if the roof would just stop leaking (I've already tried to get it fixed 2 times, and it hasn't yet worked; I now have a gallon bucket sitting in the front hallway to catch the water leaking from the hole in the roof); or, if the kids would just stop being normal teenagers, when you no longer have a husband to help you in the day-to-day coping with teenagers.

    Here is a checklist of symptoms of depressive illness:

    1) Loss of energy and interest.
    2) Diminished ability to enjoy oneself.
    3) Decreased -- or increased -- sleeping or appetite.
    4) Difficulty in concentrating; indecisiveness; slowed or fuzzy thinking.
    5) Exaggerated feelings of sadness, hopelessness, or anxiety.
    6) Feelings of worthlessness.
    7) Recurring thoughts about death and suicide.

    I remember clearly my last straw. I read the list, above, and was sure that these 7 symptoms did NOT describe me. Then, with all of my water problems at home, I went to work in my 4th (top) floor office that just happened to have a flat roof. While on the phone arguing with the roofer who claimed that my roof shouldn't be leaking, and my telling him that it still was leaking, and if he didn't believe me, he could just come over and see my bucket full of water in my entry way, when I heard the familiar pitter-patt noise that freaked me out at home. I looked up at my office ceiling just in time to see water beginning to gush out of the ceiling tiles, around the hanging lights, and pour into my office. That did it. I went home. That night, I awoke thinking that I heard the pitter-patt in the upstairs laundry room, dripping water into my living room. I got up, turned off the water to the washing machine; stuffed all of my towels around the washer, and stood with my back against the wall in my first ever anxiety attack, thinking that if this was what my life had become, why would I even want to continue living it?

    This event scared me into going to my Doctor. He had a great little depression test for me. Knowing my fragile state, he asked me the statements, and, based both on my answers and on the detailed symptom impairment document that I had started preparing for him, prescribed an antidepression medication for me.

    I learned two critical things that day - three, really. The first one is that it is critical to have a Doctor that you trust, that knows you, and that LISTENS to what you are saying. Secondly, since he knew about my MS, he told me that Depression was a frequent secondary symptom of MS. (At that time, I hadn't done my MS symptom research yet; the Disabilitykey Workbook, found at www.disabilitykey.com is the ultimate result of all of my symptom and system - Long Term Disability and Social Security Disability Insurance - research for myself.) Third, I learned that no matter how strong your personality is, and no matter how positive a person you are, Depression is NOT something you can get over by just thinking positive thoughts; by keeping a stiff upper lip. If you truely think that you are suffering from Depression, there is nothing wrong from talking to your Doctor, and seeking his advice.

    All that I have discussed so far happened over a dozen years ago. I am still taking antidepression medication, and it does help. I have searched high and low for the original test that my Doctor used on me, and finally found one at one of my favorite resources, called the Institute for Algorithmic Medicine (that's academic talk for medical condition tests). The test is The Zung Self-Rating Depression Scale. As you read the following questions, ask yourself where the statement ranks on the following scale:

    1) A little of the time for me.
    2) Some of the time for me.
    3) A good part of the time for me.
    4) Most of the time for me.

    I fell down-hearted and blue.
    Morning is when I feel the best.
    I have crying spells or feel like it.
    I have trouble sleeping at night.
    I eat as much as I used to.
    I still enjoy sex.
    I notice that I am losing weight.
    I have trouble with constipation.
    My heart beats faster than usual.
    I get tired for no reason.
    My mind is as clear as it used to be.
    I find it easy to do the things I used to.
    I am restless and can't keep still.
    I feel hopeful about the future.
    I am more irritable than usual.
    I find it easy to make decisions.
    I feel that I am useful and needed.
    My life is pretty full.
    I feel that others would be better off if I were dead.
    I still enjoy the things I used to do.

    This little test, with your self rating for each statement, and with your symptom impairment documentation, so that your Doctor knows more about you and what is going on in your life, s/he can best decide what to do to help you better achieve a higher quality of life. Perhaps antidepression medication isn't what you need, something else would be better for you. But, if you don't learn, document, seek help, and discuss with your Doctor, s/he can't help you help yourself.

    Many of you are probably asking yourselves how I can just put myself out there; just put into these bloggs what is going on in my life. I'm doing this, sharing these experiences so that you can know that I have been there; I've done that; I've got the t-shirts! For more about me, check out the about us section in the website: www.disabilitykey.com.

    About Disabilitykey.com & Carolyn Magura:

    Disabilitykey.com is a website designed to assist each person in his/her own unique quest to navigate through the difficult and often conflicting and misleading information about coping with disabilities.

    Carolyn Magura, noted disability / ADA expert, has written an e-Book documenting the process that allowed her to:

    a) continue to work and receive her ?full salary? while on Long Term Disability; and

    b) become the first person in her State to qualify for Social Security Disability the FIRST TIME, in UNDER 30 DAYS.

    Click here to receive Carolyn 's easy-to-read, easy-to-follow direct guide through this difficult, trying process. If you are disabled, don't let this disabiling process disable you. Read Carolyns Disability Key Blog.

    Disability Commissions: Where Disabled Are Heard And Cared For

    State is dutybound to protect the rights of its citizens and promote their welfare ensuring that on no occasion they are discriminated against for anything adverse that happens to them without their having played any role in it.

    Disability is one such thing that happens to people and they are many a time considered to be unequals for reasons other than merit and ability. So long as a person can perform his work as well as anyone else, he or she should not be discriminated against simply because he suffers from some kind of impairment. In order to carry out its social responsibility towards the disabled effectively, the governments all over have established the institutions, generally called 'commissions', to look after the welfare of the disabled and ensure that they are not discriminated against in any way.

    A disabled person may approach these body in case he or she needs any information or advice regarding anything that adversely affects him or his interests directly or indirectly. The body also provides all the assistance that the education providers for the disabled need.

    Not just that, if a disabled has been discriminated against, he can take his grievance to these bodies and they'll take every step necessary to secure justice for the person in accordance with the Disability Discrimination Act.

    It evaluates the problems of the disabled and if the current set of rules or policies are generally viewed by the disabled as disadvantageous to them, the body takes a serious note of it and conveys the position to the government. It makes independent suggestions to the government with respect to the operation of the disability laws and whether or not any changes in it are desirable. In order to reach any such conclusion it conducts extensive researches into the ground realities that affect and afflict the disabled in real life.

    From time to time, it launches campaigns aimed at spreading awareness regarding the disability and the disabled. This not only makes the people more sensitive to the needs of the disabled and what effects them but also makes the disabled feel cared and needed.

    In case a disabled is wronged, his case is taken up by the body and the guilty are brought to justice. Therefore, such commissions are not just the welfare bodies like so many NGOs, but also have real teeth that can be used, if and when the need arises.

    To get more information about disability, social security disability benefits and disability aids visit www.about-disability.com

    Disability Equipment

    Disability equipment can be very beneficial in helping the disabled individual to be confident despite their disability. This is significant because, unfortunately, many disabled individuals may suffer from low self esteem as a result of impaired mobility or other disabilities. Although these individuals may be highly intelligent, attractive and friendly their disability may still cause self consciousness. Equipment which minimizes the impact of the disability can help the individual to gain confidence by giving them a sense of independence.

    Those with limited mobility may be at an especially high risk for issues related to a lack of confidence. The ability to get around is important because mobility enables an individual to attend to simple tasks such as grocery shopping, banking, visiting friends and even just getting out of bed and going to the bathroom without the assistance of others. Individuals who have impaired mobility may not be able to accomplish these tasks without the assistance of others. As a result they may feel as though they are in some way inadequate.

    Equipment such as wheelchairs, scooters and adjustable beds are just a few of the items which can help those with limited mobility to feel more self confident and independent. A wheelchair can be a very important piece of equipment for an individual with impaired mobility. Some wheelchairs are designed specifically for indoor use, others are designed specifically for outdoor use and still others can be used both inside and outside. In selecting a wheelchair the individual should carefully consider the purposes for which they will be using the wheelchair. If the wheelchair will be used either exclusively indoors or outdoors it might be worthwhile to invest in a wheelchair specifically for indoor or outdoor use. However, if the individual anticipates using the wheelchair both indoors and outdoors it might be worthwhile to either invest in two wheelchairs or to invest in a versatile wheelchair which can be used in either location.

    Electric scooters can also be useful for those with limited mobility. These devices allow the individual to enjoy activities such as wandering through the neighborhood, shopping or visiting nearby friends. The ability to accomplish these simple activities can have a profound effect on the self esteem of the individual.

    Adjustable beds can also be useful for those who are mobility impaired. Some individuals may have some mobility but may be have difficulty with tasks such as getting out of bed. An adjustable bed can be useful in this situation because it incline and decline and also raise and lower depending on the needs of the individual. Adjustable beds are beneficial for those who are permanently disabled but may also be useful for those who are recovering from an injury or a surgery.

    Those with hearing impairments may also benefit from the use of equipment designed specifically for their disability. Hearing aids are beneficial because they allow the individual to be included in conversations without the use of an interpreter. This is important because many would likely feel as though they are a burden if they required assistance to participate in a conversation.

    Allen Maccey works and writes in Manchester and author for Disability and Health and Health Today

    "Frequent Fallers" One Disabled Perspective

    Since 1992, when ADA ~ Americans with Disabilities Act ~ took effect, we have witnessed an astronomical increase in community awareness. Vast numbers of handicapped persons who had rarely ventured out have come into public view. The sick have been assisted. Many broken have been made mobile. Physically unfortunates have been empowered.

    As Machiavelli said, ?Power corrupts.? Some of we disabled have come to expect everyone else to make way for us. I fear, the pendulum has swung from equal access rights ~ to special privilege civil liberties ~ which too many of us have come to expect. Errant expectation undermines appropriate appreciation.

    Beneath our somewhat successful surfaces, some of us were tyrants to begin with. We demanded instead of requesting. Rather than even ask, we answered with action! Our arrogance could masquerade as confidence.

    Pride comes before the fall if fall hard we must. Some of us Frequent Fallers routinely blame others for our shortcomings. But, when we no longer have control over our own bodies, we are frighteningly forced to revisit our selfish realities. After all, it's in our own best interest. Just because I am stubborn, I can ill afford to remain an ass.

    We that are blessed to abide in a nation that has mandated heretofore unheralded access to activities and services, making it unlawful to discriminate against us because of our Special needs, should be grateful for the lack of restrictions we now enjoy. Not that we deserve such liberty. We ought to recognize our acceptance as gifts from the benevolent, able~bodied who pay for our extended benefits.

    Please, do not misunderstand, nor find offense at my musings. I am grateful to those ?Early swimmers,? who recognized the desperation of handicapped individuals and broke new passages through which our citizenship now navigates. Whether motivated by humanity or purely personal gain, I am appreciative of their meeting a noble need for Equal Access. It is better now than it ever was. Access will yet improve. I hope that we who most benefit can develop a Have-a-little-patience perspective too.

    Often, the goodhearted & charitable only hope that we have paid a price, either through contributing in some fashion within our own lives, or that by our encouraging of others, we will extend like kindness where we can. That we learn to love better, if only because we can :))

    With Equal Access, we can Leap~out, Limp~out, or Lash~out!

    For some of us who are disabled, we are just fortunate to get what we have coming, instead of having to take what, by our wanton actions, we might really deserve.

    Russ Miles is the author of the novel, For Sale By Owners:FSBO. Seasoned Real Estate NAR? Broker Disabled by Multiple Sclerosis, FOR SALE BY OWNERS:FSBO ISBN 0-595-28703-4,in trade paperback, is available by phone or Internet:1-800-Authors to order direct! Very HOT?LINK Adobe e-book & hard cover editions also available FSBO at Amazon.com at Barnes and Noble and other fine booksellers. Comments: MilesRuss@Gmail.com. Russ extends personal referrals to his publisher, is a former radio talk show host, and the former owner of the Carriage House Paint & Art Stores in Vancouver,WA and Portland, OR. A motivational speaker, Russ avails himself to groups and organizations. He may be contacted at MilesRuss@Gmail.com

    Long Term Disability A Question Of Resources

    O.K. You've gotten the news from your doctor and gone through all the stages of grief over the loss of an ability. You could have arthritis or asthma, be blind or deaf...your disability could be mental or physical. This article isn't about a specific condition. Instead, let's consider what to do once we've emotionally processed the loss and found ourselves alive on the other side. How, then, do we live in a way that capitalizes on what we have left? If we can focus our attitude, ability and resources in a positive direction, most of us, regardless of disability, have a good chance at a happy, productive life.

    Disabled-vs-Handicapped: Attitude plays a huge role in our future. How do we see our own condition? I didn't like it when they changed the terminology from handicap to disability. Words mean things! Handicap means you're playing with a disadvantage, whereas, disabled means you can't be in the game. Do you want to be in the game? The first thing to do is to stop seeing yourself in terms of disability. I've known people who had productive jobs and happy families who were blind, deaf, suffered from Cerebral Palsy and amputation. Though they qualified, they refused to accept the unnecessary support of others. I also knew a man with vast creative talent and intelligence who used a criminal record and a dustup with a co-worker to qualify for full disability support. If you want to live a happy, productive life, you must begin to see yourself, not as disabled, but as having a handicap to overcome. Sure, there are severe physical and mental disabilities that require the full support of others to survive, but if you can understand this sentence, you don't have anything that severe...so start focusing on what you have rather than what you lost.

    Ability-vs-Impairment: To focus on your ability, you need to dump all the labels that classify you by your impairment. When my left arm was disabled, I decided to be right-handed. My writing was slow and sloppy at first, but I focused on the ability of my right arm rather than the impairment of my left. Don't focus on you blindness but on your hearing, smell, taste, touch and mental abilities. Take an inventory of all the skills, talents, and abilities you have left and begin to find things you can do to capitalize on them. My former abuse, addictions, mistakes, losses and chronic illnesses make me particularly sensitive and useful to people going through similar stuff. I guess, in a way, my disabilities have become my abilities. Take some time to make an honest inventory of what you've got, rather than what you lost. You probably have a lot more resources than you imagine.

    Getting Disability Information and Resources: After you've adjusted your attitude and assessed your abilities, it's time begin assembling your other resources. When I built my own home, it took me as long to arrange and collect the materials and subcontractors as it did to actually build the house. Developing resources will be a full-time job until you have a full-time job. You can learn a lot about resources on the Internet. Disability Info is a great place to begin your research on what resources are available to help you overcome your particular handicap. Collect and read everything you can find. Once you've decided on a field of interest you'd like to pursue, research everything you can find on it to figure out how you can work around your handicap. Don't forget your family and friend resources, with one caution...only accept help you actually need from people. Dependence is easy to develop but harmful for you and for the person helping.

    So, you've adjusted your attitude, focused on your abilities and assembled your resources. Now it's time to get out there and stub your toe, bang your head, fail, get up and try again...just like everyone else. Welcome to the mainstream!

    Glen Williams is founder and CEO of EHF, Inc. and Webmaster for http://www.e-health-fitness.com. He has done extensive research on personal and family health and fitness issues and has been helping and advising people on health since 1987.