April 2011 chemo
Comments
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PSU222 Tatooing? What is that all about? I didn't realize they do that before rads.. Eeekkkkk!
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Tats are so tiny they are no big deal. They help to line you up right each time you come in. They use a laser to point at the tats to know you are in the right position. Mine look like someone just dotted me lightly with an ink pen.
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Hi everyone, was on the thrown all day today, 2 more to go yippeeeee......
I want you all to know even if I don't make a lot of comments, I pray for all my sisters her and all the needs. My heart feels heavy with all thay you are all dealing with. Just know you are always in my heartm thoughts and prayers.
hugs to you all.....
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Windlass, babe, been wondering where you are! I'm so sorry to hear about the nodes. I've got a new round of chemo after surgery to look forward to, and I know what you mean. I was like, arrrgh...don't want to join a new group, but everyone here will be done. But then,you gals are friends, and I know you'll support me through it even if you're all done and watching your hair grow back!
So, what are they saying now? Has your treatment plan changed? Damn...just realized there's another page after this one. Must have missed some posts. Maybe you've explained there. Hang in there, kiddo. I whined earlier this week about where I'm at, whining is so totally allowed here...hell, even supported. So, go for it.
Thinking of you tonight.
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Windlass - we won't abandon you. We will rejoice along with you in every chemo you knock back. I can definitely relate to the painted picture you gave us. There will always be people who have it better or easier than us but there also will be others who have it worse. This is our challenge in life to find our joy no matter where we are at in the scale. I thank you for being so honest with us because that's what we are here for. to tell it like it is. I ditto Merliee's questions.
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Who in the group is having surgery in this September? Tomorrow I get my surgical date (I hope while meeting with my surgeon). thanks
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Windlass - whining is okay and often a necessity! When I apologize to people for whining they say they dont hear it as whining. Let's call it sharing! We want you to share - that's why we are all here together!!!
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I think my surgery will be in August. I'm waiting for them to get back to me about the date. Crazy! I finally decided to do the BMX.
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Hi gang
For those of you having surgery let me say that when I had mine it was really a breeze. I was very scared however going in. I had a BMX and no regrets there. I was surprised at how easy the recovery was. I was up out of bed the next day.
Windlass- I will never take for granted that I am a stage one. I have heard the words, "it's cancer" 3 times now in 2 1/2 years and every time I have been very lucky to find it early. Even though I HATE cancer, I count my blessing everyday. People often look at me funny when I tell them I am a very lucky lady.
It has changed my life is countless ways. It has made me really think hard about what I want to do from this point on. Time becomes precious and I don't want to live unhappy in anyway. So I have to make some changes, and one of them will be in the type of work I do. I am planning on finding something low pressure and low stress for example. I have forgiven people that I never thought I would and am trying to live a life surrounded by loving and uplifting people. I take nothing for granted these days. Any of us could be hit by a bus or any other thing. We just never know what could happen so we must make the most of, an appreciate everyday we have no matter who we are or what our bodies are going through.
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Hi, Merilee. I'm getting treatment in Boston, and I'll be done in October 2012. (Not this October, but next.)
I've looked at everyone's stats in our group, and of all the Stage III women on this thread, I believe I am the only one who is HER2+. (Please let me know if I'm not and if I overlooked someone.)
Combining Stage III with HER2 accounts for the disparity. I get one additional year of treatments for the HER2, and I get an extra two months of really nasty chemo (taxotere) - on top of the two months of really nasty chemo (A/C) I just got - because of the lymph nodes. Plus I get 33 days of radiation, again due to those lymph nodes.
I should be grateful the cancer stopped where it did - and believe me, I am!
Finally, all of this would be way easier to bear if I had good, consistent support at home. The support I have is sporadic, erratic, chaotic, and unpredictable, with love and kindness one month, and cold indifference the next.
Does anyone else out there suspect their primary relationship may have given them cancer? Or at least contributed to it? Nearly every book I've read on the mind-body connection links cancer to stress and life events, and breast cancer appears to have a particularly strong emotional component -- especially if it's the left breast, right over the heart. That's where our love relationships reside, and constant conflict and trauma there may be linked to breast cancer. (I know, that's a long and controversial topic in its own right.)
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p.s. And thanks for all the kind words, ladies! I hadn't seen there was a whole page of comments before I wrote the post above.
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I know mine was relationship/stress related. My marriage would rival a nasty soap opera.
Most of us that are er/pr will also be in treatment for 5 years with meds to zap our hormones. Those meds do not sound like much fun with the side effects either so I think we are all in the same boat as far as facing that breast cancer is a chronic ongoing thing. I hate it too and if I let myself, I can fall into the black whole of despair. I see a therapist and that helps but I have also found some new friends too. One of which has ovarian cancer stage 4. I think we help each other in a way that only another survivor/warrior can. I wonder if there is a local support group you could peak into and see how it feels.
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Windlass, I'm hoping this group won't peter out when we are all thru with out treatments! I still have 4 chemos to go. My blood counts were bad this time around too after 4th A/C. I was never diagnosed with Stage IV but probably pretty damn close and I won't be surprised if it pops up somewhere else. I hope I never have to go thru this damn chemo again. I don't know if I could do it again.
I just posted my first message in Radiation but I haven't joined a group there because I don't know when I'm going to that. I'm scared of the tattoos. I understand they are very tiny however and don't hurt much. I'm going to send you a PM
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Profbee: I am hoping I feel good enough to go see the Harry Potter Finale!!!!!!!!
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Artiecat: I can't WAIT, but I am going to. I don't want to fight the crowds and get sick. So, I'm going to wait for it to be out for a while and try to sneak out with hubby during the day someday.
I will cry like a baby though!
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How do you put info into your diagnosis box? I don't see the option when I am editing my profile!
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Linda:
* Click the black "MY HOME" tab at the top.
* Click the maroon "Edit my Diagnosis" box to change the diagnosis.
* Click the maroon "Edit my Profile" box to modify the signature at the bottom of your posts
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geocachelin**
Please don't be afraid of the tatooing. It's only little dots. That wasn't bad, I promise. Today was positioning and markings and that takes some time and patience. After that was done they proceeded with my first zap. I should have taken an Ativan before hand, only because the table was hard and you stay on it way too long.
Hoping all you ladies have a wonderful weekend.
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Windlass - so sorry to hear, and ditto that this is the safe place to whine. We're all scared and freaked and whiny at many points on this stupid, horrid journey. Your honesty was a reminder that some of us can count our blessings and pass some of them forward.
Edited: my next post is deleted cuz it was a duplicate. -
Windlass - so sorry to hear, and ditto that this is the safe place to whine. We're all scared and freaked and whiny at many points on this stupid, horrid journey. Your honesty was a reminder that some of us can count our blessings and pass some of them forward.
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Hi Ladies,
Windlass - I am at stage IV Grade 3 IDC with mets to lungs dx at the same time as primary back in Feb 2011 in my rhbreast with lymph node involvment it has spread to my lungs but I am very positive at the moment cause the chemo is working and making it all shrink everywhere which is good news. I am also HER2+ and have been told I will probably be on herceptin forever, you are not alone in this and on this thread, sending you support and hugs xxxx P.S. thanks for the info on the japanese mushroom, will be getting some of that if I can, I am in england, what brand name did you buy yours from windlass??x
RangerMom- I get my surgery in September mx with lymph node clearance I am nervous but also impatient to get rid of the mother tumour. x
Merilee - I think my cancer was to do with stress/depression/worry not relationship stuff but just life stuff, no job been going to interviews and applying for 3 years now and no luck, then the depression kicked in to add to the stress and just when I thought I'd change my life completely and finally give in to the biological clock and have a baby then this cancer comes into my life and now that seems like a far away impossible dream. Its amazing how much can change in such a short space of time.
Living for the moment is important part of my philosophy now and I agree with you Merilee we must all live as happy a life as possible I am going to make my life better, I am making plans to move nearer my family and friends back in somerset so I can get more emotional support, to get a puppy something I have long wanted, I also have 2 cats which I adore, and to be as actively creative as possible (being an artist/illustrator/designer you have to wear many many hats as a creative person).
Getting through this is sooooo tough we are all so very brave and strong who said that the female was the weaker sex? absolute rubbish eh ladies! Chemo making me heat up so bad I have too stick my head into the freezer to cool off, also really red in the face which is probably the steroids making me look like a moon face and bright red just to add insult to injury.
This made me laugh hope it cheers you all up, my friends sister has the same dx as me which is crazy eh!! she's a couple of years down the line and said "God must be a man cause all the hair on my body had disappeared except for the bikini line" LOL so true so very true.
Sending luv and light to all to guide us all through our darker times.
Sarah Sweety xxxx
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Windlass -- As many have said, don't ever think of it as whining or complaining -- you're sharing your thoughts, and this is the place to do because we are all in the "same boat" more or less. Our diagnoses may be a little different -- some better than others -- but we all have to deal with the same crap, same emotional issues, side effects.....the same awful journey. I finished my 3 months of A/C about a month ago. Had to wait to start Taxotere for a month because of getting sick and ending up in hospital. Just started my 12 weeks of Taxotere on Wednesday -- so far, no side effects. I've been told it's much milder and easier to take than the A/C. We'll see. Then I'll have to wait about a month before starting 6 weeks of radiation. And then the 5 years of whatever. I still dread it all. As Merilee, Sarahsweety and others have said -- it's important to try to live as happy a life as possible and surround yourself with positive people and stories with happy endings. It's not always easy, though. I try my best to stay positive and upbeat, but sometimes I just find myself in that "hole" of despair and have to work hard to get the hell out of it. Anyway, as always, I'm thinking of you all as we go through this together. To me, it is just so comforting to be in the same boat with so many "determined warriors," although I wish we were together for OTHER reasons, and not this.
On another note, I am truly hoping that the rain and clouds disappear this morning for the very last shuttle launch. It's not looking too promising, but we can hope. We are right across the river from the launch pad, and the view will be spectacular on a clear day. Go Atlantis!
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***Had this post queued up last night and feel asleep*** So need to go back and read all the new posts since then...we've been busy over here!
Folks, I know everyone is having their own litany of challenges. But please if for one second , could you just shout one glorious HUZZAH!!! and share my joy at the fact that they accessed my port on the first try?? One stick and they were in! You gals know my port has been H-E-double hockey sticks. So this was just one glorious break. Maybe I soaked up some of the sunshine Merilee shared. Taxol number one is done!
Windlass, I think you did such a good job expressing your fears and frustration without being hurtful to anyone else. That's a gift, friend. Especially in fora like these where emotions of all kinds run high. This should be one of your safe places. I'm glad you came back and posted. Just to share with you that these feeling of disparity in dx can go both ways. I have a dear friend who was dx with Stage 4. Survival rates beyond 2 years is very low. I got dxed three weeks after her with Stage 2. And I'm lost how to be there for her (emotionally/phone/cards/etc.) since she lives cross county which makes me pull away sometimes. And similarly, she can't fathom that at the end of this year, this will be pretty much behind me and the boys. While she is thinking about how to make memories for her 4 and 2 year old. That makes her pull away sometimes. When the answer for the both of is is to be kind, considerate, and generous to each other. At least I think that is the answer. So what a long winded why to say that you should be able to depend on us to be knd and generous to you...when you are low or when you are high. This is a soft landing place. I hope you remember that.
Rangermom, you are a shining example of listening to your body. We all try, and I know I do an awful lot of sweeping under the mat. So I appeicate the reminder to listent to my body...even though I don't really trust it right now.
Pawprint: what about "Warrior Walker Women" or "Lounging for Life" or ..."We are women, Hear us Rawr" or "Won't Work for Food, Will Walk for a Cure" as possible team names for your 5K.
Articat - one more to go. Glad the benadryl was able to get things undercontrol quickly.
SCC - Yay for a good infusion. I get really pissed waiting for doctors too. But I'm trying something out lately, especially for the doctors I really like and who take as much time with me as I need. I remind my self that at the beginning of this journey (and even still now) when I have questions, he takes his time, I never feel like his hand is on the door knob. I imagine that while I'm waiting that he is in the exam room with another woman like me, who just found this out and he is giving her the time and undivided attention that he gave me, and how important that is to her. It calms me down a bit.
Sudz - hang tough, Merilee has provided the sunshine. I'll provide some chocolates:
Scrumptious Chocolate Truffles that I imagine would increase platlets!
I hope everyone in hanging in there and getting ready for the weekend!
Much love and peace to you all.
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Thanks for the universal chocolate cure Carla!
I think this is going to be a good weekend for me. A little work Saturday afternoon, but no other plans. Last weeks 4th. of July marathon was crazy..I'm going to try and lay low this weekend.
Articat~ I love Burlington..your daughter is lucky to live around there. I'm in Southern VT in the Londonerry/Manchester area.
Sending you all the best for this weekend. Feel good~have clarity~count your blessings.
Sue
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Guilt free truffle recipe:
1/2 cup organic cocoa powder
1/2 cup organic almond butter
1/4 organic agave
stir to form a dough, make into bite size balls and refrigerate
You can add nuts, coconut , or anything you like just before you make the balls or you can top each one with a nut and flatten it.
Enjoy
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Merilee...1/4 cup of agave syrup?
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I'm going to make a batch of these when I get home Merilee...sounds so good.
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Thanks for the chocolates, Carla, and for the nice comment. And thanks for the Truffle recipe, Merilee. One word of caution, however - you might want to do a bit of research before eating a lot of agave syrup. I've read it has a higher ratio of fructose to glucose than even high fructose corn syrup (HFCS), so it may not be all that healthy. You might want to try the recipe with honey.
Sarah: I am so sorry that you learned with your diagnosis that the cancer had gone to your lungs. I have said a prayer for God to use the chemo to totally wipe it out!
Suzy: How fun to watch the shuttle! Sending hopes for sunshine and joy your way today.
Jacki: Sending blessings to you.
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I am wishing for the trufffles - but chocolate tastes horrible to me!!!! Soon, though, very soon!
Profbee - you are right about seeing HP7 in a crowd...I will be careful too!!!!
Cheers to all - I am off for the neulasta this morning! The benadryl buzz is almost worn off, so I am feeling a little steadier this morning.
Onward and upward warrior women!!!
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CarlaB -- Thanks so much for the advice on how to deal with the long waits. That really helped. And he never does make me feel rushed. And he always has me laughing by the time the visit is over. I'm going to heed your advice and not get annoyed by the wait anymore.
Truffles sound yummy, guys! Might have to try those!
Watched a successful launch of the space shuttle Atlantis -- beautiful! But so sad it's the end of the shuttle program. We've been so lucky to have lived on the Space Coast for 24 years. We've seen lots of launches, and they never get old. This one really brought some serious tears to my eyes, though -- because it's the end of an era.
I can't figure out how to insert an image or I would put a picture of the launch here.
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