my diagnosis started the same way, with a cough that wouldn't go away. I am sorry you had to find us this way but welcome to the site. I am sure you will find alot of support and info here. I have alot of the same symptoms you do so if you want to talk more about it I'm here.

Hi Lori, I too have the same problems as you do. I had a flare up in May and was told that I have Pulmonary Fibrosis. In July I was told that I also have emphysema. The first four months I thought I was actually dying, LOL. Always tired and out of breath. In August I started walking so I could strengthen my lungs. Walking actually worked. I'm not as tired as I used to be. I am on oxygen when I exert myself. I try to walk at least a mile a few times a week. It was slow starting but now it's a little better. One step at a time, then two, then three, etc. I don't need oxygen any more when I make the bed. I am not coughing as much, but I can't get excited over anything, or talk too much. When I'm talking too much, I have to shut up for a while until I get my breath back. LOL. Take care. Linda

Hi Lori..I too have had all of those symptoms. Still do to some extent. If you haven't gone already, be prepared for an extensive workup. I also have an autoimmune disease make sure you ask about that, see a rheumatologist possibly too. CT scan normal is good (probably minimal scarring). I have a type of restrictive airway disease called interstitial pneumonitis. Inhalers are useless. Will need steroids. Scary at first but really a life saver. I'm only "moderate" on the severity scale and I have been able to increase my activity level so that I can walk a "tread mile" at an incline, stationary bike 10.8 miles, swim a mile and do 30 min of weight training...all in one day if I want. I started out like you. Am NOT on any oxygen at anytime. Be aware that this can change on a dime but not everyone with restrictive airway issues is house bound. I still also work full time...there is hope!!! Hang in there... let me know if I can help you with anything.