Your doorway to information... Home about us diseases alzheimer’s disease (ad) parkinson’s disease (pd) amyotrophic lateral sclerosis (als) multiple sclerosis (ms) myasthenia gravis (mg) huntington’s chorea disease (hd) services support groups programs day care sites national links partners lending library news & events health fair the forum contact us connect with us huntington’s chorea disease (hd) huntingtonâ€™s chorea disease (hd) is a progressive, degenerative disease that causes certain nerve cells in your brain to waste away. buy cheap viagra generic viagra buy generic viagra buy generic viagra cheap generic viagra viagra without a doctor prescription floridalighttacklecharters.com/thq-sales-viagra-xh/ buy cheap viagra cheap generic viagra generic viagra online
As a result, you may experience uncontrolled movements, emotional disturbances and mental deterioration. Huntington’s disease is an inherited disease. Signs and symptoms usually develop in middle age. Younger people with huntington’s disease often have a more severe case, and their symptoms may progress more quickly. Rarely, children may develop huntington’s disease. Medications are available to help manage the signs and symptoms of huntington’s disease, but treatments can’t prevent the physical and mental decline associated with the condition. The signs and symptoms of huntington’s disease can vary significantly from person to person. Huntington’s disease usually develops slowly, and the severity of signs and symptoms is related to the degree of nerve cell loss. Death occurs about 10 to 30 years after signs and symptoms first appear. The disease progression may occur faster in younger people. Early signs and symptoms of huntington’s disease often include: personality changes, such as irritability, anger, depression or a loss of interest decreased cognitive abilities, such as difficulty making decisions, learning new information, answering questions and remembering important information mild balance problems clumsiness involuntary facial movements, such as grimacing your family and friends may notice these changes before you become aware of them. Later signs and symptoms of huntington’s disease can include: sudden jerky, involuntary movements (chorea) throughout your body severe problems with balance and coordination jerky, rapid eye movements hesitant, halting or slurred speech swallowing problems dementia young people who develop huntington’s disease may have signs and symptoms that mimic parkinson’s disease: muscle rigidity tremors slow movements seizures may also occur in those with early-onset huntington’s disease. When to see a doctor see your doctor if you notice changes in your movements, emotional control or mental ability. These signs and symptoms can be the result of many conditions, so they don’t necessarily mean you have huntington’s disease. If you have a family history of huntington’s disease, you may want to talk with your doctor about genetic testing that can tell you whether or not you carry the defective gen.