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Hi - found this site today and hope i can find a few answers - I have been on a quest to find the best place to live in the USA that is less likely to cause illness to people with bronchiectasis / NTM - also I would like to let the medical community realize that once you give a patient a diagnosis. of bronchiectasis the conversation should include what this means in the future for other illnesses that having bronc. makes you more apt to contract - i was officially dig in 2005 with bronch. after years of symptoms and now have been on meds for a year for NTM / MAI - I have been treated for puesdomonas also - I have been told that where I live is full of NTM but no one has any answers as to a better place - I found a little info on a medicare map of state with high NTM - I live on the east coast of Fl. and was told by my Dr. that this is about the worst place - any info would be great - hope this site is helpful for this community as we need some much needed answers about what life is like beyond diagnosis - thanks to all - norma
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