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I found out in late July that I am fighting for my life WITH A CONDITION CALLED Idiopathic Pulmonary Fibrosis IPF. I HAVE A LOT OF PLANS AND NOT ENOUGH TIME NOW. i AM GOING TO POST WHAT IS IPF RIGHT FROM THE FOUNDATIONS MONTHLY NEWSLETTER. THE REASON I AM EVEN POSTING THIS IS SO PEOPLE CAN HEAR ABOUT THIS AND FIND OUT IT KILLS THE SAME NUMBERS THAT BREAST CANCER DOES BUT IS RARE TO GET. SO PER CAPITA THIS IS VERY BAD. IF YOU RUN INTO SOMEONE CLOSE TO ME AND THEY ARE ACTING WEIRD OR UPSET AND YOU THINK THEIR IS NO REASON THEN READ THE POST BELOW AND GIVE THEM A BREAK.
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WagsCgo aka Scott Wagner
Idiopathic pulmonary fibrosis (IPF) is a condition in which the lungs become scarred and breathing becomes increasingly difficult.
IPF has a prognosis worse than many cancers and most sufferers go on to develop respiratory failure and die of suffocation as their lung capacity reduces.
The disease – which kills 5,300 people every year – creates a build-up of scar tissue in the lung which makes them thick and less able to take in oxygen.
Regardless of treatment, people with IPF, which usually strikes those in their late 40s or early 50s - on average only live for around three to five years from diagnosis.
Although still considered a rare disease, IPF has become more common in both the UK and the US over the last 30 years.
The symptoms of IPF tend to develop gradually and get slowly worse over time.
There is no cure and it's very difficult to predict how long someone with IPF will survive at the time of diagnosis.
Regular monitoring over time can indicate whether it's getting worse quickly or slowly.
Source: NHS Choices
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Covering Chicagoland Metro Area US