I want to put this out there as an option for implant reconstruction. Initially I had uni mx and delayed reconstruction with a TE put under my pectoral muscle. Hated, just hated it. Was painful and crampy for all the muscles of my chest. No strength because my pectoral muscle was cut. So bad I couldn't open a bag of chips. Was slowly inflated, while waiting to do DIEP. Changed my mind and did fat grafting 3 times with an inexperienced PS who took out my TE. Had infections twice and lost a lot of my grafted fat. Got a new , better, forward thinking PS who agreed to putting a new tissue expander OVER my pectoral muscle, with no cutting of my muscle whatsoever. In August 2015 I did implant exchange, to a 420cc Mentor Anatomic Implant. Then had breast lift of right side for symmetry in September 2015, about 4 weeks ago.. Plan nipple reconstruction this December, with areola tattooing in late spring with Vinnie Myers.
Looks pretty good, have a very realistic, custom made prosthetic nipple that I wear every day until I get the reconstruction done. Made by Feeling WholeAgain.com. Really nice guy named Paul created it for me. Used to be called Custom DSE.
Using Embrace Scar therapy system for the next 8 weeks on the vertical lift/breast lift incision. Hope it will minimize my scar. I will update how that goes.
Important point, had 5 weeks rads, had rad fibrosis. Got Hyperbaric Oxygen therapy in conjunction with fat grafting which healed my skin almost back to normal. Despite these setbacks I was still sucessful at Implant reconstruction. Realize is still early days. Plan to keep taking Pentoxifylline and vit E for a long while yet to prevent capsular contracture. Not perfect, but enough to make me feel nearly whole. Plan to go back to my gym and change in the locker room like a normal woman again, instead of hiding and changing in the toilet.
UPDATE : List of Plastic Surgeons doing OVER Pectoral Implant Reconstruction , ( Prepectoral Implant Reconstruction ) [This list will be duplicated in a new thread]
Dr Bryan McIntosh -Bellevue, WA
Dr. Mark Tseng - Multicare, Auburn, WA
Dr Reid Mueller - OSHU, Portland, OR
Dr Kamakshi Zeidler - Campbell, CA
Dr Karen Horton--San Francisco, CA
Dr. Charlotta Lavia - Los Angeles, CA
Dr. Michael Halls--La Jolla, CA
Dr. John G. - San Diego, CA 619-222-3339.
Dr. Jyoti Arya - San Diego, CA
Dr. Julie Park - University of Chicago Medicine, Il
Dr. William Dougherty - Santa Fe, NM
Dr. Minh-Doan T. Nguyen, MD, Ph.D -Mayo Clinic, Rochester,MN
Dr Steven R Jacobson - Mayo Clinic, Rochester MN
Dr. Bruce Chau- Berkley, MI
Dr. Marissa Tenenbaum - St Louis, MO
Dr. Richard Hainer - North Oakland Plastic Surgery, Rochester, MI
Dr Michael Bateman - Denver CO
Dr. Hardy -Northwest Plastic Surgery Associates, Missoula MT.
Dr Jeffrey Lind II - Houston, TX
Dr. Lawrence Glassman - Nyack Hospital, Rockland County NY
Dr. Tzvi Small - Valley Hospital , Ridgewood NJ
Dr. Joseph Woods - Piedmont Hospital, Atlanta GA
Dr. Samir Rao - 3299 Woodburn Rd Ste 490 , Annandale, VA 22003
Dr Mark Venturi - McLean, VA
Dr. Thomas Hahm - Charleston, SC
Dr. Kevin Delaney - Medical University of South Carolina (MUSC), SC
Dr Jason Ulm - Medical University of South Carolina (MUSC), SC .
Dr. Michelle Roughton - UNC Chapel Hill, NC.
Dr Justin Sacks - Johns Hopkins, Baltimore, MD
Dr Davinder Singh - Annapolis, MD
Dr. Eric Chang - Columbia, MD
Dr Hilton Becker - Hilton Becker Clinic of Plastic Surgery, Boca Raton, Fla
EAST COAST CANADA
Dr Mitchell Brown, Toronto Canada
RESEARCH LINKS ABOUT PREPECTORAL RECONSTRUCTION
VITAMIN C HELPS WITH HEALING FROM SURGERY/and can kill bacteria such as Pseudomonas with high dose IV Vitamin C. If you can't get Intravenous Vitamin C, Liposomal Vitamin C can be a big help if you can't afford or find IV Vitamin C.
ALSO, WANT TO BRING UP ESSENTIAL OILS SUCH AS OREGANO/THYME and GOLDENSEAL have Synergistic Effects against bacteria, alone or in combination with antibiotics. I posted this info somewhere else, but copied it to here again.
Pharmacokinetics of oral vitamin C
Purpose. To test whether plasma vitamin C levels, following oral doses in supplemented volunteers, are tightly controlled and subject to a maximum in the region of 220 µm L−1, as suggested by previous researchers for depleted subjects. To determine plasma levels following single, variable‐sized doses of standard and liposomal formulations of vitamin C and compare the effects of the different formulations. To determine whether plasma levels above ∼280 µm L−1, which have selectively killed cancer, bacteria or viruses (in laboratory experiments), can be achieved using oral doses of vitamin C.
Design. This was a single blind study, measuring plasma levels in two subjects, in samples taken half‐hourly or hourly for 6 hours, following ingestion of vitamin C. Data were compared with published results and with data from 10 years of laboratory plasma determinations.
Materials and methods. Standard 1 gram tablets of vitamin C; liposomal vitamin C. Plasma levels were analysed using the method of Butts and Mulvihill.
Results. Preliminary investigations of the effects of liposomal and standard formulation ascorbate showed that blood plasma levels in excess of the previously assumed maximum of 220 µm L−1 are possible. Large oral doses of liposomal ascorbate resulted in plasma levels above 400 µm L−1.
Conclusions. Since a single oral dose can produce plasma levels in excess of 400 µm L−1, pharmacokinetic theory suggests that repeated doses could sustain levels well above the formerly assumed maximum. These results have implications for the use of ascorbate, as a nutrient and as a drug. For example, a short in vitro treatment of human Burkitt's lymphoma cells with ascorbate, at 400 µm L−1, has been shown to result in ∼50% cancer cell death. Using frequent oral doses, an equivalent plasma level could be sustained indefinitely. Thus, oral vitamin C has potential for use as a non‐toxic, sustainable, therapeutic agent. Further research into the experimental and therapeutic aspects of high, frequent, oral doses of ascorbic acid either alone or (for cancer therapy) in combination with synergistic substances, such as alpha‐lipoic acid, copper or vitamin K3, is needed urgently.
Essential Oils and Their Components as Modulators of Antibiotic Activity against Gram-Negative Bacteria ..
Essential Oils and Future Antibiotics: New Weapons against Emerging ' Superbugs ' ?
Nicholas A Boire1, Stefan Riedel2 and Nicole M Parrish2*
1The Johns Hopkins University, Bloomberg School of Public Health, Baltimore, Maryland, USA
2 Department of Pathology, Division of Microbiology, The Johns Hopkins University, School of Medicine, Baltimore, Maryland, USA
www.microbiology5.org › book
by H Padalia - 2015 - Cited by 2 - Related articlesEssential oils can be individually effective or they may be combined with antibiotics or plant extracts. Traditional healers often use combinations of plants to treat or cure diseases and found that synergy was most
According to a report published in The Review on Antimicrobial Resistance, the government of the United Kingdom estimates that by the year 2050, more than 10 million deaths and 100 trillion dollars in global health care costs will have resulted from drug-resistant microbes.
Log in to post a reply