Washington State members?
I'm north of Seattle and would like to find someone to connect with. Support groups are a challenge since I work swing shift, so I'm hoping to connect with someone here.
Comments
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Hubby was stationed at NAS Whidbey Island for 12 yrs but he retired 20yrs ago the end of this ninth. We've been in So Dak since. -
I'm near you
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I am in Auburn Washington
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I am close to you footprintsangel.
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Hi all!I'm in Kent/Covington.
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I'm in WA state, but in Eastern WA...Spokane. We have great Docs here + an amazing group of plastic surgeons who do DIEP and other reconstruction surgeries.
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I'm in West Seattle
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I'm in Olympia, but moving to Port Angeles in a few months.
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Hi, I'm pretty close to you in Stanwood. I just joined and am looking for others near me as well
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I lived in Seattle’s U. District (1/2 bl. n. of the Ship Canal, bet. Pacific & Boat St.) for 7 years, went to law school in Tacoma, and practiced in Bellevue for 3 yrs. DH finished med. sch. at UW and matched at U of I Chicago Circle for his residency. Left Seattle kicking & screaming in ’78--if you see fingernail marks in the tarmac outside Terminal C at Sea-Tac, they’re mine.
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Does anyone in the Port Angeles area have a recommendation for an oncologist? I'm moving there next week from Olympia and am trying to get set up with the docs I'll need. Thanks in advance!
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Lynnwood...awaiting pathology reports that had to go out for a second opinion. In limbo and it sucks. Swedish pathologist won't come out and say whether its Atypia or DCIS/IDC. 39 on Saturday, so I was hoping to celebrate with some good news.
Worries me that they need the second opinion as it then it must be borderline.
mkinoly: my aunt comes to Seattle, or I think even Bremerton for her doctors - tho different cancer (she lives in Sequim)
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Tacoma here. Currently in the breast center for second look mammo and ultrasound, then an MRI guided biopsy today.
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New to the breast cancer adventure. Er, pr, negative and her+. Live in Stanwood.
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I am in Spokane!
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Been away for awhile dx 2009. I'm in mill creek. Used to be Tina_In Seattle but can't get them to send me a password reset link. So I had to set up a new account. Let me know if anyone in my area wants to meet up!
Tina
It's a nine mile skid on a ten mile ride..............Grateful Dead Treatment: Bi-lat mast, 4 rounds cytoxin/Taxotare. 40 Rounds rads which destroyed my thyroid (it's always something) , recon with implants, ooph, now on Arimedex.Dx 1/21/2009, IDC, 2cm, Stage II, Grade 2, 0/3 nodes, ER+/PR+, HER2-
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I am in Spokane. Is there anyone in Eastern Wa?
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Wife and I live in Vancouver, WA. Used to live in Tacoma and commuted to work at Ft. Lawton. What a miserable drive that was. Lived in Tacoma when the mountain blew; ash everywhere. Say, is The Dog House Restaurant still around? I liked that. Ivar's as well.
Wife's ER+ turned triple negative with numerous small mets to the spine. She's now on Xeloda as the estrogen blockers all failed her.
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I'm in Anacortes. It would be great if some of us could get together somehow.
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A get together would be great! Maybe others in the area will chime in.
Siciliana, I sent you a PM
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I live in Seattle. Still have a drain in and can't drive, but would like to meet some people soon. I figure I will meet people during chemo sessions-does that usually happen
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Hi, I live in North Seattle.
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I live in Seattle (Ballard
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I live in Wallingford, so pretty close! I start chemo July 25. I think I've seen your username in the July 2017 starting chemo thread, TWG.
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I know this is an older post but am in Lynden near Bellingham...would love to get together with anyone in area since I am so newly diagnosed...
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Just moved from Sandpoint! Would have loved to have met up
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Let's plan something! I'm out of town right now but Nov and Dec are good. We can meet in Lynden, Bellingham or Mt Vernon. Did you know knitted knockers come from Apple Yarn in Bellingham? Maybe they know of other groups.
Pm me and we'll plan something. I had the sweetest little Keeshond for many years. We can talk dogs.
Sending hugs, Lucky
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Hi, I am in Seattle, and am interested in starting a new group of women interested in complementary medicine. PM me if interested.
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I'm looking for a support group in the North Seattle/Edmonds area. I will make some calls tomorrow, but thought I would check here first. Thank you.
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For those of you in the Seattle area - I'm interested in the who, why and hows you went about selecting your providers. There are so many specialists to be seen. Did you go with Seattle Cancer Care Alliance? Swedish? Polyclinic? Virginia Mason? Elsewhere? Do you believe you made the right provider choice for you or would you change things? Many thanks.
DCIS / Stage 0 / Grade 3 / Negative ER & PR / size 5.6 / extremely dense
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