Medicaid programs are already trying to restrict access to expensive treatments, such as new hepatitis C cures. Do we really need more of this?
#KeepACA #PLWHA #healthcare
poz
Medicaid programs are already trying to restrict access to expensive treatments, such as new hepatitis C cures. Do we really need more of this?
#KeepACA #PLWHA #healthcare
#WorldAIDSDay
Gilead Sciences has begun a major trial to compare the efficacy of Descovy (emtricitabine/tenofovir alafenamide, or TAF) versus Truvada (tenofovir disoproxil fumarate, or TDF/emtricitabine) as pre-exposure prophylaxis (PrEP) against HIV.
In addition to determining how well Descovy protects against HIV compared with Truvada, the trial will compare the drugs’ effects on bone mineral density and kidney function, as well as other safety data.
The U.S. Food and Drug Administration (FDA) approved Descovy in April 2016 to be used in combination with other antiretrovirals (ARVs) to treat HIV. Researchamong HIV-positive people has shown that the drug is less toxic to the bones and kidneys than Truvada. The reason is that Descovy contains an updated version of the drug tenofovir, called TAF, while Truvada contains the older take on that drug, TDF. Both tablets also contain the drug emtricitabine.
We walked so that people infected HIV can have access to much needed services. NYC TriState area is in the top 10 of highest rate of new infections in the U.S. Money raised through such events like AIDS Walk New York will help fund Outreach and Prevention services. Again, we are all living wit HIV so, find out what you can do in your local community and/or learn more about HIV awareness and prevention.
Sponsor me for a great cause; AIDS Walk New York 2015. #photography #AIDS #hiv #cure #fightstigma #hivaids #hope #love #health #wellness #poz #instagay #instahomo #yeshomo #gayboy #selfie #gpoy https://ny.aidswalk.net/angelindiskies
So this happened…. I knew person to be Follower of mine on Facebook however, we had very little interaction (language barrier). I am open about my status and believe that everyone should know their status. This person, from what I recall, had never said anything hateful to me before. Why, suddenly, this after I changed my profile picture? I do not know and I was not able to ask him directly (the profile was not accessible immediately after the comment was left). We have come so far only to find that we have not put stigma, shaming, bullying (even by adults), bigotry, and hate behind us. With social media it (hate) is ever so present. Upsetting and sad it is indeed. Listen… I am an American… But first, let me say this… I am a Black Gay Catholic Man in Recovery LIVING with HIV in America. If you have a problem with any of those things, first go educate yourself on what means to be any of those things, then go do some soul searching ans learn something about yourself and why you have a problem with any of the above “labels”, and after that, get out into world and dive into the human condition, and express some gratitude for your very existence. I don’t hate you for hating me; your existence is the best example of what I do not want to be and for that I am grateful.
My name is Christian Ledan and I live in NYC, NY.
I learned of my #HIV status through the mail, on a Saturday, alone in my apartment, in Brooklyn, in April 2002. A few months prior I had flu like symptoms that I couldn’t shake and had gone to doctor in January, again in March, both times an HIV test was done with the results coming back negative. Due to being ill, I started thinking about what would happen if I died; who would pay for medical expenses and funeral costs? You know… all those morbid thoughts that one has when they get sick. Well, I decided to get a small life insurance plan that would help cover such costs since I was single and without children.
In March of 2002 I met with a financial advisor signed up for retirement plan/life insurance policy. Wrote a check for the deposit and scheduled the appointment for the phlebotomist to come draw blood (a requirement for the life insurance plan). April Fools’ Day of all days was the day. Twenty days later, I received correspondence from the company. In the envelope was a check equal to the amount of my deposit, a letter stating that I was denied the plan, and a copy of the blood work which appeared to indicate that I had HIV antibodies. I had to wait until that Monday to fax the results to doctor. It was confirmed two weeks later. The same week my doctor confirmed the diagnosis I was laid-off from my job.
I am what is called a nonprogressor; at the time of my diagnosis it common to suggest to wait before starting any HIV treatment. So that is what I did; waited. My t-Cells were always high and my Viral Load low. Physically, my body was doing a great job controlling the virus. Emotionally, I was torn up inside. I hid my pain very well from friends and family. I moved to Tampa to bring on a change and things started looking up. New home and a new job wasn’t enough. Suddenly I found myself using crystal meth. This became my solution to dealing with the pain. I had done plenty of club drugs for many years back when I dancing every weekend away but this time, with crystal, it was not on the dance floor. It was in my home.
My blood work still looked good even after moving back to NYC and progressing to a daily IV user of meth. By now my new doctor was recommending that I start HIV meds, due to the advancements in medicine and less side effects, and I continued to decline. I excuse was that I am allergic to so many things (which is true) and I feared having a deadly reaction to the medication. The truth, I read up on some of the medications and what I truly feared was overdosing because I was active user of crystal meth and other substances. Truly insane thinking!
Today, I am in recovery. I’ve been clean since 10-24-2010! In the Spring of 2011 I had a talk with my current doctor and, although my numbers are still great, with his help I made the decision to start HIV treatment. He told me it was time to give my body a break and to let the medication do the work for me. I’ve been on Truvada and Isentress since August 2011, I am undetectable and my t-Cells are high. Recovery has helped me feel comfortable in my own skin and there is no shame in being HIV+.
POZ STORIES: Savalas Squire
A Baptist minister uses the church to address the injustices associated with HIV/AIDS.
“I have committed my ministry and my life to addressing the injustices associated with HIV/AIDS. Being born and raised in North Carolina, I have been a student of the Civil Rights Movement of the 1960’s all of my life. The struggle for justice as it relates to HIV/AIDS has become this generations ‘civil rights’ movement.”
Op-ed: The Aftermath of Coming Out as HIV Positive
“Two weeks ago, I woke up at 3 in the morning, stumbled into the kitchen, threw on a pot of coffee and started writing the story I had written minutes ago in my sleep. I wanted to document my experience with becoming HIV positive for a couple months, but had yet to find the words, or the cojones, to do so. Quite honestly, I wasn’t sure I ever would. But here I sat, blurry eyed and bed-headed, feverishly regurgitating all of the words that came to me mid-snooze. After that manic morning, I spent several more days mulling over sentences and finessing my nuance. Then it was complete, all wrapped up with a bow on top. ‘A Reluctant Social Commentary of a Newly HIV-Positive 20-Something…’ “
read more at HIVPlusMag
The POZ Army: How We End AIDS Together
This summer, thanks to a rare confluence of events, the HIV/AIDS community will have an extraordinary opportunity to help save the lives of tens of millions of people living with the virus. In preparation, we want you to join the POZ Army. We are preparing for the final battle in the war on AIDS—the surge for the cure.
This July, the steamy, magnolia-lined streets of our nation’s capital will teem with 30,000 people who’ve traveled from the four corners of the globe to Washington, DC, for the XIX International AIDS Conference (AIDS 2012). The reality is AIDS remains a raging pandemic. But, we have the power to end it if we do the right things at the right levels right now. It is time to reawaken the world to these facts.
There is no time to waste. The good news: We have antiretroviral treatment capable of both keeping people alive and slowing the spread of the disease. The challenge? Of the 34 million people estimated to be living with HIV, only 6 million are currently in care. On World AIDS Day 2011, President Barack Obama pledged to put 2 million more in care, bringing the global total to 8 million by 2013. But that still leaves 26 million lives—about 750,000 in the United States—hanging in the balance. And new infections occur daily. AIDS can only be prevented in those who access treatment. For the rest? A diagnosis of HIV remains, ultimately, a death sentence. Which is why the HIV/AIDS community must capitalize on this rare confluence of events to reignite the fight for the real end of AIDS—the cure.
Treatment is necessary to keep people alive until we cure HIV. Treatment can slow the spread of the virus, and treatment may be a piece of the cure. But treatment is a means to an end; it should not be the endgame. Those of us living with HIV should not settle for a lifetime of pills with side effects. We should settle for nothing less than the cure.
We must take advantage of this perfect storm of opportunity. To do so, we must mobilize our community to change history for all people living with HIV.
This is where you come in. Social change happens when many advocates cry out together, loudly, in unison. It’s the only way to break through the din. To help our community amplify its collective voice, POZ is launching the POZ Army.
10 years ago today… the blood was drawn from my arm… after which… three letters changed my life.
I have survived, by the grace of God, without ever having to take medication.
Thank you to friends, family, and fellows that have been there for me.
I love you all.