Crazy Sexy Cancer in Seattle
Comments
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Typing with my thumbs here so bear with ...
Susan, sounds like your doing pretty good, complaining of hot flashes and not complications from surgery sounds like a winner.
In regards to Harmony Hill, I went to a one day session back when I was in chemo. The group setting was for all types of cancers (with some in pretty dire straights) at this point in my own txt listening to the sad stories was not necessarily a pick me up. I personally would suggest attending one of the sessions that deals with bc patients. They served a nice organic lunch.
Wedding day for my step daughter was Sat. The day was awesome and the festivities couldn't have been pulled off any better.
I am now in desperate need of getting some mileage on my feet. Our 60 mile weekend is sneaking up fast ... Yikes !!! -
So would one be insane to do elective surgery in the middle of a heat wave? I'm seriously reconsidering. Tomorrow is supposed to break the record for highest temperature EVER in Seattle. Don't you just love breaking records???
Judie
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At least the hospital would have air conditioning
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I'm thinking of checking in now. Why wait until the last minute?
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This weather is so amazing.
Judie - So your daughter's name is Heidi Sue? I don't hear of very many Heidis, let alone Heidi Sues! I work at a hospital and it was such a treat to be there in the air conditioning today. If your seriousI think you should go for it! Can't imagine a better time to have surgery.
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Heidi, I'm scheduled for Friday at 2:45pm, so doubt that I would be welcomed with open arms before then...lol. I haven't canceled yet...back and forth. I have no AC and am on the eighth floor with lots of windows. It's 91 degrees in here right now. But, it's on the books and I hate to waste all the preparations. I'll decide for sure tomorrow. I just want to be sure of having the best chance of an uneventful recovery.
I just love the way Heidi Sue sounds. Kind of like a highly sophisticated version of the Southern tradition of cutesy double names. I never liked those, but love the one your mother and I came up with...lol. My daughter was born in 1967. So who thought of the name first...your mother or me? She's also an outstanding daughter and friend. I'll bet you are, too!
Hope everyone is chillin' somehow. I'm sipping a smoothie of my own making...frozen mixed berries, frozen banana, milk, ice, Fume Blanc...all blended to slushy perfection.
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Ladies,
Just adding my two cents here from the other side of the mountains...
Towhee (Judie) is a wonderful!!!! I had the opportunity to meet her in person last year...her son goes to college in a local town to where I live....if the rest of her kids are like this young man then the world is very lucky to have them and Judie in it....
Judie-Best of luck with your surgery...you will do great....
My co-workers in Olympia have been telling me how hot it has been over there!!!! Its hot here too but we are use to it...I feel for you ladies in treatment and such during this type of heat...
Hugs to all
Jule
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Hey Jule, you make me blush!!!
I scrapped surgery. I really feel crappy in this heat. It's elective. Why would I do that to myself??? I'll re-schedule in the fall. I've agonized over it for days and am utterly relieved. It's the right decision.
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Judie - can't say I blame you....I had surgery on 7/20 at UW - (very happy with results!).
Anyway, my point is that the patient rooms did NOT have a/c. can you believe that? Now, on 7/20 it was not that hot, but if it was this week - forget it! The rest of the hospital has a/c from what I can tell (regular doctor rooms, nurses stations, hallways etc.
Today is better than yesterday but still pretty hot!
Hope you all are keeping cool!
Susan
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Hey ladies!
Where is everyone? I hope the quiet around here means that we are all out living life like we are supposed to be doing and enjoying our summer.
I am very much enjoying mine and preparing for the 3 day walk in September. Lots of walking which is good for me anyway.
Pathology from the reduction/lift all came back clean and clear and since I still have some swelling and tenderness my onc told me to wait on my next mammogram (was due in July) so I will go around the 1st of September.
Other than that, things are good around here. How is everyone?
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I'm here - thinking maybe we need to plan the next get together!! Good for you doing the 3 Day - I'm impressed. I am just waiting for my tissue expanders to do their thing, with plans for implants in the fall. Aside from work, I've been working in my yard, seeing my grandkids, getting back in to exercise - I can finally run 2 miles. The sunny weather has been so wonderful - I tried not to complain about the heat, but man it was hot there for a while. We have a vacation planned to New England in September, so pretty much staying close to home for the summer.
Can we get together after the kids go back to school? I think we might have some new people to join us.
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Libby-great idea on the get together. Here are a few dates, let me know what works for everyone for our 3rd Crazy Sexy Cancer in Seattle get together!
Wednesday September 16
Tuesday September 29
Thursday October 1
Tracy
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Hi out there!
I am around, awaiting my 6th and last T/C on Aug. 21. Can't wait. I hope I don't cry!
All those dates look fine to me, I will be in town. Good to hear from the Crazy Sexy Seattle crowd!
Peggy
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Sept 29th I'll be in New England, but the other two dates will work for me. Once we decide, I'll put it on the "Get Together" site.
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TKONE...I'm a newbie to the group, but can only make the Sept 16th date. BTW....my husband and I are headed to Harmony Hill for an overnight on Sunday then a one day retreat on Monday. Will give you a report sometime next week. I have my last TC tx on Tuesday......woohoo!!! Patti
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Hello Seattle sisters - I have had lots of house guests, and still am recovering from my reduction/reexcision that was three weeks ago.
My path report came back all clear too Tracy! Woohoo! Right now can't IMAGINE squishing "the girls" in a mammogram - ouch - so good idea to postpone.
All the dates seem good to me - if Patti can only come on 9/16 - maybe we do that date?
My sister in law and her bf (from Germany) left this morning, and my in-laws are still here. We have a friend from Canada arriving on Friday.
Lots of fun and laundry
Hope everyone is doing well and enjoying August
Susan
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Hello you Crazy Ladies ... dates look good to me ... hopefully Tracy and I won't be hobbling if the 16th is the date !!!!!
Big WhooooHooooo to Susan and Tracy for the all clear !!!!!! AWESOME !!!!!
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Hello again ladies!! I'm thrilled that Susan and Tracy are all clear!!!! I started Herceptin again last week, and am being admitted to SMC for each treatment (allergy to taxol) for long taxol & herception infusions. It takes more than 12 hrs for the treatment and I get tons of premeds. I have 5 more weekly treatments, this pushes my surgeries to the end of Oct. now. I'm glad everyone is doing so well!! I'll try to come to the get together, just depends where it falls in my chemo cycle... I'm so glad it's cooled off some here... much love!!!!!!! Jessica
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Hi Everyone,
This board is pretty quiet right now, I guess it must be that everyone is in summer mode. Maybe we'll be back to summer weather next week!
I just had #12 of 26 CMF injections yesterday and am feeling good because I'm almost halfway through. I think Susan and I might be the only ones on the Seattle forum to receive 6 months of weekly CMF. Is their anyone else? It seems to me that the people I've heard of receiving it have gotten 24 txs, not 26. I'm suddenly feeling like agitating for 24 txs with my Onc. Seems silly to quibble over 2 weeks but at the moment it feels significant. I'd appreciate hearing what anyone else has had. Susan, I think you told me you had 24.
I would be interested in trying to attend the next get together - I'm not sure about the possible dates but would try to attend anyone that works for others.
Hope everyone is doing well.
Heidi
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HeidiSue - you are correct, I had 24 weeks. i agree, you and I are the only ones that I have seen on these boards with weekly CMF, although SCCA said that is the only way they do CMF.
Congratulations on completing 12!!!! Halfway there is wonderful! I would certainly ask about 24 vs. 26 but I bet your oncologist has a reason why....they always seem to.
How do you feel overall? I was so happy to reach halfway, but the fact that I had 12 left seemed a bit overwhelming at the time. If you feel that way too, I assure you that you will be ticking those last 14 off and be done in no time.
I think you are right that we are all in summer mode. I have been so busy with houseguests and doing fun things that I haven't been on the boards much.
Jessica - only 5 more - that is wonderful too. I can't believe that it takes 12 hours - what a day. Once school starts and I start radiation I would be happy to come meet you at Swedish if you are up to it.
Hope everyone is having a great weekend!
Susan
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Susan, sounds good, I'm at SMC for at least 24hrs with each chemo, they keep me overnight, at least for now. Hopefully after the next few I'll be able to do it in the treatment center.
I hope everyone is feeling well, we are in for some nice summer weather later this week!!
Much love, Jessica
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Hi Susan - I asked my onc why it was 26, not 24, and she said it was because that was the # in the studies, but her nurse told me that they do 24 with some patients. Go figure. I have been doing pretty well, the main thing bothering me now is fatigue, which I just noticed, maybe 2 weeks ago. It's fine on a day I take it easy, but on a work day, or a day I try to cram too much in, I really notice this late afternoon slump, which is really like no feeling I've ever had. It feels good to be 12 into it. I'm feeling like the rest will go faster. I really appreciate the assurance from you - helps to hear it from someone who's done it. So you start radiation next month? Healing OK? That's alot of ferry rides!
Jessica - I haven't talked to you before but I would be happy to drop by whenever I'm a Swedish when you are having your treatments if you want some company, or someone to bring you something to eat besides their sandwiches. I have my treatment on Thursday afternoons, usually around 4pm, and I have 14 more weeks to be there. Do you have to come back in later for Neulasta shots or IV hydration or anything? Good luck.
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Hi Heidi Sue, I have chemo on Tuesdays, they admit me to 12E usually, I stay overnight. I give myself the Neulasta shot at home. If I'm there on a Thursday, I'll let you know. I bring my computer with me, it's so boring there, that way I can do research or talk to you ladies. I just got my post chemo scans scheduled, they will be Sept. 21 & 22, my bone, MRI's & PET CT, so I'll finally find out if all this chemo and Herceptin have been doing any good! My surgeries will be at the end of Oct. Much Love, Jessica
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Sounds good Jessica. Hope things go well for you tomorrow.
Heidi
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Hi everyone! Hope everyone is doing ok... I know I've been awol for several weeks...when I feel good, I just want to go-go-go. It has been busy with the kiddos and I just got back from a couple of lovely weeks on Orcas Is (my fav)!
Congrats on sucessful surgeries Tracy and Susan; oh, another get together would be great; I will try and make any of the dates work.
Jessica, good luck tomorrow.
gina
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Hi girls!
I haven't posted in soooo long - just been reading, hoping to gain more knowledge of all this.
I wanted to respond to HeidiSue and Susan: I am also on the CMF regiment. However, I am on it for 12 weeks, 2 weeks on and 2 weeks off. I take cytoxan orally (everyday for 2 weeks) and have the methotrexate and 5Fu by IV once a week for 2 weeks. Could the difference be the different type of BC I have? Looks to me like everyone here has IDC except me!
I will finish my 2nd 2 weeks tomorrow. So far it hasn't been too bad.....a little tired, bad case of diarrhea, and a kind of numb feeling in my legs some days. I do OK the day after the IV stuff, but by Friday I'm knocked out.
Been spending a lot of time in my garden...amazing amount of tomatoes this year. I think our hot spell had something to do with that.
Hope you are all as well as possible.
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Deb, HeidiSue, Susan - I did the exact same regime Deb is doing...CMF for 12 weeks... 2 weeks on, 2 weeks off. My last go around (week 8) my wbc were below 2, so rather than get 3 cytoxan pills a day, my onco cut it back to 2 per day and said it wouldn't change the outcome. I only had 3 months of it becuase I started on TC...but 6 months of CMF were one of my original options. Jeeze is CMF popular in Seattle or what????
Almost got all the laundry done. Enjoying another beautiful day in PNW!
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Deb -- Just so you don't feel alone (!)...I am and ILC'er also.
Re: tomatoes and growing season. Our apple tree is loaded down with apples, more so than usual. But the blackberries seem slow to ripen this year, most around here are still green.
Gina -- how's the hair growth going? I have a bunch of crazy white hair all over my head. Well "a bunch" is relative...most would describe it as "sparse" but I guess these comments belong on the hair hair hair thread! Glad Orcas was fun.
Take care.
Peggy
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Well, I guess we're in for another cool and cloudy stretch. Strange August. I was going to go up to the San Juans for a long weekend but instead I think I'll stay in Seattle and do a few things that need to be done - like cleaning the bathroom!
Re: CMF, it's really interesting how many different regimens there seem to be. My MF is IV weekly and C orally every day. Yesterday I had #13 and my oncologist told me that if I only finished 24 courses she would be satisfied. It's only a difference of 2 txs, but it made me so happy!
Deb, Gina and Susan - thanks for the feedback on your experiences. Deb, you mentioned the difference in your type of BC. Mine is "mixed lobular and ductal", so I've never been sure which group they use to make treatment decisions. I really should ask.
Have a good weekend everyone.
Heidi
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Hi all,
Heidi - Duh, I feel so stupid....I was going over my path report from surgery again, and noticed that they found IDC in my right breast (besides the ILC). No one mentions this when they talk about my cancer so I'm now at a loss for why I'm on the CMF regime. I can't believe I missed that. Anyway, I wonder now if I'm being treated for both or what. I did notice though that Gina's dx is IDC and she did the CMF also. Maybe it's because we're Swedish patients! I see Dr. Ellis who is in the same office with Dr Rinn. Anyway, I guess it's time for more questions. I find I can get a lot of info from the nurses.
Gina - I'd love it if the Onc would take me down to 2 cytoxan a day! I'm having a terrible problem with my stomach - not nauseated but kind of knotted up. I shouldn't complain, it's not nearly as bad as I imagined it would be.
Aug. 21 and another weird, cloudy summer day in our glorious PNW! Hope you are all doing ok.
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