Does anyone here have Pulmonary Fibrosis or know of someone? Do you know of any remedies for it ? - pulmonary fibrosis more condition_symptoms
Pulmonary Fibrosis? Do you know a cure for this, you can save what do the doctor?
Pulmonary Fibrosis More Condition_symptoms Does Anyone Here Have Pulmonary Fibrosis Or Know Of Someone? Do You Know Of Any Remedies For It ?
3 comments:
Self-care
Participate actively in their own treatment and to stay as healthy as possible is essential to the life with pulmonary fibrosis. For this reason it is important that:
Stop smoking. If you do lung disease, the best thing we can for you, you can quit. Talk to your doctor about options for quitting, including smoking cessation programs, with a variety of proven techniques to help people stop smoking. And because secondhand smoke can be harmful to the lungs, smoking Do not Let others around you.
Exercise regularly. Exercise is a double-edged sword for people with lung disease. Can worsen the symptoms, but is essential to preserve lung function, reduce stress and improve overall health and wellness. In addition, strong muscles work more efficiently than do weak muscles, so less oxygen they need to perform routine tasks.
If you already exercise, do not stop. And if you are not physically active started to examine, with gentle exercise as ridiculousng a stationary bike or on foot. For example, you could start the hike at a comfortable pace for only 10 minutes per day. When you rest the whole time without having to go, you increase the duration of the walk for one or two minutes per week. Many people with severe lung disease can easily walk at least 30 minutes without interruption. If you have oxygen prescribed for regular use, you need the exercise.
You can also ask your doctor refer you to an exercise physiologist, a training program specifically for your design. In particular, no friends and family have on the exercise you need it.
Eat well. People with lung disease May, lose weight, because it is both uncomfortable to eat and the additional energy needed to breathe. However, a diet that is rich in nutrients, which contains enough calories, essential. The kind that you eat play, time of day and portion sizes can play a role in obtaining the food they need. Because it is easier to breathe when the stomach is not completely crazyll, you can eat small meals throughout the day instead of two or three. You can also try choosing lighter foods, like fruits and salads, instead of foods high in fat or it takes more energy to digest. A dietitian can provide new guidelines for a healthy diet.
Get enough rest. Get at least eight hours of quality rest each night you can strengthen your immune system and feeling of well being.
Control of GERD. If you receive a diagnosis of gastroesophageal reflux, it is important to keep it under control. You can contribute to acid reflux, until at least three or four hours after eating before bedtime, eat small meals, avoiding foods that trigger symptoms and maintain a healthy weight.
that serious tones. You should not mess with home remedies - Why will not be treated by a doctor?
PF, and I can say that there is no cure only a lung transplant. Unfortunately, most of us do not reap a suitable candidate for lung transplantation, no organs or if they need it most. This disease is as effective as a murderer is. It is fatal to grow to 100% of the time, and killed about 50,000 people in the United States alone each year and that number. Little is known about the disease and no effective treatment available at this time.
In addition to advice he received from the previous answer, it is also necessary to control the exposure to other diseases. This means that everyone, and I want to visit anyone with a cold or flu, not the one who is sick, too. Something so cold that most people die in Benin with PF by secondary infections that follow. If you are on about someone with PF, you need to wash their hands frequently and make sure that does the question.
It is an unpleasant way to die. Life expectancy is variable, but usually 3 to 5 yearsnear the initial diagnosis. The only hope for people with PF is by research. If you want to help one of the following donation:
http://www.coalitionforpf.org/
http://www.pulmonaryfibrosis.org/
I hope this has helped, the answer to your question.
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