Posts Tagged ‘hiv’

“She grabbed me in her arms, put me in her arms, and whispered in my ear ‘we will get through this’ to hear those words by my mother were like…it was the most amazing moment in life.”

Adrian Neil Jr. Shares his heart warming story about when he was first diagnosed.

 

catharsis dec. 14

 

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Catharsis: A World AIDS Day Event

Date: Monday, November 30, 2015

I am Thomas John Davis an NMAC Youth Scholar

To kick off World AIDS Day I am collaborating with The Lula Washington Dance Theater with an event entitled “Catharsis”. The goal of this event is to raise awareness around HIV & AIDS by using performance art as the ice breaker to start conversations between parents, youth, artists, and advocates about disclosure, support, getting tested, and what living with HIV is like. The event will feature professional dancers and testimonies from people living with HIV as well as their allies.

Target Audience and Importance

The doors are open to everyone but the focused group is Parents and their children. I’ve chosen to focus on these two groups in particular because that’s where the information needs to start to make a change in how we talk about HIV when it comes to prevention. Children follow what their parents know weather they are aware of it or not. To lower stigma and increase the flow of valid information into a child’s life we have to also give parents the information so they are informed and up-to-date. By having youth attend with their families we are giving them an opportunity to ask questions about what they saw and to give them information that may be updated from what their parents know. This way the child and parent are getting information together.

 

The agenda for the evening

The event will start out with a quick “what do you know about HIV?” to figure out where the audience stands. This is meant to be a brief but informative section that will transition into the first performance. The first piece is about the challenges two friends face when one of them discloses that he is HIV+. This piece will be followed by a testimony from an ally who saw a family member pass away from HIV related complications. The second piece is about a patient going to the clinic to get their labs drawn for the first time. This piece is followed by a testimony from Thomas Davis and what it was like to be told that he was HIV+ and what he did from there. The final piece is a duet followed by a testimony from a sero-discordant couple and how they navigate their relationship where HIV is concerned. After each testimony/story questions and conversations are encouraged.

                                                                                    

Why dance?

When it comes to talking about HIV we tend to find the same conversations happening over and over again and as necessary as these conversations are we need to find more innovative and engaging ways of presenting them. Using dance as a way to communicate and tell a story is a great way to educate and inspire people. You are able to escape the idea that everything you say needs to be “Politically Correct”. It’s a way for the audience to experience a story rather then having one talked at them. To show this one of the pieces being shown is filmed below. This is a story of the struggles a couple goes through when HIV is introduced into their relationship. This piece is about the anxieties of the waiting room and was used to start conversations about testing, doctors visits, support, and dating. Do you go and get tested with your partner? When was the last time you two talked about your sexual health to each other? If one of you was positive would the other stay? All these questions and many more are asked in the heads of these two individuals as they wait.

The Long Wait

Choreographed by: Thomas Davis

https://www.youtube.com/watch?v=Zm6f1PhG5eo

 

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Adrian and Thomas share their thoughts on USCA 2015! Can’t wait for next year!

Today is National HIV Testing Day! a few of the NMAC Youth Scholars came up with a challenge for the day called “The 60 Second Challenge” The purpose is to get the message out of HIV testing to as many youth as possible. The rules are simple. When nominated you go and get tested for HIV (this is not about the results) If you decide that you would rather not get tested you are supposed to make a video showing us what you can do for 60 seconds (or what you chose to do for those 60 seconds instead of getting tested). If you already know your status you are encouraged to make a video of what you can do in 60 seconds and challenge others to know their status. Simple. Easy. Fun.  Please feel free to participate in the challenge and share with your friends!

Thomas shares the moment when he told his parents he was HIV+ and talks about what the year was like disclosing.

Sources: CDC Fact sheets (Understanding the continuum)

Initial Investment to Help Research, Identify and Apply Innovative Solutions in Baltimore, Maryland and Jackson, Mississippi – Two of the Cities Hardest Hit by HIV/AIDS 


 Research Triangle Park, NC – February 4, 2015 – ViiV Healthcare today announced the launch of a four-year, $10 million initial investment to fuel a concerted community response to the HIV epidemic among Black Men who have Sex with Men (MSM) in Baltimore, Maryland and Jackson, Mississippi, two U.S. cities hard hit by HIV/AIDS. The goal for this new initiative named ACCELERATE!, is to help speed up community-driven solutions to increase access and engagement in supportive HIV care and services by Black MSM. ACCELERATE! aligns with the National HIV/AIDS Strategy and its imperative to focus on communities most disproportionately impacted by HIV/AIDS.

In recent years, there have been increased efforts to address health disparities and social drivers that contribute to the disproportionate impact of HIV/AIDS in Black communities. However, the data continue to tell the story of an enduring and persistent epidemic among Black Americans, and Black MSM in particular. A recent study in The Lancet found disparities across the HIV Care Continuum –

the series of steps from when a person is diagnosed with HIV through the successful treatment of their infection with HIV medications – with 1 in 3 Black MSM found to be HIV-positive, compared with less than 1 in 10 White MSM. The study also found just 24 percent of Black MSM stay in care and 16 percent achieve viral suppression, compared with 43 percent and 34 percent respectively for White MSM.[i] These devastating data, along with the stories of individuals, families and communities affected, mandate the urgent need for new, community-driven approaches and solutions.

“As we commemorate National Black HIV/AIDS Awareness Day, we are proud to announce our ACCELERATE! Initiative, conceived in collaboration with national and community partners to help address the toll HIV/AIDS continues to take on Black communities,” said Bill Collier, Head of North America, ViiV Healthcare. “It’s our ambition that this investment will help build innovative, community-driven solutions to help reduce the HIV epidemic among Black MSM, and strengthen services and communities to support them.”

The ACCELERATE! Initiative leverages what ViiV Healthcare has gleaned from a range of community stakeholders and builds on available insights, community dynamics, best practices, evaluative measures and the conditions that present persistent challenges in Baltimore and Jackson.

Consistent with other ViiV Healthcare-supported programs conducted over the last five years, this initiative began with a convening of a wide range of stakeholders. The Baltimore meeting was held at Johns Hopkins University and included community representatives, allies, state and local health officials, healthcare professionals and academic researchers. The Jackson meeting was held at the Mississippi State Department of Health’s Office of Epidemiology and included a similar range of voices. These discussions, and other conversations with Black MSM and key stakeholders, confirmed the collective will and commitment to accelerating the response.

David Holtgrave, Ph.D., Professor, Department Chair, and Co-Director of the Center for Implementation Research at Johns Hopkins Bloomberg School of Public Health, welcomes the ViiVHealthcare community innovation investment. “The disproportionate impact of HIV among Black MSM in our city is a truly urgent public health issue, and there are unmet public health needs that must rapidly be addressed. We welcome an accelerated response to HIV/AIDS in our own backyard, and appreciate this unique opportunity to participate in a discussion with our colleagues and friends in community organizations, health departments, other academic institutions and those with allied concerns, to help conceive, apply and evaluate innovative and evidence-based services so that we can urgently address this critical health disparity.

“Jackson, Mississippi has alarmingly high rates of HIV infection among young Black men; our city’s infection rates are among the highest in the country. We applaud ViiV Healthcare’s commitment to investing in innovative programs to reduce HIV/AIDS-related health disparities in Jackson. We believe that participation from the private sector is an important complement to our local efforts and programs to reduce these disparities,” said Leandro A. Mena, M.D., MPH, Associate Professor of Medicine, Division of Infectious Disease and Director, Center for HIV/AIDS Research, Education and Policy at the University of Mississippi Medical Center.

The first phase of the ACCELERATE! Initiative will include ethnographic research with Black MSM and community members to identify gaps, assets, challenges and priorities, along with an intensive mapping process. ViiV Healthcare is in discussions with academic centers in Baltimore and Jackson for the Initiative’s research, monitoring and evaluation activities. The insights obtained will help determine the right approach and inform the next phase of this initiative in the effort to reduce the HIV epidemic among Black MSM and affected communities, and strengthen the systems that support and sustain programs that work.

About ViiV Healthcare 
ViiV Healthcare is a global specialist HIV company established in November 2009 by GlaxoSmithKline (LSE: GSK) and Pfizer (NYSE: PFE) dedicated to delivering advances in treatment and care for people living with HIV. Shionogi joined as a shareholder in October 2012. The company’s aim is to take a deeper and broader interest in HIV/AIDS than any company has done before and take a new approach to deliver effective and new HIV medicines, as well as support communities affected by HIV. For more information on the company, its management, portfolio, pipeline, and commitment, please visit www.viivhealthcare.com.

“I deal with stigma by speaking out about my experiences and being open to any questions people have about HIV even if it is no one else’s business. If a question or statement comes out offensive, I breathe first and try to hear where they are coming from before I respond. Stigma will only die off when we start listening and understanding exactly what it is that people are scared of.”

Check out the original piece here.

Google+

So after sending Joshua Rogers, the writer/director of Pickup, a message on Instagram I was happy to receive a response from him.I am so elated that Joshua was able to take time out of his busy schedule, promotion of the short film and fundraising to talk with ThePozLife.  I have stated my frustration with the fact that we do not tend to see many movies out there depicting the HIV experience in this new era of the virus; therefore, this movie naturally excites me.  Check out my interview below and remember to head over and donate toward the cause of seeing a movie surrounding gay characters that are HIV-positive and portraying that experience comes to fruition

Final One Sheet

What was the thought behind doing a movie that was focused on HIV?

Joshua Rogers –  I’m always looking for unique stories that haven’t been told before. I started writing this particular one, about a gay man telling a potential partner that he’s HIV-positive for the first time, when a friend came out to me as positive and I realized that I’d never seen that on film before. I never saw it as a coming out story. The more we talked about his fears and struggles, the more I understood how interesting his story was and how important it is that it’s told. Just to clarify, this is not my friend’s story, but he loves the script and I have his full support.

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Trevor Thompson

Are any of the actors HIV positive?

Joshua Rogers – Two of the three major roles have been cast, and I honestly don’t know if they’re positive or negative. All I know is that they embody these characters brilliantly and both are extremely passionate about the project.

There is a severe lack of focus on HIV in a positive light within film.  How is your film and its cast helping to address HIV and have much needed dialogue? 

Joshua Rogers – The purpose of this film is to start a dialogue. I want people to relate to the characters and situations and walk away thinking about what they just saw, talking about it with their friends. I agree that there is a severe lack of focus on HIV in a positive light within film and we want our movie to put a stop to that. We want to reach the widest audience possible so everyone can see a realistic, honest, and heartfelt portrayal of an HIV-positive person who’s happy, healthy, and looking for love, just like everyone else. This is our positive love story.

Why is donating to your film important?

Joshua Rogers – In order to reach the widest audience possible, we need to make the best movie possible. A film that looks and feels like something everyone will want to see. It’s difficult to get this kind of film made in Hollywood, which is why we choose to raise the funds on Kickstarter. We knew it was a film people would want to see made. This way we can make sure from beginning to end, that the story is authentic and true to the subject matter.

What was the biggest challenge with the film?

Joshua Rogers – Raising the money is the biggest challenge so far. We’re filmmakers who know how to make a great film, but haven’t had to raise money ourselves before. We’ve all been working really hard to get the word out (the last day to donate is December 16, 11am PST) and we’re all proud of what we’ve accomplished so far and learned so much about fundraising.

What will the audience take away from Pick up?

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Brandon Crowder

Joshua Rogers – They’ll be taken on a journey few have been on before. They will be introduced to a character and a situation only a few have ever experienced. Hopefully they will come out of it with a little more empathy, a little more understanding, and maybe it will be a step towards stopping the stigma associated with HIV.

Is there anything you would like to mention or say?

Joshua Rogers – The reception so far to the script and to the kickstarter campaign has been incredibly humbling and encouraging. I’ve had the unique pleasure of hearing some really amazing stories from HIV-positive people from all over the world who want this film made. Thank you to everyone who’s donated so far and everyone who will continue to help us reach the goal! And thank you to everyone that’s reached out, offered their help, told us their story, and reminded us of why we started this project.

Also, I learned by reading a recent post by Josh Robbins from ImStillJosh.com (Friend to ThePozLife) that in early 2015 auditions for a third important role will be taking place out in Los Angeles.  So for those actors preparing their dialogues and stage presence good luck and may the odds be forever in your favor.

For more information on Pick Up check out their Kickstarter Campaign 

12/07/2014

By Benjamin Di’Costa

IMG_0297It’s World AIDS Day, and researchers, advocates and patients are taking measure of efforts to combat the spread of HIV. The Centers for Disease Control and Prevention reports that of the estimated 1.2 million Americans who have HIV, 86 percent are aware of their status. However, just 40 percent are receiving medical care for the virus. One barrier to treatment could be the persistent stigma that many HIV-positive young people face. Here’s a relevant scene (and one that’s not uncommon in this, the Year of the Young Advocate):

World AIDS Day 2014… And here I am a  young gay male—urban, professional, culturally and politically savvy—walking down the street in the “Gayborhood” called Wilton Manors here in Fort Lauderdale. It was a beautiful day and not a cloud in sight.  in which it’s common to see men walking hand in hand to the local Starbucks, or making their way to their morning workouts when out of nowhere I hear from across the street shout, ” You are not worth life and you should die!” says the middle aged gay male.

Being a person who faced discrimination for being gay I just blew it off and kept walking down the street when another younger gay male mumbles under his breath “Dirty Faggot”. Now at this point I was taken back by this statement being that I was in a LGBT neighborhood where pretty much every lifestyle was accepted. What was it about me just walking down the street that caused such negative reactions from the community?

I look down and realize that I was wearing my No Shame in Being HIV+ Shirt from RiseUptoHIV and then it all hit me at once that this in fact had nothing to do with my sexual orientation but was solely about me wearing a shirt with HIV+ written on it? As I continue into a local Starbucks that morning and then notice the countless stares and whispers that were coming from patrons enjoying their morning cup of coffee.

Here I am a young 24 year old gay male who actually doesn’t live with HIV but I am in encountering countless acts of HIV stigma within my own community. Up until this point I had never understood what it felt like to be stigmatized and when I sat down and really reflected on what just happened a wave of emotion just hit me, I realized that at the end of the day I can take off this shirt and the stigma ends but what about those who are living with HIV? Those living with HIV don’t get to choose when the stigma comes and when it goes it is something that is commonly faced within the Gay and Bisexual community particularly minority communities.

So you may be asking, What now? Where do we go from here? 

There are many ways we can all fight HIV stigma in our lives and in our community, whether you are HIV-positive or HIV-negative:

  • Break the silence surrounding HIV stigma in our community. Talk about your experiences, fears and concerns about getting HIV or transmitting HIV with friends, a counselor, or a fuck buddy.
  • Learn how to better deal with and react when a guy tells you he has HIV.
  • Take responsibility for the prevention of HIV. The prevention of HIV is a responsibility that all gay men share – HIV-positive, HIV-negative and HIV status unknown.
  • Challenge attitudes, beliefs and behaviours that contribute to HIV stigma. Don’t be a silent witness to it when it happens around you.
  • Avoid using language that overtly stigmatizes others.
  • Treat guys with HIV as you would treat anyone else: with respect, empathy, and compassion.
  • Get informed about how to protect yourself from HIV and be confident in that knowledge. We know how to prevent HIV.
  • If you have difficulty playing safe, take charge of your sexual health and get the help you need to ensure you do not get infected with or transmit HIV.

Are there other things you can think of to fight HIV stigma?

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And remember Positivity Is Everything!