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#Virginia health care clinic
healthwellnesss · 11 days
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Glow Like Never Before: Discover Top-Rated Skin Hydration Clinics in Warrenton, VA
Hey there, skin care enthusiasts! If you’ve been battling dry, flaky, or dull skin, you’re not alone. Skin hydration is crucial for a glowing complexion, but finding the right solution can be a bit overwhelming. Luckily, Warrenton, VA, has some fantastic clinics that specialize in skin hydration treatments, including the trendy IV therapy. Let’s dive into what makes these clinics stand out and how they can help you achieve that radiant, hydrated glow.
Understanding Skin Hydration
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✦What is Skin Hydration?
Skin hydration is all about keeping your skin well-moisturized from the inside out. It’s like giving your skin a big drink of water! When your skin is properly hydrated, it’s plump, smooth, and has a youthful glow. Hydration helps maintain your skin’s elasticity, reduces the appearance of fine lines, and can even improve your overall skin texture.
✦Common Signs of Dehydrated Skin
If your skin feels tight, looks dull, or is showing flakes and dry patches, it might be time to address hydration. Dehydrated skin can be caused by various factors like environmental conditions, diet, and lifestyle choices. But don’t worry – there are effective treatments available to help restore that healthy glow.
The Role of IV Therapy in Skin Hydration
✦What is IV Therapy?
IV (intravenous) hydration therapy is a treatment where fluids and nutrients are delivered directly into your bloodstream through an IV drip. It’s a quick and effective way to hydrate your body and skin. IV therapy can boost your hydration levels faster than drinking water alone because the fluids go straight to where they’re needed most.
✦Benefits of IV Therapy for Skin Hydration
One of the biggest benefits of IV therapy is its immediate effect. You’ll notice a difference in your skin’s hydration and overall appearance right after your session. It’s not just about hydration – IV therapy can also improve skin elasticity, reduce signs of aging, and give your skin a vibrant, healthy glow.
What to Expect During an IV Therapy Session
During an IV therapy session, you’ll be comfortably seated while a healthcare professional inserts a small needle into your vein. The procedure is generally quick, and you can relax or read a book while the nutrients are administered. Afterward, there might be some mild soreness, but it’s usually nothing to worry about.
Top-Rated Skin Hydration Clinics in Warrenton, VA
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Discover Top Skin Hydration Clinics in Warrenton: Consult and Get the Glow You've Been Dreaming Of!
✦Clinic 1: Lifestyle's MedSpa
Overview: Lifestyle's MedSpa is renowned in Warrenton for its top-notch skin hydration treatments.
Services Offered: They offer a range of services, including IV hydration therapy, customized facials, and hydrating facial masks.
Unique Features: Lifestyle's MedSpa uses advanced technology and high-quality products. Their staff is highly trained, and they’re known for their personalized approach to skin care.
Location and Contact Information: Lifestyle's MedSpa | 400 Holiday ct, Warrenton, VA | (540) 680-2426
✦Clinic 2: Lifestyle Physicians
Overview: Lifestyle Physicians is a favorite for those seeking both relaxation and effective hydration treatments.
Services Offered: From IV therapy to deep hydration facials, they have a variety of treatments tailored to your skin’s needs.
Unique Features: Their soothing environment and expert staff make your visit enjoyable and effective. Plus, they often have special offers on their hydration packages.
Location and Contact Information: Lifestyle Physicians | Holiday Ct, Suite 102, Warrenton, VA | (540) 680-2426
How to Choose the Right Clinic for Your Needs
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✦Factors to Consider
When picking a clinic, make sure to check their credentials and read reviews from other clients. Look for a clinic with experienced professionals who use up-to-date technology. It’s also a good idea to visit in person if possible, to get a feel for the atmosphere and customer service.
✦Questions to Ask
Don’t hesitate to ask about the procedures, costs, and safety measures. Understanding what to expect and how the treatment will benefit you is key to making an informed decision.
✦Making an Informed Decision
Choose a clinic that aligns with your skin care needs and preferences. Remember, hydration is a personal journey, and finding the right place can make all the difference in achieving that glowing, hydrated skin you’re after.
Tips for Maintaining Skin Hydration at Home
✦Daily Skincare Routine
Incorporate products that enhance hydration, like moisturizers with hyaluronic acid and hydrating serums. Consistency is key to maintaining healthy skin.
✦Lifestyle Changes
Drink plenty of water, eat a balanced diet rich in fruits and vegetables, and avoid excessive sun exposure. These habits support overall skin health and hydration.
✦Regular Check-Ins
While home care is essential, don’t skip regular professional treatments. Schedule follow-ups with your chosen clinic to keep your skin in top shape.
Conclusion
Addressing skin hydration is crucial for a vibrant, youthful appearance. Warrenton’s top-rated clinics offer fantastic solutions, from IV therapy to comprehensive skin care treatments. Don’t wait – explore these clinics, schedule a consultation, and take the first step toward glowing, hydrated skin today!
Feel free to reach out to these clinics or follow our Blog for more tips on choosing the best skin hydration treatment. Cheers to healthier, more radiant skin!
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acorncarechesapeake · 4 months
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Occupational Health Clinic near me in Chesapeake VA
Acorn Care is the best occupational health clinic in Chesapeake, VA. We provide a wide range of occupational health services including injury care, physical therapy, pre-employment services, employee wellness, drug tests, DOT physicals, safety screenings, and more.
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Greedflation, but for prisoners
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I'm touring my new, nationally bestselling novel The Bezzle! Catch me TOMORROW (Apr 21) in TORINO, then Marin County (Apr 27), Winnipeg (May 2), Calgary (May 3), Vancouver (May 4), and beyond!
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Today in "Capitalists Hate Capitalism" news: The Appeal has published the first-ever survey of national prison commissary prices, revealing just how badly the prison profiteer system gouges American's all-time, world-record-beating prison population:
https://theappeal.org/locked-in-priced-out-how-much-prison-commissary-prices/
Like every aspect of the prison contracting system, prison commissaries – the stores where prisoners are able to buy food, sundries, toiletries and other items – are dominated by private equity funds that have bought out all the smaller players. Private equity deals always involve gigantic amounts of debt (typically, the first thing PE companies do after acquiring a company is to borrow heavily against it and then pay themselves a hefty dividend).
The need to service this debt drives PE companies to cut quality, squeeze suppliers, and raise prices. That's why PE loves to buy up the kinds of businesses you must spend your money at: dialysis clinics, long-term care facilities, funeral homes, and prison services.
Prisoners, after all, are a literal captive market. Unlike capitalist ventures, which involve the risk that a customer will take their business elsewhere, prison commissary providers have the most airtight of monopolies over prisoners' shopping.
Not that prisoners have a lot of money to spend. The 13th Amendment specifically allows for the enslavement of convicted criminals, and so even though many prisoners are subject to forced labor, they aren't necessarily paid for it:
https://pluralistic.net/2024/04/02/captive-customers/#guillotine-watch
Six states ban paying prisoners anything. North Carolina caps prisoners' pay at one dollar per day. Nationally, prisoners earn $0.52/hour, while producing $11b/year in goods and services:
https://www.dollarsandsense.org/archives/2024/0324bowman.html
So there's a double cruelty to prison commissary price-gouging. Prisoners earn far less than any other kind of worker, and they pay vastly inflated prices for the necessities of life. There's also a triple cruelty: prisoners' families – deprived of an incarcerated breadwinner's earnings – are called upon to make up the difference for jacked up commissary prices out of their own strained finances.
So what does prison profiteering look like, in dollars and sense? Here's the first-of-its-kind database tracking the costs of food, hygiene items and religious items in 46 states:
https://theappeal.org/commissary-database/
Prisoners rely heavily on commissaries for food. Prisons serve spoiled, inedible food, and often there isn't enough to go around – prisoners who rely on the food provided by their institutions literally starve. This is worst in prisons where private equity funds have taken over the cafeteria, which is inevitable accompanied by swingeing cuts to food quality and portions:
https://theappeal.org/prison-food-virginia-fluvanna-correctional-center/
So you have one private equity fund starving prisoners, and another that's gouging them on food. Or sometimes it's the same company. Keefe Group, owned by HIG Capital, provides commissaries to prisons whose cafeterias are managed by other HIG Capital portfolio companies like Trinity Services Group. HIG also owns the prison health-care company Wellpath – so if they give you food poisoning, they get paid twice.
Wellpath delivers "grossly inadequate healthcare":
https://theappeal.org/massachusetts-prisons-wellpath-dentures-teeth/
And Trinity serves "meager portions of inedible food":
https://theappeal.org/clayton-county-jail-sheriff-election/
When prison commissaries gouge on food, no part of the inventory is spared, even the cheapest items. In Florida, a packet of ramen costs $1.06, 300% more inside the prison than it does at the Target down the street:
https://www.documentcloud.org/documents/24444312-fl_doc_combined_commissary_lists#document/p6/a2444049
America's prisoners aren't just hungry, they're also hot. The climate emergency is sending temperatures in America's largely un-air-conditioned prisons soaring to dangerous levels. Commissaries capitalize on this, too: an 8" fan costs $40 in Delaware's Sussex Correctional Institution. In Georgia, that fan goes for $32 (but prisoners are not paid for their labor in Georgia pens). And in scorching Texas, the commissary raised the price of water by 50% last summer:
https://www.tpr.org/criminal-justice/2023-07-20/texas-charges-prisoners-50-more-for-water-for-as-heat-wave-continues
Toiletries are also sold at prices that would make an airport gift-shop blush. Need denture adhesive? That's $12.28 in an Idaho pen, triple the retail price. 15% of America's prisoners are over 55. The Keefe Group – sister company to the "grossly inadequate" healthcare company Wellpath – operates that commissary. In Oregon, the commissary charges a 200% markup on hearing-aid batteries. Vermont charges a 500% markup on reading glasses. Imagine spending decades in prison: toothless, blind, and deaf.
Then there's the religious items. Bibles and Christmas cards are surprisingly reasonable, but a Qaran will run you $26 in Vermont, where a Bible is a mere $4.55. Kufi caps – which cost $3 or less in the free world – go for $12 in Indiana prisons. A Virginia prisoner needs to work for 8 hours to earn enough to buy a commissary Ramadan card (you can buy a Christmas card after three hours' labor).
Prison price-gougers are finally facing a comeuppance. California's new BASIC Act caps prison commissary markups at 35% (California commissaries used to charge 63-200% markups):
https://theappeal.org/price-gouging-in-california-prisons-newsom-signature/
Last year, Nevada banned any markup on hygiene items:
https://www.leg.state.nv.us/App/NELIS/REL/82nd2023/Bill/10425/Overview
And prison tech monopolist Securus has been driven to the brink of bankruptcy, thanks to the activism of Worth Rises and its coalition partners:
https://pluralistic.net/2024/04/08/money-talks/
When someone tells you who they are, believe them the first time. Prisons show us how businesses would treat us if they could get away with it.
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If you'd like an essay-formatted version of this post to read or share, here's a link to it on pluralistic.net, my surveillance-free, ad-free, tracker-free blog:
https://pluralistic.net/2024/04/20/captive-market/#locked-in
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cartermagazine · 7 months
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Today We Honor Dr.Josephine English
Dr. Josephine English was an American gynecologist who was the first black woman to open a private practice in New York. She was also known for her work in real estate and health care, in addition to her philanthropy towards the arts.
English was born on December 17, 1920 to Jennie English and Whittie Sr. in Ontario, Virginia. She moved to Englewood, New Jersey in 1939. Her family was one of the first black families in Englewood. She attended Hunter College for her bachelor’s degree until 1949, and earned her Master’s in Psychology at New York University. She initially wanted to become a psychiatrist, but ended up choosing gynecology after discovering her interest at Meharry Medical College where she earned her medical degree in gynecology.
Dr.Josephine English opened her practice at Harlem Hospital. Once in Brooklyn, she opened up a women’s health clinic in Bushwick in 1956, as well as another in Fort Greene two decades later. During her career, English helped deliver 6,000 babies, including the children of Malcolm X, Betty Shabazz, and Lynn Nottage.
English’s interest in health care lead her establish the Adelphi Medical Center and child care programs, such as Up the Ladder Day Care and After School Program. Her passion for theater led her to establish the Paul Robeson Theater from a dilapidated church. She helped actors create performances to educate the populace on health and nutrition.
CARTER™️ Magazine
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The June 24, 2022 Dobbs v. Jackson landmark decision by the United States Supreme Court held that the Constitution of the United States does not confer the right to abortion. This decision returned to individual states the power to regulate any aspect of abortion not protected by federal law. Since this ruling, multiple states have limited or completely banned abortion care for people who are pregnant. In at least nine states, abortion is blocked with no exceptions for rape or incest.
Multiple states have banned abortion after 18, 15, or even 6 weeks gestation. These time restrictions make it impossible for patients to use medical information from ultrasounds and/or genetic testing, available later in pregnancy, to determine if a fetus has an anomaly and/or a life-threatening or lethal condition.
These abortion restrictions and laws permitting any citizen to sue anyone “aiding or abetting” an illegal abortion for up to $10,000 has created uncertainty and fear among health care providers trying to provide medical care to pregnant patients experiencing miscarriage, tubal or ectopic pregnancy (when the embryo implants in the fallopian tube, where it cannot become a full term pregnancy; can be lethal to the mother if not treated promptly and correctly), or those who need prenatal genetic counseling. Clinicians are unclear where the lines stand between providing care and committing a felony that could equal jail time, and this means that pregnant people aren’t getting the appropriate and timely care they need, even outside of a healthy, viable pregnancy.
But did you know that the Dobbs decision has also prevented non-pregnant women from receiving the medications they need to treat lupus, rheumatoid arthritis, and other conditions treated with medications like methotrexate?
Chris Stallman, MLS, MS, is a certified genetic counselor, an expert in medication impact during pregnancy, and a Clinical Instructor of Pharmacy Practice-Science at the University of Arizona R. Ken Coit College of Pharmacy. “Methotrexate is a medication used to treat many conditions, including lupus, rheumatoid arthritis, Crohn’s disease, and other autoimmune diseases. If a person who is pregnant uses methotrexate, it could increase the chance of miscarriage, birth defects, and other issues in pregnancy or after birth.”
For this reason, girls and women of child-bearing age who are taking methotrexate as treatment for their autoimmune or other diseases are not able to take methotrexate – even if they are not pregnant.
This critical problem is not hypothetical – treatment with methotrexate has already been withheld from female, non-pregnant patients with serious medical conditions in multiple states.
A 48-year-old woman in Tellico Plains, TN received an automated call from her CVS Pharmacy in July 2022 indicating that her prescription for methotrexate wouldn’t be refilled. This patient, who has inflammatory arthritis and a neuromuscular disease called myasthenia gravis, stated that methotrexate allowed her to resume simple, yet previously painful tasks like putting on her pants and rolling over in bed.
In June 2022, not 24-hours after the Dobbs ruling, a patient in Maryland who has Crohn’s disease received a call from her insurance company indicating that methotrexate, used to treat the chronic inflammation and pain associated with this condition, would no longer be available to her.
Within a week of the Dobbs ruling, a woman in Virginia who has Lupus received a letter from her doctor’s office indicating that it was pausing all prescriptions and refills of methotrexate because of the Supreme Court decision on abortion. Before taking methotrexate she experienced flares of Lupus so severe that she had trouble walking and needed to use a shower chair to wash.
Another woman from Missouri had been taking methotrexate to treat rheumatoid arthritis. When she went to the pharmacy to pick up her refill she learned from the pharmacist that they needed a specific direction from her doctor that the medication would not be used for an abortion. The pharmacy, Walgreens, confirmed with this customer that they do not require the same procedure from their male clients.
A 14-year old girl in Arizona was denied a refill of methotrexate to treat her debilitating rheumatoid arthritis and osteoporosis. Her angry physician tweeted that her patient was denied this critical medication because she was female. The withholding of life-saving or -altering medications from the women who need them has forced some of them to consider surgical sterilization.
Could denying women of childbearing age (who may or may not be sexually active, fertile, heterosexual, or pregnant) methotrexate be just the beginning of problems for women who need prescription or over-the-counter medications? Stallman says, “This certainly could lead to more medication denials – and not just for people who can get pregnant. If my husband or children need medication that could increase risks to a pregnancy, would they be denied the medication simply because they live with a person who could get pregnant? Will health care providers have to stop handling or dispensing such medications if they or their partner could get pregnant? And before saying ‘that will never happen’, remember that is what people said about the overturning of Dobbs. We don’t know how far this will go.”
Let’s take this thought experiment a step further. Is it possible that young girls will have to present a letter from their pediatricians indicating whether they’ve started having periods before they can receive the medications they need? Will adult women have to present written proof of tubal ligation, menopause, or infertility from their physicians before filling their life-saving medications? Will other medications that can affect the health of a fetus, even the highly regulated acne medication Accutane, require such additional proof? Could pharmacies use the data they have on prior purchases, like tampons and lubricant, to determine if a woman may be of child-bearing age and/or is sexually active?
The Dobbs decision is just the beginning of our government interfering with womens’ bodies, their personal choices, and their medical care. This decision is already impacting health care outside of pregnancy and could force women and their family members to disclose personal information about their fertility, sexuality, sexual and medical history with pharmacists, medical systems, the government, and the databases that all of them use. Our federal government must act swiftly to ensure that this decision doesn’t lead to further government overreach, discrimination, interference in proper medical care, and tragedy.
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Kerry Eleveld at Daily Kos:
Florida's near-total abortion ban took effect this week, marking a brutal milestone for abortion rights activists nationally: From South Carolina to Texas, the South is now a virtual abortion care desert—a once unthinkable reality that could sway votes this November. Lone outlier North Carolina has a 12-week ban that could potentially offer a glint of hope for pregnant patients in the Southeast. As Politico reported, that means a Miami resident seeking abortion care past six weeks of pregnancy would need to drive 11 hours north to North Carolina. But if they couldn't withstand the state's 72-hour waiting period, they would need to venture another four hours north to Virginia, where abortion care is still legal up to the point of viability, or roughly 24 weeks of pregnancy.
But for most patients in the South, and certainly the neediest among them, the reality is that reaching any place that could offer abortion care in a timely fashion is now out of reach.  “Our patients are screwed,” Robin Marty, executive director of the West Alabama Women’s Center, told Politico. The abortion clinic became a reproductive health center following the Supreme Court’s Dobbs v. Women’s Health Organization decision, which overturned Roe v. Wade.  “This is the point where it all starts to crumble,” Marty warned. The Biden campaign marked the South's devastating new reality by sending Vice President Kamala Harris to Jacksonville to rail against "another Trump abortion ban" going into effect. But one has to wonder if a near-total ban on abortion in an entire region of the country could impact American women’s psyches—and their votes—far more than most political analysts believe.
With the Southeastern USA a place that abortion access is nearly impossible to obtain, such policies could have a bigger impact on the elections than anticipated.
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mariacallous · 11 months
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Since 2018, conservative state legislatures across the country have proposed and passed laws targeting young transgender people’s freedom to to play on sports teams and use bathrooms that correspond with their gender, and to obtain gender-affirming health care. Advocates for trans rights argue that the increased interest in the subject has served to galvanize the energies of those who had fought an ultimately losing battle against gay marriage—and have observed how the anti-trans movement has used tactics that have proved successful in limiting abortion. As with much legislation of this type, amid the nationalized, culture-war politics, the effects are felt most acutely by the most vulnerable families and individuals.
In a startling piece of reporting in this week’s issue, Emily Witt follows a mother named Kristen Chapman who moves her family from Tennessee to Virginia, in order for her daughter Willow to continue receiving gender-affirming care. “I genuinely feel we are being run out of town on a rail,” Chapman says. “I am not being dramatic. It is not my imagination.” With nuance and compassionate precision, Witt captures the urgency of the family’s relocation, and the sense, as laws seem to change underfoot, of pursuit. As she writes, “Chapman had chosen Virginia for their new life, she said, because it was still in the South, but there would be ‘multiple avenues of escape.’ ”
On the last morning of July, Kristen Chapman was getting ready to leave Nashville. Chapman, who is in her early fifties and wears her silver hair short, sat on a camp chair next to a fire pit outside the rental duplex where her family had lived for twelve years. She was smoking an American Spirit and swatting at the mosquitoes that kept emerging from the dense green brush behind her. Her husband, Paul, who was wearing a T-shirt with the Guinness logo, carried boxes out to the front lawn. Their daughters, Saoirse and Willow, who were seventeen and fifteen, were inside, still asleep. Chapman looked down at the family’s beagle mix, Obi-Wan Kenobi, who was drinking rainwater out of a plastic bucket. “We got him when we moved in here for the kids,” she said. “He’s never lived anywhere else.”
Paul was planning to stay in town; Chapman was heading to Richmond, Virginia, with Saoirse and Willow. Chapman and Paul’s marriage was ending, but the decision to split their family apart had happened abruptly. Willow is trans, and had been on puberty blockers since 2021. In March, Tennessee’s governor, Bill Lee, had signed a bill that banned gender-transition treatment for minors across the state.
On paper, the law, which went into effect in early July, would allow trans teens like Willow to continue their medical care until March of 2024. But Chapman wasn’t sure they could count on that. Willow was determined to begin taking estrogen when she turned sixteen, in December of 2023, which would allow her to grow into adulthood with feminine characteristics. If she couldn’t continue taking puberty blockers until then, she would begin to go through male puberty, which could mean more surgeries and other procedures later in life.
At first, the family had hoped that the courts would declare the new law unconstitutional. Federal courts had already done so in at least four other states in 2023, finding that such bans violated the First Amendment and the equal-protection and due-process clauses of the Fourteenth Amendment. But that spring the Pediatric Transgender Clinic at Vanderbilt University Medical Center, where Willow had been receiving care, informed its patients that it was ceasing operations. Seeing this as a bad sign, Chapman set up a GoFundMe page in early May and began planning their departure.
Inside, the apartment was filled with abandoned objects—an old Wi-Fi router, trash bags of unwanted clothes. A Homer Simpson doll in a hula skirt lay forgotten on a windowsill. Chapman, an artist who supplements her income with social work, had recently quit her job as a caseworker. She would need their landlord as a reference to get an apartment, especially because she had bad credit, but the family still owed him back rent. She checked Venmo, waiting on a loan from a friend.
At six-thirty that morning, Chapman had gone out to her white Dodge S.U.V. and found her younger daughter asleep in the back seat. Willow had gone over to a friend’s house and stayed out late. When she got home, she realized that she had locked herself out. The Dodge’s window had been stuck open for months, so she got in. “Any other human being would have handled this totally differently,” Chapman said, shaking her head.
Willow had gone back to sleep in her room, which she once shared with her brother. (He was a sophomore in college and had already moved out.) The colorful scarves and lights that used to decorate the space had been taken down. When she woke up, she began sifting through what was left. “I feel like I’m ready to say goodbye to it,” she said, looking around. There were drawings scrawled on the wall, a desk spattered in paint. “Most of the stuff in here I’ve trashed.”
“It’s like getting a new haircut,” Chapman said. “A fresh palette.”
Chapman had chosen Virginia for their new life, she said, because it was still in the South, but there would be “multiple avenues of escape.” Paul worked nights for a large grocery-store chain; Richmond was among the northernmost cities where it had branches, and Chapman thought that at some point he might be able to transfer there. Earlier in the summer, she and Willow had driven to Richmond to see the city, and Chapman had lined up a marketing job. It didn’t pay well, but she knew she wouldn’t get a lease without a job. Willow, who had received her last puberty-blocker shot at the Vanderbilt clinic in late May, was supposed to receive her next one in late August. They didn’t have a lot of time.
Despite having taken puberty blockers for two years, Willow looks her age. She is tall and long-limbed and meticulous about her appearance. That morning, she had on Y2K-revival clothes: wide-legged jeans worn low on the hips with a belt, a patterned tank top, and furry pink Juicy Couture boots. Her blond hair was glossy and straight, her bangs held back with a barrette. She is committed to living her adolescence as a girl regardless of what medical treatment she is allowed to receive. At times she has used silicone prosthetic breasts; attaching them is an onerous process involving spray-on adhesive.
From a very young age, Willow wore dresses and gravitated toward friendships with girls. Her parents thought that she would likely grow up to be a gay man. As Chapman put it, “We knew she was in the fam.” When a homophobic shooter killed forty-nine people at Pulse, the gay night club in Orlando, in 2016, Willow, who was eight at the time, accompanied her mother to a vigil in Nashville. Willow wrote a long message on a banner in solidarity with the survivors. Chapman took a photo of her there. “It was like she was transfixed,” Chapman remembered. In the sixth grade, Willow went to an all-girl sleepover. A parent overheard the kids discussing gender and sexuality, and told Chapman. Willow says that it was around then that she began to think about her identity. “Pretty much as soon as I knew about, like, conceptualized gender, I knew I wanted to be a girl,” she said. She had been an A student, but her grades started going down. Looking back, Willow struggled to articulate what had happened. “It just got complicated, like with all my stuff physically, it just felt like a mess,” she said.
She came out to her friends first; then one day, in the spring of 2020, while she was upstairs on her laptop and Chapman was downstairs working, Willow sent her mother a three-word e-mail that said, “I am trans.” Willow told me, “I realized I have to do this sometime if I want to advocate for myself and get what I need to get.” She left it to her mother to inform the rest of the family. Chapman was accepting; Paul was more skeptical. “That’s him, you know—a man of science,” Chapman said. “It wasn’t overly positive or negative.”
Willow had already decided on her new name before coming out, and began using it with friends. She was again reluctant to tell her family. “I was, like, I’ll keep that secret,” she said—she had been named at birth for a brother of her father’s who had died, and knew the name was important to him. Her mother found out when another mom referred to Willow by her chosen name. Chapman started using it right away; it took Paul another year.
To figure out their next steps, Chapman took Willow, who was then twelve, to her regular pediatrician at Vanderbilt University Medical Center. She was referred to the center’s Pediatric Transgender Clinic. The clinic, which opened in 2018, was part of a broader expansion of gender-affirming care at flagship medical schools in the South that occurred around that time. (Clinics also opened at Duke University, the University of Mississippi, and Emory University, among other schools.) These places “attracted the kind of people who build very trusting relationships with patients and are able to establish not just the clinical competencies but also an inclusive environment,” Jasmine Beach-Ferrara, the executive director of the Campaign for Southern Equality, an advocacy group for L.G.B.T.Q. rights, told me. “All those things are nothing you can take for granted when seeking medical care in the South.” (Federal funding for health care is often funnelled through state governments, some of which have a history of withholding money from providers that offer abortion and other politicized health services.)
Care for patients who are experiencing gender dysphoria is highly individualized: some trans kids opt for a purely social transition, changing their names or pronouns; others, like Willow, seek a medical transition, which can be started at the onset of puberty. In Willow’s case, a diagnosis of gender dysphoria had to be verified before pharmaceutical treatment could begin. A course of psychotherapy was accompanied by a physical assessment at Vanderbilt, which included ultrasounds, X-rays, and blood tests. The clinic was following a protocol supported by the Endocrine Society and the World Professional Association for Transgender Health, whereby patients take puberty blockers—which have been used to treat children experiencing early-onset puberty since the nineteen-eighties—to delay the onset of secondary sex characteristics until they are ready to begin taking estrogen or testosterone.
“I’d always explain it to the families as a pause on puberty, allowing the youth to take a deep breath,” Kimberly Herrmann, a pediatrician and internist at Whitman-Walker Health, a provider in the Washington, D.C., area that offers gender-affirming care to patients aged thirteen and over, told me. (Some patients choose to go through their natal puberty.) “All of the data suggests that it is the correct thing to do for a patient with a clear diagnosis,” Izzy Lowell, a doctor who started a telehealth practice for gender-affirming care called QueerMed, said, of taking puberty blockers. “If they are going to develop the body of a grown man, it becomes difficult to undo those changes.”
Paul was worried about the blockers’ long-term effects on Willow’s health. (Studies have shown that they can affect bone density when used long term, and the protocol for hormone therapy advises doctors to discuss potential risks to fertility and options for fertility preservation.) Chapman thought the risks to Willow’s well-being would be worse if she developed male secondary sex characteristics. In one testimony against the Tennessee ban, an adult trans woman described her adolescence, in which she attempted to present as male, as “a disastrous and torturous experience.”
“Paul and I talked about it and came to the belief that we wanted her on them as quickly as possible for safety reasons,” Chapman said. “I hate that that’s true, but we know that’s the world that we live in, and that she is going to be a safer person for the rest of her life if she does not look male.” (A recent analysis of crime statistics from 2017 and 2018 found that transgender people are more than four times as likely as cisgender people to be the victims of a violent crime.)
The evaluation and diagnosis took almost a year. For Willow, the talk therapy was the most taxing part. Willow was insured through the state’s Medicaid program, TennCare, which meant that there were only a limited number of therapists she could see, none of whom were trans, or even queer. She went through three in a year. “We were in the lowest tier of care,” Chapman said, adding that at least one therapist dropped their health insurance. Willow told her mother that she wished she could just be left alone to be a “sad trans girl.”
At the age of thirteen, she was finally able to start puberty blockers. “You have an end goal,” Willow said of the experience. “And all the in-between doesn’t matter.”
In September, 2022, the conservative commentator and anti-trans activist Matt Walsh, who moved to Nashville in 2020 (along with his employer, the conservative news company the Daily Wire), posted a thread on Twitter. “Vanderbilt drugs, chemically castrates, and performs double mastectomies on minors,” it began. “But it gets worse.” Walsh—who is the author of books including “Church of Cowards: A Wake-Up Call to Complacent Christians” and “What Is a Woman?,” a polemic arguing that gender roles are biologically determined—worked in conservative talk radio before being hired by the Daily Wire as a writer, in 2017. Last year, the left-wing watchdog group Media Matters for America mapped Walsh’s origins as an aspiring radio shock jock in the early twenty-tens who once said, “We probably lost our republic after Reconstruction.” In 2022, he was one of several right-wing social-media pundits who began broadcasting misinformation about hospitals that provided gender-transition treatment for minors, which were then overwhelmed with phone and e-mail threats and online harassment. One study found that more than fifteen hospitals modified or took down Web sites about pediatric gender care after being named in these campaigns.
Walsh included in his thread about Vanderbilt a video clip of Shayne Taylor, the medical director of its Transgender Clinic, speaking of top and bottom surgeries as a potential “money-maker” for the hospital. Walsh did not specify that Taylor was mostly speaking about adults. (Vanderbilt never performed genital surgery on underage patients and did an average of five top surgeries a year on minors, with a minimum age of sixteen.) More than sixty Republican state legislators signed a letter to Vanderbilt describing the clinic’s practices “as nothing less than abuse.” In a statement calling for an investigation, Governor Lee, who was up for reëlection, said that “we should not allow permanent, life-altering decisions that hurt children.” Within days, Vanderbilt announced that it would put a pause on surgeries for minors. Jonathan Skrmetti, Tennessee’s Republican attorney general, began an inquiry into whether Vanderbilt had manipulated billing codes to avoid limitations on insurance coverage.
In October, Walsh and other anti-trans advocates held a “Rally to End Child Mutilation” in Nashville’s War Memorial Plaza. The speakers included the Tennessee senator Marsha Blackburn, the former Democratic Presidential candidate Tulsi Gabbard, and Chloe Cole, a nineteen-year-old self-described “former trans kid.” After identifying as male from the age of twelve, receiving testosterone, and getting top surgery, Cole de-transitioned to female at sixteen and is now one of the country’s foremost youth advocates of bans on gender-transition treatment for minors. “I was allowed to make an adult decision as a traumatized fifteen-year-old,” she said at the rally.
For the past four years, the number of anti-trans bills proposed throughout the United States has dramatically risen. The A.C.L.U. has counted some four hundred and ninety-six proposals in state legislatures in 2023, eighty-four of which have been signed into law. The first state ban on gender-transition treatment for minors was passed in Arkansas in 2021. It was permanently blocked by a federal judge this year, but more than twenty states have passed similar laws since then. As lawsuits filed by the A.C.L.U., Lambda Legal, and other organizations make their way through the courts, trans people are left to navigate a shifting legal landscape that activists say has affected clinical and pharmaceutical access. Lowell told me that she consults with six lawyers (including one she keeps on retainer) to best advise patients, who must frequently drive across state borders to receive care. “It’s literally a daily task to figure out what’s legal where,” she said.
In Tennessee, the Human Rights Campaign has counted the passage of at least nineteen anti-L.G.B.T.Q. laws since 2015, among the most in the nation. Some of these laws have been found unconstitutional, such as a ban on drag shows in public spaces and a law that would have required any business to post a warning if it let transgender people use their preferred rest room. But many others have gone into effect, such as laws that censor school curricula and ban transgender youth from playing on the sports teams that align with their identity.
Proposals to ban gender-transition treatment for minors were the first bills introduced in the opening legislative sessions of the Tennessee House and Senate in November, 2022. “It was Matt Walsh who lit a fire under the ultraconservative wing of the Republican Party this year,” Chris Sanders, the director of a Nashville-based L.G.B.T.Q. advocacy group called Tennessee Equality Project, told me. “It was lightning speed the way it all unfolded.” At hearings throughout the winter, parents of trans kids, trans adults, trans youth, and a Memphis pediatrician who provides gender-affirming care testified against the ban. Those who spoke in support of it included Walsh, Cole (who is from California), and a right-wing Tennessee physician named Omar Hamada, who compared such treatment to letting a minor who wanted to become a pirate get a limb and one eye removed.
L.G.B.T.Q. activists who attended described feeling disregarded by the Republican majority. Molly Quinn, the executive director of OUTMemphis, a nonprofit that helps trans youth navigate their health care, likened the experience to “being the only queer kid at a frat party.”
Three months after Governor Lee signed the ban, Vanderbilt University Medical Center informed patients that the previous November, at the attorney general’s request, it had shared non-anonymized patient records from the Pediatric Transgender Clinic, including photographic documentation and mental-health assessments. “I immediately started hearing from parents,” Sanders said. Their fear stemmed in part from attempts in states like Texas to have the parents of trans kids investigated by child-protective services. (The attorney general’s office said in a statement that it is “legally bound to maintain the medical records in the strictest confidence, which it does.”) Former patients have sued Vanderbilt, and a federal investigation by the Department of Health and Human Services is also under way. (A spokesperson for Vanderbilt declined to comment for this article.)
In July, the Sixth Circuit Court of Appeals became the first federal court in the country to allow a ban on gender-transition treatment for minors to take effect, with a final ruling planned for September. Chapman, who had spoken out for trans rights through local media outlets, and had been targeted with online threats and menacing phone calls in return, understood that Tennessee, where she had lived for most of the past thirty-five years, had become a hostile environment for her family. “I genuinely feel we are being run out of town on a rail,” she said. “I am not being dramatic. It is not my imagination.”
It was dusk by the time Paul had loaded the last of the boxes into three storage pods. Everything was ready, but the family was having trouble leaving. Someone would walk out of the house and get into the car, only to go back into the house five minutes later. Chapman suddenly remembered that she had forgotten to buy padlocks for the storage pods, which were scheduled to be picked up by U-Haul the next day. As she drove off to get them, Paul sat on the back steps and stared out at the lawn. Fireflies were winking on and off over the grass.
“Bollocks,” he said to himself, then stood up and went inside.
Although comprehensive demographic data on transgender youth are scarce, the American Academy of Pediatrics has reported that “research increasingly suggests that familial acceptance or rejection ultimately has little influence on the gender identity of youth.” But without parental consent most kids in America who wish to transition medically are legally unable to do so until they turn eighteen. Having a supportive parent or guardian as a trans child is more than a legal or practical advantage, though. A study of eighty-four youth in Ontario, aged sixteen to twenty-four, who identified as trans and had come out to their parents found that the rate of attempted suicide was four per cent among those whose parents were strongly supportive but that nearly sixty per cent of respondents who described their parents as not supportive had attempted suicide in the previous year.
Chapman’s decision to support her daughter grew in part out of her own experience as a black sheep in a deeply religious family. She was born in East Tennessee to a Baptist minister and his wife and had an itinerant upbringing, moving around the South. The last words her grandfather, who was also a Baptist minister, said to her were “I’m so sorry I’m not gonna see you in Heaven.”
Paul was raised in Dublin, Ireland, as the youngest of twelve children in a Catholic family. “We both came from communities that were super fundamentalist,” Chapman said. They agreed that they would raise their children outside of any religious tradition. If they had a doctrine, Chapman said, it was “critical thinking.” They brought their kids to Black Lives Matter demonstrations, and took them to hear the Georgia congressman and civil-rights activist John Lewis speak. But Paul and Kristen would also listen to the far-right radio host Rush Limbaugh, to know what the other side was saying. As the children got older, Paul and Kristen started to have different visions of the future—Kristen wanted to buy an R.V. and travel the country, and Paul wanted to buy a house. In 2019, they decided to separate, but they couldn’t afford to split their family into two households.
Paul at first had trouble understanding how Willow could decide about her gender so young. Kristen would argue, “If a person presents and says, ‘This is who I am,’ it is not your job to unpack that.” In the end, it was by talking to two trans women—a co-worker in her fifties and a twentysomething bartender at the pub he frequented—that Paul came to understand his daughter better. “Reading online was too much right-wing or left-wing,” he said. “I needed something more grounded.” The bartender told him that her father had rejected her, and that she had scars on her arms from self-harm. “I said, no matter what, I wasn’t doing that,” Paul recalled.
Willow had told me that one of the hardest parts of leaving town was doing so while her relationship to her father was still evolving. “I feel like my biggest unfinished business is that relationship,” she said the day before the move, over boba tea in a strip mall called Plaza Mariachi. “I think I’ve dealt with it. We’ll talk on the phone. Even if we don’t have an in-person connection, I think we’ll be O.K.”
Once they all managed to leave the house for the last time, Paul gave Chapman and each daughter a hundred dollars in cash as a parting gift. The family had dinner at Panera Bread, then sat for a while at a nearby park. Paul cancelled two Lyfts before finally getting in one and heading to the pub, where he would try to process the day. Chapman and the girls got in the white Dodge and took I-24 out of Nashville.
L.G.B.T.Q.-rights activists around the country have seen the sudden uptick in bills targeting transgender identity as a strategy to rally conservative voters after the legalization of gay marriage and the criminalization of abortion. “There was an inordinate amount of money and attention and huge far-right groups, many of which have been deemed hate groups, focussed on keeping us as L.G.B.T.Q. people from getting married, right?” Simone Chriss, a Florida-based lawyer, told me. Chriss is representing trans people in several lawsuits against the state over its restrictions on gender-affirming care. She observed that, after the Supreme Court legalized gay marriage, in 2015, “all of the people singularly focussed on that needed something else to focus on.”
She recalled watching as model legislation propagated by groups such as the Alliance Defending Freedom and the Family Research Council targeted trans people’s freedom to use bathrooms of their choice, and to play on their preferred sports teams. Health care came next. “All of a sudden, you see this surge in gender-affirming-care bills,” Chriss said. “And what’s bananas is there was not a single bill introduced in a single state legislature prior to 2018.”
The anti-trans rhetoric about protecting children mirrored that of the anti-gay-marriage movement, she continued, and new rules mandating waiting periods, for example, were familiar from the anti-abortion movement. “It’s like dipping a toe in by making it about trans children,” she said. “I think the goal is the erasure of trans people, in part by erasing the health care that allows them to live authentically.”
Beach-Ferrara, of the Campaign for Southern Equality, said her organization estimates that more than ninety per cent of transgender youth in the South live in states where bans have passed or will soon be in effect, and that between three and five thousand young people in the South will have ongoing medical care disrupted by the bans. (The Williams Institute at U.C.L.A. estimates that there are more than a hundred thousand thirteen-to-seventeen-year-olds who identify as trans living in the South, more than in any other region in the country.) Already, university hospitals such as the University of Mississippi Medical Center and the Medical University of South Carolina have discontinued their pediatric gender services before being legally required to do so.
Had Chapman stayed in Tennessee, Willow’s closest option for getting puberty-blocker shots would likely have required a four-hundred-and-fifty-mile trip to Peoria, Illinois. Willow’s TennCare insurance would not easily travel, and a single shot can cost twelve hundred dollars out of pocket. Paul had told Chapman not to be ashamed if the move didn’t work out and she changed her mind, but she already knew she would never go back to Nashville.
On their way east, the family stopped for a few days in Seneca, South Carolina, where Chapman has relatives. Back on the road, she tried not to focus on the uncertainty that awaited her and her daughters, but she had to pull over at least twice to breathe her way through anxiety attacks. There was a heat wave, and by the time they arrived in Richmond the back speakers of the S.U.V. were blown out, and everyone was in a bad mood. Willow had snapped at her mother and Saoirse for trying to sing along to the Cranberries; she had even yelled at the dog. “It was difficult?” Willow told me afterward, when I asked how the trip had been; then she added, “I’m still excited.” (Saoirse declined to be interviewed.)
Chapman had booked an Airbnb, a dusty-blue bungalow outside Richmond. It had good air-conditioning and a small back yard for the dog. She could afford only a week there before they would have to move to a motel. That night, Willow zoned out to old episodes of “RuPaul’s Drag Race” in the living room, while Chapman scrolled through real-estate listings on her phone. She asked for advice on the social-media feeds of local L.G.B.T.Q. groups, and the responses were heartening. She decided that, if she was able to find a place to live by the end of the week, she would not take the marketing job she had lined up. School wouldn’t start for a few weeks, and it was not the right moment to leave her daughters alone all day.
At eight the next morning, Chapman was sitting in an otherwise empty waiting room at the Southside Community Services Center, filling out forms to get the family food stamps and health insurance. She had put on makeup for the first time in days and was wearing wide-legged leopard-print pants and a black shirt. She had forgotten her reading glasses, however. “Do you have a spouse who does not live at home?” she read out loud, squinting her way through the questions. “Yes,” she answered to herself, checking a box. (She and Paul are not yet divorced.)
Chapman kept mistakenly writing “Willow” on the government forms—she had never officially changed her daughter’s name. (A 1977 Tennessee state law that prohibits amending one’s gender on a birth certificate will apply to Willow no matter where she moves; another Tennessee law, which went into effect this past July, bans people from changing the gender on their driver’s license.) Chapman picked up the next batch of forms, for Medicaid. “One down, one to go,” she said.
Later in the day, Chapman and her daughters went to see a house that was advertised on Craigslist, an affordable three-bedroom in the suburbs of Richmond. As they were driving, the owner texted Chapman that he had a flat tire and couldn’t meet them. But the place looked ideal from the outside, so she filled out an application and sent the landlord a thousand-dollar deposit. At five the next morning, she woke up and saw a text from the owner claiming that the money transfer had not gone through. She quickly realized she’d been scammed.
Chapman became weepy. She posted on social media about the con, then drove Saoirse to a thrift store she wanted to visit. At first, only one shopper noticed the woman crying uncontrollably in the furniture section. Then someone went to find some tissues, and someone else brought water. Soon, Chapman recalled, she was surrounded by women murmuring words of sympathy.
That evening at the Airbnb, Chapman and Willow sat at the kitchen table. “The emotional impact of the scam hit me way more than the money,” Chapman said, still tearing up at the thought of it. Willow nodded in sympathy. But for Chapman the experience was also a reminder of the advantages of talking about their situation—the women had told her that the schools near the house were not very good, anyway. “Thrift-store people will help you when you’re down and out. They’re used to broken shit,” she said, shaking her head. “If I had broke down in a Macy’s? Think how different the reaction would be.”
The next morning, Chapman was feeling a little less pessimistic. The humidity had broken, and the weather was good. People had responded to the news of the scam by donating money to replace what she had lost, and a local Facebook group had led her to a property-management company that was flexible toward tenants with bad credit.
She drove to see a three-bedroom apartment in a centrally situated part of Richmond. Though one of the bedrooms was windowless, the place was newly painted, and it had a wooden landing out back that could serve as a deck. It was also in a school district that people had recommended. “I can see this working,” Chapman said tentatively. Most of the utilities were included in the sixteen-hundred-and-fifty-dollar rent. Chapman didn’t have time to overthink it. She wrote the real-estate agent saying she would apply.
That afternoon, Chapman drove Willow to see the apartment. The door was locked, but Willow climbed through a window and opened the door so they could consider the space together. “We were, like, ‘Oh, this is nice,’ ” Willow said. She loved the neighborhood, which had vintage stores and coffee shops. “You can walk anywhere, you don’t need transportation—that’s really cool.”
The next day, Willow was sitting on a couch in the Airbnb watching a slasher film called “Terrifier.” Chapman was next to her, getting ready for a Zoom call with someone from a local trans-rights organization called He She Ze and We.
In the weeks leading up to the move, Chapman had taken time to research which schools were friendly to trans people. Willow estimated that maybe half the students in her middle school in Nashville were transphobic, and twenty per cent were explicit about it. She was bullied, but she says that it didn’t bother her. Her teachers were more supportive, such as the one who gave her an entire Lilith Fair-era wardrobe. “She was, like, ‘Do you want some of my old clothes? Because you’re so fashion,’ ” Willow said. “I had that black little bob.”
“She had Siouxsie Sioux hair for a while,” Chapman said, looking at her fondly.
The two of them agree that Willow’s personality shifted after transitioning. Once withdrawn and nonconfrontational, she began to develop a defiant attitude. “It was kind of fun to just mess with them,” she recalled of the bullies, who she said were not vicious but more into trying to get a laugh—“like, childish, immature stuff.” She would be coy; she would tell them to give her a kiss. “My only weapon, I guess, was how I chose to respond,” she said.
“She’s not a shrinking violet,” her mother added.
“I just don’t like the traditional way that you’re taught to stand up for yourself,” Willow said. “I think absurdism is the best way.” If she lets someone misgender her, she said, “it’s not because I don’t want to be the annoying trans person, it’s more like . . . you’re not gonna get to those people.”
In her freshman year, she attended a public arts high school, and began skipping class and smoking. She says there were at least ten other students who identified as trans, but she remained something of an outsider. When she was in school, she says, she almost thought of herself as a kind of character expected to perform.
Chapman is not a disciplinarian—she had enough of that growing up. But she had a conversation with her daughter after watching a video of an incident in which Willow was voguing in a school hallway, attempted to do a death drop, and ended up with a concussion. The students around Willow were clapping and egging her on even after she fell. “It’s great that you’re the kind of person who will do crazy things,” Chapman remembered saying, “but you need people around you who are not like that.” Both Chapman and Paul worry about Willow’s safety, in part because she is not easily scared herself.
“Will you turn that off?” Chapman said now about the horror film, as she logged on to Zoom. Willow took that as a cue to leave the room.
“You’re going to want to be on this thing,” Chapman said, calling her back.
Willow, who wore blue eyeshadow, a purple baby tee with a peace sign and the word “Smile!” on it, and magenta-pink shorts, plopped back down on the couch, then got up to retrieve supplies to disinfect her belly-button piercing, which she began to do with studiousness.
On Zoom, Chapman introduced herself to Shannon McKay, the co-founder of He She Ze and We, and gave a summary of their situation.
“Have you gotten connected with the medical piece yet?” McKay asked. She explained that, in Virginia, Willow might not have to wait until she turned sixteen to start estrogen. At this news, Willow looked up and made eye contact with her mother, who nodded back.
The conversation turned to politics. Earlier in the week, Glenn Youngkin, the Republican governor of Virginia, had held a town hall on parents’ rights at a school in Henrico County. A parent there had urged Youngkin to introduce a ban on gender-transition treatment for minors.
“Our governor, just to let you know, has not taken a stance,” McKay, who also has a trans daughter, explained to Chapman. “And I think he’s not conservative enough for the folks that wish he would be.”
In July, Youngkin had issued a series of rules that direct trans kids to use pronouns and bathrooms that accord with the gender they were assigned at birth, unless they have parental permission to do otherwise. Chapman asked McKay if that gave her some control over how Willow would be treated at school.
“The clincher here is, even if all parents involved do fill out the form and say, ‘We’re all on board,’ school personnel can still say, ‘I don’t believe in that. I’m not going to do it,’ ” McKay said. She did have some good news, however: if Willow learned to drive, she could determine the name and gender on her identification card.
“I’m not ready for it,” Chapman said, referring to the driving.
“Well, before this governor messes it up, I encourage people to go ahead and get these documents lined up,” McKay said.
Chapman got the apartment she and Willow had visited, and a few days later the family moved in. Willow started at her new school on Tuesday, August 22nd. She made friends with another trans girl in the first week. But, despite a letter from Chapman specifying Willow’s name and pronouns, school administrators told her they had to use the name on her registration. She was also told she should use the nurse’s bathroom instead of the girls’ bathroom, even though it was on a different floor and might cause her to be late to class. Willow ignored that rule, and asked her mother not to intervene on her behalf.
Before the school year had begun, Chapman told me that if school didn’t work out she would be fine with her daughter getting a G.E.D. When I asked Willow about the future, she said that she wants to move to New York City. She wants to go to the balls, “maybe be a model, I don’t know,” she continued. “I like doing art. I like meeting people. I don’t know how to connect all of those things and get paid.”
“You care more about personal freedom than hitting a milestone,” Chapman said. “You care less about the traditional high-school things, the traditional college things.”
“I feel like I should care about them,” Willow said.
“Oh!” Chapman said, looking surprised. “I like hearing that.”
“I’m open—like, I could potentially care about them, but if it’s not welcoming me then I won’t,” Willow said.
The day in August when Willow needed her puberty-blocker shot came and went. The family’s insurance still had not come through, and the earliest appointment Chapman could get at a clinic with tiered pricing was in mid-September. An administrator at the clinic assured her that there was a window with puberty blockers, and that Willow’s voice would not drop overnight.
I talked to Chapman the evening after the appointment. “We thought we were just going in for an intake, but they started Willow on estrogen today,” Chapman told me over the phone. “The doctor was in shock that Willow had been on puberty blockers for two years and that she was almost sixteen.” (“It’s really hard for cis people to fully appreciate the deep destabilizing physical betrayal that these kids are navigating on a day-to-day basis,” the doctor, Stephanie Arnold, told me. “It’s a period where you should be establishing confidence in yourself and your ability to interact with the outside world.”) Willow, Chapman added, “is over the moon.” They called Paul to let him know. “After every fucking thing . . . it just happened,” she said.
The following Monday, Chapman started a new job, counselling people on signing up for Medicaid. She was earning less than she had in Nashville, but hoped to rebuild her career as an artist and a community organizer.
The family was getting to know Richmond, with its restored Victorian row houses and stately parks. Using the hundred dollars from her father, Willow had bought herself a skateboard to get around town. Paul was planning a visit for October. “This city is just dang cute, let’s be honest,” Chapman said. They had found a leftist bookstore where she had bought Willow a book of poetry by trans writers. When I asked Willow how she felt on estrogen, she said that it was too early to discern any changes with clarity; what she felt, she said, was more vulnerable. A little more than a month in, Willow said that she was liking her new school and had even attended the homecoming dance. “And my grades are O.K.,” she added. “So that’s something.”
On September 28th, the Sixth Circuit Court of Appeals upheld the ban on gender-transition treatment for minors in Tennessee. The court found, among other things, that state legislatures can determine whether the risks of gender dysphoria are less significant than the risks of treating it before a patient turns eighteen. A dissenting opinion stated, “The statutes we consider today discriminate based on sex and gender conformity and intrude on the well-established province of parents to make medical decisions for their minor children.” Because the federal appeals courts have split in their findings, with other circuits finding such bans unconstitutional, the issue has the potential to proceed to the Supreme Court.
“I know what’s going on,” Willow had said, when I asked her about politics. She doesn’t see herself as an activist, though; she prefers to let the news filter through her mother rather than to consume it herself: “She’s my person on the inside.” 
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typingtess · 1 year
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Director Vance made a few phone calls so Dom's parents and sister were flown to Los Angeles on a private government jet. Col. Vail asked to see his son before the casket was closed. He regretted that decision and would for the rest of his life.
There was a funeral mass at the Cathedral of Our Lady of the Angels downtown. Dom's non-work, LA friends – there were only a handful, he wasn't in town that long – were all there. Thinking Dom worked for a fictitious NGO, Dom's friends were told he was in Afghanistan working as part of a health care initiative – a last minute addition. They were told after a long day of working in a clinic treating sick children, Dom's jeep turned over just outside of Kandahar. Three aid workers were badly hurt, Dom was killed. A fabricated tale of Dom's true hero's death.
The entire Office of Special Projects attended the funeral. Sam arrived in his Navy dress uniform. He introduced himself to Col. Vail and explained that he would travel with the family and Dom's casket back to Virginia. Col. Vail said that wasn't necessary but Sam explained it was. Dom died saving Sam's life, that sacrifice must and would be honored. Col. Vail understood.
That night, Sam flew across the country with Dom's family and Dom's casket. A day later, Sam stood at the back of the funeral home as family members, friends and the colleagues of the Vails paid their respects at Dom's wake. The following morning, Sam sat with the driver in the hearse as they drove to the Vail family plot. Dom was buried next to his grandfather Louis, a member of the 92nd Infantry Division in Italy in WWII who returned home to start a family and a career at the DoD, and near his uncle Edward who fought and died in Vietnam.
A small ceremony at the gravesite ended with the family members hugging. Once again, Sam offered his condolences to Dom's parents and sister as the family started walking to their cars.
Alone at the grave, Sam looked at the casket one last time, hoping that Dom found the peace he deserved.
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follow-up-news · 1 year
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Tens of thousands of Kaiser Permanente workers took to picket lines in multiple states on Wednesday, launching a massive strike that the company warned could cause delays at its hospitals and clinics that serve nearly 13 million Americans. The Coalition of Kaiser Permanente Unions, representing about 85,000 of the health system’s employees nationally, approved a strike for three days in California, Colorado, Oregon and Washington, and for one day in Virginia and Washington, D.C. Some 75,000 people were expected to participate in the pickets. “Kaiser has not been bargaining with us in good faith and so it’s pushing us to come out here and strike,” said Jacquelyn Duley, a radiologic technologist among the hundreds of picketers at Kaiser Permanente Orange County - Irvine Medical Center. “We want to be inside just taking care of our patients.”
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autonom-us-project · 5 months
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Abortion Rights in Virginia 
In June 2022, the United States Supreme Court overturned the ruling of the landmark 1973 case Roe v. Wade, which had previously provided federal protections of the right to abortion.
With the responsibility of protecting the right to reproductive freedom left to the states, it can be difficult to keep track of all the constantly changing laws and regulations. To help, we’ve gathered the most important information on your state’s current laws, restrictions, and related details. Below is what you need to know about Virginia’s current abortion legislation.
*Please note, information on this website should not be used as legal advice or as a basis for medical decisions. Consult an attorney and/or a physician for your particular case.
Where does the law currently stand on abortion in the state of Virginia?
Abortion is currently legal but unprotected in the state of Virginia.
When did Virginia’s current abortion legislation go into effect?
The state of Virginia repealed its Pre-Roe v. Wade abortion ban back in 1975, and, since the overturning of Roe v Wade, has continued to legally allow abortion access up until the point of viability. 
For more information on your state’s abortion legislation, see our breakdowns of various abortion bans, restrictions, and protections in the U.S.
Are there any legal restrictions to abortion access in the state of Virginia?
Currently, there are no restrictions to abortion access up until the point of viability, or the point at which a fetus is likely to survive outside of the uterus, typically occurring at 24 weeks. 
Past this point, an abortion is allowed only when “continuation of the pregnancy is likely to result in the death of… or substantially and irremediably impair the mental or physical health of,” the pregnant individual, in which case this must be confirmed by three (3) physicians. 
The specifics can be read in Virginia Legal Code 18.2-74 
What protections are in place regarding abortion in the state of Virginia?
Reproductive Health Protection Act: While the state of Virginia does not legally protect the right to abortion, several medically unnecessary restrictions to abortion access were repealed in the 2020 Reproductive Health Protection Act. 
Medical Funding: Virginia passed a law in 2021 removing the restriction on state insurance covering abortion. 
The specifics can be read in the following Virginia Legal Codes SB 733, and SB 1276
I am pregnant in the state of Virginia and wish to terminate my pregnancy. What now?
If you believe your pregnancy meets the requirements for a legal abortion in your state, schedule an appointment with a trusted physician as soon as possible. If not, you will need to arrange an appointment at a clinic providing abortion services out of state. Make sure the state you choose allows abortions at the gestational age your pregnancy will reach by the appointment date.
If you need financial assistance to do this, there are existing funds to help cover both the procedure and travel costs. 
Abortion funds can assist with the medical cost of the abortion itself. Practical Support Organizations, (PSOs), can assist with other costs incurred seeking an out-of-state abortion such as travel, lodging, childcare, provider referrals, emotional support, and judicial bypass for minors, among other needs. Here are a few resources available to those seeking support in Virginia:
Access Reproductive Care- Southeast [Fund & PSO] – Provides support for those seeking an abortion from Virginia. Offers financial aid and support for abortion, lodging, and transit. Provides Spanish language support. See their website for more information. 
Blue Ridge Abortion Fund [Fund & PSO] – Provides support for those seeking an abortion from Virginia. Offers financial aid and support for abortion, lodging, and transit. Provides Spanish language support. See their website for more information. 
Richmond Reproductive Freedom Project [Fund & PSO] – Provides support for those seeking an abortion from Virginia. Offers financial aid and support for abortion, lodging, transit, clinic escorts, food assistance, and childcare assistance. Provides Spanish language support. See their website for more information. 
Whole Woman's Health- Abortion Wayfinder Program [Fund & PSO] – Provides support for those seeking an abortion from Virginia. Offers financial aid for abortion, lodging, and transit. See their website for more information. 
DMV Abortion Practical Support Network [PSO] – Provides support for those seeking an abortion from Virginia. Offers support for lodging, transit, clinic escorts, food assistance, emotional support, and childcare assistance. See their website for more information. 
DC Abortion Fund [Fund] – Provides support for those seeking an abortion from Virginia. Offers financial aid for abortion.  Provides Spanish language support. See their website for more information. 
National Abortion Hotline [Fund & PSO] – Provides support for those seeking an abortion Nationwide. Offers financial aid for abortion, transit, and provider referrals. Provides Spanish language support. See their website for more information. 
Women’s Reproductive Rights Assistance Project [Fund] – Provides funding for those seeking an abortion Nationwide. Offers financial aid for abortion and emergency contraception (the morning-after pill). See their website for more information. 
Abortion Freedom Fund [Fund] – Provides funding for those seeking an abortion Nationwide. Offers financial aid for abortion. See their website for more information. 
Indigenous Women Rising [Fund] – Provides funding for Indigenous individuals Nationwide seeking an abortion. Offers financial aid for abortion. See their website for more information. 
Reprocare [PSO] – Provides support for those seeking an abortion Nationwide. Offers aid in the form of provider referrals, emotional support, language services, and abortion doula services. Provides Spanish language support. See their website for more information. 
The Brigid Alliance [PSO] – Provides support for those seeking an abortion Nationwide. Offers aid in the form of provider referrals, emotional support, language services, and abortion doula services. Provides Spanish language support. See their website for more information. 
Regardless of the legislation your state currently has in place, remember that safe and legal options are always available. The most important tool you can arm yourself with in these difficult times is knowledge, so stay informed about changes in legislation and policy where you live, and know that there are always resources available to help you through this ♥️
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scotianostra · 2 years
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Marie Charlotte Carmichael Stopes  founder of first modern birth control clinic, was born in Edinburgh on October 15th 1880.
At first, Stopes was home-schooled, but from 1892 to 1894 she attended St George’s School for Girls in Edinburgh, her studies  Her studies of paleobiology took her to universities in London, England and Munich, Germany, then returning to England, she became the first female member of the science faculty at the University of Manchester.  She was a very well-educated woman; she was a woman who advocated for eugenics and the women’s rights movements.
Marie Stopes was a palaeobotanist who became the United Kingdom’s greatest advocate for birth control after the 1918 publication of her book Married Love. Trained in biology and geology, she had her doctorate by the time she was 24 years old, when she became Manchester University’s first female lecturer in science. 
Marie studied and did field work in Japan and Canada, but after the annulment of her first marriage, she set out to educate women on sex in marriage. The book Married Love was a controversial bestseller (banned in the United States); she followed it with Wise Parenthood that same year. 
She and her second husband opened a clinic in London in 1921 to provide birth control and health care — but not abortions — to married women. After 1935, Stopes stopped publishing scientific articles and focused on her fame as an author and advocate for birth control. 
It wasn’t all good for Stopes in some ways was a flawed character, she was known to be a crazed fan of eugenics, in favor of sterilizing “inferior” members of society, a certain 20th century dictator and war mongered had the same idea in his nazi doctrination.According to one source  "Marie was an elitist, an idealist, interested in creating a society in which only the best and beautiful should survive”  Stopes's enthusiasm for eugenics and race improvement was in line with many intellectuals and public figures of the time.
Marie Stopes International was founded nearly 20 years after her death and provides contraception and abortion services around the world to this day.
Stopes was even remembered in a playground rhyme:
Jeanie, Jeanie, full of hopes, Read a book by Marie Stopes, But, to judge from her condition, She must have read the wrong edition.
Stopes was acquainted with many literary figures of the day. She had long-standing correspondences with George Bernard Shaw and Aylmer Maude, and argued with H. G. Wells. Noël Coward wrote a poem about her, and she edited Lord Alfred Douglas' letters. She unsuccessfully petitioned Neville Chamberlain to arrange for Douglas to receive a civil list pension; the petition was signed by Arthur Quiller-Couch, John Gielgud, Evelyn Waugh and Virginia Woolf, among others.[70] The general secretary of the Poetry Society, Muriel Spark, had an altercation with Stopes; according to Mark Bostridge, Spark "found herself lamenting that Stopes's mother had not been better informed on [birth control]
Stopes died on 2nd October 1958, aged 77, from breast cancer at her home in Dorking, Surrey.
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fluffy-critter · 1 year
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ausetkmt · 1 year
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Dexter Barry waited 12 years to get a new heart. He saw dozens of doctors, had invasive procedures and moved states to survive. In 2020, his long wait paid off. His new heart allowed him to imagine a healthy life where he could revisit his passion for motorcycles and watch his children grow and flourish in their careers. 
But in 2022, after a misdemeanor arrest kept him in jail for two days without his life-sustaining medication, his body rejected the heart.
Barry’s neighbor called 911 in November to complain that Barry, 54, had threatened to beat him up after a weeks-long fight over wifi access. A fight never occurred, but Barry was arrested on a simple assault charge. 
Barry told Jacksonville Sheriff’s Officer Jacob McKeon at least seven times that he needed to take his anti-rejection medications every day to survive, according to body camera footage that was reviewed by The Tributary. The next morning, according to the court transcript, Barry told Judge Gilbert Feltel the same.
“I am on medication,” Barry told the judge. “I just had a heart transplant, and I haven’t taken my medicine all day since I have been locked up, and I take rejection medicines for my heart so my heart won’t reject it, and I’m almost two years out.”
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On Nov. 23, Barry died.
He never got his medication, according to his son and a lawyer representing his family. A pathologist hired by the family said he died after his body had rejected the heart he had waited so long for.
Andrew Bonderud, the Jacksonville civil rights lawyer who represents Barry’s family, is worried Barry didn’t get his medications because of the extreme expense to obtain them.
“Records from jail will likely show they made a note of it,” Bonderud said. “JSO recognized it’s an extremely expensive medication and how disgusting if it turns out that this was a business decision for the JSO, that they would rather not pay for the medication. They would rather risk death over a business decision. It’s one of the most outrageous cases I’ve ever seen in this city of JSO misconduct.”
An expert with the National Commission on Correctional Health Care – under which JSO is accredited – said police and jail officials had a constitutional responsibility to care for Barry. Officials had options to get Barry his medicine.
The Jacksonville Sheriff’s Office refused to answer questions about Barry, citing an administrative review of his death, but records show that Armor Health, which operates the jail’s health care system, has not consistently given inmates health assessments within the required 14-day time frame. Because Barry had only been held for two days, it’s likely he didn’t get that assessment. It’s unknown if Barry was seen at all by a nurse during his booking because the jail declined to release medical records.
JSO spokesperson Officer Allyn Kelly declined to answer when the administrative review started or what sparked it.
‘He didn’t sound like himself’
Barry moved from Virginia to Jacksonville in 2018 when his heart started to fail. 
“He was working at Advanced Auto, and the manager said he looked real bad,” his son, Dexter Barry Jr., told the Tributary. “He had an appointment the next day, and the tube that fed oxygen to his heart had ruptured.” 
He was life-flighted that day to Mayo Clinic in Jacksonville, which was more equipped to handle Barry’s needed level of care. He was given a left ventricular assist device, or LVAD, that he carried in a bag – essentially, his heart was battery-powered. 
“He loved his little man purse,” Barry Jr. said, laughing.
Barry decided to stay in Jacksonville where his new doctors were. He was also closer to Barry Jr., who lives in Orlando. And despite his taste for his new fashion, he kept fighting for a new heart.
In October 2020 – 12 years after his diagnosis of congestive heart failure – Barry got one.
Knowing the responsibility that came with caring for his new heart, Barry was adamant about taking his anti-rejection medications three times a day as prescribed, according to his family. He was determined to keep his heart healthy. A year before he died, a biopsy showed it was in excellent condition, Bonderud, the attorney, said. 
Barry was in jail for two days and released after he posted a $503 bond. His son later remembered his dad telling him, as soon as he got out, “I didn’t get my meds.” He would have missed at least five doses. Despite restarting his medications as soon as he could, Barry said he felt unwell.
“When I spoke to him, he didn’t sound like himself, and he had shortness of breath,” Barry Jr. said. “He said he didn’t have insurance to go to the hospital, and I said, ‘You have insurance. Go.’”
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When the nurse couldn’t get Barry off the floor, he called 911. Barry died at UF Health Jacksonville. The county medical examiner declined to perform an autopsy, which left Barry’s family to get their own.
“We worked to get a GoFundMe to raise money for one, but it ended up coming out of pocket,” Barry’s daughter, Janelle King said.
The pathologist confirmed that Barry died because his body rejected the heart. He declined to make the connection between that and the days Barry went without taking his medications because he said he didn’t feel medically qualified to do so.
Dr. Maya Guglin, an Indiana cardiologist on the board at the American College of Cardiology, said organ transplant recipients have to take anti-rejection medications because their bodies view the new organ as an invasion that must be fought off. 
“If you just drop those medications, everyone is eventually going to reject that organ,” she said. 
Even if medication is restarted, it will be too late, Guglin said.
‘I’m cooled off already’
Barry’s arrest is something his kids can’t grapple with because of how minor the accusations against him were. 
Barry Jr. said that his father and a neighbor had been fighting over Wi-Fi for a few weeks. Barry told McKeon – the officer who arrested him – that his neighbor stopped paying for his half of the bill. Barry asked for payment multiple times.
That morning, Barry talked to his neighbor again. 
“At no point in time did you say you were gonna beat his ass?” McKeon asked him.
“I said I’d f— his ass up, don’t make me f— your ass up,” Barry said. 
Before he questioned Barry further, McKeon took out his handcuffs. 
“I’m going to put you in cuffs. You’re being detained. You’re not being arrested,” he said. “At this point, I do not believe you’re going to jail.”
“I’m not worried about going to jail,” Barry said. “I didn’t shake him.”
McKeon asked Barry what his disabilities were in the “event that you do go to jail.”
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It was the first time Barry told McKeon about his heart transplant. A note was made in his arrest report that Barry requested a wheelchair, but no other medical notes were made. 
Eleven minutes after telling Barry he didn’t believe he was going to jail, McKeon told him he was going to “take a ride” for threatening his neighbor. Assault is when someone makes a threat to someone else to hurt them, is able to actually hurt them and the other person has a “well-founded fear that the violence is imminent.”
When Barry was confused about the charge, McKeon told him, “I can’t in good faith leave the two of you together and be sure something’s not gonna happen later. More so it’s to separate you for a cool-off period.”
“I’m cooled off already,” Barry told the officer, explaining that he hadn’t fought with someone in decades and he wasn’t going to hurt his neighbor. About an hour had passed since the argument. Barry remained calm during the duration of his arrest.
Barry mentioned his medications six more times. 
I take rejection medicine for my heart transplant. I can’t miss those doses.
I don’t want to go to jail, because you taking me to jail and me missing my medicine means my heart will be rejected.
I’m supposed to take my noon medicine, and I didn’t take it.
He asked when the earliest he could be released would be. He asked if they could rush to get him in front of the magistrate or if he could go to a friend’s house for the night instead of jail.  
McKeon told him the jail could get him his medication. At one point made a call to his supervisor, but he continued with the arrest. He told Barry that the jail can get him his medication.
“My medication cost $2,000,” Barry responded. “I had to come from Virginia to get the transplant. This shit is no joke.”
Barry again promised McKeon that he wouldn’t escalate the fight.
“I get what you’re saying,” McKeon said. “You know how many times police in general have been told that and then the next thing that happens is someone ends up dead?”
‘A two-minute walk would’ve saved his life’
Barry was booked into jail at 1:29 p.m. – an hour and a half after he needed to take his second dose. He went in front of Judge Gilbert Feltel the following morning. Feltel declined to answer The Tributary’s questions, citing pending litigation.
Barry’s request for his medicine seemingly went ignored again. The Tributary requested any emails between Feltel, his assistant and jail management that day, but no records were found. 
The Tributary also requested copies of security video from inside the jail that would show Barry’s booking, but the Jacksonville Sheriff’s Office only sent McKeon’s body camera footage from the scene, claiming that fulfilled the request. The Tributary’s request for Barry’s medical records was denied, with the records department citing a federal health-privacy law. 
In June 2022, the Florida Model Jail Inspection noted that the Duval County Jail did not meet standards when it came to giving every inmate a health screening within 14 days of admission. 
Forty-two medical charts were reviewed with 34 patients missing those completed appraisals. This led to a backlog of appraisals. The Sheriff’s Office said it assigned staffers to address the backlog. Yet, as of April 27, a backlog of health screenings still existed. 
“Armor has determined an increase in full-time employees was required to complete assessments in a timelier manner,” Christian Hancock, a JSO spokesperson, wrote in an email about the backlog. “As per Armor’s onboarding protocols, all new medical staff will receive training and education, which includes health assessments being completed in a timelier manner … JSO, in discussions with Armor, has expressed our expectations for the health appraisals to be completed within the appropriate time frame.”
Rich Forbus, of the National Commission on Correctional Health Care, has worked in county jails before and knows that JSO could have gotten Barry his meds.
Barry should have undergone an initial health screening during his intake. Medical staff should have asked him what type of chronic conditions he had along with the type of medications he took, Forbus said. It’s unknown whether Barry underwent any screening because JSO declined to answer The Tributary’s questions.
“Typically, the provider for that facility would be notified immediately in that kind of case and told what’s going on,” Forbus said. “With medications, our standards indicate that they should be staying on the same type of medications they were receiving and the only change to a medication should be a clinical decision. It shouldn’t be based on cost savings or anything like that.”
Jails usually don’t allow outside medications in, but in the case for rare or expensive life-sustaining medications, Duval County could have made an exception, Forbus said. 
“You can verify that the pills are what they should be and that the person has a prescription,” he said. “This should’ve been something that went up to a command level to have someone make a decision on how to handle it.”
Barry’s children hope to get justice for their father.
“The police officer could’ve gone inside and got his medication,” Barry Jr. said. “This man is telling you, my heart needs those meds. A two-minute walk would’ve saved his life.”
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stephleb · 1 day
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Open Your Future: Top CNA Programs in Richmond VA Revealed
**Unlock Your​ Future: Top CNA Programs in Richmond VA Revealed**
If you’re considering a⁤ career ⁣as a Certified Nursing Assistant (CNA)⁤ in Richmond, VA, you’re on the right track to a ‌rewarding and fulfilling profession. CNAs⁢ play a vital role in the healthcare industry by providing hands-on care to patients and assisting nurses and other healthcare professionals in various‌ medical settings. To kickstart your career as a CNA, it’s essential to ⁣enroll in a‌ reputable training program ‌that will equip⁣ you with the skills and knowledge needed to excel in this role.
In Richmond, VA, there are several top-notch CNA programs that stand out for their quality education, experienced instructors, and hands-on training opportunities. To help you make an informed decision about where ⁢to pursue your CNA⁣ training, we’ve compiled‍ a list of the top CNA programs in Richmond VA.
**Top CNA Programs in Richmond‌ VA**
1. **Richmond School of Nursing**
– Location: Richmond, VA – Program Length: 4-6 weeks – Accreditation: Virginia Board of Nursing – ⁣Highlights: Small class sizes, experienced instructors, hands-on clinical experience
2. **Virginia​ Commonwealth University (VCU) Health System**
– Location: Richmond, VA – Program Length: 6-8 weeks – Accreditation:⁢ Virginia Board of Nursing – Highlights: Affiliated with a ⁤leading healthcare institution, strong emphasis on clinical​ skills
3. **Southside Regional⁤ Medical Center School of Nursing**
– Location: Petersburg, VA​ (near Richmond) – Program Length:⁢ 5-7 weeks – Accreditation: Virginia Board of Nursing – Highlights: ‍Clinical​ rotations at a bustling medical center, career placement assistance
4. **Bon Secours Memorial College of Nursing**
– Location: Richmond, VA -⁣ Program Length: 6 weeks – Accreditation: Virginia Board of Nursing – Highlights: Focus ‍on patient-centered​ care, preparation for certification ‌exam
**Benefits of Pursuing a CNA ‍Program in Richmond VA**
– Pathway to a rewarding career⁤ in healthcare – High demand for CNAs in Richmond VA – Competitive salary and ​benefits – Opportunities for career advancement‍ in the medical field – Chance to make a positive impact on patients’ lives
**Practical Tips for Success in a ‍CNA Program**
– Stay organized and manage your time effectively – Actively participate ⁣in classroom discussions and ⁢clinical experiences – Seek help from instructors or classmates‍ when⁢ needed -​ Practice good communication skills with patients and healthcare ‍team members – Prepare ⁢for the certification exam by studying diligently
**Conclusion**
Enrolling‌ in a CNA program in Richmond ‌VA is a great first step ⁢towards ⁢a successful career in ⁢the healthcare industry. By choosing one⁢ of ‍the top programs highlighted above, you can receive the necessary training and hands-on experience to⁢ excel as a Certified ‌Nursing Assistant.⁤ Take advantage of the opportunities available in Richmond VA ​and unlock your future in this rewarding profession.
https://cnatrainingcentral.com/open-your-future-top-cna-programs-in-richmond-va-revealed/
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cartermagazine · 2 years
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Today We Honor Dr.Josephine English Dr. Josephine English was an American gynecologist who was the first black woman to open a private practice in New York. She was also known for her work in real estate and health care, in addition to her philanthropy towards the arts. English was born on December 17, 1920 to Jennie English and Whittie Sr. in Ontario, Virginia. She moved to Englewood, New Jersey in 1939. Her family was one of the first black families in Englewood. She attended Hunter College for her bachelor's degree until 1949, and earned her Master's in Psychology at New York University. She initially wanted to become a psychiatrist, but ended up choosing gynecology after discovering her interest at Meharry Medical College where she earned her medical degree in gynecology. Dr.Josephine English opened her practice at Harlem Hospital. Once in Brooklyn, she opened up a women's health clinic in Bushwick in 1956, as well as another in Fort Greene two decades later. During her career, English helped deliver 6,000 babies, including the children of Malcolm X, Betty Shabazz, and Lynn Nottage. English's interest in health care lead her establish the Adelphi Medical Center and child care programs, such as Up the Ladder Day Care and After School Program. Her passion for theater led her to establish the Paul Robeson Theater from a dilapidated church. She helped actors create performances to educate the populace on health and nutrition. CARTER™️ Magazine carter-mag.com #wherehistoryandhiphopmeet #historyandhiphop365 #cartermagazine #carter #drjosephineenglish #blackhistorymonth #blackhistory #history #staywoke https://www.instagram.com/p/CpNKrgALUdK/?igshid=NGJjMDIxMWI=
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niteshratnakar91 · 4 days
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Nitesh Ratnakar: A Distinguished Leader in Gastroenterology and Hepatology
Nitesh Ratnakar, M.D., FACG, is a highly respected and experienced gastroenterologist and hepatologist, known for his expertise in the field and his dedication to patient care. With an impressive medical career that spans over two decades, Dr. Ratnakar has become a trusted name in gastrointestinal and liver health across several hospitals in West Virginia and Ohio.
A Rich Educational Background: The Foundation of Excellence
Nitesh Ratnakar’s journey to becoming a distinguished gastroenterologist began with his pursuit of extensive medical training. His dedication to mastering his field is evident from the array of fellowships and residencies he completed.
Dr. Ratnakar’s education is rooted in diverse medical disciplines, showcasing his commitment to building a comprehensive understanding of healthcare. He began his training with a Residency in Psychiatry at the University of Delhi’s Maulana Azad Medical College. This early experience in mental health gave him a holistic perspective on patient care, recognizing the importance of addressing both physical and emotional well-being.
Following this, Dr. Nitesh Ratnakar moved to the United States, where he furthered his medical education. He completed his Residency in Internal Medicine at the prestigious Chicago Medical School / Rosalind Franklin University of Health Sciences. During his time here, he honed his clinical skills and developed a keen interest in gastroenterology.
Seeking further specialization, Dr. Ratnakar pursued a Fellowship in Geriatrics and Palliative Care Medicine at the University Of South Florida College Of Medicine. This fellowship equipped him with the tools to provide compassionate care to elderly patients and those with life-limiting illnesses, emphasizing the importance of quality of life.
However, it was his Fellowship in Gastroenterology & Hepatology at the University of Wisconsin Medical School/Aurora Healthcare in Milwaukee that solidified his focus and passion for gastroenterology. From 2003 to 2006, Nitesh Ratnakar dedicated himself to understanding the complexities of gastrointestinal and liver diseases, preparing him to become a leading specialist in the field.
Nitesh Ratnakar: A Dedicated Consultant and Leader in Healthcare
Since completing his fellowships, Dr. Nitesh Ratnakar has been in private practice as a Consultant in Gastroenterology, Endoscopy, and Hepatology, serving patients across multiple hospitals in West Virginia and Ohio. His commitment to patient-centered care is reflected in his long-standing relationships with various esteemed medical institutions, including Wheeling Hospital, WVU Reynolds Memorial Hospital, Davis Medical Center, and East Ohio Regional Hospital.
Beyond his work as a consultant, Dr. Ratnakar has also taken on significant leadership roles within the healthcare community. From 2010 to 2012, he served as Chief of Staff at Davis Memorial Hospital in Elkins, WV, where he led a team of medical professionals in delivering high-quality care. During the same period, Dr. Ratnakar also contributed to the strategic direction of Davis Health System Inc. as a Board Member, helping to shape healthcare policies and improve medical services in the region.
The Expertise of Nitesh Ratnakar in Gastroenterology and Hepatology
Dr. Nitesh Ratnakar’s areas of expertise lie in the diagnosis and treatment of a wide range of gastrointestinal and liver conditions. His proficiency in endoscopic procedures allows him to provide minimally invasive treatments that can significantly improve patient outcomes. As a fellow of the American College of Gastroenterology (FACG), Dr. Ratnakar stays at the forefront of advancements in his field, continually improving his skills and knowledge to provide the best care possible to his patients.
His focus on the management of complex conditions such as hepatitis, inflammatory bowel disease (IBD), and cirrhosis has earned him a reputation as a trusted expert in these areas. Dr. Ratnakar is particularly known for his empathetic approach, ensuring that his patients feel supported throughout their treatment journeys.
A Commitment to Improving Healthcare
Dr. Nitesh Ratnakar’s dedication to the field of gastroenterology and hepatology goes beyond his clinical practice. He is passionate about contributing to advancements in healthcare and improving patient outcomes through continued education, research, and collaboration with his peers. His leadership roles within hospitals and healthcare systems reflect his commitment to driving positive change in the medical community.
Conclusion: Nitesh Ratnakar’s Legacy of Excellence
Dr. Nitesh Ratnakar’s extensive training, clinical expertise, and leadership roles have established him as a highly respected figure in the field of gastroenterology and hepatology. His compassionate approach to patient care, combined with his deep knowledge of gastrointestinal and liver diseases, has made him a trusted healthcare provider for patients in West Virginia and Ohio. Whether through his hands-on work with patients or his leadership in hospital administration, Dr. Ratnakar continues to positively impact the lives of those he serves.
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