Dysautonomia International
 
Map
Learn More
Research
Connect
Get Involved
Donate/Shop
Events
Press Room
About Us
Blog

For Patients

For Researchers

For Physicians

For Family and Friends

For Educators

For Employers



We appreciate our sponsors!

Platinum Sponsor

Gold Sponsor

Home >> Pure Autonomic Failure >> Lifestyle Adaptations for PAF

Lifestyle Adaptations for PAF



There are a number of non-pharmacological treatments and lifestyle adaptations that may help PAF patients reduce and cope with their symptoms. The following are a list of the most commonly recommended measures. It is important to remember that treatment, pharmacological or non-pharmacological, should be individualized. Speak with your doctor before making any changes to your treatment plan.

Increase Fluid and Salt Intake
It is often recommended to increase both fluid and salt intake in order to increase blood volume. This has proven to be particularly helpful in patients with blood pooling, hypovolemia, or hypotension. A fluid intake of approximately two liters and an intake of three to five grams of salt is typically recommended per day, sometimes more. Note that salt includes sodium and chloride. One gram of table salt contains approximately .393 grams (393 milligrams) of sodium. That means that five grams of salt contains approximately 1.965 grams (1965 milligrams) of sodium. This number can be useful when tracking salt in food with nutrition labels, which often list sodium content.

Smaller Meals
After eating a large meal, much of our blood is redirected to aid in the digestion process, which, for PAF patients, can increase symptoms. Therefore, it is recommended to eat several smaller meals throughout the day in lieu of two or three large ones.

Examine Your Reaction to Caffeine
Caffeine is helpful to some PAF patients and exacerbates symptoms in others. It is therefore useful to figure out if it helps you or if you should avoid it.

Avoid Alcohol
Alcohol can worsen symptoms for some PAF patients. Alcohol is dehydrating and can lead to increased hypotension through dilation of the veins and thus should be avoided by most PAF patients.

Elevate Head During Sleep
It is recommended to slightly elevate the patient's head during sleep. This is done in order to help (re)condition the patient's body to orthostatic stress, and this can also help patients that may be experiencing gastric motility problems that result in acid reflux or G.E.R.D. The best way to do this is to raise the head of the bed with a few bricks or large books. A wedge pillow is not very helpful for this. Elevating the whole body and having the feet be lower than the hip area is needed to get the intended benefit. A wedge pillow only elevates the shoulders and head, but does nothing to change the position of the hips or the lower legs. This can also help minimize supine hypertension, which is high blood pressure that results for some PAF patients in the laying down position.

Try Compression Garments
Compression support hose and abdominal binders can be helpful for some PAF patients by lessening the peripheral venous pooling and hypotension. The most effective compression hose are 30 mm Hg of ankle counter pressure and go waist high. There are many different varieties such as closed toe and open toe, knee high and waist high. All varieties are available for each gender and may be subsidized through some insurance plans as a durable medical good with a doctor's script. There are new variety of colors and patterns available for the fashion conscious patient. Some brands are more comfortable and breathable than others, so don't give up on compression stockings simply because the first pair you try are not comfortable. Getting a professional fitting at a medical supply store may help, and you may even be allowed to try on a few pairs before purchasing them.

Exercise
Exercise should be considered an essential part of treatment, to kept the body in as good a condition as possible. Reclined aerobic exercise, such as swimming, rowing and recumbent bicycling, as well as strengthening of the abdomen and legs, can be beneficial. See Exercises for Dysautonomia Patients for more information.

Counter-Maneuvers
Counter-maneuvers such as tensing the leg muscles or crossing your legs while standing have been shown to reduce symptoms of postural stress, cerebral perfusion, and oxygenation. This rarely stops PAF symptom from occurring, but may reduce symptoms and/or slow the effects of standing up. If you are feeling faint or very dizzy, sit or lay down to prevent injury from a fall.

Scheduling
PAF may require you to reduce your activity load, get more sleep, and change your schedule. It is helpful to plan activities for the time of day that is best for you. It is also helpful to keep your schedule flexible as symptoms can flare-up without much notice or forewarning.

Morning Routine
If your symptoms tend to be worse in the morning, there are a few things you can do to help mitigate your morning symptoms. It is helpful to drink a large glass of water or other hydrating fluid before you get up in the morning. It is also recommended to break down the standing up process into stages: supine to seated to standing.

Avoid Prolonged Standing
It is important to avoid prolonged standing as standing precipitates a worsening of PAF symptoms in most patients. If you must stand for a long time, try flexing and squeezing your feet, leg and gluteus maxiumus muscles, or shifting your weight from one foot to the other. The more you can move your lower half while standing, the better your blood will pump back to your heart.

Showering
Use of a shower chair can be very helpful for some patients, as it eliminates the need to stand, making showering less likely to trigger an exacerbation of PAF symptoms. It is also helpful to use lukewarm water as either hot or cold can trigger PAF symptoms. Some patients also find it better to shower just before bed, since showering can leave some PAF patinets very tired. Another technique is to avoid putting your hands above your head to wash your hair, by bending forwards and flipping your head upside down in the shower, as if you were washing your hair in the sink. This can help ward off orthostatic symptoms while allowing you to wash your hair.

Disability Parking Placard
Depending on the severity of your symptoms, you may be eligible for a disability parking placard, which for some can mean the difference between being able to partake in more daily activities and not by shortening the walk. The requirements and forms vary by state and can be located on your state's DMV website.

Mobility Scooter or Wheelchair
PAF may make some patients bed or wheelchair-bound. While it is important to try to exercise as much as your physical condition allows you to, the inability to stand or walk very far does not have to preclude you from all daily activities. In such cases, a wheelchair or mobility scooter can be very helpful for PAF patients to engage in daily life activities even while very sick or while having a flare-up.

Maintaining an Even Temperature
It is important for PAF patients to maintain an even temperature as extremes, particularly heat, can exacerbate symptoms. Air conditioning, body cooling vests, sun shirts, handheld misters/personal fans, hats, layers in case of temperature fluctuation, and quick drying clothing and sheets can all be helpful in maintaining an even temperature. Some patients use an old fashioned bag of frozen peas as an ice pack during extreme heat. The peas mold to the body, and can be used and re-frozen over and over again (but don't accidentally eat them after they have been thawed and refrozen!).

Find Your Triggers
PAF symptoms can be exacerbated by a variety of situations and activities. It's helpful to find out what exacerbates your symptoms so you can avoid or mitigate a flare-up and plan ahead.

Have A Go Bag
Since PAF patients may use many tools to help manage their symtoms, it can be challenging getting packed to leave the house. Sometimes just gathering all of your things together can be exhausting in itself, leaving you less energy to enjoy whatever activity you were going to attend. It may be helpful to have a purse or knapsack containing all of the items you are likely to need when leaving the house. That way, when you decide to go somewhere, you don't waste energy running around the house trying to find your water bottle, your salty snack, your medications and your hand held fan, etc.

Keep A List Of Medications
One important thing that should be in your Go Bag, or better yet, in your wallet, is a list of all of your current medications, dosages and time of day you take them. If you have any food or drug allergies, you can list these as well. Also, it may be a good idea to have an "In Case Of Emegency" contact name and phone number, as well as your doctor's contact information, and a very brief explanation of your important medical diagnoses. Since many EMTs and ER doctors do not know what PAF is.
 

  © Copyright 2019 Dysautonomia InternationalMedical Disclaimer