There are several people in this forum who has had bronchiectasis for most of their lives and are now in their 50s and 60s. So with taking precautions, your son will have a near to normal life.
I was told that I have it due to childhood illnesses, such as whooping cough. Along with pneumonias and other things in my life (I feel that when I worked in a sewing factory 40 yrs ago for about a year, and was inhaling fabric fibers every day did damage to my lungs). Doctors say that some people have it and never know it. Some people start having issues early in life, some later in life (mine started in my late 30s). I am now 67.
It's a progressive illness. He will progressively get worse, BUT by being proactive, you can really slow down the progression. By doing so, he will be able to live a normal life.
This is a great forum to ask questions and get information on this illness. Also to exchange ideas.
Xuanling, the improtant thing for any patient or in your case the parent of a patient with Bronchiectasis is to learn as much as you can about the illness and then how to best to treat your son as well as showing him how to treat himself.You have come to the right place to get all the support that you need for your son I belieive. I have learned so much here.) And there also other sites on the web.
You will learn more each day. I was suprised and pleased to learn that some of us on our site have had this aliment since their teens or maybe earlier and are doing well.
Some of the people on the site have found really good doctors that are up on the lasted treatments. And some have, like myself had to find somewhat better treatment.For example my Pulmonologist would not allow me to go onto long term antibiotics so I had to find a doctor who would.
It is up to you to find that one doctor or doctors or PA's or NP's who will give your son the best of care. And that may be a matter of time, but maybe not. You will get better at all of this just becasue you are so motivated I believe. I was I know.
I know you will do the your best and am looking forward to hearing you find what you are looking for, for your son.
He is getting a little better until recently the Indonesia country burn palm trees (almost annual issues that impacting most of their neighbors countries.) the Haze has worsen his condition.
He has been running with me for nearly 2 months and getting better than the last time after came put from hospital.
We are continuesly observing his diet, execersise and activities. Hope he wont get any further infection or else will have risk.
I am praying for my son and you to be able to overcome the condition. All the best
He is getting a little better until recently the Indonesia country burn palm trees (almost annual issues that impacting most of their neighbors countries.) the Haze has worsen his condition.
He has been running with me for nearly 2 months and getting better than the last time after came put from hospital.
We are doing therapy for him 3 to 4 times a day to ensure the phlegm will be able to cough out more easily.
We are continuesly observing his diet, execersise and activities. Hope he wont get any further infection or else will have risk.
Is there anyone have similar syntom "primary ciliary dyskinesia with bronchiectasis"?
I am looking for more information and find out from patient how to help my son feeling more comfortable after cough. He also always tell me many times can't smell...
Is ther eany way or any doctor who can treat "primary ciliary dyskinesia with bronchiectasis"?