Archive for the 'positive' Category

08
Jan
08

A Young Man Learns to ‘Embrace’ His HIV Status

This article is part of the Washington Post’s “A Living HIV Quilt”.

Carl, a 19-year-old Prince George’s County resident, spoke with reporter Susan Levine about finding out that he was HIV-positive — and about his life after the diagnosis. Excerpts from that conversation:

I’ve now been diagnosed for two years. Well, not two years, going on two years. January 13th. I found out on January 13th, 2006. It was Friday the 13th. I never forget, Friday the 13th, what a horrible day to find out . . .

I do not know when or where I was infected. . . . All I can give is a time period, an estimated time period anywhere between the ages of 15 and 16.

If you are what they call an at-risk person, the average teen, you kind of know, you’ve got to know, you have a feeling, look, I’m doing certain things, I’m living a certain lifestyle that can be damaging in the future.

So kind of by the age of 17, I started thinking, you know, all my friends kept saying, we’re all gonna go get tested, and we should all get tested together, but I lived with a certain fear because, a fear of knowing. You know, I kind of said to myself, I think I might have it, but I’m not sure.

To me, at the time, at the time, not knowing was waaaay better than knowing. Because if I didn’t know, I did not have to deal with the pressures or, for lack of understanding at the time, you know, ending my life. You know, it was like a death thing, what I thought at the time.

I was very uneducated about the subject. You know, when things came up on TV about AIDS or HIV, when they talked about it in school, I kind of ran away from it. You know, cut the channel, cover my eyes, ’cause I was scared of, I was scared of the facts, I didn’t want to know the facts, I wanted to stay ignorant to the subject . . . because as long as I was ignorant to the subject, I thought, Okay, I’m fine.

That kept me sane. I’m thinking, If I don’t know anything about it, I’m fine. But if I knew what was going on, it made me feel more and more guilty about the things I was doing as a teenager.

I was afraid my mom was going to throw me out, she was going to disown me as her child. . . . I did not know what the outcomes could be, you know. We didn’t grow up with the best of relationships, so I didn’t know how she was going to feel if I was positive.

Click here for the rest of this article>>

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08
Jan
08

Malawi to raise pay of civil servants with HIV

LILONGWE (Reuters) – Malawi plans to start paying civil servants suffering from HIV/AIDS about $35 a month extra to help them buy more food, Health Minister Marjorie Ngaunje said on Monday.

Malawi, with a population of about 13 million, ranks among the countries hardest hit by the pandemic in sub-Saharan Africa, home to two-thirds of those infected with HIV/AIDS worldwide.

Ngaunje told Reuters the government had sent out a circular urging all civil servants affected by the disease to come forward.

“We thought an extra 5,000 Malawi kwacha on top of their monthly salaries would go a long way in improving their nutritional requirements which are essential to their well-being,” Ngaunje said.

Civil servants in Malawi earn an average $200 per month.

Official estimates show that AIDS kills about 10 people an hour in the impoverished southern African nation, which is increasingly unable to cope with the crisis.

Health officials estimate that a million Malawians are infected with HIV and about 640,000 have died of AIDS-related causes since 1985.

Malawi spends about $13 per capita on health annually, far below the $36 recommended by the World Health Organization.

Mary Shawa, Principal Secretary for Nutrition and HIV/Aids in the president’s office, said the monthly payment would help prolong the lives of many affected civil servants.

“We know that thousands are infected in the civil service and with the new system we expect to have exact numbers when people enroll as beneficiaries,” she said.

02
Jan
08

Shift in HIV infection among men

New data from six U.S. sites show a dramatic shift by men acutely infected with HIV to choose to have unprotected intercourse only with other HIV-infected partners.

“While the findings showed condom use was up and the number of partners was down, the most startling effect was seen in men choosing to have unprotected intercourse almost exclusively with other HIV-infected individuals. This reflects a systematic shift by men, most of whom are gay, following HIV infection to behaviors that protect their sex partners,” said lead author, Wayne Steward, PhD, MPH, assistant professor of medicine at UCSF’s Center for AIDS Prevention Studies.

The findings, presented today (December 5) at the U.S. Centers for Disease Control National HIV Prevention Conference in Atlanta, were from clinics that enroll newly HIV-infected study participants in San Francisco, New York City, Los Angeles, New Haven, San Diego, and Providence. Over 90 percent of the 27 participants in this study were men who have sex with men. Continue reading ‘Shift in HIV infection among men’

01
Jan
08

Pregnant Women in New Jersey must be tested for HIV

Washington Post reports that New Jersey this week launched one of the most ambitious efforts in the country to control mother-to-child transmission of HIV, making screening tests mandatory for all pregnant women in the state beginning next year.

A bill signed into law Wednesday by the Senate president, Richard J. Codey, in his capacity as acting governor, requires two tests for pregnant women, at the beginning of the pregnancy and again in the third trimester, unless the mother objects. If the mother objects, the objection will be noted and the newborn will then be tested for HIV, with the only exception being on religious grounds. Newborns will also be tested if the woman tests positive.

Just four other states have mandated testing for pregnant women, and three more– including New York — require screening of newborns. But New Jersey’s law appears to go further by requiring both.

The mandatory screening has raised privacy concerns. The American Civil Liberties Union of New Jersey and the state’s chapter of the National Organization for Women both questioned whether the mandated tests violate a woman’s right to privacy and the right to make her own medical decisions.

Riki E. Jacobs, executive director of the Hyacinth AIDS Foundation, a New Jersey nonprofit helping people living with AIDS, said the law is unnecessary and comes when the state should be focused on expanding care for pregnant women. “I am adamantly opposed to this bill. New Jersey already reduced the perinatal rate of transmission with mandatory counseling of pregnant women,” she said. “The issue is getting those women who are not in prenatal care in for services and testing.

“I definitely think it is an invasion of privacy,” Jacobs said. She said women choose to test their babies in 98 percent of cases, so the new law’s mandatory provisions for testing children are not needed: “The fact that we assume women won’t choose to test is ludicrous and wrong.” Continue reading ‘Pregnant Women in New Jersey must be tested for HIV’

26
Nov
07

HIV/Aids at Epidemic Levels in Wash DC, Afr Americans Impacted

I read the synopsis version of this article on the cover of the Washington Post Express this morning on the train…DAG.  It’s not a secret, just something people don’t want to admit is true.  I’d like to say I’m surprised, but I’m not.  1 in 20 have HIV…that is sub-saharan Africa level, huh?  This info is based on just a sample…I wonder what a real study would find? Here’s some info from the article.  Everyone should find themselves supporting a grassroots effort or event for World Aids Day 2007 on December 1!!!!  HIV/Aids is something that we all should address and own.

The first statistics ever amassed on HIV in the District, released today in a sweeping report, reveal “a modern epidemic” remarkable for its size, complexity and reach into all parts of the city.

The numbers most starkly illustrate HIV’s impact on the African American community. More than 80 percent of the 3,269 HIV cases identified between 2001 and 2006 were among black men, women and adolescents. Among women who tested positive, a rising percentage of local cases, nine of 10 were African American.

The 120-page report, which includes the city’s first AIDS update since 2000, shows how a condition once considered a gay disease has moved into the general population. HIV was spread through heterosexual contact in more than 37 percent of the District’s cases detected in that time period, in contrast to the 25 percent of cases attributable to men having sex with men.

“It blows the stereotype out of the water,” said Shannon Hader, who became head of the District’s HIV/AIDS Administration in October. Increases by sex, age and ward over the past six years underscore her blunt conclusion that “HIV is everybody’s disease here.”

The new numbers are a statistical snapshot, not an estimate of the prevalence of infection in the District, which is nearly 60 percent black.

Read the rest of this article – Washington Post

31
Oct
07

Cascade AIDS Project: $1.2 million for positive people in Oregon

The Oregon Department of Human Services will receive a $1.2 million federal grant to support persons living with HIV/AIDS who also suffer from mental illness.

Oregon DHS was one of four applicants nationwide selected for the grant, which is funded by the U.S. Department of Housing and Urban Development.

Cascade AIDS Project and Cascadia Behavioral Healthcare will partner with the Department of Human Services to implement the project. Clients located in the five-county Portland metropolitan area and the eight counties along the Interstate 5 corridor will be eligible to receive assistance. These areas have the highest concentrations of Oregonians living with HIV/AIDS.

“For people living with HIV, having a stable place to live makes a huge difference in helping them stay as well and independent as possible,” said Dr. Susan Allan, state health officer for the Oregon Department of Human Services Public Health Division.

The Oregon Department of Human Services HIV Care and Treatment Program already receives funding through three other HUD grants that provide stable housing and other services to low-income persons living with HIV and their families who are, have been, or are at risk of being homeless. The new grant will fund housing and supportive mental health services to persons living with HIV/AIDS and co-occurring mental illness.

Cascade AIDS Project is the largest community-based provider of HIV services, housing and education in Oregon and Southwest Washington. Cascadia Behavioral Healthcare is Oregon’s largest provider of community-based outpatient and residential mental health and addictions treatment services and housing for low-income individuals and families.

21
Oct
07

How HIV man became a proud dad

LIKE a lot of men, Perry Evans had always taken for granted that one day he would become a dad.

But at the young age of 24 his world came crashing down around him when doctors told him that he was HIV positive.

Perry, originally from Aberavon, Port Talbot, was a haemophiliac and had accidentally been infected with the virus by an NHS blood transfusion.

Not only did he think it would end his dreams of starting a family – but he thought he would have just a few years to live.

The 46-year old said: “When I found out I was HIV positive at the age of 24, I felt as if I’d been handed a death sentence.

“My future just disappeared – it was assumed I’d never have unprotected sex, never father children. Worst of all, I was told I’d only have another two to five years to live before dying a painful death.

“And in my head, those few years were going to be sexless and loveless.”

But rather than resigning himself to being ill, Perry put on a brave face and resolutely decided to make the best of his life.

He said: “It was actually my mum who took it hardest though.

“Because haemophilia is passed on maternally, she already felt guilty for my health problems.

“But I’ve always faced things head-on, and I quickly came to terms with it. What choice did I have? I realised HIV didn’t have to stop me living.”

Perry was keen to start a relationship, but was fully aware that a lot of girls might have been deterred by his illness.

But he soon fell for a woman called Heather, who was 22 at the time.

He said: “I dated a couple of girls, but because I’m a Christian sex was always something I was saving for marriage.

“It didn’t become an issue until I met Heather in 1987. I knew straight away she was special – that she could be the one. I told her about my HIV status on our second date.

“I would have been gutted if she’d turned round and said, ‘Sorry, I want a man who can give me kids,’ or didn’t want to know me because of the disease. But it was a risk I knew I had to take.”

Although Heather admits that she was hesitant to begin with, she also believed that the relationship was too special to pass by.

Perry said: “Thankfully for me, Heather was brilliant about it. She didn’t freak out, and she told me soon after I dropped the bombshell that she’d decided she wanted to give things a go.

“A year later, we were married. Thinking I only had five years, tops, to live, there was no point in us hanging round.

“Of course, I worried about leaving Heather a widow and taking away her chance of becoming a mum. But I figured she’d still be young enough to meet someone else after I’d gone.”

From the very beginning Perry and Heather were constantly told by doctors that they would never be able to have children.

But despite Perry’s deteriorating health, the couple were determined to give it a go. They had heard about a pioneering technique called ‘sperm washing’ that looked like it could give them the chance to be parents.

Perry said: “Before I got HIV, I’d always thought I’d be a dad. But it was something I’d learnt not to think about. And so when I heard about sperm washing, I was really excited.”

The process allows doctors to separate the male’s sperm from the HIV virus. The sperm is then injected into the female egg using artificial insemination.

But the couple were told that there was still a three to six per cent risk of either Heather or the baby contracting the disease.

Neither did – and the couple were blessed with not one but two children.

Perry said: “Luckily it worked, and in 2001 Isaac was born. It was overwhelming. Then, in 2005 we were blessed with our beautiful daughter, Cerian.”

The couple, who now live in Worcestershire, will soon celebrate their 20th wedding anniversary. And although they don’t know what’s around the corner, they are living each and every day to the full.

Perry said: “My kids are a ray of sunshine. I try not to waste a moment and spend as much time as I can with them.

“I’ve got liver disease now, and I know I won’t be around forever. But just being here, with a wonderful wife and two kids, is a miracle.”

andrew.dagnell@mediawales.co.uk