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Archive for the ‘Social Security Disability’ Category

Erb’s Paralysis and Receiving Social Security Disability Benefits

Friday, November 11th, 2011

Your brachial plexus is made up of a network of nerves that begin near your neck and shoulder. These nerves originate at your spinal cord in your neck. Your brachial plexus controls your wrist, hand, shoulder and elbow.

Messages going from your brain to all of the other areas of your body are transmitted by way of your nerves. Your nerves are the electrical wiring system of your body. They are very much like an electrical cable that is wrapped in insulation.

The messages that go from your brain to your muscles that allow your body to move are carried by your motor nerves. Messages from different parts of your body are relayed to your brain by your sensory nerves. These are the messages that have to do with temperature, pressure and pain. Your sensory nerves and your motor nerves are both housed by your brachial plexus.

Your brachial plexus is one of your bodily structures that is extremely fragile. Your brachial plexus may be injured by means of pressure, stretching or cutting. The nerves that compose your brachial plexus may be torn out of their roots in your neck if you have an injury that is serious enough.

Erb’s paralysis comes about because of an injury to your brachial plexus. Erb’s paralysis is evidenced by the moving of your upper arm and the rotating of your lower arm being affected.

Erb’s paralysis is a paralysis of your arm that is brought about by an injury to the upper group of your arm’s main nerves. These nerves make up a portion of your brachial plexus. The paralysis that results from Erb’s paralysis can be either complete or partial.

The thing that causes Erb’s paralysis most of the time is a traumatic fall onto the side of your shoulder and head. The result of the fall is that the nerves of your plexus are violently stretched. The area that sustains the greatest damage is the upper trunk of your plexus. Do you have Erb’s paralysis? If you do, you may qualify for some type of social security disability benefits, such as SSI or SSDI. The right thing to do is to go to socialsecurityhome.com and get the advice of one of the social security attorneys. The social security attorneys at socialsecurityhome.com are skilled in matters of disability benefits and dealing with the Social Security Administration. Go to socialsecurityhome.com, now.

There are other things that may cause Erb’s paralysis. Some of these include:

  • Gunshot wounds
  • Violent traction or efforts at reducing a dislocation of your shoulder joint
  • Direct violence.

There are signs and symptoms that may be an indication of Erb’s paralysis. Some of these are:

  • The forearm of your affected arm being pronated and extended
  • The power of flexion of your affected elbow is lost
  • Your affected arm hangs by your side and is rotated medially
  • An inability to raise your affected arm from its side
  • Atrophy (wasting away) of your brachialis, biceps and deltoid muscles
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Polycythemia Vera and Receiving Social Security Disability Benefits

Thursday, November 10th, 2011

Polycythemia vera is one of a group of diseases that are referred to as myeloproliferative disorders. Polycythemia vera is a blood disease that is marked by your bone marrow producing an excessive amount of red blood cells.

Polycythemia vera may also cause an overproduction of other kinds of blood cells, such as platelets and white blood cells. However, with polycythemia vera, it is the excessive amount of red blood cells that results in the thickening of your blood and that are responsible for most of the issues that are related to this disease.

Polycythemia vera is referred to in other ways. It is also known as cryptogenic polycythemia, erythrocytosis megalosplenica, myelopathic polycythemia, polycythemia with chronic cyanosis, Osler’s disease, Vaquez’s disease, splenomegalic polycythemia, erythremia, polycythemia rubra vera and primary polycythemia.

Polycythemia vera is brought about by a defect (mutation) that takes place in one of your bone marrow cells that leads to difficulty with blood cell production. Researchers believe that this defect affects a protein switch that makes your blood cells grow. Scientists believe that it is a defect that is referred to as the JAK2 V617F mutation.

More than 95% of the people who are afflicted with polycythemia vera also have this defect. However, researchers have not yet discovered what causes this mutation to take place. They do think that the defect is something that you acquire rather than inherit from your parents.

There are some risk factors that may increase your likelihood of developing polycythemia vera. Some of these are:

  • Being exposed to intense radiation
  • Being older than age 60, although this disease may occur at any age of life
  • Being a man, because men are twice as likely to get this disease as women are
  • Having a family history of polycythemia vera.

If you have polycythemia vera, you may meet the medical requirements for social security disability like SSDI or SSI. The way to check on this is by looking at socialsecurityhome.com and getting the advice of one of the social security attorneys. The social security attorneys at socialsecurityhome.com are always ready to assist you in obtaining the disability benefits that you deserve.

In most cases, polycythemia vera does not produce any signs or symptoms at all in its early stages. However, as the disease advances, there are several different signs and symptoms that you may experience. Some of these include:

  • A feeling of bloating or fullness in your upper left abdomen that is the result of an enlarged spleen
  • Having problems with your breathing when you lie down
  • Itching that is especially prominent after you have taken a warm shower or bath
  • Headache and difficulty with your vision
  • Fatigue
  • Redness of your skin
  • Weakness, burning, numbness or tingling in your arms, hands, legs or feet
  • Dizziness
  • Shortness of breath
  • Purple patches or spots that show up on your skin
  • Blockage of your blood vessels that may lead to gangrene of your legs and arms, stroke or heart disease
  • High blood pressure (hypertension)
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Osler’s Disease and Receiving Social Security Disability Benefits

Wednesday, November 9th, 2011

Osler’s disease is a disease that is characterized by the formation of multiple abnormalities in your blood vessels (veins and arteries). These abnormal blood vessels may occur in places like your mucous membranes, skin and often times in organs like your brain, lungs and liver.

When your circulatory system is working like it ought to, blood that is transporting oxygen is pumped by your heart out of your lungs at high pressure into your arteries. By the time this blood reaches your capillaries and then flows into your veins, the pressure has gotten much lower.

If you are suffering from Osler‘s disease, some of your arteries go directly into your veins rather than being buffered by your capillaries. The high pressure has a tendency to strain and enlarge your veins due to the fact that they are not as elastic and have thinner walls than your arteries do. This may bring about compression or irritation of your adjacent tissues and frequent episodes of severe bleeding (hemorrhage).

There are different kinds of Osler‘s disease. These include type 1, type 2 and type 3. There is a higher risk for blood vessel malformations in your lungs and brain when you are afflicted with type 1 of Osler‘s disease. You are at a greater risk for malformations in your liver if you are suffering from type 2 or type 3. Women are affected by blood vessel malformations in their liver and lungs with both type 1 and type 2 more often than men are.

Osler’s disease is known by other names. It is also referred to as hereditary hemorrhagic telangiectasia and Osler-Weber-Rendu disease.

Osler’s disease is brought about by a missing or mutated (defective) gene. Researchers have been able to identify some of the genes that are responsible for leading to Osler‘s disease, but they have not yet discovered the way in which these gene defects result in these blood vessel malformations.

Osler’s disease is a disease that is passed down to you by your parents. The pattern of inheritance is what is known as autosomal dominant. What this means is that you only have to inherit a defective (mutated) gene from one of your parents in order to have the possibility of getting Osler‘s disease.

There are several different signs and symptoms that you may experience, which may be an indication of Osler‘s disease. Some of these are:

  • Black, tar-like stools
  • Unexplained, small strokes
  • Vomiting, coughing up blood
  • Dizziness, drowsiness
  • Frequent, sudden nosebleeds
  • Breathing problems, blue lips, domed fingernails (drumstick fingers)
  • Occasional paralysis
  • Fatigue
  • A pale appearance
  • Seizures (epilepsy)
  • Brain aneurysms
  • Shortness of breath when exercising
  • Lesions in your mouth and on your skin that may bleed
  • Digestive tract lesions

If you are having signs and symptoms of Osler’s disease, you may be able to get social security disability benefits. Contact the social security attorneys at socialsecurityhome.com. The social security attorneys at socialsecurityhome.com will be on your side when it comes to getting disability benefits from the Social Security Administration.

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Hereditary Tremor and Receiving Social Security Disability Benefits

Tuesday, November 8th, 2011

Hereditary tremor is a nervous system ailment. Hereditary tremor is characterized by shaking (uncontrolled rhythmic tremors) on different sides of your body and in different parts of your body. You may be afflicted with hereditary tremor. If so, you may be eligible to receive social security disability benefits, such as SSI or SSDI. The social security attorneys at socialsecurityhome.com can help you determine your eligibility for disability benefits. Do not delay. Contact the social security attorneys at socialsecurityhome.com, without fail.

Hereditary tremor is an ailment that is involuntary. What this means is that you are not deliberately trying to shake.

Hereditary tremor takes place most of the time in your hands. However, hereditary tremor may also involve your voice box (making your voice sound shaky), larynx, head, tongue, arms or chin. Although hereditary tremor does not involve your lower body in most instances, it may do so in some cases.

Hereditary tremor may cause you significant problems in trying to do some simple tasks. You may have difficulty with things like shaving, drinking from a glass, tying your shoelaces or writing.

Hereditary tremor is referred to in other ways. It is also called familial tremor, ET, essential tremor and benign essential tremor.

Hereditary tremor is a common ailment in the United States. Somewhere around 10 million people are afflicted with this ailment. About 4 to 5% of the people who are between the ages of 40 and 60 are suffering from hereditary tremor. It affects about 6.3 to 9% of the people who are over the age of 60.

While it is elderly people who are most often affected by hereditary tremor, this ailment may also affect middle-aged people and children. Hereditary tremor is not race or gender specific.

A defective gene causes around 50% of the cases of hereditary tremor. The cause is not known in the other 50%.

There are several signs and symptoms that you may have with hereditary tremor. Some of these include:

  • Problems doing simple things, such as drawing, using tools or writing
  • A shaking or quivering voice
  • Nodding of your head
  • Shaking that is usually small, rapid movements that occur more than five times a second.

the shaking (tremors) may:

  • Come and go, but usually get worse as you get older
  • Occur and be more noticeable when you move and be less noticeable when you rest
  • Begin gradually
  • Not affect both sides of your body in the same way
  • Be aggravated by temperature extremes, fatigue, emotional stress or caffeine.

Many times, hereditary tremor is confused with Parkinson’s disease. However, there are some key differences in the two ailments. Some of these are:

  • When tremors develop – Hereditary tremor usually takes place when you use your hands, while Parkinson’s usually occurs when your hands are at rest.
  • The parts of your body that are affected – Hereditary tremor affects more areas of your body than Parkinson’s does.
  • Associated conditions – Hereditary tremor does not result in other health problems, while Parkinson’s does
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Ocular Melanoma and Receiving Social Security Disability Benefits

Monday, November 7th, 2011

Your cells are the building blocks from which your body is formed. This is where cancer originates. If your body is working properly, old cells die at the right time and new cells replace them when you need them. However, sometimes old cells do not die like they ought to and new cells are produced when you do not need them.

A tumor (mass) can originate with these excess cells. These tumors may be either benign or malignant. If they are benign, they are not cancer. If they are malignant, they are cancer.

Cancer is far greater than one disorder. It is a huge category of diseases. Cancer involves cells that are invasive (they invade and destroy adjacent tissue), aggressive (they grow and divide without respect to normal limits) and sometimes metastatic (they spread to other areas of your body).

There are many different kinds of cancer. They are usually called by where they originated in your body. For example, stomach cancer begins in your stomach. Skin cancer begins in the cells of your skin. Even though the cancer may spread (metastasize) to other areas of your body, it is still designated by where it originated.

Cancer is also arranged by the type of cell that the tumor looks like. Some examples of this are germ cell tumor, lymphoma, blastic tumor, sarcoma and carcinoma.

Melanoma is a type of cancer that originates in the cells of your body that produce melanin. Melanin is the pigment that determines what color your skin will be.

Your eyes also contain melanin-producing cells. Ocular melanoma is cancer that begins in the melanin-producing cells in your eye. Are you disabled because of ocular melanoma? As a result, you may be entitled to social security disability benefits like SSI or SSDI. A great way to check on this is by going to one of the social security attorneys at socialsecurityhome.com. The social security attorneys at socialsecurityhome.com know how to help you when it comes to obtaining disability benefits.

Ocular melanoma is referred to in other ways. It is also known as intraocular melanoma and eye melanoma.

Occur melanoma develops as a result of errors that occur in the DNA of healthy eye cells. However, what causes these errors to take place has not yet been determined.

There are some risk factors that may increase your likelihood of getting ocular melanoma. Some of these are:

  • Being white
  • Getting older
  • Having a light eye color
  • Inheriting certain skin disorders
  • Prolonged exposure to the sun

As is true of some other kinds of cancer, ocular melanoma may not result in any signs or symptoms. If you do have signs and symptoms, they may include:

  • Poor or blurry vision in your affected eye
  • A change in your vision
  • A sensation of flashing lights
  • A change in the shape of the dark circle (your pupil) at the center of your eye
  • A growing dark spot on your iris
  • A loss of vision in your affected eye

    social security disability benefits and Ocular Melanoma

    You may qualify for social security disability benefits if you have Ocular Melanoma

 

 

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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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Demophobia and Receiving Social Security Disability Benefits

Friday, November 4th, 2011
Panic attack

Panic Attacks from Demophobia may qualify you for SSI or SSDI disability benefits.

The word “agoraphobia” comes from two Greek words, which literally mean, “a fear of the marketplace”. Agoraphobia is a type of anxiety disorder that is brought on by the fear of having a panic attack in circumstances or a setting from which you believe there is no easy means of escape.

Agoraphobia is a condition in which you become anxious in environments that are not familiar to you or where you think that you will have little or no control. Traveling, even if it is for short distances, wide open spaces or crowds may all be triggers for agoraphobia.

There is another phobia that can be confused with agoraphobia. This phobia is demophobia. Do you believe that you have demophobia? If you do, you may meet the requirements for social security disability benefits like SSDI or SSI. The right thing to do is to go to socialsecurityhome.com, and get the advise of one of the social security attorneys. The social security attorneys at socialsecurityhome.com are skilled in matters relating to disability benefits.

Actually, demophobia is marked by one aspect of agoraphobia. Demophobia is the fear of crowds, demonstrations or mobs. Demophobia is the fear of being in a crowded place.

Demophobia is the result of an unconscious defense (overprotection) mechanism. Demophobia is usually brought about by your mind over-protecting you from something that it considers to be a real, genuine danger to you. In many cases, demophobia is the result of an unresolved emotional conflict in your life.

In the case of demophobia, your mind sees demonstrations, mobs or crowds as being a threat or something that may harm you. Crowded places are something that you try to avoid because of this phobia.

The signs and symptoms that result from demophobia may be physical, emotional and mental in nature. The fear and anxiety that you experience may range anywhere from mild feelings of anxiety to a full-blown panic attack.

Most of the time, the closer you are to crowded situations, the greater your fear will be. However, because your fear is about crowds and not the actual crowds, themselves, you may experience a strong fear reaction just by using your mind.

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

  • An inability to function in your normal way because of your anxiety
  • A feeling of uncontrollable anxiety when you are expose to or think about crowds
  • The knowledge that your fears are exaggerated or unreasonable but feeling like you have no power to control them
  • The feeling that you have to do everything in your power to stay away from crowds
  • Fear of losing control or going crazy
  • A fear of fainting
  • Persistent worry over coming events that will involve crowds
  • Feeling dizzy, lightheaded or unsteady
  • Shortness of breath or a smothering sensation
  • A pounding heart, palpitations or an accelerated heart rate
  • Shaking or trembling
  • Stomach distress or nausea
  • Chest discomfort or pain
  • Cold or hot flashes
  • Tingling sensations or numbness
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Lower Brachial Plexus Palsy and Receiving Social Security Disability

Monday, October 31st, 2011

There is a network of nerves that begin near your shoulder and neck. This network of nerves is your brachial plexus. These nerves originate in your neck at your spinal cord. Your shoulder, elbow, wrist and hand are controlled by this network of nerves.

Your nerves are like an electrical cable that has been wrapped in insulation. Your nerves are your body’s electrical wiring system that transmit messages from your brain to every other part of your body.

Your sensory nerves are the vehicle that carry messages to your brain from different areas of your body that have to do with pain, pressure and temperature. Your motor nerves are what your brain uses to send messages to your muscles that give your body the ability to move. Your sensory and motor nerves are both located inside of your brachial plexus.

The network of nerves that make up your brachial plexus is very fragile. This means that your brachial plexus is open to damage that may result from pressure, stretching or cutting. If you suffer a serious injury of some kind, the network of nerves that is inside of your brachial plexus may quite literally be ripped out of their roots.

When you have an injury to your brachial plexus, it stops messages from being transmitted to and from your brain. In consequence of this, your hand, arm and shoulder do not function as they ought to. Another result of an injury to your brachial plexus is that you also suffer a loss of feeling or numbness in these areas.

Lower brachial plexus palsy is a kind of paralysis that involves the lower roots of your brachial plexus. Lower brachial plexus palsy affects the muscles of your forearm and hand.

Lower brachial plexus palsy mainly involves the flexors of your wrist and fingers and the intrinsic muscles of your hand. Your wrist flexors and your forearm pronators may also be affected by lower brachial plexus palsy, as well as the elevators of your eyelid and the dilators of your iris.

Fortunately, lower brachial plexus palsy is a rare disorder. The disorder affects less than 200,000 people in the United States.

Lower brachial plexus palsy usually results from traction on your abducted arm. This usually occurs by catching a branch as you fall from a tree. Have you experienced lower brachial plexus palsy? If you have, you may be able to receive social security disability benefits like SSDI or SSI. It is always a wise decision to talk to one of the social security attorneys at socialsecurityhome.com to find out what they would advise you to do. The social security attorneys at socialsecurityhome.com have experience in dealing with the Social Security Administration concerning disability benefits.

There are some signs and symptoms that are characteristic of lower brachial plexus palsy. Some of these include:

  • Weakness in your hand
  • A disturbance in your vision
  • Paralysis of your intrinsic hand muscles
  • Pain
  • Dropping of your eyelids
  • Ulnar nerve distribution numbness

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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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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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