lymph node transfer surgery
I am looking for any input from any who have had this surgery either successful or unsuccessful. I am considering it with DIEP recon with Dr Allen. It sounds like a no brainer since they harvest the lymph nodes from the fat that will be used to construct the breasts. His office reports 85% success with patients either getting complete relief from Le or at least reduction in swelling. I also am curious if insurance covered the procedure?
Maggie
Comments
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I am also interested in lymph node transfer. I have edema in right hand. I would live to get more information
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Hi Maggie! I attended a seminar in D.C. that was put on by Dr. Marga Massey. She seems to be the subject matter expert in lymph node transplants. She is a microvascular and plastic surgeon. I would recommend reaching out to her for a second opinion. She has offices in Charleston, Salt Lake City, Chicago and New Orleans. She is also trained in MLD and very much a proponent of going through therapy after surgery. I had a lumpectomy and have lymphedema in my trunk, shoulder and arm. She is fabulous! If I were to have a mastectomy in the future OR if my insurance would cover the transplant, I would absolutely travel to have her perform the surgery. She is very smart and I consider her to be a subject matter expert. I received a lot of literature from her office and I believe she may be willing to do a phone consult. Good luck!
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I just emailed her office to be contacted. Cannot hurt to have more than one consult for anything in this journey. Thanks Shady!
Maggie
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I don't have LE. But just wanted to sing praises about Dr. Massey. She did all 3 of my DIEP surgeries in Charleston. She is nothing short of amazing. She actually came in to the surgery holding area before each of my surgeries and spent about 45 minutes lightly massaging my at risk arm with the most fragrant citrus lotion. Then she put foam around it and wrapped it from hand to shoulder. She doesn't want there to be any chance of an accidental needle stick or anything done to that arm. And I don't even have LE! I remember thinking of all my previous surgeries and how the surgeon would pop in for about a minute. Dr. Massey really goes "above and beyond". I came away from all that realizing that not only had I just received care from the best surgeon possible, but I had met an angel in the flesh. You will not be disappointed in her care. She is traveling around the country doing symposiums to educate on lymphedema and reconstruction. They are free of charge, she provides a wonderful lunch, and there are several left this year. You can sign up at her website. www.drmarga.com. Wishing you all the best, Joni
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Thank you Joni. I have sent in all the paperwork for the consult and should hear from her office this week. I cannot wait to put this phase behind me and move on!! She sounds amazing.
Maggie
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check out the other topic Meeting with Dr. Becker...
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Had the surgery may 22 with dr m in chicago...all went well. Flying home today. My arm is softer with less of a heavyness. 1cm smaller around my forearm! So excited
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Yay , mags !
Sure sounds like a good sign...please keep us updated- and take care of yourself.jacee
We should all wish for such a DR- fabulous story. Thank you.
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It's amazing that you've seen results to quickly!!! Please keep this forum updated with your progress.
Hoping for swift healing.
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Maggie -
Where did she harvest the lymph nodes for the transfer? Did your insurance end up covering the surgery?
Diana -
insurance was approved...doc always gets pre authorization...says they code it as auxilla recon. The flap was taken from my neck on the opposite side from the LE
Maggie
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Thanks Maggie.
I had pt for lymphedema prevention, have a sleeve and gauntlet that I wear when flying and most of the time when I run, do MLD on left side (arm and breast) Beginning to believe that I may have slight (if there is such a thing as 'slight') truncal lymphedema.
Truly want to learn more about the lymph node transplant surgery.
Diana -
Diana
Were you taught to do MLD that focuses more on the truncal area than the arm ? This might be important for you. And also- do you wear a compression cami - that does help me.
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I had a lymph node transfer 11 weeks ago.. I have created a blog to document this and others transfers .. I wanted to create a place where new surgeries for Lymphoedema were talked about from the patients point of view
http://lymphnodetransplant.wordpress.com/about-me/
I hope this has some useful information for you and I would love to hear and share others experiences.. My email is helenbrd@bigpond.net.au Thanks Helen
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