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Archive for the ‘Impairments that Affect Multiple Body Systems’ Category

Myelodysplastic Syndromes and Getting Social Security

Thursday, February 9th, 2012
BONE MARROW: THERAPY-RELATED MYELODYSPLASTIC S...

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Myelodysplastic syndromes, as the name implies, are not one disease. Myelodysplastic syndromes are a group of disorders that are evidenced by your bone marrow not producing enough healthy blood cells.

Myelodysplastic syndromes are diseases that affect your bone marrow and blood. When your bone marrow is functioning like it should, it produces cells that are immature (blood stem cells) that go on to become mature blood cells with the passage of time. You may have been diagnosed with one of the myelodysplastic syndromes. As a result, you may meet the requirements for social security disability benefits like SSDI or SSI. The thing to do is to turn to one of the social security attorneys at socialsecurityhome.com to check this out. The social security lawyers at socialsecurityhome.com know about what it takes to get disability benefits.

Your blood stem cells may become either a lymphoid stem cell or a myeloid stem cell. If your blood stem cell develops into a lymphoid stem cell, it will eventually become a white blood cell.

Myeloid stem cells may go on to become any one of three kinds of mature blood cells. They may develop into:

Ÿ  White blood cells, which fight against disease and infection

Ÿ  Platelets, which work to stop bleeding by leading to the formation of blood clots

Ÿ  Red blood cells, which transport oxygen and other nutrients to all of the tissues of your body.

Myelodysplastic syndromes are marked by your blood stem cells failing to become mature, healthy platelets, white blood cells or red blood cells. The blood stem cells that do not mature are known as blasts.

These blasts do not work in the way normal, healthy blood cells do. They either die soon after they get into your blood or while they are still in your bone marrow. What this results in is less space for red blood cells, platelets and white blood cells that are mature and healthy to form in your bone marrow. This, in turn, may lead to things like anemia, easy bleeding or infection.

There are several kinds of myelodysplastic syndromes. Each one of these types of the disease is characterized by not having enough kinds of healthy blood cells in your blood or bone marrow.

Myelodysplastic syndromes are caused when something occurs that disrupts the proper making of blood cells in your body. In some cases there is no known cause for myelodysplastic syndromes. In other instances, these diseases result from chemical exposure or treatments for cancer like radiation and chemotherapy.

There are some risk factors that may increase your likelihood of being afflicted with myelodysplastic syndromes. Some of these include:

Ÿ  Being male

Ÿ  Exposure to heavy metals

Ÿ  Being over the age of 60

Ÿ  Exposure to certain chemicals

Ÿ  Treatment with radiation or chemotherapy.

There are several signs and symptoms that myelodysplastic syndromes may cause. Some of these are:

Ÿ  Getting infections frequently

Ÿ  Fatigue

Ÿ  Petechiae (pinpoint-sized red spots right beneath your skin that result from bleeding)

Ÿ  Shortness of breath

Ÿ  Bruising or bleeding easily

Ÿ  A pale appearance due to anemia

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Fanconi Renal Tubular Syndrome and Receiving Social Security Disability

Saturday, November 5th, 2011

Fanconi renal tubular syndrome refers to a group of kidney problems that are due to a variety of seemingly unrelated disorders. These kidney difficulties lead to thirst and excessive urine production. This brings about deficits of potassium, calcium, magnesium, water and other substances in your body. This, in turn, may cause stunted growth and bone disease.

When your kidneys function in the way that they ought to, they maintain your blood’s acidity, water and salt in balance, and they cleanse your blood. The acidity, water and salt that your body does not require is placed into urine. This is so that it may get out of your body. The water, salt and acidity that your body has to have is left behind in your blood.

This essential work of your kidneys is performed in two steps. First, your blood is filtered through a kidney structure that contains small holes that enable the large molecules and cells to stay in your blood. Second, some of the small molecules in the filtrate that your body has to have are reabsorbed and placed back into your bloodstream.

Fanconi renal tubular syndrome is marked by a defect in this second step of reabsorption. As a result, substances that are supposed to be reabsorbed, such as phosphate, calcium, bicarbonate, glucose, potassium, magnesium, small proteins and water are lost. What this results in is your body becoming overly acidic.

Fanconi renal tubular syndrome can be the result of genetic defects. This syndrome may  also be brought about by different environmental elements.

Fanconi renal tubular syndrome may also be caused by several genetic disorders. Some of these are:

  • Tyrosinemia
  • Wilson disease
  • Lowe syndrome
  • Galactosemia
  • glycogen storage disease
  • Medullary cystic disease
  • Hereditary fructose intolerance.

There are also several environmental factors that may lead to Fanconi renal tubular syndrome. Some of these include:

Ÿ  Exposure to heavy metals like uranium, mercury, lead, cadmium and platinum

Ÿ  Exposure to substances, such as toluene, the amino acid lysine when taken as a nutritional supplement, paraquat and Lysol

Ÿ  Kidney transplantation

Ÿ  Certain drugs like outdated tetracycline and gentamicin.

There are several signs and symptoms that you may have, which may be an indication of Fanconi renal tubular syndrome. Some of these are:

  • A decrease in the levels of calcium and phosphate in your blood, along with excessive blood acidity and increased levels of chloride in your blood
  • Anorexia nervosa (eating disorder)
  • Vomiting
  • An increase in the levels of phosphate, calcium, glucose, uric acid, amino acids and protein in your urine
  • An excessive amount of urination and urine being produced
  • Dehydration
  • An excessive amount of thirst

You may have been diagnosed with Fanconi renal tubular syndrome. If this is your situation, you may qualify to receive social security disability benefits like SSI or SSDI. A smart move on your part would be to consult one of the social security attorneys at socialsecurityhome.com about this. The social security attorneys at socialsecurityhome.com are standing ready to help you receive the disability benefits that are rightfully yours.

 

 

 

 

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Developmental Reading Disorder and Receiving Social Security Disability

Wednesday, October 26th, 2011

One of the most important skills that anyone can come to possess is the ability to read. In many different areas of life and learning, reading is a skill that is necessary and basic.

Developmental reading disorder is an impairment in your brain’s capacity to translate written images that are taken in by your eyes into meaningful language. Developmental reading disorder is a learning disability that may hinder your ability to read, spell, write and sometimes speak. If you have been diagnosed with developmental reading disorder, you may meet the requirements for obtaining social security disability benefits like SSDI or SSI. The SSI and SSDI attorneys at socialsecurityhome.com are the ones who can help determine this. Do not delay or put this off. Contact socialsecurityhome.com, today.

Developmental reading disorder is referred to in other ways. It is also known as specific reading disability and dyslexia.

There are different types of developmental reading disorder. Some of these are:

  • Primary developmental reading disorder – This form of the disorder is marked by a dysfunction of the left side of your brain (your cerebral cortex).
  • Secondary developmental reading disorder – This type of the disorder is believed  to be brought about by hormonal development in the early stages of fetal development.
  • Trauma developmental reading disorder – This kind of the disorder is usually the result of some type of trauma or brain injury to the part of your brain that controls reading and writing.

Developmental reading disorder is a common condition in the United States. It is estimated to affect somewhere around 2 to 30% of the general population of the United States. The most accepted estimate for this disorder is about 10%.

As just mentioned above, trauma developmental reading disorder is brought about by some kind of trauma or brain injury to that part of your brain that controls reading and writing. The other types of developmental reading disorder look as if they are caused by a malfunction in certain parts of your brain that have control of language. It is also possible that genetics (heredity) may have a part in leading to developmental reading disorder due to the fact that the disorder frequently runs in families.

There are several different signs and symptoms that may indicate that you have developmental reading disorder. Some of these include:

  • Reading at a level that is well below your expected level
  • Seeing letters or words in reverse when you read
  • Having problems processing and understanding what you are hearing
  • Having difficulty with spelling
  • Having problems with rhyming
  • Having problems with remembering the sequence of things
  • Not having the ability to sound out the pronunciation of an unfamiliar word
  • Having difficulty following more than one command at a time
  • Having trouble hearing and seeing similarities and differences in the letters and words that you look at
  • Having problems with learning a foreign language
  • Having difficulty with comprehending and understanding instructions that are given fast
  • Having problems determining the meaning (content, idea) of a simple sentence.

 

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Degenerative Spine Disease and Receiving SSDI or SSI Disability

Wednesday, October 19th, 2011
receiving social security because of degenerative spine disease

Image via Wikipedia

When it comes to degenerative spine disease, there is a good deal of misunderstanding and confusion about what it is. Some of the confusion centers around the fact that degenerative spine disease sounds like a disease that gets progressively worse. However, the term, “degenerative spine disease,” is really a misnomer.

The word degenerative carries with it the idea that something is going to get worse as time goes by. This would mean that degenerative spine disease would get progressively worse with the passage of time. However, the pain that comes as a result of degenerative spine disease often times gets better instead of worse as time goes by.

Also, degenerative spine disease is not really a disease, but rather a condition that at times can produce pain from damage to your spine. Finally, there is misunderstanding and confusion concerning degenerative spine disease due to the fact that medical professionals do not agree on what does or does not constitute a diagnosis of degenerative spine disease.  Because of these few factors, it is a smart choice to enlist the help of a SSI or SSDI disability lawyer when choosing to file for disability.  An attorney can work with you to strengthen your case and give your disability the validity it deserves.

Your spinal discs are soft, compressible discs that function to separate the interlocking bones that compose your spine. These discs work in a way that is similar to shock absorbers for your spine. These discs enable your spine to flex, bend or twist.

As you grow older, these discs experience wear and tear, or they deteriorate. This is something that takes place in all of us as we age, but not everyone experiences pain along their spine with the deterioration of these spinal discs.

Degenerative spine disease may occur at any point along your spine. However, usually, this condition takes place in your neck (cervical region) or lower back (lumbar region).

As mentioned above, degenerative spine disease is a part of the aging process as you grow older. In fact, it has been said that degenerative spine disease is as sure as death and taxes, but, again, not everyone has pain with these degenerative changes in the spine.

The signs and symptoms that result from degenerative spine disease usually consist of neck pain or lower back pain, but it is not the same in everyone. Some people experience no pain, while other people with the same degree of spine damage have to endure severe pain that greatly affects and hinders their daily activities.

The location of the pain that you have with degenerative spine disease depends on where your affected disc is. For example, If you have a disc that is deteriorating in your neck, you may have pain in your arm or neck. If the disc that is affected is in your lower back, you may experience pain in your buttocks, leg or back.

The pain that you experience with degenerative spine disease, many times, becomes much more intense when you twist, bend over or reach up.  It is also possible that you may have numbness or tingling in your leg or arm with degenerative spine disease. The effects of degenerative spine disease and/or complications that develop from it can be disabling and debilitating.

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Barbeau’s Disease and Receiving Social Security Disability

Sunday, September 11th, 2011

Muscular dystrophy is a term that is used to designate a group of hereditary, genetic muscle diseases. These diseases lead to progressive muscle weakness in the muscles that enable you to move.

Muscular dystrophy means that you have missing or incorrect information in your genes. There are certain proteins that you need in order to have healthy muscles. Muscular dystrophy keeps these proteins from being produced. Muscular dystrophy is something that you inherit from your parents. It is not contagious. You cannot “catch it” from someone who has it.

Muscular dystrophy causes your muscles to get weak over time. People who are afflicted with muscular dystrophy may gradually lose the ability to do things that most of us take for granted like walking or sitting up. These problems that are caused by muscular dystrophy can begin at birth or shortly after. However, they can also take place later on in childhood, adolescence or adulthood.

There are several different forms of muscular dystrophy that affect different muscle groups in different ways. Barbeau’s disease is one of the kinds of muscular dystrophy.

Barbeau’s disease is usually an adult form of the disease. The onset of Barbeau’s disease is usually when you are in your 40s or 50s. It can even occur up to around the age of 70.

Little was known about what causes any kind of muscular dystrophy until the 1980s. Then, researchers found out that it is caused by a mutated (defective) gene. There is an insufficient amount of dystrophin because of the defective gene. Dystrophin is a protein that aids in keeping your muscle cells intact. In the case of Barbeau’s disease, there is a faulty gene that is believed to make extra chemical material that causes the development of clumps in your muscle cells.

Barbeau’s disease progresses slowly. The first sign or symptom of Barbeau’s disease is usually muscle weakness of your throat and eyelids. You may have difficulty swallowing. Your may have trouble keeping your eyes open or with drooping eyelids.

As Barbeau’s disease advances, you may have other signs and symptoms. Some of these include:

  • Characteristic face
  • Progressive muscle weakness in your limbs
  • Progressive weakness in your facial muscles
  • Progressive ptosis (drooping of your eyelids)
  • Weakness and wasting (loss of muscle tissue) of your tongue.

 

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Dystrophia Myotonica and Receiving Social Security Disability

Thursday, September 8th, 2011
Histopathology of gastrocnemius muscle from pa...

Image via Wikipedia

Muscular dystrophy refers to a group of genetic (hereditary) muscle diseases. Progressive muscle weakness in your muscles that enable your body to move is what characterizes these diseases.

Muscular dystrophy involves incorrect or missing information in your genes. Proteins are stopped from being produced that are needed for healthy muscles. Muscular dystrophy is a disease that is passed down to you from your parents. It is not something that you can catch from someone who has it. Muscular dystrophy is not contagious.

Muscular dystrophy weakens your muscles with the passage of time. You may gradually lose your ability to do things that most people do not even think about, like sitting up or walking. These difficulties may have originated when you were a baby, or they can start in childhood, adolescence or adulthood.

There are several different kinds of muscular dystrophy that affect different muscle groups in different ways. Dystrophia myotonica is one of the forms of this disease.

Dystrophia myotonica is the most common kind of muscular dystrophy that starts in adulthood. It usually develops between the ages of 20 and 40. However, there is an infantile form of dystrophia myotonica. In fact, this disease can begin at any age from birth to old age.

Until the 1980s, there was not much known about what causes any type of muscular dystrophy. Then, researchers discovered that muscular dystrophy is caused by a defective gene. Not enough dystrophin is made because of the faulty gene. Dystrophin is a protein that helps keep your muscle cells intact. In the case of dystrophia myotonica, there is a repeated section of DNA on either chromosome 3 or chromosome 19.

The progression of dystrophia myotonica is slow. The disease can span 50 to 60 years.

The first signs and symptoms of dystrophia myotonica are usually generalized weakness and loss of muscle tissue (muscle wasting) in your hands, forearms, lower legs, face and neck. This is in conjunction with difficulty relaxing muscles after contracting them. Other signs and symptoms that you may experience are:

  • Mild diabetes
  • Difficulty breathing and swallowing
  • Frontal balding in men
  • Dizziness or fainting
  • Inability to concentrate
  • Problems with your digestive tract like diarrhea and constipation
  • Daytime sleepiness
  • Difficulty sleeping well at night
  • Clouding of the lenses of your eyes (cataracts).

You or your loved one may have decided to apply for the financial help that you need from the Social Security Administration by applying for Social Security disability benefits or disability benefits because of the disability that has resulted from dystrophia myotonica and/or complications that have been brought about by it or other ailments that you have in conjunction with this disease. You may have already applied and been denied by the Social Security Administration.

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MD and Receiving Social Security Disability Benefits

Thursday, September 8th, 2011
Collage of varius Gray's muscle pictures by Mi...

Image via Wikipedia

Most people have heard of MD (muscular dystrophy) because of the Labor Day telethon that is held each year. However, other than this, most people do not know much about MD.

 

MD refers to more than one single disease. MD is used for a group of hereditary (genetic) muscle diseases that result in progressive muscle weakness in the muscles that enable your body to move.

People with MD have incorrect or missing information in their genes that keep them from producing the proteins that are required for healthy muscles. Because MD is congenital (something you are born with), it is not something that is contagious, that you can get from someone who has it.

MD weakens your muscles over time. Children, teens and adults with this disease may gradually lose their ability to do the things that most people take for granted, like walking or sitting up. The muscle problems resulting from MD can begin when you were a baby, or they may start later on. Some adults acquire MD.

There are several different kinds of MD that can affect different muscle groups in different ways. Some of these include Duchenne MD, distal MD, Becker’s MD, myotonic MD, congenital MD, limb-girdle MD, facioscapulohumeral MD, oculopharyngeal MD and Emery-Dreifuss MD.

Somewhere around 250,000 children and adults have MD in the United States. Some forms of MD like Becker’s and Duchenne affect primarily boys.

As mentioned earlier, MD is a genetic (inherited) disease. This means that it is passed down through families. It is caused by defects (mutations) that occur in the genes that are passed down to you from your parents. Each one of the various kinds of MD is caused by a genetic mutation that is particular to that form of the disease.

There are many signs and symptoms that you may experience with MD. They will depend on the type of MD that you have. Some possible signs and symptoms include:

  • Frequent falls
  • Progressive muscular weakness or wasting
  • Poor balance
  • Pain in your calf
  • Drooping eyelids
  • Walking difficulty or waddling gait
  • The inability to walk
  • Gonadal atrophy
  • Muscle contractures
  • Scoliosis
  • Respiratory problems
  • Limited range of movement.

Some types of MD can also affect your heart. These kinds of MD can cause arrhythmias or cardiomyopathy.

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Syracuse-related study raises serious questions about fairness of SSA disability judges

Saturday, July 30th, 2011

TRAC finds wide disparity among ALJ  rulings

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No study about SSA Disability in recent memory deserves more attention than the one recently released (and subsequently pooh-poohed by the SSA) from Syracuse University’s Trans­ac­tional Records Access Clear­ing­house (TRAC), a non-profit research orga­ni­za­tion.

Don’t let the system beat you down

If you (or a family member or friend) are one of the unlucky minions to feel trapped and ignored by the federal government’s program to aid disabled persons, please don’t let the findings of this admittedly bleak report stop you from pressing forward with your claim. If anything, this report should legitimize the idea that disability judges can be arbitrary in their rulings and therefore a trained, experienced disability attorney could be your best ally in this notoriously time-consuming process.

Huge disparity among judges’ approval rates

The following is from a Baltimore news site called Baltimore City Paper Blogs; it begins with a district centered in San Antonio, Texas–but the grim numbers apparently apply across the nation:

In San Anto­nio, Texas, peo­ple hop­ing to get Social Secu­rity dis­abil­ity pay­ments could see their cases assigned to any of 17 judges. The luck of this draw mat­ters a lot. One of the judges grants ben­e­fits in just 14 per­cent of cases. Another judge hands over benefits—which range from about $700 per month to about twice that—92 per­cent of the time.

That 78 per­cent dis­par­ity rate makes San Anto­nio the sec­ond most lottery-like sys­tem in the Social Secu­rity Administration’s arch­i­pel­ago of hear­ing offices, accord­ing to a data analy­sis by the Trans­ac­tional Records Access Clear­ing­house, a non-profit research orga­ni­za­tion housed at Syra­cuse Uni­ver­sity. (Dal­las is num­ber one, with 83 per­cent disparity).

“To a sur­pris­ing extent the records on dis­abil­ity deci­sions show again and again that even within the indi­vid­ual offices there is not a clear con­sen­sus among the judges about which claims should be awarded ver­sus which should be denied,” the authors of the report , David Burn­ham and Sue Long, write. “The prob­lem today is some­what worse than it was four and a half years ago.”

This study is from a group aligned with Syracuse University

In case you missed the in-line link, here it is again, the link to the report summary by TRAC, the research outfit aligned with Syracuse University, which reports studying nearly two million claims filed with the Social Security Administration. The report starts thusly:

A court-by-court analysis of close to two million Social Security Administration (SSA) claims has documented extensive and hard-to-explain disparities in the way the administrative law judges (ALJs) within the agency’s separate hearing offices decide whether individuals will be granted or denied disability benefits.

These findings — discussed in detail below — suggest that in many SSA hearing offices today, the chance a disability claim is granted or denied is often determined more by the particular judge assigned to handle it than by the facts and circumstances presented in the case. The findings further document that the problem is not simply the result of a few judges whose decisions are far out of line with those of other judges on the bench. Rather, the agency’s own case-by-case evidence demonstrates that the problem is systemic. To a surprising extent the records on disability decisions show again and again that even within the individual offices there is not a clear consensus among the judges about which claims should be awarded versus which should be denied.

Systemic.

That doesn’t sound good, as anyone with a systemic disease knows and understands. That means whatever the problem is, it’s not localized but instead spread throughout the entire system.

USA Today reports on ‘disparity’

Following is an excerpt from a recent USA Today report, illustrative of the perception of the status quo in such matters:

Congress and the agency’s inspector general have begun looking at the disparity. Yet both Social Security officials and advocates for the disabled say they are reluctant to interfere with the judges’ independence.

“Congress has been pretty enthusiastic about the idea of ALJ independence,” said Social Security Commissioner Michael Astrue, adding that only “a handful” of judges have approval ratings above or below average.

“They can’t tell an ALJ how to decide cases, but they can make sure they follow the agency’s policies.” said Ethel Zelenske, government affairs director for the National Organization of Social Security Claimants’ Representatives.

The Social Security Administration reports about 8.4 million disabled workers nationwide get an average monthly benefit of $1,069. Another 8.1 million low-income disabled people with little work history get about $500 a month in Supplemental Security Income. More than 2.9 million people applied for disability-worker benefits in fiscal year 2010, up 38% over the past five years, agency figures show.

To cope with the increase, Social Security has added about 200 judges in the past five years and streamlined the process of reviewing claims. The average wait time for a decision has steadily dropped, from a peak of 532 days in August 2008 to 354 days last month, agency data show.

TRAC responds to SSA’s response

To be fair, the SSA did respond to TRAC’s study-report, and TRAC’s response to that can be found here.

Just remember, we can help connect you with a compatible, trained attorney who can help you with your case–if nothing else, it’s possible that an experienced attorney might be able to steer your case toward a more reasonable outcome.

 

 

End-Stage Kidney Disease and Receiving Social Security Disability

Tuesday, June 14th, 2011
Kidney

Image via Wikipedia

Healthy kidneys are vitally important because they clean your blood by filtering out extra water and wastes. Your kidneys also produce hormones that help to keep your bones strong and your blood healthy.

Excess fluid accumulates in your body when both of your kidneys fail. Your blood pressure goes up. Harmful wastes build up. Your body will not produce enough red blood cells. When both of your kidneys fail, fatigue, nausea and loss of appetite begin to occur.

If both of your kidneys fail, you must have treatment that will do what your kidneys are not able to do. The prospect of dialysis or a transplant because of kidney failure is not something that anyone looks forward to. End-stage kidney disease is when this occurs.

End-stage kidney disease is a complete or near complete failure of your kidneys to work and function. It is marked by your kidneys failing to regulate electrolytes, concentrate urine and to excrete wastes.

To give you an idea of how big a problem end-stage kidney disease is, more than 400,000 people in the United States are on long-term dialysis. Over 20,000 people have a working transplanted kidney.

The number one cause of end-stage kidney disease is diabetes. End-stage kidney disease almost always occurs after chronic kidney failure. In fact, end-stage kidney disease is the final stage of chronic kidney failure. In addition to diabetes causing your kidneys to fail, heredity and prolonged medical conditions like high blood pressure may also play a role in causing kidney failure.

There are many signs and symptoms that you may have with end-stage kidney disease. Some of these include:

  • Blood in your vomit or stools
  • Unintentional weight loss
  • Fatigue
  • Headaches
  • Vomiting or nausea
  • Frequent hiccups
  • Muscle cramps or twitching
  • Greatly decreased urine output
  • No urine output
  • Decreased sensation in your hands, feet or other areas
  • Generalized itching
  • Increased skin pigmentation
  • Easy bleeding or bruising
  • Skin that may appear brown or yellow
  • Nail abnormalities
  • Decreased alertness that may involve lethargy, drowsiness, confusion, delirium and coma.
  • Seizures.

You or a loved one may be suffering from end-stage kidney disease. End-stage kidney disease and/or complications that have resulted from it or other disorders that you have in addition to this disease may have brought about you or your loved one’s disability and be the reason why you are not able to work.

You may need assistance if this is your situation. You may need financial help.

You or your loved one may be intending to apply for the financial assistance that you need from the Social Security Administration by applying for Social Security disability benefits or disability benefits because of the disability that has resulted from end-stage kidney disease and/or complications that have come about because of it or other disorders that you have in addition to this disease. You may have already done this and been turned down by the Social Security Administration.

If you or your loved one is planning on reapplying or appealing the denial, you really ought to think about an important fact that you may not know about. It is an established fact that people who are represented by a disability attorney like the one you will find at socialsecurityhome.com are approved more often than people who do not have a disability lawyer working for them.

Please do not hesitate. This is something of great importance to you or your loved one. Contact the disability attorney at socialsecurityhome.com, today.

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A Stroke and Receiving Social Security Disability Benefits

Wednesday, April 27th, 2011
Brain

Image via Wikipedia

Your brain is the center of your nervous system. Your brain monitors and regulates your body’s actions and reactions. It continuously receives sensory information. Your brain rapidly analyzes this data and then responds by controlling your bodily actions and functions.

In order for your brain to function like it should, it requires a constant supply of blood from which it receives the glucose and oxygen that it needs. A stroke is when the supply of blood to a part of your brain is interrupted or severely reduced.

A stroke is also referred to in other ways. It is also referred to as a cerebrovascular accident (CVA), brain attack, cerebrovascular disease, cerebral hemorrhage, ischemic stroke, stroke- ischemic and CVA.

There are two main types of stroke. They are ischemic stroke and hemorrhagic stroke.

Ischemic stroke is the most common, accounting for about 80 to 90% of all strokes. Hemorrhagic stroke accounts for the other 10 to 20% of strokes.

There are two common types of ischemic stroke. They are thrombotic stroke and embolic stroke.

There are also two types of hemorrhagic stroke. They are intracerebral hemorrhage and subarachnoid hemorrhage.

A TIA (transient ischemic attack) is sometimes referred to as a ministroke. It is a brief episode in which you experience signs and symptoms that are similar to what you would have in a full-blown stroke. It should be thought of as a warning that you may be in danger of having a major stroke.

Somewhere around 600,000 strokes occur in the United States each year. Around 150,000 of these strokes are fatal, making stroke the third leading cause of death in the United States and the number one cause of disability.

The incidence of stroke is the same for men and women. However, women are more likely to die from stroke than men. Ischemic stroke occurs more often in people over the age of 65, while hemorrhagic stroke occurs more frequently in people of a younger age.

There are some signs and symptoms that may be an indication of a stroke. These include:

  • Having difficulty seeing with one or both of your eyes
  • A sudden, severe headache
  • Difficulty walking
  • Numbness or paralysis on one side of your face or body
  • Problems with talking or understanding.

You or a loved one may have had a stroke. A stroke and/or complications resulting from it may have resulted in you or your loved one’s disability and need for financial help.

You or your loved one may be thinking about applying for the financial assistance that you need from the Social Security Administration by applying for Social Security disability benefits or disability benefits because of the disability caused by a stroke and/or complications resulting from it. You or your loved one may have already applied and been denied by the Social Security Administration.

If you or your loved one considers reapplying or appealing the denial, think carefully about this fact. The simple truth is that people who have a disability lawyer fighting for them like the one you will find at socialsecurityhome.com are approved more often than people who are not represented by a disability attorney.

Please do not hesitate. Contact the disability lawyer at socialsecurityhome.com, today.

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