Anyone from Canada?

Posted by amn17 @amn17, Sep 19, 2018

I would like to connect with anyone from Canada...

Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.

helpme33 | @helpme33 | 3 days ago

In reply to @mholm "Thanks" + (show)

I will call you tomorrow. When is a good time?
Esther

helpme33 | @helpme33 | 3 days ago

In reply to @payette78 "Esther can you post the Canadian group meeting info here?" + (show)

I will do my best. The next meeting is tentative for June 16th with Dr. Marras, well known physician/researcher with Mac/Bronchiectasis. I am also working on a support group meeting.
Thanks

payette78 | @payette78 | 3 days ago

In reply to @helpme33 "I will do my best. The next meeting is tentative for June 16th with Dr. Marras,..." + (show)

That would be awesome.

Colleen Young, Connect Director | @colleenyoung | 3 days ago

In reply to @helpme33 "I will do my best. The next meeting is tentative for June 16th with Dr. Marras,..." + (show)

Hi @helpme33 Esther and all. Mayo Clinic Connect is a public forum. Personal contact information have been removed from your posts. It is recommended to use the secure private message function to share phone numbers, emails and other personal info.

helpme33 | @helpme33 | 3 days ago

In reply to @colleenyoung "Hi @helpme33 Esther and all. Mayo Clinic Connect is a public forum. Personal contact information have..." + (show)

Thank you

mholm | @mholm | 3 days ago

In reply to @helpme33 "I will call you tomorrow. When is a good time? Esther" + (show)

Just text first. Sunday, Pacific Time after 11 a.m. Anytime Tuesday.

attracta | @attracta | 4 hours ago

In reply to @helpme33 "We have an Education and Support Group in Canada - our meetings are on zoom. Contact..." + (show)

Hello Esther,
I believe I replied to you privately and you responded but I can’t find your mail. Where might it be hiding?
I live in Toronto with NTM!

cjsummer13 | @cjsummer13 | 4 hours ago

Hi everyone. I’m new to this so I hope I can connect with anyone that has bronchiectasis and Mac. I’m living in Ajax, Ontario Canada. I found out that I had bronchiectasis last fall and now recently have been told I have Mac. Does anyone have ideas of how to deal with the fatigue?