Starting chemo January 2009?
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Hello everyone. Hope you all had a nice weekend.
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Jess--Hope your weekend was good too!
Mine--well I didn't go to GG park for the ACS walk. Did it last year and it was hard, walking in memory of 2 young moms and my grandma. My co-workers went, and maybe I'll do it next year. But instead I did go to a great workshop at Cal (teaching writing) focusing on helping kids understand children with differences (immigrants, special needs, alternative families) and write about their own "safe places."
Brenda--congrats on the walk! Sounds great.
KM47--I read your blog. Love the go away "f...ng" pain idea. Wow--a half marathon!!! I'm impressed. My feet hurt just thinking about running that far.
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Well, went in to see my Onc today about that area on my chest wall bothering me. I have a CT scan next week. Suspicion is "low" but we need to check it out. That low suspicion is enough to keep me sleepless right now
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Think of you kmmd!!!
(((HUGS)))
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I have a day off today! Slept in till 7am! Felt wonderful.
Aw, Kmmd- I hate the waiting and all the wondering and the worrying. HUGS! I still am bothered by the low blood counts-every cold foot,hand or headache, every bruise.....i have to check out. I think I am slightly nuts over this. Thank goodness I have exercise.
DD- has to drive in Detroit next week! Yikes! Country girl and the city! Should be interesting. I am praying as we type this. Let her be safe and no accidents.
KM47- I agree with BK, my feet hurt thinking about a half marathon. I am impressed. Been years-no decades - since I've done one.
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Strange day today. It was the elementary school halloween party and last year a volunteered to work the prize table. I was just a week or so out from my reconstruction surgury and thought that would be an easy job. Forgot about chemo brain and trying to keep tabs of a hundred kids pushing tickets in my face demanding prizes. This year I was just a parent taking their kid, but I can remember how hard it was last year.
Things are weird at work. My boss whom we all love and has been devoted to being a shield for us against unreasonable demandes from above has been suddenly transferd to a new post. They told him in a 4 minutes meeting on Wednsday, he told me yesterday (since I would be out of the office in the morning today) and e everyone else was told today. He starts his new position on Monday, but they have not told him where he will e working, who he will be working for, or who will be filling his shoes. My office is in mourning and shock over this. My boss is as well, but as a survior of prostate cancer he reminded me that we both know this is just work, there are more important things in life. But the many hours of life spent at work are likely to be get alot less pleasant in the near futures. Sigh. I really have to pay attention to the stress this will cause, because I think stress had alot to do with my BC.
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Must be the week for it Renrel, I've had to deal with some buttheads this week myself. DH asked last night why I didn't push harder in a meeting I had and I told him I just didn't have the stomach for it. I just couldn't work up any anger or passion and fight. I'll have to not let it stress me and if I can't do that move on.
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Broke out my pink wig for halloween and could barely get all my curls under it. I had to wear a swim cap to come anywhere near getting on my head. DS had an awesome day. Sunday school in the morning where the learned about the tower of Babal by building tall leg building together but without being allowed to talk. Then in the afternoon his best friend came over to play for a hour or so before they went trick or treating. First time his friend has gone. DS went out again after his friend left and is convinced that he has gather more look than any one else ever. He had to hide at every house and yell boo when the openned the door, so he earned his candy.
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Renrel, stories about your DS always make me smile
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Getting pretty nervous for that CT tonight. Can't wait to post here by the end of the week saying it was all nothing.
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Dear all
need your good thoughts. mammogram and onc visit today. The mammogram took two hours! they kept taking more and more film, then finally an ultrasound. Bottom line-- found a .5mm calcification on left side (lumpectomy was on my right). radiologist said he thought it was not cancer, but because of the location (under my arm up high) he could not biopsy it and thought it should come out. I have to say, I was just pissed off. Two years after dx, chemo, radiation, damn hormonal therapy---- this better NOT be cancer.
I went to onc- had a list of questions we never got to..... I realize I am jumping the gun here, but I am a worst case scenario kind of girl. Told her I was NOT doing chemo again, ever... and if this indeed was breast cancer, I wanted to get off all the meds since they are wreaking havoc on my life...lupron and femara. I was so cranky.
Then I marched down to the records, ordered up my last mammos and MRI's, called the breast surgeon- will march those damn records right over there tomorrow.... then go see what she says. I have to tell you I am hopping mad.... I will not let cancer have one more minute of my life... it took half of 2008 and all of 2009...... no more....
Now, I know I have to take this in steps, and the radiologist is probably right, but am just done.....
Now, on a different note- I went to the sexual health clinic at the onc's as well. I was going to blow it off because of all this, but since I am not letting cancer take any more of my time, I went. It was so helpful.... they had some good suggestions for the vaginal dryness and made some suggestions about the lack of desire--all of which I will share in another post.
BUT, I am so mad..... I am not doing this again...I just won't (does that sound stubborn enough??) I will go through the diagnostics, but I cannot see a situation where I could stand any more treatment.....
thanks for letting me vent
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momand2kids. I'm so sorry this is happening to you. I hope its noghtin. We're here for you either way
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My scans were good, I'm so relieved
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momand2kids, Hoping the best for you.
(((HUGS))).
kmmd, YEAH!
((HUGS)))
My PET & Mammo is the 18th
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momand2kids and mnmom, please keep us updated
what would we do without each other?
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momand2kids - Totally sucks! We are here for you what every you need. You know that. Keep us informed.
kmmd - Great news!
I am planning to get my Reiki masters certification in two weekends. I am amazed at home much I use it in my life.
We had a major shake up at work end of last week. Our boss for about the last 10 year or so, whom we all love because he fights for us against upper management demands, was suddenly reassigned to a special project with no notice. Everyone thinks it is a way to get him out of the way so that they can whip our department into shape. I think that is a side benefit and that do really need him on this project. But one workmate took me aside and asked for advise on how I remain so calm. She comment that first I took BC with such grace and now I am calm through this upheaval. She said she was just so mad she could not think straight. I was not sure what to tell her. I mentioned yoga and breathing and reiki, and my choice to believe that there was more to the decision than an evil desire to abuse us. But I have been thinking that part of it may be that I am gaining some ground on the how "non attatchment" concept. i accept, to some degree, that everything changes and that to try to hold on the the present will be a source of suffering. Good health and bad health will both pass with time. The people we love and those we dislike will pass through this life and on to what comes next. All we have is the acutally experience of the present moment. We can take all that it has to offer, or we can waste it in an unproductive comparasion to the past that is no more or the future that we are only imagining.
OK, I am diving in to the deep end again and taking you on a swim when you did not even ask to get wet, so I will sign off now. I have a phone call I need to make. Sweet dreams my Jewels. I will be sending some energy toward you in the next few days. Feel for it.
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Dear all
thanks for your kind words.
I raced around the city yesterday moving films from Farber to MGH. When I got to MGH they told me that I had an appt with surgeon tomorrow morning at 8:30--now there is a benefit of being in the system.
I think they are going to do a needle loc biopsy/surgery--- I will know more tomorrow. I went to the wig store next door. If I have to do this all again, I am going to get a new wig in a different color. I am also going to share more and get more help.
While I hope none of this comes to pass (I keep reminding myself that the radiologist said "I don't think it is cancer') I am preparing for the worst.
In the meantime, unlike last time, I am not falling into an emotional heap. Last time I cancelled all non-essential activities during the diagnostic phase, did not want to see or talk to anyone unless it was about bc, which left me a small group since I told so few people.
Now, going to my college reunion, dinner with friends, work, professional conference..... I simply refuse to let a .5 mm spot on my mammogram dictate my entire life. There will be plenty of time for that after a diagnosis. For now, I consider myself a healthy person who had a questionable mammogram. Last time I could NOT sleep for weeks-- last night I slept like a baby.
I am delighted that we can see her tomorrow--maybe we can schedule this in the next week or two then recover and wait for results to make a plan..... again, which I hope we won't have to do.
It is what it is and I cannot change it..... I am sure I will need to lean on you as we go forward.
thanks for the great support
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momand2kids - (((HUGS))) Keep us posted on the biopsy. I like your attitude (not letting a .5mm spot dictate your life).
kmmd - woohoo! Glad to hear about the clear scans!
Renrel - "that everything changes and that to try to hold on the the present will be a source of suffering. Good health and bad health will both pass with time. The people we love and those we dislike will pass through this life and on to what comes next. All we have is the acutally experience of the present moment. We can take all that it has to offer, or we can waste it in an unproductive comparasion to the past that is no more or the future that we are only imagining." I love this, how true and profound.
Had my 2 year cancerversary yesterday and to be honest I didn't really even think about it much, I wasn't emotional at all, I think I was happy. I had a great Nov 3rd this year. We had an annual meeting for our department (150 staff) and I won an award for office comedian, we had these silly awards for strange things, mine was the 'you really could quit your day job award'. I work in healthcare and apparently nobody is funny for them to vote for me, if I'm the funniest person in the office.....we're in trouble lol. For my prize, I won a Slap Chop and a Graty - like on the commercials - zucchini, martini, bikini. Anyway, it was a much better day than it was 2 years ago!!!
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momand2kids - remember that i work in boston and live not far out if you need something. IMGH was my home away from home during treatment and beyond. If you haven't been already definately check out the resource room and the healing garden on the 8th floor of Yawkey. If you are there around 11 I believe my favorite gentle yoga class will be going on. If you pop in say hello for me. And there are some really tasty sandwichs in the cafeon the first floor. I love the bean burritto.
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Thanks
I am drafting my list of questions for the surgeon..... gearing up the voice recorder, getting the kids' stuff ready for the am-we have not said anything to them yet--no point...... they will know when they have to know......
I never got to see the healing garden when I was at MGH because I only had my surgery there and was treated at the Farber.... I will check it out tomorrow.... maybe I will see the yoga class!
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I did indeed see the healing garden today-- it looks great Renrel....
Surgeon does not think this is cancer, but is going to do an excisional biopsy and pathology. I have such respect for her skills and opinions that I just felt so much relief at her assessment.
Should be having it done in the next couple of weeks.
thanks for all the good thoughts.
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Let me know when you are back at the hospital and maybe we can meet up for lunch or something. I have not been able to stop by there for a class or anything in ages.
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momand2kids, keep us posted, we'll be thinking of you.
Had the nicest "night in" with DH last night. Just sat and talked and reflected on the year and how we want to work on getting back to a little more balance and normal next year. Just very sweet and romantic. I do love that man.
The scans being clear was a relief, but, still left with a lot of chest and shoulder pain. We think its the lymphedema acting up. So, back to LE therapy for me. I'm also increasing the accupuncture appts. Hope this gets better soon
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Momand2kids--thinking of you. I'm glad your surgeon thinks it's nothing, but will put your worries to rest with the biopsy. I had calcifications and a biopsy on my "good" breast 2 years before my ca diag. It was nothing, and is still fine.
kmmd--Great news!! I just got approved for a tighter sleeve and more massage. I've been bad about doing self-message, and I can see it. Also, while swimming has helped my neck pain, my underarm pain is worse. Onc. just said to take Advil, but then I read that isn't good for LE.
Had my 3 month onc visit last Thurs., which was frustrating because I had to wait for 1.5 hours, and almost was ready to leave for a meeting when she walked in. She had a patient with issues, and while I appreciate her taking the time with patients who need her, I felt at least someone should have alerted me to the wait. Oh well--didn't have time for questions. I guess I'm fine--at least the bloodwork seemed ok, although my tumor marker when up a bit (my support group leader said not to worry about the small rise). So, I'll breathe easier for 3 more months.
Happy weekend!
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Two years ago this Thursday I had my bilat. I thought I would feel good about that, two years cancer free, but I am feeling all on edge. Maybe cause my boss was transfered to another position and now they are changing all sorts of little things which make everything feel different, plus I have a backlog I could drown in. And I found out today that an agent who used to appear before me died over last week from pancreatic cancer. He only found out about a year ago and we not that old. I would guess in his 50's or 60's.
But I am off on Thursday for the Veterns day and took off Friday to make a long weekend. The downstairs is company clean since we took part in a progressive dinner this past weekend. Wednsday we are going out to see a play if we can find a babysitter and Sunday I am doing my 3rd level of Reiki. I just wish I could show a little will power and stop eatting halloween candy and other junk. My sweet tooth is getting the best of me.
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Well, I managed to figure out how to hook up a web camera and am now using Skype. I have talked to my daughter. I am pretty proud and am amazed I figured out how to download all the stuff for Skype. I am not the most savy when it comes to utilizing computer technology.
Ug, ate too much today- so much for trying to lose the tamoxifen weight! Sigh.
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Jess, that post chemo tamoxifen weight has been a discussion in my household a lot the last few days. Getting some help for the neuropathy so I can move more, and, getting off of the gabapentin has helped. The hot flashes are miserable but the scale and mirror were worse
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Speaking of weight......I have the extra Tamoxifen weight as well. I joined Weight Watchers 2 weeks ago and have lost 7 lbs. I don't have very much to lose, maybe 15 total, so I'm halfway there. I am 5'2 and started at 141 lbs and now 134 lbs. I'd like to get down to 125 but even 130 would be great. I haven't been doing too much for exercise, basically just following the WW points system and eating better/less. I have joined a gym that has a running track so I go there and walk for an hour about 2 to 3 times a week at my own pace and it's nice.
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On my way tomorrow to Ann Arbor to take dd to U of Penn to speak at a Model UN conference. This is all so cool. I decided to take the day off, and it isn't because of the F-ING cancer!!! Ha !!! Then in about a month or so , she is off to Harvard- gets to speak there as well. Isn't that the coolest of cool? I do hope this will yield fruition for her when she is out and about on her own. I am as excited as can be. I feel like I am playing hookie (sp?) for senior skp day or something!
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Jess, you have to post back and tell us how the day went. Yay for DD, that is so cool, you must be busting out with pride! Hope playing hooky was awesome. Will be thinking of you.
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