Wednesday, December 31, 2008
What Are Your Health Issues?
Thursday, December 11, 2008
Labrador Lung
Symptoms of Labrador lung are lung opacities, pleural thickening, impaired lung function, lung fibrosis, breathing problems, cough, tight chest and wheezing. There may be no symptoms during the early stages of the disease. Read More...
Wednesday, December 10, 2008
Klein-Levin Syndrome
Sunday, November 23, 2008
Signs and Symptoms of Paine Syndrome
Paine syndrome is a rare genetic condition that is present at birth. A baby with Paine syndrome is born with a smaller than average head. There are also several abnormalities in the brain that cause severe mental and physical retardation, movement disorders and vision problems. Babies with this syndrome rarely live past a year.
Signs and symptoms of Paine syndrome are poor swallowing, physical and mental retardation, myoclonic jerks, opisthotonic fits, seizures, disinterest in environment, small head, low birth weight, low birth height, spastic limbs, increased reflex response, optic atrophy, underdeveloped cerebellum and mild aminoaciduria. Read More...
Symptoms of Progeria: The Rapid Aging Syndrome
Progeria is a rare and fatal disease that affects approximately 1 in 8 million children. The name is derived from the Greek and means “prematurely old”. Progeria is also known as Hutchinson-Gilford Progeria Syndrome. It was named after the doctors who first described it. Dr. Jonathan Hutchinson described it in 1886 and Dr. Hastings Gilford described it in 1887.
Progeria usually begins to show around 6-12 months. The first noticeable symptoms are a failure to gain weight and skin changes. Other symptoms of Progeria are failure to grow during the first year, narrow, shrunken or wrinkled face, baldness, loss of eyebrows and eyelashes, short stature, large head for size of face, delayed, absent or abnormal teeth formation, open soft spot, small lower jaw, dry, scaly and thin skin, limited range of motion, prominent scalp veins, high pitched voice, prominent eyes, hip dislocation and loss of body fat and muscle. The symptoms of Progeria strongly resemble normal human aging. Signs of Progeria include the presence of insulin-resistant diabetes and early atherosclerosis of blood vessels that causes abnormal stress tests of the heart. Read More...
Thursday, November 20, 2008
Symptoms of Orthostatic Intolerance Syndrome
Have you ever stood up and felt extremely dizzy? This is caused by a sudden drop in blood pressure and something those suffering with Orthostatic Intolerance Syndrome deal with on a regular basis along with a multitude of other symptoms. Those who suffer from Orthostatic Intolerance Syndrome may also have difficulty taking showers, brushing their teeth or doing the dishes.
Approximately 5,000 Americans suffer from an Autonomic disorder that is not understood. Orthostatic Intolerance Syndrome or Dysautonia is caused by a malfunction of the autonomic nervous system, which controls the involuntary bodily function. Orthostatic Intolerance Syndrome causes an excessive increase in heart rate when standing up. This causes the cardiovascular system to work harder in order to control blood pressure and blood flow to the brain.
Orthostatic Intolerance Syndrome affects people under the age of 35 and it affects women more than men. The onset is usually sudden and can majorly affect lifestyle and the ability to work. There are three categories that are used to describe Orthostatic Intolerance Syndrome; Postural Tachycardia Syndrome, Mitral Valve Prolapse Dysautonomia and Idiopathic Hypovolemia. Read More...
Wednesday, October 1, 2008
The Symptoms and Treatment of Leptospirosis
Leptospirosis was first recognized as an occupational disease of sewer workers in 1883. Occupational exposure accounts for approximately 30-50% of human cases. Occupational groups that are at risk include farm workers, veterinarians, pet shop owners, field agricultural workers, abattoir workers, plumbers, meat handlers and slaughterhouse workers, coal miners, workers in the fishing industry, military troops, milkers and sewer workers.
In 1970 Leptospirosis was also recognized as a recreational disease. Recreational activities that put you at risk include traveling to tropical areas, canoeing, hiking, kayaking, fishing, windsurfing, swimming, waterskiing, wading, riding trail-bikes through puddles, whit-water rafting and other outdoor sports that are played in contaminated water. Camping near and traveling to endemic areas also add to the risk of exposure to Leptospirosis.
Leptospirosis can cause a wide array of symptoms in humans, but some infected persons may have no symptoms at all. Symptoms include high fever, severe headache, chills, muscle aches and vomiting. Other more severe symptoms include jaundice (yellow skin and eyes), red eyes, abdominal pain, diarrhea and rash.
Clinical signs that have been reported in dogs include fever, vomiting, abdominal pain, diarrhea, refusal to eat, severe weakness, depression, stiffness, sever muscle pain and inability to have puppies. Sometimes pets do not have any symptoms. Younger animals are more seriously affected than older animals.
If no treatment is received kidney damage, meningitis, liver failure and respiratory distress could develop. Meningitis is an inflammation of the membrane around the brain and spinal chord. Leptospirosis usually begins abruptly with high fever.
Diagnosis is made by reviewing the history of exposure and clinical suspicion. Blood tests rarely confirm illness in time to affectively treat it, but they can be used to confirm presence of the disease later on. Diagnosis can be confirmed early by identifying Leptospira in cultures of blood, urine or cerebrospinal fluid samples. Diagnosis is also made by detecting antibodies against the bacteria in the blood.
Infected people who don’t develop jaundice usually recover. Jaundice indicates liver damage. This increases the death rate to ten percent. The death rate increases more in people over Sixty years of age. Doxycycline, an antibiotic, can prevent the disease. It is given to people that are exposed to the same source as an infected person. Penicillin, ampicillin and similar antibiotics are given to treat the disease. The more severe infections are treated intravenously with antibiotics.
There are one to two hundred cases of Leptospirosis reported every year in the United States. Fifty percent of these cases occur in Hawaii.
Female Genital Mutilation
Most girls undergo Female Genital Mutilation between the ages of 7 and 10. Female Genital Mutilation seems to be occurring at earlier ages in several countries because parents want to reduce the trauma to the children. Parents also want to avoid government interface and/or resistance of the children as they get older and form their own opinions. Some women undergo Female Genital Mutilation during early adulthood when they marry into a community that practices Female Genital Mutilation or just before or after the birth of their first child. This is common in Mali and Nigeria.
Female Genital Mutilation is practiced in at least 26 of the 43 African countries. Female Genital Mutilation is also found among ethnic groups in Oman, the United Arab Emirates and Yemen. It is also found in parts of India, Indonesia and Malaysia. Female Genital Mutilation has become an important issue in Australia, Canada, England, France and the United States due to continuation of the practice by immigrants from countries where Female Genital Mutilation is common.
THE FOUR TYPES OF FEMALE GENITAL MUTILATION
TYPE I This is the most common form of Female Genital Mutilation. The clitoris is held between the thumb and index finger and then pulled out and amputated with one stroke of a sharp object. The bleeding is stopped by packing the wound with gauze. A pressure bandage is then applied. Modern trained practitioners may insert one or two stitches around the clitoral artery to stop bleeding.
TYPE II The degree of severity varies a lot in this type. The clitoris is amputated as in Type I. The Labia Minora are partially or totally removed, often with the same stroke. The bleeding is stopped with packing and bandages or by circular stitches that may or may not cover the urethra and part of the vaginal opening. Types I and II account for 85% of all Female Genital Mutilation.
TYPE III An extensive amount of tissue is removed. This is the most extreme form. It involves a complete removal of the clitoris and labia minor along with the inner surface of the labia majora. The raw edges of the labia majora are brought together to fuse. Thorns, poultices or stitching are used to hold them together for two to six weeks. The healed scar creates a hood of skin that covers the urethra and part or most of the vagina. This acts as a physical barrier to intercourse. A small opening is left at the back to allow the flow of urine and menstrual blood. The opening is surrounded by skin and scar tissue. It is usually 2 to 3cm in diameter and may be as small as the head of a matchstick.
TYPE IV This type is unclassified and deals with a variety of procedures. (1) Pricking, piercing, stretching or an incision of the clitoris and/or the labia. (2) Cauterization by burning the clitoris and surrounding tissues. (3) An incision is made to the vaginal wall. (4) Scraping or cutting of the the vagina. (5) An introduction of corrosive substances or herbs into the vagina. Some of these procedures often result in vesicovaginal fistulae and damage to the anal sphincter.
THE HARMFUL PHYSICAL EFFECTS OF FEMALE GENITAL MUTILATION
Female Genital Mutilation does irreparable harm. It can result in death through severe bleeding leading to hemorrhagic shock, neurogenic shock as a result of pain and trauma and severe, overwhelming infection and septicemia. Female Genital Mutilation is routinely traumatic. Many girls enter a state of shock that is induced by severe pain, psychological trauma and exhaustion from screaming.
Other harmful physical effects include failure to heal, abscess formation, cysts, excessive growth of scar tissue, urinary tract infection, painful sexual intercourse, increased susceptibility to HIV/AIDS, hepatitis and other blood-borne diseases, reproductive tract infection, pelvic inflammatory disease, infertility, painful menstruation, chronic urinary tract obstruction, bladder stones, urinary incontinence, obstructed labor, increased risk of bleeding and infection during child birth.
THE REASONING BEHIND FEMALE GENITAL MUTILATION
Female Genital Mutilation is practiced for several reasons. (1) To control or reduce female sexuality. (2) An initiation for girls into woman-hood, social integration and for the maintenance of social cohesion. (3) Hygiene and aesthetic reasons because it is believed that the female genitalia is dirty and unsightly. (4) It is believed that it enhances fertility and child survival. (5) It is believed that Female Genital Mutilation is a religious requirement.
Since 1998, 16 states have instituted criminal sanctions against the practice of Female Genital Mutilation in the United States. The states include California, Colorado, Delaware, Illinois, Maryland, Minnesota, Missouri, Nevada, New York, North Dakota, Oregon, Rhode Island, Tennessee, Texas, West Virginia and Wisconsin.
A federal law criminalizing the practice was passed in 1996 and became effective in April, 1997. Female Genital Mutilation that is performed on a person under the age of 18 is a federal crime, unless the procedure is necessary to protect the health of a young person or for medical purposes that are connected with labor or birth. The penalty is a fine or imprisonment for up to five years or both. The law specifically exempts cultural beliefs or practices as a defense for conducting Female Genital Mutilation.
It is estimated that 130 million girls and women have undergone Female Genital Mutilation. Approximately 2 million are subjected to this practice worldwide each year worldwide. Female Genital Mutilation is a violation of the rights of girls. It is discrimination and it violates the rights to equal opportunities, health, freedom from violence, abuse, torture, cruel or inhuman and degrading treatment, protection from harmful traditional practices and to make decisions concerning reproduction. These are all rights that are protected in international law.
Sunday, September 21, 2008
Ten Most Popular Aromatherapy Oils
Tea Tree is a natural anti-fungal oil. It is good for treating fungal infections such as vaginal yeast infections, jock itch, athlete’s foot and ringworm. It also boosts the immune system.
Friday, September 19, 2008
Types of Diabetes
Diabetes is a disease where the blood glucose levels are abnormal. Diabetes restricts the body’s ability to convert food to energy. There are three types of Diabetes; Type I, Type II and Gestational Diabetes.
TYPE I DIABETES
Type I diabetes use to be called Juvenile Diabetes and Insulin-Dependent Diabetes. This type of Diabetes develops because the beta cells of the pancreas are no longer able to make insulin because the immune system has attacked and destroyed them.
The symptoms of Type I Diabetes are increased thirst, increased urination, weight loss despite increased appetite, nausea, vomiting, abdominal pain, fatigue and the absence of the menstrual cycle.
TYPE II DIABETES
Tuesday, September 16, 2008
Heart Attack Symptoms in Women
Friday, September 12, 2008
Sexsomnia: The Causes of Sleep Sex
Sexsomnia or Sleep Sex is sexual behavior that occurs during sleep. It appears to occur predominantly among males, but there are reported cases of women who initiate the sexual behavior while sleeping. The condition can range in severity from disruptive moaning to unwanted, sometimes violent sexual advances. Those who experience sleep sex usually do not remember what happened. Sexual behaviors that can occur during sleep include sexual vocalizations, masturbation, fondling another person, intercourse and even sexual assault.
The exact cause of Sexsomnia is unknown, but is possibly caused by abnormalities in the brain’s arousal mechanisms and is believed to be a variant of sleepwalking. Sexsomnia could also be caused by other sleep disorders that are combined with emotional problems. Those who suffer from Sexsomnia may also suffer from other sleep disorders such as sleepwalking, REM behavior disorders, apnea, bed wetting, seizure disorders and night terrors. Some may also have substance abuse problems and other psychological issues such as undefined emotional problems.
There are at least 11 different sex-related sleep disorders and they are easily treated with medication. If Sexsomnia is not treated there can be very negative consequences such as the person suffering from the disorder may actually rape their spouse or someone else.
Thursday, September 11, 2008
Health Risks of Pica, A Behavorial Eating Disorder
Pica is a serious behavioral problem that is characterized by a persistent craving and a compulsive urge to eat items that are not food. It is classified as a feeding and eating disorder of childhood. The disorder affects children, pregnant women, certain cultures and the mentally disabled. Substances that may be ingested include, but are not limited to, chalk, hair, glue, paper, toothpaste, soap, baking soda, cigarette butts, vinyl gloves, light bulbs, needles, string, wire, matches, erasers, fingernails, coal, plastic, feces, pebbles, stones, clay, paint, wool, ashes, dirt, ice and laundry detergent.
RISK FACTORS AND HEALTH RISKS
Risk factors for developing Pica include developmental disabilities, mental retardation, children between ages of 2 and 3, nutritional deficiencies and cultural factors. It has also been associated with Sickle Cell disease. Pica is more common in tropical countries because of cultural practices and diets. It is actually a culturally sanctioned practice in some societies. It is also more common in deprived and neglected children. Symptoms in children are poor weight gain or weight loss, constipation, excessive crying, irritability and apathy.
There are many health risks associated with Pica including poisoning that results in death, abdominal problems, teeth damage and parasitic infections. Pica can also result in lead poisoning and Anemia.
SUBGROUPS OF PICA
There are several subgroups of Pica that define what is ingested: Acuphagia (sharp objects), Amylophagia (starches), Cautopyreiophagia (burnt matches), Geophagia (sand, dirt and clay), Lithophagia (stones), Pagophagia (ice), Trichophagia (hair), Xylophagia (wood), Urophagia (urine), Hyalophagia (glass), Hematophagy (blood), Plumbophagia (lead), Mucophagy(mucous), Emetophagia (dust) and Bibliophagia (pages of a book).
DIAGNOSIS AND TREATMENT
A person must ingest non-food for at least a month before a diagnosis of Pica can be made. There is no single test that can confirm Pica, but blood tests can be done to see if nutrient levels are abnormal and if Anemia is present. Both of these are associated with Pica. Medications may help reduce abnormal eating and other therapies such as Aversion Therapy may also be used to treat Pica. The symptoms of pregnant women with Pica usually go away after the child is born.
CAUSES
The exact cause of Pica is unknown. Possible causes include vitamin, mineral, iron or other dietary deficiency, underlying physical or mental illness or stress.
PROGNOSIS AND PREVENTION
Prognosis depend on the substances ingested and if treatment works. Severe cases of pica can result in death due to complications such as bowel perforation or infection. There is no way to prevent Pica.
Saturday, September 6, 2008
Irritable Bowel Syndrome or Gastrointestinal Stromal Tumor
Have you been diagnosed with Irritable bowel Syndrome? Are you still experiencing your symptoms even with treatment? It may not be Irritable Bowel Syndrome, but a tumor in the gastrointestinal tract. Gastrointestinal Stromal tumors are tumors of the
gastrointestinal tract. They are the most common mesenchymal tumors. The gastrointestinal tract consists of the esophagus, stomach, small intestine and the colon.
Gastrointestinal Stromal Tumors begin in special cells that are called interstitial cells of Cajal (ICC’s). They are found in the intestinal tract and are part of the autonomic nervous system, which sends signals to the intestinal tract. Not all of Gastrointestinal Stromal Tumors are cancerous. They stay in one place when they first develop and are referred to as localized tumors. Advanced Gastrointestinal Stromal Tumors can spread to other parts of the body and are then referred to as metastatic tumors. The size of the tumors can range from a few millimeters to over thirty centimeters.
The symptoms of a Gastrointestinal Stromal Tumor may mimic those of Irritable Bowel Syndrome, but the symptoms do not respond to the IBS treatment. There is also a possibility of there being no symptoms at all. Symptoms include vague abdominal pain, early feeling of fullness, vomiting, abdominal bleeding (blood in stool or vomit), fatigue due to anemia, anorexia, nausea, weight loss, fever, bloating, flatulence and constipation. The bleeding occurs because of an ulcer that forms in the gastric mucosa that is above the tumor. A palpable abdominal mass in the abdomen may be found during an examination if the patient has an exogastric tumor. The symptoms usually depend on the size and location of the tumor.
Gastrointestinal Stromal Tumors are hard to diagnose and treat because the tumor is often hidden in the abdomen and it may not cause any physical symptoms. They often become very large before they are diagnosed and there becomes a risk of them spreading to other organs such as the liver. The tumors are resistant to chemoradiation so surgical removal of the tumor is the only effective treatment.
Gastrointestinal Stromal Tumors where considered to be a rare occurrence at one time, but now there are 4,500 to 6,000 new cases each year in the United States. The tumors most often occur between the ages of 40 and 80, but they can occur at any age. Fifty percent of the tumors occur in the stomach, twenty-five percent occur in the small intestine, ten percent in the colon and fifteen percent occur in other parts of the gastrointestinal tract.
There are no known risk factors for developing a Gastrointestinal Stromal Tumor, but there may be a slight risk if there is a family history of the tumor. With no known risk factors, there is no way to prevent the tumor from occurring.
Large Vestibular Aqueduct Syndrome
Large Vestibular Aqueduct Syndrome (LVAS) is an uncommon disorder described as sudden and progressive sensorineural hearing loss. The vestibular aqueduct is a narrow, bony canal that connects the inner ear and the cranial cavity. It is related to the bony labyrinth of the inner ear. LVAS is also known as Enlarged Vestibular Aqueduct syndrome (EVAS) and Vestibular Aqueduct syndrome (VAS). LVAS received its name in 1978 simply because the large vestibular aqueduct was the only part of the disorder visible on a CT scan.
LVAS develops when the vestibular aqueduct becomes larger than it is suppose to be. It should not be larger than 1.5 millimeters. This is the result of an abnormal or delayed development of the inner ear. LVAS usually begins in infancy, but it also can occur in childhood and more rarely adolescence. In a patient with LVAS progressive hearing loss may be triggered by head trauma or anything else that may cause a sudden fluctuation in the cerebrospinal fluid.
CT Scans are the test of choice to provide the evidence needed to make a diagnosis of LVAS. Other tests that may be used to confirm diagnosis include Magnetic Resonance Imaging (MRI) and a Axial CT Scan.
LVAS can be associated with Pendreds syndrome and Mondini’s syndrome, but it can occur by itself. Characteristics of LVAS include large vestibular aqueduct on a CT scan, hearing loss, sudden hearing loss after minor head trauma and vertigo or dizziness.
Symptoms of Fibromyalgia
As many as 12 million Americans suffer from a pain no one else can see. They are called lazy and sometimes crazy because no one understands what they are going through. It’s overwhelming and very lonely. It’s Fibromyalgia. Fibromyalgia is a chronic arthritis-related syndrome and while it affects a lot more, only 3.7 million Americans have been diagnosed with the condition. Unlike arthritis, Fibromyalgia affects the muscles and ligaments, not the joints. Fibromyalgia has also been referred to as fibrositis, chronic muscle pain syndrome, psychogenic rheumatism, tension myalgias, fibromyositis and myofacial pain syndrome.
The symptoms of Fibromyalgia are multiple tender points on the neck, shoulders, sternum, lower back, hips, shins, elbows and knees, fatigue, sleep disturbances, body aches, reduced exercise tolerance, chronic facial muscle pain or aching. Other symptoms may include headaches, irritable bowel or bladder, temporomandibular joint disorder, pelvic pain, noise sensitivity, temperature sensitivity, restless leg syndrome, depression, anxiety, numbness or tingling sensations in hands and feet, difficulty concentrating, mood changes, chest pain, dry eyes, skin and mouth, painful menstrual periods, dizziness and anxiety.
It can take up to five years for a Fibromyalgia diagnosis to be made because it is so misunderstood and there are no tests that can diagnose it. There are 18 tender point sites on the body and a diagnosis is based on having at least 11 of these tender points. The tender points are located in the neck, shoulders, chest, rib cage, lower back, thighs, knees, arms/elbows and buttocks. Tests are done to rule out similar conditions such as Ankylosing spondylitis, Lupus, Carpal tunnel Syndrome, Multiple Sclerosis, Polymyalgia rheumatica and Restless Legs syndrome.
Fibromyalgia affects more women than men and usually develops during early to middle adulthood. If you have a family history of Fibromyalgia or if you have a rheumatic disease such as Lupus or Rheumatoid arthritis then there is a higher risk for developing Fibromyalgia. Other possible causes include sleep disturbances, injury, infection, abnormalities of the autonomic nervous system and changes in muscle metabolism. Ninety percent of Fibromyalgia patients have severe fatigue and sleep disorders.