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I did a search and it appears that very few people have had a lobectomy - is it not common? For those of you who have had one, what research did you do or have available that helped you make your decision? Are you glad you had the lobectomy? Is there anyone with CF who decided not to have it? For those of you who have had transplants was a lobectomy an option first? My SIL and husband are having to make a decision about a lobectomy for their 6 year old daughter with CFRD and any input would be appreciated.
I am having a lobectomy (Right upper lobe) on Feb 7th (2006) What questions did u have specifically about the lobectomy. Maybe I can help anwer them. let me know you can email me if u dont want to talk about it on here
Lauren M Kelly
Proverbs 3:5-6
Trust in the Lord with ALL of your heart and rely not on yourself, in all times, acknowledge him. And he will make your paths straight.
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I was offered a lobectomy or transplant. I chose the transplant only for the reason that my pft's were to low as it was. Taking a part of my lung would have made it worse. but since my Transplant I feel better than I've ever felt.
pour on the fat and hope for the best
pour on the fat and hope for the best