CF WIVES SUPPORT GROUP

Newly married to my cfer would love to have someone to talk to about all these scary motions coming up in our lives January 28th getting our assessment for his double lung transplant and im freaking out. .. not sure how I should feel.. would love to talk to ppl who have experienced the same thing we r dealing with
 

vgonthier

New member
Hi Lacey,
I have been married to a Cfer for 12 years. I am not sure we have had the exact experience, but I know how trying some of the medical issues can be. Wishing you the best of luck with the transplant!
 

Mathews

New member
Been married to a CFer for over 20+ years. Transplanted in 1992 - double lung. I'd be glad to answer any questions.
 
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