Justinsmom
New member
Hi,
My 7 year old has been going through the diagnostic process for the past year. He became pancreatic insufficent from January of last year to June of this year with fecal elastase levels going from 148 to 25. He did not have a positive sweat test. Last Friday night he complained of nausea and tummy pain as well as pain in the back. During the night he spiked a fever of 103.5. Taking the advice of "Bill" who posts here about pancreatitis, I took him to the ER. They did a CT scan looking for pancreatitis or appendix issues. They found an "infiltrate in his postular intererior left lung base. We were told he has pneumonia and he was kept about 36 hours and given 2 iv doses of antibiotic and sent home on 875 of amoxicilin 2x day. We were strongly advised to seek a second opinion and were given a copy of the scan on disc. Meeting with the new CF doctor, she said this was somthing that is not a run of the mill pneumonia but is linked or common to CF. I appologize, it was a lot of information to get a one time. She will be repeating the scan (or x-ray I am not sure yet) next week for to make sure it has gone away. Otherwise, she will be doing a broncoscopy to make sure he does not get bronciectasis.
Could anyone please tell me their experience with infiltrate in the lungs? What does this mean and is it more common/specific to CF? Again, I received so much information at once and am not sure I have kept it straingt.
Thank you in advance.
My 7 year old has been going through the diagnostic process for the past year. He became pancreatic insufficent from January of last year to June of this year with fecal elastase levels going from 148 to 25. He did not have a positive sweat test. Last Friday night he complained of nausea and tummy pain as well as pain in the back. During the night he spiked a fever of 103.5. Taking the advice of "Bill" who posts here about pancreatitis, I took him to the ER. They did a CT scan looking for pancreatitis or appendix issues. They found an "infiltrate in his postular intererior left lung base. We were told he has pneumonia and he was kept about 36 hours and given 2 iv doses of antibiotic and sent home on 875 of amoxicilin 2x day. We were strongly advised to seek a second opinion and were given a copy of the scan on disc. Meeting with the new CF doctor, she said this was somthing that is not a run of the mill pneumonia but is linked or common to CF. I appologize, it was a lot of information to get a one time. She will be repeating the scan (or x-ray I am not sure yet) next week for to make sure it has gone away. Otherwise, she will be doing a broncoscopy to make sure he does not get bronciectasis.
Could anyone please tell me their experience with infiltrate in the lungs? What does this mean and is it more common/specific to CF? Again, I received so much information at once and am not sure I have kept it straingt.
Thank you in advance.