Anyone from Canada?
I would like to connect with anyone from Canada...
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Note from the Moderating Team
In addition to connecting with fellow Canadians here on Mayo Clinic Connect, you can also reach out to the
Bronchiectasis/NTM Organization of Canada
Esther Steinberg, Lead
Canada@ntminfo.org
See the contact information for Canada and other country support groups here: https://ntminfo.org/local-support-groups/
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Thanks Margie
Hi amn17,
Does being in coastal & moderate temperature help you? If you dont mind me asking, how often do you get infected?
@rampa Yes Vancouver has clean air because its very green and clean. I don't get infected much really due to environment. Good city, good choice. Does your son has NTM or just bronchiectasis?
Good to hear that you dont get infected often. Hoping my son feels better too once we are there. My son has bronchiectasis. BTW what is NTM?
@rampa It's Non tuberculosis mycobacteria a bacterial lung disease and has different strains of bacteria like Mac, etc. Usually if you have Bronchiectasis you might have other lung diseases but not sure in your case. Would be good to get checked when he is here.
@rampa Hello, and welcome to our group. I have not had amember report such a young person as your son with bronchiectasis. There is another member here in Vancouver, she is @amn17. I am curious, what made you choose Canada to move to?
Hi, recently been diagnosed with Bronchiectasis. Is anyone from Atlantic Canada? I'm from Nova Scotia.
I am in Vancouver area..would love to connect!
I am in the Vancouver area - Squamish, B.C. I am interested in connecting with anyone from BC..it seems the treatment in Canada - West Coast is different from the US..re mild bronchiectasis, no MAC..my pulmonologist prescribes low dose Symbicort.
I am in Ontario, near Toronto. I have bronchiectasis and mac, both diagnosed just over 5 years ago.