Good morning, I write you from France. I m 37 years old and I have cysticfibrosis. I used to use saline solution with a bronchodilator by aerosol, 2 time a days. I saw a lot of research with manuka ...
can you tell me as much information on cysticfibrosis. Is able to be passed on by gene ? What is it like living with it every day? What are the medical procedures and medication taken for it? Is it able ...
My 13 year old son has cysticfibrosis and type 1 diabetes, He returned form a hospital Tune up a week ago, where his lung function was over 100% . he is sleeping all day, very tired most of the time ...
dear doctor, my mom have 2 fibroids in her uterus.... doctors recommended to take the uterus... as the fibroids couldn't be decreased in size by using injections.... so is there any risk of continuing with this surgery...?
I need a list of all the meds my son might be taking for cysticfibrosis. I know most are enzymes for digestive purposes. I do know that he s required to take about 45 meds/day. GF Yourselves. this is a matter ...
if no one in my family has ever been diagnosed with Cysticfibrosis should I be worrying about it? cuz I had some chest discomfort today and short of breath?
cysticfibrosis is a very serious disease that can be inherited. If you had it, you would have symptoms for (and from) a long time. If you had symptoms "today", then this is so very much against cysticfibrosis, that you shouldn't worry about it.
Was there any family member with cysticfibrosis? If yes, then perhaps couples that want to have children should be tested for it.
Salty bitter cum? Why is this , my bf has cystic vibrosis
this can be due to cysticfibrosis. His sweat and secretions will be slightly salty
I am suffering from breathing problem a lotdue to excess accumulation of mucus in my lungs due to allergy just want to know what the name of this disease.
Hello! It may be cysticfibrosis, astma or a chronic bronchitis.