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Archive for the ‘Skin’ Category

Weber-Cockayne Syndrome and Getting Social Security Disability

Saturday, February 11th, 2012

Epidermolysis bullosa refers to a group of inherited conditions that are evidenced by the presence of extremely fragile skin. Because of the extremely fragile skin, skin blisters start to form as a response to minor injury, heat or friction that occurs because of rubbing or scratching.

There are a number of kinds of epidermolysis bullosa. Most of the time, these types of epidermolysis bullosa originate in infants and young children. However, the signs and symptoms that come from the various forms of epidermolysis bullosa may not take place until adolescence or early adulthood in some of the people who have the mild kinds of the condition. The milder types of epidermolysis bullosa are those that may get better with age, but the severe forms of epidermolysis bullosa may lead to serious complications and can be fatal.

Epidermolysis bullosa is a condition that does not show any predilection for ethnic and racial groups. Men and women are affected about equally with this condition. Fortunately, epidermolysis bullosa is a rare condition that is estimated to occur in somewhere around 50 out of every one million live births.

Weber-Cockayne syndrome is one of the types of epidermolysis bullosa. Weber-Cockayne syndrome is marked by noninflammatory bullous eruptions that form primarily on your feet and less prominently on your hands. If you have been diagnosed with Weber-Cockayne syndrome, you may qualify for social security disability benefits, such as SSI or SSDI. It is always a good idea to consult a social security attorney at socialsecurityhome.com concerning your disability benefits options. The attorneys at socialsecurityhome.com are experienced in these matters.

Weber-Cockayne syndrome gets its name from Frederick Parkes Weber and Edward Alfred Cockayne. Weber described this syndrome in 1926 and Cockayne described it in 1938.

Weber-Cockayne syndrome usually starts during early childhood as the result of mechanically induced blisters (trauma). However, Weber-Cockayne syndrome may also originate in adults, especially during the warm season of the year.

The cause of Weber-Cockayne syndrome has not yet been determined. There have been reported instances where the condition has run in families.

Weber-Cockayne syndrome is an inherited condition. The pattern of inheritance may be what is known as either autosomal dominant or autosomal recessive. When the pattern of inheritance is autosomal dominant, only one of your parents has to have the defective (faulty) gene in order for you to have Weber-Cockayne syndrome. When the pattern of inheritance is autosomal recessive, both of your parents have to have the faulty gene in order for you to have this condition.

As mentioned above, the main sign or symptom of Weber-Cockayne syndrome is the formation of noninflammatory bullous eruptions on your skin. These eruptions take place primarily on your feet, but may also occur on your hands.

When bullae burst (rupture), you usually experience significant pain. The bullous eruptions usually heal without leaving residual scarring or other changes to your skin, such as hyperkeratosis (thickening of your skin). Sweating unpredictably and excessively (hyperhidrosis) is sometimes connected with Weber-Cockayne syndrome.

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Dropsy and Receiving Social Security Disability Benefits

Monday, November 14th, 2011

Dropsy is swelling that takes place as a result of fluid becoming trapped in the tissues of your body. Dropsy refers to large amounts of fluid that are retained in your circulatory system or the spaces between the cells of your body.

In most cases, dropsy takes place in your feet, legs and ankles. However, dropsy may also develop in other areas of your body, such as your face and hands.

It is important to understand that dropsy is not a disease or a disorder. Dropsy is a sign or symptom of an underlying problem that is causing it. In fact, dropsy may be the primary sign or symptom of the underlying difficulty that is responsible for it. If dropsy is chronic (long-term, ongoing) and widespread, it may be a sign of a serious underlying medical problem.

Dropsy is an older term that is used for swelling in your soft tissues. This condition is also known by other names. It is referred to as fluid retention, edema, swollen legs, hydropsy and swelling.

Dropsy is a condition that can take place in anyone at any time. However, dropsy occurs most of the time in women who are pregnant and older adults.

Dropsy is a result of tiny blood vessels (capillaries) in your body leaking fluid. This fluid leakage may be caused by damage to or increased pressure in your capillaries. This leakage may also be the result of lowered levels of serum albumin. Serum albumin is one of the proteins in your blood. The fluid that leaks from your capillaries gets into your surrounding tissue. When this happens, the tissue begins to swell.

As mentioned earlier, dropsy is a sign or symptom of an underlying problem that causes your capillaries to start leaking. There are several things that can do this. Some of these include:

  • Congestive heart failure
  • Medications, such as corticosteroids, calcium channel blockers and NSAIDs
  • Brain tumors or head trauma
  • Pregnancy
  • Nephrotic syndrome
  • Cirrhosis of the liver
  • Allergic reactions
  • Critical illness, such as life-threatening infections or burns
  • Obstruction of the flow of liquid from a body part

Even though dropsy is a sign or symptom of an underlying problem, there are also signs and symptoms that may be an indication of dropsy. Some of these are:

  • Stretched or shiny skin
  • Swelling or puffiness of the tissue that is located under your skin (subcutaneous tissue)
  • An increase in the size of your abdomen
  • Your skin continuing to keep a dimple even after it has been pressed for several seconds.
  • Indications of dropsy in your lungs include:
  • Shortness of breath
  • Chest pain
  • Having trouble breathing

If you are experiencing dropsy, the underlying difficulty that is responsible for it may make you eligible to receive social security disability benefits like SSDI or SSI. A good decision would be to turn to one of the social security disability lawyers at socialsecurityhome.com. The social security attorneys at socialsecurityhome.com will help you explore your options in regard to disability benefits.

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Hemidesmosomal Epidermolysis Bullosa and Receiving Social Security Disability

Thursday, October 27th, 2011

 

Epidermolysis bullosa is a medical term that applies to a group of inherited disorders that are characterized by your skin becoming extremely fragile. As a result of this, skin blisters begin to occur in response to friction, heat, or minor injury that is due to scratching or rubbing.

There are several types of epidermolysis bullosa. Most of these forms of epidermolysis bullosa develop in infants and young children. However, the symptoms that are produced by the various kinds of epidermolysis bullosa may not appear until adolescence or early adulthood in some of the people who are affected by the mild types of epidermolysis bullosa. The milder kinds of epidermolysis bullosa may improve with age, but the severe types of the disorder may result in serious complications and may even prove to be fatal.

Epidermolysis bullosa is a disorder that occurs in all ethnic and racial groups. The disorder develops about equally in men and women. Thankfully, epidermolysis bullosa is a rare disorder that is estimated to take place in about 50 out of every one million live births.

Hemidesmosomal epidermolysis bullosa is one of the major forms of epidermolysis bullosa. Hemidesmosomal epidermolysis bullosa is usually present when you are born. This means that it is usually congenital. Hemidesmosomal epidermolysis bullosa is usually one of the severe forms of this disorder.

As stated earlier, hemidesmosomal epidermolysis bullosa is a genetic inherited condition. What this means is that it is handed down to you by your parents. The pattern of inheritance for hemidesmosomal epidermolysis bullosa is what is referred to as autosomal recessive. This means that both of your parents have to have the faulty (defective) gene in order for you to have the possibility of getting hemidesmosomal epidermolysis bullosa.

You may qualify for disability benefits with epidermylosis bullosa

The hallmark sign or symptom of hemidesmosomal epidermolysis bullosa is the eruption of fluid-filled bullae (blisters) on your skin. They usually begin to form on your hands and feet because of friction. These blisters typically take place in different areas on you body. With the milder forms epidermolysis bullosa, these blisters may heal without scarring. If you are experiencing this hallmark sign of hemidesmosomal epidermolysis, you may meet the requirements for some type of social security disability benefits like SSDI or SSI. The thing to do is to get in touch with one of the social security attorneys at socialsecurityhome.com. The social security attorneys at socialsecurityhome.com understand what it takes to get you the disability benefits that you deserve.

There are other signs and symptoms that you may have as an indication of hemidesmosomal epidermolysis bullosa. Some of these include:

Ÿ  Internal blistering that may take place on your intestines, stomach, esophagus, throat, urinary tract or upper airway

Ÿ  An excessive amount of sweating

Ÿ  Atrophic (wasting) scarring

Ÿ  Small cysts or tiny white bumps that develop on your skin (milia)

Ÿ  Dental abnormalities

Ÿ  The deformity or loss of your fingernails and toenails

Ÿ  Scarring alopecia (baldness, complete lack of hair)

Ÿ  Abnormal thickening of the outer layer of your skin (Hyperkeratosis)

Ÿ  Difficulty swallowing (dysphagia).

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Mummification and Receiving Social Security Disability Benefits

Monday, October 24th, 2011

Gangrene is a medical term that is used to refer to the decay and death of an area or part of your body. Gangrene may take place in any area of your body, but the parts of your body that are affected in most instances are your hands, fingers, toes and feet.

There are several different kinds of gangrene. Some of these are gas gangrene, wet gangrene, Fournier’s gangrene and internal gangrene.

Mummification is one of the types of gangrene. Mummification usually develops and progresses slowly.

Mummification is referred to in several other ways. It is also known as secondary gangrene, senile gangrene, Pott’s gangrene, native artery gangrene, dry gangrene and arteriosclerotic gangrene.

Mummification is characterized by dry and shriveled skin that ranges in color from brown to purplish-blue to black. In the case of mummification, your tissue becomes black and cold. Eventually, in time, your tissue that is affected by mummification will slough off.

Fortunately, mummification will not spread to other healthy tissue. Also, infection does not take place with mummification.

Mummification is the most prevalent kind of gangrene. Mummification takes place most of the time in people who have a blood vessel disease, such as diabetes or atherosclerosis.

Gangrene occurs when the blood supply to a part or area of your body is cut off. Any underlying condition or injury, or especially a combination of these two, may lead to gangrene of some kind.

In the case of mummification, it is a result of a reduction of blood flow in and through your arteries. This may be caused by several things. Some of these are:

Ÿ  Hypertension (high blood pressure)

Ÿ  Being exposed to extreme cold

Ÿ  Having some form of blood vessel disease

Ÿ  Having an arterial blockage that is the result of a thrombosis

Ÿ  Being a smoker

Ÿ  Having human immunodeficiency virus (HIV)

Ÿ  Having an arterial blockage that has been brought about by an embolism

Ÿ  Taking immunosuppressive medications

Ÿ  Taking chemotherapy treatment for some type of cancer

Ÿ  Having arteriosclerosis or atherosclerosis

Ÿ  Having circulatory problems

Ÿ  Having some kind of surgery

Ÿ  Having diabetes mellitus

Ÿ  Experiencing some kind of trauma

Ÿ  Having high blood cholesterol.

There are some signs and symptoms that you need to watch out for that could be an indication of mummification. Some of the possible signs and symptoms include:

Ÿ  The area of your body that is affected becoming numb and cold

Ÿ  Pain that may start out as a dull ache but that quickly becomes extremely severe

Ÿ  The affected part of your body becoming black and shriveled

Ÿ  The area of your body that is affected becoming red at the beginning

Ÿ  Later on, the affected part of your body being a brown discoloration.

Mummification may be a disorder that has happened to you. As a result, you may need to check on getting social security disability benefits, such as SSDI or SSI. It would be worthwhile to call one of the social security attorneys at socialsecurityhome.com. The attorneys at socialsecurityhome.com can help you get the disability benefits that are rightly yours.

 

 

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Allergic Cutaneous Vasculitis and Receiving Social Security Disability

Thursday, October 13th, 2011
possible acute allergic cutaneous vasculitis

Image via Wikipedia

Vasculitis is a broad medical term that is used to refer to a group of uncommon diseases that are characterized by inflammation of your blood vessels. Your blood vessels are what make up the vascular system of your body.

Your blood vessels are composed of arteries that take oxygen-rich blood to the tissues of your body and veins that carry back oxygen-depleted blood from your tissues to your lungs to get more oxygen. Vasculitis is evidenced by inflammation in and damage to the walls of different blood vessels in your body.

Each one of this group of diseases under the heading of vasculitis is characterized by certain patterns of particular organ involvement, distribution of blood vessel involvement and laboratory test abnormalities. Another way in which this group of diseases is referred to is that they are also called vasculitides.

Allergic cutaneous vasculitis is one of the forms of vasculitis. Allergic cutaneous vasculitis is marked by the development of cutaneous lesions, such as vesicles, small ulcers, papules, purpura, macules and urticarial wheals.

Allergic cutaneous vasculitis is characterized by the inflammation of blood vessels in your subcutaneous tissue and skin. Allergic cutaneous vasculitis especially involves your small and medium-sized blood vessels. These are blood vessels, such as your venules, arterioles and capillaries.

Three Types of Vasculitis

There are three types of allergic cutaneous vasculitis. They are chronic, acute and subacute allergic cutaneous vasculitis.

Chronic allergic cutaneous vasculitis is an ongoing, long-lasting disease. It is evidenced by the occurrence of macules and papules in areas of your body where blood vessels are dominant. This may include areas, such as your back, abdomen, upper and lower limbs, buttocks and arms.

Acute allergic cutaneous vasculitis is a short-term disease. It may damage the blood vessels and tissues that are involved. Acute allergic cutaneous vasculitis may also hinder blood supply to your surrounding tissues and result in tissue death.

Subacute allergic cutaneous vasculitis is usually not as serious. It is usually resolved in around a week.

As you would expect from the name, allergic cutaneous vasculitis is caused by an allergic reaction. It results from an allergic reaction or hypersensitivity to a drug, foreign substance or infection. However, even though your doctor has your complete medical history, what causes this hypersensitivity or allergic reaction to take place has not yet been discovered.

Signs and Symptoms that you have Vasculitis

There are several different signs and symptoms that you may experience, which may be an indication of allergic cutaneous vasculitis. Some of these include:

Ÿ  A rash that develops on the surface of your skin that consists of small red blotches that are referred to as petechiae or large bruises that are known as ecchymosis

Ÿ  The formation of papules and macules, lump or wheal formations on your skin

Ÿ  Swelling that takes place in your lower legs

Ÿ  Itching or pruritus (a sensation that causes the reflex or desire to scratch)

Ÿ  Redness

Ÿ  Irregular fever

Ÿ  Muscle pain

Ÿ  General fatigue

Ÿ  Weakness in your lower legs

Ÿ  Malaise (a general sick feeling that you just do not feel well).

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Granulated Eyelids and Receiving Social Security Disability Benefits

Friday, September 16th, 2011
Eyelash

Image via Wikipedia

Your eyelid is a thin fold of skin that covers and protects your eye. Your eyelid is made up of the thinnest skin on your body except for the labia minora (lips of the female external genitalia) and the fold of skin that covers the head of the penis (prepuce).

It is extremely important for the front surface of your eyeball and cornea to remain moist. Your eyelids do this all-important task for you by sweeping the secretions of your lacrimal (tear gland) apparatus and other glands over the surface at regular intervals while you are awake. Your eyelids cover your eyes to help stop evaporation while you are asleep.

Your eyelids are what permit you to blink your eyes. This blinking aids in keeping dirt and dust out of your eyes. Blinking also helps guard your eyes from injuries that are the result of foreign bodies.

Your eyelashes are a fringe of short hairs that grow on the edge of your eyelids. Your eyelashes function as a screen that keeps dust particles and insects from getting in to your eyes whenever your eyelids are partially closed.

Granulated eyelids is a chronic (long-term) disease that is marked by inflammation of your eyelids. Granulated eyelids is a common inflammatory disease. It is also evidenced by your eyelids becoming scaly and flaky.

There are two kinds of granulated eyelids. They are anterior and posterior granulated eyelids. Anterior granulated eyelids involves the outside front of your eyelid. This is where your eyelashes attach to your eyelids.

Posterior granulated eyelids affects your inner eyelid. This is where your eyelid comes in contact with your eye.

Granulated eyelids is caused by tiny oil glands not working like they ought to. These tiny oil glands are located near the base of your eyelashes. There are several disorders and conditions that may bring this about. Some of these are:

Ÿ  Allergies that include reactions to eye medications, contact lens solutions or makeup

Ÿ  Some type of bacterial infection

Ÿ  A skin condition that is evidenced by redness in your face (rosacea)

Ÿ  Oil glands in your eyelid that do not work properly

Ÿ  Dandruff of your scalp and eyebrows (seborrheic dermatitis)

Ÿ  Eyelash mites (tiny parasitic mites that infest the roots of your sebaceous glands and eyelashes).

There are some risk factors that may increase your chance of developing granulated eyelids. Some of these include:

Ÿ  Anything that weakens your immune system, such as chemotherapy, diabetes, AIDS or an organ transplant

Ÿ  Yeast infections

Ÿ  Acne

Ÿ  Seborrhea, an oily, scaly skin rash.

There are several different signs and symptoms that you may experience, which may be an indication of granulated eyelids. Some of these are:

Ÿ  The loss of your eyelashes

Ÿ  Frothy tears

Ÿ  Burning, itching

Ÿ  Crusting or flakes on your eyelashes

Ÿ  Redness, warmth and swelling of your eyelids

Ÿ  A sensitivity to light (photophobia)

Ÿ  Eyelashes that grow abnormally (misdirected eyelashes)

Ÿ  Dry eyes

Ÿ  Watery eyes

Ÿ  A blurring of your vision

Ÿ  A gritty (foreign body) feeling

Ÿ  Redness of your eye itself

Ÿ  Infections that keep on recurring

Ÿ  Your eyelids looking dark like raccoon eyes

Ÿ  A yellow or green colored fluid/discharge from your eyes.

Are you being kept from working because you have become disabled as a result of complications that have developed from granulated eyelids and/or other underlying conditions that you have besides this disease? Because of this, you may be seeking financial help.

Have you filed for Social Security disability benefits or disability benefits from the Social Security Administration? Did the Social Security Administration reject your application?

If you plan on reapplying or appealing your denial, you really ought to have the disability lawyer at socialsecurityhome.com fighting for you. The disability lawyer at socialsecurityhome.com may be able to get you the disability benefits that are rightfully yours.

Do not delay. Turn to socialsecurityhome.com, now.

 

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Fifth Disease and Receiving Social Security Disability

Wednesday, September 14th, 2011
A 16 month old child with Fifth Disease (aka S...

Image via Wikipedia

Fifth disease is a highly contagious childhood disease. It is a common ailment that, historically, was one of the five common childhood diseases that was marked by a rash.

Even though fifth disease is a common childhood illness, adults can get it, also. For people with a weakened immune system, women who are pregnant or people with certain kinds of anemia, fifth disease can result in serious health problems.

Fifth disease is caused by one of a family of small single-stranded DNA viruses that is referred to as parvovirus B19. This virus only infects humans. It is not the same parvovirus that can infect your dog or cat. Also, this virus cannot be passed from humans to animals or from animals to humans.

Fifth disease occurs all over the world. This ailment can develop in anyone at any time of the year. However, fifth disease takes place most of the time in elementary school-age children during outbreaks in the spring and winter months.

As mentioned at the start, fifth disease is highly contagious. It is spread from person to person in the same way as a cold. This may involve respiratory secretions and hand-to-hand contact.

Many adults with fifth disease do not experience any signs or symptoms. This is borne out by the fact that studies show that anywhere from 40 to 60% of adults all over the world have laboratory evidence of a past parvovirus B19 infection, but most cannot remember having any signs or symptoms of fifth disease. When signs and symptoms do occur, they vary greatly by age.

Adults with fifth disease do not usually have the distinctive slapped-cheek rash that children have, but you may have a lacey rash on your body. Instead, one of the main signs and symptoms that you may experience as an adult is swelling, pain and soreness in your joints that may last for weeks. The joints that are affected most often are your wrist, hands, ankles and knees.

As an adult, you may also have flu-like signs and symptoms, such as chills, fever, headache, fatigue and muscle aches. These flu-like symptoms are usually more severe than they are in children with fifth disease.

You or a loved one may have fifth disease. Fifth disease and/or complications that have developed from it or other conditions that you have in addition to this ailment may have brought about the disability of you or your loved one and be what is keeping you from being able to work.

As a result of this, you may need assistance. You may need financial help.

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Alkaptonuric Ochronosis and Receiving Social Security Disability

Friday, August 12th, 2011

Alkaptonuric ochronosis is an inherited (genetic) disease that is marked by your urine turning black when it is exposed to air. Alkaptonuric ochronosis is also characterized by ochronosis. Ochronosis is where there is an accumulation of dark pigment in your connective tissues, such as your cartilage and skin. This blue-black pigmentation usually takes place after you reach the age of 30.

One of the difficulties that is connected with alkaptonuric ochronosis is that most people who have this disease begin to develop arthritis. The onset of arthritis is usually in early adulthood. This is arthritis that takes place especially in your spine and large joints. Alkaptonuric ochronosis may also cause prostate stones, kidney stones and heart problems.

Alkaptonuric ochronosis is referred to by other names. It is also known as black urine disease, homogentisic acidura, AKU, alkaptonuria and homogentisic acid oxidase deficiency.

Somewhere around 1 in 250,000 to 1 million people in the United States are affected by alkaptonuric ochronosis. The incidence of this disease is much higher in the Dominican Republic and Slovakia. In Slovakia, the rate of incidence of alkaptonuric ochronosis is 1 in 19,000. Women and men are affected equally by this disease.

Alkaptonuric ochronosis is caused by a mutation (defect) in the HGD gene. This faulty gene results in your body not being able to correctly break down tyrosine and phenylalanine. These are two of your amino acids. What results from this is that a substance referred to as homogentisic acid builds up in your skin and other body tissues and goes out of your body when you urinate. When it mixes with the air, your urine turns brownish-black.

As mentioned at the beginning, alkaptonuric ochronosis is a genetic (inherited) disease that you get from your parents. The pattern of inheritance is what is known as autosomal recessive. What this means is that you have to inherit a defective HGD gene from each one of your parents in order to acquire this disease.

Because alkaptonuric ochronosis is a genetic (inherited) disease, there is only one risk factor that is known. It is a family history of this disease.

It is possible for the urine in a baby’s diaper to get darker and turn to almost black after several hours, if the baby has alkaptonuric ochronosis. However, it is also possible for you to have alkaptonuric ochronosis and not be aware of it until you reach close to the age of 40 in mid-adulthood. It is around this time when arthritis and other problems begin to develop with alkaptonuric ochronosis.

There are several other signs and symptoms that you may experience with alkaptonuric ochronosis. Some of these are:

Ÿ  Limited range of motion of your joints

Ÿ  Calcification of your heart vessels

Ÿ  Pain, swelling and stiffness in your joints

Ÿ  Sweat that is dark-stained

Ÿ  Dark spots that show up on your cornea and sclera (the white of your eye)

Ÿ  Artherosclerotic plaques

Ÿ  The darkening of your ear

Ÿ  Erosion of your peripheral joints

Ÿ  Degenerative changes in your peripheral joints

Ÿ  Swelling, stiffness and pain in your thoracolumbar spine.

There are some serious, disabling complications that can result from alkaptonuric ochronosis. These may include:

Ÿ  Coronary artery disease

Ÿ  Kidney stones and prostate stones

Ÿ  The need for heart valve replacement

Ÿ  Arthritis.

Are complications that have resulted from alkaptonuric ochronosis responsible for your incapacity and disability? Are you not able to work?

Have you requested Social Security disability benefits or disability benefits from the Social Security Administration? Were you turned down for these disability benefits?

The lawyer at socialsecurityhome.com can assist you in obtaining Social Security disability benefits or disability benefits from the Social Security Administration. Do not put this off for another day. Get in touch with socialsecurityhome.com, without delay.

 

 

 

Barlow’s Syndrome and Receiving Social Security Disability

Monday, August 8th, 2011
Base of ventricles exposed by removal of the a...

Image via Wikipedia

The center of your cardiovascular system is your heart. Your heart uses your body’s blood vessels to pump blood to all of the cells of your body. Your blood has oxygen that your cells require. Heart disease is a medical term that is used in reference to a group of diseases that develop when your blood vessels and heart are not working like they ought to.

Your mitral valve is also known as the left atrioventricular valve or bicuspid valve. It is a dual-flap valve that separates the upper (atrium) and lower (ventricle) chambers of the left side of your heart. Your mitral valve has the task of regulating blood flow from your left atrium into your left ventricle.

Barlow’s syndrome occurs when your mitral valve fails to close the way it ought to. This can lead to blood leaking back into your left atrium. This is a condition that is known as mitral valve regurgitation.

Barlow’s syndrome is the heart valve abnormality that develops most often. As much as 10% of the general population of the United States may be affected by some type of this syndrome.

No one knows the exact cause of Barlow’s syndrome. However, it is associated with many things. Some of these are:

  • Minor chest wall deformities
  • Heredity
  • Medical conditions like Marfan syndrome, scoliosis, polycystic kidney disease, Graves disease, Ehlers-Danlos syndrome and osteogenesis imperfects.

A vast majority of the time, Barlow’s syndrome does not cause any difficulties and does not need any treatment. However, when Barlow’s syndrome does cause signs and symptoms, it can have serious, life-threatening complications.

If you do experience signs and symptoms with Barlow’s syndrome they can vary greatly from person to person. Some of the possible signs and symptoms are:

  • Dizziness or lightheadedness
  • Depression, anxiety and panic attacks
  • Fatigue
  • Shortness of breath or having trouble breathing that often occurs when you are lying down flat or doing physical activity
  • Migraine headaches
  • Chest pain that is not caused by a heart attack or coronary artery disease
  • An irregular or racing heartbeat (arrhythmia)
  • A cough
  • Heart murmur
  • Low blood pressure when you are lying down.
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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.