Looking for Plastic Surgeon in Twin Cities

Options
leslie1024
leslie1024 Member Posts: 5
edited November 2016 in High Risk for Breast Cancer

I am considering a bilateral mastectomy and I am looking for recommendations for a plastic surgeon in the Minneapolis/St Paul areas ofMinnesota. Not sure yet whether I want implants or a flap procedure. Thanks

Comments

  • Dejaboo
    Dejaboo Member Posts: 2,916
    edited February 2009

    Leslie I sent you a  pm  (Private Messages)...Find the Link at the top Right

    Pam

  • Dejaboo
    Dejaboo Member Posts: 2,916
    edited March 2009

    Hi Leslie- Just checking to see how you are doing & if you have made any Decisions.

    Did you get my pm?

    Pam

  • robyn33
    robyn33 Member Posts: 99
    edited March 2009

    Hi Leslie,

    I live in the Mpls. metro area and had a bilateral mastectomy followed by tissue expander placement last June done by Dr. George Landis.  He, by all accounts, is one of the top physicians in the metro area and has won the "Top Physician in Minneapolis St. Paul" award and has been a runner-up in other years.

     I have always found him to be sensitive to my frame of mind, willing to hear my wishes, kind, thorough, and possessing a good sense of humor.  His work so far (I'm a work in progress) has been very good, and I'm anticipating a great conclusion.  I had radiation on one side, so the plan is to place an implant on the "good side" and do a lat flap procedure on the radiated side--sometime in June or July (or 6 months after completion of radiation).

     If you would like more info, PM me anytime...

    Good luck in your search!

     Robyn

  • Dejaboo
    Dejaboo Member Posts: 2,916
    edited March 2009

    Robyn,

      Dr Landis Was my Plastic Surgeon also.  I do hope everything goes very well with your Exchange this summer.

    I no longer am seeing Dr Landis.  He wished me Good Luck at my 2 week Post Op.  I will be having my Symmastia Fix with a New Plastic Surgeon hopefully this summer.

    Pam

  • robyn33
    robyn33 Member Posts: 99
    edited March 2009

    Pam,

    Did you have the same experience with Dr. Landis that I have so far, or are you leaving his care because of something that went wrong?  I guess I ask because I don't know what symmastia is.Undecided

  • Dejaboo
    Dejaboo Member Posts: 2,916
    edited March 2009

    Hi Robyn,

    Symmastia Is When your 2 Implants are placed Way to close together.  So they appear to be one.  I have no definition between my implants.  The skin on my sternum Sticks out about 1.5 " from my Chest.  I have pictures Posted on Timtams Picture forum if you want to see them.  Do you have access there?  if not- You can pm Timtim & aske for permission to access it.

    It is caused by Surgeon Error.  That is why I am having someone else fix it.  it is a Major Complication that is hard to fix.

    I also sent you a pm.

    Pam

  • lamuso
    lamuso Member Posts: 123
    edited April 2009

    Hi Leslie...... did you find a good plastic surgeon?  I am in Duluth and I am still considering my options here.  I've had a double mastectomy with radiation on my right side.  We have a handful of good plastic surgeons here but I've put off making the appointment to see mine.  I did go in before my mastectomy and spoke with him.  It's all a bit scary.  I know the lat flap is quite involved.

  • leslie1024
    leslie1024 Member Posts: 5
    edited April 2009

    I have not met with anyone yet. The more I research, the more freaked out I get.

  • Minnesota
    Minnesota Member Posts: 923
    edited April 2009

    Leslie and Lamuso,

    Just to throw something else into the mix - I'm from St. Cloud, and I went to New Orleans for my recon. They have the most experience at this. Experience with these procedures, especially if you go the flap route (I had DIEP), is critical. Don't think your options are limited to the Twin Cities area or even to Minnesota. Lots of ladies have traveled for this, and others from Minnesota. It's very doable. For me, it was an incredibly positive experience.  You'll find plenty of discussion about surgeons and procedures on the breast reconstruction part of this forum.  Here's the website of where I went: http://www.breastcenter.com/welcome/   

    Good luck with your research and your final results!

  • ktn
    ktn Member Posts: 181
    edited April 2009

    Hi! When I was diagnosed I was referred by my Gyn to the Piper Breast Center in MPLS for my care. I had tumors in each breast so she wanted me to have specialized care. I had my mast at Abbott and Eric Johnson was my surgeon and was great (also listed in the top MD's in the Twin Cities). When the nurse from Piper called to tell me I had been assigned to him I asked her to recommend a plastic surgeon for me. As a nurse myself, I was upfront, said I was a little vain but wanted a really good PS. She said she had 2 favorites and would get me set up. I am going to Tim Schaefer of Midwest Plastic Surgery. He has offices in Edina(next to Fairview Southdale) and Robbinsdale ( next to North Memorial). He has been great! He specializes in breast reconstruction after breast cancer. My regular surgeon said that Dr Schaeffer has 'the gift'. I have bilateral expanders, went through radiation and even had to have some saline removed for radiation and then was reexpanded again after. I'll probably have the exchange surgery 6 months after radiation ended (last Feb). I have always felt he is very knowledgable and skilled. I know of 2 people who had problems after their surgeries done by a female PS and i sure want to avoid that!

    Good luck in your search!

  • tifan
    tifan Member Posts: 19
    edited April 2009

    Hi,

    I would like to second the recommendation for Tim Schaefer (at Midwest plastic surgery). He did my reconstruction and is meticulous and patient and just all around wonderful. My husband also said that post-mastectomy, Dr. Schaefer spent more time with him to explain everything than did my regular surgeon. Dr. Schaefer's partner, Dr. Ruebeck is also highly regarded and lots of women in the chemo room had him and loved him as well.

  • ktn
    ktn Member Posts: 181
    edited April 2009

    Tifan- Quite a coincidence that you had the same PS! I agree that my husband and I have spent so much time talking with him. there are alot more appts with him than with the surgeon. The weekend I had my surgery my surgeons partner made rounds very briefly. Dr. Schaeffer came in each day and was the one to remove the dressings and explain things. My husband thinks I like him because he's so cute but whatever!!!! Did you have expanders? I will be so happy when I can finally get the exchange done. These expanders are so hard!

  • tifan
    tifan Member Posts: 19
    edited April 2009

    HI KTN,

    I was diagnosed right around the same time as you (May, 2008), with a 4.9 CM ILC, 3+ nodes, I was going to have a mastectomy with LAT flap reconstruction but a number of things during the mastectomy surgery, led to the thought that I would need rads so Dr. Schaefer and I had agreed up-front, if it looked like I'd need radiation, I wouldn't get the flap procedure, just simple expanders with implants later.  

    As it turned out, I didn't need radiation so for awhile I was upset about just having implants after expanders, I had hoped for something more sophisticated - and I really hated the expanders, they were always painful and I hated the way they looked - in clothes or out of clothes.

    I had my exchange surgery in March 2009, and  I am sooo happy with the results.  They are soft and comfortable and I frequently forget I have anything foreign inside of me  - they feel great and they look very good. 

     Dr. Schaefer IS cute as can be of course, and that doesn't hurt anything, certainly.

  • lamuso
    lamuso Member Posts: 123
    edited April 2009

    ktn and tifan, the two of are incouraging me to check out  Dr. Schaefer.  I am still worried about the radiation I've had and if expanders are even an option.  He sounds like he knows what he's doing.

  • ktn
    ktn Member Posts: 181
    edited April 2009

    Tifan- Did you get silicone implants??? And are they a special kind?? That's what I am thinking. Dr. Schaeffer said they are the softest but if the thought of silicone would keep me up at night I should do saline. (I think I have bigger issues to worry about!) These expanders with saline are so hard! I'll see him later in May and he'll check out my skin. The radiation ended mid Feb and he said he'd check me every 2 months until he feels the skin is ready for the exchange. He mentioned I would need 2 weeks off work for the surgery but most people only need pain meds the first week. What did you think??? Any helpful hints?

    Lamuso- Getting an appt to get checked out can't hurt- rather with Schaeffer or in Duluth. I had radiation to both sides but my skin healed well. There is always a risk to reconstruction after radiation but to me it's worth it. I had a 'skin sparing mast' so there was extra skin to use for expanders. I'm sure they will have options for you too!     Kathy

  • tifan
    tifan Member Posts: 19
    edited May 2009

    ktn,

    I had 2 weeks off post-surgery but I think I could have gone back to work after 1 week. I was mostly just tired, not at all sore after the first 2 or 3 days. It was incredible how little pain there was.  I think if you are having the surgery shortly after chemo or radiation, it is the exhaustion you have to worry about, not the pain.

    I did get silicone, I was sure I wouldn't want silicone because I happen to know an awful lot about the silicone implant litigation, but, rather last minute, I went ahead with silicone and I'm so glad I did.   It is just so nice to have something soft filling out my shirts again.  It does so much for the spirit.

  • ktn
    ktn Member Posts: 181
    edited May 2009

    tifan- thanks for the info! Do you know when the next part happens as far as the nipples and tatooes if you are choosing that too? Early on I was told there that they did the scar tissue for nipples. Some on the boards have said they had procedures with general anesthesia and others said local. I'm wondering if you have more info than me???

  • tifan
    tifan Member Posts: 19
    edited May 2009

    I am getting nipples in early June - so, 3 months after exchange. Dr. said they give you the very light sedation for the procedure. 

  • ktn
    ktn Member Posts: 181
    edited May 2009

    Tifan- Thanks for letting me know. It seems some people must have more involved procedures. After all this the easier the better! I just want things to feel completed. I'm not planning to go topless anywhere anyway!! I'll be anxious to hear how things go in June. Where will they do the procedure at??? Thanks!

Categories