Wheelchair Gloves and Carpal Tunnel Syndrome

The hands of a manual wheelchair owner hold tremendous power. They are ?the engine?, ?the steering?, and ?the brakes?. They are the heart of a chair owner?s mobility.

They also take a great deal of abuse.

A wheelchair owner?s hands are exposed to constant friction and heat generated by pushing, stopping and turning. They are numbed and desensitized in cold and wet weather. Active and athletic owners are particularly vulnerable to the damage and irritation caused by constant use and exposure. In fact, At least 18% of all wheelchair users experience blisters, abrasions, and lacerations. Many more develop thick, rough calluses.

Carpal Tunnel Syndrome: A Wheelchair User's Enemy

Even more importantly, according to studies performed by Dr H.Gellman and his team from Rancho Los Amigos Medical Center in California, 49% of parapalegic patients showed signs and symptoms of carpal tunnel syndrome, a potentially debilitating condition. Dr. Coopers and Dr. Robertson of California State University report, ?Research in this area suggests that carpal tunnel syndrome may be the result of nerve compression which occurs during forceful exertions with the hand and wrist in hyperflexion or hyperextension. Repetitive strikes of the heel of the hand against the push rim may cause pain and numbness of the thumb and fingers.?

Hands were simply not designed to withstand the repetitive impact and constant contact with wheelchair pushrims. Fortunately, there are ways to minimize the effects of constant stress and exposure to the hands. Many researchers strongly recommend the use of properly designed wheelchair gloves to minimize hand injury.

Wheelchair Gloves Can Provide Relief

Properly designed wheelchair gloves can provide:

? Protection against skin damage caused by starting, stopping and turning the wheelchair.
? Protection against injury caused by vibrations and repeated impact.
? Improved stopping and maneuverability
? Comfort in cold or wet weather

Unfortunately, many gloves marketed as ?wheelchair gloves? fail. They fall apart under intense usage, or worse, are inappropriate for the lifestyles of their owners. The requirements of an athlete can be different from a moderately active person who is using a wheelchair in cold weather, while the needs of a person with limited hand function are different from those of a person who is experiencing a great deal of vibration or impact to the hand. Therefore it is important that a wheelchair user buys high quality, gloves that were designed for their specific needs.

To meet the unique needs of active wheelchair users, Med Services Europe has launched RehaDesign Gloves. For more information click here: RehaDesign Gloves or contact us at www.NewDisability.com

Dr. Gene Emmer is President of Med Services Europe GmbH a Zurich, Switzerland registered company. In addition to RehaDesign Wheelchair Gloves(http://www.newdisability.com/gloves.htm), the gloves designed for Active Wheelchair Users) we represent Colours Wheelchairs in Europe and the Middle East. We are seeking distributors and dealers for our products. Dealers are encouraged to contact us for more information.

Pain Management

Even the word pain hurts to those of us who endure levels of pain each day. Pain management is what the doctors tell us to do. This sounds great in theory, but what does it mean, and how does one go about doing it? These are excellent questions. It probably sounds logical, but the better you are at describing your pain to others, the better you can get help in managing pain. And, pain management is the key!

The best way to document and comunicate pain is to use what I call a pain scale. I set this up in what I call a matrix, where I have a chart with four columns as follows: The left column is for pain level, from 0 being NO PAIN (right, like that's gonna happen!) and 10 being so painful that NOTHING YOU DO seems to decrease the pain level.

In the next column, you describe the pain at different levels. I use the following: 0 = No pain; 02 = low levels of pain, an Over the Counter (OTC) remedy can get rid of it; 04 = moderate pain, need double the strength of the OTC remedy to dull the pain; 06 = heavy moderate pain, need double the strength of OTC remedy, but the pain isn't dulled, and activities are curtailed (decreased); 08 = heavy pain, need something stronger than an OTC remedy, and one must sit/lie still; and, finally, level 10.

The next column is the most important one, where you describe specifically what the pain feels like, and use many VERY SPECIFIC examples of how this specific level of pain impacts your normal daily living activities. I cannot stress how important it is to be as specific, and as complete with your examples as you can be. Also, you need to guesstimate the % of time a day/week that you routinely have this pain.

Here are some examples that I use:

02 - The low levels of pain are primarily headaches and backaches. I can take an OTC remedy, and rest for about 30 minutes, and the pain goes away. This level of pain comes about 2X a week, and only lasts for the 30 minutes until the OTC remedy kicks in. This level of pain does not keep me from doing my daily activities. BUT, I need to get on this level of pain immediately, or it will increase in level if not addressed and removed.

04 - This level of pain occurs in my hands, arms, legs, feet, and head. It is like the muscles are hurting, and the joints hurt. This level gets my attention; I take double the advised level of OTC remedy, and get some hot tea, and rest lying down. This level usually takes about an hour to manage, and I have to stop whatever I am doing to lie down until I get it under control. This level occurs about 10% of the time, every other day, usually in the evening. This level makes me depressed, and when depressed, the level of pain often increases to the 08 level.

08 - I usually go straight from 04 to 08, skipping the 06 level. This level is incapacitating. It feels like the worst flu you have ever had, where EVERY muscle and joint in my body hurts! Even my teeth and scalp hurt. Light hurts my eyes; sound hurts my ears; movement makes me nauseous. I take triple the OTC remedy, and a hot shower. I have a stool in the shower where I can sit and let the hot water shower down on me until I run out of hot water (I do this after I take the meds, and try to stay in the shower until I feel the pain beginning to receed). When out of the shower, I have room temperature ginger ale (hot or cold liquids hurt my head), and lie down with soft music - no words; with a cool washcloth over my eyes in a darkened room. This level of pain occurs 2 or 3 times a week, and lasts for about 20 - 30% of the day. I cannot function in any activity at this level of pain. When the meds kick in, the pain is only reduced to the 04 or 02 level.

10 - at this level, no OTC remedy helps; the shower doesn't help; nothing helps; the pain is just reduced to the 08 level. Need greater help than an OTC remedy. This level occurs about one time each week, and literally knocks me out. Now for the last column, and, this one is very important for long term pain management. In this column, you document what, SPECIFICALLY you were doing just before this level of pain was triggered! This will help both you and your Doctor determine what will help you.

For me, the doctor really noticed the comment about depression linked with pain, and the comments about taking above recommended levels of an OTC remedy. He prescribed for me an anti-depressant, and a pain medication in lieu of the OTC remedy. These meds, in conjunction with the meds for joint pain and for the tingling pains, allows for me to regain some of the normal daily living activities.

Good luck for you in documenting your pain levels!

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.

Medicaid vs Medicare

Just like there's confusion over the difference between SSDI and SSI, there's confusion over the difference between Medicare and Medicaid.

So, here in a nutshell, is the definition of each.

Medicare - the very same health plan that retired people over 65 enjoy - can be obtained after receiving SSDI for 24 months. (NOTE: ONCE YOU QUALIFY FOR SSDI, YOU HAVE TO WAIT FOR 29 MONTHS BEFORE RECEIVING YOUR FIRST CHECK.) Medicare has two parts: Part A, which you pay for through your payroll taxes, and which covers overnight hospital bills, hospices, home health care and very limited, partial nursing home care. And Part B, three-fourths of which is paid for by federal income tax, and one-fourth ($84.00 a month in 2006, deducted from your SSDI check) by you. It pays for doctor, ambulance, emergency room, clinic and most other outpatient care (except drugs and nutritional products).

As of May 15th, 2006, Medicare now has a Part D which covers partial payment of prescriptions. Most people who qualify for Medicare select a Supplement package that covers additional things such as Doctor visits (minus the co-pay) and other things usually covered by a Health Insurance Plan. You have to pay extra for this. If you become eligible for Medicare after May 15th, 2006, you have to select a carrier for Part D. This can be included in your supplemental package, as mine is, or it can be a separate coverage.

Medicaid is run by the state and local governments. It completely covers hospitalization, clinic visits, emergency room visits, doctors' visits, hospices, home health care, nursing home stays, ambulance and outpatient prescription drugs. Medicaid has very small co-payments for prescriptions, doctor visits and some other care. While all hospitals and almost all drug stores accept Medicaid, most doctors don't, and many home health agencies, nursing homes, and hospices are also reluctant to accept Medicaid. People on SSI are eligible for Medicaid, and in most but not all of the states in the nation, SSI sends lists of recipients to the local government, which then automatically sends Medicaid cards out to them. But in some states, you must always apply separately for Medicaid at the welfare office, even if you're on SSI.

It's possible - indeed, sometimes it's absolutely necessary - to be on both Medicare and Medicaid. In that case, Medicare first pays medical bills up to whatever its rules allow, then Medicaid pays the rest. Always get Medicaid, if you can, to supplement Medicare, because with it, you'll have a way to pay deductibles and co-payments that you would otherwise face without it. Moreover, Medicaid pays for some things Medicare doesn't cover at all. Conversely, always get and keep Medicare (including Part B) even if you are already on Medicaid. Medicare pays doctors and hospitals more than Medicaid does, and therefore will make them more likely to accept you as a patient and devote adequate time to your case. Don't be afraid of the Part B monthly premium, either. Once you're on Medicaid, it will start paying the Medicare premium for you, and your SSDI check will go up by $84.00.

According to the Social Security Administration some assets are considered exempt (not countable) toward SSI eligibility such as:

? The house an individual lives in and the land it is on;

? Personal and household goods (depending on their value);

? Life insurance with a face value of $1,500 or less;

? Burial plots or spaces for the individual and immediate family; burial funds for the individual;

? A car with a current fair market value up to $4,500. The car may be of any value, however, if it has been modified to accommodate a person?s disability or if it is needed for necessary activities.

Some of an individual?s income is also not counted toward SSI eligibility such as: The first $20 of most income received in a month (from any source); the first $65 a month earned from working and half the amount over $65; food stamps; most food clothing and shelter from non-profit organizations; most home energy assistance. If the individual with a disability works, any wages used to pay for items needed for work related to the disability are not counted as income. (Source: Social Security Administration.) Since eligibility for government benefits is dependent on these financial restrictions, a person with a disability would be in jeopardy of loosing those benefits if he or she amasses any resources above the limit.

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

Asthma Education Information You Must Consider Before Marriage... If Both Of You Are Asthmatic

Love can be a very strong feeling that can survive any difficulty that comes to a relationship. Think carefully though when it comes to deciding if children are right for you if both you and your intended spouse have asthma. Hereditary issues can increase the risk of having children who will end up suffering with asthma!

Is it love if two people knowingly bring a child into the world to go through life with the physical and psychological challenges because of asthma? There are many stresses and strains on a marriage without the problems of dealing with asthmatic children.

As you already know, asthmatic children, like you, can radically change the dynamic of a family. One of the major causes of asthma are hereditary factors. In many cases, asthma is passed from a parent to the child. So, if both of you have asthma, it is most likely that one will pass it over to your children if greatly increased. This is not a certainty, but the chances of it happening are very high and something that should be considered.

It has been confirmed by some experts that a person who has a parent with asthma is three to six times far more likely to develop asthma during his life time than a person who doesn't have a parent with asthma.

If this statement is true, then it is true also that if both parents have asthma, the chance of the child having asthma goes up dramatically. Statistically speaking, 40% of children who have asthmatic parents will eventually grow up and develop asthma!

So, am I saying couples who have asthma should not get married?

Not necessarily.

Instead couples with asthma need to recognize that this may be a very real possibility in the future. They should have a complete understanding of what could be the result of their getting married and be prepared to handle it.

There is no point regretting later in life when you start having children who have asthma. It is best to know what to expect and be prepared to handle it.

Talk to your doctor and get his or her advice and be prepared on the things to do to make the condition favorable if you eventually give birth to children with asthma.

This is necessary because early detection of asthma can help protect your baby's life than if you were not aware of it at all.

If couples with asthma know what to expect, they would be better prepared to deal with it than if they were ignorant.

So, before getting married as asthmatic victims, understand what to expect regarding the possibility of asthmatic children.

Abigail Franks writes on a variety of subjects which include family, health, and Home. For More information on Asthma and Asthma treatment options go to http://www.asthma-treatment-resources.com and http://www.asthma-treatment-resources.com/asthma-education.html

Autism: Disease Disorder Handicap or Disability?

As the parent of two young children with the Autism Spectrum Disorder, I have learned a lot since the initial diagnosis with my son. Like most people, Autism used to mean that people affected by it lived in their own world. In my mind, I used to associate the picture of ?Rain Man? with ASD. Now, I now a lot more, thank God.

Nowadays, when I mention the word ?Autism? to others, the main questions that people tend to ask are: ?What is Autism? Is it a disease? Will it get better? Isn?t it when people rock and are mentally challenged? Aren?t they in their own world?? Some of these questions are on the right path while others can be downright offensive and/or plain wrong.

In fact, I even heard of people avoiding being near people with Autism simply because they thought it could be an infectious disease. Well, they could not be more wrong.

A disease is based either on a viral or bacterial infection, on the malfunctioning of body organs or even radiations. Its source is often exterior or eventually appears on its own as for ASD it is quite different. A disorder such as the Autism Spectrum Disorder is in fact a genetic condition that is part of the DNA of the individual as soon as the egg and the sperm cell became one, creating a new life.

You see, the organs such as the brain even developed differently affecting its processing of information and managing all bodily functions. In some cases, like in my son?s, the brain also does not make enough Melatonin, which is the hormone that is responsible of both the cycle and quality of sleep. This is why often; individuals with ASD suffer from sleep problems.

Since Autism is also physical, does it become a handicap? Well, first of all, being a disorder which level of severity varies as it is on the spectrum, the effects on people?s lives vary as well. For example, my son is considered non-verbal which prevents him from communicating verbally his needs, questions and emotions and may even become a safety issue. In this case, I would say that Autism can be a handicap.

My daughter, on the other hand, is verbal but has difficulty understanding questions. Well, as long as you say it differently, she will be able to give or understand a message. In her case, her problems with communication skills would be more of a disability.

What is the difference between a disability and a handicap? A disability is basically a task that you are unable to do without assistance. A handicap is something that is usually physical, that cannot allow someone to complete a task on their own or without the help of a mechanical device such as: a wheelchair, a special computer or technology, etc.

Since the Autism Spectrum Disorder is not always as obvious as a paraplegic sitting in a wheelchair, how can you identify and even assist someone with ASD? Well, unfortunately people with Autism are often misjudged as eccentric, a hermit or for children, little brats trying to get their way with their parents. And in other cases, when the parents remain calm and loving with a screaming child, they are being judged as bad parents.

Nowadays, some parents will either explain briefly to you or give you an explanatory card about their child?s Autism. Unfortunately, unless you know what Autism is because you happen to know someone that is affected by ASD, it can be difficult to identify, most of the time.

So, just in case, never judge others? behavior as you may not be aware of what lies beneath the surface.

As the mother of two young children living with Autism, both my husband and I have learned an impressive amount of information since their diagnosis was made. If you wish to learn more about Autism Spectrum Disorder, I invite you to visit the following sites: http://autism-spectrum-disorder.com , http://autism.findoutnow.org or http://autismsymptoms.blogspot.com

Assistive Technology Explained

Assistive technology, sometimes known as Adaptive Technology, includes devices or equipment used to maintain, increase or improve the abilities of individuals with disabilities. It is important to realize that assistive technology is NOT only computer programs or electronic devices. Since many people think of computers when thinking of technology, this is a common mistake. Assistive technology doesn?t have to be high-tech, but it should serve the purpose of ?assistance? and can include anything from a stick one uses to reach for something to a walker or a wheelchair, or more complex items such as environmental controls or adapted vehicles.

This means that assistive technology has existed since the first homo sapiens picked up a branch to help himself over rough terrain. Sophisticated forms of assistive technology date back for centuries as well, as the 6th century saw an image of a wheelchair being carved in stone on a Chinese sarcophagus. Today, assistive technology is available to support many common disabilities. For example assistive technology may:

?Provide help with communication, such as speech, writing and typing aids

?Help people with difficulty accessing a computer with the standard keyboard and mouse. They include software programs such as a screen reader or on-screen keyboard and hardware, such as a head operated mouse.

?Provide exercises that stimulate train and assess cognitive functioning.

?Assist with daily living such as cooking, dressing, toileting, bathing, eating

?Provide assistance with hearing or visual limitations such as flashing light system for the doorbell, hearing aids and closed caption decoders for TV.

?Provide assistance with mobility such as wheelchairs, walkers and canes.

?Help with missing or disabled limbs such as artificial limbs, braces, supports

?Allow disabled individuals to take part in sporting or leisure activities.

?Support the muscular-skeletal systems and maintain positions needed to perform desired activities, such as moulded seats, lumbar supports, and modifications to wheelchairs would fall into this category.

?Improve access to print materials such as Braille devices and translators, and large button telephones.

If you are a disabled person or you know a disabled person, perhaps you have some thoughts about assistive technology. Perhaps you know of a cool disability product or you have some ideas about what you would like to see.

A new website has been created at http://www.NewDisability.com which is meant to be a platform for communication between the disabled community and the assistive technology industry. There is a forum where you can express your feedback about all kinds of innovative assistive technology. What are your experiences? What disability products are you using that you like? What disability equipment or disability aids would you like to see on the market? Don?t limit yourself to what you already know. Tell us what you would like to see.

About the Author: Dr. Gene Emmer is President of Med Services Europe (http://www.MedServicesEurope.com). Med Services Europe markets disability products in Europe and has built the European distribution network for Colours Wheelchairs (http://www.ColoursWheelchair.com). Manufacturers and Distributors of Innovative Disability Products and Assistive Technologies are encouraged to contact us at: http://www.NewDisability.com

Chronic Fatigue Syndrome: Are You Often Tired? Searching for a Cure?

Chronic Fatigue Syndrome is probably one of the most misunderstood diseases in existence today. Many doctors continue to doubt that CFS is even a real disease. Some doctors think CFS is no more than a psychological disorder, or an extended symptom of another disease. CFS is an insidious disease with no absolute connection or root cause being yet discovered. On top of that, there are no constant biological determinants to open the way to objective measurements like brain scans or blood tests for conducting an absolute diagnosis of CFS. So clearly and frustratingly for those who suffer from Chronic Fatigue Syndrome, have great barriers stacked against them from the very beginning.

Surveys indicate that Chronic Fatigue Syndrome impacts more than four in every 1,000 Americans. According to a U.S. study, women suffered the highest rates of CFS. Individuals ages between 40 to 50, suffered CFS more often than any other age group. CFS affects both sexes of all ages, and across all ethnic and racial groups.

What are some of the most common symptoms of Chronic Fatigue Syndrome?

The most identified and common symptoms of CFS are the following:

--A severe exhaustion lasting over six months and which doesn?t get better even after sleep.

--Periods of forgetfulness, memory loss, confusion, or difficulty concentrating

--Tender lymph nodes in the neck or armpits.

--Joint pain without redness or swelling.

--Unrefreshing sleep, or unable to fall asleep

--Fatigue lasting more than 24 hours after exercise.

--Fatigue that significantly disables a person?s ability to behave and function regularly at work, at home, and in social events.

--When minimal exercise intensifies other CFS symptoms.

--Sensitivity to sunlight.

What Can I Do Right Now to Better Cope with CFS?

Here are a few steps you can begin implementing in your life for coping with CFS:

Tip #1: Before you fully accept CFS, be 100% certain that you have it. Locate a clinic that treats CFS and request a diagnostic test to determine if you have this disease.

Tip #2: Eat a well-balanced diet consisting of fresh fruits, vegetables, and fiber. Try to eliminate as much as you can sugar, salt, saturated fat, and animal protein in your meals.

Tip #3: Exercise regularly everyday but do not over do it. Stay within your limits. How? If you cannot tolerate a whole hour of walking, jogging, or cycling without adverse consequences such as sleeping more than your usual, do less.

Tip #4: If you find yourself unable to sleep soundly, consider taking a safe natural remedy that treats insomnia.

Tip #5: If you feel depressed, discouraged, and even defeated because of chronic fatigue syndrome, consider taking a safe natural remedy that treats depression.

Tip #6: CFS patients suffer from a weak immune system. That is why they catch a cold or flu so easily. Supplement your diet with something that strengths your immune system.

Tip #7: Whenever you have time, educate yourself about CFS online and offline. Type in ?chronic fatigue syndrome? in the search engine window and browse. The more you know about CFS, the better you?ll cope with this disease.

I personally have done battle with this enduring and merciless beast. I can honestly confess that Chronic Fatigue Syndrome is an affliction not easily identified, or treated. I have learned a great deal through trials and errors what works and what doesn?t. Often I have wasted my hard-earned money on products that did nothing for me.

George Alarcon at http://www.chronic-fatigue-aid.com reveals his personal CFS story, how he fought and learned to boost his energy level back to normal. He freely offers the suffering CFS patient a remarkably easy, fast-acting 2-step remedy for successfully treating CFS. Under More Help at his site you'll also learn how to treat insomnia, depression, and a weak immune system.

Control Your Chronic Pain and Reclaim Your Life

Be honest now, you're one of those people who pushes yourself as hard as you can to complete an activity, aren't you? And then suffer terribly from the pain? Well you are not alone. It's a common coping strategy for people who have chronic pain. And it's completely ineffective.

Chronic pain is much more common than most people realize. It can be caused by repeated back or neck injuries, arthritic change in joints, high level sports activity, road accidents, operations or illness. It can take over your life and make it so much less satisfying than you hoped.

If you answered yes to the question at the beginning you are a person who likes to get things done. A person who needs to finish things once they are started, who doesn't like loose ends. I used to be able to.. will be a common theme going through your mind as you determine not to give in, not to be beaten. So when you have to get something done, you do it and hang the consequences.

And oh yes, there are consequences. Your pain is much worse for the rest of the day, a few days or a week. During this time you are limited in what you can do and feel frustrated at your inability to function in what you see as a normal manner.

This is the Over-Under Activity Cycle, where you swing from doing too little to doing too much, trapped in an endless cycle. It is a counterproductive behaviour which can make you more disabled with time.

And yes, there is a way you can break out of this cycle and reclaim some of your life. It's called Pacing. Follow these simple rules and you too will start to get your control back.

1. Choose an activity you tend to overdo and suffer badly afterwards. Choose your worst one.

2. Time (yes, with a watch!) how long you can do the activity before the pain comes on or worsens. You might need to do it a few times to get the average right.

3. Take 20% off that average time and record that as your quota.

4. Next time you do the activity, do not go over your quota. Stop when the time is up no matter where you are in the activity.

5. When you stop, rest for at least twice your quota time. Do another activity if you want, but not related to the original one.

6. Continue with your paced activity sessions until you have finished the task. Sometimes you may have to leave longer periods between sessions to avoid a pain increase. And you may not get it all done in one day.

7. When you can do the paced time without problems, decide to increase your quota by no more than 10%.

8. Always decide how much of an activity you are going to do before you start.

9. Stick to the times, not how you feel. Your emotions are a trap, don't let them mislead you.

10. Beware good days in particular, that's when you get overconfident and tend to push too hard.

Is this process easy? No! It's very hard to do and very annoying. It goes against all the ingrained habits you may have been brought up with. But my patients say it's the single most useful pain management strategy my team teaches them.

Yes I know, things have got to be done. And it is the Eleventh Commandment after all, that thou shalt not leave anything undone. Or at least it seems that way. However, you can find a better way, a way which puts you in control of your life. You do not want your pain in control. I could never do that people say. I know it's hard, but we all have the choice of how we behave and you can choose to do things the old way or try something new.

To be really good at pacing you need to accept the difficulties in your life. That's not the same as resignation to your fate. None of us are as we were, and we often have to accept the limitations which our pain or other difficulties place upon us. You cannot break through the Pain Barrier, it's too deep to get through. Work with, not against, your body and you will get results.

Pacing is a simple concept but a complex and difficult skill. There's a lot more to it but you can apply these principles today and improve your life. There's a lot more to it than I can cover in a short article, for further information see below.

Jonathan Blood Smyth is author of Secrets of Pacing and a Superintendent Physiotherapist in an NHS Hospital in the South-West of the UK. With over 15 years experience of managing orthopaedic conditions and looking after joint replacements, he now specializes in the management of chronic pain conditions. For more information on these and other subjects see The Physiotherapy Site. Copyright J Blood Smyth 2006.

SSDI vs. SSI

I have had, and continue to have, numerous questions about the difference between SSDI and SSI. Summarized below are the key differences.

The SSDI and SSI programs are the largest of the Federal programs that provide assistance to people with disabilities. Generally, the medical requirements for disability eligibility are the same under SSDI and SSI programs, but the way these programs are funded differs.

The SSDI program is funded by the Social Security taxes paid by employed individuals. Therefore, the SSDI program is based on a person?s work experience. The SSI program is funded by general tax revenues and pays benefits to people with disabilities who have limited income and assets, and is based on a person?s financial need.

SSDI: Social Security Disability Insurance is an insurance program that sends out monthly checks to disabled workers who have paid Social Security taxes (called FICA on your paycheck stubs). You must have worked for at least 5 of the past 10 years before you apply to be currently insured, or covered, but the minimum time is less if you're under age 31 when you become disabled. The amount you get depends upon how much you have paid in taxes and for how long, since SSDI is an insurance - not a welfare - program. In general, the higher your earnings have been and the longer you have earned them, the higher your SSDI check will be. Benefit amounts vary from a low of about $200 monthly to a high of about $1,600; the average SSDI check is about $850, but this average does reflect low wages paid in the South, in rural areas, and in small towns.

SSDI checks start at the end of the fifth month after the date of onset, the day you became disabled under the Social Security rules by meeting the medical rules as well as not engaging in substantial gainful activity (SGA?). The number of work credits you need for disability benefits depends on your age when you became disabled. Generally you need 20 credits earned in the last 10 years ending with the year you became disabled.

However, younger workers may qualify with fewer credits. The rules are as follows:

? Before age 24?You may qualify if you have six credits earned in the three-year period ending when your disability starts.

? Age 24 to 31?You may qualify if you have credit for having worked half the time between age 21 and the time you become disabled. For example, if you become disabled at age 27, you would need credit for three years of work (12 credits) out of the past six years (between age 21 and age 27).

? Age 31 or older?In general, you will need to have the number of work credits shown in the chart shown below. Unless you are blind, at least 20 of the credits must have been earned in the 10 years immediately before you became disabled.

Born After 1929, Become Disabled At Age Credits You Need

31 through 42: 20
44: 22
46: 24
48: 26
50: 28
52: 30
54: 32
56: 34
58: 36
60: 38
62 or older: 40

The easiest way to check your financial eligibility is to request a Summary of Earnings and Benefits. You can obtain a request form as well as apply on-line at http://www.ssa.gov/howto.htm and click on: ?How To Request a Social Security Statement of Earnings and Benefits.? You may also obtain a form to request the Statement at any Social Security office and most post offices. Ask for: ?Request for Social Security Statement (SSA-7004).?

SSI: Supplemental Security Income is a welfare program for disabled people who meet the Social Security medical and SGA disability rules and whose income and assets are below the eligibility levels. SSI allows assets of $2,000 liquid; a separate bank account of up to $1,500 for burial; a vehicle of any value, if used to go to medical care; household furnishings; certain self-employment business equity and equipment; and a lived-in home of any value. The SSI income level in 2002 is $545 per month (but it's higher in most wealthy industrial states, which supplement this amount). All gross income counts against this level: SSDI, earnings, pensions, gifts, contributions, bank interest, dividends, veterans' benefits, etc. If your SSDI check is below the SSI level, you can get SSI as well as SSDI. Before comparing gross income to this level, SSI disregards (i.e., doesn't count) $20 per month of any income, out-of-pocket Impairment Related Working Expenses (IRWEs: medical costs you pay to enable you to work) and $65 and half the rest of any earnings. If the resulting countable income is above the SSI income level (again, $545 in most---but not all-- states), you're not eligible. If it's computed to be less, you get an SSI check for the difference between your countable income and the SSI level - and, as a fringe benefit in most but not all states, a Medicaid card.

SSI?This is known as Title XVI (16) Supplemental Security Income. This program is for people who either:

? Have not paid enough quarters (earnings) into Social Security for any reason.

? Have limited resources and income.

Although you must be disabled according to SSA?s definition, you must first meet SSA?s strict resource eligibility test prior to your medical condition being considered. If your resources exceed SSA?s limit, you cannot collect SSI irrespective of your medical disability.

Do You Qualify For SSDI???

The Social Security Administration has provided this online test for people to use so that they can decide for themselves if they are eligible.

BENEFIT ELIGIBILITY SCREENING TOOL (BEST)

https://s044a90.ssa.gov/apps12/best/benefits/

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

Rigid Versus Folding Wheelchairs Explained

Disabled athletes are rarely seen competing in a folding wheelchairs. Why? The reason is increased performance of rigid wheelchairs. All athletes seek to optimize performance. But performance is not only important for sports wheelchairs, it is important for active everyday users as well. A well designed rigid wheelchair becomes part of the body of a disabled user allowing easier access and freedom of movement. What are the features of a rigid wheelchair that give superior performance?

?Reduced Maintenance and Weight: Folding chairs have lots of movable parts that undergo strain. These parts must often be regularly adjusted or replaced to keep the chair in alignment. Because of this strain, thicker walled aluminium is required and therefore the wheelchairs are usually heavy. Rigid wheelchairs have fewer movable parts and fewer things to go wrong. Rigid wheelchairs are generally more durable and age better than folding wheelchairs.

?Much of the energy from the push on the wheels is lost in the flexing parts of the folding wheelchair. Since the rigid wheelchair has fewer movable parts, most of the energy from the push on the wheels is translated into forward motion. In short, the rigid wheelchair may be easier to push than a folding wheelchair.

?Due to the need to fold, the folding wheelchair design might not be optimized for performance. For example, the casters of the folding wheelchair are usually placed well behind the foot-rest, in order to allow the wheelchair to close properly. This design puts a lot of weight on the casters. With the rigid wheelchair, the distance between the footrest and casters is usually much shorter; placing more of the weight on the rear wheels. Less weight on the casters makes the rigid wheelchair easier to turn.

?Because rigid wheelchairs are lighter and more manuverable than folding wheelchairs they, perform better, that is, they are easier for the user to move in. But this is not an advantage only for athletes. Imagine a wheelchair user going up a wheelchair ramp without assistance. This can be more difficult in a heavy folding chair, than in a manuverable, ultra-light, which can be lighter by 10kg or more.

?In summary, due to weight, design, and fewer moving parts, the performance of a rigid wheelchair is usually better than a folding wheelchair. This difference may become even more noticeable as the wheelchairs age.

Performance is only one of the advantages of a rigid wheelchair over folding wheelchairs. Below is a partial list of advantages of rigid wheelchairs over folding chairs:

Better Body Fit (Design): The primary design of a rigid wheelchair is to fit the body of the user. The primary design of a folding wheelchair is to fold. Folding wheelchairs are generally boxy, while rigid wheelchairs conform to the shape of the body. For example, with a rigid chair, one can taper the design to conform to the body shape (large at the hips, narrow at the knees) which can hold the users? body in place. Also the frame between the knees and footrest can be tapered (wider at the knees, narrow at the feet) holding the feet in place. With a folding chair, you can not taper it or it would not close completely.

After Market Adjustments: Rigid wheelchairs generally have more configurations and adjustments then folding chairs. Most folding wheelchairs have limits in their configurations and adjustments. For example, many folding wheelchairs do not allow for adjusting the angle between the backrest and the seat.

Independence: Users can easily make transfers from rigid wheelchairs into some cars independently. With a folding wheelchair, the user usually requires a companion to fold the wheelchair and put it in the car trunk. With some forms of rigid wheelchairs, the user can transfer into the car and from the inside of the car, remove the two wheels, fold down the back rest and bring the wheelchair inside the car and place it either in the back seat or on the floor. An independent transfer would be more difficult in a folding wheelchair.

Esthetics: Some rigid wheelchairs are designed to be attractive. Folding wheelchairs are rarely considered attractive, only functional

What is the advantage of a folding wheelchair? Mainly there is one advantage: a folding chair can be stored in a trunk of an automobile without removing the wheels. Rigid wheelchairs are not for everyone, but many people who are now using folding wheelchairs are better off in a rigid wheelchair.

Who is the right customer for a rigid wheelchair? Someone who:

?Has good upper body strength

?Wants to be independent

?Is young and active (5-50 years)

?Sees their wheelchair as part of their body and not just a piece of furniture

Who is the right customer for a folding chair? Someone who:

?Will never be independent or has no upper body strength

?Has minimal upper body strength or coordination

?Is very young (0-4) or older (60-90)

In summary: A rigid wheelchair is generally purchased for the users? convenience. Folding wheelchairs are generally purchased for companions? convenience.

Dr. Gene Emmer is President of Med Services Europe (http://www.MedServicesEurope.com). Med Services Europe develops sales in Europe for Medical Manufacturers. Med Services is the Europe Representative for Colours Wheelchairs (http://www.ColoursWheelchair.com). Colours is a US manufacturer of ultra-lightweight, active Wheelchairs. Med Services Europe has recently launched ?New Disability? a website dedicated to innovative disability products and assistive technology. Manufacturers of innovative disability products who are seeking distributors in Europe are encouraged to contact us at http://www.NewDisability.com.

Stroke Rehabilitation: A Novel Treatment Pays Off

In a landmark study, researchers at the University of Alabama at Birmingham used a randomized controlled trial -- the gold standard method for evaluating the effectiveness of a treatment -- to show that immobilizing the good arm of stroke patients and intensively exercising the weakened arm actually improved recovery, even when performed long after the stroke occurred. At one level, randomized controlled trials in the field of rehabilitation medicine have been so rare that the publication of each and every one should be applauded. At another level, the outcome of this study is so satisfying in terms of what we think we know about brain physiology (function) that even if the results turn out not to be true, they ought to be.

A controlled trial is one in which there is a comparison group of patients that is either untreated or is treated differently. When a controlled trial is also randomized, it means that upon entering the study, participants agree to be assigned to one group or the other based on the equivalent of a coin-toss. Randomization eliminates bias that might otherwise come from (knowingly or unknowingly) assigning more promising patients to one group and less promising patients to the other.

Publishing their results in the March 2006 online issue of Stroke, a medical journal, Edward Taub, PhD, and co-workers studied 21 patients treated with constraint-induced movement therapy (CI) and compared their outcomes to those of another 20 stroke patients who received placebo treatment.

In strokes a loss of circulation damages a portion of the brain, resulting in impairment of whatever mental or bodily function that part of the brain controls. Strokes often cause weakness in an arm with or without concurrent numbness. Strokes are the leading cause of long-term disability in the U.S.

The researchers included stroke victims in their study who had mild to moderate impairment in use of their affected arms, but excluded those with severe impairment. The research subjects varied widely in age, averaging in their fifties. The investigators selected patients whose stroke had occurred a minimum of one year earlier with an average interval between stroke and treatment of 4.5 years. Patients with concurrent numbness were included, but those with poor walking or balance were excluded, as were patients with excessive confusion or too much additional impairment caused by other medical conditions.

The CI treatment was administered over a 2-week span, during which the good arm was immobilized about 90% of the time with an arm-sling and a hand-splint. CI patients had 10 weekday sessions with therapists, lasting 6 hours each. During those sessions, patients received one-on-one therapy that was individualized to their needs and abilities and involved specific, practical tasks of gradually increasing difficulty. The therapists praised patients each time their performances improved even just slightly. By contrast, placebo-treated patients received a more general program of physical fitness, cognitive and relaxation exercises over the same schedule.

The abilities of CI and placebo-treated patients were compared in two main ways. In one, the research subjects were videotaped in the laboratory while attempting specific tasks like holding a book, picking up a glass and brushing teeth. Their performances were rated by viewers who were purposely not told which treatment the subject received. The other rating, called the real world outcome, came from structured interviews of the patients and their caregivers concerning performance outside the treatment facility.

The researchers found significant improvements in CI-treated patients compared with both their own initial abilities and those of patients receiving placebo treatment. The CI patients showed a moderate improvement in their laboratory skills and a large improvement in use of the affected arms in their daily lives. Improvement was still evident 4 weeks after treatment, and even after 2 years in the 14 of 21 CI patients who could be retested at that time.

The researchers interpreted the improvement as due to two factors. The first factor, probably more important for faster gains, was in overcoming learned non-use of the weaker arm. The idea is that after a stroke, patients quickly learn to avoid using the weaker arm to a greater extent than its impairment might warrant, and CI training forces them to put it back into action. The second suspected factor, developing more slowly, was neural plasticity or actual rewiring of the brain. In neural plasticity surviving brain cells -- previously uninvolved or less involved in controlling use of the arm -- attempt to make up for the lost brain cells either by creating new contacts with other brain cells or by modifying the effectiveness of existing links.

In 1992 researchers at the Hammersmith Hospital in London used positron emission tomographic (PET) scans to examine patterns of brain use in stroke patients. PET scans are good at showing which parts of the brain are most engaged by specific tasks. Investigators compared PET scans in 10 patients who recovered from a stroke to those of 10 patients who never had a stroke. In this study subjects repeatedly moved one hand (which in the stroke patients was the affected hand) while their brains were being scanned. Compared to non-stroke patients, stroke patients used more areas on both sides of the brain to perform the requested movements, as if the surviving brain cells were trying to fill in for their fallen comrades.

Taub and collaborators at the National Institute of Neurological Disorders and Stroke used similar methods to compare patterns of brain activation in 9 CI-treated stroke patients with those in 7 less-intensively treated stroke patients. In this 2003 study, CI-treated patients showed a shift in the extent to which different parts of the brain participated in moving the fingers of the weakened hand. Thus, CI treatment seemed to modify the brain pathways responsible for the finger movements.

(C) 2006 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 websites at: http://www.cordingleyneurology.com and http://www.neurologyarticles.com

Make The Best Use Of The Services Of Disability Lawyer

Even under the most perfect terms and conditions, to get your claim settled in a scheme like Social Security Disability is not that easy. Only when you begin to fill up the prescribed form and read the listing of the documents required- that too, when you are disabled, you feel the necessity to engage the services of a disability lawyer.

If your claim is once rejected, you don't wish to take a chance at the time of the appeal. In filling up any form, the technical points are more important and all such technicalities can be solved with the assistance of the lawyer.

The obvious benefits of engaging a lawyer to look after your claim are:

Better chances of winning the benefits- the lawyer will not miss any likely benefit.

The lawyer is an experienced man in the line. He is a skilled personnel and has dealt with such cases in the past.

He has trained staff for all the departments.

He makes smooth and quick movement of the file possible. Your precious time and expenses on conveyance is saved. Some lawyers don't charge anything, unless you receive your benefits. To that extent, you can consider their services free.

If you have any doubts, he has professional answers.

Take a note, Social Security and Social Security disability should not be confused. The former is a retirement plan while the later is a plan to assist the seriously disabled. Some of the disability plans drawn by the Government of USA are indeed unique and show a high sense of social responsibility. They are discussed below.

Cincinnati Social Security Disability Physical and mental disability is the last thing one wants to live with. Along with physical pain, you suffer emotionally in every moment of your life. You compare persons with normal health with that of yours and suffer all the more. You can support yourself and can do anything for the welfare and happiness of your loved ones. Under this Scheme, the Federal Government has made two separate provisions to support such children/ individuals.

Pittsburgh Social Security Disability USA is the land of plenty and prosperity, and this opulence of the materialistic civilization has also showered them with sufferings of many types. Those suffering from disabilities and impairments resulting from chronic diseases, accidents and congenital defects are in plenty. The Americans with Disabilities Act passed in the year 1990, provides regular income to such persons by the Federal Government.

Do not be under the false notion that you are entitled to get social security disability benefits, only in case of accidents and other very serious ailments. If you have recurring attacks of any one of the following, contact your disability lawyer and he will be able to find a way out to secure you the benefits under the existing legal provisions. We are listing below, some of them only:

Aids, arthritis, autism, bipolar disorder or manic depression, cancer, cardiomyopathy, cerebral palsy, clinical obesity, congestive heart failure, cystic fibrosis, depression, dizziness, epilepsy, fatigue, head trauma, hepatitis, learning disability, memory loss and mental retardation.

To get more information about disability, disability insurance and disability and civil rights visit http://www.about-disability.com/

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.

The Appearance of Disability What Does Disability Look Like After All?

I found a remark on a blog recently and the remark basically said this (I'm paraphrasing): I'm tired of people who aren't disabled but try to get benefits from the government.

I guess it goes without saying that, today, we live in a fairly judgmental climate. And regarding individuals with disabilities, perhaps it has always been that way. However, for those who think like the person who made the statement above, consider the fact that many individuals with disabilities have conditions that allow them to work, but only on a limited basis, or for short durations. In other words, just because you see someone at the grocery store pushing a cart, don't assume that they're not being truthful about being disabled. For all you really know, after making a short trip to the store, they may be flat on their back when they get home, and in a considerable amount of discomfort.

This example, of course, raises the question: Can you necessarily see a disability? And the answer is no, of course not. And, in fact, when it comes to most mental and physical impairments, even when the condition is truly disabling, the average watcher won't be able to determine that's the case. Contrary to myth, most disabilities are not apparent to the untrained eye, making them effectively invisible.

To use a personal example, I have an in-law with bipolar disorder. My brother-in-law has had electroconvulsive therapy on an outpatient basis for nearly two years, which is fairly significant as far as treatment goes (this was enough to qualify him for social security disability benefits). By any thoughtful consideration of his impairment he is certainly disabled. But you can't see his various deficits when you see him putting gas in his car, or when he is picking up milk at the grocery store. In the same manner, you can't see the disability of a person who has depression, anxiety, fibromyalgia, or migraines.

The mere concept that a person with disabilities should have to pass a visibility test belies a depressing degree of ignorance on the part of those who are not disabled. That a person with a physical disability should have to possess a limp, or a person with a mental disability should have to carry on a conversation with himself in public before a non-disabled person can accept that a disability, in fact, exists shows just how far the disability rights movement still needs to go.

The author of this article is Tim Moore, who also publishes answers to questions about social security disability.

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.

"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

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.