Maintaining optimal nutrition may be difficult for the person with Huntington disease, particularly as the disease progresses. The disease involves chorea (jerky, involuntary movements), difficulty swallowing, and psychological problems, all of which can make eating a challenge. In addition, because of their constant muscle activity, people with Huntington disease require more calories to maintain their body weight. They are also at an increased risk for aspiration (inhaling food into lungs) and suffocation due to difficulties with swallowing.
The individual with
will most likely want to maintain their independence in eating. However, as the disease progresses, they will become more dependent on others. If you are responsible for the nutritional care of a person with Huntington disease, the following tips can help. Registered dietitians, speech-language pathologists, and occupational therapists can provide additional help.
In the Early Stages
You may find more clumsiness in the early stages.
are also quite normal as the affected person adjusts to the diagnosis.
There may be a decrease in eating or changes in eating habits.
Depression may contribute to eating problems:
Be aware that depression may develop. Look for symptoms such as a loss of interest in most activities, or fatigue as the person struggles to
accept the diagnosis.
Seek psychological care from a therapist who is
familiar with Huntington disease if symptoms last more than 2 weeks.
Food cravings, particularly for
high carbohydrate foods.
There is little need to worry about food cravings, as long as
the individual eats an overall well-balanced diet.
A multivitamin and mineral supplement may be beneficial.
Frequent, smaller meals may be easier to tolerate. Talk to a dietitian with experience in Huntington disease nutrition.
In the Middle Stages
In this stage, you may find more involuntary movements, less dexterity, and slow reaction times. Keep in mind that it may be common for the person to be unaware of hunger until it is time to eat. However, their body still needs regular meals. Skipping or missing meals can lead to exhaustion and uncontrolled emotions because of unrecognized hunger. Scheduling meals over set periods of time can help avoid these problems. Here are some other tips that may make meal time easier:
Difficulty swallowing; choking
Avoid eating when tired or upset.
Sit upright during all meals, snacks, and drinks.
Try to avoid foods that cause coughing, choking, or throat
irritation. These may be foods that are dry, crumbly (chips, dry
cereal), acidic (citrus fruit/juice, tomatoes/juice), spicy
(chili powder, red and black pepper, curry powder), or stringy
Avoid talking while eating or swallowing.
Eat foods that have been blended or pureed.
Add sauces, gravies, liquid dressings, and moist toppings (sour cream, butter, mayonnaise) to foods.
Choose foods that are soft and moist, such as yogurt, pudding,
scrambled eggs, mashed potatoes, macaroni and cheese, oatmeal,
gelatin, milk shakes, frozen yogurt, or ice cream.
Buy a commercial thickener to thicken liquids. Liquids with a
milkshake consistency are easier to swallow.
Eat food that has been cut into small pieces. Take small bites (½ teaspoon or
less) and chew well.
Between bites of food, sip a beverage.
Use a straw.
Drink homemade vegetable and fruit juices.
Stay seated upright for at least 30 minutes after eating.
Jerky movements and poor coordination
make eating slow and messy.
Use cups with covers and straws, such as sports cups, to
Get forks and spoons with rubber handles or larger handles for
For the slow eater, use a warming tray to keep food warm.
Use bibs, aprons, and moisture-resistant table covers.
Increased caloric needs
Have more high-fat, high calorie foods such as:
Sauces (creamed or cheese) and gravies
Creamed soups and bisques
Plain, whipped, or sour cream
Ice cream (without chips, nuts, or chunks)
Mayonnaise (add to sandwiches and salads)
Butter (add to vegetables, pancakes, and hot cereals)
Smooth peanut butter or other smooth nut butters
Full-fat salad dressings
Avocados in guacamole dip, sliced in salads, or as a side
Full fat milk or yogurt
Soft cheeses, cheese spreads, dips, or sauces
The individual becomes distracted or upset
Eliminate possible distractions, such as the TV and radio.
Avoid arguments or discussions that may be upsetting.
Provide a pleasant and relaxing setting with adequate lighting,
attractively arranged food and decor, and a comfortable seating
Be flexible and consider the changing needs of the person with
In the Advanced Stages
As the disease progresses, nutrition will need to be delivered by a family member or other caregivers.
Caregivers with patience, sensitivity, and a sense of humor tend to
find the experience enjoyable and loving rather than stressful.
When eating becomes extremely difficult, tube feeding is an
option. Family members and other caregivers may be trained to
provide tube feeding at home.
Things to Remember
There is a lot of information here, so take a minute to remember some key points:
This information helps with nutrition tips only. There are other aspects of the disease, like medications, and medication side effects. Learn as much as you can.
Counseling may be part of the treatment process for the individual and family and caregivers.
As the disease progresses, swallowing and eating become more difficult.
During the late stages, person may need 24-hour care.
The best way to manage Huntington disease is to be informed and take advantage of professional help when you need it.
Huntington disease. EBSCO DynaMed website. Available at: http://www.ebscohost.com/dynamed. Updated July 25, 2016. Accessed August 4, 2016.
Huntington disease and diet issues. Better Health Channel website. Available at: http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Huntingtons_disease_diet_issues?open. Updated August 2014. Accessed August 4, 2016.
Major depressive disorder. EBSCO DynaMed website. Available at: http://www.ebscohost.com/dynamed. Updated June 13, 2016. Accessed August 4, 2016.
Nutrition. Huntington Disease Society of America website. Available at: http://hdsa.org/living-with-hd/nutrition/. Accessed August 4, 2016.
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