
Woman can no longer walk, talk or feed herself after Brazilian butt lift cosmetic surgery went horribly wrong
Daidys Pena Garces, 50, underwent the procedure, also known as a BBL, at A&E Med Spa in Miami on May 15, 2023.
The operation was performed by Dr. Fermin Morales, who only weeks later caused another BBL patient's death following the procedure, state health officials said.
The operation involves taking fat from the hips, abdomen and other areas via liposuction, before injecting it into the buttocks.
Recipients hope for a bigger, more pert behind, but experts have long warned of the dangers of BBLs, which can prove fatal.
Less than a month after her procedure, Garces suffered a pulmonary embolism that caused severe brain damage and left her unable to walk, talk or feed herself, according to her husband, Jorge Fernandez.
'She was my first, like my first love,' he told WSVN. '[Now] she never more will talk or walk or eat by herself.'
Fernandez filed a medical malpractice lawsuit against A&E Med Spa and Morales, who is certified as a general surgeon, not a plastic surgeon, in June.
The lawsuit claims Garces was not made aware of the risks associated with the elective surgery or of Morales' qualifications because the med spa withheld information from her.
'This pulmonary embolism occurred because of this surgery,' Fernandez's attorney, Lavenia Santos, told WSVN.
According to the lawsuit, Garces was never made aware that Morales was not a plastic surgeon.
'From representations made by the agents at A&E Med Spa, any reasonable person would be led to believe that Fermin Esteban Morales, M.D., was Board Certified in Plastic Surgery when, in fact, he was not,' the court document said.
'Garces would not have undergone the high-risk plastic surgery procedure had she known that [Morales] was not a trained and board-certified plastic surgeon.'
In Florida, there is no legal requirement that a doctor be a board-certified plastic surgeon to preform a BBL.
'The woman has no idea that she is not being cared for by a board-certified plastic surgeon. That's just wrong,' Santos said.
'If the public knew that, they probably not be so willing to go, regardless of price. What happened to her shouldn't happen to anyone.'
A GoFundMe page set up for Garces and Fernandez said that she 'had no idea the surgeon was unqualified.'
'Daidys required emergency medical care and was hospitalized for seven months due to the pulmonary embolism,' it read.
'Now, Daidys is unable to perform any activities of daily living without assistance. Along with facing an extended recovery process, she is now burdened with growing medical bills and ongoing treatments.'
Additionally, the lawsuit argues that Garces was not properly made aware of the medical risks of the operation because all of the informed consent documents she signed were in English, not her primary language of Spanish.
In their response filing, A&E Med Spa denied all of the allegations. Their attorneys told the local news station that Morales no longer works there.
The Daily Mail contacted A&E Med Spa, their attorneys, Morales and his current employer, New Life Plastic Surgery, for comment.
In February, Morales was accused by the Florida Department of Health of causing a BBL patient's death in 2023, the same year as Garces' operation, the Miami Herald reported.
On June 7, 2023, Morales allegedly injected fat into the wrong area during a 40-year-old woman's BBL procedure at Doral's Venus Cosmetic Institute/DASO Plastic Surgery, located in a strip mall.
The woman died the next day and her autopsy found 'copious globules of lacerated fat throughout her left and right superficial and deep gluteal muscles' and 'fat globules in blood' in her left lung vessels.
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Daily Mail
13 minutes ago
- Daily Mail
Woman who was told by doctors that symptoms were 'all in her head' for YEARS lays bare gruesome health battle
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'But when I lost over 20 pounds in just a few months without trying, I knew something was seriously wrong. 'The signs were subtle at first – bloating after eating, fatigue, upper abdominal pressure and pain, especially after caffeine or carb-heavy meals. 'I started by changing my diet, thinking it was something I could fix on my own. 'When that didn't help, I went to a GI specialist who quickly dismissed my concerns, chalking it up to anxiety from nursing school.' But Hannah's pain became 'relentless' – and impossible for her to ignore. She continued: 'It felt like my upper abdomen was being squeezed from the inside like there was a tight fist around my organs that never let up, especially when I ate or drank anything. 'It wasn't just discomfort, it was debilitating. Every meal felt like a punishment. The pressure would build so intensely that it made it hard to breathe or think straight. It completely took over my life.' 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'But along the way, I've also discovered a strength I didn't know I had. I've learned to slow down, to listen to my body, and to find beauty in small moments of peace. 'My greatest wish in sharing my story is that other people will feel seen, understood, and reminded that even in the hardest seasons, healing is still possible.'


The Independent
an hour ago
- The Independent
Hundreds of CDC employees get layoff notices just days after workers return to HQ in wake of shooting
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Reuters
an hour ago
- Reuters
Leading Researchers Reject FDA's Position, Find No Evidence of Harm From 7-OH in Response From Shaman Botanicals to FDA
WASHINGTON, DC, August 21, 2025 (EZ Newswire) -- Shaman Botanicals has issued a formal response to the FDA's recent warning letter on its 7-hydroxymitragynine (7-OH) products, backed by reports from leading researchers at Johns Hopkins, Harvard, UCLA, and other institutions. The company argues that current scientific evidence supports the safety of 7-OH, directly countering FDA's claims. Experts consulted — including those previously cited by FDA — stress that 7-OH should not be considered a public health crisis and that available data shows no evidence of overdose deaths, respiratory depression, or widespread dependence. The experts also emphasize that 7-OH is a naturally occurring kratom-derived compound, not synthetic, and that preclinical studies commissioned by Shaman found no serious toxicity. Collectively, the findings point toward a favorable safety profile and call for continued study rather than scheduling. Shaman Botanicals maintains its commitment to scientific transparency and consumer safety, urging FDA to follow the science. Key Points See the full Shaman Botanicals, LLC response below: Shaman Botanicals, LLC Responds to FDA Warning Letter with Scientific Reports by Renowned Experts Shaman Botanicals, LLC, a leading innovator in botanical wellness, has formally responded to a recent warning letter from the U.S. Food and Drug Administration (FDA) regarding its 7-hydroxymitragynine (7-OH) products. In support of its mission and to defend its products, attorneys for Shaman Botanicals have assembled an interdisciplinary team of renowned researchers, scientists, and clinicians to prepare reports that directly address the FDA's claims concerning 7-OH. "The FDA asserts that there is insufficient information about the safety of our 7-OH products. However, the scientists consulted by our legal team have found that the evidence to date supports the safety of our products,' stated Stephen 'Vince' Sanders, II, founder of Shaman Botanicals. Scientists Cited by the FDA Express Concerns About the Scheduling of 7-OH Scientific reviews were provided by Dr. Kirsten Smith, PhD, widely regarded as the leading clinical researcher on kratom in the United States and an Assistant Professor at Johns Hopkins University, and Dr. Edward Boyer, MD, PhD, a Harvard-educated medical toxicologist with extensive experience in kratom research. The support for further study and regulation of 7-OH products by Drs. Smith and Boyer reflects a growing and dynamic shift in the scientific community's perspective on 7-OH. Work by Drs. Smith and Boyer was cited by the FDA in their recent report recommending the scheduling of 7-OH. Both Drs. Smith and Boyer are currently leading projects to better understand 7-OH use patterns in the United States. But, having looked at the latest data, they do not agree with FDA's position. Other scientists cited in Shaman's response to the FDA include Dr. Michael Levine, MD, a medical toxicologist educated at Chicago Medical School and an associate professor at the University of California-Los Angeles, recognized for his research in botanical toxicology, and Dr. Jackob Moskovitz, a Technion-Israel Institute of Technology-trained biochemist and internationally recognized expert in molecular biology. Drs. Levine and Moskovitz were provided with three preclinical studies commissioned by Shaman and asked to comment on them. Shaman's response also cited Dr. Glenn Prestwich, PhD, a Stanford-educated chemist and internationally recognized authority on natural products chemistry and chemical biology, and Dr. Andrew Monte, MD, PhD, the Associate Director of the Rocky Mountain Poison & Drug Center in Denver, Colorado, and an expert in nationwide monitoring for adverse events from opioids. 7-OH Should Not Be Considered a Public Health Crisis Dr. Smith strongly disagrees with the FDA's recent recommendation to schedule 7-OH. According to Dr. Smith, the use of 7-OH does not constitute a public health crisis. Furthermore, Dr. Smith asserts that, much like kratom, 7-OH currently offers a net benefit to its users. According to Dr. Smith, who estimates that at least 4 million adults have tried 7-OH, there are no confirmed human cases of respiratory depression caused by 7-OH. Additionally, reports of physical dependence or substance use disorder related to 7-OH are even rarer than those associated with kratom. 7-OH Is Not Causing Widespread Illness or Injury Dr. Boyer reviewed nationwide toxicology databases, including poison center data, and found limited evidence of acute overdose risk from 7-hydroxymitragynine. No deaths have been attributed to 7-hydroxymitragynine, a finding confirmed by America's Poison Center in their August 12, 2025 report. As Dr. Boyer stated, 'A signal arising from overdose death from 7-hydroxymitragynine is absent. Based upon data available at this time, given the degree of population exposure, the lack of findings suggests that 7-hydroxymitragynine carries no unreasonable risk of overdose death.' Dr. Monte arrived at the same conclusion as Dr. Boyer, that there is currently no evidence of a safety signal regarding 7-OH as reported by independent poison control and toxicology centers across the United States. Dr. Boyer also disagreed with the FDA's report regarding the putative safety or danger of 7-OH. According to Dr. Boyer, the FDA assessment relies on animal studies receiving intravenous 7-hydroxymitragynine (a route of administration never used in humans) and overlooks existing data indicating low bioavailability, rapid clearance, and poor brain penetration characteristic of oral 7-hydroxymitragynine. 7-OH is a Natural Product; Not Synthetic Opponents of 7-OH often mistakenly label these kratom-derived products as 'synthetic.' According to Dr. Prestwich, '7-OH is not manufactured synthetically.' Instead, 7-OH is a naturally occurring selective oxidation product of mitragynine, already present among the indole alkaloids in kratom plant extract. These products contain 7-OH that is chemically identical to the natural metabolite of mitragynine produced by the kratom plant and through metabolism in the human body. Thus, 7-OH is a natural product. Pre-Clinical Data Conducted by Shaman Botanicals Supports the Favorable Safety Profile of 7-OH Drs. Levine and Moskovitz each reviewed three preclinical studies commissioned by Shaman: (1) 'Acute Toxicity Assessment of 7-Hydroxymitragynine in Rodents,' (2) 'Pilot Safety Study of Escalating Doses of 7-Hydroxymitragynine and Mitragynine Pseudoindoxyl Administered Daily for 7-day Intervals to Mature Dogs,' and (3) 'An In-Vitro Pre-Clinical Safety Comparison of Mitragynine and its Oxidative Metabolites: 7-Hydroxymitragynine and Mitragynine Pseudoindoxyl.' In the two animal studies, no serious clinical toxicity or adverse events were observed. Dr. Levine stated these studies support initial safety and warrant further evaluation. Dr. Moskovitz concluded, 'Based on all the obtained data (i.e., in vitro studies, mice and dogs' models), it seems that the therapeutic potency and safety profile of 7HMG are either the same or better compared to mitragynine.' Current Science Supports a Reasonable Basis of Safety and Recommends Continued Study, Not Scheduling Full copies of each expert report have been provided to the FDA. 'The FDA pledged to follow the science. The aforementioned experts, some of the top scientists in the world, maintain the science supports a reasonable basis of safety in our 7-OH products,' said Sanders. Commitment to Transparency and Consumer Safety Shaman Botanicals remains deeply committed to transparency, scientific rigor, and consumer welfare. The company welcomes continued dialogue. About Holistic Alternative Recovery Trust (HART) Holistic Alternative Recovery Trust (HART) is a national nonprofit organization advocating for science-based policy, regulatory transparency, and access to safe, plant-based alternatives to opioids and other pharmaceuticals. 7-hydroxymitragynine (7-OH), a metabolite of mitragynine, the most abundant alkaloid found in kratom, is a new tool being used to combat opioid misuse and improve public health. HART strongly supports robust regulation to mandate that all 7-OH products are manufactured safely, are marketed transparently, and are kept out of the hands of children. Learn more at opens new tab. Media Contact HART Mediamedia@ ### SOURCE: Holistic Alternative Recovery Trust (HART) Copyright 2025 EZ Newswire See release on EZ Newswire