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Mark S. King

Mark S. King

Mark S. King and his very funny site "My Fabulous Disease" must share some DNA with Positive Lite, because his light-hearted approach to living with HIV feels just like family. "My Fabulous Disease" has the authority of Mark's lifelong HIV activism mixed with the wit of your favorite gay uncle.

Apr13

Remembering, and Saying Her Name

Written by // Mark S. King - My Fabulous Disease Categories // Gay Men, Social Media, Living with HIV, Media, Population Specific , Mark S. King

Mark S. King on his blogging career with TheBody.com, the woman who helped him start and a look back at his very first video effort.

Remembering, and Saying Her Name

In the Summer of 2008, I received a curious package from Bonnie Goldman, the editor of TheBody.com. Inside was a Flip video camera, what was then a new-fangled device that allowed you to take video footage with a camera the size of a pack of cigarettes.

It came with a simple note. “I think you should try this,” it said.

How did she know? I wondered. I had never mentioned to her that I once taped a special for my newborn niece, back when video cameras were the size of footballs and editing consisted of painstakingly recording segments from one VCR to another. “Carly’s Video” consisted of magic tricks, songs and a dramatic reading of “Yurtle the Turtle.”

And yet, Bonnie had the notion that I might have some fun documenting my life as a gay man living with HIV. Immediately, I bought editing software online and started to learn it. But I had my doubts.

There wasn’t anything particularly special about my life, I complained to her in a phone call to her New York office. And a lot of it, like my ongoing struggle with drug addiction, was downright seedy.

 “Tell the truth,” she said. “The more honest you are, the better it will be.”

I trusted her judgment. In my writing for TheBody over the previous years, Bonnie had always demanded the best of me. We regularly debated topics and my approach to my written pieces, and anything that sounded too easy, that contained more platitudes than honest emotion, was questioned. The same would hold true for the video episodes that I quickly began producing.

In September of 2008, “My Fabulous Disease” premiered on TheBody.com. The first episode was an introduction to my life, and already I was being playful with the camera and the potential of video. It concluded with the mantra that Bonnie had instilled in me. “I can’t promise this will always be entertaining,” I said. “But I can promise I will always be honest. So. Let’s see what happens…”

Since then, plenty has happened. When I spent time in Michigan caring for a brother dying of cancer, the camera was there. When I was treated for facial lipoatrophy by getting injections of facial filler, I brought the camera. For everything from my thoughts on barebacking to touring a gay sex club to drug relapses to HIV criminalization to the international AIDS conference in Vienna, I documented everything using the inventive gift sent to me by Bonnie Goldman.

When Bonnie left TheBody a few years ago, I missed her counsel and her friendship. She was maddeningly hard to reach in the two years after, and I wondered if our friendship had been purely professional.

And then the news, in January of 2011, that Bonnie had died after a long struggle with cancer. She had fought it privately, and I felt ashamed for having wanted more contact during what was clearly a difficult time.

Only now, more than a year after her passing, am I finally writing about her death, something so deeply felt I haven’t found the words. I am searching for them still. Life keeps showing up. New people populate it, projects come and go, video episodes of My Fabulous Disease are made. And it has been too long since I have said her name out loud. Bonnie. Bonnie Goldman.

We all come across things, tokens from a person, from a life we treasured but has faded from view. A photograph on a shelf that we pass in the hallway. A shirt in the closet. A book. A recipe.

A broken video camera that has outlived its purpose, that I cannot bear to throw away.

This article first appeared on Mark's blog, My Fabulous Disease.

Apr06

The Unfortunate Pursuits of the Idle Blogger

Written by // Mark S. King - My Fabulous Disease Categories // Gay Men, Arts and Entertainment, Lifestyle, Living with HIV, Population Specific , Sex and Sexuality , Mark S. King

Writer Mark S. King is asked to critique some “gay erotic fiction” aka porn sent to him. “Using standard literary analysis felt like watching a skin flick and wondering if the wooden floors they’re flailing around on are bamboo.”

The Unfortunate Pursuits of the Idle Blogger

Being a writer is not without its perks. I can’t exactly name one at the moment, but I’m certain they exist. Hold it, here’s one. Starting sentences with “Being a writer…” Oh, and receiving gay erotic fiction from a guy who wants feedback on his work.

This morning as I chomped down my Raisin Bran Crunch, I opened email from an aspiring writer and read his gay sex story called “Jason’s Awakening.” The title has kind of a grand sweep, don’t you think? Very English Patient. Or The Sheltering Sky.

Anyway, Jason is 25 and textbook hot, if textbooks gauged such things, and happily engages in his first homo experience in the gym sauna with another muscled hottie. Everything goes along swimmingly, so they do it again in the gym shower. And then again twenty minutes later back at the house. I kept hoping they would grab some bottled water to stay hydrated. Our characters are both frighteningly endowed and no one complains about rectal spasms or asks the guy to please slow down for one damn minute, for God’s sake. But I’m projecting.

I had hoped to be transported, as good writing often does. But my critical eye kept getting in the way.

What kind of gym was this, anyway? Certainly not LA Fitness. That sauna has more of a Jewish deli flavor, with older men wearing ill-considered briefs and complaining about the poor selection at the juice bar.

This Jason fellow was mighty accommodating during his “awakening” in the dry sauna, I must say. Why was it that now, at his age, he was just waking up? From the descriptions of his maiden sexual voyage he looked wide awake to me. Maybe it simply took the right sauna. The wooden planks at LA Fitness are murder.

Reviewing porn over breakfast was crushing to my perceived position in the literary universe, I will admit. I would have preferred, say, examining a potential submission to OUT Traveler on the rustic beaches of Croatia. Hell, they could be nude beaches, I wouldn’t mind. Instead I get enthusiastic Jason, with orgasms launched with such range they confound physics as we know it.

Worse yet was writing my response. Aside from the existential crisis I endured over morning coffee, wondering how it had come to this and ruefully damning my life choices, there was the matter of deciding what to say in my role as the experienced wordsmith. First, deconstructing porn takes all the fun out of it. And once engaged in the task, using standard literary analysis felt like watching a skin flick and wondering if the wooden floors they’re flailing around on are bamboo.

I tried to be helpful in my email to the fledgling writer, pointing out the lack of backstory for Jason and actually using phrases, so help me, like “character flaw” and “conflict.” He also had the irksome habit of using language that “removes the reader from the scene at hand,” as I dutifully explained. You know, like mentioning the many flavorful selections provided by the Keurig gourmet coffeemaker on the kitchen counter, which I suppose you might spy if you looked just over the shoulder of the man getting boinked against the sink.

There are also words that are a smidgen overused in writing for this particular milieu. (Yes. I said milieu. Allow me to exercise my vocabulary after the soul crushing morning I’ve had.) Words like “engorged,” for example. There are others, and they are probably crossing your mind about now. Sorry about that.

Some words seem to exist almost solely in the context of porn. Case in point: I defy you to find the word “perineum” outside The Physician’s Desk Reference. And yet there it was, nestled in the text of Jason’s adventures, a ten dollar word stranded amidst sticky loose change.

Twice.

Go ahead, Google the word. I got all day. It’s not like I have stacks of porn to wade through. Nope. I only had the one.

With my literary critique complete, I charged on through lunch with other vital business, like finding pictures online of my friends to attach to their names on my phone. I love to see their happy faces appear when they call, all of them smiling reassuringly, as if to say they believe in me, they applaud my brave and transformative work, that I couldn’t possibly be sipping coffee and bemoaning the lack of synonyms for “scrotum.

I will trust those happy faces. They needn’t know of my morning reading. I will simply consider it an exercise in “expanding my skill set” and “pushing the envelope.” Yes. I like the sound of that.

And now I have some further work to do on my phone’s contact list. I need to assign a photo to the author of today’s reading, and it may take some time to find an image of a perineum.

This article first appeared on My Fabulous Disease, Mark S. King’s regular – and fabulous - blog. 

Mar25

Dealing with Shame can be a Drag

Written by // Mark S. King - My Fabulous Disease Categories // Gay Men, Arts and Entertainment, Performances, Living with HIV, Population Specific , Mark S. King

Mark S. King says “Being a drag queen, even for a night, terrified and delighted me. But the performer in me won out, wouldn’t you know, and Anita Mann was born.” The rest is history!

Dealing with Shame can be a Drag

We’re born naked… and the rest is drag.” — RuPaul

When I was nine years old, I took my parents’ album of the Broadway musical “Damn Yankees” and memorized every syllable of Gwen Verdon’s show stopper, “Who’s Got the Pain When They Do the Mambo?” Once I was satisfied with my lip-synching and choreography (I decided that a mambo was a dance in which young boys gyrated and flung themselves on and off the living room sofa), the number was ready for public display.

The premiere was a simple affair, exclusive and unannounced. Mrs. May from across the street had stopped in for afternoon coffee, and opportunity knocked when Mother busied herself in the kitchen for a few minutes.

 Not a smart move, Mother, leaving Mark alone with the company.

“Mrs. May, would you like to see me do a song?” The unsuspecting woman gave a polite “yes, that sounds nice” and before Mother could run interference I had turned on the stereo and dropped the needle at the precise moment where Gwen breaks into song.

Mrs. May stared and stared, her hands folded neatly in her lap, as I brought out every sashay, twist and thrust in my dancing arsenal. My moves may have been imperfect but I vocalized brilliantly, thanks to Gwen. As I struck my final pose, arms reaching for the heavens, frozen and triumphant, I saw mother standing in the doorway, holding a plate of cookies and breathing heavily through her nostrils.

Future performances would be limited to my bedroom, where I could conjure an audience cheering with acclamation and mothers wouldn’t put you on restriction.

It is that boy, the cheerful but feminine performer, that I always feared would creep out of me as I navigated young adulthood as a gay man. I worked to shed his characteristics, to replace every soft gesture with a wooden one, to embrace the gym and tank tops and Levi jeans with the same fervor I once had for my beloved Broadway musicals, with mixed success.

And then, a lifetime later, as I worked for an AIDS agency in Atlanta in the 90’s, destiny called. An upcoming drag contest to benefit our agency was suffering from poor participation, and my boss asked if I would consider entering.

Being a drag queen, even for a night, terrified and delighted me. But the performer in me won out, wouldn’t you know, and Anita Mann was born. I created an interactive video rendition of Donna Summer’s “This Time I Know It’s for Real,” (even then, long before this blog, I was toying with the possibilities of video) and won the contest.

 Soon I was performing with “the camp drag queens of the south,” The Armorettes, who hosted a Sunday night show to raise funds for AIDS organizations. Over the years they have raised over $1 million, and their show was a sellout every week. But my own phobic notions lingered.

I didn’t want to be known as a drag queen (“It’s comedy! I’m a performer!” I would insist). I never appeared anywhere in drag but on that stage – I would always get dressed at the show, and was often out of drag for the final curtain call, in a bid to display whatever masculine credentials I had to offer.

I would hear other gay men make disparaging remarks about drag and I withered, unable to admit I was playing to a packed room every Sunday.

The nexus of shame and shamelessness is a complicated one. Each week I put on full display the very things about myself that I had worked so hard to reject – my femininity, my silly pursuit of acceptance through laughter and applause. And just as I gained confidence in what I was doing and why, I would lose a potential boyfriend when he learned of my weekend talents.

As a growing drug addiction encroached on my free time, I abandoned Anita Mann to its demands. For many years thereafter, Anita’s dress and wig would be relegated to a duffel bag hidden in the back of the hallway closet. I had found a vocation in drugs that offered twice the shame and every bit of the need to keep quiet about it.

It took a few years in recovery from my addiction before Anita would make her comeback. Armed with a TV set and a sense of the absurd, Anita performed at a benefit for those of us in recovery, in what may have been her finest hour. Her rendition of “Don’t Get Around Much Anymore” grows more insane by the moment, and perfectly embodied my interest in multi-media performance.

And yes, I am aware that I speak of her in the third person. Maybe it is because I view her as a character I have created, and perhaps it is the remnants of shame, and of my need to keep her at a distance.

It’s strange, how those things about which we have drawn the most shame are also able to liberate us, not to mention help others. My HIV status. My drug addiction. My drag personality. As I have embraced each of these, I’ve found self-acceptance and a way to carry a message of hope, and even joy, to others.

Anita Mann limits her performances these days to recovery-related engagements. It seems fitting that these two aspects of my life, both once secretive, have found their place together. Anita has a voice now as well, doing a sort of recovery stand-up and even singing live when the occasion permits. Anyone in recovery might enjoy watching the highlights of her recent stint at the Crystal Meth Anonymous conference in Atlanta, which includes her bittersweet rendition of “Happiness is…”

Meanwhile, I still struggle with the need to project as much masculinity as I can muster. I swagger more than I sashay. I sport a beard when possible. And I work to maintain a strict gym regimen.

It’s important for me to stay in shape if I expect to fit in that dress.

This article first appeared in Mark S. King’s own blog My Fabulous Disease.

Feb24

Living with Hep C

Written by // Mark S. King - My Fabulous Disease Categories // Gay Men, Hep B and C, Health, Living with HIV, Population Specific , Mark S. King

Mark S King has been there. But he says “The good news, thank God, is that the treatment plan worked, and I cleared hepatitis C from my body. There has been no recurrence. “

Living with Hep C

The image in my mind has never left me, even after many years of trying, of applying layers of wallpaper to that corner of my mind. I am in someone’s bedroom — it could have been anyone, really — and I am offered a syringe to inject crystal meth. The syringe has been used. I take it. I consider the consequences for a brief moment, but I am cavalier. And very, very high. I use the syringe.

It wasn’t the threat of HIV that gave me pause. It was hepatitis C, which I knew was serious… and that’s about it. But I can tell you this, now, my friends: More U.S. residents are now dying of hepatitis C complications than HIV-related illnesses, as reported recently by Tim Horn in Hepatitis News.  

Within days of using that syringe, maybe two weeks, I become horrifically ill. The acute infection swept through me like a freight train, exhausting me, turning my urine brown, making it impossible to perform routine tasks. Doctors diagnosed it quickly, and then gave me the grave treatment plan: 11 months of interferon, coupled with ribavirin. The interferon, a ferocious chemotherapy, would cause mood swings, deep depression, and would be administered, ironically, by injecting myself with it each week.

Depression is so severe among interferon patients that they do not allow pilots to fly who are being treated with it, for fear they will deliberately crash the plane.

The months I endured with hepatitis C and the treatment protocol remains the worst period of health in my life. The mental side effects were as devastating as the illness. Everything hurt. Everything made me angry. Or want to cry. Or convinced me you were against me. Those eleven months crawled by without mercy.

The good news, thank God, is that the treatment plan worked, and I cleared hepatitis C from my body. There has been no recurrence.

I’ve said that the disease most likely to kill me is addiction, not HIV, and hepatitis C was a terrible by-product of my addiction.

While I am drug-free today and maintaining good health, the report that hepatitis C has overtaken HIV as a cause of death brought up some strong emotions. It reminded me of the insanity of the interferon treatment, and then, of course, the insanity of my drug addiction. And it made me wonder how many of those who are dying of hepatitis C acquired it the same way I did.

My life is filled with unlikely rescues. To have lived with HIV for thirty years and to be here typing on my laptop is amazing. To have thumbed my nose at that fact, and reward my good fortune by sticking needles in my arm, well, that is as alarming and sad to me as it must be to you. It’s tough to feel worthy of the grace that has saved me, again and again. So I’ll simply be grateful to be clean and alive today.

Get tested for hepatitis and get the vaccine for A and B if you have not already been exposed. And should you be an injection drug user, bring your own clean needles wherever you use. You and I both know that, when the choice is a used needle or getting high, all of our good fortune can disappear in a flash.

Mark

p.s. May I sneak back on my HIV criminalization soap box for a moment? If 26 U.S. States have laws criminalizing the potential exposure of HIV to another person, than why don’t they have laws against exposing someone to hepatitis C, which is now officially more deadly than HIV? Thank you. That will be all.

You can read more of Mark S. King on his own blog My Fabulous Disease here

Feb13

HIV Criminalization Face-Off: One Poz Man and His Accuser

Written by // Mark S. King - My Fabulous Disease Categories // Activism, Legal, Living with HIV, Mark S. King

Mark S. King” What if you could witness a face-to-face confrontation between a man living with HIV and the sex partner accusing him of not revealing his status? Wouldn’t you like to be a fly on that wall?

HIV Criminalization Face-Off: One Poz Man and His Accuser

The fireworks could be mighty, as emotions raged between the furious accuser and the positive person trying to defend his actions. What might that meeting look like, exactly?

In this video, you’re about to find out.

Amidst the highly charged emotions of the HIV criminalization debate, “sides” are developing. One side believes that those with HIV who do not tell their sex partners about their status should go to jail. Period. But others claim that there is little public health benefit to laws against non-disclosure because they discourage people from getting tested – you can’t be prosecuted if you don’t know your status — and there are often prosecutions in which the risk of transmission is remote or even non-existent.

But taking firmly entrenched sides helps no one. We’ve simply got to get educated beyond our gut reactions to these prosecutions. We all could use more understanding about HIV criminalization laws, how they are being applied, and whether or not they are truly serving the public good. It’s also important that we understand the anger of those who feel they were put at risk and are seeking retribution.

A full list of HIV criminalization laws – and convictions globally (including for each of the states of the USA ) can be found at http://www.gnpplus.net/criminalisation/. To find multiple resources on what to do if one is at risk of prosecution, who to call for help, what the law is in every state, or get palm cards with links to resources, visit The Positive Justice Project.

But back to the video: I couldn’t help but wonder what might happen if an HIV positive man had to sit down with his accuser and explain himself. So, through the magic of some creative editing, I produced this video episode of “My Fabulous Disease” to give a voice to the opinions and feelings of both parties. You can decide if I was successful.

I used this editing technique to comic effect in the “My T-cells Could Use a Facelift” episode (the infamous video about butt padding, among other things). I’ve been looking for a good reason to do it again, and I thought this topic fit the format perfectly.

Thanks for watching, and please be well.

Mark

You can read more of Mark S.  King on his own website My Fabulous Disease 

 

Jan21

On Milford, and Finding Home Again

Written by // Mark S. King - My Fabulous Disease Categories // Activism, Lifestyle, Living with HIV, Mark S. King

After his break-up, Mark S. King is visiting renowned POZ founder, activist Sean Strub. Here is his portrait of the small town life that Mark discovers Sean Strub is an integral part of – and his tale of looking for drag queens there.

On Milford, and Finding Home Again

Even in darkness, in the bitter cold of northern Pennsylvania on a January night, the town of Milford can’t help displaying its charm. I’m walking through Main Street and the shops splash warm light in my path as strolling shoppers offer smiles and salutations.

This isn’t a night for shopping, however. It’s Bingo Night, and I am making my way down a side street for the local church. I follow the sounds of a boisterous crowd that lead me to the fellowship hall.

The tables in the small hall are stuffed with people and the elevated sounds of good cheer reverberates throughout. Many in the crowd turn to me, the bundled up stranger, and they call out welcomes, whoever I am. Tables are littered with bowls of chili and chips and salsa.

I give a woman in an apron my ten dollars, which affords me chili, all the brownies I can eat, and a bingo card.

A chorus of cheers suddenly rings out, and there in the doorway is my host Sean Strub. But the crowd isn’t celebrating the AIDS activist of queer history, but rather the civic pioneer who has done so much for the restoration of Milford in the fifteen years he has lived here. The cheers give way to a round of friendly applause, and Sean makes his way to me as chili and brownies and soda are enthusiastically offered him from every direction.

If these townspeople are living a Frank Capra fantasy, then Sean is their George Bailey, popular and humble, a friend to all. I keep waiting for someone to raise a toast “to the richest person I know.”

It’s impressive and sincere. The entire scene is imbued with the kind of openheartedness that a jaded gay man like myself hardly recognizes anymore. I’m a bit dumbstruck.

“Really, Sean?” I ask him as he finally arrives at my table. “I mean, really. Applause?”

Sean blushes and beams in equal measure, both convincingly. He steps to the head of the room to take his position calling the numbers, naturally.

markmilford1

For a week I’ve been in Milford, Sean‘s idyllic town a short drive from New York City, to stay with him and work on the issue of HIV criminalization. There has been a startling rash of new prosecutions of people with HIV who did not disclose their status to sex partners. It is a topic Sean has been passionate about for years now, but only recently have people like myself paid much attention. It’s an uphill battle, not simply convincing lawmakers that these prosecutions are bad for public health because they discourage HIV testing, but, surprisingly, because a majority of people, even gay men, support the laws.

As HIV as an issue has aged, stigma has risen. Younger gay men who find themselves infected are judged far more than were men of my generation. The shame of becoming infected “when you should know better” and the certain rejection they will face from their peers (“I’m drug and disease free, you be too”) make them more likely to want to hold someone else responsible for their infection.

It’s a sad blame game, fueled by vengeance and humiliation. With lawyers and jail sentences involved.

A ten year old girl, all curls and colorful hair clips, cries “bingo!” and the crowd responds enthusiastically. She approaches the prize table to select her reward with the careful discernment of a grocer choosing the most perfectly ripened fruit.

Beside me, a gay couple, one of many who split their time between careers in New York and a home in Milford, are bringing me up to speed on gay life in the bucolic town.

“There’s gay dances about once a month in a hotel basement up the street,” one is saying. “We even had a drag show last year.” I’m skeptical of the local drag talent pool, but the couple assures me that corporate attorneys and physicians aren’t the only highly skilled professionals that make weekend escapes to the serenity of Milford. “It was an all-star lineup,” he continues. “Matter of fact, there’s a birthday party tonight at a lounge on main street for one of the drag queens. Should be lots of fun. You should check it out! It‘s probably already started.”

The incongruity of church bingo and a drag queen birthday is too much to resist. I surrender my bingo card to one of the kids and give a wave to Sean.

markmilford2

The lounge resides in the parlor of one of the town’s handsome, renovated hotels, but the crowd isn’t what I had hoped. A pair of men are playing pool, dividing their attentions between the table and college football skirmishes on the overhead monitors. They are clearly unaware of any drag festivities afoot, and I wasn’t about to be the one to inform them.

And then, sitting at the bar with his hands folded neatly in his lap, I find evidence of another party attendee. He is a gay man of a certain age, with frosted hair and a small, sparkling package on the bar before him. It is bejeweled from the efforts of a hot glue gun and a dozen or so rhinestones.

He is sitting patiently with his offering, and I wonder of his relationship with the drag queen in question, deciding that he is a devoted fan ready to pay his respects. He appears unfazed by the nonexistent party turnout and sips from his white wine glass without care.

The gay couple from the bingo game appear, and their apologies are written across their faces. “It’s okay, it’s probably too early for a party anyway,” I say. I’m sure the drag queen will eventually make an entrance, but something about an outrageous wig, sequins and enormous eyelashes on the scene feels as if it will spoil the natural environment. It’s time to head out. I don’t want to break the spell of Milford.

That spell is one of belonging, of community, of home. After a couple of months living a nomadic existence, visiting family and now Sean after the breakup of my relationship and exit from Ft Lauderdale, my spirits have been lifted just as my longing for my own sense of community has heightened. I see the settled, peaceful faces of the residents here and want that for myself. I know that my work with the criminalization issue is valuable, and yet I wonder if Sean knew that he was also giving me safe haven and a chance to be valued beyond our project, all in the warmth of new friends and domestic tranquility after a few difficult months.

The more my spirits are raised, the more I know I must move on, to Atlanta, where friends and an anxious realtor await me, where my belongings are boxed and stored and ready to find their place.

I want to know that place, too. It’s time to find home again.

You can read Mark S. King’s regular blog, My Fabulous Disease, here.

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