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NY Times article: This is Not A Cure for My H.I.V.
 
 
  https://www.nytimes.com/2019/03/09/opinion/sunday/cure-hiv-aids.html
 
"The news last week that a second person seems to have gone into long-term remission from H.I.V. after a stem cell transplant is a real scientific advance. But I fear the sensationalism with which this report was received could do more harm than good. It obscures the actual struggles we face in combating this epidemic.
 
In reality, a cure for H.I.V. remains a distant dream and the focus on the two "cured" patients is a distraction from the work that we still have to do, that's more pragmatic and not as high-profile as news that someone is possibly free of the infection."
 
From Jules: of course Gregg is correct, HIV cure remains a distant dream, it has been over-hyped and sensationalized, and it distracts from the actual struggles we face and one of those problems not mentioned in this article, probably the most pressing problem for HIV+ certainly in the USA is the aging & HIV problem. In the USA where about 1.2 million have been diagnosed with HIV, 50% are over 50 years old, and 25% are over 60 years old. In NY & SF 55% to 63% are over 50 and perhaps 30% are over 60. We know that older HIV+ people are often suffering severe ravages of accelerated or premature aging, meaning they have earlier onset of & many more comorbid conditions than HIV-negative people. Many are suffering 2-5 times the number of these comorbid conditions as HIV-negative people of comparable older age. Many older HIV+ are suffering premature mental & physical disability and impairment resulting in inability to function normally, they suffer impaired or disabled ability to shop, maintain their home, engage & communicate well, greater social isolation & loneliness than HIV-negatives of comparable age. They suffer from greater immobility so often have great difficulty in navigating transportation & getting to doctor visits. The impaired cognitive function they experience & often low health literacy limits how much they even understand their health conditions. The comorbid conditions for which they suffer premature I onset & in greater prevalence include bone disease (osteoporosis), kidney disease, numerous different types of cancers, cognitive impairment, frailty, higher rates of diabetes, cardiovascular disease is 50% greater among HIV+ compared with HIV-negative. They experience very poor quality of life with the prospect for premature death, I expect death rates to increase soon. Never discussed is housing & care for this group. As more older HIV+ get increasingly more disabled & unable to care for themselves, where will they be housed & who will provide the care for them they need. To negotiate now through daily living this group desperately needs greater support services than they receive now or are available for them. The billion$$ Ryan White Care Act (RWCA) is not addressing this need for services. They have essentially ignored the problem. These services should be available for all older suffering HIV+ who need them. As well the HIV clinics supported by the RWCA should be providing the support to offer these services. These issues are obviously not recognized by many who work in HIV or by advocates & states, city and federal HIV officials. Healthcare costs are doubled for older HIV+ due to the extra costs beyond just the ART HIV drugs for medications for these comorbid conditions, and the extra care & hospitalizations due to these comorbid conditions. This problem was ignored too in this article in the NY Times reflecting the under appreciation & lack of recognition of the problem, all that was mentioned was access to HIV ART drugs which is not the only problem, which is mostly a global issue, but here in the USA the aging & HIV problem is paramount yet clearly ignored.
 
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Opinion
 
This is Not A Cure for My H.I.V.
 
The news about a second person who may be free of the infection is a distraction from the work we need to keep focusing on.
 
By Gregg Gonsalves
 
Mr. Gonsalves is a longtime AIDS activist and a researcher.
 
• March 9, 2019
 
H.I.V. is not going away anytime soon. I've been living with it for more than 20 years and have seen the overhyped stories promising a cure around the corner pop up regularly, particularly around the time of big AIDS conferences. The news last week that a second person seems to have gone into long-term remission from H.I.V. after a stem cell transplant is a real scientific advance. But I fear the sensationalism with which this report was received could do more harm than good. It obscures the actual struggles we face in combating this epidemic.
 
In this most recent case, cancer was an opportunity that offered the chance to cure two diseases at once. The individual, known as the "London patient," received the transplant from a donor with a genetic mutation that conferred resistance to the H.I.V. infection. He was the second person ever to sustain long-term viral suppression in the absence of antiretroviral treatment. Timothy Ray Brown, also known as the "Berlin patient," underwent a similar procedure 12 years ago, with the same remarkable results.
 
But stem-cell transplants from these rare donors are unlikely to be used for the average H.I.V.-positive patient without cancer, because of the risks involved and the impracticality and costs of these procedures. In reality, a cure for H.I.V. remains a distant dream and the focus on the two "cured" patients is a distraction from the work that we still have to do, that's more pragmatic and not as high-profile as news that someone is possibly free of the infection.
 
In 1995, I was at the bedside of my cousin Carl, who was dying of AIDS. His siblings, my aunt and I tended to him during his illness. It was the most terrible period in my life. That year was also the year I also found out I was H.I.V.-positive. I was 32. My first laboratory results were not encouraging. My T-cell levels were quite low, which meant my disease was already progressing toward the danger zone where I would be at risk of infections like those that killed my cousin. Since 1981, this disease had been a death sentence for most people who were H.I.V.-positive, and I had few hopes for my own survival.
 
But then a miracle happened. There was a great leap forward in AIDS treatment soon after Carl's death. People desperately ill came back from the brink, and the new treatment began to offer a normal life span for others of us living with H.I.V. Within a few years, the death rate from H.I.V. plummeted in the United States and in other rich countries. By the end of the decade, a sweeping campaign began to reduce the prices of these new drugs and to get them to patients across the globe. This all came too late for Carl, but just in time for me and a generation of people living with the virus.
 
It is one of the great honors of my life that I got to work with the activists who battled governments and drug companies to make this all happen. From the late '80s, along with my colleagues in ACT UP and the Treatment Action Group, I fought for investments in AIDS research and drug development and changes in the way both were done. By 2000, I had moved on to pushing for access to medicines in poorer countries. However, I made the decision in 2008, in my mid-40s, to go back to college.
 
Since then, I have been working on solving the fundamental problems facing the delivery of H.I.V. care and dealing with the opioid epidemic and infectious diseases like hepatitis C that, along with H.I.V., can travel in its wake.
 
While we should continue to dream big and hope for a cure, my own history has shown that a few months in the here and now can make the difference between life and death. As researchers and activists, we have to urgently focus on what works, on overcoming barriers to scale up H.I.V. treatment and prevention, which will need both scientific and political solutions.
 
The recent study may be an important step in getting us a cure for all. But, there is so much more to do to ensure that the promise of discoveries now more than 20 years old — these powerful AIDS drugs — become a reality for millions today who will perish, like my cousin Carl, without them.
 
Gregg Gonsalves is an assistant professor at the Yale School of Public Health.
 
The Times is committed to publishing a diversity of letters to the editor. We'd like to hear what you think about this or any of our articles. Here are some tips. And here's our email: letters@nytimes.com. 


 
 
 
 
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