People living with HIV/AIDs,YNGP y not go public?

This is the post excerpt.


I’m SherryShavon ..I started the SherryShavon Network as the Founder and CEO of LOOP establish since 2007

My voice will be heard, now 🎢 carry on!

I started this blog because its alot of people living in silence worried about what others may think when dealing with way bigger, super extraordinary hot epic issues. Yes lets not hold back no more I’m coming with the cure of breaking silence. When you are passionated about what you do and what you believe in, its not work to me its research, its resources in the palm of your hand. I’m the founder of LOOP. Yes the CEO of Lives Of Ordinary People. And the question to you Y Not Go Public on important topic and break the silence.

I want to come into your home…lets talk lemonade…

Be more carefulΒ 

Important message from Metropolitan Police 


For the next few weeks do not drink any products from Pepsi , as a worker from the company has added his blood contaminated with HIV (AIDS). It was shown yesterday on Sky News. Please forward this message to the people who you care about that’s why I stress to go PUBLIC because of issues like this. Follow my blog 🚨ynotgopublic@wordpress.com Lives Of Ordinary People. Since 2007🚨

Ryan White Program

The Ryan White HIV/AIDS Program provides a comprehensive system of care that includes primary medical care and essential support services for people living with HIV who are uninsured or underinsured. The Program works with cities, states, and local community-based organizations to provide HIV care and treatment services to more than half a million people each year. The Program reaches approximately 52% of all people diagnosed with HIV in the United States.

The majority of Ryan White HIV/AIDS Program funds support primary medical care and essential support services. A smaller but equally critical portion is used to fund technical assistance, clinical training, and the development of innovative models of care. The Program serves as an important source of ongoing access to HIV medication that can enable people living with HIV to live close to normal lifespans.

August 18, 2015 marked the 25th anniversary of the Ryan White Comprehensive AIDS Resources Emergency (CARE) Act, the legislation that created the Ryan White HIV/AIDS Program. First authorized in 1990, the Program is funded at $2.32 billion in fiscal year 2016. The Program is administered by the U.S. Department of Health and Human Services (HHS), Health Resources and Services Administration (HRSA), HIV/AIDS Bureau (HAB).

About The Ryan White HIV/AIDS Program Parts

The Ryan White HIV/AIDS Program is divided into five Parts, following from the authorizing legislation.

  • Part A provides grant funding for medical and support services to Eligible Metropolitan Areas (EMAs) and Transitional Grant Areas (TGAs). EMAs and TGAs are population centers that are the most severely affected by the HIV/AIDS epidemic.
  • Part B provides grant funding to states and territories to improve the quality, availability, and organization of HIV health care and support services. Grant recipients include all 50 states, the District of Columbia, Puerto Rico, Guam, the U.S. Virgin Islands, and the 5 U.S. Pacific Territories. In addition, Part B also includes grants for the AIDS Drug Assistance Program (ADAP).
  • Part C provides grant funding to local community-based organizations to support outpatient HIV early intervention services and ambulatory care. Part C also funds planning grants, which help organizations more effectively deliver HIV care and services.
  • Part D provides grant funding to support family-centered, comprehensive care to women, infants, children, and youth living with HIV.
  • Part F provides grant funding that supports several research, technical assistance, and access-to-care programs. These programs include:

Date Last Reviewed:  October 2016

Must Read Living


On a late night in Atlanta’s Old Fourth Ward, lots of people were leaving and going to bars. Out there on the side of the street was Gary Jerkins of the AIDS Healthcare Foundation. He was standing in front of a large HIV testing van.

“Get tested! Get your result in one minute,” Jerkins shouted as people passed him. “Participate. Raise awareness.”

Jerkins passed out condoms and candy.

“So, we pass out lifesavers and we tell people that the test can be a lifesaver, he said. “We pass out dumb dumbs and we say don’t be a dumb dumb. Know your status. And we pass out Smarties. Smarties get tested. Know your status.”

Jerkins says every status is good whether positive or negative if it means halting the spread of HIV. Atlanta is the fifth highest metro area for rates of new HIV diagnoses, according to the Centers for Disease Control and Prevention.

“In many ways the South is the epicenter of the epidemic and really Atlanta is the epicenter of that,” said Nic Carlisle, executive director of the Southern AIDS Coalition.

LaMar Yarborough, 23, remembers his diagnoses. It was on his 18th birthday. A couple days earlier, he had been rushed to Atlanta’s Grady Hospital.

“Two days before my birthday, I fainted in the shower,” Yarborough recalled. “And my mother, she rushed me to the hospital. I went to doctors, and I had everyone standing around me. You know, Grady partners with Emory. So, you know you have a whole bunch of medical students. So, it was like eight people around me you know asking me questions. They told me I had AIDS, and then they were asking me if I knew what that is and things of that nature. At the time, I did not.”

Yarborough said the virus was sexually transmitted. At the time, he was sleeping with both men and women. He also developed a type of cancer tied to HIV. Yarborough said within his family, talk about sex was confined within heterosexual relationships. Sex Ed in school wasn’t much better.

“Pretty much within the south we do an abstinence only teaching,” he said. “If you were to catch an STD, I remember the video, it was like the steam rising from the ally, the girls with the short skirts on, guys with the sagging pants. I remember friends and I we kind of checked out cause that’s not us. We talk proper. We do what we’re supposed to do. It just didn’t apply to us.”

Now he is more vocal about the importance of being able to identify with someone on how to handle HIV.

“You don’t have a lot of people who are advocates who are African American men that I’ve seen growing up,” he explained. “We are dying from this and therefore it makes me step up to the plate and say I need to be a leader, and to educate my fellow people of color so that we don’t die from this epidemic.”

Death from AIDS is still a reality for many young African-Americans. Dr. Abigail Hankin-Wei oversees the H-I-V testing program at Grady Hospital, where Lamar Yarborough was diagnosed.

“We’ve had patients who were diagnosed on the same-visit that they died of their complications, which is not the way we should be doing it in 2015,” she said.

Hankin-Wei said at Grady, there are anywhere between 15-and-20 new HIV diagnoses a month. In about half of all cases, the patient already has AIDS, which she says for some patients can take about a decade to develop.

“We do have the patients that despite the possibilities of treatment are going to get diagnosed extraordinarily late and too late to get the benefits of treatment,” she noted.

According to the CDC, the South has the greatest number of people living with the disease and dying from it, and that in Georgia, 613 people died with AIDS in 2012. Emory researcher Patrick Sullivan used to oversee HIV surveillance at the CDC. He said black men who have sex with other men in Atlanta are three times more likely to become HIV positive than whites. That is despite having a similar number of sex partners.

“That finding was related to two things,” Sullivan explained. “One was the racial composition of their sexual network. In other words, they had more black partners. Those black partners were more likely to be living with HIV, and the other was access to health insurance.”

Medicaid is the largest source of coverage for persons living with HIV/AIDS, said Nic Carlisle of the Southern AIDS Coalition. Carlisle said not expanding Medicaid under the Affordable Care Act, which is the case in Georgia, keeps some people from getting tested.

“The bigger issue and I think the bigger issue where Medicaid comes in is so many people are being diagnosed late,” he said. “I think that’s one of the signs of not having access to routine health care. Not being part of a culture that establishes a primary care doctor and encourages folks to have an annual checkup.”
For those already diagnosed with HIV, there is a safety net. It is the federal Ryan White CARE Act, and it’s available to people who are HIV positive and don’t have any health coverage.

“But that safety net is vulnerable,” Carlisle said. “It’s subject to appropriations every year and if and when the Ryan White Care Act goes away and Medicaid hasn’t been expanded, you’re talking about a disaster for people living with HIV in the south.”

LaMar Yarborough relies on the Ryan White CARE Act to cover the cost of his antiretroviral medication. He is unemployed and does not qualify for Medicaid in Georgia.

“For me just personally if Ryan White ever went away then hopefully God willing, I would be financially stable to pay for them myself,” Yarborough said.

Georgia’s Department of Public Health reports that a disproportionate share of the more than 50,000 people with HIV in Georgia who are low-income and black.

“If they don’t have enough money, for example, to put a roof over their head, they’re not going to spend a lot of attention thinking about taking the medication for HIV,” said Patrick O’Neal, the director of Health Protection for the Georgia Department of Public Health. “They’re going to be thinking about the basic needs of getting a roof over their heads. Poverty definitely plays a role, and obviously throughout the southeast we have severe poverty issues.”

Georgia is one of several states that’s part of a pilot program with the CDC to boost HIV testing and prevention, particularly among minorities.

Meanwhile, Yarborough doesn’t live out his days as a death sentence. He said he feels good. He is taking his medication and this summer started a support group to help youth and young adults living with HIV.

What is HIV?

What Is HIV?

HIV stands for human immunodeficiency virus. It is the virus that can lead to acquired immunodeficiency syndrome, or AIDS. Unlike some other viruses, the human body cannot get rid of HIV. That means that once you have HIV, you have it for life.

No safe and effective cure currently exists, but scientists are working hard to find one, and remain hopeful. Meanwhile, with proper medical care, HIV can be controlled. Treatment for HIV is often called antiretroviral therapy or ART. It can dramatically prolong the lives of many people infected with HIV and lower their chance of infecting others. Before the introduction of ART in the mid-1990s, people with HIV could progress to AIDS in just a few years. Today, someone diagnosed with HIV and treated before the disease is far advanced can have a nearly normal life expectancy.

HIV affects specific cells of the immune system, called CD4 cells, or T cells. Over time, HIV can destroy so many of these cells that the body can’t fight off infections and disease. When this happens, HIV infection leads to AIDS.

HIV stands for human immunodeficiency virus. It is the virus that can lead to acquired immunodeficiency syndrome or AIDS if not treated. Unlike some other viruses, the human body can’t get rid of HIV completely, even with treatment. So once you get HIV, you have it for life.