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Uterine fibroids are the most common benign tumors and can affect one in three in Canada. While most fibroids are asymptomatic, they can cause heavy and painful periods, urinary frequency and urgency and pelvic discomfort and pain. A new treatment is available that doesn’t involve invasive surgery. With Fibristal, you can treat fibroids, relieve symptoms and finally live your life the way you want to!

http://www.paruresistreatment.norisk101.com Having trouble urinating in the presence of others? Is a friend or family member struggling with this problem? The following article offers some insight into this social anxiety disorder.
What is Shy Bladder Syndrome?
shy or bashful bladder syndrome, is properly titled Paruresis.It is a phobia that involves fear and avoidance of using public toilets. It should be mentioned that this form of urinary retention is not the result of a physical blockage in the body. People who suffer from paruresis have trouble urinating in the presence of others or put another way paruresis is the fear of not being able to urinate unless one is in absolute privacy.The symptoms can vary in severity . This social anxiety disorder can affect a person's quality of life in many ways. Paruretics are confronted with problems at work with a prime example being when they have to submit a urine sample for drug testing, traveling on long journeys via airplane or train to every day social situations that the rest of us take for granted.
What causes paruresis?
The cause of paruresis is hotly debated and not easily determined in some cases. It could start as a toddler in preschool, in adolescence, or even in adulthood. While not all paruretics can point to an event in their life that could have lit the fuse to their shy bladder syndrome, some look to a traumatic incident in their past including embarrassment by a parent, teasing by schoolmates or freinds and siblings, harassment in public bathrooms or even sexual abuse as the catalyst.
How common is Shy Bladder?
While definitive numbers are hard to find with regard to how many people suffer from shy bladder surveys performed over the last few decades show that the numbers could range from less than one percent to more than 25 percent of Americans. There was a study done in 1994 called the National Comorbidity Surveywhich showed that 6.6 percent (17 million people) of the populationare fearful of using the toilet away from home, although it is uncertain how many of these fears were related to the difficulties initiating urinating in public bathrooms.
Paruresis symptoms?
A common scenario for how shy bladder syndrome evolves in a person's life is as follows: After an initial unpleasant experience, the person anticipates difficulty urinating whenever entering a bathroom. After trying to make themselves overcome this fear and failing, the associated anxiety with performance reduces the individual's chances even further of the possibility of urinating in a public restroom. The sufferer then adjusts to the condition by urinating as much as possible while at home, restricting how much they drink and avoiding social events that will keep them away from home for too long.

How is Shy Bladder Syndrome treated?
It is recommended that a sufferer of paruresis should first visit a urologist to make sure there is nothing physically wrong with them.
The urologist will:
A) make sure there are no underlying physical problems.
B)Let the patient know they are not alone and that any other people suffer with the same problem
C) Offer guidance as to approaches for coping with the condition such as scheduling urination, and, for men making use of an enclosed cubicle as opposed to the urinal.
4) Discuss the possibility of self-catheterization if the patient feels that would work for them. It is a way to offer an instant way to improve their quality of life through being able to be more social.
5) Referring them out to a specialist dealing with anxiety disorders for cognitive and graduated exposure therapy.

There is new hope for sufferers of shy bladder syndrome with the "Paruresis Treatment System" which is helping people lead different and better lives.
To learn more visit:-
https://www.youtube.com/watch?v=j6TpU_0-ufw
~N

This video narrates the story of a girl who travels to Iran for doing a nose surgery.

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Twin girls joined at the head who share the same brain and so much more

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Your baby's sex is set at conception. At around 7 weeks, your baby's internal sex organs – such as ovaries and testes – begin to form in the abdomen. Male and female sex organs and genitalia look the same at this stage because they're derived from the same structures. At around 9 weeks, boys and girls begin to develop differently. In girls, a tiny bud emerges between the tissue of the legs. This bud will become the clitoris. The membrane that forms a groove below the bud separates to become the labia minora and the vaginal opening. By 22 weeks, the ovaries are completely formed and move from the abdomen to the pelvis. They already contain a lifetime supply of 6 million eggs. In boys, the bud develops into the penis and starts to elongate at around 12 weeks. The outer membrane grows into the scrotal sac that will later house the testicles. By 22 weeks, the testes have formed in the abdomen. They already contain immature sperm. Soon they'll begin their descent to the scrotum, but it's a long journey. They'll reach their destination late in pregnancy, or for some boys, after birth. If you're eager to find out whether you're having a girl or a boy, you'll have to wait until you're at least 17 weeks pregnant. That's when the genitals have developed enough to be seen on an ultrasound.

This is the incredible moment a new-born baby arrived still inside its amniotic sac, completely intact. The tiny infant can be seen moving and stretching still inside the sac, as medics prepare to snip the new born free. The amniotic sac is a thin but durable membrane filled with fluid which helps keep a baby warm and safe from bumps during pregnancy. When it breaks, this is typically referred to as a woman's 'waters breaking' shortly before she gives birth. But in rare cases, less than 1-in-80,000 births, the baby is delivered with the membranes still intact and this is known as a 'caul birth'. Some babies are born with part of the membrane still attached to them, but to be born completely encased in the intact membrane is incredibly rare. Many people still believe the phenomenon to be a good omen for the child's infancy and it is has even been suggested, but not proven, that caul babies will always have a natural affinity for water. The video was taken in Spain on Saturday and captures the rare moment the baby was born with the membrane covering its entire body, just minutes after its twin was delivered normally.

LDL (Bad) Cholesterol LDL cholesterol is considered the “bad” cholesterol because it contributes to plaque, a thick, hard deposit that can clog arteries and make them less flexible. This condition is known as atherosclerosis. If a clot forms and blocks a narrowed artery, heart attack or stroke can result. Another condition called peripheral artery disease can develop when plaque buildup narrows an artery supplying blood to the legs. View an animation of cholesterolHDL (Good) Cholesterol HDL cholesterol is considered “good” cholesterol because it helps remove LDL cholesterol from the arteries. Experts believe HDL acts as a scavenger, carrying LDL cholesterol away from the arteries and back to the liver, where it is broken down and passed from the body. One-fourth to one-third of blood cholesterol is carried by HDL. A healthy level of HDL cholesterol may also protect against heart attack and stroke, while low levels of HDL cholesterol have been shown to increase the risk of heart disease.

Medial medullary syndrome, also known as Dejerine syndrome, represents less than 1% of brainstem stroke syndromes. Thrombotic or embolic occlusion of small perforating branches from vertebral or proximal basilar artery supplying the medial aspect of medulla oblongata cause this rare syndrome. It is characterized by contralateral hemiplegia/hemiparesis as well as hemisensory loss with ipsilateral hypoglossal palsy (ipsilateral tongue weakness and atrophy) from involvement of CN XII nucleus. Other manifestations e.g. vertigo, nausea, ipsilateral limb ataxia are also reported.

EKG Interpretation Part 1

Before the angioplasty procedure begins, you will receive some pain medicine. You may also be given medicine that relaxes you, and blood thinning medicines to prevent a blood clot from forming. You will lie on a padded table. Your doctor will insert a flexible tube (catheter) through a surgical cut into an artery. Sometimes the catheter will be placed in your arm or wrist, or in your upper leg or groin area. You will be awake during the procedure. The doctor will use live x-ray pictures to carefully guide the catheter up into your heart and arteries. Dye will be injected into your body to highlight blood flow through the arteries. This helps the doctor see any blockages in the blood vessels that lead to your heart. A guide wire is moved into and across the blockage. A balloon catheter is pushed over the guide wire and into the blockage. The balloon on the end is blown up (inflated). This opens the blocked vessel and restores proper blood flow to the heart. A wire mesh tube (stent) may then be placed in this blocked area. The stent is inserted along with the balloon catheter. It expands when the balloon is inflated. The stent is left there to help keep the artery open

Inflammatory bowel disease (IBD) involves chronic inflammation of all or part of your digestive tract. IBD primarily includes ulcerative colitis and Crohn's disease. Both usually involve severe diarrhea, pain, fatigue and weight loss. IBD can be debilitating and sometimes leads to life-threatening complications. Ulcerative colitis (UL-sur-uh-tiv koe-LIE-tis) is an inflammatory bowel disease that causes long-lasting inflammation and sores (ulcers) in the innermost lining of your large intestine (colon) and rectum. Crohn's disease is an IBD that cause inflammation of the lining of your digestive tract. In Crohn's disease, inflammation often spreads deep into affected tissues. The inflammation can involve different areas of the digestive tract — the large intestine, small intestine or both. Collagenous (kuh-LAJ-uh-nus) colitis and lymphocytic colitis also are considered inflammatory bowel diseases but are usually regarded separately from classic inflammatory bowel disease.

A salivary gland stone -- also called salivary duct stone -- is a calcified structure that may form inside a salivary gland or duct. It can block the flow of saliva into the mouth. The majority of stones affect the submandibular glands located at the floor of the mouth. Less commonly, the stones affect the parotid glands, located on the inside of the cheeks, or the sublingual glands, which are under the tongue. Many people with the condition have multiple stones. Salivary Gland Stone Causes and Symptoms Salivary stones form when chemicals in the saliva accumulate in the duct or gland. They mostly contain calcium. The exact cause is not known. But factors contributing to less saliva production and/or thickened saliva may be risk factors for salivary stones. These factors include: dehydration, poor eating, and use of certain medications (such as antihistamines), blood pressure drugs, psychiatric drugs, and bladder control drugs. Trauma to the salivary glands may also raise the risk for salivary stones. The stones cause no symptoms as they form, but if they reach a size that blocks the duct, saliva backs up into the gland, causing pain and swelling. You may feel the pain off and on, and it may get progressively worse. Inflammation and infection within the affected gland may follow. Salivary Gland Stones Diagnosis and Treatments If you have symptoms of a salivary gland stone, your doctor will first check for stones with a physical exam. Sometimes tests may also be ordered, such as X-ray, CT scan, or ultrasound.

Is My Chest Pain a Sign Of a Heart Attack?

Colorectal cancer screening tests Screening is the process of looking for cancer in people who have no symptoms of the disease. Several tests can be used to screen for colorectal cancers. These tests can be divided into: Tests that can find both colorectal polyps and cancer: These tests look at the structure of the colon itself to find any abnormal areas. This is done either with a scope put into the rectum or with special imaging (x-ray) tests. Polyps found during these tests can be removed before they become cancerous, so these tests may prevent colorectal cancer. Because of this, these tests are preferred if they are available and you are willing to have them. Tests that mainly find cancer: These tests check the stool (feces) for signs of cancer. These tests are less invasive and easier to have done, but they are less likely to detect polyps.