Hi everyone,
Would love to hear some reassurance from anyone here who has also been diagnosed with bronchiectasis. Bit of a hit to be honest after everything with UC. Very worried about the long-term outlook and survival?
Dr seems to have diagnosed me and sent me away with an inhaler and 'dont get sick' advice and that's about it. They don't seem to understand the link and need to see a UC specialist.
Anyway, any advice, or just anyone who is in a similar boat would really appreciate hearing from you!