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Archive for June, 2011

Three recent books address ‘mental health epidemic’

Thursday, June 30th, 2011

Numbers of reported afflicted great cause for concern

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A disturbing trend

A June 23 review of recent books at The New York Review of Books begins with this startling observation:

It seems that Americans are in the midst of a raging epidemic of mental illness, at least as judged by the increase in the numbers treated for it. The tally of those who are so disabled by mental disorders that they qualify for Supplemental Security Income (SSI) or Social Security Disability Insurance (SSDI) increased nearly two and a half times between 1987 and 2007—from one in 184 Americans to one in seventy-six. For children, the rise is even more startling—a thirty-five-fold increase in the same two decades. Mental illness is now the leading cause of disability in children, well ahead of physical disabilities like cerebral palsy or Down syndrome, for which the federal programs were created.

The review, entitled “The Epidemic of Mental Illness: Why?,” addresses three new works:

 

‘Astonishing 46 %’ meet criteria

You’ll have to read the whole thing to decide whether these books might be useful to you or someone you’d like to help, but we’ll leave you with one more passage from the review, before more commentary on the same:

A large survey of randomly selected adults, sponsored by the National Institute of Mental Health (NIMH) and conducted between 2001 and 2003, found that an astonishing 46 percent met criteria established by the American Psychiatric Association (APA) for having had at least one mental illness within four broad categories at some time in their lives. The categories were “anxiety disorders,” including, among other subcategories, phobias and post-traumatic stress disorder (PTSD); “mood disorders,” including major depression and bipolar disorders; “impulse-control disorders,” including various behavioral problems and attention-deficit/hyperactivity disorder (ADHD); and “substance use disorders,” including alcohol and drug abuse. Most met criteria for more than one diagnosis. Of a subgroup affected within the previous year, a third were under treatment—up from a fifth in a similar survey ten years earlier.

If any of this is close to the target, these are trends we can not ignore. The stats on children have to be particularly disturbing, even for the most hard-hearted among us.

Skepticism: ‘Researchers come up empty-handed’

However, what may be most disheartening for those whose loved ones suffer from these ailments is that all the modern hoo-haw about science and pharmacology might be just that: hoo-haw. Writing about the same three books, and the review itself, Jacob Sullum writes June 13 at Reason.com:

As those questions suggest, Angell seems to share the skepticism of the authors whose books she reviews: University of Hull psychologist Irving Kirsch, who in The Emperor’s New Drugs shows that antidepressants are only slightly more effective than placebos, so slightly that the difference may be attributable to stronger expectations of improvement primed by the drugs’ side effects; the journalist Robert Whitaker, who in Anatomy of an Epidemic argues that the “astonishing rise of mental illness in America” can be understood largely as an outgrowth of the desire to sell psychiatric drugs; and Daniel Carlat, a Boston psychiatrist who confesses his profession’s shortcomings in Unhinged: The Trouble With Psychiatry. Angell notes that “none of the three authors subscribes to the popular theory that mental illness is caused by a chemical imbalance in the brain.” She adds that “the main problem with the theory is that after decades of trying to prove it, researchers have still come up empty-handed.”

None of this can be comforting to anyone connected to a friend or loved one affected by mental illness. Imagine being stuck “in the system” trying to get SSI or SSDI benefits for someone so afflicted.

Delays in system back in the news

The system in general is infamous for its delays and backlog, although some announced efforts we’ve covered here have been targeted at reducing the wait times, which can linger from many months to years. Sadly, recent reports indicate those efforts are losing headway. According to a June 22 report in Baltimore City Paper:

The Social Security Administration (SSA) may be losing its battle against the backlog of disability cases, according to an analysis of its data by a New York-based nonprofit.

“In particular, the data show that while progress had initially been made, the hoped for reduction in backlogged matters ground to a halt in the last 12 months,” a report by the Transactional Records Access Clearinghouse (TRAC) says. “Since then the number of pending cases grew by 5 percent. More success has been achieved in reducing average wait times.”

We can help find an attorney

That’s good news about reducing wait times, but the backlogged cases is definitely not improvement. If you’re feeling “stuck in the system” after having trying to make a go of it by yourself, we understand. And we can help. Perhaps it’s time you reach out to a trained, experienced attorney who can guide you through the maze of federal bureaucracy. If so, please scroll down and, under the heading “Need Help With Your Disability Case?” please complete the online form to get a personal response to your case.

 

Early-Onset Glaucoma and Receiving Social Security Disability

Thursday, June 30th, 2011
Blebitis - infection and inflammation of the g...

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Early-Onset Glaucoma and Receiving Social Security Disability

Glaucoma has the nickname “sneak thief of sight” because the loss of your visual field often takes place gradually over a long period of time and may only be discovered when it is already well advanced. In fact, as many as half of the people with glaucoma are not aware that they have this disorder.

Glaucoma is a major problem all over the world. Worldwide, glaucoma is the number one cause of irreversible blindness. In fact, as many as 6 million individuals are blind in both eyes because of this disorder. In the United States alone, it is estimated that over 3 million people have glaucoma.

Glaucoma occurs most often in older adults. The risk of older adults developing glaucoma can be affected by several different medical conditions. These include family history, hypertension (high blood pressure) and diabetes mellitus.

When an individual develops glaucoma before the age of 40, it is referred to as early-onset glaucoma. The risk of getting early-onset glaucoma is primarily determined by heredity.

There are different forms of early-onset glaucoma. These include primary congenital glaucoma and juvenile open-angle glaucoma.

Early-onset glaucoma occurs most often as a result of inheriting a defective (mutated) gene from your parents. Depending on the type of early-onset glaucoma that you have, you may inherit the possibility of developing this disorder in either an autosomal dominant or autosomal recessive pattern. If you get the defective gene from one of your parents, it is autosomal dominant. It is autosomal recessive if your get the mutated gene from both of your parents.

Although early-onset glaucoma is usually due to inheriting a defective gene from your parents, for reasons that doctors do not totally understand, intraocular pressure (increased pressure within your eye) is what is associated with the damage to your optic nerve that marks early-onset glaucoma. You could think of it in this way. The defective gene is what causes the increased pressure to take place in your eye. The increased pressure is what actually damages your optic nerve resulting in early-onset glaucoma.

There are several signs and symptoms that you may have with early-onset glaucoma. Some of these are:

  • Excessive tearing
  • Abnormal sensitivity to light
  • Eventual blindness
  • Reduction in peripheral (side) vision
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Cranial Arteritis and Receiving Social Security Disability Benefits

Wednesday, June 29th, 2011
The arteries of the face and scalp.

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Arteritis is a condition that involves inflammation in the walls of your arteries. Your arteries are the blood vessels that carry oxygen-rich blood from your heart to the rest of your body. This usually results from an auto-immune system response or an infection.

Cranial arteritis is a serious disease that is evidenced by an inflammation of the lining of the arteries in your head, specifically those arteries in your temples. These are the medium-sized arteries that supply your optic nerves, eyes and head.

Cranial arteritis may also be marked by jaw pain, headaches and blurred or double vision. Blindness and stroke may also result from cranial arteritis.

Cranial arteritis develops most often in people who are over the age of 50. This disease becomes more and more common as people age. In fact, about 20 out of every 100,000 people over the age of 50 are afflicted with cranial arteritis.

Women are twice as likely to be affected by cranial arteritis as men. Caucasians, especially those who are Scandinavians, are also affected by this disease more than people in other races.

Cranial arteritis develops when your arteries become inflamed. However, no one knows what causes this to happen. It is thought that this may be due in part to an incorrect response by your immune system. Cranial arteritis has also been associated with the use of high doses of antibiotics and severe infections.

The hallmark signs and symptoms of cranial arteritis are head tenderness and pain that are usually severe. This usually occurs in both of your temples. However, you may experience the pain in the front of your head or in one of your temples.

Other signs and symptoms of cranial arteritis may vary from person to person. Some of the possible signs and symptoms include:

  • Blurred or double vision
  • Pain in your jaw (jaw claudication) when you chew
  • Unintended weight loss
  • Pain in your tongue (tongue claudication) when chewing
  • Acute tinnitus (ringing in your ears)
  • Stiffness and pain in your arms, hips or neck that is usually more severe in the morning before you get out of bed
  • Sudden, permanent loss of vision in one eye
  • Tenderness of your scalp so that it hurts to lay your head on a pillow or comb your hair
  • Fever
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Peptic Esophagitis and Receiving Social Security Disability Benefits

Tuesday, June 28th, 2011

Peptic Esophagitis and Receiving Social Security Disability Benefits

Heartburn is a common difficulty for people in the United States. It is also a common problem in the rest of the Western world. Somewhere around 7% of the population have heartburn on a daily basis. Probably 20 to 40% of the people who experience heartburn on a daily basis have peptic esophagitis.

Most people know about acid reflux, heartburn and indigestion. However, if you have heard of peptic esophagitis, it is probably because you have been diagnosed with this condition. If so, you know that peptic esophagitis can be a serious problem.

Peptic esophagitis is a condition in which the liquid content of your stomach regurgitates (backs up or refluxes) into your esophagus. This liquid can inflame and damage the lining of your esophagus. Fortunately, this only occurs in a minority of people.

This regurgitated liquid usually contains acid and pepsin that are made by your stomach. Pepsin is an enzyme that starts the digestion of proteins in your stomach. The regurgitated liquid may also contain bile that has backed-up (refluxed) into your stomach from your duodenum. (The duodenum is the first part of the small intestine that attaches to your stomach.)

Acid is thought to be the most harmful component of the refluxed liquid. Bile and pepsin also may injure your esophagus, but their part in the production of esophageal damage and inflammation (esophagitis) is not as clear as the role that acid plays.

Doctors think that there are multiple causes of peptic esophagitis. Different things may cause this condition in different people. There are a small number of people who make unusually large amounts of acid, but this has not been found to be a contributing factor in the majority of people with peptic esophagitis.

Doctors believe that there are several factors that may result in the development of peptic esophagitis. Some of these are:

  • Emptying your stomach
  • Your lower esophageal sphincter
  • Hiatal hernias
  • Esophageal contractions

Regurgitation and continuing heartburn are the primary signs and symptoms of peptic esophagitis.  Other possible signs and symptoms of this condition include:

  • A feeling of choking that may awaken you from sleep
  • A dry cough
  • The feeling of burping acid into your mouth
  • Bad breath
  • The frequent sour taste of acid, especially when you are lying down
  • The feeling that food is stuck in your throat
  • Trouble swallowing
  • A raw, sore throat or hoarse voice.

You or a loved one may have been diagnosed with peptic esophagitis. Peptic esophagitis and/or complications that have developed from it or other illnesses that you have in conjunction with this condition may have resulted in you or your loved one’s disability and not being able to work.

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Hereditary Spinal Ataxia and Receiving Social Security Disability

Monday, June 27th, 2011

Hereditary spinal ataxia is an inherited disease that results in progressive damage to your nervous system. This damage affects your spinal cord and the nerves that control muscle movement in your legs and arms.

Ataxia is usually a sign or symptom of coordination problems, such as unsteadiness or awkward or clumsy movements. Ataxia is present in many different diseases and conditions.

The ataxia in hereditary spinal ataxia results from the degeneration of nerve tissue in your spinal cord. In particular, this is your sensory neurons that are required (through connections with your cerebellum) for directing muscle movement of your legs and arms. Hereditary spinal ataxia causes your spinal cord to become thinner and nerve cells lose some of their myelin sheath (the insular covering on some nerve cells that helps conduct nerve impulses).

Hereditary spinal ataxia affects around 1 in 50,000 people in the United States. This disease affects men and women equally.

As mentioned earlier, hereditary spinal ataxia is an inherited disease. It results from an abnormality in one of your genes, called X25, located in the ninth chromosome pair. The pattern of inheritance is what is known as autosomal recessive. What this means is that hereditary spinal ataxia can only occur when you inherit the defective (faulty) gene from both of your parents. If you get a defective gene from only one of your parents, you become a carrier of the disease.

The signs and symptoms of hereditary spinal ataxia usually start between the ages of 5 and 15. However, with late onset of the disease, signs and symptoms may begin in your 20s or 30s.

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

  • Your feet becoming deformed and rigid
  • Muscle weakness in your arms and legs
  • Diabetes
  • Paralysis of a lower limb
  • Hearing loss
  • Curvature of your spine
  • Vision impairment
  • Heart disorders
  • Slurred speech
  • Problems swallowing
  • Trembling when you are standing still
  • Progressive weakness of your legs that may appear as a staggering, lurching gait when you are walking
  • Clumsiness
  • Partial loss of your sensitivity to pain and temperature or your sense of touch
  • Loss of coordination.

You or a loved one may be afflicted with hereditary spinal ataxia. Hereditary spinal ataxia and/or complications that have been caused by it or other disorders that you have besides this disease may have led to you or your loved one’s disability and inability to work.

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

You or your loved one may be intending to apply for the financial assistance that you need from the Social Security Administration by applying for Social Security disability benefits or disability benefits because of the disability that has been caused by hereditary spinal ataxia and/or complications that have resulted from it or other disorders that you have besides this disease. You may have already tried this option, and your claim was turned down by the Social Security Administration.

If you or your loved one is planning on reapplying or appealing the denial, here is an important fact that you really need to keep in mind that you may not know about. The fact of the matter 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.

Please do not delay or wait until tomorrow. This is a matter of great importance to you or your loved one. Contact the disability attorney at socialsecurityhome.com, today.

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Myofascial Pain Syndrome and Receiving Social Security Disability

Sunday, June 26th, 2011
Collage of several of Gray's muscle pictures, ...

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Myofascial Pain Syndrome and Receiving Social Security Disability

Myofascial pain syndrome is a chronic kind of muscle pain. The pain that results from myofascial pain syndrome is located around sensitive points in your muscles that are known as trigger points.

These trigger points may be painful to the touch. The pain may then radiate throughout your affected muscle.

Nearly all people have occasional muscle pain at one time or another that goes away in a few days. However, if you have myofascial pain syndrome, you experience pain that gets worse or will not go away. In some cases, the pain may be quite severe.

The pain that is associated with myofascial pain syndrome that results from trigger points has been linked to many different kinds of pain. Some of these are pelvic pain, leg pain, jaw pain, arm pain, low back pain, neck pain and headaches.

Women are more likely than men to develop myofascial pain syndrome, but the reason for this is not clear. Also, myofascial pain syndrome is more common in middle-aged adults than in younger adults. The reason is thought to be that the muscles of younger adults are better able to deal with strain and stress than those of older adults.

Myofascial pain syndrome may be caused by a muscle injury or strain on a tendon, ligament, muscle group or individual muscle. Other possible causes of myofascial pain syndrome are:

  • Repetitive motions
  • A lack of activity from having something like a broken arm or leg
  • An injury to an intervertebral disc
  • Medical conditions like stomach irritation or a heart attack
  • General fatigue.

There are several signs and symptoms that you may experience with myofascial pain syndrome. These include:

  • Pain that worsens or persists
  • A problem with sleeping because of pain
  • Deep, aching pain in one of your muscles
  • An area of tension in your muscle that may feel like a tight spot or knot and that may be very sensitive to touch
  • Joint stiffness that is near your affected muscle
  • Muscle stiffness
  • Fatigue
  • Behavioral disturbances
  • Depression.

 

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Bowel Incontinence and Receiving Social Security Disability Benefits

Saturday, June 25th, 2011
Diagram of the rectum and anus.

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Bowel incontinence is the term that refers to the involuntary loss of gas, liquid stool or solid stool. If it is the loss of liquid stool or gas, it is called minor incontinence. When it involves the loss of solid stool, it is known as bowel incontinence.

Bowel incontinence can be a leakage of stool that occurs once in a while as you are passing gas. Or, it can be a complete loss of control of your bowel movements.

Bowel incontinence affects over 5.5 million people in the United States. This figure represents anywhere from 2 to 7% of the general population. The actual incidence may be much higher because many people are embarrassed and ashamed to talk about bowel incontinence, even with their doctor.

Men and women are affected equally by minor bowel incontinence. However, women are two times more likely than men to acknowledge major bowel incontinence.

Bowel incontinence is found most often in older adults. Almost half of all nursing home residents are affected by bowel incontinence.

Bowel incontinence may have a devastating effect on your life. It may undermine your self-confidence, cause you great anxiety, prevent you from working and bring about social isolation by causing you not to want to participate in any social activities.

There are several different disorders that can cause bowel incontinence. Some of these include:

  • Abnormalities of your pelvic floor muscles and nerves
  • Muscle damage to your anal sphincter
  • Loss of the ability of your rectum to stretch and accommodate stool
  • Cancer of the anus or rectum
  • Surgery that involves your anus and/or rectum
  • Diarrhea
  • Chronic abuse of laxatives
  • A loss of muscle strength that comes with advancing age
  • Constipation
  • Damage to the nerves that control rectal sensation or your anal sphincter.

Bowel incontinence is evidenced by the fact that you are not able to get to the toilet in time to prevent an accident. Another sign or symptom of this condition is that you cannot control gas or stools, liquid or solid, from your bowels. You may also have other bowel difficulties along with your bowel incontinence. Some of these are:

  • Constipation
  • Bloating and gas
  • Abdominal cramps
  • Diarrhea.
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Renal Fanconi Syndrome and Receiving Social Security Disability

Friday, June 24th, 2011
Structures of the kidney: 1.Renal pyramid 2.In...

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Renal Fanconi syndrome is a group of kidney difficulties that are caused by a variety of seemingly unrelated disorders. These kidney problems result in excessive urine production and thirst. This leads to deficits of water, calcium, potassium, magnesium and other substances in your body. This may then result in bone disease and stunted growth.

When your kidneys work like they should they cleanse your blood and keep its salt, water and acidity in balance. This puts what your body does not need into urine so it can get out of your body and leaves what your body needs in your blood.

This vital work of your kidneys is done in two steps. First, your blood is filtered through a kidney structure that has small holes that keep the large molecules and cells in your blood. Second, some of the small molecules in the filtrate that your body needs are reabsorbed and returned to your bloodstream.

Renal Fanconi syndrome is evidenced by a defect in this reabsorption step. Because of this, substances that are normally reabsorbed like water, magnesium, small proteins, amino acids, potassium, glucose, bicarbonate, calcium, and phosphate are lost. This results in your body becoming overly acidic.

Renal Fanconi syndrome can result from genetic defects. It can also be caused by different environmental elements.

There are several genetic diseases that are known to result in renal Fanconi syndrome. These include glycogen storage disease, vitamin D dependency, hereditary fructose intolerance, medullary cystic disease, galactosemia, Lowe syndrome, Wilson disease and tyrosinemia.

There are also several environmental factors that can lead to renal Fanconi syndrome. Some of these are certain drugs like outdated tetracycline and gentamicin, kidney transplantation, exposure to heavy metals like lead, platinum, cadmium, uranium and mercury and exposure to other substances like Lysol, paraquat, toluene and the amino acid lysine when taken as a nutritional supplement.

There are several signs and symptoms that you may experience with renal Fanconi syndrome. Some of these include:

 

  • Vomiting
  • Excessive thirst
  • Anorexia nervosa
  • Excessive urine production and urination
  • Elevated levels of glucose, amino acids, calcium, uric acid, protein and phosphate in your urine
  • Dehydration
  • Decreased levels of phosphate and calcium and elevated levels of chloride in your blood, along with excessive blood acidity.

You or a loved one may have been diagnosed with renal Fanconi syndrome. Renal Fanconi syndrome and/or complications that have developed from it or other illnesses that you have in conjunction with this syndrome may have resulted in the disability of you or your loved one and be what is preventing you from working.

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 the disability that has developed from renal Fanconi syndrome and/or complications that have been brought about by it or other illnesses that you have in conjunction with this syndrome. You may have already applied and been denied by the Social Security Administration.

If you or your loved one is considering reapplying or appealing the denial, you really need to remember this important fact that you may not know about. The fact is that people who have a disability lawyer like the one you will find at socialsecurityhome.com are approved more often than people who are not represented by a disability attorney.

Please do not delay. This is something that may affect you or your loved one for the rest of your life. Contact the disability lawyer at socialsecurityhome.com, today.

 

 

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Landouzy-Dejerine Dystrophy and Receiving Social Security Disability

Thursday, June 23rd, 2011

Muscular dystrophy is also referred to as (MD). The term muscular dystrophy refers to a group of genetic, hereditary muscle diseases. These diseases cause progressive muscle weakness in the muscles that enable your body to move.

If you have muscular dystrophy, you have incorrect or missing information in your genes. Because of this, the proteins that are needed for healthy muscles are not made. Muscular dystrophy is a disease that you are born with (congenital). You cannot catch it from someone else.

Muscular dystrophy causes your muscles to weaken over time. You may gradually lose your ability to do things that are taken for granted by most people. These are things like sitting up or walking. The problems caused by muscular dystrophy can start anywhere from infancy to adulthood.

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

Landouzy-Dejerine dystrophy is evidenced by progressive muscle weakness and wasting (loss of muscle tissue). This usually originates in childhood or by the age of 20. However, these signs and symptoms may not be revealed until later in life or not at all. The signs and symptoms of Landouzy-Dejerine dystrophy usually progress very slowly.

Not much was known about what causes any form of muscular dystrophy until the 1980s. Then, researchers discovered that it is caused by a defective (faulty) gene. There is an insufficient amount of dystrophin that is produced because of this faulty gene. Dystrophin is a protein that helps keep your muscle cells intact.

When it starts, Landouzy-Dejerine dystrophy affects the muscles around your lower legs, upper arms, shoulders, mouth and eyes. Later, you may experience weakness in your abdominal muscles and sometimes your hip muscles.

There are other signs and symptoms that you may have with Landouzy-Dejerine dystrophy. Some of these are:

  • Shoulder deformities
  • Problems with pronouncing words
  • Angry or depressed facial expression
  • An inability to whistle
  • Decreased facial expression
  • Abnormal heart rhythms
  • Difficulty walking
  • Drooping of your eyelids
  • Hearing loss
  • Difficulty raising your arms.

You or a loved one may be afflicted with Landouzy-Dejerine dystrophy. Landouzy-Dejerine dystrophy and/or complications that have been caused by it or other disorders that you have besides this disease may have led to the disability of you or your loved one and be what is keeping you from being able to work.

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Charcot Arthropathy and Receiving Social Security Disability Benefits

Wednesday, June 22nd, 2011
Diffuse swelling is noted to the left foot in ...

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Arthropathy is a broad term that is used in reference to joint diseases. This is because arthropathy is taken from two Greek words that mean “joint” and “feeling or disease”.

However, the term arthropathy does not specify the type of joint disease that you may have. Arthropathy may refer to an infectious joint disease, osteoarthropathy or some other kind of joint disease.

There are several different kinds of arthropathy. These include facet, enteropathic, diabetic, crystal, neurogenic and reactive arthropathy. Each of these results from different causes and requires different approaches to treat them.

The incidence and prevalence of the various forms of arthropathy are not known. This is because arthropathy is usually secondary to an underlying disease. Because of this, it is not known how common the various types of arthropathy are.

Charcot arthropathy is a progressive musculoskeletal disorder that is characterized by fractures, deformities and joint dislocation. This leads to progressive destruction of soft and bone tissue of your weight-bearing joints. This occurs most often in your ankle and foot.

It used to be believed that syphilis was the number one cause of Charcot arthropathy. Now, however, diabetes mellitus is considered to be the main cause of this disorder. In addition, any condition that causes autonomic or sensory neuropathy at one of your joints can result in this disorder. These conditions include:

  • Spinal cord injury
  • Renal (kidney) dialysis
  • Leprosy
  • Chronic alcoholism
  • Congenital insensitivity to pain
  • Syringomyelia
  • Meningomyelocele.

Depending on the stage that Charcot arthropathy has reached, the signs and symptoms that you have may vary widely. The main sign or symptom of this disorder is mild to severe swelling, along with moderate deformity. Other signs and symptoms that you may experience with Charcot arthropathy include:

  • Pain
  • Degenerative changes in your affected joint
  • Increased skin temperature
  • Joint effusion (escape of fluid)
  • Instability and loss of joint function
  • Bone resorption
  • Inflammation
  • Concomitant (naturally occurring or associated) ulceration
  • Erythema (redness of your skin).

You or a loved one may be suffering from Charcot arthropathy. This disorder and/or complications that have been brought about by it or other conditions that you have along with this disorder may have caused the disability of you or your loved one and be the reason why you are not able to work.

If this is your situation, you may need help. You may need financial assistance.

You or your loved one may be intending to apply for the financial help that you need from the Social Security Administration by applying for Social Security disability benefits or disability benefits because of the disability that has been brought about by Charcot arthropathy and/or complications that have developed from it or other conditions that you have along with this disorder. You may have already taken this step, and your application was denied by the Social Security Administration.

If you or your loved one is planning on reapplying or appealing the denial, here is an important fact that you really ought to carefully consider that you may not be aware of. The fact of the matter is that people who have a disability lawyer working for them like the one you will find at socialsecurityhome.com are approved more often than people who are not represented by a disability attorney.

 

Please do not hesitate or wait until tomorrow. This could mean so much to you or your loved one. Contact the disability lawyer at socialsecurityhome.com, today.

 

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