Category Archives: Health

Diabetes type 2: Treatment for blood sugar includes onions suggests study

Type 2 diabetes means the pancreas does not produce sufficient insulin to regulate blood sugar levels or the insulin it does produce is not taken up by cells. Insulin regulates blood sugar – the main type of sugar found in blood. Deprived of this mechanism, blood sugar levels can soar to dangerous levels. Fortunately, there is an effective countermeasure at hand.

According to findings presented Thursday at The Endocrine Society’s 97th annual meeting in San Diego, extract of onion bulb, Allium cepa, strongly lowered high blood glucose (sugar) and total cholesterol levels in diabetic rats when given with the antidiabetic drug metformin.

“Onion is cheap and available and has been used as a nutritional supplement,” said lead investigator Anthony Ojieh, MBBS (MD), MSc, of Delta State University in Abraka, Nigeria.

“It has the potential for use in treating patients with diabetes.”

To three groups of rats with medically induced diabetes, Mr Ojieh and his colleagues gave metformin and varying doses of onion extract- 200, 400 and 600 milligrams per kilograms of body weight daily (mg/kg/day)- to see if it would enhance the drug’s effects.

READ MORE: Diabetes: The red juice that can ‘fight’ diabetes by ‘consistently’ improving blood sugar

They also gave metformin and onion extract to three groups of nondiabetic rats with normal blood sugar, for comparison.

Two control groups, one nondiabetic and one diabetic, received neither metformin nor onion extract.

Another two groups (one with diabetes, one without) received only metformin and no onion extract. Each group contained five rats.

Two doses of onion extract, 400 and 600 mg/kg/day, strongly reduced fasting blood sugar levels in diabetic rats by 50 percent and 35 percent, respectively, compared with “baseline” levels at the start of the study before the rodents received onion extract, Mr Ojieh reported.

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Allium cepa also reportedly lowered the total cholesterol level in diabetic rats, with the two larger doses again having the greatest effects.

Onion extract led to an increase in average weight among nondiabetic rats but not diabetic rats.

“Onion is not high in calories,” Mr Ojieh said. “However, it seems to increase the metabolic rate and, with that, to increase the appetite, leading to an increase in feeding.”

“We need to investigate the mechanism by which onion brought about the blood glucose reduction,” Mr Ojieh said. “We do not yet have an explanation.”

READ MORE: Diabetes: The cheese to ‘significantly’ reduce blood sugar without increasing cholesterol

The study, which also involved scientists from Cranfield University in the UK, found that the brown skin and external layers of onions contain useful amounts of fibre and flavonoids, and that the bulbs contain sulphurous compounds and fructans.

The research showed that because the brown skin of the onion was high in dietary fibre it could be used as a functional ingredient, and that two outer fleshy layers also contain fibre and flavonoids, and have a high antioxidant capacity.

Researcher Vanesa Benitez commented: “One solution could be to use onion waste as a natural source of ingredients with high functional value, because this vegetable is rich in compounds that provide benefits for human health.”

She added: “Eating fibre reduces the risk of suffering from cardiovascular disease, gastrointestinal complaints, colon cancer, type 2 diabetes and obesity.”



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Percutaneous Revascularization for Ischemic Left Ventricular Dysfunction

Abstract

Background

Whether revascularization by percutaneous coronary intervention (PCI) can improve event-free survival and left ventricular function in patients with severe ischemic left ventricular systolic dysfunction, as compared with optimal medical therapy (i.e., individually adjusted pharmacologic and device therapy for heart failure) alone, is unknown.

Methods

We randomly assigned patients with a left ventricular ejection fraction of 35% or less, extensive coronary artery disease amenable to PCI, and demonstrable myocardial viability to a strategy of either PCI plus optimal medical therapy (PCI group) or optimal medical therapy alone (optimal-medical-therapy group). The primary composite outcome was death from any cause or hospitalization for heart failure. Major secondary outcomes were left ventricular ejection fraction at 6 and 12 months and quality-of-life scores.

Results

A total of 700 patients underwent randomization — 347 were assigned to the PCI group and 353 to the optimal-medical-therapy group. Over a median of 41 months, a primary-outcome event occurred in 129 patients (37.2%) in the PCI group and in 134 patients (38.0%) in the optimal-medical-therapy group (hazard ratio, 0.99; 95% confidence interval [CI], 0.78 to 1.27; P=0.96). The left ventricular ejection fraction was similar in the two groups at 6 months (mean difference, −1.6 percentage points; 95% CI, −3.7 to 0.5) and at 12 months (mean difference, 0.9 percentage points; 95% CI, −1.7 to 3.4). Quality-of-life scores at 6 and 12 months appeared to favor the PCI group, but the difference had diminished at 24 months.

Conclusions

Among patients with severe ischemic left ventricular systolic dysfunction who received optimal medical therapy, revascularization by PCI did not result in a lower incidence of death from any cause or hospitalization for heart failure. (Funded by the National Institute for Health and Care Research Health Technology Assessment Program; REVIVED-BCIS2 ClinicalTrials.gov number, NCT01920048.)

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‘I didn’t care if it killed me’

After feeling deep, aching pain in her right lung for two years following COVID-19, Lily Godsoe of Half Moon Bay is grateful to the woman who made the anguish go away.

Her savior wasn’t the doctor who peered at her X-rays and prescribed inhalers that didn’t help. It was the Costco vendor who sold her an elixir of turmeric, extra-strength, on sale for $20.

Godsoe never got her name. But in April the vendor prescribed three daily teaspoons of the orange liquid — always chilled. In a week, Godsoe was a believer.

“I realized that I felt well. It was really shocking,” said Godsoe, 54, an interfaith minister so debilitated by long COVID that she had to quit her job. “I had forgotten what it felt like to feel normal.”

Godsoe didn’t know that the Food & Drug Administration had its eye on the turmeric maker, Quten Research Institute in New Jersey, whose “therapeutic anti-inflammatory” claim for the plant-based product earned a rebuke in 2020 for “misbranding.”

But it might not have mattered. To Godsoe and thousands of other long-COVID sufferers whose doctors have been unable to relieve their mysterious symptoms, such unproven, poorly tested, or just off-label remedies provide hope and — sometimes — help.

The names read like cure-alls touted by 19th-century hucksters: hyperbaric oxygen, intravenous ozone, herbal tollovid, the Patterson Protocol. Some are under serious study by scientists seeking verifiable treatments. Others could be quackery, or even harmful.

“There’s always the danger that people will try things they shouldn’t,” said Lisa McCorkell of Oakland, a co-founder of the Patient-Led Research Collaborative, a nonprofit seeking to speed up the search for good long COVID treatments.

Colin Bennett, 34, has already spent a remarkable $100,000 on untested therapies and do-it-yourself remedies in hopes of conquering the barrage of post-viral symptoms that turned the financial analyst and golfer into a de facto old man since he got the virus a year ago.

But he only went rogue — even flirting with the notorious horse de-wormer, ivermectin — after doctors at Stanford, the University of Southern California, three University of Californias and various ERs failed to alleviate his ailments: brain fog, maddening tinnitus, varicose veins, hair loss, rapid heartbeat (a common long COVID symptom called postural orthostatic tachycardia syndrome, or POTS) and chest pain that, at its worst, “felt like someone was stabbing me with a super-heated poker.” The list goes on.

“I never had any problems before COVID,” said Bennett, of Los Angeles.

His desperation led him to drop $1,500 on hyperbaric oxygen therapy to rejuvenate his tissues. A double-blind Israeli study of 73 long-COVID patients, published in July in the peer-reviewed journal Nature Scientific Reports, suggests this can actually work. Researchers found much improved brain function in the half who got oxygen.

Bob Lambertsen, safety director, monitors a patient in a hyperbaric chamber at Hyperbaric Medical Services on August 25, 2022 in San Francisco.

Lea Suzuki/The Chronicle

At Hyperbaric Medical Services and Wound Care in San Francisco, patients lie in a clear chamber with oxygen equal to scuba diving at 30 feet — then watch Netflix for 90 minutes. Patients often have vascular damage from diabetes, said Dr. Jamie Bigelow, the pulmonologist who runs the center. Oxygen can stimulate new growth in the tiniest capillaries.

But it can take many sessions. Each now costs $500 and isn’t covered by insurance. Of three long-COVID patients who sprang for them, a man with neuropsychological symptoms needed 60 sessions, Bigelow said. That’s $30,000. A man with POTS benefited after 10 tries, while a woman with the same condition found no relief after 20.

Bennett went 10 times in Southern California. “I didn’t really notice much,” he said. He then tried popping pineapple enzyme pills to “help with blocking the ACE2 receptors” that are implicated in opening cell doors to COVID-19, and took N-acetyl cysteine, a supplement popular with long-COVID sufferers and sold as NAC. It promises “free radical protection.”

In November, Bennett heard about exosomes, which carry molecules between cells in service of the immune system. A friend bought Bennett a $5,000 infusion when he was in bad shape.

“He wanted his golf buddy back,” Bennett mused. But the exosomes didn’t help. Nor did the electromagnetic therapy, though he slept better for awhile.

“When you’re this screwed up, you try everything,” he said. Even stem cells. At Christmas, Bennett spent $5,000 on 500 million of them that a doctor friend picked up in Mexico. “Sounds kind of shady,” he admitted. “I was so desperate that I didn’t care if it killed me.”

Bennett’s tour de treatments wouldn’t have been complete without a visit to the one doctor in the Bay Area, perhaps the country, who claims to cure nearly all long COVID patients.

“Eighty-five percent of patients get better. Maybe more,” said Dr. Bruce Patterson, who developed the “Patterson Protocol” at his San Carlos company, IncellDX, Inc.

There are no peer-reviewed studies to verify this. But that hasn’t stopped long-COVID sufferers — 30,000 of them, Patterson says — from requesting test kits, virtual consultations, and scores measuring the severity of five common symptoms.

Yet everyone gets the same two drugs: A cholesterol-lowering statin and Maraviroc, an HIV anti-viral. “Six to 12 weeks” is all it takes to get better, he claims. Patterson, an associate professor at Stanford University in the 2000s who directed a virology lab there until 2011, works with other doctors who prescribe the drugs.

One is Dean Mitchell, a New York immunologist who has monitored 20 people on the Patterson Protocol over six months. “I’m cautiously optimistic that some of have improved,” Mitchell said. “I’m watching and waiting.”

One happy customer referred to a reporter by the company, Susan Pi of Oakland, said she was so pleased that she canceled her appointment at Stanford’s long-COVID clinic. A ghost writer who got sick in 2020, Pi, now 40, suffered fatigue and post-exertional malaise for a year. “I’m fully recovered, thanks to the Patterson group,” she reported.

Colin Bennett, 34, who spent about $100,000 on everything from stem-cell infusions to the animal de-wormer ivermectin to try to cure his many long COVID symptoms, is seen here in an Orange County emergency room last year during an especially difficult period. His do-it-yourself methods worked no better than standard medical therapies, he said.

Courtesy of Colin Bennett

Bennett, though, quit halfway through. “I didn’t think it was helping,” he said. Insurance covered most of the protocol, but he’s out $1,000 for the tests. Now he takes only fistfuls of ginkgo biloba pills (a plant-based supplement reputed to sharpen thinking) and has improved enough on his own to return to work part time.

Dr. Lekshmi Santhosh, co-director of UCSF’s post-COVID clinic, cautioned against embracing unproven treatments. She offered a car analogy: If your car’s brakes failed, would you fix them with a new steering wheel?

“Because long COVID encompasses so many different symptoms, one size usually doesn’t fit all when it comes to treatment,” Santhosh said, acknowledging that research is “frustratingly slow.”

McCorkell, of the Patient-Led Research Collaborative, agreed. “We try to push for things that have been researched or validated by the community,” she said. “But it’s a tricky balance.”

Anisha Sekar of San Francisco ran ultramarathons before getting COVID two years ago. Now 31, she needs a wheelchair to go through the airport.

The tech entrepreneur says there is “exactly one” doctor who has earned her trust because she is open to trying novel but safe treatments, including prescriptions approved for other purposes. Such “off-label” uses are gold in the long-COVID community.

Sekar takes four that have helped, despite their having been approved only for narcolepsy, heart ailments, muscle weakness and allergies.

She gets most of her treatment ideas from long-COVID forums on Reddit and Body Politic. “I keep my ear to the ground,” she said. “And if I hear it enough, I’ll take it to my primary care physician and she’ll chime in with, ‘the science makes sense,’ or it doesn’t.”

Her nine over-the-counter remedies include, yes, turmeric.

Godsoe, whose relentless lung pain vanished after she began sipping turmeric, also credits six months of acupuncture with calming other post-COVID symptoms, from rapid heartbeat to joint pain. The needle treatment — in her arms, legs, torso and head — cost $140 a week.

“I really had given up hope that I was ever going to feel OK,” Godsoe said, her voice filling with emotion. Acupuncture wasn’t a total cure. But making her own treatment choices has felt therapeutic in itself.

“A sense of wellness came over me,” she said. And as symptoms eased, “I was so elated.”

Nanette Asimov is a San Francisco Chronicle staff writer. Email: nasimov@sfchronicle.com Twitter: @NanetteAsimov



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What pet owners should know

Laboratory tests from sick or dead dogs in Northern Michigan have come back positive for canine parvovirus, a highly contagious virus that can affect all dogs.

Unvaccinated dogs and puppies younger than four months old are most at risk. The virus affects a dog’s gastrointestinal tract and is spread by direct dog-to-dog contact and contact with feces, environments or people, according to the American Veterinary Medical Association.

“This situation is complex because although the dogs displayed clinical signs suggestive of parvovirus, they consistently test negative by point-of-care tests performed in clinics and shelters. Screening tests for parvo are done to help guide immediate isolation, disinfection, and treatment protocols. While those tests are valuable in the clinical setting, they are not as sensitive as the diagnostic tests we can perform here in the laboratory. We continue to further characterize the virus in hopes of better understanding why those animals were testing negative on screening tests,” MSU VDL director Dr. Kim Dodd said.

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According to Otsego County Animal Control, the 30+ dogs that died came from different areas and different owners. A puppy mill was not involved and the dogs were not one type of dog breed.

Animal control officials urge people to make sure their dogs are properly vaccinated. They also said when traveling to consider not allowing their dogs to go potty in areas where numerous other dogs have gone. It’s also very important to clean up after your dogs.

They also made the following statements on Facebook, hoping to clear up any confusion:

  • The illness does not affect certain breeds more than others

  • They have heard of many counties around northern and central Michigan with reports of illnesses

  • They have not seen any properly vaccinated dogs die

  • Those affected have been puppies under two and elderly dogs

Read: Here’s how Parvo-like illness is affecting young dogs in Michigan

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How you can protect your dog from parvovirus

The most important way to protect your dog is to keep up with routine vaccinations, especially if you plan on traveling.

Ensure your dog is vaccinated against canine parvovirus, rabies, canine distemper, adenovirus, parainfluenza, and leptospirosis.

If you have a puppy, make sure it has been fully vaccinated before you allow it to interact with other animals. You should keep all dogs and puppies away from other dogs if they have any signs of illness.

Make sure you clean up after your pet when you’re walking them in public to prevent the spread of illnesses. The virus can spread from place to place on the hair or feet of dogs, or through contaminated cages, shoes or other objects.

Parvovirus is resistant to heat, cold, humidity, and drying. It is known to survive in the environment for long periods of time, which is why it’s so important to get your dog vaccinated.

Parvovirus is not contagious to people or other animals.

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Symptoms of parvovirus in puppies

Most deaths from parvovirus occur within 48 to 72 hours following symptom onset, according to the AVMA. There aren’t any specific drugs that can kill the virus in infected dogs and treatment is to support the dog as it fights the infection.

The American Kennel Club said the following are symptoms of parvovirus in puppies.

  • Bloody diarrhea

  • Vomiting

  • Fever

  • Lethargy

  • Anorexia

  • Weight loss

  • Weakness

  • Dehydration

  • Depression

If your puppy has any of these symptoms you should contact your veterinarian.

How to clean after parvovirus

It is very difficult to completely eliminate the virus in your home after an infection has been present.

According to McEwen Animal Clinic, freezing is completely protective to the virus so if your yard is frozen you have to wait for it to thaw before you introduce a new puppy. Shaded areas should be considered contaminated for seven months and sunny areas should be considered contaminated for five months.

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According to the University of Wisconsin-Madison School of Veterinary Medicine, bleach works for inactivating the virus. Bleach can be used on surfaces such as stainless steel or sealed floors but another option should be used for porous surfaces.

Read: All 4 Pets coverage

Copyright 2022 by WDIV ClickOnDetroit – All rights reserved.

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I Had Monkeypox, and the Physical and Emotional Pain Were Excruciating

  • Insider’s Joel Marino got monkeypox in July. The pain was so bad he couldn’t lie down at times.
  • Marino said the stigma was awful — with monkeypox, people look at you differently.
  • This is Marino’s story, as told to Insider reporter Hilary Brueck.

I spent most of June isolating with COVID-19, a disease I’d managed to avoid until this summer. Frustratingly, as an out gay man, the diagnosis meant spending nearly all of Pride Month by myself, pacing my New York City apartment. I canceled plans with friends and stayed in.

This was supposed to be the year that nothing was going to stand in my way. The start of the pandemic in 2020 and the 2021 Delta surge had put a damper on two Pride celebrations; I didn’t want to miss out on a third. 

So once my week of fever, fatigue, and chills was behind me, and I tested COVID negative for three days in a row, I made a beeline for a queer dance party in Manhattan on the last Sunday in June. 

It was a fantastic night. Finally, after so many months of being careful, getting vaccinated and boosted, and taking necessary pandemic precautions (which, honestly, meant less dating), I was able to touch strangers again and we could enjoy it. I danced, I kissed, I conquered. I met someone and we asked each other coyly, “Your place or mine?”

Monkeypox feels like something that happens to other people. Until it’s not.

Monkeypox lesions visible near my hairline.

Joel Marino


There wasn’t much talk about monkeypox going around the club then. People briefly mentioned it, if nothing else to laugh at the bad name, but it still felt like something that was happening to other people, somewhere else. 

My mom, who was already worried about me recovering from COVID, had texted me and suggested that maybe I should get vaccinated with Jynneos, but there were barely any monkeypox vaccines available in the city at that time. It was so hard to get an appointment, people often waited hours and hours in the blistering sun, and I just thought, “What are the chances, really, of catching this thing?” I hadn’t heard of anybody who had caught monkeypox yet in my social circle, or even on social media.

I spent a week feeling good after the party, reconnecting with friends after my COVID infection, and soaking up summer. 

Then, about nine days after the dance, I started to feel a strange itch in the back of my throat. The tickle progressed into swelling over the next several days. I went to urgent care. No one even mentioned monkeypox. It wasn’t on my mind, or anyone else’s. I was tested for strep, syphilis, and other diseases. Nothing came back positive. 

My monkeypox appeared overnight



I counted at least 25 lesions on my body, including on my face, arms, legs, glutes, and in my mouth.

Joel Marino


On Sunday, a full two weeks after the party, I woke up and suddenly realized my throat was so swollen I couldn’t swallow properly. I couldn’t talk. I rushed to the mirror and, to my horror, my body was covered in little pimples and blisters. They had surfaced overnight like a bunch of mosquito bites. 

I had little red bumps all over my body — I counted more than two dozen on my face, hands, arms, legs, abdomen, and butt. I knew instantly that I had caught monkeypox. The incubation period lined up neatly with the dance party. 

The monkeypox diagnosis was so much harder on me than COVID, not just physically (the lesions were so painful at times that I could not even sit or lie down) — mentally and spiritually, the disease also really took a toll.

COVID didn’t hurt me in the same way emotionally. The disease has been intensely studied for more than two years, there are vaccines, booster shots, and treatments available, plus I knew what to expect. I have so many friends who’ve shared what it feels like to get COVID, so my loss of smell and taste weren’t a surprise, and mercifully the US now has a bountiful supply of free, at-home tests to confirm a diagnosis.

Surviving monkeypox meant dealing with internalized homophobic thoughts I hadn’t acknowledged in years

Monkeypox felt like my punishment for being a proud gay man. Having grown up in a fundamentalist Christian family, the son of a Pentecostal minister, I found thoughts that I’d abandoned long ago racing back into my fever dreams.

As I sweat through my sheets and my temperature climbed to 104 degrees Fahrenheit, I briefly considered going to the hospital, but I worried about putting others at risk, or getting stuck at the hospital for days on end, and eventually I thought, “Well, I just got through COVID by myself. I can get through monkeypox by myself, too.” 

Being home alone with monkeypox gave me a lot of time to think, overthink, and dissect my own thoughts about the diagnosis: “Is this a punishment from God? Have my wanton ways caught up to me? Have I been too hedonistic, and this is the universe’s cruel way of telling me so?”

Ideas about being gay that I hadn’t grappled with since my father put me into a single session of “reparative therapy” at age 19 all came swirling back. 

I wasn’t the only one having them.  

A lot of people have been spewing nasty rhetoric, both clear and coded, about the ways that people are getting monkeypox, suggesting monkeypox spreading to kids is something predatory and pedophilic, or even just that the disease isn’t their concern. Marjorie Taylor Greene’s comments that monkeypox is “not a threat” to “most of the population” were probably some of the most upsetting for me — such a classic othering of gay people, much like what happened during the AIDS crisis when I was a kid. It’s painful to see people still react this way when gay people get sick.

Watching episodes of “RuPaul’s Drag Race” and “Love, Victor” as I recovered really helped me counterbalance the apocalyptic, religious thoughts going on in my head. “Hey, it’s OK being gay, Joel,” I told myself. “Keep remembering that.”



“RuPaul’s Drag Race” was my salve for internalized homophobia.

VH1


My colleagues sent me pints of ice cream as a get-well gift, and the cold treat really helped with swelling in my throat (so did gargling salt water, although it was too painful at first). 

My scars, both the physical and emotional ones, are still healing

As I recover from monkeypox, I’ve been spending time visiting my family, and it’s nice to be together in person with the people I love after spending so long by myself sick and in isolation this summer. But there are things we do not mention. 

I haven’t pointed out to them the still-healing monkeypox scars on my body, the pinkish new skin left where lesions have scabbed off. Acknowledging the scars would be acknowledging my gayness in front of them. We don’t do that anymore. I came out to my family as a teenager, and after many contentious years in my 20s, we’ve reached a place now where nobody really wants to talk about my homosexuality. It’s too upsetting for everybody, including me. Seeing the visible scars of my infection as I type on my computer makes me wonder: “Is this something I have to address?” 



What my thumb looked like on July 13, left, and July 21, right. I named this particular lesion “Postule Malone.” There was also “Susan Boil” on my leg, a cluster on my torso I called “Legions of Tomorrow,” and “Blister Mistoffelees” on my nose.

Joel Marino


Once you have monkeypox, people start looking at you differently. A lot of my friends have asked me some version of a raised-eyebrow “How did that happen?” — which is something no one ever wondered about my COVID diagnosis. 

Now I tell all my gay friends, “Please get vaccinated as soon as you can.” Some have, others say “I’m careful” or “I’m in a relationship,” suggesting they aren’t worried about getting infected yet. 

People need to realize monkeypox is happening to people they know and love. And it isn’t a punishment for any moral misdeeds.

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Detransitioner says he was ‘brainwashed’ into having gender reassignment surgery by woke doctors

A detransitioner has told how he was ‘brainwashed’ into having gender reassignment surgery after believing himself to be a woman trapped in the wrong body.

Going by the name Shape Shifter, the 32-years-old who lives in Massachusetts grew up in a Muslim country in the Balkans where even being gay was frowned upon, but he believed that if he transitioned to female he would finally feel happy with himself.

He was given a referral letter by Fenway Health in Massachusetts, which he claims has been taken over by biased pro-trans activists.

The surgery itself was performed by Dr Sherman Leis of the The Philadelphia Center for Transgender Surgery. Leis is regarded as the United States’ most experienced gender reassignment surgeon.

But soon after the operation was complete in 2015 in his mid-20s, Shape Shifter quickly realized he had made a terrible mistake, and that he was just a gay man who enjoyed presenting in a feminine way. 

The procedures he has undergone – which include the removal of his penis and the creation of a ‘neo-vagina’ are irreversible.

They have left him with osteoporosis, scoliosis, a ‘vagina’ which his body believes is a wound, and which it tries to close up, as well as a host of mental health conditions including depression and a reduced sex-drive.  

Shape Shifter believed that making the initial switch to a woman would make him finally feel happy in his own body.

But he ended up feeling even more depressed than before the surgery, ultimately realizing that he was simply a man who enjoyed expressing his femininity. 

He still wears makeup, and has long hair, but says men like him need to be encouraged to feel comfortable in their femininity, without feeling pressured into medically transitioning.  

Shape Shifter, 32, was born male, transitioned to female but then reverted back. The surgeries have left him without a penis and without a working vagina also

Speaking to Blaire White, 28, herself transgender, during a more than hour-long interview, he explained how after the initial surgery to become female he suddenly fell into a deep depression.

During the interview, which has been posted to YouTube and received almost 500,000 views, Shape explained how the new vagina that had been constructed for him using tissue from his penis fell far short of expectations and left him unable to have intercourse.

‘I was happy maybe for a month or two but then got even more depressed after surgery. My neo-vagina started constricting. I thought I was going to spread my legs and get f****d and that never really happened after I gave away my penis.   

‘I was online telling people how depressed I was. A lot of people thought it was because of the surgery… but I had no energy, I was so lethargic, I had brain fog and no sex drive at all. I then found that all the tranny-chasers stopped following me and I was competing with other women for men.’

Shape believes a lot of people would reconsider having surgery in the first place if they knew of the possible complications and regret that can follow

White asked Shape what it was like to ‘miss your penis’.

‘I just wanted to have my surgery and then blend in and complete my transition. When I started taking testosterone I had no sex drive. I went from enjoying sex to avoiding it,’ Shape explained.

‘I miss just being an average dude and obsessing over sex, money and my career. It sucked being heteronormative and doing the whole emotional thing. Now I feel like a man trapped in a woman-lookalike body.

‘I will never be able to get my penis back which is extremely traumatic for me. I want it back and I can’t. Sex is traumatic for me now because I’ve had botched surgeries.’

Shape says he even dreams about having a penis, while before his first transition he would dream about having a vagina.  

Host, White, asked how difficult it was for Shape to revert to being male. 

Speaking to Blaire White, 28, right, herself transgender, Shape warns others who may be considering transitioning to think carefully of their options beforehand

Shape, pictured, says he even dreams about having a penis, while before his first transition he would dream about having a vagina

‘These detransitioners regret the surgeries and then because they’ve got the surgeries they’re seen as like an enemy by these activist doctors and then they can’t even get help to revise the surgeries because trans surgeons hate detransitioners?’ White suggested. 

‘Pretty much’, Shape responded. 

‘What they don’t tell you is because they’ve labelled them as difficult patients but even beyond that, the one thing they don’t tell you is once your first surgery didn’t go right and second one didn’t go right, after a while nobody wants to touch other surgeons work because they don’t want to attach their name to a complicated case.  Every time you go in there is more scar tissue and more complications.’

Shape said that despite wanting to detransition he is happy to present as female and appear like a woman in terms of how he dresses.

‘I just declared myself to be a woman but when i changed my paperwork or when it was all libbed out and drinking kool-aid and was brainwashed by the trans community. I simply enjoy presenting as feminine and having long hair.’

In a more than hour-long interview, Blaire White, herself trans, asked Shape Shifter what it was like to ‘miss your penis’ now that he is male once again

Shape says that he is trying to navigate his sexuality moving forward.

‘Looking back I don’t think my mind was able to comprehend what was happening. Even when I was a woman, I only knew what it was like to be a man on estrogen. And now I can’t go back to being a traditional man.’

‘I will never know what it’s like to be a woman, at least biologically,’ added host, White, agreeing with him.

Shape explained how there is no long-term research as to what taking all of the artificial hormones will do to his body in the long term.

‘I’ll have to have some kind of hormone in my body so it’s going to be estrogen only because if I don’t take any hormones, I already have osteoporosis and it will continue to get worse. I went almost seven years without any hormones. The hormones I am taking are similar to what women get during menopause.’ 

Shape explained how having undergone the surgeries, neither having a working penis nor a vagina that functions and now required to take hormones for the rest of his life, feels like a medical experiment gone horribly wrong.

Shape explained how neither having a working penis nor a vagina that functions and required to take hormones for the rest of his life, feels like a medical experiment gone horribly wrong

‘It’s transphobic to say it but after I’ve been through the system, I 100 percent feel like I was part of some cruel medical and social experiment – except nobody checked in on me,’ Shape explained. 

‘If I’d killed myself I would not have even been included in any statistics. I’m sure they would just write me off as the cause being some other issue. Moreover, I’ve spent thousands of dollars. I’ve traveled across the country and did all the consults trying to get help.’

Shape believes that a lot of people might reconsider having surgery in the first place if they knew of the possible complications and regret that can follow in the moments following transitions. However, he believes it would be ‘bad for business’ if surgeons alluded to such realities. 

After his first surgery to become female, Shape Shifter quickly realized he had made a terrible mistake, and that he was just a gay man who enjoyed presenting in a feminine way

Shape has blamed Fenway Health, an LGBT health care and advocacy organization based in Boston, Massachusetts for the position he finds himself in currently.

‘One of the biggest mistake is because I went to Fenway Health. A lot of their staff is LGBT and one of my therapists was trans as far as I know. Initially I thought it was good because she would understand me but now looking back she was biased. You know it’s kind of an activist hospital in a way.

‘I feel like my life would have been better and more productive if over the last 10 years I spent expanding definition of what it is to be a man instead of trying to just blend in like society wants and trying to be a heteronormative woman. 

‘I don’t really know what the future holds. But we need to go back to the science lab to work out what true trans is. Do you want to be on hormones or have surgery?’

‘I f****d up my life, I could have been so much more.’

Shape feels his time might have been put to better use by defining what it is to be a man instead of trying blend into society as a woman

The whole issue of gender reassignment surgery has been the subject of heated debate recently after Boston Hospital was forced to defend itself over its Gender Multispecialty Service Program, or GeMS, which it claims provides gender-affirming care to ‘eligible adolescents and young adults’. 

The hospital prides itself on being ‘home to the first pediatric and adolescent transgender health program in the US’ and has been accused, it says falsely, of performing hysterectomies to underage children as part of that care. 

Much of the controversy stems from an allegation on right wing social media sensation LibsofTikTok – who was doxed as Brooklyn real estate agent Chaya Raichik – that the hospital offered such treatment, in a still public tweet.

The claims are based off of videos from the hospital’s YouTube account that discusses medical care provided to transgender patients. The video has since been removed.  

The story gained traction among activists critical of gender affirming care for underage kids, even going as far as former advisor to President Trump Stephen Miller, who called it ‘monstrous’. 

Podcaster David J. Harris called one of the videos ‘pure evil’ and made the claim of underage hysterectomies. 

Activists Christopher Rufo and Matt Walsh also slammed the hospital, with Walsh saying: ‘Every sane and decent human being in the country must unite against it’. 

Posters on right wing message boards have even allegedly called for the doctors to be ‘executed’ and to call the hospital on the phone, according to Vice.   

Boston Children’s Hospital prides itself on being ‘home to the first pediatric and adolescent transgender health program in the US’ says it’s faced threats and false claims

Boston Children’s told DailyMail.com in a statement: ‘The commentary and the online attention that followed was based on the incorrect statement that Boston Children’s performs genital surgeries on minors in connection with transgender care’. 

‘For hysterectomies and other genital surgeries performed as part of gender-affirming care, Boston Children’s requires a patient to be capable of consenting for themselves. Age 18 is used to reflect the standard age of majority for medical decision-making. Boston Children’s does not perform genital surgeries as part of gender-affirming care on a patient under the age of 18.’

Multiple fact-checkers, including PolitiFact and Lead Stories, both debunked the idea that they perform hysterectomies on children. 

The hospital’s statement continues: ‘We are deeply concerned by these attacks on our clinicians and staff fueled by misinformation and a lack of understanding and respect for our transgender community.’

Libs of TikTok then went on to claim that the hospital’s denial was a lie and said that they had materials allowing girls to get surgeries as young as 17 in a Substack post. 

The account wrote: ‘Although I never mentioned a specific age, Boston Children’s does in fact provide ‘gender-affirming’ surgeries for minors. After the videos went viral, they quietly updated their website. They changed the age of requirement for a vaginoplasty from 17 to 18 and added ‘we only perform gender-affirming hysterectomies on patients who are age 18 or older.’ 

A molecular geneticist participating in a UC Berkeley debate argued that trans women are not women and should not be legally treated as such, citing women’s safety fears of trans women in changing rooms and prisons

Issues over trans women also became a topic of discussion earlier this month when a female molecular geneticist participating in a UC Berkeley debate argued that trans women were not women and should not be legally treated as such, citing examples of women’s safety fears of trans women in changing rooms and prisons.

The geneticist argued that legally treating trans women as women, and allowing them into changing rooms and prisons, means women have put a man’s comfort ahead of their own safety – claiming that the behavior of men is inherently different than that of women.  

‘Women have internalized misogyny to the point where the man’s comfort takes precedence over the woman’s safety,’ she said. ‘This is the most insane thing that has happened in my life, that women are a feeling now.’

‘There’s a reason why they (trans women) don’t want to be in men’s prisons,’ she said. ‘Men beat each other to death. Women don’t do that.’

The debate, moderated by Peter Boghossian, author and professor of philosophy, was held in April at UC Berkeley that posed the phrase: ‘Trans women should be treated as women.’

The geneticist strongly disagreed with the claim, first arguing that trans women are not women, because ‘being male or female is developmental, and you cannot go backwards.’

Another participant, a woman, an aspiring molecular geneticist, agreed with the claim, and the third participant, a man, initially stood on the ‘disagree’ line but moved over to ‘strongly disagree’ by the end of the discussion. 

When asked by the moderator why she strongly disagreed in the claim, the geneticist responded without hesitation: ‘Because I’m a molecular geneticist.’

She continued: ‘Being male or being female is a developmental process. You can’t go backwards. You cant change your sex, like you cannot do that.’ 

The geneticist appeared to get emotional while talking about the subject, telling the moderator: ‘I’m sorry this bothers me so much. My heart is pounding.’

She then gave her stance on trans women in changing rooms and prisons. 

‘I go to the women’s changing room at my gym and there’s a dude there and he’s putting on makeup and hoop earrings and this is not something a woman does when she goes to work out,’ she explained. 

The moderator said he’s not familiar with women’s changing rooms and asks, is this behavior not common?

She responds: ‘No, nor do women beat each other to death. But men do.’  

The geneticist claimed that in prisons in California and across the country, women are getting raped and impregned by other ‘women.’

‘There’s a reason why they (trans women) don’t want to be in men’s prisons,’ she said. ‘Men beat each other to death. Women don’t do that.’

In an August 18 post on her ‘Justice 4 Demi’ blog, transgender inmate Demi Minor revealed she ended up in the emergency room after trying to remove her testicle with a razor

The 27-year-old has claimed she has been abused at her new prison, the Garden State Youth Correctional Facility (GSYCF), where staff are refusing to acknowledge her gender identity

Minor was born Demetrius Minor, a boy, and was just 16 when she broke into the home of her stepfather Theotis Butts’s home in Gloucester Township, New Jersey 

Meanwhile, a transgender prisoner who impregnated two of her fellow inmates at a women’s prison in New Jersey has revealed she tried to remove one of her testicles with a razor after being misgendered at her new men’s facility. 

Demi Minor, 27, was moved from Edna Mahan Correctional Facility for Women in Union Township to the Garden State Youth Correctional Facility (GSYCF) with male inmates in June after guards learned of the pregnancies. 

Minor, who is serving a 30-year sentence for stabbing her former foster father to death, has since complained that she has been mistreated and abused at her new prison, where staff are refusing to acknowledge her gender identity. 

In an August 18 post on her Justice 4 Demi blog, she revealed she ended up in the emergency room after using a razor to cut out one of her testicles in an apparent suicide attempt.  

‘When I began to bleed, I did not even think about dying. I just thought about finally having relief from the pain that I felt,’ Minor wrote. 

‘Being here in a male prison, amplifies the harm that I once felt… I hate it all.’ 

Minor, who was first jailed at the age of 16, started to transition into a woman in 2020 and was transferred out of the male prison system to Mahan. 

The 800-inmate Mahan facility began housing transgender women – including those that have yet to undergo gender reassignment surgery – last year after a lawsuit brought by an inmate and the ACLU. It now has 27 trans prisoners. 

Minor was first jailed at the age of 16, but started to transition into a woman in 2020 and was transferred out of the male prison system to Mahan

Minor explained she began feeling ‘hopeless’ and ‘ignored’ at GSYCF on July 28 after she was asked to prove she was transgender despite having provided staff with medical records stating she had been ‘on hormones for years.’

She claims she was later told by the committee chair that there were some things that ‘we can biologically not change’, suggesting that ‘regardless of my transition without surgery I am a man.’

‘I ignored her comments. But the truth is everything she said hurt, and was hard not to cry in the meeting it was hard to know that the same people who I once admired were now responsible for placing me in harms (sic) way,’ she wrote. 

‘I started cutting again, and with a razor I begin (sic) making a incision to remove my testicle. In my head, I just wanted the pain to stop. I just wanted out of this. They don’t know what the hell that I am going through. 

‘Instead, if you have a penis, you deserve to be in a male prison. That is all central offices cares about,’ she added. 

Minor added that she has been diagnosed with gender dysphoria, meaning she is ‘five times more likely’ to die by suicide, but admitted she sometimes ‘would rather not be here.

‘I have been diagnosed with gender dysphoria, and it makes me 5 times more likely to die by suicide. I hide these thoughts. I have often not told anyone how I truly feel, and how sometimes, I would rather not be here’.

Since her transfer, Minor claimed men write her letters asking for sexual favors and that she finds herself in some ‘dark places’.



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Recently Discovered Molecule Kills Hard-To-Treat Cancers

The study was carried out in isolated cells, in human cancer tissue, and in human cancers grown in mice.

The new compound called ERX-41 kills a broad spectrum of hard-to-treat cancers.

A new molecule created by a researcher at the University of Texas at Dallas kills a variety of difficult-to-treat cancers, including triple-negative breast cancer, by taking advantage of a weakness in cells that was not previously targeted by existing drugs.

The research, which was conducted using isolated cells, human cancer tissue, and mouse-grown human cancers, was recently published in Nature Cancer.

A co-corresponding author of the study and an associate professor of chemistry and biochemistry in the School of Natural Sciences and Mathematics at the University of Texas at Dallas, Dr. Jung-Mo Ahn has dedicated more than ten years of his career to developing small molecules that target protein-protein interactions in cells. He previously created potential therapeutic candidate compounds for treatment-resistant prostate cancer and breast cancer using a method called structure-based rational drug design.

Dr. Jung-Mo Ahn, associate professor of chemistry and biochemistry at The University of Texas at Dallas, synthesized a novel compound called ERX-41 that kills a broad spectrum of hard-to-treat cancers, including triple-negative breast cancer, by exploiting a weakness in cells not previously targeted by other drugs. Credit: The University of Texas at Dallas

In the current work, Ahn and his colleagues tested a novel compound he synthesized called ERX-41 for its effects against breast cancer cells, both those that contain estrogen receptors (ERs) and those that do not. While there are effective treatments available for patients with ER-positive breast cancer, there are few treatment options for patients with triple-negative breast cancer (TNBC), which lacks receptors for estrogen, progesterone, and human epidermal growth factor 2. TNBC generally affects women under 40 and has poorer outcomes than other types of breast cancer.

“The ERX-41 compound did not kill healthy cells, but it wiped out tumor cells regardless of whether the cancer cells had estrogen receptors,” Ahn said. “In fact, it killed the triple-negative breast cancer cells better than it killed the ER-positive cells.

“This was puzzling to us at the time. We knew it must be targeting something other than estrogen receptors in the TNBC cells, but we didn’t know what that was.”

To investigate the ERX-41 molecule, Ahn worked with collaborators, including co-corresponding authors Dr. Ganesh Raj, professor of urology and pharmacology at the Harold C. Simmons Comprehensive Cancer Center at UT Southwestern Medical Center, as well as Dr. Ratna Vadlamudi, professor of obstetrics and gynecology at UT Health San Antonio. Dr. Tae-Kyung Lee, a former UTD research scientist in Ahn’s Bio-Organic/Medicinal Chemistry Lab, was involved in synthesizing the compound.

The researchers discovered that ERX-41 binds to a cellular protein called lysosomal

“For a tumor cell to grow quickly, it has to produce a lot of proteins, and this creates stress on the endoplasmic reticulum,” Ahn said. “Cancer cells significantly overproduce LIPA, much more so than healthy cells. By binding to LIPA, ERX-41 jams the protein processing in the endoplasmic reticulum, which becomes bloated, leading to cell death.”

The research team also tested the compound in healthy mice and observed no adverse effects.

“It took us several years to chase down exactly which protein was being affected by ERX-41. That was the hard part. We chased many dead ends, but we did not give up,” Ahn said.

“Triple-negative breast cancer is particularly insidious — it targets women at younger ages; it’s aggressive, and it’s treatment-resistant. I’m really glad we’ve discovered something that has the potential to make a significant difference for these patients.”

The researchers fed the compound to mice with human forms of cancerous tumors, and the tumors got smaller. The molecule also proved effective at killing cancer cells in human tissue gathered from patients who had their tumors removed.

They also found that ERX-41 is effective against other cancer types with elevated endoplasmic reticulum stress, including hard-to-treat pancreatic and ovarian cancers and glioblastoma, the most aggressive and lethal primary brain cancer.

“As a chemist, I am somewhat isolated from patients, so this success is an opportunity for me to feel like what I do can be useful to society,” Ahn said.

Reference: “Targeting LIPA independent of its lipase activity is a therapeutic strategy in solid tumors via induction of endoplasmic reticulum stress” by Xihui Liu, Suryavathi Viswanadhapalli, Shourya Kumar, Tae-Kyung Lee, Andrew Moore, Shihong Ma, Liping Chen, Michael Hsieh, Mengxing Li, Gangadhara R. Sareddy, Karla Parra, Eliot B. Blatt, Tanner C. Reese, Yuting Zhao, Annabel Chang, Hui Yan, Zhenming Xu, Uday P. Pratap, Zexuan Liu, Carlos M. Roggero, Zhenqiu Tan, Susan T. Weintraub, Yan Peng, Rajeshwar R. Tekmal, Carlos L. Arteaga, Jennifer Lippincott-Schwartz, Ratna K. Vadlamudi, Jung-Mo Ahn, and Ganesh V. Raj, 2 June 2022, Nature Cancer.
DOI: 10.1038/s43018-022-00389-8

Ahn is a joint holder of patents issued and pending on ERX-41 and related compounds, which have been licensed to the Dallas-based startup EtiraRX, a company co-founded in 2018 by Ahn, Raj, and Vadlamudi. The company recently announced that it plans to begin clinical trials of ERX-41 as early as the first quarter of 2023.

The study was funded by the National Cancer Institute, the Cancer Prevention and Research Institute of Texas, and The Welch Foundation.



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Vets urge caution for dogs experiencing severe case of pneumonia :: WRAL.com

— There is a mysterious and severe case of pneumonia affecting dogs, and some veterinarians are already seeing it in Raleigh.

It’s impacting how vets are accepting new dogs for boarding.

Doctors are still trying to figure out what it is. At Care First Animal Hospital at Oberlin, they see 15-20 dogs per day with the infection.

With the Labor Day holiday weekend approaching, some boarding facilities are being careful.

Upper-respiratory diseases are common in shelters because dogs that come in aren’t usually vaccinated.

“Late spring [and] early summer, we did have a few severe cases, but that has calmed down,” said Wake County Animal Center animal services director Dr. Jennifer Federico. “So now, we’re not seeing that as much in our world.”

Federico said private practices are now the ones seeing this kind of infection more.

“This one seems pretty scary because of how sick the dogs are coming in,” said Care First Animal Hospital’s Dr. Page Wages.

Since May, Care First Animal Hospital has seen 450 dogs with pneumonia. In the last two or three weeks, they’ve seen about 20-50 dogs with a more severe case.

“The scary thing is the dogs with this pneumonia,” Wages said. “Some dogs are dying from it …

“It’s young dogs. It’s dogs [that are] a year or 2 years [old]. We have one right now that’s at a hospital that probably won’t survive. It’s really sad.”

An X-ray of a dog with pneumonia shows the animal’s lungs fully infected.

Dogs who are more active with other dogs are at a higher risk.

Symptoms include:

  • A runny nose
  • Cough
  • Diarrhea
  • Eye discharge

Wages said they’re being extra careful boarding dogs because the infection can spread easily.

“[If they are] coughing [and] sneezing, they cannot come in the kennel,” Wages said. “Just people that want to board their dogs that are sick, just please don’t board them here or any other place it’s just going share it to other dogs.”

Doctors encourage pet owners to keep their dogs away from other dogs for a couple of weeks until the infection dies down. Also, doctors recommend dogs stay up to date with their vaccines.

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What parents need to know to keep children safe

Though cases remain few, monkeypox has already hit children from New York City to Seattle and many communities in between.

Currently in the US there are just under 17,000 cases of monkeypox, mostly among adults. Though no fatalities have yet been recorded, there’s some evidence that an early strain of the virus is more likely to be severe in children under 8, according to the Centers for Disease Control and Prevention, particularly in those with immunocompromising conditions or certain skin conditions, such as eczema.

As school bells ring to call kids back to class for the fall, it’s important for parents to know everything they can about protecting their children from the painful disease.

Those potentially exposed to monkeypox should be watched closely for 21 days, and isolate away from peers and wear a mask if they begin to show symptoms.
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What does monkeypox in children look like?

The symptoms of monkeypox in kids presents in a similar way to adults, according to the CDC.

It will most likely begin with a bodily rash that may resemble the signs of an allergic reaction, chickenpox, or hand, foot, and mouth disease.

The rash quickly forms lesions, which progress over the course of two to four weeks, into blisters, pustules, then scabs. Meanwhile, patients are also likely to suffer fever, swollen lymph nodes, fatigue and headache.

The risk of children and adolescents contracting the virus remains low as the few known cases among them have been quick to treatment and quarantine. Moreover, infections in US children and teenagers have been mild so far, according to the American Academy of Pediatrics.

How does monkeypox spread in children?

Monkeypox spreads in children and teens the same way it does in adult: through close personal contact. For kids, this could mean hugging another, skin-to-skin, with the infectious rash; or swapping spit, such as through kissing or very close-talking, with a sick patient.

The CDC also notes the potential for the virus to spread through contaminated objects or surfaces, including clothing, towels and linens, that were used by someone with with the virus.

It’s not known whether children are more susceptible to monkeypox than adults or whether the virus will affect them in the same way.

What should you do if a child is exposed to monkeypox?

Unlike with COVID-19 and other contagions, people exposed to the virus will not necessarily have to isolate. However, during monitoring, the health department may limit their participation in activities if investigators are unable to pinpoint where or with whom exposure first occurred, or if the exposure setting presented particularly high risks. They’ll also consider the child’s age and ability to recognize or communicate symptoms and the risk to others.

Babies are advised to stay in a separate room and not have contact with parents or caregivers who are infected or may have been exposed to monkeypox. 

If your child comes in contact with someone with monkeypox, they should be watched closely for 21 days. If symptoms should arise, they should isolate away from peers and wear a mask.

On a case-by-case basis, vaccination and prophylactic antiviral treatment may be available to children who are suspected to have been exposed.

The CDC recommends that anyone — children and adults — with a known case of monkeypox should isolate until all scabs from the rash have fallen off, which could take up to 4 weeks after symptoms first started.

There’s no vaccine available for children unless they’ve been directly exposed to the virus.
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Can children be vaccinated for monkeypox?

At the moment, most children are not eligible for monkeypox vaccine — unless they’ve been directly exposed to virus. If you suspect your child is at risk of contracting the disease while at home, school or elsewhere, contact your doctor or local health department to learn about the options available in your area.

Is monkeypox fatal to children?

So far, no deaths related to monkeypox have occurred in adults or children. However, the disease can be excruciating and continue for the better part of a month, so it’s nothing to take lightly.

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‘Monkeypox does not wait for anyone’: Virus hitting Black community hard in metro Atlanta – WSB-TV Channel 2

ATLANTA — WSB-TV is getting real about monkeypox and its impact on minorities.

The disease is hitting the Black community hard, but the good news is that anyone can now get tested for the virus without leaving your car.

Channel 2′s Audrey Washington was at a new drive thru monkeypox testing site opened on North Druid Hills Road in DeKalb, where it was busy on Friday afternoon.

The site tests for both the COVID-19 and monkeypox viruses.

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But workers told Washington that around 25% of the people who showed up Friday came for monkeypox testing.

One-by-one, they drove up and got tested. According to the Centers for Disease Control Prevention, there are more than 16,000 confirmed monkeypox cases nationwide and nearly 1,300 cases right here in Georgia.

Dr. Jayne Morgan, the executive director of the COVID-19 task force at Piedmont Heathcare, said she expects cases to keep climbing.

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“What is happening is exactly what we should have expected to happen, because we saw this occur in COVID, and we certainly saw this occur in HIV as well,” Morgan said.

Morgan said infectious agents generally take hold in populations that have the fewest resources and that are at the most disadvantaged. She said that factor explains why research now shows a growing racial disparity pertaining to new monkeypox cases.

“Here in Georgia we see about 82% of the monkeypox cases have been in Black men,” Morgan said. “It really depends on whether you have health access and what your resources are.”

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Camille Seaton is the first woman in Georgia to have been diagnosed with monkeypox. She said it took about three-and-a-half weeks to recover.

“It’s still all over my body, but the stuff is scarring up and everything,” Seaton said.

She said it’s important to remember that monkeypox doesn’t discriminate, despite the rise of the virus in the Black community.

“Monkeypox does not wait for anyone,” Seaton said. “It does not care who it attacks.”

People at risk for the virus are urged to get vaccinated.



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