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Still fighting for parental rights in Ireland

Every child of an LGBTQ parent deserves equality under the law

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parental rights, gay news, Washington Blade
Ranae von Meding

My name is Ranae and I live in Dublin, Ireland with my wife Audrey. Our daughters Ava and Arya are 4 and 2. Our girls have two mothers, yet I am still seen as a single parent.

Audrey and I were an unlikely couple from the start. She was in her fourth and I was in my first year of acting in a theater school in Dublin. We were paired together at an open day and became friends. We were so different, yet we immediately clicked. I knew Audrey wasn’t straight, but over the course of the next year, I had no idea that I was developing feelings for her. The day before my 21st birthday the realization hit me like a bolt of lightning. The feelings I had for her were so much more than just friendship. The rest, as they say, is history.

We have been together for 12 years now, and married for five. Audrey and I always knew we wanted to have kids and talked about this from the moment we started dating. We both have lots of siblings and knew that life wouldn’t be complete for us without having our own kids. I always dreamed about being pregnant and going through the process of growing and birthing a baby. Audrey, on the other hand, didn’t really want to be pregnant as long as she could become a parent. It was almost an unspoken thing that I would be the one to carry our child, should we go down the IVF route.

One night in early 2015, after a few glasses of wine, I had an idea. Wouldn’t it be cool if we could use Audrey’s eggs but I would carry the baby? This way, our children would genetically be Audreys, but I would be the birth mother. At the time it was just a silly idea we had. Little did we know that conversation would change the course of our lives. We decided to Google it and lo and behold, we found out that it wasn’t that crazy of an idea. Reciprocal IVF was actually an incredibly popular fertility treatment option for same-sex couples. At that moment, we knew that Reciprocal IVF was right for us.

When we tried to book a clinic appointment in Dublin, we were disappointed to find out that they wouldn’t treat us in Ireland. Back in 2015, Reciprocal IVF wasn’t licensed yet. In fact it’s only been licensed in the last year. We were given the option to do IUI/IVF with my own eggs, but at that point we had our hearts set on using Audrey’s eggs. Despite the setback, it made us more determined to find a way. We found a clinic in Spain and to be honest it was a bit of a crazy time for us. We didn’t know any other LGBTQ+ parents, let alone any who had undergone treatment abroad. We had no clue what we were doing, and made so many mistakes along the way. A few months later, we conceived our first child with the help of an anonymous sperm donor.

Conceiving our first child in the wake of marriage equality in Ireland was like a dream. Wrapped up in our little bubble of happiness, we went through that pregnancy with a sense of hope for our future. We got married when I was five months along and we celebrated a future that was finally equal. Little did we know what lay ahead of us.

Toward the end of my pregnancy, we learned something that devastated us. LGBTQ+ parents in Ireland were still not equal. I remember feeling so overwhelmed with emotions and going through various stages of shock. My first reaction was ‘but we are married and we voted for marriage equality last year.’

After consulting with a solicitor, we found out more. From the moment our daughter was born I would be a married woman but considered a single mother. I would be forced to register myself as a sole parent and our family would not be recognized under the law, simply because we were a same-sex couple. The simple difference was that I was married to a woman and not a man and because of this, Audrey would be a legal stranger to her own child.

There are some moments that stick with me. Moments that were stolen from us as a young family and ones that we will never get back. The day we registered Ava’s birth, we walked into the registration office and saw all the proud parents with their babies. When they called us into the room, the registrar sat down behind her desk. Without looking up she asked, ‘OK, so which one of you is the mother?’ We said, ‘We both are.’ ‘But which one of you gave birth?’ I said, ‘I did!’ She looked at me and said, ‘OK Ranae, I will be directing all my questions at you, if that’s OK?’ From that point on, she didn’t even look at Audrey. It felt like a kick in the gut. It was just all wrong.

That was the day I promised Audrey I was never going to stop fighting until we fixed this. I joked and said, well at least this will all be sorted out by the time we have another baby. How wrong I was. Fast forward to New Year’s Eve 2018 and I lie bleeding in the recovery suite with a second daughter, listening to fireworks, my heart breaking because I knew we were still in the same position as before. As it stands today, I am considered a single parent to our daughters. Our children, along with countless others in Ireland, are denied the right to a legal connection with both of their parents simply because their parents are a same-sex couple.

Much has changed in the last five years. In 2019, following on from an online petition that I started, we started a campaign called ‘Equality For Children’ along with a group of other LGBTQ+ parents. Since then we have been successful at lobbying the government for change and raising awareness of these issues within Ireland. Legislation was finally passed in 2020 that would allow certain LGBTQ+ families to have both parents legally recognized. Sadly it’s legislation that will only cover certain methods of conception. It’s great to see progress in the right direction, but it’s galling for anyone who falls outside of this and is still being actively discriminated against. Only female couples who have conceived in an Irish clinic with a non anonymous donor and a child born in Ireland are covered.

I can’t really put into words how damaging this has been for our family. To be reminded every day that you are ‘less than.’ That you are not equal. For your kids to be punished because their parents aren’t straight. In practical terms it’s an issue for children when one of their parents is unable to give medical consent, unable to travel freely with them, unable to make decisions on their behalf. But it goes beyond that, the emotional and physiological damage it has done to our families is immeasurable.

Following on from lengthy legal proceedings, our family soon hopes to be recognized. If we are, we will be one of the lucky ones. What about all those who fall outside of this? Are their children less deserving of equality? Because they have two dads? Because they were conceived outside of a clinic? Because they have a known donor? Because they weren’t born in Ireland?

This fight will never be over until every child of an LGBTQ+ parent in Ireland has the same rights and protections as any other child in the country.

Ranae von Meding is a writer and a same-sex parent to two young daughters with her wife Audrey. They live in Dublin, Ireland where she has become an outspoken advocate for equal rights for children of LGBTQ+ families. She is the co-founder and CEO of ‘Equality For Children.’ You can find her on Instagram at @ranaevonmeding.

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Finding community through tragedy

Death of my dog opens floodgates of condolences

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(Photo by Liliya/Bigstock)

I recently lost my dog, Argo.

He was a pit bull, big, sweet, endlessly cuddly, and for 15 years he was my constant. The kind of presence you stop consciously noticing until they’re gone and the quiet hits you all at once. Pit bulls have a reputation. Argo never got the memo. He just loved people, completely and without condition, from the moment he met them until his last day.

I wasn’t prepared for what happened next.

My phone filled up. Instagram lit up. Texts came in from people I hadn’t heard from in months, in some cases years. Hugs from neighbors. Messages from colleagues. Condolences from people I’d lost touch with, some through nothing more than the slow drift of busy lives in a busy city, and some honestly through small tiffs and misunderstandings that neither of us ever bothered to resolve.

And sitting with all of that love pouring in, I found myself asking a question I wasn’t expecting: Why has it taken this long?

We do this in D.C. We get caught in our heads, our calendars, our ambitions. We let weeks turn into months. We let a small misunderstanding calcify into distance because nobody wants to be the first one to reach out, nobody wants to seem like they need something. We perform resilience so well that sometimes the people who care about us most don’t know we need them.

And then something breaks open, a loss, a moment of real vulnerability, and suddenly people show up. And you realize the connection was always there. It just needed permission.

Argo gave people permission. Even in dying, he did what he always did when he was alive. He brought people together.

I’ll be honest with you about where I’ve been lately. As I’ve climbed the entrepreneurial ladder, something quietly shifted. People stopped seeing Gerard. They started seeing a title, a resource, someone who could give them something or who owed them something. A character. Not a person. And when most of your day is spent inside other people’s problems and crises, you can start to feel it, a slow creep of cynicism that you don’t even notice until one day you realize you’ve gone numb.

And I’m not alone in that. Look around. We just watched innocent people die while those in power looked us in the face and called it something else. We watched people erupt over a 10-minute halftime performance like it was the greatest threat to our country. Everywhere you look there is something designed to make you angry, or exhausted, or both. Anger and numbness have become survival strategies. I understand it. I’ve lived it.

But here is what Argo reminded me.

The world is not what the loudest voices say it is. The world is what shows up when something real happens. And what showed up for me, after losing my sweet boy, was people. Caring, loving, present people who put down whatever they were doing to reach out to a friend. Some of them I hadn’t spoken to in too long. Some of them I’d had friction with. All of them showed up anyway.

That is the world. That is what it actually is underneath all the noise.

I think we’ve forgotten that. Or maybe we haven’t forgotten it, maybe we’re just so tired and overstimulated and battle-worn that we’ve stopped letting ourselves feel it. Because feeling it requires vulnerability, and vulnerability feels dangerous right now. It’s easier to scroll. It’s easier to stay mad. It’s easier to keep a wall up and call it wisdom.

Argo spent 15 years showing me a different way. He never met a stranger. He never held a grudge. He never saved his love for people who deserved it on paper. He just gave it, freely, every single time. Not a reward. Not a transaction. Just the most natural thing in the world.

Grief burns off everything that isn’t essential and leaves only what matters. What’s left for me is this: the world is full of good people. You may be surrounded by more of them than you know. And if you’ve gone numb, or angry, or so busy surviving that you’ve stopped connecting, I want you to know that the feeling can come back. It came back for me.

Reach out to someone today. Close a distance you’ve let grow. Tell someone they matter. Not because everything is perfect, but because connection is how we survive when it isn’t. Living disconnected, mad and closed off isn’t living at all. It’s a slower kind of dying.

Death came to teach me how to live. I hope this saves you some time.


Gerard Burley, also known as Coach G, is founder and CEO of Sweat DC.

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Why innovation matters for Black health

Making healthcare more affordable is vitally important

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(Photo by 18percentgrey/Bigstock)

Black Americans are more likely than Americans of other races to live with chronic conditions like HIV. They also disproportionately struggle to afford the often expensive treatments needed to manage those conditions.

So it’s hardly surprising that Black voters care about politicians’ proposals to bring down healthcare costs more than any other group.

Most of those proposals — from leaders in both parties — are well-intentioned. But they are not all equally beneficial. Recent efforts to impose price controls on prescription drugs threaten to harm the very patients they are meant to help.

Consider former President Biden’s signature Inflation Reduction Act, which gave Medicare the power to set prices on brand-name medicines for chronic conditions like diabetes, autoimmune disease, or cancer — all diseases that Black patients disproportionately struggle with.

These price controls promise short-term cost savings. But they threaten to erase the much larger savings that patients with chronic illness would otherwise see over their lifetimes. That’s because price controls disincentivize companies from developing new medicines to compete against existing popular treatments for serious conditions.

Consider HIV. According to the CDC, more than 1.2 million people in the United States are living with HIV, and roughly 31,000 new infections still occur each year. In the 1980s, these diagnoses would have been a death sentence. Today, they represent a manageable chronic illness — a direct result of decades of sustained research and investment in antiretroviral development, long-acting injectables, and prevention tools like PrEP.

HIV treatments are cheaper and more accessible now than ever. That’s not because of government intervention, but because of the price wars that resulted as companies introduced competing therapies and battled for market share.

In fact, had the government prematurely intervened, those competing treatments might never have reached patients, who would still be stuck paying vastly higher prices.

That is precisely the risk our leaders are now taking. Many companies are already scaling back research because of the IRA’s price controls. Since the law’s passage in 2022, biotech firms have canceled at least 55 research programs.

That is especially dangerous for the Black community. Black patients have historically been overlooked by the research establishment, from the underrepresentation of Black participants in clinical trials to underinvestment in conditions like sickle cell disease that disproportionately affect Black patients. If companies are forced to scale back research, it is likely that treatments for smaller and more marginalized patient populations will face the greatest risks of being cut.

The Trump administration, meanwhile, continues to push for its so-called “Most Favored Nation” policy that would tie U.S. drug prices to the lower prices arbitrarily set by foreign governments.

The consequences could be severe. “Most Favored Nation” pricing would dramatically reduce companies’ revenues on both new and existing medicines, decimating resources for future research and development. Researchers project that, if imposed on Medicare and Medicaid alone, such policies could cut research spending nearly in half, leading to more than 200 fewer new medicines over the coming decade.

Developing treatments for HIV has historically required long timelines, complex trials, and sustained capital. Any policy that compresses revenues for breakthrough medicines must be evaluated not only for short-term savings, but also on its potential long-term effects on the pipeline that brings new survival and prevention advances to patients.

And there are also access risks. In countries that rely heavily on price controls, patients often face delayed and restricted access to drugs. Black communities in the United States already face barriers to consistent care and adherence to treatment. Importing foreign countries’ price controls would inevitably have ripple effects across our healthcare system, worsening these disparities.

Making healthcare more affordable is vitally important. Black families feel the pressure of rising costs every single day. But price controls carry severe tradeoffs. Breakthroughs in HIV treatment, long-acting prevention, cancer treatment, and chronic disease management rely on steady research — and if policymakers weaken the economic engine that drives that research, Black patients will feel the consequences first.

Health equity is not just about lowering today’s price tag. It is also about protecting tomorrow’s cures. Black communities deserve reforms that do both, not price controls that promise cost relief while sacrificing future breakthroughs.

Guy Anthony is president and CEO of Black, Gifted & Whole.

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Kansas passes bathroom bounty hunter bill

A move reminiscent of slave catcher laws

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Kansas State Capitol (Photo by jzehnder/Bigstock)

Republican representatives in the Kansas Legislature recently passed a bill that bans people from using restrooms in government buildings that do not align with their sex assigned at birth. The bills SB 224 and HB2426 initially focused on rewriting legislation surrounding driver’s licenses but after amendments, the bill would not only stop trans people from updating their gender on these driver’s licenses but force people to surrender their existing licenses. These bills also carry the most severe anti-trans bathrooms ban of any state. 

According to Erin Reed for Erin In The Morning (EITM), “the measures would now even empower private citizens to act as bounty hunters — entering private business to search for transgender people in bathrooms and sue them for alleged violations.” 

The bills would allow anyone to report any people who utilize any bathrooms that do not align with their gender assigned at birth. Anyone who believes that someone has entered a restroom not in alignment with their gender assigned at birth can complain and pursue $1,000 in damages. The first time that someone complains about a person using the “wrong” bathroom, that person can face a written warning for their first violation. The second violation would require them to pay a $1,000 fine, and with each additional violation, they could receive a misdemeanor resulting in another fine or up to six months in jail. 

The Kansas Attorney General’s office is then responsible for determining whether the person has to pay the fine. Allowing people to police bathroom spaces is reminiscent of Florida’s bathroom law that allows transgender people to face criminal penalties, but even more dangerous, the bills extend this enforcement from “government-owned buildings” to private spaces. 

Government entities that manage bathrooms and locker rooms at public schools and universities, highway rest areas, and public parks are now required to assign a gender designation to multi-occupancy private facilities or face a $25,000 fine for the first violation and a $125,000 fine for any additional violations.

There is a section, Reed notes, that creates a “private right of action,” making it the first law to penalize trans people directly for using the restroom and would extend bathroom bans into private spaces. “Without the option of single-person or family alternatives, this essentially forces trans people out of public life by denying us the right to even relieve ourselves or wash up,” Isaac Johnson of Trans Lawrence Coalition told EITM. 

“Denying access to basic public amenities doesn’t just inconvenience people; it relegates them to second class citizenship,” Allison Chapman of Lawyers for Good Government told EITM. 

The legislation flew through the Kansas Congress (and by using procedural maneuvers, Republican lawmakers ensured that there was no public input on the bill). The bill is now heading to the Kansas Gov. Laura Kelly’s desk for signature. Thankfully, Kelly, a Democrat who has consistently vetoed anti-trans legislation, vetoed it, but even so, it could be passed if Kansas Republicans get the support of two-thirds of lawmakers in both chambers. 

The quick passage of these bills, and using the “gut-and-go” measure to ensure people had no opportunity to provide feedback after the bathroom elements were added, has drawn swift criticism.

The bills themselves have deeply unsettling historical parallels to slave catcher laws that allowed “bounty hunters” to track down and return escaped enslaved individuals to their enslavers for a cash reward. Federal laws, like the Fugitive Slave Acts of 1793 and 1850, enabled “bounty hunters” to operate even in free Northern states. These “bounty hunters,” also known as “slave catchers” or “kidnapping clubs” frequently kidnapped free Black people and sold them back into slavery, in what has been called the “Reverse Underground Railroad.” 

Both of these acts provided little to no protection to free Black Americans; in fact, these acts aided and abetted this violence by incentivizing the kidnapping and sale of people of color into slavery. Even if free people had official “freedom papers,” many kidnappers destroyed these documents, and even free people of color typically could not testify in court. Free and previously enslaved Black children who had escaped to the North were especially vulnerable to “slave catchers” because they often did not know how to assert their rights.

In fact, ICE’s kidnapping of five-year-old Liam Conejo Ramos echoes this long history of child snatching in the U.S., from bounty hunters capturing and selling Black children into slavery. 

This legislation also reeks of Texas Senate Bill 8 (SB 8), enacted in September 2021, that allowed private citizens to sue anyone who aids or performs an abortion after the detection of a fetal heartbeat, around six weeks of pregnancy. At the time, this was the most severe anti-abortion legislation on the books. It has remained there for five years, leading to a number of Rule 202 petitions that aim to collect more information that would provide a person who has violated SB 8. 

Just this past month, the Texas Supreme Court heard oral arguments for Sadie Weldon v. The Lilith Fund, a case where a private Texas citizen sought to depose Neesha Davé, deputy director of the Lilith Fund, a nonprofit that supports people seeking abortions. The case will not rule on SB 8’s constitutionality but would open a path to challenge the law. 

Bathrooms have long been a battleground to police people’s bodies, and this new Kansas soon-to-be law is no different. Think of segregation in the Jim Crow South between the 1890s and the mid-1960s when some White people acted as vigilantes ensuring that Black people remained out of “white-only” restrooms and other “white-only” spaces.

Just as Rep. Susan Hemphries, a Wichita-based Republican who brought the bill to the House floor said that the legislation is about the privacy for and safety of women, bathroom segregation was often justified by painting Black male sexuality as a threat to white women.

This even extended to the perceived threat of Black women in white women’s restrooms, with one group of white women in Detroit going on strike to protest the order prohibiting discrimination of people working in government and defense industries. These white women argued that they would contract syphilis from sharing toilet seats with Black women.

These new bills and all other anti-trans bathroom legislation, as many have argued, are the continuation of these racist bathroom restrictions.

There is deep historical precedence not only for policing public (and private) bathroom access but also enabling private citizens to act as bounty hunters. This form of bounty hunting threatens not just trans women but all women who anyone does not “assume” is cisgender who may be subject to legal complaints. As Orien Rummler reported for the 19th and them, anti-trans legislation and rulings threaten the rights of all women, especially cis women of color. And as science has long proved, gender is not binary–so it raises the question of how intersex people will be policed in these restrooms. 

And by commodifying the bounty, it emboldens anti-trans violence, and misogynistic violence writ large, in the most intimate of public and private spaces. 


Emma Cieslik is a museum worker and public historian.

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