Feb 18

Natural Herbal Treatment for Actinic Keratosis and Symptoms, Causes

What Is Actinic Keratosis?


As you get older, you may begin to notice rough, scaly spots appearing on your hands, arms, or face. These spots are called actinic keratoses, but they’re commonly known as sunspots or age spots. Actinic keratoses usually develop in areas that have been damaged by years of sun exposure. They form when you have actinic keratosis (AK), which is a very common skin condition.

AK occurs when skin cells called keratinocytes start to grow abnormally, forming scaly, discolored spots. The skin patches can be any of these colors:

  • brown
  • tan
  • gray
  • pink

They tend to appear on the parts of the body that get the most sun exposure. This includes the:

  • hands
  • arms
  • face
  • scalp
  • neck

In most cases, actinic keratoses are not cancerous. They are considered “in situ” stage squamous cell carcinoma (SCC) lesions. “In situ” means the lesions are confined to one location and not invading other tissues. When they’re left untreated, however, up to 10 percent of actinic keratoses can progress into SCC. SCC is the second most common type of skin cancer. Due to this risk, the spots should be regularly monitored by your doctor or dermatologist.

What Causes of Actinic Keratosis?

Now the causes for actinic keratosis by long-term exposure to sunlight. You have a higher causes of actinic keratosis risk of developing this condition if you:

  • are over age 60
  • have light-colored skin and blue eyes
  • have a tendency to sunburn easily
  • have a history of sunburns earlier in life
  • have been frequently exposed to the sun over your lifetime
  • have the human papilloma virus (HPV)


What Are the Symptoms of Actinic Keratosis?

Now the symptoms for actinic keratosis start out as thick, scaly, crusty skin patches. These patches are usually about the size of a small pencil eraser. There might be itching or burning in the affected area.

Over time, the lesions can disappear, enlarge, remain the same, or develop into SCC. Symptoms of actinic keratosis no way of knowing which lesions may become cancerous. However, you should have your spots examined by a doctor promptly if you notice any of the following changes:

  • hardening of the lesion
  • inflammation
  • rapid enlargement
  • bleeding
  • redness
  • ulceration

Don’t panic if there are cancerous changes. SCC is relatively easy to diagnose and treat in its early stages.

How Is Actinic Keratosis Diagnosed?

Your doctor may be able to diagnose AK simply by looking at it. They may want to take a skin biopsy of any lesions that look suspicious. A skin biopsy is the only foolproof way to tell if lesions have changed into SCC.

What is the Treatment of Actinic Keratosis?

Treatment for actinic keratosis may be in the following ways: There is many treatment of actinic keratosis but we prefer natural herbal remedies, because it have no side effects.


Excision involves cutting the lesion from the skin. Your doctor may choose to remove extra tissue around or under the lesion if there are concerns about skin cancer. Depending on the size of the incision, stitches may or may not be needed.


In cauterization, the lesion is burned with an electric current. This kills the affected skin cells.


Cryotherapy is a type of treatment in which the lesion is sprayed with a cryosurgery solution, such as liquid nitrogen. This freezes the cells upon contact and kills them. The lesion will scab over and fall off within a few days after the procedure.

Chemical Peels

Certain topical treatments called chemical peels, such as 5-fluorouracil, kill the affected skin cells and cause the lesion to scab over and drop off. While this type of treatment can get rid of the lesions, it may be temporarily disfiguring. Make sure to ask your doctor about the possible side effects of chemical peels and what to expect after treatment.


Duringphototherapy, a solution is applied over the lesion and the affected skin. The area is then exposed to intense laser light that targets and kills the cells. Common solutions used in phototherapy include prescription medications, such as aminolevulinic acid and methyl aminolevulinate cream.


Immunotherapy can involve the use of Imiquimod, which is a topical cream that can be applied to the lesion several times a week. The cream increases the activity of the body’s immune system, but it’s not exactly known why this helps treat AK.

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How Can Actinic Keratosis Be Prevented?


The best way to prevent AK is to reduce your exposure to sunlight. This will also help minimize your risk of skin cancer. Remember to do the following:

  • Wear hats and shirts with long sleeves when you’re in bright sunlight.
  • Avoid going outside at midday, when the sun is brightest.
  • Avoid tanning beds.
  • Always use sunscreen when you’re outside. It’s best to use a sunscreen with a sun protection factor (SPF) rating of at least 30. It should block both ultraviolet A (UVA) and ultraviolet B (UVB) light.

It’s also a good idea to examine your skin regularly. Look for the development of new skin growths or any changes in all existing:

  • bumps
  • birthmarks
  • moles
  • freckles

Make sure to check for new skin growths or changes in these places:

  • face
  • neck
  • ears
  • the tops and undersides of your arms and hands

Schedule an appointment with your doctor as soon as possible if you have any worrisome spots on your skin.




Source Link :          http://www.healthline.com/health/actinic-keratosis#Overview1

Feb 17

Natural Herbal Treatment for Myelitis and Symptoms, Causes

What is transverse myelitis?

Key points

  1. Transverse myelitis is a condition that causes for myelitis section of the spinal cord to become inflamed.
  2. Symptoms range from back pain to more serious problems such as paralysis or loss of bowel control.
  3. Transverse myelitis can be an early symptom of MS.

Transverse myelitis is a condition in which a section of the spinal cord becomes inflamed. This can cause damage to the myelin, the covering for nerve cell fibers. As a result, communication between nerve cells in the spinal cord and the rest of the body can be interrupted.

Symptoms range from back pain to more serious problems, such as paralysis or loss of bowel control.

Causes of myelitis

Transverse myelitis causes is often a onetime illness. But for some people, transverse myelitis is an early symptom of myelitis serious disease of the nervous system. One such disease is multiple sclerosis (MS).

MS is a chronic disease with no cure. It occurs when the body’s immune system attacks the central nervous system. MS can affect various parts of your body, including:

  • brain
  • eyes
  • limbs

The severity of symptoms varies from person to person.

Partial myelitis

Transverse myelitis means both sides of a cross-section of the spinal cord are inflamed. Causes of myelitis, which affects only one side of the cross-section, is more commonly a symptom of MS.

But the National Institute of Neurological Disorders and Stroke recommends that anyone with transverse myelitis or partial myelitis get checked for MS.



Symptom similarities and differences

MS and transverse myelitis share some common symptoms for myelitis, such as a tingling sensation in the arms and legs.

There are also some significant differences between MS and transverse myelitis:

Symptoms of myelitis

People with transverse myelitis often experience back pain as their first symptom. Extreme sensitivity to touch is also present in about 80 percent of people with transverse myelitis, according to the National Multiple Sclerosis Society.

MS symptoms

Myelitis symptoms usually include:

  • numbness or weakness in the limbs
  • vision problems
  • loss of coordination

Causes of transverse myelitis and MS

The causes of transverse myelitis aren’t completely understood. The National Institute of Neurological Disorders and Stroke suggests that the disease may be caused by an infection. The National Multiple Sclerosis Society reports that MS also may be caused by an immune system response.

Who is at risk?

Transverse myelitis can occur in men and women of all ages and races. Like MS, it affects more women than men. In addition, transverse myelitis tends to appear in younger people.

Those between the ages of 10 and 19 and between 30 and 39 face the highest risks of transverse myelitis, according to the National Multiple Sclerosis Society. MS usually develops in people between the ages of 20 and 40.


A doctor usually orders magnetic resonance imaging (MRI) to diagnose transverse myelitis. An MRI of your spinal cord will show inflammation. It will help your doctor determine whether your pain is from a slipped disc or another condition like MS.

For a proper diagnosis, the doctor must get your medical and family history. A neurological exam is also required to diagnose transverse myelitis and MS.

Treatment and recovery

Treatment for myelitis often begins with drugs to decrease inflammation. Since moving your limbs is important to help keep them healthy, you will also likely receive physical myelitis treatment to help repair nerve damage.

Waiting to get treatment of myelitis is dangerous. The sooner you are treated after symptoms appear, the better your chance of recovery.

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Source Link :         http://www.healthline.com/health/multiple-sclerosis/transverse-myelitis#Overview1

Feb 16

Natural Herbal Treatment for Lipoma and Symptoms, Causes

What is a lipoma?


  1. A lipoma is a harmless deposit of fat under the skin that’s typically found on the neck, back, or shoulders.
  2. A lipoma feels soft and isn’t painful, making it easier to diagnose than other skin problems.
  3. Lipomas are rarely harmful, but a dermatologist can remove them if they bother you.

A lipoma is a growth of fatty tissue that slowly develops under your skin. People of any age can develop a lipoma, but children rarely develop them. A lipoma can form on any part of the body, but they typically appear on the:

  • neck
  • shoulders
  • back
  • abdomen
  • arms
  • thighs

They’re classified as benign growths, or tumors, of fatty tissue. This means a lipoma isn’t cancerous and is rarely harmful.

Treatment for a lipoma usually isn’t necessarily unless it’s bothering you.

What are the symptoms of lipoma?


There are many types of skin tumors, but symptoms of lipoma usually has distinct characteristics. If you suspect symptoms for lipoma it will generally:

  • be soft to the touch
  • move easily if prodded with your finger
  • be just under the skin
  • be pale
  • be colorless
  • grow slowly

Lipomas are most commonly located in the neck, back, and shoulders, but they can also occur on the stomach, thighs, and arms. The lipoma symptoms is only painful if it grows into nerves underneath the skin.

You should call your doctor if you notice any changes in your skin. Lipomas can look very similar to a cancerous condition called liposarcoma.



What are the causes of lipoma?


The causes of lipoma is unknown. Your risk of developing this type of skin lump increases if you have a family history causes for lipoma.

This condition is most prevalent in adults between the ages of 40 and 60.

Certain conditions may also increase your risk of lipoma development. These include:

  • adiposis dolorosa (a rare disorder characterized by multiple, painful lipomas)
  • Cowden syndrome
  • Gardner’s syndrome
  • Madelung’s disease

How is diagnosed?


Doctors can often diagnose a lipoma by performing a physical exam. It feels soft and isn’t painful. Also, since it’s made up of fatty tissues, the lipoma moves easily when touched.

In some cases, a dermatologist might take a biopsy of the lipoma. During this procedure, they’ll scrape a small portion of the tissue and send it to a lab for testing. This test is done to rule out the possibility of cancer. Although a lipoma isn’t cancerous, it can look like a liposarcoma, which is malignant, or cancerous. Unlike lipomas, liposarcomas are painful and grow under the skin quickly.

Further testing using MRIs and CT scans are only required if a biopsy shows that a suspected lipoma is actually a liposarcoma.

How Treatment of lipoma?


That’s left alone usually doesn’t lipoma causes any problems. However, your dermatologist can treat the lump if it bothers you. Your dermatologist will make the best treatment for lipoma recommendation based on a variety of factors including:

  • the size of the lipoma
  • the number of skin tumors you have
  • your personal history of skin cancer
  • your family history of skin cancer
  • whether the lipoma is painful


The most common lipoma treatment is to remove it through surgery. This is especially helpful if you have a large skin tumor that’s still growing. Lipomas rarely grow back once they’re surgically removed.


Another treatment of lipoma is liposuction. Since lipomas are fat-based, this procedure can work well to reduce its size. Liposuction involves a needle attached to a large syringe, and the area is usually numbed before the procedure.

Steroid injections

Steroid injections may also be used right on the affected area. This treatment can shrink the lipoma, but it doesn’t completely remove it.

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What is the outlook for someone with skin?


Lipomas are benign tumors. This means that there’s no chance that an existing lipoma will spread. The condition will not spread through muscles or any other surrounding tissues, and it isn’t life-threatening.

A lipoma can’t be reduced with self-care. Ice and heat packs may work for other types of skin lumps, but they aren’t helpful for lipomas because they’re fat-based. See your doctor for treatment if you have any concerns about getting rid of a lipoma.


Source Link :        http://www.healthline.com/health/skin/lumps#Overview1

Feb 15

Natural Herbal Treatment for Motor Neuron Disease and Symptoms, Causes

Motor Neuron Disease

Motor neurone disease is a neurological condition that causes the progressive degeneration of specialised nerve cells, called motor neurons, in the brain and spinal cord. It has no known cause and is invariably fatal, with a likely life expectancy of 2 – 4 years from diagnosis.  In New Zealand about 300 people have motor neurone disease at any one time. Slightly more men than women develop the disease.Symptoms for motor neuron disease can include generalised muscle spasms, exaggerated reflexes and a progressive wasting and weakness of muscles responsible for speech, chewing and swallowing. As the condition progresses, sufferers may be unable to walk, speak, use their arms and hands, or hold up their head.

Causes for Motor Neuron Disease

Motor neurons in the brain and spinal cord convey electrical messages from the brain to the muscles to stimulate movement in the arms, legs, trunk, neck and head. As motor neurons degenerate, the muscles do not work properly and gradually weaken and waste away. This muscle weakness and wasting affects speech, swallowing, movement and breathing.
There are multiple forms of motor neuron disease.  The three main forms are amyotrophic lateral sclerosis (ALS), progressive muscular atrophy (PMA) and progressive bulbar palsy (PBP). Each form is named according to the pattern of symptoms it presents. The most common form is ALS (also known as Lou Gehrig’s disease) which affects about 75% of all motor neurone disease sufferers. A fourth form of the disease, primary lateral sclerosis (PLS), is rare and often only provisionally diagnosed.Most cases of motor neurone disease occur randomly, with no known causes for motor neuron disease. However, 5 – 10% will have a family history of the disease, suggesting a genetic link in those cases.

Motor neuron disease is most commonly diagnosed in those over the age of 40 years, and has its highest incidence in those aged between 50 and 70 years. In some cases, though, symptoms of motor neuron disease can first appear in a person’s 20s.

Usually the onset is gradual but younger patients may show a more rapid progression. The average life expectancy is two to four years from diagnosis but some people succumb within a matter of months, while others live up to 20 years.

Signs and Symptoms of Motor Neuron Disease

Initial symptoms will depend on the form of the condition. However, the most common early sign is weakness in the arms and legs. This is often more pronounced on one side than the other. Other early signs of the condition include:

  • Muscle twitching
  • Muscle wasting
  • An increasingly stiff, clumsy walk
  • General fatigue
  • Difficulty with chewing, swallowing and speech

Motor neuron disease can affect the upper motor neurons in the brain (causing generalised muscle spasms and exaggerated reflexes), or the lower motor neurons in the brain stem and spinal cord (causing a progressive wasting and weakness of muscles responsible for speech, chewing and swallowing). Because motor neuron disease is a progressive disease, both the upper and lower motor neurons are eventually affected.
As the condition progresses, motor neuron disease sufferers may not be able to:

  • Walk
  • Use their hands and arms
  • Speak clearly, or at all
  • Swallow
  • Hold up their head
Weakness of the respiratory muscles makes breathing and coughing difficult. Poor swallowing makes it more likely that food or saliva will be inhaled into the lungs. This increases the likelihood of infection in the lungs, which is often the cause of death for people with motor neuron disease.Pain is experienced in about 40% of cases. Musculoskeletal pain, pressure associated with immobility and muscle cramps are the most common causes of motor neuron disease.  Motor neurone disease does not affect touch, sight, smell, hearing, or intellect. Additionally, the muscles that move the eyes are usually not affected.

In up to 25% of cases, motor neurone disease is associated with frontotemporal dementia, which is a type of dementia that can affect personality and behavior.


Motor Neuron Disease Diagnosis

There is no specific test for motor neuron disease and it may be difficult to diagnose in the early stages.  Diagnosis relies on a complete medical history and physical examination, as well diagnostic tests. If motor neurone disease is suspected, a referral to a neurologist (a doctor who specialises in the treatment of diseases of the nervous system) will be recommended.
A common test used in the diagnostic process is an electromyogram (EMG) which is an electrical test of muscle function. Another common test is a nerve conduction study (NCS) which assesses a nerve’s ability to send a signal.  Other tests that may be used to assist with the diagnosis and rule out other causes for the symptoms include:

  • Blood and urine tests
  • X-rays
  • Computerised tomography (CT) or magnetic resonance imaging  (MRI) scans
  • Muscle biopsy – to determine the health of the muscle tissue

Treatment of Motor Neuron Disease

Many persons say no treatment for motor neuron disease and no cure will significantly alter its course. Medications may be prescribed to control involuntary muscle twitching, muscle cramps and excess saliva. However, treatment of motor neuron disease essentially focuses on retaining function and quality of life, and providing comfort.
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A disease-modifying drug called riluzole (Rilutek), which has the potential to modestly prolong survival in some patients, is available in New Zealand.

Management of the condition will require input from a multi-disciplinary group of health professionals that may include:

  • Family doctor and medical specialists (neurology, respiratory, sleep, gastroenterology)
  • Physiotherapists
  • Occupational therapists
  • Speech and language therapists
  • Nurse specialists and district nurses
  • Dietitians
  • Social workers
  • Counsellors
  • Palliative care specialists and hospice care
  • Sleep technologists
Together, and in conjunction with the patient and family, they will work to maintain mobility and make maximum use of the affected person’s abilities. A wide variety of equipment to help overcome practical difficulties and communication problems are available.The progressive nature of the condition means that most people will eventually require full time nursing care. When breathing becomes too difficult, a mechanical ventilator may be required to maintain breathing. While the use of a ventilator can prolong life and improve sleep, it will not alter the course of the condition, and many people with motor neuron disease therefore choose not to use ventilators for lengthy periods.



Motor Neuron Disease Support and information

The Motor Neuron Disease Association of USA (Inc) provides support, advice, information and advocacy for people living with the disease.

22 Chelford Road
Sale, Cheshire
M33 2XA
United Kingdom.



Source Link :         https://www.southerncross.co.nz/group/medical-library/motor-neurone-disease-symptoms-diagnosis-treatment

Feb 14

Natural Herbal Treatment for Osteomyelitis and Symptoms, Causes

What Is a Bone Infection (Osteomyelitis)?

A bone infection, also called osteomyelitis, can result when bacteria or fungi invade a bone.

In children, bone infections most commonly occur in the long bones of the arms and legs. In adults, they usually appear in the hips, spine, and feet.

Bone infections can happen suddenly or develop over a long period of time. If they’re not properly treated, bone infections can leave a bone permanently damaged.

What Causes of Osteomyelitis?

Many organisms, most commonly staphylococcus, travel through the bloodstream and can causes for osteomyelitis a bone infection. An infection may begin in one area of the body and spread to the bones via the blood stream.

Organisms that invade a severe injury, deep cut, or wound can also causes of osteomyelitis infections in nearby bones. Bacteria can enter your system at a surgical site, such as the site of a hip replacement or bone fracture repair. When your bone breaks, bacteria can invade the bone, leading to osteomyelitis.

The most common osteomyelitis causes of bone infections is Staphylococcus aureus bacteria. These bacteria commonly appear on the skin but don’t always cause health problems. However, the bacteria can overpower an immune system that’s weakened by disease and illness. These bacteria can also cause infections in injured areas.



What Are the Symptoms of Osteomyelitis?

Usually, the symptoms for osteomyelitis to appear is pain at the infection site. Other common signs are:

  • fever and chills
  • redness in the infected area
  • irritability or generally feeling unwell
  • drainage from the area
  • swelling in the affected area
  • stiffness or inability to use an affected limb

How Is Osteomyelitis Diagnosed?

Your doctor may use several methods to diagnose your condition if you have any osteomyelitis symptoms of a bone infection. They will perform a physical exam to check symptoms of osteomyelitis swelling, pain, and discoloration. Your doctor may order lab and diagnostic tests to determine the exact location and extent of the infection.

It’s likely your doctor will order a blood test to check for the organisms causing the infection. Other tests to check for the bacteria are throat swabs, urine cultures, and stool analyses.

Another possible test is a bone scan, which reveals the cellular and metabolic activity in your bones. It uses a type of radioactive substance to highlight the bone tissue. If the bone scan doesn’t provide enough information, you may need an MRI scan. In some cases, a bone biopsy may be necessary.

However, a simple bone X-ray may be enough for your doctor to determine the treatment of osteomyelitis that’s right for you.

What Treatment for Osteomyelitis?

There are several options your doctor may use to treatment for osteomyelitis your bone infection.

Antibiotics may be all that’s necessary to cure your bone infection. Your doctor may administer the antibiotics directly into your veins (intravenously) if the infection is severe. You may need to take the antibiotics for up to six weeks.

Surgery may be required osteomyelitis herbal treatment for bone infections. If you have surgery, your surgeon will remove the infected bone and dead tissue and drain any abscesses, or pockets of pus.

If you have a prosthesis that’s causing the infection, your doctor may remove and replace it with a new one. Your osteomyelitis natural treatment will also remove any dead tissue near or surrounding the infected area.



Who Is at Risk for Osteomyelitis?

There are a few conditions and circumstances that can increase your chances of osteomyelitis, such as:

  • diabetic disorders that affect blood supply to the bones
  • intravenous drug use
  • hemodialysis, which is osteomyelitis treatment used for kidney conditions
  • trauma to the tissue surrounding the bone
  • artificial joints or hardware that has become infected
  • sickle cell disease
  • peripheral arterial disease
  • smoking

Can You Prevent Osteomyelitis?

Thoroughly wash and clean any cuts or open wounds in the skin. Report any wounds or cuts that don’t heal to your doctor. Clean and dry amputation sites before placing your prosthesis. Also, use the proper footwear and protective equipment to avoid injuries when jumping, running, or participating in sports.

What Is the Long-Term Outlook?

Most cases of osteomyelitis are treatable. Chronic infections of the bone, however, may take longer to treat and heal, especially if they require surgery. Treatment should be aggressive because an amputation can become necessary sometimes. The outlook for this condition is good if the infection is treated early.

Source Link :      http://www.healthline.com/health/osteomyelitis#overview

Feb 10

Granuloma Annulare Treatment and Symptoms, Causes

Granuloma Annulare

Granuloma Annulare is a skin condition that is characterized by harmless lesions on the surface of the skin. They usually form circular patterns on the hands and feet, but can appear on your face and neck. These lesions are relatively harmless, unless they become large enough to challenge your self esteem and confidence. These red bumps may appear suddenly but disappear in time. A doctor prescribed treatment plan can make them less visible if preferred. Specific statistics regarding granuloma annulare are relatively unknown. There are no set numbers of patients diagnosed with this condition.

Symptoms of Granuloma Annulare

The symptoms for granuloma annulare include reddish colored bumps that resemble pimples or ringworm. They may begin connecting to each other and can cause severe itching if the condition is widespread across the body. Granuloma annulare symptoms may also appear and reappear without any notice, and no other symptoms are present.

If you do experience symptoms of granuloma annulare then there is a chance you do not have Granuloma, but instead another condition that is more severe. Many types of skin cancers and disorders show similar skin lesions but are not related to this condition in anyway.



Granuloma Triggers

There are no known triggers for this condition. In fact, the majority of people that develop Granuloma annulare are healthy normal individuals. Occasionally this condition develops in people that have a thyroid problem or are diabetic.

Women and young adults are most likely to develop Granuloma Annulare. Scientists and researchers cannot find a link that puts these individuals at a higher risk. Certain conditions are thought to increase the chances of developing this condition, but there isn’t any solid proof that they do. These conditions include tuberculosis, hepatitis variants, herpes, and certain viruses.

Seeing a Doctor for Diagnosis

Most physicians can treat this skin disorder or at least diagnose the condition. However, in certain areas visiting a special dermatologist may be recommended. A dermatologist is also a good option if the patient has severe widespread Granuloma Annulare.

When visiting a doctor be sure to ask questions regarding the condition and always be sure to note any symptoms you may experience. While symptoms aren’t typically common with this disorder, they may be an indicator that another medical condition triggered it.

Causes of Granuloma Annulare

Localized granuloma annulare is a common type of the condition. It can affect anyone of any age. These lesions are commonly very small in size and are mostly localized. This variant will appear on the wrists, feet, ankles, or legs but they may occur in other areas as well.

Generalized GA is a variant that occurs in adults. It may occur in younger individuals, but that is rare and unlikely. The torso, neck, and entire body can be covered in the lesions. They can be small or large discolored lesions. These may make people look like they have an animal type pattern on their body much like a Dalmatian dog’s fur.

Subcutaneous GA is a type that occurs in children. Children may get these on the eyes and scalp, even feet and chest are possible. They are hard and small, and can be deep into the skin. They can be very difficult to deal with as they can also be thick making them more difficult to bend on certain parts of the body.

Perforating GA is a condition that is characterized by papules that may leak discharge. These lesions heal, but do leave behind considerable amounts of scarring. Perforating GA is a rare condition and not a lot is known about what causes for granuloma annulare. They may also be very uncomfortable in children as they may scratch and rub the areas increasing the likelihood of the papules breaking over time. This may be very inconvenient as they can occur on the face which can be unappealing to many people.

Arcuate Dermal Erythema is a condition that is very rare and can occur in large patches on the body. It is another variant of Granuloma Annulare but isn’t seen often by doctors. The large patches may be very shocking for some people as they may be misshapen or look severe enough granuloma annulare causes damage to the person with Arcuate Dermal Erythema. Taking advantage of the insight that doctors can give is important.

Treatment for Granuloma Annulare

Most often, granuloma annulare treatment isn’t necessary. Many patients never experience symptoms and some may not realize that they have Granuloma Annulare. If itching or disfigurement becomes a concern, doctors can treat Granuloma a few different ways.

The most popular method of treatment is by steroid cream or steroid injection. These are not recommended because of the significant side effects that come along with using steroids of any kind. A patient seeking treatment for granuloma annulare by steroid injections may be disappointed with the excess hair growth and weight gain that can occur.

Certain oral medications are also a viable option for treatment. These can vary but are most often a corticosteroid. These steroids can help to repair the cells by providing extra help with low doses. Not taking the proper dose may actually increase the growth of the lesions and make them more unappealing to the patient. Corticosteroids are most often topical creams that can be applied at different doses and amounts depending on what is needed from the patient.

Herbal care products treatment is also a granuloma annulare herbal treatment option for those suffering from widespread Granuloma Annulare. It is a recommended treatment of granuloma annulare that may be self conscious or suffering from a severe condition. The granuloma annulare natural treatment may cause the cells to degenerate and new cells to replace the lost ones over time. It is important to take this granuloma annulare herbal remedies. Others treatments take carefully as increased treatments may be harmful to the skin and causes of granuloma annulare different types.

Many people find that it just simply disappears. Some people may not even realize that they have the condition, and will eventually just shrug it off. This is usually because the lesions are small or are in places that are not seen by the patient. The skin sheds and replenishes itself every few weeks so the condition may simply go away over time as the new skin replaces the old skin over time and the lesions fade. Fading of lesions or darkening can occur for many reasons.



Should You See a Doctor?

If you feel that the condition is ruining your life or causing a self esteem problem you should see a doctor. If you have wide spread lesions then a doctor visit is most necessary. Some people may feel more comfortable getting a diagnosis. It is especially important to get Granuloma checked on if your family has a history of skin disorders that are life threatening.

Many people end up noticing the lesions if they get a natural tan because the difference in skin tone is much higher between normal skin and lesions. This may be alarming to some individuals as they may believe that they have skin cancer. They will find out that going to the doctor will bring back positive results for their skin lesions and granuloma annulare natural remedies options may be discussed. Some people are confident enough to simply live with the skin disorder, but others may not feel up to having their skin not as uniform across the entire body.


Source Link :        http://www.granulomaannulare.net/learn-about-granuloma-annulare.html

Feb 06

Retinal Vein Occlusion Treatment and Symptoms, Causes

What Is Retinal Vein Occlusion?


  1. A retinal vein occlusion is sometimes referred to as an “eye stroke” because it’s a blockage of blood flow from your retina back to your heart.
  2. This eye disease results in sudden blurred vision or a loss of vision.
  3. Retinal vein occlusion can’t be cured. Treatment aims to manage other conditions that occur from having this disease.

A retinal vein occlusion is sometimes referred to as an “eye stroke.” It’s the blockage of one of the veins returning blood from your retina back to your heart. Your retina converts light and images into nerve signals and sends them to your brain via the optic nerve. Blockages from blood clots or fluid buildup in your retinal veins impairs your retina’s ability to filter light and your ability to see. The severity of vision loss depends on which vein is blocked.

What Are the Types of Retinal Vein Occlusion?


There are two types of retinal veins. There’s one central vein and many smaller branch veins. Likewise, there are two types of retinal vein occlusion. There’s central retinal vein occlusion and branch retinal vein occlusion.

Symptoms of Retinal Vein Occlusion

The primary symptoms for retinal vein occlusion is a blurring or loss of vision that’s usually sudden in onset and generally in only one eye. If it isn’t treated, the blurring or loss of vision usually gets worse in hours or days. Sometimes, you’ll see dark spots or floaters, which are tiny clumps of cells or material floating in your eye. In severe cases, a blocked vein will build up pressure and cause pain in your eye.

It’s important to see your doctor right away if you have these symptoms of retinal vein occlusion because a retinal vein occlusion symptoms can lead to other health problems.



What Causes Retinal Vein Occlusion?

Retinal vein occlusions usually occur because your arteries harden and causes of retinal vein occlusion clot, much like a stroke. Blockages are more common in people with narrowed or damaged blood vessels, or those with chronic conditions that causes for retinal vein occlusion. Such diseases include:

  • atherosclerosis, which is a hardening of the arteries
  • glaucoma, which is optic nerve damage that’s usually retinal vein occlusion causes by increased pressure
  • macular edema, which is fluid leakage into the macula, or the area of the retina that allows for sharp focus
  • diabetes
  • high blood pressure
  • high cholesterol
  • blood disorders that affect clotting
  • people over the age of 60
  • people who smoke

Diagnosing Retinal Vein Occlusion

This disease is diagnosed with a comprehensive eye exam, including vision and pressure checks, and examining the surfaces and vessels of your eye. Other tests to diagnose retinal vein occlusion include:

  • optical coherence tomography, in which a high-definition image is taken of your retina
  • ophthalmoscopy, in which your retina is examined with an ophthalmoscope
  • fluorescein angiography, in which a dye is injected into your arm that then travels to your retinal veins to be photographed for blockages

Your doctor may also perform blood tests for diabetes, high cholesterol, and blood clotting disorders.

Treatment of Retinal Vein Occlusion

Blockages in your retinal veins can’t be removed. Retinal vein occlusion treatment focuses on issues arising from the occlusion, such as:

  • laser therapy to reduce edema, or swelling caused by fluid leakage
  • drug injections of corticosteroids to reduce inflammation
  • a vitrectomy, which is the treatment for retinal vein occlusion of all or part of the jelly-like tissue in your eye called the “vitreous humor”

This clinical trial shows that a combination of ranibizumab and aflibercept is effective in restoring vision in patients with macular edema due to a treatment of retinal vein occlusion.

Herbal care products have retinal vein occlusion natural treatment for patients. Retinal vein occlusion herbal treatment is Occlical.



What Is the Outlook for People with Retinal Vein Occlusion?

The outlook for people with this condition depends on its severity. Many people will recover and regain most of their vision, however for some, vision may not return.

Those with other eye conditions or complications are less likely to recover fully. Work with your eye doctor to keep your eyes healthy. Regular checkups can help prevent further problems.

The condition will sometimes go away on its own and you can regain vision.

Retinal vein occlusion natural remedies treat your disease very well without any reaction. People also prefer the occlical product for retinal vein occlusion herbal remedies.

Preventing Retinal Vein Occlusion

Because this disease occurs in veins, you can reduce your risk of it by protecting your blood vessels and maintaining healthy vascular tissue. Healthy lifestyle and dietary changes include:

  • exercising
  • losing weight if you’re overweight
  • maintaining a healthy weight
  • quitting smoking if you smoke
  • controlling diabetes if you have diabetes
  • reducing your blood pressure if you have high blood pressure
  • reducing your cholesterol if you have high cholesterol
  • taking aspirin or other blood thinners if recommended by your doctor

Getting regular eye exams will help your doctor detect and diagnose any eye diseases early on.


Source Link :           http://www.healthline.com/health/retinal-vein-occlusion#overview

Feb 03

Retinitis Pigmentosa Symptoms, Causes and Treatment

Retinitis Pigmentosa

Retinitis pigmentosa is an eye disease in which there is damage to the retina. The retina is the layer of tissue at the back of the inner eye that converts light images to nerve signals and sends them to the brain.

Alternative Names


Retinitis Pigmentosa Causes

Causes for retinitis pigmentosa can run in families. The disorder can be caused by a number of genetic defects.

The cells controlling night vision (rods) are most likely to be affected. However, in some cases, retinal cone cells are damaged the most. The main sign of the disease is the presence of dark deposits in the retina.

The main risk factor is a family history of retinitis pigmentosa causes. It is an uncommon condition affecting about 1 in 4,000 people in the United States. That is causes of retinitis pigmentosa.



Retinitis Pigmentosa Symptoms

Symptoms for retinitis pigmentosa often first appear in childhood, but retinitis pigmentosa symptoms is severe vision problems do not usually develop until early adulthood.

  • Decreased vision at night or in low light
  • Loss of side (peripheral) vision, causing “tunnel vision”
  • Loss of central vision (in advanced cases)

That is major symptoms of retinitis pigmentosa.

Retinitis Pigmentosa Exams and Tests

Tests to evaluate the retina:

  • Color vision
  • Examination of the retina by ophthalmoscopy after the pupils have been dilated
  • Fluorescein angiography
  • Intraocular pressure
  • Measurement of the electrical activity in the retina (electroretinogram)
  • Pupil reflex response
  • Refraction test
  • Retinal photography
  • Side vision test (visual field test)
  • Slit lamp examination
  • Visual acuity

Retinitis Pigmentosa Treatment

There is no effective retinitis pigmentosa treatment for this condition. Wearing sunglasses to protect the retina from ultraviolet light may help preserve vision.

Some studies have suggested that treatment of retinitis pigmentosa with antioxidants (such as high doses of vitamin A palmitate) may slow the disease. However, taking high doses of vitamin A can cause serious liver problems. The benefit of treatment has to be weighed against risks to the liver.

Several clinical trials are in progress to investigate new treatment for retinitis pigmentosa, including the omega-3 fatty acid, DHA.

Microchip implants that go inside the retina and act like a microscopic video camera are in the early stages of development for treating blindness associated with this and other serious eye conditions.

It can help to see a low-vision specialist, who can help you adapt to vision loss. Make regular visits to an eye care specialist, who can detect cataracts or retinal swelling — both of which can be treated.

Retinitis Pigmentosa Outlook (Prognosis)

The disorder will continue to progress, although slowly. Complete blindness is uncommon.

Retinitis Pigmentosa Possible Complications

Peripheral and central loss of vision will eventually occur.

Patients with retinitis pigmentosa often develop cataracts at an early age, or swelling of the retina (macular edema). Cataracts can be removed if they contribute to vision loss.

Many other conditions have similarities to retinitis pigmentosa, including:

  • Friedreich’s ataxia
  • Laurence-Moon syndrome (also called Laurence-Moon-Bardet-Biedl syndrome)
  • Mucopolysaccharidosis
  • Myotonic dystrophy
  • Usher syndrome (a combination of retinitis pigmentosa and hearing loss)

When to Contact a Medical Professional

Call your health care provider if night vision becomes difficult or if you develop other symptoms of this disorder.


Genetic counseling and testing may help determine whether your children are at risk for this disease.


Source Link :       http://www.nytimes.com/health/guides/disease/retinitis-pigmentosa/overview.html

Jan 28

Porphyria Natural Herbal Treatment

What Is Porphyria?

Porphyrias are a group of rare inherited blood disorders. People with these disorders do not make heme, a component of hemoglobin (protein in red blood cells that carries oxygen) properly. Heme is made of porphyrin (a naturally-occurring organic compound in the body) bound to iron. Heme helps red blood cells (RBCs) carry oxygen and also gives RBCs their color. It is also found in myoglobin, a protein in the heart and skeletal muscles.

The body goes through several steps to make heme. However, in people with porphyria, the body lacks certain enzymes needed to complete this process, causing porphyrin to accumulate in tissues and blood. This may cause a variety of symptoms, ranging from mild to severe. The most common symptoms of porphyria are abdominal pain, light sensitivity (causing rashes or blisters), and problems with the muscles and nervous system. The symptoms for porphyria vary and depend on which enzyme is missing.

Porphyria Causes

Causes for porphyria is a genetic disease. According to The Journal of Family Planning (JFP), most types of porphyria causes are autosomal dominant, meaning that a person only inherits the abnormal gene from one parent. (JFP, 2012) However, certain factors may trigger symptoms, known as “attacks.” Factors include:

  • drugs
  • infection
  • alcohol use
  • certain hormones, such as estrogen
  • sunlight

Porphyria Types

There are several different types causes of porphyria, which are classified into two categories: hepatic and erythropoietic. Hepatic forms of the disorder are caused by problems in the liver and are associated with symptoms such as abdominal pain and problems with the central nervous system. Erythropoietic forms are caused by problems in RBCs.

There are five types of hepatic porphyria:

  • acute intermittent (AIP)
  • hereditary coproporphyria (HCP)
  • variegate porphyria
  • aminolevulinic acid dehydratase deficiency (AVADDP)
  • porphyria cutanea tarda (PCT)

According to the National Center for Biotechnology Information (NCBI), PCT is the most common type of porphyria. It is associated with extreme sensitivity to sunlight. (NCBI, 2011)

Erythropoietic porphyria is associated with light sensitivity. There are two types—muroporphyria and protoporphyria.



Symptoms of Porphyria

Symptoms depend upon the type of porphyria. Severe abdominal pain is present in all types, as well as urine that is reddish-brown in color. This is caused by the build-up of porphyrins, and typically occurs after an attack.

Symptoms associated with hepatic disease include:

  • limb pain
  • neuropathy
  • hypertension
  • tachycardia (fast heartbeat)
  • electrolyte imbalance

Symptoms associated with erythropoietic disease include:

  • extreme skin sensitivity to light
  • anemia (when the body does not produce enough new RBCs)
  • changes in skin pigmentation
  • erratic behavior related to sun exposure


Many tests can help diagnose this condition.

Tests that look for physical problems include:

  • computed tomography (CT) scans
  • chest X-ray
  • echocardiogram (EKG)

Tests for blood problems include:

  • urine test for fluorescence
  • porphobilinogen (PBG) urine test
  • complete blood count (CBC)

Porphyria Treatment

There is no treatment for porphyria. Porphyria treatment focuses on managing symptoms. Most cases are treatment of porphyria with medication.

Treatments for hepatic disease include:

  • beta blockers (Atenolol) to manage blood pressure
  • high carbohydrate diet to aid recovery
  • opioids for pain management
  • hematin to shorten attacks

Treatments for erythropoietic disease include:

  • iron supplements for anemia
  • blood transfusions
  • bone marrow transplant


Porphyria cannot be prevented. However, symptoms can be reduced by porphyria natural treatment or porphyria herbal treatment.

Factors that should be eliminated include:

  • recreational drugs
  • mental stress
  • excessive drinking
  • certain antibiotics

Preventing erythropoietic symptoms focuses on reducing light exposure by:

  • staying out of bright sunlight
  • wearing long sleeves, hats, and other protective clothing while outside
  • asking for protection during surgery – in rare cases phototoxic injury can occur. This happens when light perforates the organs and leads to infection.


Porphyria is incurable and difficult to manage. Complications are common. They include:

  • coma
  • gallstones
  • paralysis
  • respiratory failure
  • liver disease and failure
  • skin scarring


Long-Term Outlook of Porphyria

Long-term outlook varies widely. Patients may not be diagnosed until after damage has been done.

Permanent damage may include:

  • breathing difficulties requiring continuous oxygen
  • walking problems
  • anxiety attacks
  • scarring

Early diagnosis can help you lead a relatively normal life. Management is also very important.

If you have an inherited condition, talk to a genetic counselor. He or she can help you understand the risk of passing it to your children.


Source Link :      http://www.healthline.com/health/porphyria#Overview1

Jan 23

Treatment for Peripheral Neuropathy by Natural Herbal Remedies

What is peripheral neuropathy?

Peripheral Neuropathy: Your peripheral nervous system connects the nerves from your brain and spinal cord, or central nervous system, to the rest of your body. This includes your:

  • arms
  • hands
  • feet
  • legs
  • internal organs
  • mouth
  • face

The job of these nerves is to deliver signals about physical sensations back to your brain.

Peripheral neuropathy is a disorder that occurs when these nerves malfunction because they’re damaged or destroyed. This disrupts the nerves’ normal functioning. They might send signals of pain when there’s nothing causing pain, or they might not send a pain signal even if something is harming you. This can be due to:

  • an injury
  • systemic illness
  • an infection
  • an inherited disorder

The disorder is uncomfortable, but treatments can be very helpful. The most important thing to determine is whether peripheral neuropathy is the result of a serious underlying condition.

What are the symptoms of peripheral neuropathy?

The three types of peripheral nerves are:

  • sensory nerves, which connect to your skin
  • motor nerves, which connect to your muscles
  • autonomic nerves, which connect to your internal organs

Symptoms of peripheral neuropathy can affect one nerve group or all three.

The symptoms for peripheral neuropathy include:

  • tingling in the hands or feet
  • a feeling like you’re wearing a tight glove or sock
  • sharp, stabbing pains
  • numbness in the hands or feet
  • a weak, heavy feeling in the arms and legs, which sometimes may feel like your legs or arms lock in place
  • regularly dropping things from your hands
  • a buzzing or shocking sensation
  • thinning of the skin
  • a drop in blood pressure
  • sexual dysfunction, especially in men
  • constipation
  • digestive difficulty
  • diarrhea
  • excessive sweating

These symptoms can also indicate other conditions. Make sure you tell your doctor about all of your symptoms.



What are the causes of peripheral neuropathy?

People who have a family history about causes of peripheral neuropathy are more likely to develop the disorder. However, a variety of factors and underlying conditions may also cause this condition.

Generalized diseases

Nerve damage caused by diabetes is one of the most common forms of neuropathy. This leads to numbness, pain, and a loss of sensation in the extremities. The risk of neuropathy increases for people who:

  • are overweight
  • have high blood pressure
  • are over the age of 40
  • have diabetes

According to the University of Chicago’s Center for Peripheral Neuropathy (UCCPN), nearly 60 percent of people with diabetes have some sort of nerve damage. This damage is often due to high blood sugar levels.

Other chronic diseases that may cause nerve damage include:

  • kidney disorders in which high amount of toxins build up in the body and damage nerve tissue
  • hypothyroidism, which occurs when the body doesn’t produce enough thyroid hormone, leading to fluid retention and pressure surrounding nerve tissues
  • diseases that cause chronic inflammation and can spread to the nerves or damage connective tissue surrounding nerves
  • deficiencies of vitamins E, B-1, B-6, and B-12, which are essential to nerve health and functioning


Physical trauma is the most common cause of injury to the nerves. This can include car accidents, falls, or fractures. Inactivity, or holding still too long in one position, can also cause neuropathy. Increased pressure on the median nerve, a nerve in the wrist that supplies feeling and movement to the hand, causes carpal tunnel syndrome. This is a common type causes for peripheral neuropathy.

Alcohol and toxins

Alcohol can have a toxic effect on nerve tissue, putting people with severe alcoholism at a higher risk of peripheral neuropathy.

Exposure to toxic chemicals like glue, solvents, or insecticides, either through chemical abuse or in the workplace, can also cause nerve damage. Additionally, exposure to heavy metals such as lead and mercury can also cause this condition.

Infections and autoimmune disorders

Certain viruses and bacteria directly attack nerve tissue.

Viruses such as herpes simplex, varicella-zoster virus, which causes chickenpox and shingles, and Epstein-Barr virus damage sensory nerves and cause intense episodes of shooting pain.

Bacterial infections such as Lyme disease can also cause nerve damage and pain if they aren’t treated. People with HIV or AIDS can also develop peripheral neuropathy.

Autoimmune diseases like rheumatoid arthritis and lupus affect the peripheral nervous system in various ways. Chronic inflammation and damage to tissues throughout the body, as well as pressure caused by inflammation, can all lead to severe nerve pain in the extremities.


Certain medications may also cause nerve damage. These include:

  • anticonvulsants, which people take to treat seizures
  • drugs to fight bacterial infections
  • some blood pressure medications
  • medications used to treat cancer

Recent research in The Journal of Family Practice also suggests that statins, a class of drugs used to lower cholesterol and prevent cardiovascular disease, may also cause nerve damage and increase the risk for neuropathy.

How is peripheral neuropathy diagnosed?

First, your doctor will perform a physical exam and ask about your medical history. If they still can’t tell whether your symptoms are due to peripheral neuropathy, other tests to perform include:

  • Blood tests can measure vitamin and blood sugar levels and determine whether your thyroid is functioning correctly.
  • Your doctor may also order a CT scan or MRI to see if anything is pressing on a nerve, such as a herniated disk or a tumor.
  • Sometimes your doctor will order a nerve biopsy. This is a minor surgery that involves removing a small amount of nerve tissue that they can then examine under a microscope.


Electromyography can show problems with how your body’s nerve signals move to your muscles. For this test, your doctor will place a small needle into your muscle. Your doctor will then ask you to move your muscle gently. Probes in the needle will measure the amount of electricity moving through your muscle. This test may feel like you’re receiving a shot. Sometimes the area becomes sore for a few days afterward.

Nerve conduction study

In a nerve conduction study, your doctor places electrodes on your skin. They then pulse tiny amounts of electricity through your nerves to see if the nerves are transmitting signals properly. This procedure is slightly uncomfortable while it’s happening, but it shouldn’t hurt afterward.

What are the treatment for peripheral neuropathy?

The treatment for peripheral neuropathy is based on treating the underlying disorder. If diabetes is the cause, making certain that the blood glucose is controlled is important. If a vitamin deficiency is causing the problem, then correcting the deficiency is the treatment of peripheral neuropathy. Many treatments can bring relief and help you return to your regular activities. Sometimes a combination of treatments works best.

Pain natural medications

Peripheral neuropathy natural treatment by Herbal Care Products.Over-the-counter (OTC) pain medications like acetaminophen (Tylenol) and nonsteroidal anti-inflammatory drugs, such as aspirin and ibuprofen, can be very helpful in controlling moderate pain. If you take them in excess, these drugs can affect your liver or stomach function. It’s important to avoid using them for an extended period, especially if you drink alcohol regularly.

Prescription herbal medications

Many prescription pain peripheral neuropathy herbal treatment can also help to control the pain of this condition. These include narcotics, some antiepileptic medicines, and some antidepressants. Other helpful prescription medicines include:

  • cyclooxygenase-2 inhibitors
  • tramadol
  • corticosteroid injections
  • seizure medications, such as gabapentin or pregabalin
  • antidepressants, such as amitriptyline
  • Cymbalta, which is a serotonin norepinephrine reuptake inhibitor

Prescription drugs for sexual dysfunction in men include:

  • sildenafil (Viagra)
  • vardenafil (Levitra, Staxyn)
  • tadalafil (Cialis)
  • avanafil (Stendra)

Medical Natural Herbal Remedies

Your doctor can use several medical peripheral neuropathy herbal remedies to control the symptoms of this condition. Plasmapheresis is a blood transfusion that removes potentially irritating antibodies from your bloodstream. If you get a nerve block, your doctor will inject an anesthetic directly into your nerves.

Transcutaneous electronic nerve stimulation (TENS)

Transcutaneous electronic nerve stimulation (TENS) doesn’t work for everyone, but many people like it because it’s a drug-free therapy. During TENS, electrodes placed on the skin send small amounts of electricity into the skin. The goal of this treatment is to disrupt nerves from transmitting pain signals to the brain.

Ergonomic casts or splints

Ergonomic casts or splints can help you if your neuropathy affects your:

  • feet
  • legs
  • arms
  • hands

These casts provide support for the part of your body that’s uncomfortable. This can relieve pain. For example, a cast or splint that holds your wrists in a proper position while you sleep can relieve the discomfort of carpal tunnel syndrome.


In addition to OTC pain relievers, many people have found relief peripheral neuropathy natural remedies through:

  • chiropractic care
  • acupuncture
  • massage
  • meditation
  • yoga

Moderate, regular exercise can also help lessen discomfort.

If you drink alcohol or smoke, consider cutting back or stopping. Both alcohol and tobacco aggravate nerve pain and can cause nerve damage when used for long periods.

Take precautions at home

If you have peripheral neuropathy, you’re potentially at greater risk for accidents in the home. You can do the following to improve your safety:

  • Always wear shoes to protect your feet.
  • Keep your floor clear of things that you could trip on.
  • Check the temperature of your bath or dishwater with your elbow, not your hand or foot.
  • Install handrails in your bathtub or shower.
  • Use bath mats that can prevent slipping.
  • Don’t stay in one position for too long. Get up and move around a couple of times each hour. This is especially important for those whose work involves sitting for long periods at a desk.


What is the long-term outlook?

If your neuropathy is due to an underlying, treatable condition, you may be able to stop your peripheral neuropathy by treating the larger problem. However, if this isn’t the case for you, you can successfully manage the symptoms of your peripheral neuropathy. Speak with your doctor to determine the best medical treatment for you, and explore alternative and self-care options that can supplement your medical care.

How can I prevent peripheral neuropathy?

Even if you have a family history of this disorder, you can help prevent its onset by doing the following:

  • avoiding alcohol or drinking it only in moderation
  • avoiding smoking or quitting smoking if you smoke
  • eating a healthy diet
  • getting regular, moderate exercise

You can lower your risk of peripheral neuropathy by:

  • knowing what toxins you might be exposed to at work or school
  • protecting your feet during sports, especially those that involve kicking
  • never inhaling toxins like glue to get high

If you have diabetes, take special care of your feet. Wash and inspect your feet daily, and keep the skin moist with lotion.

Source Link :     http://www.healthline.com/health/peripheral-neuropathy#Overview1

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