As a caregiver, you play an important part in helping people with Parkinsons disease. Youll provide essential day-to-day care, take patients to and from healthcare-related appointments and, most importantly, provide essential physical and emotional support.
Who is a caregiver? A husband, wife, partner, son, daughter, or neighbor to name a few. Essentially, a caregiver is anyone willing and able to assume the responsibilities of helping a person with Parkinsons disease manage the disease and its symptoms and live a more active life.
The goal of Parkinsons disease treatment is managing the symptoms so the patient can try to maintain daily activities. Although the patient and the doctor will make decisions regarding treatment, caregivers provide essential physical and emotional support. Here are a number of ways you can help:
Assist With Medicine
Keep a list of all prescription and nonprescription medicines, vitamins, and herbal supplements the patient is taking, including dosage and frequency taken. You may want to use the Doctor Visit Worksheet (PDF) found here to record this information and share it with the doctor. Ask the doctor for specifics about each medicine, and what to expect as the disease worsens.
Help the patient organize medicines each week into a medicine organizer, which makes it easier to keep track of multiple medicines. To learn how to reduce the number of doses required to manage Parkinsons symptoms, ask the doctor about REQUIP XL, a once-daily treatment for Parkinsons patients.
Encourage Activities
Ask the doctor if simple, enjoyable exercises like walking or gardening, or group programs like yoga or massage, are right for the person under your care. If balance is a problem, ask the doctor about seated exercises.
Suggest a Healthy Diet
If the patient has trouble swallowing, be sure to cut food into small pieces, and have him or her drink plenty of water during meals.