Amyotophic Lateral Sclerosis Case Study

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Amyotrophic Lateral Sclerosis Case Study

On December 1, 2012, a patient by the name of John Dough walks into the medical assistant’s office. The patient is five foot 11 inches tall, currently he is 70 years old and weighs approximately 211 pounds. The patient has no known allergies does not smoke and has a relatively clean health record. After filling out the patient medical history forms, the patient is seen by the doctor. The patient explains to the doctor that lately he has had trouble lifting object he would not normally have trouble with, as well as walking short distances, and being very fatigued. After further examination the patient explains how he recently found a tick on his back and removed it, but now there is a red bullseye on his back. The physician suggests a blood sample be taken and sent to the laboratory. To help with weakness and fatigue he recommends the patient to get a good nights sleep and drink plenty of fluids to avoid dehydration. He also wants the patient to limit medication intake that could contribute to fatigue such as cold and allergy medicines and make sure to finish all daily exercising three to four hours before bed. The patient schedules a check up two weeks later.

On December 15, the patient comes in for his check up. The physician tells the patient his blood test was positive for Lyme and prescribes the patient antibiotics. However the patient now tells the doctor that he is still experiencing the weakness and fatigue even after the doctor’s advice. He also says he is having slight trouble swallowing foods and speech has become slurred and nasally at times. Due to the patients broad range of symptoms, the physician suggests the patient either get an electromyography o...

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... patient complete daily living activities and maintain mobility. Pulmonary function information should be recorded and used for reference as the disease progresses. As time passes you may need to resort to the use of a ventilation system or feeding tube which will only make things harder. There is no permanent treatment for ALS but there is a medication that slows the effects and degeneration of the disease. Riluzole is taken twice a day by mouth in 50mg tablets and has shown to increase life expectancy by 20%. If you decide to take Riluzole you must complete a complete blood count and liver function test every three months for nine months. The medicine works by slowing the time it takes for glutamate mediated motor neuron cells to die. And lastly if you have any other concerns, questions or problems you can always speak to your family therapist or physician.

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