Do You Need Help With Your Disability Claim?

Social Security Disability Attorneys and Advocates can help you in all phases of the social security disability claim process. Contact an advocate today for your FREE case evaluation!

Archive for December, 2010

Four Chilean Miners victim to own fame; Governor’s furloughs blamed for SSDI delays in California

Friday, December 31st, 2010

By Mike Hinshaw

Normally, we don’t post about issues that are outside the realm of most U.S. citizens or family members who may have a legit claim to disability payments.

However, in today’s first case, we make an exception. Then we look at more trouble for SSDI recipients in California.

The first case concerns those miners from Chile, who were wildly cheered throughout the U.S. every time another one of them popped to the surface in that German-made rescue device.

Four of the the 33 have lost their disability payments.

But apparently they’re not victims of some nefarious scheme or bumbling bureaucracy.

Medical review appointments missed

Nope, their own fame did them in, via invitations abroad, which led to their missing scheduled medical review appointments.

According to a Dec. 31 piece at Inquirer.net:

Omar Reygadas, Edison Pena — who practiced for the New York City marathon while trapped deep underground with his colleagues — Dario Segovia and Carlos Bugueno lost their medical leave payments, officials said.

“Article 33 of the work accident law clearly states that if the worker does not comply with medical instructions, he will be suspended from the allotted payments,” said Jorge Diaz, medical director for the Chilean Insurance Association (ACHS), which is treating the miners.

After their 69-day ordeal deep in the San Jose mine, many of the miners traveled abroad to tell their story, preventing them from attending their required checkups.

Reygadas, who has since dedicated his time to delivering motivational speeches, criticized the move, saying most of his colleagues have yet to recover psychologically.

Earlier this month, according to the article, 14 of the men were reviewed and declared fit to return to work.


Governor’s furloughs: delays without benefit?

We’ve covered Gov. Arnold Schwarzenegger’s various run-ins with disability and workers’ comp programs before (here’s one, from November).  Now, a Dec. 27 piece at Contra Costa Times describes how the governor’s furlough practices have caused delays for SSDI recipients, without generating benefits to the state in return. Worse, the furloughs may continue even after the Guv’nater leaves office in a few days–with approval ratings barely above 30 per cent.

Former rail-yard worker waits almost four years

The Contra Costa piece reports that former rail-yard worker Grant Sterling began suffering symptoms of a heart condition in June 2006, painful enough to keep him from working. So he began the application process for Social Security Disability Insurance that same month.

He began receiving payments in March–almost four years later. According to the CC Times:

Part of that long delay was that applying for disability benefits is a complicated process that requires plenty of doctor visits and paperwork. But another part was that, for more than a year, the state workers who go through disability applications were ordered by Gov. Arnold Schwarzenegger to take two or three unpaid days off each month.

That’s a practice that disability advocates say has hurt disabled workers and state employees but hasn’t helped the state. But it’s a practice that could continue, although to a lesser degree, after Schwarzenegger leaves office.

“As of Nov. 30 of this year, 84,000 initial applications for SSDI have been delayed” because of the furloughs, said Dan Allsup, communications director for Allsup Inc., a firm specializing in SSDI claims. “That’s more than $23 million in monthly benefits that have been held up.”

In December 2008, amid a state budget crisis, Schwarzenegger ordered most California state employees to take two unpaid days off each month. In June 2009, he ordered a third furlough day per month.

SSDI workers were not paid by state

Here’s the really hinky part: among those affected by the furloughs were the state workers in the Department of Social Services’ Disability Determination Service Division, which are those who handle applications from people like Sterling. Well, they’re not paid by the state; they’re paid by federal funds.

Says the CC Times, ” ‘The state of California never saved any money by furloughing those employees,’ said Lowell Kepke, a spokesman for the Social Security Administration’s San Francisco office. ‘That has been brought up to the governor’s office and it was never changed.’

“The furloughs are now down to one day per month rather than three, but the Social Security Administration still has a backlog of about 30,000 applications. For now, the administration is sending about 1,400 applications per week to processors in other states.”

New contract would be required

The Social Security Administration has contacted Jerry Brown, who gets sworn in on Monday, asking for assurances that SSDI processors will be no longer exposed to state furloughs, freezes or overtime limitations.

But, according to the article, “Brown spokesman Evan Westrup pointed out that the once-per- month furloughs are now part of a new contract between the state and the union representing SSDI processors and that undoing those furloughs could require renegotiating that contract.”

Auditory Neuropathy and Receiving Social Security Disability

Thursday, December 30th, 2010
An illustration of one of the three semicircul...
Image via Wikipedia

The term “neuropathy” is used to refer to any and all malfunctions or diseases of your nerves. For example, peripheral neuropathy is a condition in which your peripheral nervous system is damaged. It is the vast communications network that transmits information from your brain and spinal cord (the central nervous system) to every other part of your body.

Auditory neuropathy (AN) is a hearing disorder that is marked by sound entering your inner ear normally, but the transmission of signals from your inner ear to your brain is impaired. It is a variety of hearing loss where your outer hair cells within your cochlea are present and functional, but the sound information is not faithfully transmitted properly to your auditory nerve and brain.

Auditory neuropathy is known by other names. It is also known as Auditory Neuropathy/Auditory Dys-synchrony (AN/AD) or Auditory Neuropathy Spectrum Disorder (ANSD).

Auditory neuropathy is a disorder that can affect anyone at any age. The number of people with this condition is unknown. What is known is that auditory neuropathy affects a relatively small percentage of people who are hearing-impaired or deaf.

Auditory neuropathy is a condition that is not fully understood at the present time. Researchers believe that this disorder may have more than one cause. Possible causes include:

  • Faulty connections between your inner hair cells and the nerve that goes from your inner ear to your brain
  • Damage to the nerve going from your inner ear to your brain
  • Damage to your inner hair cells (specialized sensory cells in your inner ear that transmit information sounds through your nervous system to your brain).

There are signs and symptoms that may be an indication of auditory neuropathy. Some of these include:

  • Normal Hearing, but trouble understanding
  • Anywhere from mild to severe hearing loss
  • Poor speech-perception abilities (trouble understanding speech correctly)
  • Speech perception that is worse than the degree of hearing loss would indicate
  • Hearing sounds, but difficulty recognizing spoken words
  • Sounds fading in and out and seeming out of sync.

You or a loved one may have auditory neuropathy. Auditory neuropathy and/or complications that have resulted from this disorder or other disabling conditions that you have along with it may be why you are disabled and in need of financial assistance.

You or your loved one may intend 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 caused by auditory neuropathy and/or complications that have resulted from this disorder or other disabling conditions that you have along with it. You or your loved one may have already applied, and your claim was turned down by the Social Security Administration.

If you or your loved one plans on reapplying or appealing the denial, always remember. People who have a disability lawyer standing with them like the one you will find at Social Security Home are approved more often than people who are not represented by a disability attorney.

Ectropion and Receiving Social Security Disability Benefits

Wednesday, December 29th, 2010
The tarsi and their ligaments. Right eye; fron...
Image via Wikipedia

Your eyesight is one of the most precious and important of all your senses and abilities. What price would you put on your eyesight? It is truly priceless.

Ectropion is a condition in which your eyelid turns out. This is usually your lower eyelid. This leaves the surface of your inner eyelid prone and exposed to irritation.

When this condition is mild, only one segment of your eyelid turns out, away from your eye. When ectropion is severe, the entire length of your eyelid is turned out.

Ectropion is a condition that usually develops in older people. It is more common in men than in women.

There are seven different types of ectropion. These are:

  • Involutional (age-induced horizontal elongation of your eyelid)
  • Cicatricial (scar, trauma or tumor induced contracture of the outer layer of muscle and skin in your eyelid)
  • Paralytic (resulting from a nerve palsy like Bell’s palsy)
  • Punctal (eversion of the medial portion of your eyelid)
  • Mechanical (eversion of your lower lid due to inflammation or the weight of a tumor)
  • Congenital (evident at birth or shortly after)
  • Mixed mechanical (a combination of two or more causes).

Ectropion is often caused by the process of aging and the weakening of the connective tissue of your eyelid that causes it to turn out. Other possible causes of ectropion include:

  • Facial palsy like Bell’s palsy
  • Scar tissue from burns
  • A  birth defect like Down syndrome
  • Muscle weakness
  • Growths on your eyelids whether malignant or benign
  • Previous radiation, cosmetic procedures or surgery
  • Skin problems like dermatitis.

There are several signs and symptoms that may be an indication of ectropion. Some of these are:

  • Excessive tearing with weeping or watery eyes
  • Excessive dryness where your eyes feel gritty, sandy or dry
  • Irritation from dryness or stagnant tears that causes redness and a burning sensation in the whites of your eyes and your eyelids
  • Chronic (long-term) conjunctivitis
  • Your eyelid turns out
  • Keratitis (inflammation of the tissue of your cornea).

You or a loved one may have been diagnosed with ectropion. This disorder and/or complications that have resulted from or other underlying conditions along with it may be the cause of your disability.

You may need assistance if this is true. You may need financial help.

You or your loved one may be considering 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 ectropion and/or complications that have resulted from or other underlying conditions along with it. Have you or your loved one already applied and been turned down by the Social Security Administration?

If you or your loved one has decided to reapply or appeal the denial, remember this important fact. 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 standing with them.

Brucellosis and Receiving Social Security Disability Benefits

Tuesday, December 28th, 2010
Swine brucellosis in wild pigs
Image via Wikipedia

Brucellosis is a serious infectious disease. It comes from one of four different species of bacteria that are a part of the genus Brucella.

Brucellosis can be local, which means that it affects only a certain area of your body. However, what makes brucellosis dangerous is that it can have serious widespread complications that affect different organ systems in your body. This includes your central nervous system.

Brucellosis is usually an acute (short-term) disease. However, it can become chronic (long-term) with long lasting complications.

Brucellosis is known by several other names. It is also called Maltese fever, Neapolitan fever, Mediterranean fever, undulant fever, Crimean fever, Gibraltar fever, Bang’s disease, Cyprus fever, brucellemia, goat fever, brucelliasis, melitococcosis and rock fever.

Brucellosis affects hundreds of thousands of animals and people each year in Mediterranean countries and other areas of the world. Brucellosis is not common in the United States. There are about 100 to 200 cases that are reported each year.

Brucellosis is a disease that affects many different domestic and wild animals. There are at least six strains of bacteria that cause this disease in animals, but not all of these strains cause brucellosis in people. Brucellosis is spread from animals to people in three ways. They are:

  • Direct contact with infected animals through a cut or wound that you have
  • Eating raw dairy products that come from infected animals or eating undercooked or raw meat from an infected animal
  • Inhaling the brucella bacteria in the air.

The signs and symptoms of brucellosis may start anywhere from a matter of days to a few months after you have been infected with the brucella bacteria. There are several signs and symptoms that you may experience. Some of these are:

  • Muscle, back and joint pain
  • Weakness
  • An undulating fever (fever that rises and falls)
  • Chills
  • Headache
  • Fatigue
  • Sweats.

The signs and symptoms of brucellosis may go away for weeks or months and then come back. If you have chronic brucellosis, signs and symptoms include arthritis, fatigue, fevers and spondylitis (an inflammatory arthritis that affects your spine and joints that are close by).

You or a loved one may have or have had brucellosis. Brucellosis and/or complications that have been caused by this disease may be responsible for you or your loved one’s disability and being unable to work.

You may need assistance if this is true. You may need 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 brucellosis and/or complications that have been caused by this disease. You or your loved one may have already tried this option and been denied by the Social Security Administration.

If you or your loved one is considering reapplying or appealing the denial, think about this. People who are represented by a disability attorney like the one you will find at Social Security Home are approved more often than people who do not have a disability lawyer fighting for them.

A Pheochromocytoma and Receiving Social Security Disability

Thursday, December 23rd, 2010
The adrenal glands sit atop the kidneys.
Image via Wikipedia

Your adrenal glands are two triangular shaped glands that are located on top of your kidneys and are made up of two parts that work separately. The first part is your outer layer (cortex). The second part is your inner area (medulla).

Your adrenal glands make hormones that give instructions to practically all of the tissues and organs in your body. These hormones affect your ability to deal with stress, help to regulate your kidney function and impact your growth and development.

A pheochromocytoma is a rare tumor that originates in the core (medulla) of your adrenal gland. Most of these tumors are benign (non-cancerous). However, some can be malignant (cancerous).

A pheochromocytoma causes your adrenal glands to produce too much of the hormones epinephrine and norepinephrine. These hormones regulate your heart rate and blood pressure. In addition to regulating your heart rate and blood pressure, these hormones play a vital role in what is known as the “fight-or-flight response”. When too much of these hormones is produced, your heart rate and blood pressure can be elevated, which can lead to serious problems and conditions.

Fortunately, as mentioned above, a pheochromocytoma is rare. It affects about 1 to 2 people per 100,000 adults each year in the United States. A pheochromocytoma develops most often in people who are in their 40s and 50s. Men and women are affected equally by these tumors.

Researchers do not know the exact reason why cells inside of your adrenal glands form into a tumor. What is known is that a pheochromocytoma starts in special cells that are called chromaffin cells. These cells are located in the medulla or inner part of your adrenal glands. These are the cells that produce the hormones epinephrine and norepinephrine.

There are several signs and symptoms that you may experience with a pheochromocytoma. Some of these are:

  • Profound sweating
  • Nervousness
  • Palpitations
  • Abdominal pain
  • Hypertension (high blood pressure)
  • Unintended weight loss
  • Chest pain
  • Difficulty sleeping
  • Severe headaches that come on suddenly
  • Irritability
  • Feeling of extreme fright
  • Rapid heart rate
  • Forceful heartbeat
  • Hand tremor
  • Flushing
  • Increased appetite
  • Pale skin
  • Feeling of anxiety.

You or a loved one may have a pheochromocytoma. A pheochromocytoma and/or complications that have resulted from it may have brought about you or your loved one’s disability and being unable to work.

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

You or your loved one may be considering 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 pheochromocytoma and/or complications that have resulted 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 decides to reapply or appeal the denial, consider this. People who have a disability lawyer on their side like the one you will find at Social Security Home are approved more often than people who are not represented by a disability attorney.

Proposal to reform SSDI based on private disability insurance, belief that new health-care law will stand

Wednesday, December 22nd, 2010

By Mike Hinshaw

As promised, we are tracking developments about proposals to streamline or otherwise improve the SSDI/SSI system.

The joint report from the Brookings Institution’s Hamilton Project and the Center for American Progress referenced in a previous post was released earlier this month. The authors, David H. Autor and Mark Duggan, are professors of economics, Autor at the Massachusetts Institute of Technology and Duggan at the University of Maryland. Both are research associates for the National Bureau of Economic Research (the outfit charged with pronouncing the official beginnings and endings of recessions).

‘Twin problems’ for SSDI

A Dec. 17 piece at Investors.com describes the 48-page report as a proposal aimed at “reforming SSDI to solve its twin problems of impending fiscal shortfalls and poor employment incentives.”

The SSDI program has been projected to be in the red by 2018. From the report:

Due to its rapid growth, SSDI has come to encompass an ever-larger share of the Social Security system budget. In 1989, approximately one in ten Social Security dollars was spent on SSDI. By 2009, this number had risen to almost one in five Social Security dollars (18 percent), as shown in Figure 3. SSDI expenditures currently exceed the payroll tax revenue the program collects, and analysts project that the SSDI trust fund will be exhausted in 2018, twenty-two years ahead of the trust fund for Social Security retirement (the so-called Old-Age and Survivors Insurance, or OASI). The rapid expansion of SSDI contributes significantly to the deteriorating financial health of the overall Social Security system since both depend on the Social Security payroll tax.

A new ‘front end,’ using private disability insurance

Autor’s and Duggan’s idea, says the Investors.com piece, is to create “a new ‘front-end’ universal program of private disability insurance (PDI) paid for out of a new payroll tax to be shared by employers and employees. PDI would provide employment supports to disabled workers with a view of keeping them on the job. It would also provide new subsidies to employers to retain disabled workers on the job.

“Under their reform, applications to SSDI by those with disabilities but who could continue working with assistive technologies would be statutorily delayed by 22 months, during which time they would continue to receive PDI’s employment supports.”

Borrowing from unemployment and workers’ comp programs

Part of the idea is to model a new approach based on workers’ compensation and unemployment benefits programs. From the report:


Our proposal envisions extending PDI coverage to the vast majority of U.S. workers, in much the same way that UI and WC benefits are universally provided to workers who participate substantially in the labor market. PDI coverage under our proposal would form the first line of defense in the U.S. worker disability system. Its primary goal would be supporting work. Thus, in contrast to the traditional SSDI system—but similar to the PDI plans numerous employers purchase—it would treat disability and gainful employment as potentially compatible conditions rather than mutually exclusive states.

The proposed policy would support workers from 90 days to 2.25 years following onset of disability, providing partial income replacement and supports geared toward helping individuals maximize work readiness and self-sufficiency. After receiving PDI benefits for twenty-four months, individuals who are unable to engage in substantial gainful employment would transition into the SSDI system. The screening criteria for SSDI would be unchanged.


It is instructive to consider the average amount paid for private long-term disability coverage in the market at present. Using data from the Bureau of Labor Statistics on the average hourly cost of PDI coverage ($0.04) and the fraction of workers with long-term disability coverage (32 percent), we estimate that the average policy costs approximately $250 per year—about $20 per month.

This is likely an upper bound on the average cost of policies under our proposal, as current PDI policies are, on average, significantly more generous than the one we propose. For example, the median maximum monthly benefit of these policies is $7,500, which is three times greater than the corresponding maximum in our plan. Additionally, our proposed coverage would pay benefits for a maximum of just two years, while existing policies are typically long-term and may provide at least partial benefits to the worker until he or she reaches full retirement age.

Questions to be answered

Of course, the plan is not without hurdles. For one, enough variations exist among the various states’ workers’ compensation systems that finding a single “role model” to copy is unlikely. For example, Texas doesn’t even require employers to carry workers’ compensation insurance.

On the other hand, according to the report, five “U.S. states already mandate that employers provide temporary disability insurance to their workers.  Although little studied, the available data on these mandates suggest that they have not substantially hindered labor market operation but have provided valuable insurance to workers.” Furthermore, a program similar to that one proposed already has been seen some success in the Netherlands.

Another rough spot may be persuading employees to go along with paying for a share of a program that does not provide for medical care, which the authors view as unnecessary because of the passage of “Obamacare.”  According to the report: “Alongside lost income, medical care is one of the most costly aspects of disability. Private-sector disability policies do not pay for medical care. Instead, they serve to partially insure lost earnings as well as reimburse workplace accommodations and certain rehabilitation services that a traditional health insurance plan would not cover. Our proposed PDI coverage likewise would not cover medical care. Such coverage is unnecessary because health insurance is slated to become nearly universal and much more affordable for American workers over the next several years as a result of the recently enacted Patient Protection and Affordable Care Act.”

However, several states have filed suit against health care law, and a federal judge recently ruled a portion of the law unconstitutional, and many observers expect the final word on the law will come only with a ruling from the U.S. Supreme Court.

Gaucher’s Disease and Receiving Social Security Disability

Monday, December 20th, 2010

Gaucher’s disease, which is also sometimes referred to as glucocerebrosidase deficiency, is a genetic disease. This means that it is an inherited disease. Gaucher’s disease is marked by the accumulation of a fatty substance (lipid)that is called glucocerebroside in your cells and certain organs, including your spleen, liver, kidneys, brain, lungs and bone marrow.

Gaucher’s disease is the most common of the lysosomal storage diseases. It occurs in about 1 in 20,000 live births.

Lysosomal storage diseases are a group of about 40 inherited metabolic conditions that are rare. They result from defects in lysosome function.

Gaucher’s disease can develop in anyone at any age. It is most common in Ashkenazi (Central and Eastern European) Jewish people.

Gaucher’s disease is named after the French doctor Philippe Gaucher. He first described this disease in 1882.

There are three types of Gaucher’s disease. They are:

  • Type 1 – This is the most common type of the disease. This type of Gaucher’s disease causes spleen and liver enlargement. Sometimes it involves kidney and lung difficulties. It does not affect your brain.
  • Type 2 – This type causes severe brain damage. It occurs in infants. Most children with this type of the disease die before reaching 2 years of age.
  • Type 3 – This type involves spleen and liver enlargement. The brain is affected gradually.

The signs and symptoms of Gaucher’s disease may vary greatly from person to person. This is especially true with the different types of this disease. Signs and symptoms that you may experience include:

  • Excessive fatigue
  • Pingueculae (yellow spots in your eyes)
  • Nosebleeds
  • Skeletal abnormalities that include bone fractures, bone pain and osteopenia (thinning of your bones)
  • Cognitive deterioration that includes dementia or mental retardation
  • Delayed puberty
  • Loss of muscle coordination
  • Anemia (decrease in healthy red blood cells)
  • Abnormal eye movements
  • Splenomegaly (enlarged spleen) or hepatomegaly (enlarged liver), or both
  • An increased risk of bruising, which may mean that you have thrombocytopenia (low number of blood platelets).

You or a loved one may have Gaucher’s disease. Gaucher’s disease and/or complications that have resulted from this condition may be the cause of your disability and not being able to work.

You may need assistance because of this. 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 caused by Gaucher’s disease and/or complications that have resulted from this condition. You or your loved one may have already done this and been denied by the Social Security Administration.

If you or your loved one plans on reapplying or appealing the denial, remember this important fact. The truth is 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 standing with them.

Restrictive Cardiomyopathy and Receiving Social Security Disability

Friday, December 17th, 2010
Hypertrophic cardiomyopathy
Image via Wikipedia

Your heart is at the center of your cardiovascular system. Your heart is the organ that pumps blood to all of the cells in your body through your body’s blood vessels. Your blood has oxygen that your cells have to have.

Cardiomyopathy literally means “heart muscle disease”. It refers to the deterioration of the working of your myocardium (heart muscle).  This medical condition hinders your heart’s ability to pump blood.

There are three major types of cardiomyopathy. They are dilated cardiomyopathy, hypertrophic cardiomyopathy and restrictive cardiomyopathy.

Dilated cardiomyopathy is the most common form of this disease. It is when your heart’s main pumping chamber becomes dilated (enlarged), and its pumping ability becomes impaired.

Hypertrophic cardiomyopathy (HCM) is a form of cardiomyopathy where your heart muscle (myocardium) becomes hypertrophied or abnormally thick. The result is that your heart may have a harder time pumping blood. This disease can also affect the electrical system of your heart.

Restrictive cardiomyopathy is the rarest kind of cardiomyopathy. It is a disease where the walls of your ventricles (lower chambers of your heart) become abnormally rigid. They do not have the flexibility to expand as they fill with blood. With the passage of time, restrictive cardiomyopathy can cause your heart to lose its ability to pump blood properly. This can then lead to heart failure.

You may experience several signs and symptoms that may be an indication of restrictive cardiomyopathy. These include:

  • Fatigue
  • Swelling of your ankles and feet
  • Poor exercise tolerance
  • A persistent cough
  • Swelling of your abdomen
  • Difficulty breathing when you are lying flat, at night and especially with exertion
  • Weight gain
  • Chest pain or pressure
  • Fainting
  • Palpitations (fluttering in your chest because of abnormal heart rhythms)
  • Bloating, nausea and poor appetite that is related to retention of fluid.

You or a loved one may have restrictive cardiomyopathy. Restrictive cardiomyopathy and/or complications that have resulted from this disease may be the reason why you or your loved one is disabled. It may be preventing you or your loved one from working.

You may need assistance if this is the case. 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 caused by restrictive cardiomyopathy and/or complications that have resulted from this disease. You or your loved one may have already taken this step, and your application was denied by the Social Security Administration.

If you or your loved one plans on reapplying or appealing the denial, you really ought to consider this important fact carefully. The fact of the matter is that people who have a disability lawyer standing with them like the one you will find at Social Security Home are approved more often than people who are not represented by a disability attorney.

Fibrous Dysplasia and Receiving Social Security Disability

Thursday, December 16th, 2010

Fibrous dysplasia is a chronic (long-term) bone disease where a portion of bone develops abnormally. Fibrous (scar-like) tissue takes the place of normal bone. As your bone grows, this softer fibrous tissue expands. As it does so, your bone is weakened.

Fibrous dysplasia can cause your affected bone to become deformed. This makes it more likely to fracture (break).

Fibrous dysplasia begins before you are born. However, it may not be discovered until childhood, adolescence or adulthood.

Fibrous dysplasia is responsible for about 7% of all benign bone tumors. Although any bone in your body may be affected, this disease occurs most frequently in your skull, upper arm bone, pelvis, thighbone and shinbone.

Most of the time fibrous dysplasia only affects one bone. When it does so, it is referred to as monostotic fibrous dysplasia. Polystotic fibrous dysplasia is when this disease affects two or more of your bones. This can be two bones in the same limb or several bones throughout your skeleton.

Fibrous dysplasia affects men and women, equally. It also affects all races about the same.

Fibrous dysplasia is caused by a gene defect (mutation) that affects the cells that produce bone. However, no one knows what causes this gene defect. It is known that this disease is not inherited or passed on to the children of affected parents. There is also no known environmental or dietary cause of fibrous dysplasia.

Your doctor may suspect fibrous dysplasia from the signs and symptoms that you are experiencing. If so, your doctor will probably do a physical exam and want X-rays of your affected bones. In order to confirm a diagnosis of fibrous dysplasia, your doctor may want you to have additional diagnostic tests and procedures. Some of these are:

  • Bone scan
  • Bone biopsy
  • MRI (magnetic resonance imaging) scan
  • CT (computerized tomography) scan.

Fibrous dysplasia may cause little or no signs and symptoms. However, if the disease is severe, you may experience:

  • Bone deformities
  • Bone pain that increases with activity and lessens with rest
  • Fractures (breaks)
  • Problems with walking
  • Bone sores (lesions)
  • Endocrine gland difficulties
  • Pigmentation (unusual skin color).

You or a loved one may have fibrous dysplasia. Fibrous dysplasia and/or complications that have resulted from or other debilitating conditions that you may have along with this disease may be the cause of your disability and need for financial help.

You or your loved one may have applied 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 fibrous dysplasia and/or complications that have resulted from or other debilitating conditions that you may have along with this disease. Were you or your loved one denied by the Social Security Administration?

If you or your loved one reapplies or appeals the denial, remember this. People who are represented by a disability attorney like the one you will find at Social Security Home are approved more often than people who do not have a disability lawyer on their side.

Gastroenteritis and Receiving Social Security Disability Benefits

Wednesday, December 15th, 2010

Your stomach is a crescent-shaped hollow organ that is made-up of several strong, muscular layers. Your stomach is located and protected under your rib cage. It is connected at one opening to your esophagus and at the other opening to your small intestine.

Your stomach stores, mixes and digests the food that you eat. It also functions to protect you from infectious organisms that you may have ingested.

Gastroenteritis is a disease that is marked by inflammation and irritation of your stomach and intestines (gastrointestinal tract). Gastroenteritis is also marked by dehydration (your body not having enough fluids and water).

Gastroenteritis is referred to by other names. It is also called stomach flu or gastric flu, although this condition has nothing to do with influenza.

There are different types of gastroenteritis. These include viral gastroenteritis, bacterial gastroenteritis, bacillary dysentery and amebic dysentery.

Gastroenteritis is a very common disease in the United States. Each year, gastroenteritis accounts for 8 million doctor visits and 250,000 hospitalizations.

Gastroenteritis has many different causes. However, viruses and bacteria are the most common causes of this disease. Viruses and bacteria are extremely contagious. They can spread by means of contaminated water, food or improper handwashing.

A less common cause of gastroenteritis is protozoans and parasites. These tiny organisms are usually found in contaminated water. You may become infected with them at a public swimming pool or by drinking contaminated water.

Gastroenteritis that is not contagious may be caused by chemical toxins that are usually located in seafood. Antibiotics and other medications, heavy metals and food allergies may also cause non-contagious gastroenteritis.

There are several different signs and symptoms that you may experience with gastroenteritis. Some of these include:

  • Stomach pain or spasms
  • Abdominal cramps
  • Loss of appetite
  • Vomiting and nausea
  • Diarrhea
  • Bloody stools
  • Weakness and fainting
  • Headaches
  • Fever
  • Abnormal flatulence (gas)
  • Abdominal pain
  • Heartburn.

You or a loved one may have gastroenteritis. Complications that have resulted from gastroenteritis and/or an underlying condition that you have along with this disease may be the reason for your disability and not being able to work.

You may need help as a result of this. You may need financial assistance.

You or your loved one may be thinking about applying for the financial help that you need from the Social Security Administration by applying for Social Security disability benefits or disability benefits because of complications that have resulted from gastroenteritis and/or an underlying condition that you have along with this disease. You or your loved one may have already taken this step and been denied by the Social Security Administration.

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