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Imgp1207

Member Since: October 5, 2008
Last Login: November 20, 2008
Location: MI
Occupation:

Biography

Diagnosis

Diagnosis: Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Diagnosed: October 3, 2008
Type: Ductal Carcinoma In Situ
Recurrent? No recurrence
Metastatic? No
Stage: Stage 0
Lymph Nodes Removed:
Positive Lymph Nodes:
Tumor Size: Less than 1cm
Tumor Grade: Grade 3 or high grade
Hormone Receptor Status: Tumor has both estrogen and progesterone receptors
HER2/neu Status:

Recent Posts by stronger27

Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Nov 10, 2008 10:35 pm

34 and just DX with DCIS

Rebecca go with your gut feeling:)  I'm glad you have a multi-disciplinary team I did too, sounds like you are in great hands.  So I was not a candidate for tram flap implants using my tissue I think thats what they called it so I have expanders in ughhh they are not comfortable but I'm not complaining either:)  I go for my second fill at the end of the week and hopefully by March they will be long gone and my implants in.  My PS told me I could choose between saline or silicone implants and I'm pretty sure he said the silicone implant was the more real feeling of the 2 that would not ripple or pucker.  I guess the saline ones are known to do that sometimes.  I'm not 100% I felt both and I know that one was a lot smoother and had nicer fluidity to it.  I will have to confirm that this week so many decisions!  Good luck to you I will send positive thoughts and strength your way!

Melissa 


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Nov 9, 2008 09:31 pm

I'm 27 and just dx with DCIS

Hi ladies can anyone fill me in on the HER2 test.  My doc did not mention anything about it and I don't think they tested for it.  There was nothing regarding it in my final path report.  She did say that her team was meeting to discuss if they felt I should have any further treatment like the tamoxafin, but she felt there would be no need but wanted to consult with her Onc??? Is this HER2 test something that should have been done???  Thanks

Melissa 


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Nov 9, 2008 09:22 pm

34 and just DX with DCIS

Hey there,  I'm so sorry to hear of your recent DX, I saw your post and wanted to share a little of my story because I was there posting the same thing 1 month ago.  First, you have come to the right place this board helped me cope through the days and nights when I first found out. I am hear to tell you that the waiting and the unknown is the hardest part, but it gets easier and it gets better.   I am 27 years old and I pretty much had the same DX as you and found out on 10/3.  Right away I got to work.  Luckily I work at a hospital so I was able to get information from Co-workers on the best of the best as far as surgeons, oncologists and plastic surgeons go so I made my appointment with the chief of general surgery where I work who had much experience with breast cancer.  Going into the appointment I had my mind made up 95% that I wanted a bilateral mastectomy.  I had a gut feeling and strong intuition to do this.  I was scared but not scared of loosing my breasts.  I am young and the grade was aggressive and the research I did just lead me that direction, there were so many stories out there of recurrence and I have a lot of years ahead of me to enjoy, but I hadn't seen a doctor yet and needed ones opinion.  After meeting with the surgeon and given the same options of Lumpectomy+ rads or a unilateral mastectomy I told him of my choice of a bilateral mastectomy.  He felt I was being extreme and somewhat radical.  I was annoyed that he had said this to me and that he was very brief and general in my treatment options.  Needless to say I did not go with him there was no connection there, he may have had the best hands in the county but he was too general for my liking and I needed more.  Even more Luckily my work is affiliated with a cancer institute and they were going to be my second opinion and my choice in the end.  Point being, choose a breast specialist I would never go anywhere else.  The whole team was amazing.  To make a long months story a lot shorter my surgeon agreed on the Bilat. Mastectomy with reconstrution which I had on 10/24 and I also had a sentinel node biopsy.  Things went great I'm home and doing so well.  My final path report showed no invasion and my nodes were clear.  They did find a second area of DCIS that was so small it did not show on my Mammos MRI or ultrasounds the only place it was found was in my intuition to do this surgery:) and I'm so greatful I did.  Bottom line is get second opinions, do your research, know your gut and intuition, your young take control of your life you make the decisions, be strong, stay positive and keep family and friends close.  I will be thinking of you and praying for you. If you have any questions please contact me or check out my posts there were some great things sent and shared with me from the most compassionate women ever.  Keep breathing:)

Best to you

Melissa 


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 31, 2008 08:44 pm

SNB with DCIS: What's the point?

yes it is a separate procedure usually done in nuclear medicine.  They have to inject the dye so that it goes straight to the SN.  They mark your body once its found with a marker and then snap images for your surgeon.  The surgeon while in surgery uses a probe that alerts them to the exact node they will take.  The injection and photos process takes about 30 min.  then they will take you back to your family or maybe straight to surgery depending on your scheduled OR time.  I had my SNB injections at 1030 surgery at 1230.  Close your eyes blow your deep breath out when they inject the dye and squeeze someones hand, it helps especially if its a family member.  they didn't let me have my family but the student nurse lent her hand:)They will walk you through it all step by step, before you know it they are snapping the pictures and its over.  Don't be freaked out if I did it you can too!!!!  Did you ask about the numbing cream,  I really believe it helped me.  They said I may feel burning( thats the dye moving through the tissue and I did not) Good luck to you.  Deep breaths and stay strong:)  YOU CAN DO IT!!!


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 30, 2008 03:20 pm

I'm 27 and just dx with DCIS

I finally got great news!!!!  I had my post op appointment today and my path report showed no microinvasion and my SNB was clear!!!!!! It remained stage 0 and I couldn't be happier.  I'm SOOOOOOOOOOOO relieved.  I did have 2 places of DCIS and the mammo nor the MRI found the second area, it was very small but was starting in another duct.....so crazy but I'm so happy I went with my gut and did the bilateral mastectomy,  I know I have a long road ahead but the path looks so much smoother and brighter.  Thank you ladies for your support and the power of prayer works!!!!  I have to say my thank you prayers now best to al of you:) xoxo


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 29, 2008 09:54 pm

SNB with DCIS: What's the point?

I too had left mastectomy for DCIS with SNB and prophalactic mastectomy on my rt breast.  I want to share that the SNB is not bad at all but I also had numbing cream prescribed to me from the surgeon that prevented the stinging pain of the injections.  I believe its called emla cream.  Have your doc write a script for it.  It does not interfer with the procedure its topical.  Make sure you apply it 2 hours prior to the appointment this is very important for it to be effective.  Also do not use the tagaderm to cover it to absorb it hurts worse then the procedure itself to pull it off.  Slather it on the whole breast do not rub it in and cover with seran wrap it will absorb into the superficial layers of your skin.  Best to you it will be okay,  I am 5 days out of surgery and everyday gets easier:)


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 26, 2008 08:38 am

I'm 27 and just dx with DCIS

Hi! I'm home, well at my parents and feeling pretty good ( I have my long moments lol). Surgery went well and I bounced back very quickly,  but the next morning was a diffrent story.  I managed to get home that affernoon and with the help of my parents(thank god my moms a nurse) husband and friends I'm on the road to recovery.  The pain is starting to subside now too.  I have this cool pump that keeps the area numb for about 4 days so I'm coming off the vicodins slowly.  Motrin and muscle relaxers seem to work better.  I guess the only pain I'm feeling now is the muscle that the expanders are behind but I should be feeling better in a couple of days.  Thank youf or all your prayers, they have helped:) I will be in touch!

Melissa


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 23, 2008 11:37 am

1 year anniversary tomorrow! Yikes

Wow Congratulations I'm so proud of you and appreciate you reaching out to me.  I have found the strength inside and I'm ready to beat this disease!  I wish you the best life has to offer.  We all deserve it!  Enjoy!!!!!


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 23, 2008 11:31 am

I'm 27 and just dx with DCIS

I'm starting to get those knots back in my stomach I can't believe my surgery is tomorrow morning.  Please pray for me that the cancer has stayed contained.  There is NO MICROINVASION.  I'm miss positivity:) and my fists are up Dani thanks for the support.  I love my shepherds they are my"kids" they really are the best dogs:)Thanks again for all the support.

Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 21, 2008 07:45 pm

I'm 27 and just dx with DCIS

I met with the PS today, it was so great to go to an appointment within all this chaos and actually laugh instead of cry.  I'm so ready for this surgery now, I can do this and I'm gonna be okay.  Friday is the big day ladies 8am please keep me in your prayers you are all in mine thank you for your support thoughts and prayers during the most difficult and scary time in my life!  Only better things to come:)

Melissa 


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 14, 2008 10:21 am

I'm 27 and just dx with DCIS

P.S.  Amy- my shepherds name is Heidi I have 3 german shepherds all puppies still!  Recovery is gonna be tricky since they love to jump on me when I get home every day we got a baby gate to block them when I come home lol:)


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 14, 2008 10:08 am

I'm 27 and just dx with DCIS

Hi ladies just wanted to share that I am seeing the PS on 10/21 and as long as he gives the thumbs up surgery for bilat mast is scheduled for 10/24!  OMG am I nervous but I'm ready to get this cancer out of my body I'm so greatful they were able to get me in this month, I just pray that the DCIS is still contained like my original path report stated please keep praying for me I need some good news after surgery.  God bless you all. This thread has really helped me cope!


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3, ER+/PR+
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 11, 2008 12:02 am

I'm 27 and just dx with DCIS

So today I spent 5 hours at the comprehensive breast center at Karmanos Cancer Institute.  I now know that my treatment will continue there and not with the chief of general surgery ( my first opinion).  I was so impressed with Karmanos.  It is kind of a scary place because there were so many people and it was very much a "cancer institute" but once I got inside the breast center I felt better.  From the moment I walked in the door they catered to my every need. They had a team of specialist all ready and waiting for me. Right a way they got to work on my slides and pathology the Doctor popped in my MRI CD and she already knew my entire case and reviewed all of my history from my first appointments with the general surgeon.  My new doctor is a professor of surgery at Wayne State University a breast surgeon specialist and oncologist and was so comforting compassionate and explained every last thing step by step.  Within 30 min of talking with me and my family she got a page, it was the pathology dept with their own findings of my slides and they were not happy with my biopsy results.  I was very nervous at this moment I was hoping the first path was all wrong and I was cancer free and it was all a bad dream:) however that was not the case.  She hung up the phone and explained to me that the sample they had to work with was minimal and that the core of calcifications they had was such a small sampling and seemed to be from the very edge of the approximate 1cm tumor and not the center. They told my doctor they were highly suspicious of microinvasion.  How could this of happened?  What does this mean exactly?  Why did my final path report say DCIS if the sample was not from the center, why did the first surgeon tell me its all contained they got a great sample? She told me not to panic and of course I did but she said that they didn't confirm this and couldn't until surgery.  I explained to her I wanted the Bilat Mast and to just skip all the lumpectomy talk and she didn't blink an eye, where the other Doc told me I was being extreme.  I feel she just understood me and where I was coming from she related to my feelings and it all just felt right.  Right away she wanted Mammos of both breasts again she didn't understand why they didn't do both after DX to begin with. They also did a lt underarm ultrasound to check for lymph node abnormalties and everything came back normal thank god.  They were so pro active and on top of things where my first opinion was not.  So now I am meeting her plastic surgeon in 17 days I wish it was sooner and surgery will be close behind that.  She reassured me nothing would change in this time because I was asking her to call if someone cancels to move my appointment up:)  I guess I'm just still confused about the micro invasion part and how much it changes things???  I'm much more confident now though than I was after my first opinion and glad I went to a breast center.  No matter how great a general surgeon may be I now know a specialist is the place to be.  Wish me luck ladies!  Best to all of you fighters out there we are going to be OK!!!


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 7, 2008 03:29 pm

I'm 27 and just dx with DCIS

redheadace1 thankyou for your prayers:)  I met with the surgeon today still feeling somewhat lost.  He told me today that my options were a partial mastectomy (lumpectomy) with 8 weeks mon-fri radiation bringing my chance of reacurrance to 6-7%  or a full mastectomy of the left breast and no radiation.  My dad jumped in knowing my feelings of just having a double mastectmy and asked him what he would suggest being a surgeon if he had a daughter with my same scenario.  He was very hesitant to answer saying he had to know what his daughters feelings were first.  He felt that a double mast was extreme but a mast for my left was not.  The way I see it is that I've had breast issues forever and my rt breast was the one being watched to begin with now something popped up in my lt breast within 6 months of my last ultrasound and its a DCIS grade 3 and I feel like they really didn't even get a great sample during my biopsy from what my reports all read ( my mom is a nurse best friend is a cancer survivor and Doctor they both read it)  anyway my intuition says that my rt breast isn't healthy like he seems to think and he even recommended a blind core needle biopsy for the rt side even though nothing showed on the MRI but I don't want to do that.  With this all said my MRI only shows what we already know in the lt breast the DCIS and nothing else.  He did tell me also that he did want an SNB at the time of surgery he mentioned that in the MRI it stated that they could see the sentinel Node?????  and tried to stress that it would just be precautionary.  That didn't sit well with me either. AAHHHHHHHHHHH   He told me that If I still wanted to do the double mast that I would have to see a psychologist first.  I really feel like this is the right option for me do any of you think I'm being extreme I keep going back to this outcome.  please give me your feedback. Thanks love and hugs


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3
Posted in: Support & Community Connections + Get Togethers, Created: Oct 7, 2008 11:02 am

MI Survivors

Hi Michigan ladies!  I was referred to this thread because I live in Michigan in oakland county and have been posting under the just DX with DCIS.  I'm 27 years old and just found out on 10/3 that I have stage 0 grade 3 DCIS.  I'm seeing the chief of general surgery today at HVSH through Detroit Medical Center.  (I work there)  I've been asking around the other thread about the general surgeon who comes highly recommended vs. a cancer center like Karmanos. I have an appointment there also this week for a second opinion.  I'm so lost in where to begin and would love any advise you gals may have or could share about options or great experiences in Michigan.

Thanks 


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 7, 2008 09:24 am

Karmanos Cancer Institute???

Has anyone had treatment, researched, been to with a loved one the Karmanos Cancer institute in Detroit Michigan.  I have an appointment there this Friday and I've heard great things about this hospital.  I  made an appointment for this Friday they are sliding me in and want all my reports including the slides.  They take a multi disciplinary approach here and have back to back doctors ready for each step.  I'm still going to meet with the highly regarded chief of general surgery today at the hospital near home which is affiliated with Karmanos through the 8 hospitals of Detroit Medical Center, but is it better for me to be at a cancer institute that specializes?  I'm 27 scared out of mind and want the best pathologists and surgeons that will be aggressive.  What do you think even if you haven't heard of this hospital.  


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 7, 2008 09:01 am

I'm 27 and just dx with DCIS

Rockwell_girl and PSK07 thank you for the positive thoughts.  I know after surgery everything will stay non invasive, I believe this I have too, not looking forward to having my teenage days period back:)  please pray for me as I do for all of you!!!  Meeting my surgeon today, yikes


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 6, 2008 09:38 pm

I'm 27 and just dx with DCIS

Thanks for the response beesie, wow thats scary to think about I've been on birth control for 12 years.  On my path report it says ordered next to er/pr so I don't know yet.  God I just want to have this surgery already.  I wouldn't know if there was microinvasion until after the lumpectomy right?  

Thanks 


Dx 10/3/2008, DCIS, <1cm, Stage 0, Grade 3
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 6, 2008 02:59 pm

I'm 27 and just dx with DCIS

I just got my actual path report today from the hospital.  It states that the nuclear grade is high a grade 3 what does this mean in relation to the non invasive DCIS?  Also I take birth control pills should I stop taking them? Does anyone know if they effect BC and if they are related in anyway, I've read many conflicting reports regarding birth control and breast cancer.

Thanks 


Dx 10/3/2008, DCIS, <1cm, Stage 0
Posted in: Connecting With Others Who Have a Similar Diagnosis + DCIS (Ductal Carcinoma In Situ), Created: Oct 5, 2008 05:10 pm

I'm 27 and just dx with DCIS

Thank you so much for all of your responses.  This board is great and I'm glad I found it.  I am going to try and relax until I find out more with my MRI and go from there. I'm sure I will have many more posts as I go through this scary time.  Thanks again, god bless us all:)


Dx 10/3/2008, DCIS, <1cm, Stage 0

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