May 2010 Chemo
Comments
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Had my PET scan yesterday (fri). I meet with onc on Monday to find out the results. I'm trying not to worry, but the thought of the cancer still being there or having spread would be such a nightmare at this point. I started all of this back in december and I'm just about at the end of what I can take. I still haven't done my last tx. I called last Monday and told them I couldn't physically even come in so I wasn't doing it. Onc said having a week off would be good, but I want to be done damnit. The thought of having one more tx makes me want to just crawl in a hole.
I just all of a sudden stopped wearing head wraps. Its weird because I was so embarrassed and wouldn't even do it around bf. I just hit this, I don't give a #@**. Its hot and I don't care. I've went shopping and everything. I just don't care.
makes me laugh.Today was nice. Bf's parents bought this castle playhouse and slide deal so we sat outside and watched the little guy play. Yesterday was a nightmare. Bf had the flu and there was nobody around to help with the baby so I did my best to watch him. I thought I was gonna die. I've been nearly bedridden for several weeks, only a few days being up and about.
I'm still working on eating healthy. I feel like I know what smokers feel like. I had a dq blizzard in town yesterday while thinking how the sugar could be fueling my cancer. But I couldn't stop myself. I juiced a bunch of vegetables when I got home, but still.
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Hi Paxton! Why do they do those scans on Fridays.... ugh, don't they know that it is awful to wait! Good on you for being comfortable to go commando! It is very hot covering our heads! Good for you on your healthy eating too... and I wouldn't worry about having a little ice cream! I know what you mean about treatment... I have to go Tuesday... and I am dreading it, but I just want this over too! I hope you BF feels better soon! ((HUGS))
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Hi Ladies,
Sorry to disappoint you, but I won't be able to make it to NJ for your party. I start rads on Monday and go to 10/5. On top of that my DH is going away for 3 weeks during September. I am dreading that. I put out a call to arms message on my blog and have several people who are offering to help as well as my sister-in-law possibly flying in.
This week I had to arrange for my kids to be picked up every day from school because the time of the rads is too close to the time they get out of school and over an hour away. Fortunately several friends have stepped up.
I am 7 weeks past my chemo and still having effects. Some trouble breathing, voice still not back to normal, often itchy skin, water retention. That doesn't even take in to account the hot flashes and the fact that I can not fit into any of my pants! Man, I'm a mess in a satin dress.
I see my GP Monday to discuss the breathing thing. Onc says it can't be from the chemo, because chemo was so long ago. But I didn't have it before the chemo, so WTF?
Oh well, enjoy your weekends. Hubby and I got to have a few hours without the kids to celebrate our 10th wedding anniversary today (16 yrs together but only married 10. I had to threaten him to get him down the aisle! Maybe that's why he prefers to celebrate the anniversary of the day we met).
Jen
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Packjen This is our anniversary too..28 years married going on 29
paxton I haven't had craving for sugar..not so much ...but love the salt..but the ONC got me getting a vanilla shake after my 7day blood test, she told me to stop and get one after I complained about the yucky tongue. It was sure good and felt great on my tongue..but milk does it too..but shake is frozen and feels better..
This is day 2 and I'm still hyper from the steroids. going to take a sleeping pill tonight, didnt get much sleep last night and really getting slap happy with no sleep ..
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Sacphotomom ~ post a pic of Brandy sometime - would love to see her. And happy anniversary! I bet you keep DH laughing - love your sense of humor. Leanna ~ so nice to hear you enjoyed 5 Guys. Sorry the SE of the AC are so brutal. You mentioned your webpage - are you on CaringBridge? Irishtess ~ congrats on your final tx!!! How are you holding up emotionally? Day ~ wonderful wonderful news re: nodes! I'm so happy for you
. Kim ~ DO IT! Are you shaving stubs since you're sporting the bald look or are you just going to let them come in as they are? I wish it would all come in at once - vs. patches here and there. Patricia ~ glad you got some anti-depressants. I just returned to my therapist - so helpful! Kudos for continuing to walk - don't know how you do it! You're so right that this is exhausting mentally as well. I think that's why I want to drink alcohol so often because it gives me a break. I'm working on changing that - not a healthy escape. Paris sounds wonderful! Drim ~ 3 wks already? Btw, why am I not surprised you went to bed after working 50 hrs.?! I hope you're giving your body some time to rest and recover. Are you still experiencing any SE from chemo? Hope not! Paxton ~ hoping and praying for a good report. I bet you feel liberated taking off the headwraps! My head has been sweating like it's nobody's business! Jen ~ 7 wks and still SE? SO sorry to hear that! I feel your pain about the weight gain - I'm shocked by how much I've put on. Hope the docs can figure out the breathing issues. Happy anniversary to you! How did you celebrate? Wellsey ~ you hanging in there? Summer ~ are you hanging in there? I better try your biscotini before I start my liver cleanse (after last tx). It seems we have quite a few martini girls in our group.I just discovered that my family designed t-shirts for my last chemo day. They have pink boxing gloves on the back with my name on them - along with the final chemo date 9-02-10 (just like the show that used to be on). It's nice to be on this end of this part of the journey. Think about all the women logging on to BCO for their first time right now. If anyone ever has free time, it might be worth jumping in on one of the newer groups with a word of encouragement. Remember how scary and overwhelming it was at first? Off to "try" to get some sleep... Hugs to each of you!
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Daiva,
We went to a little town on the coast called Bolinas. Funky, little hippy town sort of like our own town but smaller and by the water. We had lunch and went and sat on the beach and watched the tide come in through the channel between 2 beaches. The water was soaring in and several sea lions were riding the surf. Watched the surfers and the boogie boarders. Mostly soaked in the sun (though I was covered from head to toe) and enjoyed the negative ions of the water and calming effect of the waves.
Jen
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Is it too late for me to join your group? It looks like most of you have been trudging through this together for months already... I just tripped across you today... wish I'd found you months ago!!
At any rate, just quick introduction... I'm Stacey. 42 years old, wife to a retired Marine and Mom to 10 yo son. We live in the Pacific Northwest where I'm a software analyst for a local healthcare system.
I was DX'd March 16th 2010 with Invasive Carcinoma with Ductal and Lobular features (IDC), 1.7 cm, Stage IIa, Grade 3, 3/36 nodes (two of the nodes were sentinal nodes the third was a "regular" node and showed only isolated tumor cells), ER (4+) / PR (1+) / HER2 (3+).
I opted for a bilateral mastectomy.... even though the surgeon tried to convince me to just do a lumpectomy, I just couldn't face doing this again, and wanted a nice even reconstruction later. I haven't begun any reconstruction because the Military doesn't recommend any until 6 months after radiation and they did my surgery...
I've just finished my last (6 of 6) rounds of TCH (since I've heard that there are several "versions" of TC, mine was the standard Taxotere (aka Docetaxel) and Carboplatin) and Herceptin). I'll continue of course to receive Herceptin (every three weeks) for a year.
Two weeks from now I'm having a full hysterectomy as I have history of ovarian cysts and heavy bleeding, so my Oncologist believes getting it all out - reducing my Estrogen levels... good thing.
Then, immediately following I'll begin radiation (28 treatments).
This last round kicked my butt and I'm really struggling to climb back out of the terrible fatigue! Exhaustion and dizziness. Had some terrible acne issues this round. The "usual" stuff as well, gastro issues (I had controlled IBS before cancer which Taxotere irritated beyond belief), neuropathy in hands and feet, never ending runny nose, oh and did I say exhaustion?
I'm so relieved that this part of my treatment is over but now this week started returning to the "what if it comes back" thoughts... Digging through statistics, blah, blah... that's how I ended up here!
At any rate, It's good to "meet" you all - and I'm sorry if I'm jumping in here really late, but hope that you're open to another?
Praying you are all doing well -
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Hi May Friends My sister visited me this weekend and has just gone home. I have kept up with you all by email on my phone, but my achey pain has kept me off the computer. I am also developing my first signs of numbness in my feet and hands, and my digestive issues are back. Joy Joy!!!
Stacey - you are welcome here. Thanks for catching us up on your treatment, etc. I am so glad you found us. We are a great group of women and you will find a lot of support here.
Leanna You are so awesome! I think your friends are missing such a wonderful opportunity to spend time with you and support you. My friends are older, and better understand chronic pain and illness. When we are younger, we just have no idea what this kind of treatment is like. I know my adult children are that way. I just think that they have a hard time seeing me struggle, and it is easier for them to go on with their "life" as usual. Part of me is happy they do not know the details. Anyway, thanks for all your hugs and support. I am sending you love and energy for your next treatment.
Sacphotomom I laughed till I cried when I read your Freudian slip of BS instead of BC. You are so much fun. I always Christmas shop on my trips too, and I have nothing this year, so I do know what you mean about feeling behind. I hate the malls and crowds. I like to get small gifts from museum shops, galleries, etc. Also, I love the salt too! I just do not dare have anything in the house that is a salty treat.
Pacjen Your anniversary celebration sounds beautiful.Congratulations to you and sacphotomom on your anniversaries.
Daiva How neat about the t-shirts. It is exciting that you are getting so close to the last chemo. I am so happy for everyone who is finishing and I pray that each of you You are right about this journey, and how we have all come a long way. Thanks for the reminder to check in with some of the newer groups. You are a wise woman!
Paxton I am sorry you have to wait on test results. I think that is the hardest part for me. I am praying for everything to be clear, and I wish you could just be finished with chemo. About eating healthy, it is a process of making better choices and there is nothing wrong with an occasional sweet. I find most things are too sweet, and only a taste is enough for me. You have been doing great to make the changes in your diet and you will continue to do well. I am so proud of you for getting rid of the head gear. It is a pain. My sister said I looked like the first queen elizabeth due to no eyelashes and eyebrows. She said I looked regal. I think I look like an alien. Ha.
Drim did you feel okay on your trip to PR? I have felt so bad this week that I hope I am not being overly optimistic about going to Paris in October. I think I just feel so weak because of my hemoglobin. I hope I bounce back after the transfusion. How are the rads going?
Irishtess Your trip to Ireland sounds great. I love to read your posts. You are so thoughtful
Day Thanks for sharing your art with us. You are awesome. I miss your folk wisdom and hope you will be writing more soon. Can't wait to see pictures of your hair. I have felt too bad to worry about mine. Nothing seems to be happening on my head or elsewhere. It is nice not to shave my legs or pull chin hair!
KIm I hope work is going okay and the heat is not to bad for you. I look forward to your humor and miss you.
Hugs and prayers for everyone of you, and anyone I missed. I pray for all of us daily, that we will heal and bring more love and wisdom to those we touch along the way.I know you all have done that for me. Patricia
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Here I am writing after a blah week and a very full week-end.
So, last week was very unproductive for me. the routine was like this: wake up, eat something, take pills, have some coffee (with a cigarette of course, yes I am a smoker and didn't quit through all this). Then do the exercises prescribed to avoid lymphedema. Big pain. Take Percocet. Snooze from Percocet. Rinse and repeat.
My pain is getting better in a way and worse in another way. The pain from the surgery itself has subsided. But now I have pain on the exact line cording is forming. And it seems to get worse every day. I can't stretch my arm without pain or lift my arm above shoulder level without pain.
I had my friends over Saturday, and we stayed up late - they left close to 2 am. Considering they usually come over around 3:30 pm, you can image what a good time we usually have. Also, it was cooler Saturday, so we could be out in the backyard, instead of stuck in the house because of the heat. That afternoon I gave up on Percocet in favor of beer. *wide grin*
Then Sunday I had one of them coming over to work on polymer clay sculptures (she is an artist too, but never tried it, and wanted to learn) so we had fun on that too. No, I still didn't tackle my humongous and totally messy computer desk to find the cable - to be honest, mostly because of the arm pain, because I keep forgetting how much it hurts and I reach for stuff and then I have to stop for a few minutes to catch my breath from the shooting pain.
That is also the reason I couldn't use my hair-re-growth potion. Well, that and the fact that I still have the bandages and the drain - I wouldn't want to rinse something made of alcohol and garlic right over the incision, at least not at this point. I should be able to start using it by the end of next week.
My schedule is all busy, as I said, until the surgery I will have on the 22nd of September. I am trying real hard to make more stuff to sell at the fair. I definitely need to find my cable for the camera as I will NEED to upload som e of the stuff I've made so it can be shown.
Also, my bone density scan results came back - osteopenia in the hips; and the endocrinologist ordered a Vit. D level test done - and it came back quite low, at 18 only, when it's supposed to be in the 30's. So now I am on extra Vit. D - 50,000 U.I. a week and more cheese in my diet. With all the chemo flashes and me not being able to be outside in a smoldering heat - no wonder my Vit. D levels plummeted.
I cant' believe how much has been going on here! I wish I could go fishing with all of you, I so miss fishing, I couldnt' go this year at all. My boyfriend had promised me that if I get recovered enough in October we'll go then.
I will not even try to address each and every one of you, as I know I will miss someone. But I wish I could be near each of you to give you hugs, for your bravery through all this. For all your kind hearts, for all your suffering, for all the tears, for all the sleepless nights, for all the worries, I wish I could have a magic wand and erase everything so you can be healthy, smiling and happy again.
Hugs all
Day
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Hi Ladies! Yep, I finished chemo on Friday! Went shopping on Sat with my sisters. Later, Mom, sibs & spouses went to dinner & then back to my sister Margi's house. Mom entertained us with a wild story about the night before my sister, Judy, was born (her birthday was Sun so we were celebrating that as well). Oddly, I didn't ~ & still don't ~ feel as excited as I had expected about finishing. Anyone else have that reaction? I'll probably be a lot happier in 2 weeks when I don't have to drive to NYC for an appearance at the chemo lounge!
Day: So sorry you're having such a hard time, esp with the cording & the lymphedema. Your ability to put that all aside to help a fellow artist is inspiring.
Drim: Wow, it's hard to believe you're so far into the rads regimen! Hope you don't overdo it at work.
Kim: I triple dog dare you! Thanks for the website info ~ I'm going to check it out!
Leanna: Kim is right ~ hang in there! AC is really tough, but you're almost done. Pretty respectable showing at the bowling alley ~ sounds like a lot of fun!
njbhwgirl: Thanks ~ I did enjoy my wkend! Speaking of which, what dates do you have in my mind for our visit? Please let us know what we can bring.
Packjen: Sorry to hear about the ongoing SEs ~ hope you get some answers. Happy Anniversary!
Patricia: Glad you had some time with your sister, but sorry to hear about the numbness starting up. It's no fun! I think you're right about the transfusion making you feel better. I will pray that you are in tip-top shape for your Paris trip.
Paxton: Your pain and frustration are palpable. I hope you get good news today.
Sacphoto: Isn't it great when you hear about survivors, & doubly great when they and their family reach out to you? Happy Anniversary!
Summer: We didn't make the biscotti martinis this time, but decided we'll try them next time we're together. I forget ~ when do you start rads? I see the rad oncologist this Fri & hope to get started soon.
x-ray: Your family sounds awesome ~ love the T shirts! What a wonderful suggestion about reaching out to new members here. It's so easy to forget how scared & isolated we all felt. I'm so looking forward to meeting you and some of the other ladies from our group!
usmcwife: Welcome, Stacey! I had a bmx in April. Sloan-Kettering docs also want a 6-month post-rads waiting period before seeing the PS for recon. I developed neuropathy in my hands & feet from the Taxol, so I know what you're going through. Ditto on the runny nose!
Everyone else: Hope you're ok & continuing to improve. Here's to a good week for all!
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A week after T/C #5 and I am still dragging. I did pretty good through the first four, but this one seemed to him me like a Mack truck. Stomach issues, indigestion, fatigue, severe aches--it just didn't seem to want to go away. Now I am dreading #6 since the last one was so bad.
I am starting to get a growth of fuzz on my head. Is that really hair while I am still in treatment or is it just an attempt at hair that will fall out after the last chemo?
I saw an ad for Rapidlash. Anyone try it?
Day I hope you are recovering well from your surgery. I saw your faries and trolls. You are amazing.
Packjen & Sacphotomom Congrats on your anniversaries. We just celebrated our 40th.
Paxton I can't imagine going through this with a litlle one.
Drim Congrats on finishing chemo and forging ahead and keeping us all informed.
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usmcwife- it's never too late to join our little group. We are always happy to have another, even if it means you had to have cancer to join. I too chose bilat mx for the same reasons you did. I have tissue expanders and will finish reconstruction sometime after rads.
I started rads today 1/25 done. I am using Emu Oil on my breasts and also rubbing a little on my stubby hair as I heard it helped it grow.
wellsey - my hair started growing back sometime before my 4th TC (I only had 4) and didn't fall out again. I now have a dark fuzz all over my head. Sort of blackish with grey. I used to be reddish brown. It has been 7 weeks since my last TC and the hair seems to be fairly aggressively coming in. Also had to shave my legs and underarms and pluck a chin hair today. Boo.
Jen
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Hi All! Sorry I've been bad about posting. I've been keeping up on my cell phone, but can't post from there. Work has been crazy and my BF got a new job. It's his dream job, so that is great, but his commute is about an hour one way on a good day (and in MI we don't get those most of the year!) and he's been logging 12 hours day, so we've been a little stressed. He is going to rent a little flat to stay at during the week so he doesn't have to drive so much while we try to figure out where to live long term. It's temporary, but I miss him
I have finished 21 of 33 rads and so far, so good! I would say use the lotion and be generous! So far I have not had any skin issues, but I slather that stuff on at least 3 times a day. I feel so bad for those of you who will have to drive so far for rads 9summer, LibraryJen, etc). It's so quick; you will be spending so much more time in the car than is rads. Wish you could find closer places. I also started tamoxifen about the same time I started rads. So far, it's not been too bad. Definitely has made the hot flashes more often and a little hotter, but that's about it. Had some plumbing issues at first, but those worked themselves out after a day or so. Overall, I don't notice being on Tamoxifen which is a relief since its for 5 years!
Day- hope you are feeling better and the pain is subsiding. I had a lumpectomy and SND and the SND was the worst part for me. Felt like a had a tennis ball under my arm for a while.
Paxton, patricia, wellsey, leanna- Hang in there! I really hope you feel better soon. Each of you is usually so positive and uplifting for the rest of us, its hard to see you feeling down. I hope things get better soon. Like the others, wish I lived close enough to help you out! Sending you ((hugs))
Packjen I had to pluck chin hairs today, too! Boo! Funny thing, my eyebrows are still kind of thin, but there are all kinds of out of place hairs up there. Definitely need some tweeing/plucking, but they are still thin so I hate to do it!
Irishtess and Patricia, your trips sound great! I know someone else is going to Vietnam in Jan, was that njwbhgirl? I can't remember and I can't o back or I'll lose my post...anyway, you girls have the right idea! i could really ue a vacation and need to seriously think about one. But with the BF's new job, not sure he'll be able to get away anytime soon. maybe I can join you all on the Coast in Sept? Let me know what weekend and if I can swing it, I will! Martinis, the beach and a group of May warriors sounds great to me!
Drim - glad to see rads is ging well for you, too. Hope the tamoxifen goes wel, too. I did not know there is a test on the effectiveness, I'll have to ask about that next visit.
One more thing, on the chemo weight gain. I ended up gaining about 12lbs.
My rads doc said people tend to lose weight on rads, so that made me happy! Then I told her I had started tamoxifen and she said "oh that can make it harder to lose the weight" Boo! But, surprisingly, without even really trying, I am losing weight, slowly but surely. My rad onc actually asked me last weekif I was eating or if there was a problem because I lost 2lbs in one week. But really it's just that my appetite is definitely (thankfully) back down to pre-steriod levels, so hopefully by the end of rads, I'll be close to my pre-chemo size again. Phew! I was dreading having to do weight watchers again, but looks like I'll be able to avoid that 
I know I missed people and I am sorry! I still have chemo brain and though I read all our posts, I swear i can't retain anything other than what I am typing at the moment. Oh, that reminds me of Kim- MONKEY BRAINS- I double dog dare you too! Hope your return to work is going well and you are feeling good!
Ok, off to cool off before I have another hot flash...((((hugs to all))))
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I AM CANCER FREE and I AM DONE WITH CHEMO!!!!!!! Onc said I didn't have to have my last tx. I told her I wouldn't do any more Taxol because of the neuropathy so she said there really wasn't much point in doing the carboplatin by itself. I was almost as excited as hearing my scans showed no cancer. Its like a gigantic weight has been lifted. BF and I went out for pizza and ice-cream.
They told me not to have recon for at least 6 months, too. I don't know for sure when I'll do it. I was thinking next summer when my parents are up for 3 months so they can help. But we'll see.
My chemo acne is slowly improving but yeah, I'm having facial hair issues, too. I had that the first time I went thru chemo and I don't think it lasted very long. I've been running bf's buzz clipper over it. Seems to work well. I really didn't think using a regular razor was a good idea. The clipper leaves enough that it looks more normal and no 5 oclock shadow to deal with. Why do we have to deal with all of this weird crap??
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PackJen - I'm glad your friends are being so great helping with your children. I am going to have to think about a schedule around school times when it comes! Hope the breathing improves... and I agree, if not from chemo, then what??
Denise - I hope you slept well!
Daiva - No, my website is Lotsa, um, I think Lotsa helping hands, or something like that. Love your t-shirts! What great support!
Hi Stacey! Welcome my sister! In a lot of ways... I'm 41... also triple positive.... I have not had surgery yet... I had a big monster tumor with at least one pos node, so I started with the chemo first! How's your family doing through all of this? Have you been working? We'll be here! Just jump right on in! We've vowed to stay together through rads... and I'm sure past that - we have a great group and we just love each other alot!!
Patricia - Thank you for that big hunk of support!! I need it! I'm going to my first chemo alone tomorrow. It is DH's 2nd day at his new job. My BF is not off work, #2 choice is in Aruba.... #3 is working also; family is watching my youngest... so, that just leaves me! It's AC, so none of the hard pre-meds; it will be fine. Just sad. One of my GF said that she assumed (and then did the ass-u-me thing) that I had a big support system with friends and family.... and I said that I DID, but chemo has drug on for so long, that I feel like all my friends feel like they have already done enough!!! Oh, the irony!!
But, I have people to cover the kid for my bad days on Thursday and Friday....dinner Wednesday and Friday.... and Monday is a holiday so DH will be home, so that gets me through the hump of the bad SE from this treatment, then just one more to go!
I'm glad you got to see your sister! I hope your tummy gets better.... those are some of the worst feelings!! Ick! ((HUGS)) and ((PRAYERS))!!!!!! Day - great to hear from you!! Glad you had a good time with your friends in spite of the LE and stretching issues and pain! You are an inspiration always!! I am an ex-smoker btw... quit sometime around jan last year (off and on smoker through the years before that... usually more of a social smoker) - I have a vapor (electronic) cig.... it works fine when I'm stressed. Ever tried one?
Tess - YAY for finishing chemo!! I'm waiting for everyone to make a big deal in 2 weeks about me being done... and me waiting to be excited when the SE have passed, not just the actual infusion!!!! Sounds like you had a great day with family!!!
Wellsey - hang in there!!! That stinks that your SE were worse this time.... but you are almost done... getting there... so close!! Funny about your hair. I still have fuzz ALL over my head! I'm going on AC #3 and still have hair! Haven't had to shave my legs or underarms in a long time.... have like 3 hairs down "there"and hair still left on my arms, but considerably thinner. But, how do I still have so much hair on my head??? I buzzed it while I was on taxol, and it still feels the same, but def not growing. Strange!
Good to hear from you!! ((HUGS)) GG - Congrats on BF job.... hope you figure out the living thing soon! Almost done with rads, wow!! Congrats on losing a couple of pounds. I go up and down between each AC! The first week, I lost 7 pounds... had gained it back by infusion day. I think its all water that first week, and then I gain it back as soon as I start eating, so for now, I've been steady as a rock with my weight on weigh in days!!
It's good, because it means they will have donor tissue from my belly... they are going to have to do both sides to make one boob at 5'6-5'7" and 140. I've been working hard on my Komen Race sight... I can post the link if any of you want to check it out. I made a pretty big .... what's the word.... goal? Anyway... I'll post it so you guys can see it. Our day is 10/16/10.... that's going to be close to my surgery day possibly, so I'm hoping I can do it that day!!
Here's the link, if it works: http://race.komenlowcountry.org/site/TR/Race/General?px=1359159&pg=personal&fr_id=1050
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Paxton, Oh that is such great news!!!!! I know how good it feels, just been through it myself! It's like a huge weight is lifting off your chest.
This is so awesome! I am so happy for you!
Leanna, yes, we thougth about it, and he was going to get me one last year, then the BC struck. Once I'm out of all these surgeries, I'll definitely get one.
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Paxton ... Wooohoooo I'm so happy for you...got to start those cart wheels again...what a giant relief...and no more chemo..even better...
USMCWife... sorry I never said welcome to our family of Warriors..
Day What surgery are you having in Sept?
I have had to pluck out chin hairs more and more...I don't remember there being so many . I could swear there were only 2 that gave me trouble before???? My head hair is still growing..but the other day I noticed my arm hair, the right arm has lost some hair...weird my left arm started right after he first AC and still had lots on my right I hope that doesn't mean I'll loose more hair before I Am done with Taxotere.
Today starts my decline..feeling very tired today..hate the thought that tomorrow will be worse.. taking a Valium and going to bed hoping that more sleep will help..
Have a great day tomorrow everyone!.
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sacphotomom - I'll have a revision to my reconstruction. After that I'll take a loooong break, for now I had about enough of surgeries and treatments lol.
usmcwife - yes forgot to say welcome too. *hugs*
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Hey, everybody! As I see it's never late to join your group, let me introduce myself. My name is Magda and I was diagnosed with IDC at the beginning of May. I live in Prague, Czechia (Europe) and I never thought this would happen to me at my age - I'm 33 years old - but after the initial shock I decided to fight and take this as a valuable experience. I am currently in neo-adjuvant chemo, finished my four rounds of AC and had my first round of T last Wednesday. My tumor is melting litterally every day and the outlook is very good, but I thought I might join to share my experience, because even if I'm pretty robust and don't give in so easily, the SE's sometimes take my courage away. It's great to see such a community of lovely ladies sharing your experience here!
*hugs*
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Paxton: WOW ~ that's such great news! We all are so happy for you.
GG: Glad to hear from you. Sounds as if the BF is happy about the job, but I can imagine that you are worrying already about commuting in the winter. Good luck on the "where to live" issue, & congrats on getting through so many rads with so little SEs.
wellsley: Sorry to hear about the SEs ~ how many more tx do you have?
Magda: Welcome! Sorry you have to be here, but you've definitely come to the right place. These ladies are wonderful! Hope the positive outlook outweighs the SEs. I just finished my last T (x 4; had AC x 4 before that) ~ still dealing with neuropathy & bone/joint pain, but at least I'm done with chemo. Now, on to rads!
Sac: Feel better soon.
Leanna: Just checked out your link ~ good luck with the fundraising! What date is your surgery?
Gotta run ~ have a good day, girls!
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Irishtess: Thanks a lot for your welcome! I have three more T therapies to go and I'm still battling a slight "dissapointment"; Days 1 and 2 went remarkably well so I thought the final stretch would be a breeze, but then I had some unbelievable pains from my neulasta shot + stomach cramps and a slight diarrhoea and symptoms of UTI. Today is Day 6 and I'm finally getting a little better, but worn out and I'm just wondering if the cardboard mouth will persist until next time or if I need to get used to this loss of taste until the end of the treatment (thanks to this forum I can now use the salt/soda mouthwash, so I hope it will help). However, I try to focus on the end of my chemo, I've gone through worse (the nauseas from AC were no fun at all, so what am I complaining about, really?) and I made it my signature to be lighthearted about my treatment, so I guess this is no time to give it up
. Best, Magda -
Irishtess-I only have one more to go. #6 will be my last.
I have another bull riding story to share. They had a contest to rename the twitter site. I had submitted a few ideas. One of my ideas made the top 10. I had a rough time after my last chemo and it got the best of me. I was really wondering if I could go through it one more time when I got word that my name had won! The name I sent is PBR Get Tough. How ironic! I need to "get tough" and make it through one more treatment and I will be done. I won 4 tickets to a PBR event but the fact "get tough" won and I see the words of encouragement every time I go on twitter really gave me the boost I need to get through one more treatment.
This weekend we are going to NC to see a Touring Pro event. I have heard that my favorite rider JB is going to be there. I am so excited that I am going to have a chance to meet him!
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Irishtess ...that pic is adorable...
Majdula...Is your T, Taxol or Taxotere... because if its Taxotere I have found that your taste buds come back for about a week before the next treatment..which makes me try to eat everything I have not been able to taste for the last few months..
wellsey... nice job on the the contest win ..you will have so much fun in NC
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Hey May Warriors So much is happening for all of us! Paxton Congratulations on your scans and being finished with chemo. Yeah! Magda Welcome to our group. This is a great place to get courage and to give it. BC is not for sissies! GG Good luck with BF's new job, and deciding about where to live. I am the one going to Vietnam, Cambodia, Thailand, China in January. That trip was planned before BC. I will be going with my sister, if all goes well. The Paris trip is with my Sweetie, and it is only about 7 weeks away. I am so excited. It is one of my very favorite places. Wellsey It is so fun that they picked your name. I love it! I hope you get to meet JB. Irishtess I love your new pic. Sacphotomom and Pacjen I found chin hairs today. Yikes. I think I have more than before. Still not hair. I don't miss my underarm or leg hair. Day I hope you get a chance to go fishing in October. Thanks for all the wishes and good thoughts you are sending. Leanna Congratulations on your Komen site. I hope you reach your goal! I hope everyone else is okay. I continue to pray for each of you and your families. Thanks for being in my life. Have to go, my Yoga teacher will be here soon. Keep walking and exercising and eating well. Hugs to all.
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Sacphotomom: Thanks so much for your reply, mine is Taxotere, so I'll wait for another week (I'm scheduled every three weeks)... this treatment does require patience!
Patricia48: Thanks for your warm welcome, it's great to be able to share my joys and trials. You're right, chemo is not for sissies, so I'm trying my best to be a man
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afternoon all my friends...and new friends too! welcome Majdula and usmc...sorry your part of this group but glad you found us....
Paxton: Horray for you! Finally you can now hopefully make a fast recovery. pizza and ice cream..yummm
packjen: wow you have alot going on..regarding the shortness of breath.. I had that for so long and they told me it couldn't be from the chemo either.. then I got really sick and was put on antiobiotics...Breathing cleared up...I am drug free 2 weeks and my breathing has def improved..I believe it is from the chemo as well. hands down believe it. ps nice way to spend your anniversary. sounds peaceful and fun....glad you enjoyed. Also liked that your hair is growing back..7 weeks out...well I guess I have 5 more to go.
xraygirl: glad your last time is in 2 days. Are you counting the hours till it is over? I did
Day:what a sweet thing to write to all of us...made me teary eyed.
Irishtess: congrats on being DONE>..I cried all day when it was my last treatment. I wasn't at all happy. I think somehow it is all the anger, fear, uncertainty built up in me. The fact that I knew I had 4 months to trudge through it all and that I had to stay strong...I am just coming to grips with the reality of it all.. I am more looking forward to the day when I can say : It has been one month since I had to ingest or have drugs flow through my body:.
wellsely: is rapidlash the same thing as Latisse..you know the one that Brooke Shields advertisies. I wanted to try it by my onc said my lashes would grow back about the same time. I think the prescription is about $200. would aslo be interested to know if anyone used. Hope #6 is better for you than #5..Will this be your last one?
golfergirl: wish I was going to Vietnam.. Heard remarkable place..I am going to wait and do my yearly trips with my girlfriends to next May.. looking into either AZ to see grand canyon or Jamaica or Mexico.. can't make up my mind
Going over calendar now for weekend trip to beach. My son just told me he might get home one weekend next month so I am waiting for his call on Sunday to see if that will happen. If not then I am looking at end of September or early October...
Going in an hour for my pelvic, chest abdomen scan..have to drink that yucky stuff...hopefully t his will be my last scan for awhile..
Enjoy the rest of the day ladies
Jean
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Jean: I'm hoping for a good outcome from your last scan. I understand completely about the tears, the uncertainty, etc. Bet your visit with your son will help put that all aside. Denise & Patricia: Thanks! I got so tired of the bald and scarf pics. This one always made me feel good ~ an ice cream cone and my dog looking out the window! wellsley: Meeting your fave will be quite the thrill. Hope you can get his autograph!
I just got the results from the blood sample they drew before the last chemo. Seems my ALP (part of the liver panel) is way high (onc wants to repeat the testing before I start rads). Researching it today just gave me the shivers, so I'm going to do a Scarlett O'Hara and think about it tomorrow!
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Denise - Sleep well... HUGS for you to feel better, and well, sorry about your beard! haha!

Day -Sounds like you have had your share of surgeries, and deserve a break!!
Magda! Welcome!! So young! I'm sorry you find yourself here!! You are through the AC, so the big dog is down, so to speak! Are you on taxotere or taxol? I did taxol first, and am now (today) done with 3 of 4 AC treatments. So great to hear that your tumor is responding to chemo! We'll be here - when will you finish your T treatment? Welcome again and (((HUGS))). Are you taking Claritin for the pain from the Neulasta?? I take 1 the day before my shot and continue for about 4 or 5 days each day, and have had NO bone pain issues!! I like to think it's the Claritin that helped! Just an off-label use I picked up from the ladies on this board that has worked for me! (and you already answered the T question!!

Paxton - How did I miss your post??? It crossed mine because it took so long (mine did).... CONGRATULATIONS!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! That is sooooo great!! I am so happy for you!!!!! That sounds like a great plan for your recon... when you will have family there to help you! You must feel so relieved!! (((((((HUGS))))))
Hi Tess - thanks for looking at my site!!
I'm not sure... onc said surgery will be about 3 weeks after my last chemo which is Sept 14th. That would be sometime 1st or 2nd week of October..?? But, I'm seeing that it seems like it take them longer to coordinate everyone, so it will probably be more like 5 or 6 weeks, so I should be able to do the walk! Funny, 6 months ago I wouldn't have hesitated about running a 5K... but, now I'll do the walk proudly!!!
... regarding your liver tests..... no research!! Just wait for a retest!!!! Wellsey - How awesome!! Get Tough! I love it!! Have a great time this weekend, and I hope you get to meet JB and give him a big ol' hug!! And, if you do, get pictures!!
I'll be laying on my couch all weekend! Denise - great minds think alike....

Patricia - Thanks for being a great inspiration - and enjoy your yoga!!!
Jean - I hope you get to see your son next month! Your trip sounds great - if you've never seen the Grand Canyon, I'd say, put it at the top of your list, but if you had, I'd go with one of the other! (if it were me!!). I hope your yucky drink went down well, and your scan was good and clean, and you get quick results!!! (((HUGS))). PS - Another one of your neighbors just moved into our neighborhood!! We joke that our neighborhood should be called "Little Jersey" because so many people move here from Jersey.. and seems like a lot into our neighborhood!! LOL Oh yes, and today was my 3 or 4 AC, and I cried 3 times during the infusion talking about it, and made 2 other ladies there cry with me!! I think its a combinatinon that I'm almost done, and that everyone keeps saying that I only have 2 more, but the SE are so bad, I am dreading them and think I'm not seeing the light at the end of the tunnel yet!!
So, you all know today was #3 AC. I may still be ok tomorrow, and I know you all understand I go to my bad place for a while!!
If I do.... I will see you on the other side!!! ((HUGS & PRAYERS))) to each and everyone of you.... I'm going through the list... even everyone who doesn't post!!! 
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Leanna - Good luck to you and sending you lots of (((HUGS))) to help you through the tough days. Hopefully they won't be so bad this time. If others get you down, just remember us gals on here and know that we are all pulling for you and sending you positive vibes
Paxton - WoW! Great news!!!! So happy for you!
Jean - I went to Cancun just before my surgery way back in February. It was soooo nice to escape the cold and reality for a while, too. I hope you get to go! Hope the scan went well!
Majdula, welcome! Sorry you have to be here, but glad you found us!
Wellsley- have a great time this weekend. Hope you can post some pics of you and JB!
I'm supposed to be googling a blu ray player for my BF but find myself here instead...you guys are way more fun than a blu ray player! Ok, back to it....xoxox, GG
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Ok so my new obsession is rubbing my head..the hair is so soft..I find my self feeling it all day long..
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