Bronchiectasis

Kristen

New member
I had a CT scan last fall that showed mild bronchiectasis in one location - my CF doctor said it was likely caused by a collapsed lung I got with a really bad pneumonia when I was 12.
 

Kristen

New member
I had a CT scan last fall that showed mild bronchiectasis in one location - my CF doctor said it was likely caused by a collapsed lung I got with a really bad pneumonia when I was 12.
 

Kristen

New member
I had a CT scan last fall that showed mild bronchiectasis in one location - my CF doctor said it was likely caused by a collapsed lung I got with a really bad pneumonia when I was 12.
 

iwantmypup

New member
I was diagnosed with CF at 2 months and I just recently found out that I have "severe" bronchiectasis (I'm 15 now). It bothers me that until we changed doctors, not one person had ever told me that I have it. I actually had a bronch this morning and he told me it was one of the worst cases he's ever seen...
 

iwantmypup

New member
I was diagnosed with CF at 2 months and I just recently found out that I have "severe" bronchiectasis (I'm 15 now). It bothers me that until we changed doctors, not one person had ever told me that I have it. I actually had a bronch this morning and he told me it was one of the worst cases he's ever seen...
 

iwantmypup

New member
I was diagnosed with CF at 2 months and I just recently found out that I have "severe" bronchiectasis (I'm 15 now). It bothers me that until we changed doctors, not one person had ever told me that I have it. I actually had a bronch this morning and he told me it was one of the worst cases he's ever seen...
 

greatbay

New member
I have it and it is one of the reasons my current lung Dr. finally agreed to test me for CF. It shows in all but 1 lobe of my lungs...so I guess you could say I have a severe case.
 

greatbay

New member
I have it and it is one of the reasons my current lung Dr. finally agreed to test me for CF. It shows in all but 1 lobe of my lungs...so I guess you could say I have a severe case.
 

greatbay

New member
I have it and it is one of the reasons my current lung Dr. finally agreed to test me for CF. It shows in all but 1 lobe of my lungs...so I guess you could say I have a severe case.
 
W

windex125

Guest
I was diag. with Bronch. at 21 and the right lung is now completly destroyed from the bronch and CF with Mac on top of it all which came around 2000 so looking at a xray of me you think wow how is this person walking around without o2 all day? I am not sure? I guess it was a grad. decay of the lung even though on meds constant once their is nesting ground for infection anything is possible. I campare it to trying to get rid of roaches and you live in a apartment complex and not everyone is agreeing to use the RAID to kill them They just keep coming back. Casue it's dark,moist lots to eat. Pat-56/CF-MAC other stuff as well
 
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windex125

Guest
I was diag. with Bronch. at 21 and the right lung is now completly destroyed from the bronch and CF with Mac on top of it all which came around 2000 so looking at a xray of me you think wow how is this person walking around without o2 all day? I am not sure? I guess it was a grad. decay of the lung even though on meds constant once their is nesting ground for infection anything is possible. I campare it to trying to get rid of roaches and you live in a apartment complex and not everyone is agreeing to use the RAID to kill them They just keep coming back. Casue it's dark,moist lots to eat. Pat-56/CF-MAC other stuff as well
 
W

windex125

Guest
I was diag. with Bronch. at 21 and the right lung is now completly destroyed from the bronch and CF with Mac on top of it all which came around 2000 so looking at a xray of me you think wow how is this person walking around without o2 all day? I am not sure? I guess it was a grad. decay of the lung even though on meds constant once their is nesting ground for infection anything is possible. I campare it to trying to get rid of roaches and you live in a apartment complex and not everyone is agreeing to use the RAID to kill them They just keep coming back. Casue it's dark,moist lots to eat. Pat-56/CF-MAC other stuff as well
 

Treewife

New member
My non-CFer has it - ABPA as well.

Ashley my CFer has it too but they they seem to describe it more as a symptom or something that goes along with the CF... not a lot of attention to it.
 

Treewife

New member
My non-CFer has it - ABPA as well.

Ashley my CFer has it too but they they seem to describe it more as a symptom or something that goes along with the CF... not a lot of attention to it.
 

Treewife

New member
My non-CFer has it - ABPA as well.
<br />
<br />Ashley my CFer has it too but they they seem to describe it more as a symptom or something that goes along with the CF... not a lot of attention to it.
 

zoe4life

New member
This hospital stay...6 days ago (still on home iv's), Zoe was diagnosed with Bronchiectasis.<img src="i/expressions/face-icon-small-sad.gif" border="0"> She will be 7 in April. She had a chest ct done while in. The doc went over it with me. It's not a great thing to hear when your 6 yr. old is diagnosed with it. Unfortunately, Zoe is on albuterol, hypertonic, and pulmozyme nebbed. CPT twice a day. Without fail. She has NEVER missed a treatment or CPT. The only thing they added due to this new diagnosis is Zithro MWF, to help with inflammation.
Soooo...do all cf'ers get it...when does it show up??? Who knows. Another gray area with CF. Yay.
 
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