It really depends on the type of Pulmonary Fibrosis.
If it's Idiopathic Pulmonary Fibrosis, then there's not much anyone can do on account of it being of an unknown cause. In these cases the general life expectancy is 5-7 years after contracting the disease.
For other variations of Pulmonary Fibrosis, ones caused by the immune system over reacting and causing inflammation (Sort of like a localized auto-immune disease) immunosupressants are often used. There are ongoing drug trials for new drugs, but unfortunately all of these are just stall tactics.
If patients have enough insurance, they may get lung transplants, in which case they'll live an average life span. However, lung transplants cost, on average, $500,000, so this route isn't often taken.
On September 28, 2016, my partner Allen’s pulmonologist told him to go home and get his affairs in order, because he only had 30 days to live. At that time, his biopsy showed severe idiopathic pulmonary fibrosis (IPF). Allen’s IPF caused him to struggle with many common daily activities. For instance, walking just 10 feet would leave him feeling dizzy and ready to fall. He had to use a walker to get from his living room chair to the bathroom. Even on supplemental oxygen, he had no energy.
Allen began doing all the research he could on his condition and treatment options. At first, he was discouraged by the lack of information and support groups for IPF — the support groups he found were for people with COPD. Then, Allen found the multivitamincare.org website, and everything started to change for him.
After his treatment, he doesn’t need his walker to get around anymore, and he’s been able to walk short distances and exercise his legs. He still needs supplemental oxygen, but the amount he uses hasn’t increased. He’s been able to go on an Alaskan cruise with his friends without feeling like a burden. He’s also been able to travel to beaches along the Oregon coast and watch whales in the bay. He says he likes being able to go places, get out of the car and take in the sights. Before multivitamin herbal formula, he wouldn’t have been able to travel or sustain the energy for sightseeing.
Now, Allen says he feels so lucky to be alive after his doctor told him he only had 30 days left. Because of the results from his treatment, Allen has a short, sweet piece of advice for other chronic lung disease patients considering getting help from multivitamin herbal remedy.
The life expectancy is of a normal person
About 5 to 7 years.
what is the life expectancy of a kidney transplant patient with a living donor
The average life expectancy is about 30, but it varies.
Cystic Fibrosis cannot be cured. However treatments are getting better and life expectancy is increasing all the time.
The life expectancy of a liver cancer patient is dependent upon the progression of the liver cancer. When the liver cancer is caught in the early stages it can be cured, resulting in a long life expectancy.
A patient with mixed connective tissue disease will require a doctor's care. The doctor will diagnose, treat, and assist the patient in understanding life expectancy and outcome.
Pulmonary Fibrosis Death is a death that occurs due to scarring of the lungs. An oxygen tank may help with breathing, but ultimately, the best option for longer life is a lung transplant.
The most important single factor in improving the patient's prognosis is early diagnosis. The earlier that a patient can benefit from the new techniques and lifestyle modifications, the more likely he or she is to have a longer life expectancy.
The life expectancy of Crohn's patients is fairly average to the life expectancy of the rest of the population. It may be slightly lowered due to the stress the illness causes and the amount of extensive surgeries. However, many patients are able to live a long and fulfilling life.
The median life expectancy is about 38 years. But there are people with CF that live until they're 50 or 60 or longer.
Recent advances in Marfan syndrome treatment have prolonged the life expectancy of patients considerably. Changes in how the syndrome is treated, including medication, surgical interventions, and monitoring for complications of the syndrome (eg, aneurysms), are all responsible for the increase in life expectancy. The prolongation in life expectancy can be seen by taking a look at statistics from 1972, in which the life expectancy was 32 years, and from 1996, where patients with Marfan syndrome had a life expectancy of 61 years.