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Amyotrophic lateral sclerosis
Alternative Names: Lou Gehrig's disease; ALS Treatment: There is no known cure for ALS. Riluzole may prolong life, but does not reverse or stop disease progression. Text Continues Below Treatment is aimed at controlling the symptoms. Baclofen or diazepam may be used to control spasticity that interferes with activities of daily living. Trihexyphenidyl or amitriptyline may be prescribed for people with impaired ability to swallow saliva. Physical therapy, rehabilitation, use of appliances (such as braces or a wheelchair) or orthopedic intervention may be required to maximize muscle function and general health. Choking is common and there may be an early need for placement of a tube into the stomach for feeding (gastrostomy). A referral to an otolaryngologist may be advised. A nutritionist is helpful to prevent weight loss, especially for patients with limited ability to swallow. The use of devices to assist in breathing includes machines that are only used at night as well as mechanical ventilation. Patients should discuss their wishes regarding artificial ventilation with their doctors. Support Groups: Emotional support is vital in coping with the disorder, because mental functioning is not affected. Groups such as the ALS Association may be available to assist in coping with the disorder. See ALS - support group. Expectations (prognosis): There is progressive loss of ability to function or care for oneself. Death often occurs within 3 to 5 years of diagnosis, although there are some rare cases of patients living decades. Complications: Loss of ability to care for self Inhaling food or fluid Pneumonia Respiratory failure (see adult respiratory distress syndrome) Skin breakdown (pressure sores) Weight loss Calling your health care provider: Page:  1 | 2 | Next >>