Crazy Sexy Cancer in Seattle
Comments
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Is anyone here involved with the support groups in Everett? I hope to go to my first meeting next Wed.I also plan on attending the event on the 6th of June in seattle.
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Hi Laurie
I am a south end girl so unfortunately I can't help you. I hope someone can and that the support groups work well for you.
Annie, let us know when you are in town. We are due for a get together probably in June.
Tracy
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Hello Gals,
My goodness I guess life in lil' Poulsbo is cruising along as its been a while since I've popped in. Finally feel like I'm over the hump in the recovery process, golf in April was definitely not one of my smarter choices. Dealt with a bit of infection on the new hoot (not on the flap itself, but on the outer area), hoping an aggressive course of antibiotics has done the trick. Been starting some short walks (5/6 milers) on the weekends for my 3 Day training. Been pretty lazy when it comes to weekday walking .... need to get my hiner in gear.
Just read your post Annie, and if it's of any help I too do a Zometa infusion (like Tracy) every 6 mo. I realize we may all have different dosages, I did want to reiterate what Tracy mentioned that I too had much more of a reaction after my first txt then I have with the subsequent 3. I will hope that your se's take themselves a hike and your txts do nothing but kick some cancer pa-tootie!
I'm planning on walking at the RFTCure on the 6th and hoping to see some familiar faces ! Has anyone else participating received their T-shirt yet ? Was just reading on the website for the race about picking up your T-shirt the day before??? Think/hope I paid to have it sent to the house ?!?!?!?
Time to hit the "galley" ! Take care my friends, Carol
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Carol -- I'm walking with my family at RFTC and just read where they changed the date and location for shirt pick-up. Now it is at Seattle Center the day before the race. Oh well.
I hooked up with Team Survivor NW and have been doing the walk/run team weekly. My daughter and I did 8.5 miles last weekend. They also have some programs over water. www.teamsurvivornw.org. It's nice to have a group to walk with and many of them are bc survivors.
Annie - I'm so sorry to hear about your bone mets. My thoughts go with you.
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golfer, I'm going to the event on the 6th too. I'm not registered but gonna be there any way. hope to get a chance to meet some of you in person.
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Hi, everyone..I posted last a couple of months ago..I have been catching up on the posts and I agree, Swedish Dr. are great. I live in Olympia also, and have just went to Swedish for the surgery part of treatment. I am going in on Thursday to get my Recon started on my left side with a Lat flap and tissue expander. Dr. Chatal is my PS...has anyone had her or know someone who did? She did my right side and IMO did a great job, but I am just wondering about others opinion?
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Hi Colette. I had surgery last week with Dr. Chatal. I had tissue expanders put in, so I can't comment on her work as a finished product. I did want to tell you, though, that my Swedish PT recommended her work and she sees mastectomy patients pretty much exclusively. She gave me a list of about 5 drs and said she thought Chatal was the best of the lot. Best wishes for Thursday!
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Is anyone attending the walk on the 6th of Jnue? If so can you let me know what time it starts, and is it at Quest feild or grrrrr can't remember the other ones name? But you guys know what I mean I hope. Thanks for your help.
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kyasou...Thanks for the reply..I agree she did good work on my right side, but it is my left side that has the rads and much less tissue. It is nice to know I chose a great surgeon and that she does many of these kids of surgeries. She can be anal and really reminds me of my sister..but you WANT that in a surgeon! LOL
Thanks for the well wishes, I will be glad when this one is over because then it seems like it is down hill with the exchange and nipple construction. Sigh...this has been a long treck hasn't it!
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HI Ladies,
I just signed up for the Race for the Cure. Wasn't sure before if I would be feeling up to it. But, this last weekend, I went mountain climbing and I figure if I can do that, I can certainly handle a 5K. I have my last round of chemo on Friday. YEAH!!! So, I may be a little tired, but I figure I should be able to do it. Hope I will see some of you ladies there.
Hope everyone is doing well,
Verene
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Laurie R - they moved to Seattle Center and it starts about 830am. http://www.komenpugetsound.org/ will get you the details. You have to pick up your shirt the day before unless you chose to have it mailed to you.
Verene -- have you noticed the creeping fatigue? It really hit me hard on #4 and found that the 5.5 miles I walked this past weekend was almost too much. Just did #5 today. YAYYYY!!! One more to go!
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frosty,
I'm not sponcered but I want to attend anyway. I just finished my chemo so now I feel up to getting more involved in the other activities involved with this desease. Thank you so much for your help with the place and time. Do you happen to know where everyone is gathering?
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Hey folks,
Haven't posted for a long time; been dealing with my mother's illnesses and then she passed away in March from a combination of liver disease, liver cancer and breast cancer. I'm still sad but it's getting a little easier. I'll be at RFTC with my colleagues from work (our team is Group Health Poulsbo Jean's Beans), raised more than 1000$ so far!
Carol--sorry to hear about your infection, hope it clears up quickly.
Welcome to all newcomers to this club; you'll find amazing support and inspiration here.
Jean
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We should try to figure out a spot to meet -- maybe before the survivor's walk?
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I'm going to be there but not up to the walk yet. I'll be getting there about 11:00. Everyone knows about the location change to Seattle Center?
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Frosty-yes, the fatigue is getting worse. I had my last round of nasty chemo yesterday. Whoo Hoo. I have joines Anne E's Army team. So, I will find out next week where we are meeting. I just singed up for the walk on Thursday, so not sure about all the particulars.
Verene
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I went to pick up our shirts yesterday at Road Runner and met the woman who runs the program. She is a hoot! The survivor walk starts about 11am on top of the pavilion. I'm trying to find the particulars and will post and maybe we can all meet up ...
Day 5 and defintely have the yucks. You know it's bad when even a shower is tiring. Oh well. One more!
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Congrats on everyone doing the 5k next week. Thinking back to last December/January when I was doing AC....yes, I still could have done a 5k walk. In fact, I did do this up Queen Anne Hill regularly. Was seriously dragging though. (I am not a runner but cycle, ski and hike.)
Taxol was easier, and I did the short course of the Chilly Hilly (22 miles) on Day 7 following an infusion.
I need to get my butt out the door and cycle to Alki and back. Getting ready for LIVESTRONG which is three weeks from today. I am doing the 70 mile course, but suspect I will be walking the hill that goes up Cougar Mountain.
I froze my tail off doing the 35 miles on the Centennial Trail yesterday. But my cycling friend and I had the place to ourselves.
I have 6 more radiation to go, then I am done with active treatment. I can't wait.
So thrilled at alll the exercisers in the group as that is the single best thing we can do for ourselves going forward. - Claire
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I will be at the 5k - with kids so not running!
Would love to meet up -
I have not registered yet, so I guess will have to go in on Saturday?!
S
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Let's post a place for those of us who may not do the run to meet up.
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Do any of you know any support groups for YOUNGER women down in the Lacey/Olympia area? When I first was diagnosed I tried finding a breast cancer group and the lady point blank told me that the group here was targeted towards older victims and was not really appropriate for younger women with young kids..And so I was wondering if any of you know of any groups directly in the area? I know that I am 14 months after diagnosis, but I am still dealing with the emotional baggage from losing my breasts, to now slowly getting them back. I am 38 and have 3 kids (9, 5, and 2)
It is hard for me to believe that there is only one group in an area the size of Olympia that is targeted towards breast cancer.
How many people on this board are from the Olympia/Tumwater/Lacey area? Would you be interested in getting a group together to meet and chat once a month or every other month?
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Does anyone know where one can purchase one of those Micro bead forms locally. I really don't like the idea of buying from a catelog until I get better about how to get the right size.
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hi all - when I wrote not running, I meant - walking in the co-ed 5k walk. So, I will be there, and will be participating, just not RUNNING.
For sure, let's meet up somewhere - we can exchange cell phones BUT it is really loud (as you can imagine) so it was virtually impossible to hear anyone who called. Anyone have a good meeting place in mind?
Colette - I would either contact Gilda's club or the Young Survivor group and see if they have groups in your area. I went to one cancer support group on Bainbridge when I just started chemo. I was 44 and the rest of them were over 70. Subsequently I found Carol (Golfer779) on the boards who lives close, then Jean, then Peg etc. etc. So we kind of formed our own little support group locally. Your local support group contact does not seem very supportive! There has got to be other groups.
Hope everyone is enjoying Memorial Day weekend - I am having fun with cozy fires inside instead of the outdoor bbq's that were planned! Either way - have a good time!
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Aprilgirl...That is a good idea..thank you for that. No, they really weren't supportive..the sad thing is there are more and more young women developing breast cancer and if they did that to me, then they are probably doing the same to other women, which isn't good. Who knows, maybe start a group on my own..I will have to call the hospital to find out what is needed to do it.
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I met Jeri on Saturday who was handing out the t-shirts at Road Runner and she asked me to carry the 0-1 year survivor banner. So look for me with the 0-1 year banner in the survivor march. I'm walking as well ... working my way up to running, but still a ways out. Since the walk is at Seattle Center this year, I'm not really sure of the layout, so hard to figure out where to meet. Jeri said there is a Celebration Tent that you gather at 1040 before the parade and the parade is on top of the pavilion.
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Hi All - I'll be there (sans pink wig!) with daughter and another bc survivor and her son. And we are walking the co-ed 5 too. Susan - good point about the noise level! I seem to remember that now!! The walk starts at 9ish, right? We are going Saturday to pick up shirts et al. Anyone with an idea: feel free to identify a meeting place.
Jean - I am so sorry to hear about your mom.
Colette - if you are interested in meeting half way...I'd be happy to get together. I am 42 with a 7 yr old and 3 yr old. Sometimes...these things just need to start small!
g
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Good luck to all of you walking/running this weekend. Actually sounds fun (which is not something I would have said a year ago). I am in the middle of training for the 3 day. My sister and I walked 6 miles twice this weekend which is a good accomplishment. I also had an "Thank You/ End of Chemo / Fundraiser" Party a week or so ago. We had 70 people and my husband set a challenge that if we raised $2000 for the 3 day walk, he would shave his head. We ended up raising $3500+ and both he and my son shaved their head. It was an amazing party and now when I don't want to go out for a walk, I remember all my friends and women on this board.
I am having my hysterectomy on Friday (BRCA1+) and then I am taking the summer off from surgery and treatments. My surgery will be done via the DaVinci Robotic Surgical System. The recovery is supposed to be pretty quick.
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Issymom-Sounds like a fantastic party! Love what you husband and son did! My neice had the same surgery that you are having and it really was a super quick recovery.
Frosty-very cool on carrying the survivor banner!
Hopefully, we will get to see one another at the 5K
Verene
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Lorrie -- best of luck on your surgery and a speedy recovery!
I hope to see many of you on the walk Sunday.
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Hi ladies,
I haven't posted in awhile so I won't attempt to address all the previous posts. I will just say congrats to those who are finishing chemo and surgeries, bravo to those who are doing the race for the cure and hang in there to those that are struggling. Love, love, love the head shaving at the party! Good for you for raising the funds. I am at about 2800.00 raised for the 3 day. My goal is 5000.00 so we will see how I do. My team's goal is 250,000 and I think we are just under 100,000.00 right now. Love my team.
I am in the process of interviewing for a consulting job that I REALLY, REALLY want. I have been through 2 interviews and have 2 back to back on Thursday. Keep your fingers crossed for me. I have been unemployed now for 15 months and it is starting to get a little old.
Gina-cute hair girl! You look smokin' hot! You inspired me to change my avatar since I cut off all my chemo curls and now have a big girl haircut!
Hugs to all.
Tracy
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