Is there a MInnesota Group
I have noticed a few from MN and just wondered if there was a thread yet...anyone meeting up etc. or in need of support. I live in the outer SW burbs of Minneapolis.
Comments
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Hi nowords,
I am not from MN, but, I do go to the Mayo clinic for tx. Where are you being treated?
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I go to the Mayo. Just went yesterday for 1 year checks and all clear!
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I am in the Stillwater area. I was just diagnosed yesterday. Wow, that feels like about 100 years ago. There is supposed to be a free group at Lakeview Hospital in Stillwater (651-430-4549) or www.lakeview.org. I haven't checked it out yet. I just printed the .pdf file. My surgeon also gave me a number for the American Cancer Society that pairs newbies with experienced bc volunteers: 1-800-227-2345 was the number in the brochure I just got.
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Congratulations nowords! That is great. I am up there next week and will start my every 3mo visits (again) for the next who knows how many years! I would love to meet survivors at Mayo if you are ever interested. Take care and enjoy another free and clear year!
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Hi,
I am from MN and i go to Mayo in every 3 months, my next visit will be on January 28. I love to meet BC survivar sisters from MN.
Thanks.
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curious, HAVE ANY ONE TRIED MEETING, mn GROUP. iF SO LET ME KNOW.
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Louvjja- I am in Minnesota. You probably can guess my area by my name. :-) Where are you located? I've seen a few others from Minnesota on here. Are you being treated right now? I am in chemotherapy and then have radiation to follow.
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HI mankatostat…,
I am located to twin cities. Best of luck on your Radiation therapy. make sure skin don't get burn. At the end i got moderate burn on my chest. By the way, Where you are getting your treatment? I love to have a MN group so we can have meet ups, sharing and fun.
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