Medical ID Cards offering communication help for stroke survivors and people with traumatic brain injury or aphasia http://clinicaltrials.gov/ct/gui/c/a2 r/action/SearchAction/screen/OpeningScreen%3FJServ SessionIdcs%5

So far, no treatment has proved effective for patients with this form of MS. However, you can join one of several ongoing research trials.

this time RPC is not believed to be hereditary, however there are several families with documented and diagnosed RPC in them. Siblings are the most commonly found grouping, although several twins only one twin developed RPC. The next factor seen is parent and child, then grandparent and child.

Aphasia is difficulty expressing oneself verbally (expressive) and/or understanding language (receptive). It is a direct result of the brain injury (typically an injury to the left hemisphere of the brain), not of the muscles of speech or hearing. (RK) The problem of substance abuse in TBI survivors has been well-documented in the literature. In her review article, Mtiguy (1991) cites alcohol as a major contributing factor in over 50% of head injuries sustained in the United States.

There appears to be a predisposition based on heredity for some people when they are exposed to loud sounds, but whether or not tinnitus is genetically indicated is not certain. Scientists working on the Human Genome Project, for example, have not discovered a "tinnitus gene," but they have identified genes that are responsible for a few rare varieties of hearing loss, temporomandibular joint (TMJ) dysfunction, Ménière's Disease, and acoustic Neuroma.

Hereditary hemochromatosis is a genetic disease that is the result of inheriting two defective copies of a particular gene, one from each parent. The mutation in this gene causes the intestine to absorb too much iron. Over time, usually several years, this excess iron is deposited in the cells of the liver, heart, pancreas, joints, and pituitary gland. If left untreated, organ damage can result.

Hereditary Angioedema (HAE) is a very rare and potentially life threatening genetic condition that occurs in about 1/10,000 to 1/50,000 people. HAE symptoms include episodes of edema (swelling) in various body parts including the hands, feet, face, and airway. In addition, patients often have bouts of excruciating abdominal pain, nausea, and vomiting that is caused by swelling in the intestinal wall. Airway swelling is particularly dangerous and can lead to death by asphyxiation.

Heredity does seem to play a role. Ten percent of lupus patients have a first-degree relative (sister, daughter, son, mother) or a second-degree relative (aunt, uncle, first cousin) with lupus. Therefore, 90 percent of lupus patients DO NOT have relatives with lupus. Even in identical twins, when one sibling has lupus and the other twin does not, it is believed there are environmental factors that play an important role.

Each of us is the result of genes inherited from our parents, and the influence of our environment on the functioning of the genes and body components encoded in our genes. Sometimes an error occurs during replication of genes as part of the reproductive process. Most of the errors are analogous to typos in printed text - a single wrong character appears in an instruction in a gene. The defective gene results in the production of a faulty component for the body.

No, hammertoes and bunions are caused by pathomechanics, although shoe gear can aggravate the symptoms that can cause these problems.

Research indicates that genetic factors may play a part in causing autism in some individuals. Most researchers agree that autism probably results from many separate causes.

The most common cause of aphasia is stroke (about 25-40% of stroke survivors acquire aphasia). It can also result from head injury, brain tumor or other neurological causes.

Aphasia affects about one million Americans -or 1 in 250 people- and is more common than Parkinson's Disease, cerebral palsy or muscular dystrophy. More than 100,000 Americans acquire the disorder each year. However, most people have never heard of it.

While aphasia is most common among older people, it can occur in people of all ages, races, nationalities and gender.

You need to be evaluated for scoliosis fusion. There are different ways to perform this type of surgery, all customized to the curvature present. For adolescents with less degree curves, bracing may be recommended.

Progressive" is an political term used loosely to identify activists of the left, favorable to sound and fair economic and social policies, equality of chances, and the defense of personal rights. The European Tribune is broadly progressive, but welcomes all contributors regardless of political self-identification, provided that they be respectful of the mission of this site, provide principled disagreement and don't engage in trollish behavior. (click to see the definition of a troll)

No. A person with aphasia may have difficulty retrieving words and names, but the person's intelligence is basically intact. Aphasia is not like Alzheimer's disease; for people with aphasia it is the ability to access ideas and thoughts through language - not the ideas and thoughts themselves- that is disrupted. But because people with aphasia have difficulty communicating, others often mistakenly assume they are mentally ill or have mental retardation.

No. There are many types of aphasia. Some people have difficulty speaking while others may struggle to follow a conversation. In some people, aphasia is fairly mild and you might not notice it right away. In other cases, it can be very severe, affecting speaking, writing, reading, and listening. While specific symptoms can vary greatly, what all people with aphasia have in common are difficulties in communicating.

There is no proof that Social Phobia is hereditary. Some epidemiologic data suggest it, but there are not enough elements to warrant a conclusion. The same occurrence in one of the parents cannot be regarded as evidence. A person's self-concept, values, and beliefs, as well as many current feelings and emotions, may have their roots in childhood, when the self was being formed.

Yes, heredity plays a role. In one out of five persons with alopecia areata, someone else in the family also has it. Those who develop alopecia areata for the first time after the age of thirty years have less likelihood that another family member will have it. Those who develop their first patch of alopecia areata before the age of thirty have a higher possibility that other family members will also have it.

There is an increase in AMD among children of AMD patients. This is one more reason why your children, after age 40, should have regular eye exams at least every other year.

To some extent, but this does not mean that it is impossible to treat. Environment, stress and even your personality can play a role. Genetics are also said to play a part in baldness. However, Hair Fantastiques success rate with thinning hair and male patter baldness is very high.top

According to estimates, approximately 29.5 million people in the United States suffer from migraine. Four out of five (80 percent) of them report a family history of migraine, but scientists are not sure if this is genetic or a family predisposition. Despite the uncertainty, a child has a 50% chance of having migraine if one parent suffers and a 75% chance if both parents suffer.

It is more correct to say that there is evidence of a strong family history and genetic relationship to bipolar disorder.