Calling all ladies in their 20's
Comments
-
Hi ladies!
So I had my last chemo a year and 5 months ago and I started taking prenatal vitamins about 6 months ago since my husband and I are trying to conceive.. Anyways ever since I started taking prenatal vitamins (jamieson brand), my hair has been growing like crazy!! It is already past my shoulders!! Everyone always can't believe how long my hair is. Anyways I don't know if it's all my parental but it's worth a try! And if you are young there is no harm in a parental, they are packed with good vitamins that people our age need! -
Here it´s the normal treatment plan for women under 40 with an er+/pr+ bc to get 2 years of zoladex together with 5 years of tamoxifen. It seems to work better.
To be honest, I didn´t really think too much about it, because even if I was triple negative I would not try for a baby until 2 or 3 years are over (personal decision)...and under tamoxifen I won´t try either, so I have to wait 5 years anyway and in that case it does not matter if I get zoladex for 2 years or not :-)
And for now it´s ok not to have periods...although I will be happy when they come back, because I still want to have children.
-
Amanda: I also don´t want to complain about the hot flashes, we all now, there are more worse things than that. Of course it´s annoying. They come every night at the same time ( 2:00 a.m.) and I wake up with a wet head and the feeling that I have to drink all the water in the world!
I forgot to ask when your hair grew back? I´m 4 weeks out of chemo and still look like Yoda. So I started using indian oil ond shampoo with coffein to advance hair growth. I hope I can go wigless when rehabilitation starts ( here we go to a rehabilitation facility after treatments for 3-4 weeks, so this would be in april). I can´t stand my wig anymore. It the same thing eyery day.
-
KK- I only have 6 treatments I go once every 3 weeks but then after I get done with chemo I have to do radation 5 days a week for 35 days so I should be done around the end of July and I cannot wait! The hot flashes are not to bad Ijust adjust according to what my body feels at the time lol! I feel very blessed that I dont have to do to much chemo like I have heard from some people I dont know how much of that I could handle!! My grandmother had bc in her early 40s the first time, and I have 2 girls so I am hoping that my insurance will pay a good bit of the testing so that we know for sure, but I know that Im gonna teach my kids to be aware and to start learning their bodies early not wait until they "think" they should pay attention. My oldest is only 10 and her and I have already discussed that no matter what she is at risk and needs to be aware of that the older she gets! I think I would rather know its gentic to to wonder why I got it in a way Im sorry you dont know in a way I think I would love knowing my kids dont have as much to worry about!!
-
Amanda - Regardless of whether you do the test, the recommendation is typically that your daughters would start getting mammograms (and if appropriate, MRIs) 10 years before your diagnosis. As for chemo, you're one down and 5 more to go! It will feel good once you hit the halfway mark, because at that point, you have been doing it longer than you have left! As for whether it's better to know if it's genetic vs not genetic, I don't know which is better or worse. I think there are pluses and minuses to both. It would be better if none of us had this at all, but unfortunately that's not the case.
SKD - I agree that prenatal vitamins can help with hair growth. I had some really healthy hair just before and during my pregnancy (well, the 10 weeks of it). When are you going to start trying, or have you already started? Wishing you the best of luck!
Moonflower - I guess that makes sense about the Zoladex and Tamoxifen together. I think I had that option as well, but decided against it. Can't remember why anymore! But I'm also not THAT ER+. Just 10% was ER + and the rest was triple negative. Since I'm not doing Zoladex I'm trying to keep the estrogen lower in other ways. Eating more fiber and increasing exercise.
-
Kk11: we have already started trying but I miscarried 8 weeks into the pregnancy so we are hoping to try again once I am physically and emotionally ready to again. I was on tamoxifen for 10 months and my onc okay'd me to take a break to have babies and I had been off it for about 5 months when we found out we were pregnant. I don't know why I miscarried but I'm really hoping it doesn't happen again!!
-
SKD - So sorry about your miscarriage. Hugs. I had one at 10 weeks, so I know how hard they can be. Just know you did nothing to cause it and you waited the right amount of time after you stopped Tamoxifen to get pregnant. Sadly enough, miscarriages are very common, and most of the time we don't know why they happen. That doesn't make it any easier to have one though. I struggled with mine all the way up until my cancer diagnosis (partly because it took 6 months to resolve) and still have my moments, especially when others around me get pregnant or have their babies. I hope the next time you will have a healthy pregnancy and a take home baby. You will know when you're ready to try again. I'm rooting for you!
-
skd so sorry about you miscarriage, I have watched my bf and my sister go through them and I know how hard it can be, my prayers are with you to heal from you loss and to be able to have a healthy pregnancy and a happy healthy baby!!
Kk I agree about wishing none of us had to deal with this but I know that in the end we are stronger and wiser for it!!
-
hey girls
kristien I hav a question?
my hormone report is still nt ready i still dnt knw if am a tripple negative or not but I read tht tripple negative comes only in Grade3 BC n am Grade 2 means am not tripple negative isnt it?
I asked my oncologist but didnt give me a clear answer n then the FEC didnt shrink my tumor I will do TAXOTERE now I hope this works . some girls here told me tht TAX is so efficient n will shrink the tumor is tht true? I feel down :''''(
-
Rosaa I can tell you that I am a triple negative and my stage is 2b, so whoever told you that it was only in 3 was wrong!! Taxotere is 1 of the chemos that I am doing do now, but I had a mystectomy so idk how well it works for shrinking tumors, you are in my prayers!! I pray that it does what you want it to do!! Dont feel down we are here with you!! ((HUGS))
-
Amanda - Stage 2 is different from Grade 2. There are grades 1, 2, and 3 with 3 being the most aggressive. Grades basically just tell you how fast growing the cancer is, but the stage is defined by lymph node involvement, tumor size, and any metastasis. I just thought I'd clarify it for you. Or maybe you misread grade for stage due to chemo brain?

Rosaa- I'm not 100% sure about whether being grade 2 means you aren't triple negative. If your oncologist doesn't know, I would ask the person who did your biopsy whether you would be considered triple negative or not. Personally, I feel like your oncologist SHOULD know and should be able to answer your questions. I'm sorry if the FEC doesn't appear to be helping much. Do you know why they are giving you FEC rather than AC? Do you have any heart conditions? I hope Taxotere kicks the crap out of this thing! Hugs!
-
I though Epirubicin and Adriamiacin were cousins like taxol and taxotere.... I didn't think there was a ton of difference. The F is 5 FU or 5 Fluoro.. something tacked on. The F and A are usually a push and the C is an infusion. I start FAC on Monday after finishing weekly taxol. Rosaa, I get my US to check my Lymphs to see if they shrunk so I will let you know...
I have heard taxotere can be more difficult than taxol and the DD or x3 weeks are harder than the weekly treatments I was on. I was pretty much side effect free through it all till I got a Virus this week 
Rosaa, I hesitate to ask since I am not trying to insinuate anything but I know counterfeit drugs have been in the news a lot right now in the US. Vials of counterfiet avastin are being found. Is it possible that you got a counterfiet drug. MDA, one of our best cancer care centers here uses FAC and FEC as part of most of their standard chemo, so its got to be pretty good. Regardless, that really sucks that its not working for you and I really agree that you should be getting answers on your hormone status, mine was ready within a week of both the biopsy and later my UMX. Hugs!
-
i found that tripple negetive often occurs in grade 3 n i asked most women in tripple negative thread n they confirmed it.
I didnt say tht FEC didnt work with i just got two rounds n just took the third injection
My breast is no longer shaped and no inflammation or inverted nipple it s changing evryday n the tumor might start to shrink sooner i still have one FEC and four TAXOTERE so i wiill pray tht my tumor will shrink soon

-
KK thank you for clearing that up for me cause honestly I didnt know there was a grade in all of this I have never been told anything about a grade, so in saying that Rosaa I am sorry that I opened my moruth and said anything lol!!!
-
It's okay Amanda! I wasn't sure if it was a chemo brain moment or not, so I figured I'd clarify either way. Glad you learned something in the process. Maybe you can ask your onc for that info?
Rosaa - I'm glad you are seeing some changes in your breast (in a good way). I personally feel that it's okay if the tumor doesn't 100% go away as long as it's responding to the chemo, because they will still do a lumpectomy/mastectomy and remove the tumor anyways. Of course, if it shrinks away completely, that's even better.
MMM - I know a few people that were not able to get Adriamcyin due to the cardio toxicity because their heart function tests showed it wasn't strong enough, so they got FEC instead. I know there are different treatments for Triple Negative than for ER+, so that may be another reason someone would get FEC rather than AC.
-
Rosaa,
it´s strange that it takes so long for your hormone report. Mine took 3 days. Did you ask your oncologist why it still isn´t ready? And, i hope i don´t scare you, but a friend of mine is triple negative and had a Grade 2 bc. So triple negative is not always Grade 3 ( and I also think your oncologist should be able to answer this question. Can I ask you where you live?).
-
Wooohooo. Undetectable chest lymphnodes after taxol... lets let the fac clean it up.
Kk. I have heard the epirubicib can be gentler on the heart but i still thought they were related. No worries regardless. -
hi ladies,
i have been on tamoxifen for a year and was on zoladex for a year. i just stopped the injections.
can anyone shed on some light on how my body will start changing? has anyone gotten their period after stopping zoladex/lupron while on tamoxifen?
i'm starting to really regret not freezing my egg and i'm getting myself paranoid about my fertility

-
Hi Rosaa ~ I was triple negative. My biopsy path report said Grade 2 triple negative. And after chemo, my surgical path report changed to Grade 3 triple negative. Grade can change. Sometimes the cancer cells are dormant or multiply very slowly (Grade 1), and some multiply very quickly (Grade 3). I would not worry about the FEC and "being different". It is very similar to AC. C are both cylophosphamide. A is adriamycin and E is epirubicin, which are similar drugs. And F is Fluorouracil which is the only difference. I also did Taxotere and had an excellent response! When do you start Taxotere?
-
Oh yeah I forgot to say that triple negative isn't necessarily "worse". So don't stress out about that.

-
I agree with Nanna. My onc told me that for pre-menopausal women, it can actually be better to be triple negative.
MMM - Congrats on a good report!
Shiramg - I never did the lupron shots, but I did get my period back while on Tamoxifen. I got it back about 3 1/2 months after my last chemo infusion. I was told by the fertility specialist that you can expect it to take up to a year to get your periods back. I'm not sure with Lupron, but I would definitely give it at least 6 months. It's possible it could take even longer since your ovaries need to "wake up". How old are you? The younger you are, the better in terms of your future fertility.
-
Hey Girls,
I got my hormone report came positive am not tripple negative
i will have to take medcines for five years as a hormonal therapy 
-
Rosaa - I'm glad you were able to finally get your answer regarding pathology and that you're happy with the results. When you have all of the facts, you know where you stand, and can make the best decisions for your care.
-
Just want to stop in and ask you ladies to keep me in your prayers today, my hair is starting to fall out so Im gonna try to shave it. Idk that I will actually pull it off given that Ill probably start crying
so just please say a prayer for me that my emotions will stay in control!! Thank you ladies!! -
Amanda: I'm right there with you. My hair didn't fall out all the way for taxol so I just got a really short (though thin) pixy cut. I got my first FAC monday and I have already noticed more fallout. They said within 2 weeks I should be bald. I am not looking forward to it either, but hey It is just temporary. I think I am going to let my son and his buddy paint my head when I do it, gotta get a little giggle in there somehow. Big Hugs!
Rosaa: Yay for getting your reports. There is a forum on here about the side effects for the different brands of tamoxifen. SOme brands seem to have more side effects, so I am going to definately try different ones.
Also, has anyone seen any of the forum posts about the diabetic drug metformin. I am thinking about getting an RX for it. I have PCOS, so I can be on it, but never have been in the past. The prelimary articles show lots of promise.
-
MiniMacs: I agree at least it is temporay, and Im gonna have fun with it to, we re talking about taking pics of with a mowhawk and all kinds of silly stuff. For me I just dont want to see it fall out so I feel like if I shave it myself I will have more control over it! Either way it sucks but I will get through it just like I am everything else, and I know you will also! As for the drugs I cant help you there, I am not taking anything but the chemo so I dont know about all the other drugs, sorry I cant help!!
-
Amanda: I am not on Tamoxifen yet, but I am pretty anal retentive when it comes to research
I like to be prepared for almost everything (BC DX excluded). I'm glad you are doing ok with the hair thing. I was all prepared to shave my head in December but it didn't fall out as fast as I thought, so when I made it through Christmas and New Years I decided to play chicken with the taxol
I know I am going to loose with the FAC but my hair is so short now, I'm not really worried about it. Keep on chugging through!!! When are you going to be done with your chemo. My last is at the end of April!!! -
Hey ladies,
So I wrote in a few times here and there, but now am at another decision point and emotionally drained once again. My stats: 26 years old, IDC, grade 2, NSM mastectomy with immediate implant, 2 negative nodes, clear margins, BRCA 1/2-, oncotype 14 (9% reoccurence with Tamoxifen). I had the same problem with making a surgical decision where my first opinion said no to radiation and to do the mastectomy, and the second said the opposite. Now that I am over with surgery and happy with my more drastic surgical decision, I have to decide about the rest of the course. My first and original MO said last week that based on everything he would just recommend Tamox. He did get into chemo and said he would also do that if I wanted to. He said he would do TCX4, but again said he would feel safe to do just Tamox.
I went for a second opinion today and this Dr. was very ADAMANT about doing chemo. He said based on my age alone that he was extremely concerened. He said that oncotyping doesn't look at age (and doesn't even think the study had any 20 year olds in it) and said that based on age he would be much more aggressive.
Now I have two conflicting opinions (once again) and do not know what is safer. My biggest concern first is fertility. I am young and newly married no kids. We would like kids someday and I don't know exactly if doing the whole egg harvesting, etc. is right for me. Do I risk doing chemo and hope my function comes back after? The benefit is like a 3-6% difference adding in chemo to my hormone therapy. I am so terrified and do not want to make the wrong decision obviously. I know I have to be the one to live with it etc, but it is just not so cut and dry. Any thoughts?? I would appreciate anything! I need to make my decision by next week..
-
Not to sound snobby, but where did you go for your opinions. If at all possible make it to one of the top in the nation. MDAnderson, Sloan Kettering, Cleveland clinic. As important as regional docs are, they just are not as current on breast cancer research and data. I do agree though that the longer you have to live the higher your lifetime risk. We are a rare breed of breastcancer, one that doesn't have many specific studies. We mostly get lumped with pre-menopause...and thats not really fair. I do know that the risks associated with chemo and fertility may seem high, but it does seem like many women do get their periods and such back. Now, being stage 3 I had no chemo choice, but I also already have a son, so I can only sympathise with your delima. (sorry for the spelling I am on day 4 of FAC and its rough
) Whatever you decide we are all here with you. Have you had any scans to definately rule out mets. I know I had infected lymphnodes further down the chain, they removed 4 infected, 9 clear, then I had more infected. -
I thought I'd chime in on the periods... I was told that it is uctually uncommon for young women to go into permanent menopause from chemo. But, it is a risk. In our 20s, our hormones are really working at their peak and can rebound quite well. It is probably the estrogen regression meds that cause fertility delays. I had LOTS of chemo (check signature) and my period is back on on schedule better than before

At such a young age, I wouldn't refuse chemo. Especially a mild TCx4
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