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Topic: Breast Cancer Specialist -Triple Neg

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  • Posted on: Sep 14, 2009 03:46 pm
Minersville, PA
Joined: Jan 2008
Posts: 43
Kim_888 wrote:

Hello,

I'm interested in exploring treatment with a  new doctor.  Can anyone recommend a Tri-neg breast cancer specialist on the East coast???  I'm in PA, but would be willing to travel.

Thanks in advance!

Kim

Kim
Diagnosis: 10/3/2007, IDC, Stage IV, Grade 3, 3/9 nodes, ER-/PR-, HER2-
Posts 1 - 11 (11 total)
hope123108
Joined: Jul 2009
Posts: 14
Oct 20, 2009 01:54 pm hope123108 wrote:

Hello,

I see you are from the PA. area.  Was wondering how you made out with your visit to John Hopkins? Or if you found another specialist you are happy with?

 Thanks,

unklezwifeo…
Union County, NJ
Joined: Aug 2009
Posts: 965
Oct 22, 2009 01:22 pm unklezwifeonty wrote:

Univ of Penn in Philly has some good oncologists.

Onty
Diagnosis: 7/31/2009, IDC, 3cm, Stage IIb, Grade 3, 1/9 nodes, ER-/PR-, HER2-
hope123108
Joined: Jul 2009
Posts: 14
Oct 22, 2009 04:11 pm hope123108 wrote:

Hello Unklezwifeonty,

Thanks for the advice , have you been to U of Penn?  I went to Fox Chase but was not impressesd by no means.  Have about the same DX as you do, only tumor was a little bigger.

Thanks

PatMom
Joined: Jul 2008
Posts: 664
Oct 26, 2009 07:43 pm PatMom wrote:

This site did an ask the expert online conference in July 2008, which was before any of you joined the boards.  http://www.breastcancer.org/symptoms/types/ask_expert/2008_07/

You can read transcripts of many of the ask the expert conferences at the link in the site's home page. 

Dr DuPree, one of the experts in that particular conference practices in Bucks County, just north of Philadelphia, and her office is only a few minutes from Route 1, the PA turnpike, and I-95.

Until the time when someone comes up with a definitive "cure", we each have to cobble together what we believe will be the most effective treatment that we can live with, not merely survive.
hope123108
Joined: Jul 2009
Posts: 14
Oct 27, 2009 09:06 am hope123108 wrote:

Hello PatMom,

I am aware of Dr.DuPree's name from the conference.  I live north of Phil. She may not be all that far, perhaps something i should look into.  I am seeking a Dr. that will give some scans, my Dr. does not seem to have time for me. Are you aware of any women that have seen her?

All you sisters are great,great, great !!

Elliemae32
Calabash, NC
Joined: May 2008
Posts: 61
Oct 27, 2009 09:48 pm Elliemae32 wrote:

I went to see Dr. Lisa Carey at UNC chapel hill NC.  She has been referenced many times in articles about tnc.  Hope that helps,

Ellen

My treatment buddy was born October 23rd and is a perfect little boy!
Diagnosis: 5/28/2008, IDC, 3cm, Stage IIb, Grade 2, 3/18 nodes, ER-/PR-, HER2-
Kim_888
Minersville, PA
Joined: Jan 2008
Posts: 43
Oct 28, 2009 12:16 am Kim_888 wrote:

Hi All,

I appreciate the feedback.   

To hope123108:  I went to Johns Hopkins on October 2nd and met with Dr. Robert S. Miller.  Overall, it was a good visit, however, I will not be treating there.  In fact, you cannot receive treatment at JH for BC unless you are currently in a clinical or phase trial.   This was a surprise to me.  I was impressed by Dr. Miller though.  It was evident to me that he truly had reviewed my lengthy and complicated medical/cancer history.  He spent about 90 minutes with me and my husband and was not at all rushed in our discussions.  Unfortunately, for me, there aren't any clinical trials available for me there.   He pretty much affirmed for me that the care I am currently receiving is what I would receive if I were treating with him.  He indicated that the chemo approach my current onc has taken is very good.  That made me feel somewhat better, but overall, I was disappointed that some 'miracle' approach wasn't available.  Dr. Miller did promise to do research to see if there were any trials nationally for which I may be eligible.   He kept his word.  He's found a trial at the National Cancer Institute in Bethesda, MD and put me in touch with the researcher overseeing the trial.  At this juncture, I am going to remain on Doxil for as long as I possibly can.   When the time comes that we determine Doxil is no longer effective, I will be contacting this researcher to gain access to this study.  I'm hoping the Doxil will work for a LONG time, but in reality, I've only been getting 3-4 months out of drug before the progression starts up.  So, I'll keep my fingers crossed.

To Unklezwifeonty, I visited UPenn in May and was seen by Dr. Kevin Fox.  He was very professional, thorough, etc., but didn't offer any great insight into my case.  He did suggest that perhaps I may be a candidate for proton therapy (some form of radiation) in the future.  He also indicated that a new proton center was being built at UPenn and is anticipating a Jan 2010 launch.  He did recommend that my oncologist change my Taxotere from once every three weeks, to once weekly for three weeks with one week off.  In doing so, my fatigue was greatly alleviated.  Dr. Fox also affirmed that for my case, I was receiving very good chemo agents, but he didn't have any other recommendations.  

 As for Fox Chase, I sought a second opinion there in both 2001 and again in 2007.  In fact, in '07, it was Fox Chase that confirmed my cancer recurrence.  I met numerous times with Dr. Lori Goldstein (she's the head of the BC division) and her fellow, Dr. Ben Neggin.   Ben was very informative, helpful, calming, thorough.  Dr. Goldstein was an odd duck.   Although Fox Chase is a fine institution, for personal reasons I decided to stay with my private oncologist.  I know many people who treated there or have treated at FCCC and reviews are mixed.  To each his or her own.

Elliemae32- Thanks for sharing this.  I have her information bookmarked and may be someone I seek guidance from in the future.  

For now, I'm going to stay with my current oncologist.  However, I think that its important to seek additional opinions from time to time.  By doing so, I found out about the clinical trial that may be of help to me in the future.  In the future, I may change docs/facilities, etc., but for now, I'm just going to keep things status quo.

I wish you all well and thank you for the info!   Stay strong!

Kim 

Kim
Diagnosis: 10/3/2007, IDC, 6cm+, Stage IV, Grade 3, 3/9 nodes, ER-/PR-, HER2-
hope123108
Joined: Jul 2009
Posts: 14
Oct 28, 2009 11:31 am hope123108 wrote:

Thanks Kim,

Glad you are happy where you are. Maybe having second opion may put your mind a ease.  I somewhat heard the same about Dr. Goldstein at Fox Chase. I am also surprised that Hopkins's would not treat you.  Fox Chase is the most convenient for me, if i could find the right DR.

Take Care

Kim_888
Minersville, PA
Joined: Jan 2008
Posts: 43
Oct 28, 2009 03:14 pm, edited Oct 28, 2009 03:17 PM by Kim_888 Kim_888 wrote:

Hello again,

Yes, Goldstein was very strange.  Prior to my cancer being confirmed, she grabbed both of my hands and held them in hers.  While holding my hands, she says that although I have something serious going on, she was 99% sure that it WAS NOT cancer.   She then said perhaps it was lupus or some auto-immune disorder or something.   My husband than chimes in and in a somewhat exasperated voice, asked why I was having so much pain.   She (I kid you not), yelled very loudly..."We may never know the source of her pain!".  I was a bit startled, as was he.  Dr. Negin seemed very embarrassed.  It was just an odd display of behavior for a doctor.   All this aside, this is not why I don't treat there.    

My sister-in-law passed away there 10 years ago from T-cell lymphoma.  I saw her the night before she died and I really wish I had not.  Overall, the place to me just seems gloomy.  Or, like I said, it may be just negative feelings I have because of my sister-in-law's death.   Its just a personal choice for me.  

I wish you well, too.   Feel free to keep in touch via private messages if you like.  Take care,

Kim 

 Ps.  I treat with Dr. Michel Hoessly at Paoli Hematology and Oncology.   He shares a practice with Dr. Jennifer Armstrong.  I see her on her from time to time with expert advice.   He is located just 1/4 west of Paoli Hospital on Route 30, in Paoli, PA.  Phone number is 610-725-0650.   It is a small office, with a small chemo 'clinic'.   Very homey.  The oncology nurses are great.  Office staff very friendly and helpful.  Always lots of goodies to nibble on while getting treatment.  Very intimate environment.  Not sure where in the Philly area you are, but you may want to consider a consult with Hoessly.    

Kim
Diagnosis: 10/3/2007, IDC, 6cm+, Stage IV, Grade 3, 3/9 nodes, ER-/PR-, HER2-
hope123108
Joined: Jul 2009
Posts: 14
Oct 28, 2009 04:13 pm hope123108 wrote:

Thanks Kim,

I don't know how to PM anybody, new at this.  I saw Bleicher (surgeon) at Fox Chase and told him i was interested in BMX, he replied why don't i CUT your right arm off  too just in case. I was trying to decide what to do when the nurse tapped on the door asked if everything was O.K. i said yes just trying to make a decision, she said we need the room, please get dressed.  Wow now i'm standing in a hallway crying waiting for a room..Glad your happy where you are being treated.

Have a good evening.

Kim_888
Minersville, PA
Joined: Jan 2008
Posts: 43
Oct 28, 2009 11:37 pm Kim_888 wrote:

I just sent you a Private Message.   When you log onto the Discussion Boards....near the top of the screen, you will see Forum, My Home, My Favorite Topics and Private Messages.   You have a message waiting there from me.  Also, you can just click on a users name and send them a message.   The Private Messages area is just like an email inbox.

 That nurse sounded like an inconsiderate jerk.  

Kim
Diagnosis: 10/3/2007, IDC, 6cm+, Stage IV, Grade 3, 3/9 nodes, ER-/PR-, HER2-

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