Posted on: Nov 6, 2009 02:53PM, edited Nov 23, 2009 02:18PM by Warrior517
I am so thrilled we finally have a place to call HOME here! I was diagnosed w/IDC last year at the age of 39. It was in 2/6 lymph nodes. I was also HER2 and Estrogen Positive.I had dbl mastectomy w/implants. This summer, one of the implants failed. So, I underwent a DIEP procedure w/Dr. Massey and Dellacroce in New Orleans. Great Outcome!! I did TCH for six rounds, rads and a year of Herceptin. I am currently on tamoxifen and Boniva (study).
I just wanted to start this thread for those that had it spread to lymph nodes. I can't tell you how many threads I have read that said "thank God, my nodes were clear"...we all weren't as lucky. BUT I believe God puts people in our path when we need them most. Last year during Rads,I met an older lady(she was there for her hubby) who told me that she was a 30 year survivor and Yes..It was in her lymph nodes! The job of the lymph nodes is to catch that little sucker!Log in to post a reply
Posts 1 - 30 (2,159 total)
Nov 6, 2009 03:02PM Warrior517 wrote:
Stage IIA can be a smaller tumor w/lymph node involvement, or a single larger tumor. My tumor was 1.9cm(one of three) w/lymph node involvement which made me Stage IIA, if it would of been 2cm, then I would of been IIB. Tomato...Tomata...lol Stage II UNITE!
Nov 6, 2009 03:06PM stef58 wrote:
Hello, I just got done with chemo and finally a place to get answers for our stage. I had 2A with 1 node and multifocal with the biggest being 1.5. The other spots were less than 1mm. Had a mastecomy in June 4A/C dd then 4 taxtoere. Had neualsta after every chemo and that was the worst part of the treatments. They told me the node catches the cancer and that it did its job. Looking forward to life just wish the hair would grow. Started coming back on taxotere. Hope life is good, I thinking it is great. Hugs dianne
Nov 6, 2009 03:07PM Warrior517 wrote:
Welcome Jackie..or should I say Wacky! lol I love it!! With all the threads on here, it is amazing that we never truly had a place to go! This thread needs to be the place we can go for understanding, friendship and most of all, advice for those w/this diagnosis. Glad you are here.
Nov 6, 2009 03:16PM Warrior517 wrote:
Congrats on finishing chemo!! Yeah...I going to share a poem with you that I wrote after treatments were done. You may be able to relate to the many feelings...ENJOY! PS..My pic is me now and chemo ended last July...it will grow back!!
The Chapter Closes...
It has been over a year since I received the call
You have breast cancer...I remember starting to bawl.
Surgery was needed, chemo and rads, too.
Don't forget the IV med, Herceptin, which is new!
My journey is written but I don't know the end....
But do any of us really, my friend??
I have written each chapter in my heart and my head,
From every tear to hope to all of the meds.
My surgery has temporaily changed me frm a C to an A
Thank goodness for pump ups in this modern day!
I made it thru surgery, waking up w/4 drains.
Taking my Vicodin to get thru the pains.
I heal and get stronger each and everyday
So, I finish that chapter w/success, I say!
A new chapter starts, the one we all dread...
Chemo begins and I know it will affect my head.
Soon, my brush was filled w/chunks of hair
I was sad, but I was prepared to look in the mirror.
Fun wigs..short wigs...sassy ones, too!
No one knew which one I would do!
Made it through chemo w/support of family and friends
Time to close that chapter, thought it would never end!
So, the new chapter begins of radiation for over 6 weeks
The burn and the pain would eventually peak
Again, I make it thru w/everyone's love and prayers.
Each day, I live in Faith and Hope, NOT fears.
I close the chapter of my new burnt skin.
Grateful my expanders did not give in!
I do my IV med, Herceptin, every 3 weeks for a year.
The Oncologists staff know you by name and truly care
The access was made easier by inserting a port
But it's been over a year, not very short!
So, when does this chapter get to close for me?
In 2 weeks, and my heart needed these words to be free
You won't hear this often, but it gets stuck in our mind.
We get fearful, as safety nets are removed one at a time.
This is where I learned to control what I think
Positive thoughts can turn a black world to pink!
I also have learned to not live in fear, but hope
It is love, faith and believing that helps us cope.
So, here I sit two weeks before my final surgery day
Looking forward to silicone, port out and an overnite stay
I felt the need to write down my words for others to hear.
Maybe you will read them and want to share
I am a fighter, a warrior at war.
I have my battle wounds to even the score
I wear my pink boxing gloves and continue to fight.
So, pray for all of us each day and each night!!
Nov 6, 2009 03:49PM stephanie1 wrote:
Stage II is divided into subcategories known as IIA and IIB.
Stage IIA describes invasive breast cancer in which:
Stage IIB describes invasive breast cancer in which:
Nov 6, 2009 04:23PM AnnaM wrote:
Wow, this is great. You guys are so on top of things. Warrior, I love your poem! I had DIEP reconstruction, too.
I went into the MX thinking I had widespread DCIS. It was such a shock when they found the micromets in my nodes. The pathologist had to do three studies on my breast tissue because they couldn't figure out where the cancer cells came from. They were all less than 3 mm. There was no tumor in the breast tissue. My BS advised against going back and taking out more nodes. That's why I got chemo.
Dianne, your hair will indeed come back. Mine came back very very curly and it stayed curly for about one year. It's back to where it was before now, but there seems to me more of it. Weird, huh? I really can't complain. I got myself a cheap wig during chemo and it was very cute, but I only wore it a handfull of times. I got lots of compliments and couldn't figure out why people didn't see it was a wig. I was bald during winter, so it was nice to wear soft fleece caps all the time.
I don't know anything about extranodal nodes, 5graces.
Anyway, nice to meet all of you!
Nov 6, 2009 04:28PM stephanie1 wrote:
Miss WARRIOR :) I figured might as well just put the facts up for any newbies. TO THE RESCUE
I am supergirl everyday of the year. My superpower is the ability to fly as given to me by my radiation treatments LOL.
I got that because a male friend of mine asked me to let him know which superpower I was given because of the radiation. I thought that was too cute.
It came to me in a dream that I am now SUPERGIRL
Perhaps you have xray vision?
so glad to have you girls to talk to,
Nov 6, 2009 04:38PM Warrior517 wrote:
Anna..Glad you liked the poem! Some have a tumor, some don't...this disease is never the same for each of us, is it? My lymph nodes didn't just have micromets, it has MACRO, nearly 1cm tumor in one of them!! Aggressive little stinker...but I kicked its butt and then some!
Grace-Being that our Forum is so new, it may take a bit of time to get your answer. I am confident you will find someone that can explain it better. In the meantime, YOU ARE HEALED. Simple as that, my friend!!
Stephanie...hmm..my super power?? Lets see....I glow! I glow in the darkest of hours by trying to be positive and finding the silver linings. (Lots of practice..didn't always come easy..lol)
Look fwd to many threads, ladies! Kathy aka Warrior
PS Any Moms out there? I have a 8, 11 and 14 year old!
Nov 6, 2009 05:08PM Ainm wrote:
It's great to see we got our own home at last
Nov 6, 2009 06:30PM AnnaM wrote:
Yep, a mom and a grandma, 30 year-old daughter, 39 year-old stepson and 37 year-old stepdaughter. 16 month-old grandson (I simply can't resist):
Nov 6, 2009 06:45PM stephanie1 wrote:
I haven't started it yet. I have my last radiation on Tuesday. I had 33 treatments and I missed 3 of them one week as my doc let me go to Orlando for work so I am trying to catch back up. I am not scheduled to go to the oncologist until early December so I will be starting then. Not too thrilled out about it. Funny I would be scared of anything after everything we have been through right but for some reason I am nervous about the side effects of it. I am sure it will be fine though. Guess I am fearful of menopausal type symptoms or something. I am 36 now and I guess I am not ready for all of this. But this too shall pass right :)
I started taking clodonrate a month ago for a trial.
Nov 6, 2009 07:35PM , edited Nov 6, 2009 07:36PM by Lauren3
I am so glad to find this thread.
I'm was diagnosed in May at age 32, I'm 33 now. Finished TAC chemo a few weeks ago and began rads this week (3 down and 32 or less to go). I had my first Lupron injection on Wednesday and will be starting Tamox. soon too.
I know what you mean about reading "thank goodness the nodes were clear" on posts. It always puts a pit in my stomach. I guess I was close to 2B also since my tumor was 1.8.
I have a 2 year old son. We were going to begin trying for another soon (this was the month we planned to start actually) but I guess God had other plans.
Nov 6, 2009 08:53PM Warrior517 wrote:
Reen......Age limit?? Neeeeeverrrrr!! lol You are young, silly!!
Anna- BEAUTIFUL Grandson!! I love his little scarf! ha ha
Welcome Mamita! Is that you with your daughter? So cute!
Stephanie- I was 39 at dx. I did have chemo induced menopause. Basically some hot flashes, but my cycles did come back and I am back to pre menoupausal. Obviously, its hard to predict if your cycles come back but just look ahead in shorter segments. As my favorite saying goes..."Faith is taking the first step when you can't see the whole staircase" Just take your first step and believe the rest will fall into place!
Lauren..Welcome!! How is rads going for you so far? How long does the dr want you do to Lupron? any side effects from it??
Nov 6, 2009 08:55PM mmm5 wrote:
lymph node - schmymph node
I know I don't have positive lymph nodes but I just wanted to tell all of you ladies that every lady I know personally that has had breast cancer (friends and family) have been lymph node positive and all are doing great.
My stepmom (3 positive nodes 14 years out)
My stepaunt (too many to count dxed at 40 says atleast 10 positive nodes) going strong 23 years later
Director of HR at my company (1 node large 5cm tumor 7 years out)
Close friends Godmother (6 nodes one big tumor in node) 6 years out
Longtime friend of family (8 nodes highly Her2) 6 years out
Mom at my sons school (3 nodes 5 years out)
Hope I did not intrude but wanted you to remember what L Nodes are for 'catching the Cancer"
Stay Well, and BELIEVE
Nov 6, 2009 09:20PM MAMAQ wrote:
Warrior... I liked your poem alot. It's nice to be able to get your feelings out. I am a mom with kids close to the same age. I have a 13, 12, 9 and 3 year old.
Anna... I had a microinvasion with a micromet in my SNB. It was a little shocking to be told this info when you weren't expecting it.
Stephanie... I don't have a superpower, no rads here. I always wanted a superpower.
Lauren... Wow, you are young. I hope that fate brings another child to you somehow.
Reen... 51 is young, nowhere near to an age limit.
Nov 6, 2009 09:32PM samiam wrote:
It is wonderful to hear all the positive stories from women with lymph node positive BC. I (much to the surprise of myself and my physicians) was diagnosed with IDC and one positive node. I had a tumor less than 1 cm, grade 1, very low KI-67 ... and guess what? I still had a positive node. It has been one year since I finished chemo and I'm doing great. Now if I could only figre out how to manage this curly hair!
Nov 6, 2009 10:48PM AnnaM wrote:
Enjoy those curls, samiam, those days were great cause I never had to fiddle with my hair. Now I'm back to blowdrying. I never once had a badhairday when I was bald either. Now my hair is back to normal and serves as my own private barometer.
How great is this to meet women who have such similar node/micromet/"tumor" stats! I've been on these boards for four years and always felt sort of alone in that department.
I do have some superpowers, but I already had them way before my diagnosis. I can write upside down and backwards at the same time and that's a sign I'm far out on the dyslexia scale. Great conversation starter. I'm also a puzzle wiz. That's about the extent of it though.
So many of you have young children. That's the one sure thing that can bring me to tears: that this disease can disrupt the lives of such young women.
Hugs to all of you!
Nov 6, 2009 10:53PM Warrior517 wrote:
Anna...your writng skills! Classic!! It sounds like chemobrain didn't take your talent away!! lol
I agree with you...it was hard finding similiar dx in one area and I am glad we have this thread!
When I had those "curls", I used to dress them up a bit w/a cute thin head scarf worn like a bandana...one way to keep those curls under control...lol
Nov 6, 2009 11:56PM , edited Nov 6, 2009 11:57PM by Lauren3
Warrior - so far the rads are ok. I get uncomfortable staying in the same position without being able to move but I'm getting used to it. As long as it works I'd lay on that table all day! I loved your poem, especially the part about the pink boxing gloves! I too have many different "hairstyles" these days, although I'm really starting to get sick of being bald! The hair is growing back a tad but soooo slowly.
MMM - thank you so much, I really needed that today. What you posted really gives me so much hope!
Everyone - nice to "meet" you. Have I mentioned, I love this thread?
Nov 7, 2009 06:32AM GOGOT1 wrote:
HI, IAM 48 YEARS YOUNG !!!!!
THREE YEARS SURVIVOR, STAGE 2A, GRADE 2, NODES 1/14 POS.
I HAD 3 ROUNDS EPIRUBISIN,3 ROUNDS TAXOL AND 3 ROUNDS CMF
MAST WITH IMMEDIATE RECONSTRACTION ON LEFT BREAST
EVERY DAY NOLVADEX
I'M FINE BUT SOME TIMES AFRAID AND SOME TIMES FEELING JUST GREAT.
LOVE THIS TREAD!!!!!!!!!!!!!!!!!!!