Calling all ladies in their 20's
Comments
-
hey again
I read in a thread that some pple died out of chemo doses can this happen really??
-
My oncologist told me that 1% of chemo patients get infections from chemo and a small percentage can die from the infection. Its a risk but its rare. Considering most of the people with cancer are significantly older than us and have weak immune systems. Its a side effect I am aware of, but not as concerned with as something else. THats why we are supposed to take our temps all the time and be very observent of everyone else being sick.
-
Rosaa I was a candidate for either surgery. My radiation oncologist was very concerned about the long term effects of radiation with the lumpectomy. Long term effects are low but serious. There are no studies done in our age group on what long term risks are and if we are at an even higher risk. We decided to go into surgery trying to avoid radiation. They did the sentinel node biopsy first with the frozen cut in the or. From there while in surgery I told them if there were positive nodes to just do lumpectomy cuz I would have had to get radiation. My nodes were negative so did the mastectomy do I didn't need to do radiation.
-
wat are the side effects of radiation? do u know that there is a new technique of doing radiation during surgery? i can send u the link if u want
-
hey again
is it normal that i have had my period today and am through chemo???
-
Hey Rosaa ~ My hair started to grow back while I was doing Taxotere
And I also had a couple "periods" during chemo. It's normal as long as it's only a few days and not heavy. And congrats on the shrinkage!!! 
-
Hi ladies....I'll have to post my 4 month post chemo picture tomorrow. I'm starting to look like I just had a really short "boy" cut! Hoping to ditch the scarf soon!
MissRC - Awesome picture! It's hard to tell how long your hair is now. Mine is over an inch. How come you haven't been started on Tamoxifen? Usually they like to start it relatively soon after finishing chemo or radiation.
Melanie_Ann - Do you constantly feel tired since starting Tamoxifen? I feel like I have less energy than I did during Taxol!
Rosaa - I remember a stronger sense of smell too. I also had that when I was pregnant. When you're nauseous, anything that doesn't smell good just makes it worse. I swear I could smell the alcohol coming through my husband's pores after just one beer, so I made a rule of no drinking during my chemo weeks because it was just too awful. And then of course, I that I stunk like chemo, but he didn't think so, so I think as long as others don't smell it, there's no reason to worry. Oh, and I also had my hair grow back somewhat during Taxol, but it was VERY slow and really not many hairs. I didn't have periods during chemo, but it's definitely possible. I can't remember what my fertility specialist said, but I think he said it didn't matter whether you did or didn't as far as future fertility is concerned. You can always ask your oncologist what it means for your chemo treatment. What chemo regimen are you on again?I know you said Taxotere right now, but did you have other chemo first? Some chemos are harsher on the ovaries than others. I think Taxol/Taxotere is less harsh than AC (Adriamycin and Cytoxan). I started with AC. I had my period a week before starting it and then never got another one until 10 days ago.
amandabiv - I had a bad skin reaction after my mastectomy, but it came the day after surgery. There are a number of different potential reasons...The material they used to disinfect my skin during surgery, the antibiotics they gave me, and also the gown and sheets in the hospital. They switched me to hypoallergenic sheets and gown and also gave me Atirax because Benadryl didn't help. Hope you feel better soon. It's awful when you're itching in an area you can't even scratch!
sjenson - I didn't get to keep my nipple. I asked my surgeon, but the tumor was too close, so it wasn't possible for me. You may find that with the expansions, your nipple isn't quite symmetrical to the other side. They can definitely make adjustments to move things around though, so don't worry too much about that. Also, it's normal to have a hard time looking. I found that by forcing myself to look early and often, I adjusted more quickly. What you're seeing now though is the worst of it. It should look better through expansions and your implant swapout. It will take time, but it will look more and more normal. As for the oncotype, my oncologist suggested I NOT have the test done. He felt I would benefit from chemo anyways so there was no reason to do the test. He also said that the margin for error in younger women is greater and that if came back saying that I didn't need chemo, my insurance may not end up paying for chemo. So I would definitely think about that because they might just deny coverage if the oncotype comes back saying you don't need chemo and you may wish to have it anyways. Totally up to you, but I wanted to share the reasons I didn't get it done.
-
kk11: My hair is also about an inch. Also, I found out today that I do not have to take Tamoxifen, and I only have 5 Herceptin treatments left!
I just wanted to give y'all a quick update. Have a great day!
-
Hey kristien
am right now on FEC chemo it s my third injection then i will have Taxotere after
-
Rosaa ~ Taxotere is what murdered my tumor! It shrunk drastically! If ur already having a response to FEC, you may not have much of a tumor left by the time u get surgery
-
Nanna: I can't remember are you BRCA pos? And now many lymphs involved. We are fairly similar except for I am ER pos. Anyway. Why the extra chemo? The cisplatin is a platinum drug right? Sorry, I just wanted to know how they knew you neede more chemo post rads?
-
I'm BRCA1 & 2 negative. But I am still getting ++ gene testing for PALB2, TP53 and Li Fraumani syndrome, and will be participating in a genetic research study. Because my mom and her brother both got cancer before they were 40 and her sister got eye cancer. But no breast cancer in the family, just a bit of everything else.
I did chemo before surgery and it must have totally destroyed my lymph nodes, as they couldn't count any, it was a clump of mush. Which was all negative for malignancy

I needed the extra chemo, because the tumour grew really fast in the 6 ish weeks between my last chemo and surgery. I couldn't feel any tumour after my 3rd Taxotere. And then it came back
... 4.5 cm mulifocal area. And since I'm triple negative, with no targeted therapies available, chemo was the only last option. Because they were worried that cancer cells could still be living in my blood/lymph systems.Cisplatin is an "old fashion" platinum drug. And was very harsh! Side effects were the worst out all the chemos I've done. Nausea +++++!! And I also got lots of clotting issues and a pulmonary embolism during last chemo regime.
-
Yuck. I am sorry that sucks really bad. But you are almost at two years!!! Thats amazing
I will keep sending my good wishes your way
Keep us updated! DId you see the article where Miriad Just patented a new BC gene? It was on the forums a week ago. I think its called RAD51C. I know its more money
but its kind of exciting too. So you did test positive for li fromeni?We are still trying to figure out if I am the orignator of my BRCA 2 gene. It didn't come from my dad, and my mom is resistant to testing. My older sister is now on high risk testing until my moms results come back positive.
-
Hi ladies sorry I havent wrote in awhile been with out a computer!! Hope everyone is doing well just wanted to say that I started my chemo today and so far I am doing really well, matter of fact when I got done I was hyper as all get out lol!! Now I am calming down but I am still doing good and I am thanking God for that!! Sjensen,it is very hard to look in a mirror for a little while but know that it does get easier as time goes on but you will have good days and bad just remember you are allowed to get upset just dont allow it to hold you down to long!! I had a double mystectomy Jan 11th and after a couple of weeks it was easier for me to look at myself and not just cry though I dont like it for me its easier to make a joke and then go on. I will pray for you as I do all of you!!
-
Amanda definately enjoy the steroid high but dont overdo it... the crash will be much worse
but im glad to hear u r feeling beter. Big hugs ur way. -
You ladies are absolutely incredible!
I'm hoping I could maybe get some advice...
Like some ladies in previous entries I have been diagnosed with fibrcystic breasts. 2 years ago I found a lump, after much persuasion I decided to get it checked out. I went to the normal student clinic and they didn't even exam me because of my age (I'm 20). They said not to worry about it. After getting engaged my fiance encouraged me to go see someone else. I went to my gyno and she was concerned. We got a biopsy of one of the 4 lumps in my left breast. Gratefully it was benign.
However, since then some of my other ones have gotten a little bigger and new ones have been found. Most girls have breast pain during their period and thats about it. I have very intense breast pain everyday of the year. It gets so bad I sleep with heaters on my breast or icepacks to numb the pain. I can barely give hugs without them being incredibly sore.
But, since the last biopsy and ultrasound only proved to be extremely expensive and benign I'm VERY hesitant to go in at all. I know I have several lumps in both my breasts now but, I feel like this is probably just how fibrocystic breasts are, and if they are all like the first tumor and all benign there is no point of going in or even considering surgery. Chronic breast pain is not usually a sign of breast cancer. But, the pain is increasing bringing me to tears often, but I don't want to waste money on something unsubstantial. If I ever did get them removed, due to the size, I would have to remove 2/3 of my breasts..leading to reconstruction. Which if benign doesn't make sense to do but...
Idk what should I do?
-
Thanks Mimmacs and I am taking it easy today I have noticed being more tired then ususal and thankfuly my crash was not bad just went to bed!! Chelsi26 I have no clue what to tell you to do I wish that I did but I am praying for you that you can find some help and much needed relief!!
-
Yay for bed. I have a now 19 mo old and its hard to just go to bed so I have to divy out my energy during the day wisely
When I have help though I definately enjoy going to bed and sleeping in! D is not appreciative of mommy's need to nap
Chelsi: I also have no help for you. It might be better to post in the not diagnosed but worried forums. Some of the ladies may not be as young but you'll prolly get more eyes lookin at your posts

-
Gene testing takes a LONG TIME in Canada. Because the government pays for health care and has to aprove funding etc. It has to jump thru lots of hoops. It takes 4 months or so for results!! So I don't know if I tested positive or negative for Li Fraumani syndrome??? If I test positive, it's no big deal really... it just means more screening for other cancers.
CHELSI ~ I had breast pain. My tumor was so big and surrounded with edema. My tumor was 8cm. Plus the fluid! No wonder it was painful, it was like my boob was going to explode! I had fibrocystic breasts before getting diagnosed. Pain is very common. Did u get both breasts ultrasound? Y did they only want to biopsy 1 lump? y not all 4?
-
Hello girls!
Just popping in to say hi, wow I had lots of reading to do to catch up! Welcome to all the newbies! Im 2.5 years out since cancer diagnosed, and 2 years on tamoxifen. Im doing fantastic! No complaints whatsoever, BRCA negative & busy planning my wedding for 6 weeks time!!!!! EEK!!
its funny, Im thinking about cancer less and less these days, in fact, some days I might not think of it at all, until I take my nightly pill of tamixifen. I have extremely light periods, approx 1 every 5 or 6 months, then only lasting 1 - 2 days. My onc said I can take a break from the tamoxifen any time now to try to conceive. Its definitely something we will do, might wait for another 6 - 12 months though & enjoy our time as newly married!!!
best of luck to all those undergoing treatments, it will soon seem like a distant memory xx
-
Hey treadSofly- I was just dx a month ago and waiting to see my MO on Monday. I don't think I will be having to do chemo from what he said on the phone, but will know for sure then. My oncotype was 14. I am 100% Er/Pr and will be definitely doing Tamoxifen. I have been reading about all these women with side effects..have you had any problems? Anything that helped? Also, how does your MO deem it safe to go off of it before the 5 years to conceive??
-
MissRC - Did they tell you why you don't need to take Tamoxifen? My oncologist is so PRO Tamoxifen that he even has a friend of mine (who was diagnosed as Triple Negative) taking it. I've been on it for 4 months now, but if I didn't have to take it, I probably wouldn't either (or I'd do it for only 1 to 2 years total).
Rosaa - Taxotere is similar to Taxol. It's of course different for everyone, but most people I've talked to do find Taxol/Taxotere to be less uncomfortable than FEC or AC. That's not to say it's a cake walk (though I've heard for some "lucky" people it was), but hopefully it holds true for you too that it's a bit easier.
Nanna - So are you P53 positive? I also had that test done and fortunately I was negative. Haven't heard of PALB2. What is that one?
Treadsoftly - Welcome back! And congrats on the upcoming wedding! How awesome that your oncologist is on board with you stopping Tamoxifen any time now to have a baby. I wish my Tamoxifen would be on board with that. Right now it looks like I'll have to go against his advice because I'm not waiting another 5 years!
Amanda - How are you doing this week? The steroids can make you a bit crazy and then the crash comes. Hope it wasn't too bad for you.
Chelsi - Not sure either what you should do. I know it's expensive to have biopsies and ultrasounds, but your peace of mind is so much more important. I hope you get the other lumps checked out.
MMM - I hope you can send your daughter with family for a few hours every now and then so you can take a nap! Or can you have your husband take over some responsibilities once a week so you can sleep in? Your health is important and sleep is part of staying healthy!
AFM - I've had a headache for the last few days and I've got lower back pain and abdominal cramping. It's too early for my period..and it's lasted too long for it to be ovulation pain. I'm trying not to worry about it until after I see my oncologist again, which is in 2 weeks, but it's not easy considering my history (Gestational Trophoblastic Disease and then Cancer).
Oh, and I'm gearing up to go to New Orleans for the Young Women's Breast Cancer conference that's from the 24th-26th of February. I'm going with 4 other girls from my local young women's support group and I'm excited! I'll let you all know what I think and what I find out. I know some of you wanted to go this year but can't.
-
Ok....so it's been 3 weeks since my first post chemo "period", which was very light. Now I'm spotting, so I have no idea what's going on. But I guess it's hormones being out of wack that caused my headache and the back pain is now explained as well, though I'm hoping that my next cycle is closer to 28 days. I go back to the fertility specialist in a month, so I can talk about all of this with him then. I know he will do an ultrasound to check on things, so I feel good knowing that if something is wrong, he will find it.
-
kk i have to say that this week has been blah!! I have not felt good at all, my head has been killing me and the more days pass the more that hurts its as if my whole body is hurting now and I have no clue how to stop it!! I really hope all of it passes soon, however I dont want to complain to much cause I think I have had it better then I could have asked for! I hope things go good with your fertility specialist and that everything turns out ok!! Have fun and be careful on your way to New Orleans!! As for everyone else I hope that you are doing well my prayers are with all of you!
-
Amanda - What chemo regimen are you on? I had AC followed by Taxol. AC really kicked my butt. I had a lot of headaches (I really think it was from the Neulasta shot), almost always starting the day after my Neulasta shot. I was told some of the medicines they have you on for the nausea, like Zofran, can cause headaches, so you may want to mention it to your onc to see if they can give you something else. In my case, it didn't help, but it's worth a try. In any case, it did help more with the nausea to switch, so I got something out of the switch.
Oh, as far as my period goes, yesterday spotting, today full flow. On the one hand, I'd rather not have it every 3 weeks, but on the other, I am happy to have it all, plus happy I won't have it next week in New Orleans!
-
Hey girls,
I´m done with week 1 of radiation and on Tamoxifen and Zoladex since Friday.
It´s ok, nothing in comparison to chemo. I don´t recognize any special SEs (maybe they need more time to develop :-/ ) The hot flashes at night are still there but I had them also during chemo, so it´s nothing new to me and I can deal with it.
But the needle of the Zoladex shot is really big and it hurts! And I will get this shot every month and I´m not looking forward for the next one. My gyn said I was very brave, because she also does not like Zoladex. I don´t want to scare anyone. In case of things like shots I´m actually a big baby and my gyn knows that ;-)
kk: Have fun in New Orleans!
And best wishes to all the girls who are going through chemo now.
-
KK I am on 3 differnt kinds for the chemo: Taxotere, Adriamycin, and Cytoxan. I havent taken the Zofran in a few days because you are right it has not helped with the nausea at all and I dont remember the name of the shot that I get the day after my treatments but I will deff ask if it may cause headaches! I am feeling much better today but I still have the mild headache!! I understand about not missing your periods cause I had a hysterectomy 2yrs ago and I do not miss them at all, however for you I am happy that you are getting yours again, since you are wanting to have children and I pray that any of you who want them that God will bless you all with them. I would not give anything for my children and I thank God everyday for them, they are my rocks in all of this!! God bless you all!
-
Amanda - Are you ER or PR +? Since you've had a hysterectomy (I assume with the removal of the ovaries as well), they likely would not put you on Tamoxifen but rather an Aromatase Inhibitor. Are they giving you all 3 chemos at once? Usually the AC goes together and Taxol is by itself. Thanks for your kind words about the kids thing. I hope everyone here is blessed with having the # of chldren they wanted before all of this happened.
moonflower - How come you're still getting Zoladex shots after chemo? Or is it that they wanted to do both because you're extremely ER/PR +? I did want to mention that my hot flashes improved after chemo (it took a little while) and I think it coincided with my getting my period back because I don't have them much at all anymore, even though I'm on Tamoxifen. Thank goodness because I was waking up in full sweat quite often towards the end of chemo!
-
KK I am a triple negative we believe mine is genetic due to my grandmother having bc but I have not done the test yet. I do all 3 chemo on the same day but they each go in seperately I believe! My hysterctomy was due to another problem I was having but yes my ovaries were removed, and it is a decision that I do not regret at all!!
Moonflower I have been having problems with hot flashes also though they dont bother me so much except at night, I dont know if the hot flashes are my sleeping problems are if just being plain uncomfortable is
however like I said somethings I will not complain to much about given that I am not sick all the time and I have been able to eat! Best of luck to you with your shots sorry they hurt so bad! -
Amanda - I hope you can get the test so you can have peace of mind. My grandmother also had bc, but not until her late 70s. My mom has 3 cousins (all sisters) who had it in their 40s, so I was also tested for BRCA and p53 because of my young age and tested negative. It's nice to know I don't have the mutated gene, but then I look for other explanations. As for the hot flashes, I think it's the Taxol or Taxotere. It should start to get better once you're done with treatment. How many cycles do you have and how often? I had 4 cycles (dose dense) of AC every 2 weeks, followed by 4 cycles (dose dense) of Taxol every 2 weeks, so a total of 16 weeks. I already had 9 weeks of chemo before that for a molar pregnancy, so it all adds up to nearly 6 months of chemo in less than a year.....but I know there are others who have had even more, so I'm just happy to be done with it!
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team