Calling all ladies in their 20's
Comments
-
MiniMacsMom: My first MO is not a top institute, my second one is..Froedtert Memorial Lutheran Hospital and the Medical College in Milwaukee, Wisconsin. I agree, I think it is annoying that we are just clumped together when being on here it seems like there are so many of us...I know in the whole picture of BC we are small, but still. I have thought of a third opinion, but I am pretty sure they are going to be telling me the same thing. It is a toss up basically.
I had just an MRI before my surgery and showed no other sites from the one we found..no lymph nodes and the SNB confirmed. I asked both MOs about doing a PET scan, but both agreed it isn't the standard and at this point, my BC does not have any other factors warranting them to go and do other scans. I really want to get rid of any random floating cells obviously, but am i willing to go through all the side effects when it is such a low risk...yet a real risk? ugh I just don't know. I hope to God if I do end up doing chemo that my period would also return. One has no idea how badly they want children when they don't have the choice..I hate it. I hate this. I am so exhausted and just want to wake up and be over.
-
So when they say TC do they mean taxol and cisplatin or taxol and cytoxin. I just finished weekly taxol and really it wasn't bad. I started FAC on monday (5 FU, A, and Cytoxin) monday and I won't lie, it sucks. I didn't help that I was sick last week and traveled to MDA monday for Chemo, Tuesday was duable, but yesterday was awful. Today is much better but not great. I have tons of help between friends and family who help with the house and the baby and that has allowed me to rest alot. If you are comfortable with everything you can always look into fertility preservation. Fertile hope and livestrong (combined organization) Help with the costs. They give you the medicines for free and then negotiate with the clinic for a 25% discount on fees. I started the process, but ended up not going through with it. They were fast and AMAZING to work with!!!
-
Minimacs: Idk how well Im actually gonna take my hair being gone,I have a feeling that when I go to shave it I will cry A LOT!! I should be done with my chemo May 24th, at least that should be the day I get my last treatment! Then I will get about 3 weeks before I have to start the radiation!! I understand about the research, when they told me what chemo I was gonna be taking I sat there and read the papers then looked up things on the internet, asked my Onco questions and every thing!!
sjensen29: I think you should try to get another opinion from the best!! You should not be walking into this as confused as you are about what plan you should take. Dont be afraid to ask for 2nd opinions until you feel you found the right dr to go with, I knew my Onco was the right 1 just with the way he talked to me and explained things from the get go. Just dont let them pressure you to do anything do what you feel is right for you! You are in my prayers
-
Mini macs: tc is taxotere and cytoxan?? Sorry for spelling, but it would be 4 rounds three weeks apart. I don't know about the first one but did you do cytoxan with other chemos? If not, what kind of side effects? Why did you stop going through with fertility preservation? I am nervous to go through with that part as well..
Amandabiv: I think i might because two opinions isn't enough, but I am nervous to just keep asking drs. My first MO who I love, talked with his whole group of MOs and he said it was 50/50. He said despite what my second opinion was he still feels comfortable doing just hormone therapy. I don 't know..does anyone feel 100% ok with what they choose? They all just say everything is in my favor except my age...all this research isn't done on your age..even oncotyping..it's so frustrating and I am already ready to be done with this nightmare and wake up... -
sjensen: I understand I was the same way I just wanted it to be over and I still have days that I wish it was, but when my doc told me what he wanted to do and that he would recomend his wife to do it if she was in my shoes then I felt 100% ok with his decision. Dont feel bad about asking drs if that is what makes you feel better,right now it is all about you and you do what you feel the best about!! I understand that you like your 1st MO but that dont mean you have to do what he is comfortable with just dont forget that!! ((HUGS)) and prayers to you
-
Cancer treatment will be over soon. Once you get started, the time just flies!
Hang in there ladies and stay strong!
-
hey ladies. I just wanted to second NannaBaby's comment.
Cancer treatment will be over soon. Once you get started, the time just flies!
I was diagnosed back in August and now I only have 8 more radiation zaps left. Hold on tight and ride this roller coaster. You'll be on the other side before you know it.
-
hey Girls
Hope that u r doing well
yup I agree tht time just flies!!!!Amandaviv: Be strong but hair will grow back againn sooner. am without hair it s been two months now still have 3 months before my hair starts to grow back. it s hard smts i feel tht am more tomboy
and i keep starring at ither girls' hair when am out. I miss my hair very much n I compare it to other hair when i see a girl with a long lovely hair i always sigh and say i used to hav a better one

Anyway when I think that i lost my hair not my life I feel stronger Am fightin somethin so bad a cancer!!! it s not easy but i feel that i will win the battle I always pray when i feel down i stopped to cry and am taking it as it is even my onc as surprised how much I changed He said that cancer is helpin me becomin tough yes it is

Girls u all in my prayers God bless u
-
Rosaa I can understand how seeing others with beautiful hair makes you stop and think! I actually got through today with out getting upset about my hair, Im not gonna say that I am getting use to it but I knew it was something I was gonna have to go through and your right its better loosing my hair for just a while then loosing my life! I know that you will beat this also! We always surprise our selves on how strong we can be when we have no choice! I have always been tough and felt as if I can handle anything so for me this is teaching me how to depend on my husband more and not feel like I have to do everything for the kids! I guess our expierence teaches us something about ourselves and those around us!
Praying for you all each and every day!!
-
KK- Sorry I'm so late in responding. I just went on vacation for a week in Mexico and am catching up! It was nice to truly relax for a change. But YES...I am pretty tired most days. I'm not sure if its from the Tamoxifen but I've been this way since chemo and radiation. I've noticed that I have to get at least 8 hours of sleep a night to be worth anything during the day. Even on vacation this week, while my friends were going out at night, I went back to the hotel at like 9:30 to go to bed. I don't mind though as I'm not a drinker. I got lots of sleep and I feel so rested now. I try to explain my need for sleep to my friends but I just don't think they get it. They say...well, I only need 5-6 hrs a night..you sleep so much. And my response is...well sorry, but I've been through a lot that you will probably never understand. I don't think I can be compared to who I was before.
Nanna- I saw that you were getting all of the additional genetic testing done. I am too. My genetic counselor at the center I go to asked me to do it a couple weeks ago at my last appt. I was BRAC neg too. I was kind of shocked when she said they wanted to do more genetic testing..but I said go for it. I'm also being tested for Li fraumani...and I had never even heard of it. I have no idea when the results will be in, but I'll keep everyone posted. I'm having them done b/c I've had a lot of cancer in my family as well...not my immediate family, but lots of aunts and uncles.
-
KK- also, I heard something great in church today and thought of you immediately. It's so funny b/c I don't really know any of you personaly but trust me when I say, I think of you all often. We are a true sisterhood...
Anyways, there is a woman that comes to sing at our church sometimes with her band. A few years ago she went through a molar pregnancy that I believe turned into some sort of cancer. I'm not 100% sure..you prob know more about it. But anways..she had chemo and everything. And they announced in church today that she is pregnant! She's about 12 weeks along. I just wanted to send a little encouragment your way.

-
Hey
Melanie Ann : How long u have been diagnosed ? why you still feel tired? what kind of side effects u r getting ?
-
Melanie Ann: I say your friends should be a little more understanding, your body has been put through it and I can say that this is even harder on your body the pregnancy!! Glad you had a relaxing trip!! I agree with you, you all are my sisters!!
-
On another forums someone posted this about the "spoon theory" its a way to explain our tiredness to others who are not sick or haven't gone through something as devastating as this. The women who came up with this doesn't have cancer but it still applies. It has been very helpful, especially when explaining to people who don't think I look sick (with a hat on of course
)Melanie Ann: my genetic counsellor told us if BRCA came back neg to try Li Fromeni. Anyway, its just another genetic mutation that increases your risk of BC. The scary thing is that it can have some increased risk of true childhood cancers also. So, the prospect of that and having a son was truely terrifying. But knowledge is power. Also, there has been some info about how Miriad just patented the testing for a new BC gene thats not BRCA or LF. I hope it was just a fluke for you guys though and you don't have to deal with this again.
-
Hi! Another 20 something (27) who's SO glad to have found this thread. I just started reading through, will definitely have to go back and catch up on goings-on but just thought I'd drop a line and say hi! Got diagnosed in Nov, had a lumpectomy and about half way through chemo now to be followed by radiation and tamoxifen too. I also opted to have the ovarian suppressant shots druing my chemo. So hopefully it'll all work out fertility wise as I'm still single and very much want to be able to have kids still when I do find someone.
-
Hey Girls
My report showed that am HER2+
and they will do a further test called FISH to see whether i will take Herceptin for a whole year or nt m 2+ if i become 3+ i will eventually take it
can anyone explains more ? will this gene kill me? -
Rosaa, Yay for finding out all you stats, it will definately make it better to finalize your treatment. I honestly don't know anything about being Her2 positive, but there is a forums on here for her 2 + people (of all ages). You will probably get better answers there. You can also try the Young survivor coallition. Its a BC forums only for women under 40, and you may find more women there with Her 2+ cancers. I hope this bump in the actives list gets you more answers.
On a side note, I get FAC #2 today. Not looking forward to it, but its only a few days of not feeling good and then a couple weeks of normal. I also still have the hair I had left after finishing taxol. Weird, but kinda interesting
Nikk, welcome, no one wants to be here, but we are a nice group of ladies
I hope your fertility also goes well. There are many women here who definately have been in your shoes and can give you some great advice and stories. -
Hi everyone! I am new here and just wanted to stop by to share my story. I am 28 and BRCA1 positive. I was diagnosed in Oct 2011 and since they did 4 rounds of chemo with Cisplatin amd Gemsidomine (probably spelled wrong) and they did not cause me to lose my hair. On Feb 22 I underwent a bilateral mastectomy and DIEP surgery. The second part of my reconstruction will be in a few months. Before I did chemo I went trough IVF as a back up just in case. I am married and we were starting to try for a baby just a month before I found out I had cancer. My docs believe I will be fine to have a baby normally so the IVF is there in case. We have 7 frozen embryos and joke that we already have 7 kids. Later this month I will find out results of my mammoprint to see if I am high or low risk for reoccurance. If high risk I will need to do 3 more rounds of "bad" chemo that will make me lose my hair and get sick. I had a relatively easy time with original chemo but would have to do "bad" kind 2nd time around. Trying to prepare myself for the worst... If it comes back low risk it's up to me if I want to do chemo (9 weeks less invasive and won't lose hair) and lower my risk of reoccurance by a few % or just move on. I haven't decided what I would do yet. trying to just wait and get results first. I just want it to be over so we can start trying for a baby again!
-
Welcome Sarah though wish you didnt have to be here!! I agree with waiting until you know everything before you decide what to do. I am so ready for mine to be over also, I have 4 more rounds of chemo and then radiation and Im just so tired of having to do it all and worry about getting sick. I just got out of the hospital Monday after being in there for 5 days it made me wish it was all over sooner..My prayers go out to every one, and extra prayers for those wanting kids!
-
hey girls
how re u??
AM FINE my HER2 test turned only her2++ so they treat it same us negative i wont take herceptin
-
Rosaa: Yay for not needing herceptin
Thats great, so when you are done with TAC, you can actually be done. Woot!Sarah: thats a super hard decision to make
Let us know how your test goes! But yay for being done with the other chemo. I am BRCA 2 positive and I wanted to add cisplatin or carboplatin but my 2 oncs said there wasn't enough research. From what I have read though the platinum drugs do a great job with BRCA cancers, and supposedly (from one onc) BRCA responds better to chemo than non BRCA cancers... go figure. Amanda: Boo for being in the hospital. I was in the hospital about a month ago for 3 days and it sucked. A stupid virus that gave my son 12 hours of vomitting and my hubby one case of diahrea knocked me out. I hope everything is under control and the warm weather will help kill all the flu germies that are out there so you don't end up in the hospital again.
I just had FAC #2 on Monday, so 2 more to go at the beginning and end of April!!! Then on to more surgery and Rads. They gave me IV Emend on infusion day with this round and i was SOOO much better. Not nearly as sick as with the first round. Plus the insurance is supposed to pay for IV emend, the pills are really expensive! Ask for it if you need it, it made all the difference in the world. I was even out planting my spring garden this weekend!
Hope everyone is getting the awsome weather we are having! -
Minnimacs the bad part is we have no clue what caused the fever or my wbc to bottom out like it did so now I will be taking antibiotics after every treatment!! I go for my 3rd treatment tomorrow so please keep me in your prayers tomorrow, I am so ready for this to be over with!! I hope all of you has had this warm weather I have been getting and been able to enjoy it!!
-
Amanda: Boo for not knowing. They really threw the book at me when I was at the hospital, since I am immune compromised. I had a hospitalist, infectious disease, and my onc all visiting me
So popular. The hospitalist said in about 80% of the cases they never know what causes it. Its just conjecture in my instance that it was a virus... I also had a rogue fever. No fever when admited, but it would come and go after and it didn't always respond to tylanol. Regardless, I hope the antibiotics take care of preventing everythign in the future! Its also prolly hard to keep under chemo quaratine with kiddos in school. That was one bonus of having such a young baby, less germ exposure. Good luck at your treatment tomorrow. They gave me IV emend as a premed on this last round and it was AMAZING. I felt so much better so much faster. The insurance apparently pays for it via IV, but not pills. I didn't get any of that terrible day 3 stuff I had last time. I didn't feel great, but it was much more managable.
Hugs! -
Minimacs: Yea they told me that we would probably never know what caused of it but he felt like it was my body not something I got from anyone, I pray the antibiotics help also, I hate hospitals!! The germ exposure is harder with all 3 kids in school but I will say they are pretty good about not getting in my face and washing their hands and all. I wish they could give me something that would help me feel better faster, I guess I shouldnt complain to much since Im not sick as dog just feel like I have the flu for about 4 days, sore, and just plain ugh but I can survive it just really wish all this would go faster so I can say Im done
Thanks for the well wishes and Hugs I can always use those!! I hope all is well with you HUGS to you also! -
MiniMacsMom - Thanks! My appointment is tomorrow morning. I am trying to expect the worst but hope for the best. I keep assuming it will come back high risk cause I have been "difficult" in every other aspect of all of this. I was very very happy to have taken the cisplatin. My doctor does a ton of research and is the head of a company that does all the testings on stuff (Caris) so he wanted me to try it. It worked well enough to lower my tumor from 2.2 to 1.5. I had a good response from it, just not as good as if I did Adreomyocin (sp?). Hoping to avoid it again but if I have to, I have to...
-
Amanda ~ Do you take neulasta or neupogen? My WBC crashed almost every chemo, even with the neulasta shot. I went to emerg a few times, but was never admitted. I am sorry you had to stay for 5 days! Ugh! I didn't really go out during my nadir days... to avoid catching something. I don't have kids. I bet kids bring home lots of germs! My friend's hubby would bathe the kids as soon as they got home from school, everyday.
Rosa ~ i don't understand HER2++ ? Here they test by the FISH test and 50% positive and over qualifies you for herceptin.
My HER2 test was 0%.
I saw my plastic surgeon again today! We decided to go ahead with a free abdominal flap. Either DIEP SIEA or free TRAM. It will depend on my anatomy once I'm opened up. He discouraged the ab flap because I still want to get pregnant in the future. But, he thinks it may be fine if I wait long enough to heal. July 13th is the tentative date. I'm on a waiting list in case something earlier becomes available

-
Nannababy: I take the neulasta shot and my onco said it wasnt that my WBC dropped it was the fever to why the put me in the hospital, so now I have to take an antibiotic for 10 days to try and prevent it from happening again. My thoughts and prayers are with you with your PS I know its alot to take in!!
Sarahmfallo: You are in my prayers today ((HUGS)) I pray that you do well with your treatment and have no problems at least none to bad!!
-
hey amandaviv
my her2++ is nt qualified fr herceptin it s a small amount of proteins on cells cnt take herceptin almost 20% means like negative n will b killed by chemo to get to 0% only few pple hav such sitution cz most test positive fr herceptin but it s good

-
Thanks everyone for your well wishes. I got the mammaprint test back yesterday and it came back high risk
I will have to do 9 weeks of weekly chemo and on the bright side after that, I will be done! I start up again next Thursday. Ill be doing Cytoxin and something else I cant remember. I am just barely over what is considered negative for her2 but not positive either. My doctor doesnt want to give me herceptin because it doesnt cross the brain membrane barrier just in case any cell ever got to there. Ill be taking a pill form of something else that I also cant remember the name of, it starts with an L. Insurance doesnt usually cover it unless herceptin didnt work so hopefully they do or Ill have to just pay out of my own pocket to use it. He said I can probably negotiate how long I have to take it, he originally said a year but possibly as low as 2 months. I just want to be off this chemo so I can try and get pregnant.The good news is I only have to do 9 weeks and by doing it I will lower my chances of a reoccurence from 22% to 10%. And after this Ill be done. My doctor is hoping that by doing the chemo weekly instead of once every three weeks it will lessen my chances greatly of losing my hair. Well just have to wait and see I guess. The chemo will have similar side effects to the cisplatin which wasnt too bad at all for me. The main thing it just made me tired and not much of an appetite. But I didnt have naseua or anything like that.
-
@NannaBaby - congrats on getting a surgery date! Im still recovering from my DIEP 4 weeks ago but doing really well and much better than I expected. Let me know if you have any questions, Id be happy to answer!
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