The gall bladder stones or cholelithiasis, is the formation of stones in the gallbladder, the organ that stores bile secreted by the liver. The formations, sometimes called "stones", actually look like small rocks. In about 80% of cases, they are composed of crystallized cholesterol. Stones made from bile pigment can be formed, especially in cases of serious liver disease or sickle cell anemia, but this will not be discussed here.

Also, unusual symptoms of gall bladder disease are hard to spot, because they are, as the name says, unusual. If you believe you are feeling unusual symptoms of gall bladder disease, then you should go to a doctor as soon as possible. Aside from that, here is a general description of a common gall bladder disease.

The shape and number of stones (there may be several hundred) differ from one individual to another. They can be as small as a grain of sand or as big as a golf ball. In about eight out of ten cases, the stones involve no discomfort. However, they can block the bile ducts that carry bile to the liver and intestines. If it can no longer be emptied, the gallbladder begins to swell, which can cause violent stomach pains. This is called biliary colic. When the stones do not cause colic, they are sometimes found incidentally during an ultrasound or CT scan of the abdomen.

Note that the intensity of symptoms does not depend on the size of the stones. Indeed, small stones can cause intense pain, and large stones go unnoticed. They may be too large, for example, to get out of the gallbladder and block the channels.

The gallbladder is a small sack located between the liver and intestine. It stores bile, a yellow liquid produced by the liver. During meals and at other times, the gallbladder contracts and releases bile, which then flows into a canal to the intestine where it helps digest fats.

Causes - Bile is composed primarily of water, bile salts (which, emulsifying fat, play an important role in digestion by the gut), cholesterol, phospholipids, pigments and electrolytes. The cholesterol gallstones are formed when:

Bile contains too much cholesterol; Bile does not contain enough bile salts; Gallbladder does not contract regularly (a "lazy" bladder). It is not known exactly what triggers the formation of gallbladder stones, but various risk factors have been identified, such as obesity and having given birth to several children. Note that there is no link between blood cholesterol and the concentration of cholesterol in bile.

Symptoms - In the vast majority of cases, gallstones do not cause symptoms or complications. During a fit - Biliary colic typically lasts 30 minutes to 4 hours. Here are the main symptoms. Intense pain is felt in the middle or upper right abdomen. The pain sometimes radiates to the shoulder and right shoulder blade. Nausea and vomiting. Signs of complications: in the presence of these symptoms, consult a doctor urgently. Fever. Jaundice. A very intense and sudden pain right side of the abdomen, which persists beyond six hours. Persistent vomiting.

What is Cushing's syndrome? The state in which the body produces too much cortisol is called Cushing's syndrome. Cortisol is also sometimes known as a hormone whose production increases in times of stress and is a natural steroid hormone that is like the "cortisone" in some medicines. Cushing's syndrome can be caused because the body produces too much cortisol or for taking too many drugs on the type of cortisone.

What causes Cushing's syndrome? The most common cause of Cushing's syndrome is the type of drugs taking cortisone orally (by mouth) every day for months or weeks. Prednisone is the most common medicine that is taken in this way.

Steroid medicines for asthma and inhaled steroid creams for eczema and other skin conditions do not cause Cushing's syndrome. Even oral medicines taken daily for short periods of time or every other day for longer periods do not often cause Cushing's syndrome.

The second most common cause of Cushing's syndrome is Cushing's disease. Tumors in the adrenal glands or elsewhere in the body can also cause Cushing's syndrome.

What is Cushing's disease? Cushing's disease is the name doctors use when Cushing's syndrome is caused by a pituitary gland tumor. The pituitary gland is located at the bottom of the brain that controls the body's production of cortisol. These small tumors can cause the adrenal glands, located near the kidneys, produce too much cortisol.

Tumors in the pituitary gland in Cushing's disease are usually not cancerous. However, if the tumors grow too much they can cause problems with your vision. What are the Cushing’s disease symptoms and the Cushing’s syndrome signs?

Cushing’s disease symptoms can form fatty deposits around your stomach and your upper back, but arms and legs stay thin and do not usually get fatter. Your skin gets thinner and is easily bruised. Cuts, scrapes and insect bites are slow to heal. You can form streaks of pink or purple skin. The face may become round and bloated. You may feel tired and have muscle weakness. You may feel depressed

Women usually have irregular menstrual periods and they may grow thick or body hair that is more visible than usual. High blood pressure, osteoporosis (weak and brittle bones) and the levels of blood sugar above normal may be signs of syndrome or Cushing's disease. Often you are given skin infections or other infections, and they take longer to heal.

How does my doctor know if I have Cushing syndrome or disease? Your doctor may start by asking some questions and a physical examination. If the cause is a medicine you are taking, no tests are needed. If your doctor thinks you have Cushing syndrome or disease, but does not include drugs that are causing this, you may need to have some blood tests and urine tests.

You may be asked to collect your urine for 24 hours. Your doctor will explain how to do this test. You may also be given a medicine called dexamethasone before collecting the blood or urine. This tests your response to steroids. At some point you may need a computed tomography (CAT or CT scan) or examination (magnetic resonance imaging or MRI). These tests show a "snapshot" of the inside of your body. Looking at these pictures, your doctor can determine whether there are tumors on the pituitary gland or other parts of your body.

Lyme disease is an infectious disease caused by a bacterium (Borrelia burgdorferi) to humans by tick bite (not all ticks are carriers of the bacterium Borrelia burgdorferi). The name of Borrelia burgdorferi sensu lato (ie -in the broad sense) is generic and can be about one or more strains of Bb involved in infection.

Lyme is known as -the disease with 1000 faces- because of that, affecting the entire body, its symptoms mimic those of other diseases, individual reaction to the pathogen is very different from person to person, hence the multitude of events, making lyme disease onset symptoms hard to spot.

The infection is systemic, affecting the entire body, through the 3 stages that are more or less distinct:
-Stage 1 - Chronic migratory erythema (CME) - Lyme Borreliosis usually begins with a characteristic skin lesion, chronic migratory erythema (stage 1).
-Stage 2 - Disseminated infection - After several days to weeks, spirochaetes can spread through blood to other organs in the body.
-Stage 3 - persistent infection - months to years later may show signs of serious complications.

We could define a common core of lyme disease onset symptoms, which applies to all patients, otherwise every patient reacts differently, depending on many parameters: length of illness, number of pathogens that cause infection, characteristics of the individual's own immune system, etc..

If the disease is treated quickly, immediately after the tick bite, the chances of recovery are greater. Otherwise you can reach a disseminated borreliosis, chronic borreliosis, with damage to the joints, cardiac problems and chronic ophthalmologic and neurological problems. In general, after 6 months of symptoms, we can talk about chronic Lyme disease.

Allopathic treatment is limited to antibiotics (repeated courses with high dose antibiotics combined periods of time / course - 4-8 weeks / course). SPA focuses more on boosting immunity, intake of antioxidants, vitamins and enzymes through a diet of raw vegetables or enriched fruit juices and vegetables and salad, green leaves, herbal teas, bee venom bites, pollen, etc..

-Symptoms of Lyme disease: -spot / spots which move around the body (ECM - chronic migratory erythema - early stage disease - Lyme stage 1); -sweating, strong fever; -muscle pain (like after a flu); -headache (like after a flu); -red spot at the tick bite; -weakness, fatigue; -sleepiness; -vision problems (the blurred, double, even disappearance of the visual field); -joint pain (Lyme stage 2 - already chronic phase / age of onset over 6 months); -pain in the tendons, the Achilles heel, etc..;

Other symptoms are as follows: -painful and / or burning muscle; -cardiac and neurological disorders (stage 3); -numbness of the limbs, head, etc..; -sting (as those of cactus); -tingling (like the skin had ants on it); -rashes as if you came in contact with nettles; -swallowing disorders; -urinary disorders (often urgent feeling to urinate); -dizziness; -headache; -sensation of -sand in the eye- or -itchiness in the eye-, etc..; -paralysis of the face or limbs; -psychiatric disorders, depression, anxiety, panic attacks, obsessions, phobias, emotional disturbances (which mimic bipolarity), etc..

The gallbladder is one of the most important organs of the body, but there are many problems associated with it. The gallbladder diseases are surprisingly common, and it is important to be aware of the various causes and gallbladder disease symptoms, so that you can tell right away if you are developing the disease yourself.

Bile is made in the liver and the gallbladder stores and releases in a controlled manner to help the body digest fats. If the flow of bile is slowed or blocked then the ball bladder can become infected and inflamed. The gallbladder disease is a condition that affects men and women but a lot more grain than most women. There are many gallbladder disease symptoms, some to be consistently more common and severe pain in the upper abdomen that increases rapidly and lasts for several hours, under the right shoulder pain, nausea or vomiting, colic, belching, and indigestion.

There are actually several different diseases with which one can suffer from acute cholecystitis. It is an infection or inflammation of the gallbladder, causing pain and usually a fever as well. The pain experienced usually tends to get worse coughing and moving around and if you ever experience the symptoms of gallbladder disease you should get in to see your doctor as soon as possible.

Then there is also chronic cholecystitis, which is a chronic inflammation of the gallbladder and causes sporadic pain in the middle of upper abdominal pain that may be accompanied by nausea and vomiting, and the frequency and severity of attacks is variable. Attacks can be triggered by a variety of factors, including foods such as chocolate and cakes.

Jaundice is also considered to be one of the most common diseases of the gallbladder. It is a condition that can occur when there are gall stones present, and the earliest symptoms of the condition include the same as those associated with acute cholescystitis. Jaundice is caused when there is an obstruction to the flow of bile from the liver.

All diseases of the gallbladder are considered as being serious and can even be potentially dangerous if left untreated. It is important that you seek medical attention if you begin to experience any of the symptoms known here and that you get treatment as immediately as possible.

There are many treatments you can use to relieve symptoms associated with these diseases, even things you can do right at home. The attacks can usually be treated with the counter painkillers, and even do something as simple as putting something hot like a hot water bottle on your stomach- this can bring relief.

Vitamins and over the counter products can help with treating gall bladder problems such as vitamin A, vitamin C, garlic and ginkgo- these vitamins are more common. The deficiency of vitamin A may increase the risk of cancers of the lung, larynx, bladder, gall bladder, esophagus, stomach, colon, rectum and prostate.

Vitamin C is nature's protective nutrient, essential for defending the body against pollution and infection and enhances the body’s immune system. Take 1,000 to 5,000 mg daily. Garlic counteracts the usual result of high fats in the diet and helps reduce high blood pressure. Ginkgo further widens the blood vessels, increases circulation and speeds blood flow in the capillaries.

Batten disease is a fatal, hereditary disorder of the nervous system that begins in childhood. The first symptoms of this disorder usually appear between the ages of 5 and 10 years, when parents or doctors warn that a previously normal child has begun to have seizures or vision problems. In some cases the early signs are subtle. The early symptoms of Batten disease manifest in changes in personality and behavior, slow learning, clumsiness or stumbling while walking.

Over time, the symptoms of Batten disease can lead to mental impairment, more severe seizures and progressive loss of sight and motor skills. Eventually, children with Batten disease become blind, bedridden and even insane. Batten disease is often fatal to reach the final years of adolescence or reach the age of 20.

Batten disease is named after the British pediatrician who first described it in 1903. Also known as Spielmeyer-Vogt-Sjogren-Batten is the most common form of a group of disorders called neuronal NCL (NCL by its acronym in English). Although Batten disease is generally regarded as the juvenile form of NCL, doctors often use the term Batten disease to describe all forms of NCL.

There are three main types of neural NCL (NCL), including two forms beginning by early childhood and a very rare form that strikes adults. The symptoms of these three types are similar to those of Batten disease, but become apparent at different ages and progress in different ways.

The child neuronal NCL (Santavuori-Haltia disease) begins about 6 months to 2 years of age and progresses rapidly. Affected children usually do not develop and have an abnormally small head (microcephaly). Also typical are short and sharp contractions of the muscles called myoclonic jerks. Patients usually die before the age of 5 years, although some have remained in a vegetative state a few years.

The late infantile neuronal NCL (Jansky-Bielschowsky disease) begins between ages 2 and 4 years. The typical early signs are loss of muscle coordination (ataxia) and seizures that do not respond to medication. This form progresses rapidly and ends up being lethal in the ages between 8 and 12.

The adult neural NCL (Kufs disease or Parry's disease) usually begins before age 40, causes milder symptoms that progress slowly and does not cause blindness. Although age of death is variable among patients with this disorder definitely shortens life expectancy.

Until now, there is no known specific treatment that can halt or reverse the symptoms of Batten disease or other neural NCL. However, in some cases can reduce or control seizures with anticonvulsant medications and other medical problems can be treated appropriately as they arise. At the same time, physical and occupational therapy can help patients preserve the functioning of your body for as long as possible. Some reports have noted delays of the disease in children with Batten disease who were treated with vitamins C and E and with diets low in vitamin A. However, these treatments did not prevent patients died because of disease.

Helping and encouraging patients can help themselves and their families to face serious situations of disability and dementia caused by neural NCL. Often, support groups allow children, adults and families affected to share common experiences and concerns. Meanwhile, scientists continue to research for something that could result in an effective treatment in the future.

Peyronie's disease is a disorder that is manifested by abnormal curvature of the penis during an erection due to scarring of erectile tissue. This scarring prevents straightening of the penis, and some people may have their penis curved so severe that penetration is almost impossible. Those suffering from this disease experience pain during intercourse.

The disease is most common among middle-aged men and elderly. Symptoms of Peyronie’s disease - Signs and symptoms of Peyronie's disease can occur instantly or may be developed in time. Some symptoms include: - Curved penis during erection; - A bulge along the penis on one part or both parts of the penis; - Painful erections, some men do not feel pain than swelling reached; - Inability to maintain an erection; - Inability to penetrate; - Shorten penis

In most cases the pain caused by Peyronie's disease may disappear, but a curved penis will persist even if no pain is felt. Causes leading to disease - Currently, doctors do not know with certainty the exact causes of the disease, but existing theories include cases such as:
- Injury to the penis: an accident in the penis area can cause blood vessels in the penis to break and cause internal bleeding, which in time lead to severe wounds that may develop fibrosis or calcium deposits that have resulted in a curved penis
- Autoimmune disorders: the scar might be a reaction of immune system factors
- Inheritance of an abnormalities
- Drugs: some drugs may cause Peyronie's disease because of side effects. Most drugs are responsible for the occurrence of disease like high blood pressure, heart disease, or glaucoma

Diagnosis and treatment - Through a physical exam, your doctor can tell if you have the Peyronie's disease. Because Peyronie's disease differs from person to person, treatment should be prescribed by the doctor. Some treatment methods include:
1) oral medication - If the disease does not show signs of improvement, the doctor may prescribe oral drugs, increasing treatment applies to the first 12-18 months when the wound is in training. Medicines recommended for this disease include:
- Colchicine, medicament increase may inhibit the growth of collagen and improve symptoms. Side effects of this medicine are digestive problems and diarrhea.
- Aminobenzoate Potassium: taken after medical advice, this medicine can cure you of disease. No studies have been conducted to determine the exact efficacy of this product.
- Vitamin E: Studies show that vitamin E can help alleviate disease, although in this case be conducted more thorough research

2) injections - Your doctor may encourage all treatment consisting of drugs such as Verapamil injected directly into the injured. Injections are meant to destroy the scar.

3) Surgery - If no drug treatment helped in the case of this disease and the penis still remains curved, you can opt for surgery. Doctors recommend this last method when the patient has painful sexual acts or of poor quality sexual acts. Surgery is necessary to restore the normal erection functions. Surgical options are: remove scars or cutting portion affected. In some cases, the use of prosthesis can help maintain the erection during the sexual act. And this method has side effects, because the penis might shorten n time.

Behcet's syndrome is a multi-systemic disease, chronic, characterized by mouth ulcers, genital lesions and eye lesions. At some people appear arthritis, skin problems, inflammation of the gastrointestinal tract, brain and spinal cord. The disease was discovered in 1973 by Dr. Hulusi Behçet, a dermatologist in Turkey.

This is common in the Middle East, Japan and Asian countries where the syndrome affects more men, and tends to develop especially in the second - the third decade of life, but may be encountered at other ages. Researchers do not yet know the causes of this disease, but it is believed that genetic and environmental factors have an important role in triggering it. The disease is not contagious, that is not transmitted between people.

Causes - Inflammation: Most Behcet's disease symptoms are caused by inflammation of the blood. The inflammation of vessels is a characteristic of the body when attacked, and is marked by these signs: pain and local heat.

Doctors think that an autoimmune reaction would cause inflammation of blood vessels, but do not know what triggers them. A normal immune system protects the body conditions of infection and disease and removes harmful foreign substances like germs that enter the body. In an autoimmune reaction, the immune system mistakes and attack the body's own components.

Genetic and environmental factors - Are thought to be hereditary, and some bacteria or viruses could trigger this disease.

Behcet's disease symptoms - Symptoms of Behcet's syndrome vary from person to person another. Some have mouth ulcers, others have a more severe vision loss. They show periods of remission and reactivation. The 5 common symptoms of the disease are: -mouth ulcers; -genital ulcers; -skin problems; -impaired different parts of the eye; -arthritis.

Genital ulcers resembles the mouth ulcers, they appear on the scrotum in men and the vulva in women. Skin lesions are a common symptom in the syndrome, they include folliculitis, erythema nodosa, exanthema. Patients have acne more frequently on the legs and the thorax, and in some people injury occurs when the skin is scratched.

When a person is suspected of the Behcet's syndrome, they are submitted to take a test in which the skin is punctured with a needle. Arthritis- swollen joints, deformed legs and knees. It causes swelling and pain. Other symptoms are: - Central nervous system comprising meningitis and Encephalitis (brain inflammation) -formation of clots -affecting the gastrointestinal tract -blindness.

The central  nervous system includes brain and spinal cord function to include information processing and coordination of thinking, behavior, sensation and movement. The Behcet syndrome can cause inflammation of the brain, the spinal cord and the thin membranes that surround these organs. These conditions are translated into encephalitis and meningitis and they determine: -fever -headache -stiff neck - difficulty in coordinating movements. These symptoms should be immediately found by the doctor, because if they are left untreated can lead to a stroke (blockage or rupture of blood vessels in the brain).

The Gaucher disease is represented mainly by the accumulation of fat in the organs, especially spleen, liver, bone marrow, bones and brain. The accumulation of these fat deposits lead to lower operating capacity of these structures, some being very serious damaged.

What is Gaucher disease? - Gaucher disease is the accumulation of fat especially in internal organs. This accumulation of fat is somewhat specific, in the sense that patients do not accumulate any kind of fat, but only a particular type: glucocerebrosidase. They accumulate in deposits that the person presents a deficiency of the enzyme to metabolize these fats.

What are Gaucher disease symptoms? - Gaucher disease symptoms vary depending on each person, which organs are affected, the degree of impairment of their age, etc. Thus, the events keep the damage to the liver, bone marrow and bone, brain, kidney even: - Anemia due to marrow and spleen damage that destroys red blood cells; - Predisposition to bleeding and bruising of the skin (bruises) due to the decrease in the number of platelets, blood components that occur in repairing broken vessels; - Skeletal abnormalities and frequent fractures, bone pain, change in position;

- Disorders of nerve function that can lead to deep behavioral disorders, including retardation; - Hepatomegaly (liver volume increase) and splenomegaly (spleen volume increase) or both (hepatosplenomegaly); - Yellow fat in the eye and abnormal eye movements (by affecting the optic nerve); - Renal Dysfunction but other organs (e.g. lungs); - Brown staining of the skin (jaundice staining liver damage).

What causes this disease? - The causes are mainly genetic. The Gaucher disease is a genetic disease with autosomal recessive transmission (is transmitted from parents to children, but the disease manifestation skip generation, for example grandparents have the gene, a forward and children, but grandchildren have the disease). Is most common in Jews of Central and Eastern Europe. Both parents must be carriers of the gene that produces the enzyme deficiency.

Types of Gaucher disease - Classification is done on several criteria, depending on age and affected organs.

Type 1 - This form does not affect the brain. The disease may occur at any age but is most common between 19-25 years. Manifestations are progressive and the disease can be kept under control if diagnosed early and treatment begins on time.

Type 2 - Type 2 is very rare and is manifested in infants in the first three months after birth. Presents serious liver diseases, spleen, marrow, brain. The disease evolves quickly and aggressively.

Type 3 - It is also rare and occurs in childhood or adolescence. Is less aggressive than type 2 and evolves more slowly, and affects the brain.

How is the disease diagnosed? - The doctor discussed with the patient and if there is suspicion of this disease, the doctor will take some blood tests to reveal the glucocerebrosidase enzyme dosage. Then investigations are pointing to this disease in the family. The diagnosis of Gaucher disease is made with imaging analysis that shows whether or not an enlarged liver, spleen, marrow and bone density and the doctor must also monitor the developments.

There are pathogens of fat or ring system that in certain stages of their development may mimic cellulites condition. Below are described some of the most popular types of diseases that present similarities with the cell and may be confused by an eye less informed. Also this chapter is intended to criminalize behavior which is minimized as clear symptoms of serious UNPR illness, usually because of insufficient preparation in the field which provides such therapies. It is again clear the important role of cellulite and the medical diagnosis at early stages of this disease that may have a very serious evolution.

Differential diagnosis is made by the following elements: 1. Growth of lymphatic stasis; 2. Venous stasis; 3. Abnormal fat can be: A. minus (lipodystrophy) b. in excess of fat (located fatness). In this disease, sometimes extremely serious, legs and feet are swollen. The edema is initially depressed, the skin maintains its properties, the disease is painless, is accompanied by paresthesia, the sensation of tension and weight in the legs and feet. Symptoms of Dercum disease include: swelling of the lymph- characteristic fingers, which start looking like sausages. In more advanced stages, the lymph becomes hard, and often achieves asymmetric sizes (elephantiasis).

Lipodystrophy - Appears in various diseases or may be constitutional. Lipodystrophy is characterized by altering the distribution of fat tissue, with poor conjunctive support system, with the consequence of impaired vascular system. It is characterized by fibrosis tissues and their subsequent dehydration. The symptoms of Dercum disease accentuate with age and consists in losing fat masses in some favored areas, sometimes uneven, especially on the face, but not only. Arrangement of fat in the body is dictated by each type separately and is strongly dependent on sexual hormones.

Lipomatosis - It is a benign pathology, easily identified on ultrasound, and which can be removed only by surgery. Recidivism is possible. The exact cause which induces tumors it is not regarded as a known disorder. Multiple symmetric lipomatosis is a genetic disease associated with diffuse lipomatosis represented by systematic increases of the body. Restrictive diet is welcomed in association with exercise programs.

Such a diagnosis is certainly incomplete and limited, other pathologists can cause symptoms that simulate cellulite, and this is why your target should be a specialist. All this demonstrated the importance of establishing accurate diagnosis before beginning any form of therapy.

There is no single type of cell, but several. There is no single treatment, but one integrated complex, comprising various methodologies. Surgical procedures should be combined with non-surgical, diet and physical exercises programs, so that the results are far superior.

Many beauty therapists or centers proposing improvement of aesthetic appearance especially by hot packing techniques, methods that promise to reduce inches in circumference. But you must be very careful, because this reduction is obtained by loss of water, often repeated therapies may lead to chronic dehydration of the tissue, with subsequent destruction of collagen and elastin fibers and early aging. This process is often irreversible.

It is therefore better to work in a team-surgeon, physical therapist, to talk together about diagnosis and treatment. And last but not least, this team should take into account the patients needs and desires regarding treatment and alternative treatment methods.

Some people believe that animals are bearers of all sorts of dangerous diseases. Sometimes these assumptions are justified, especially if we are dealing with wild or exotic animals. But the truth is that animals are not carriers of diseases that are dangerous to humans, especially if the pet is cared for and vaccinated. If we get sick from animals, why do we keep them in our house?

I will try tell you some of most common diseases that can occur in cats, as well as feline disease symptoms. Also, it is important that when you see these feline disease symptoms, you know how to solve them and how dangerous they are for your meowing friends.

What diseases can cats get? - Before you know which are the most common diseases, we need to do away with several myths. There are several problems with pompous names, which sound very serious and can scare the cat owners.

-Feline Leukemia (FeLV) is an incurable disease that affects only cats! It is not transmitted to humans and can not survive in the human body. If you have a cat diagnosed with Leukemia, you should know that there is no risk for you to get sick.

-Feline Immunodeficiency Virus (FIV) sounds very similar to Human Immunodeficiency Virus. Both viruses belong to the same class of viruses, which is the only similarity between the 2 disorders. FIV does not harm humans and can not cause AIDS. Some veterinarians have called FIV - feline AIDS to better explain the effects on the cats who are holders of the virus. Unfortunately, that name has scared people but the conclusion is the same: FIV is a specific disease, feline and human AIDS are two different types of diseases!

Also, the chances of a cat cold to be transmitted to humans are next to zero. The virus that causes cold in humans, sneezing, coughing, tired and bloodshot eyes stuffy and running nose, can not infect cats in the same way as any feline virus does not harm humans. In fact, cats may be diagnosed with human diseases such as diabetes, arthritis, heart disease, cancer, but these diseases are not contagious so they can not be transmitted from cat to man!

The general mind frame of people, cats are less dangerous than dogs (when is the last time you saw a postman chased by a cat?) and their reputation of clean animals should gives the impression that they are healthy as bulls. In fact, many veterinary doctors would rather treat an angry dog than an angry cat (cats claw and scratch much worse than a dog). There are some diseases that can be transmitted from cats to humans.

-Fleas. These tiny insects feed on the blood of cats as well as that of humans. Fleas are so small that their bite is almost invisible (at first), but if the man and the cat are is allergic to fleas, every bite will be felt as an injection after which it will irritate the area.

There are concerns about diseases that can be transmitted through fleas but that would mean that the fleas have bitten a healthy person after biting an ill person, and the odds are against that. In most cases, the effects of flea bites are nothing more than itchiness and perhaps a rash. End of part one. (part two, coming soon)