Sunday, December 1, 2013

Not Alone

Quinton Harper, NCAAN Community Organizer
When I was a sophomore in college, a good friend who left college and moved back home the previous year confided in me his HIV positive status. 
That year, Black men represented 88% of the new HIV infections among male college students in North Carolina, according to a report by UNC-Chapel Hill researchers. As a Black man reared to fight becoming simply another statistic, what hurt me the most was knowing that that my friend had become a statistic in that report. And that he had gone through this alone.  
I made two promises to him – and I’ve kept them.  I was tested for HIV, and I have worked diligently ever since to make sure that no one close to me has to deal with this alone.
He is my friend. She is my friend’s mom. He was my classmate. He was my uncle. She is an ex-girlfriend’s home girl.  He is an ex-lover.  She was a colleague’s mother. These people, nameless to you, are the reason why I began my work with HIV/AIDS.  They are why I do what I do. HIV has no name, but their reflection increasingly reflects an image similar to mine. They are me.
We are all affected by HIV and AIDS. Our strength is in our collective power; we must continue to fight together.  
After a summer of “having that conversation” with friends, and the recent passing of “a soldier” in the war, my heart is heavy. But what I told my friend as an undergraduate, what I’ve told my brothers over the past years since then, and what I would tell anyone fighting this war is this: “You are not alone.”

Thursday, June 27, 2013

National HIV Testing Day Congressional Call-In to Support Domestic HIV/AIDS Programs

image by pouwerkerk via Flickr Creative Commons
Can join people around the country for this national call-in day? Just call your Senators today, June 27, and ask them to fully support programs vital to people living with HIV/AIDS in Fiscal Year 2014.

Members of the Senate Appropriations Committee plan to vote on the federal spending bill that supports Fiscal Year 2014's domestic HIV/AIDS programs in early July. As a part of National HIV Testing Day today, June 27, we need to let Senators know that in addition to HIV testing, they should support full access to HIV prevention, care, treatment and research. Urge Congress to fully fund these programs now!

CALL YOUR SENATORS NOW: 
Dial the U.S. Capitol Switchboard at 202-224-3121 and ask for one of your Senators. Our NC Senators are Kay Hagan and Richard Burr. If you don't live in NC, you can find out who your Senator is here.

Use this message:
Hello, my name is [you name] and I am a constituent in [your hometown]. I am calling on National HIV Testing Day to ask my Senator to fully fund and prevent additional cuts to HIV prevention, care, treatment, and research programs.

[Please add one or more of the messages below]
  • Supporting access to HIV testing means supporting access to the full continuum of HIV programs needed, including HIV prevention, care, treatment, and research.
  • Early identification through HIV testing, and reliable access to effective HIV care and treatment helps people with HIV live healthy and productive lives and is cost efficient. Investing in HIV prevention today translates into fewer new infections and less spending on care and treatment in the future.
  • In my state, such programs already have been cut and are greatly needed, because (insert local details or tell personal story).
If you have questions, please contact Donna Crews, Director of Government Affairs at AIDS United, at dcrews@aidsunited.org or (202) 595-4165. Thank you!

This alert is being sent by the AIDS Budget and Appropriations Coalition (ABAC), a working group of the Federal AIDS Policy Partnership (FAPP). ABAC is a coalition of over one hundred national and community-based HIV/AIDS and public health organizations that represent people living with HIV/AIDS, HIV medical provider and researchers, and advocates, as well as community organizations that provide critical HIV related health care and support services. ABAC advocates for increased resources for domestic HIV/AIDS programs across the federal government.

Sunday, June 23, 2013

We can't stop now: Why I'm defending ADAP

Guest post by Michelle Stinson, CNA


I wouldn’t be here if it wasn’t for the AIDS Drug Assistance Program and if it wasn’t for people who believed in me when I didn’t believe in myself. Now the General Assembly might cut $8M from that program. We can’t let that happen.

I just came back from a retreat where many people were newly diagnosed with HIV, and I was struck by how much they are hurting – not because of stigma, but because of fear. Fear of their diagnosis. Fear of telling others. I have been there. I know what it was like. We were able to rally around those people. We told them “Life is going to be OK.” We told them “You will be able to go on.”

This is my fear – without enough funding for ADAP, how are we going to be able to help people who are newly diagnosed to live? We’re going to have to put them on a wait list.

When you’re dealing with an HIV diagnosis, it can be hard to get up out of the bed, put on a smile, and face life. If you have too many stressors, it makes it so you can’t put that smile on. It makes it harder to lead a healthy life. If you have to worry about where your medications are coming from – that’s big.

And if the state cuts certain kinds of medications out of the program, that’s big too. I know first-hand that when the state cut mental health medications, a lot of people got sick, got scared, hurt other people – but if the meds had just been there, those people would have been OK. It all ties together – mental, emotional, physical. If one piece is missing, it can make your whole life out of balance.

I’m living a healthy, happy life right now. I’m getting off many of my medications because my body is getting stronger. I’m getting healed from the inside out. I’ve got my CNA certification. I’ve been in the same home for seven years now. I voted for the first time last year. At one time, I didn’t think my life was that important. But now I am in the fight. I am not going back. I am here to stay. And I’m not afraid, because I’ve got too many people on my side.

This is not over. If we can get the General Assembly to put even part of that $8 million back in the AIDS Drug Assistance Program, that will be worth fighting for.

Please send a message now. Tell our Representatives and Senators that we need ADAP. 

Make sure that our legislators notice us and know that “no” is not an option.

Monday, June 3, 2013

Think Tax Reform Isn’t an HIV Issue? Think Again.

original photo by justinsomina via Flickr Creative Commons
Access to health care is important for people living with HIV/AIDS - but so is having groceries, housing, childcare, and transportation. If these basic needs aren’t met, keeping up with HIV/AIDS treatment is much harder. According to the National AIDS Strategy, the best way to guess someone’s chances of getting to their doctor’s appointments and taking their medications is to know is whether they have a stable housing situation. In North Carolina’s HIV needs assessment, housing and transportation rank just below medication in the top needs for people living with HIV, and food is not far behind.

That’s why NCAAN is paying close attention to the tax reform plans currently under debate at the NC General Assembly. One Senate plan includes tax hikes on food, medication, and medical services, all of which are critical for people living with HIV. Under the House tax plan, all of us with incomes below the top 20% would pay more in taxes. The top 20% would pay less. And all three plans being discussed by lawmakers point our state in the same direction: less revenue from income taxes and more from sales taxes, which would place a heavier burden on the shoulders of lower and middle-income families.

As HIV advocates, we can’t sit idly by while elected officials take our state down a path that will make it harder for people living with HIV and communities disproportionately affected by HIV to lead healthy, productive lives. Over 5,000 people living with HIV in our state are at or below 150% of the poverty level. The AIDS Drug Assistance Program ensures they have access to medications, but they need more than medications to survive, let alone thrive. These tax proposals make it harder for people living with HIV to afford the stable life they need to stay healthy and keep up with their medical care. And these proposals put a heavy burden on communities worst hit by HIV, including rural, African American, and Latino communities across North Carolina.

Can you write a letter to the editor in your local paper about how the tax shift would affect your community? We can help! Email Claire Hermann at claire@ncaan.org.

Thursday, May 30, 2013

Another step forward for harm reduction in NC

More good news from our friends at the NC Harm Reduction Coalition! A bill that will reduce the risk of transmission of HIV and hepatitis has passed the house and is on it's way to the Senate. Here's what they have to say about this great bill and how you can support it:
The NC House [has] passed HB 850, a partial syringe decriminalization/ needle stick prevention bill which NCHRC supports. The bill basically decriminalizes possession of syringes and other sharps if a law enforcement officer asks a person if he or she is carrying syringes or sharp objects prior to a search, and the person gives them up. This is a goodbipartisan bill and we need your continued support!  The bill will now go to the senate.

We are asking our members to call their Senate members to ask them to support the bill.  To find out who represents you, please go to:  http://www.ncleg.net/representation/WhoRepresentsMe.aspx

If you make a call please let me know.  Please ask them to support the bill and needle stick prevention efforts in NC.  Please send me a quick email to robert@nchrc.net if you can make a call.
 
Thank you,
 
Robert Childs
Executive Director
North Carolina Harm Reduction Coalition (NCHRC)

Friday, May 17, 2013

Up to the Challenge


We did it.
We stopped the bill that would have made NC the only state in the nation to require parental consent for an HIV test and any other prevention, testing or treatment related to STDs, pregnancy, mental health or substance abuse – House Bill 693.
When the clock ticked over to midnight last night, the parental consent bill had still not come up for a vote in the General Assembly. Yesterday was the crossover deadline in the NC General Assembly. If a bill didn’t pass either the House or the Senate by yesterday, it won’t become law this year. We won.
We just proved that when thousands of committed people stand together, we can stop our lawmakers from making a dangerous, shortsighted decision. Action Team members sent a record number of emails and personal notes, made phone calls, wrote letters to the editor, blogged, tweeted, and went to the General Assembly in person to defeat this bill. As doctors, counselors, parents, students, and advocates, they spoke out about why the bill was bad for their clients, their families, and the young people of our state. 
We were joined by an amazing set of partners and friends: Planned Parenthood Action Fund of Central NC, Covenant with North Carolina's Children, ARC of NC, ACLU-NC, NARAL NC, the NC Psychiatric Association, Adolescent Pregnancy Prevention Campaign of NC, The North Carolina Chapter of the National Association of Social Workers, and others.
The legislative session isn’t over. We still have the state budget fight ahead of us. We’ll need to protect funding for the AIDS Drug Assistance Program, which is threatened with huge cuts. We’ll need to fight for the basic voting rights of the people who are most affected by HIV in our state. And we’ll need to keep building power.
It’s sad that our state’s lawmakers would even consider a bill like HB 693. It’s scary that a bill like HB 693 would pass through committee and be scheduled for a floor vote. I don’t know what we’ll face next. But I know we are up to the challenge.

Thursday, May 16, 2013

Not Broken: Why NC's parental consent bill is bad for teens


Guest Columnist Kevin Varner

My father had a saying, “If it ain’t broke, son, don’t fix it.”

House Bill 693 is an attempt to tinker with something that isn’t broken. North Carolina law already requires parental consent for teenagers to get an abortion. The new House Bill 693 would require parental consent for a minor to receive, among other things, testing or treatment for HIV and STDs. If passed, it would be the first law of its kind in the United States.
As Director of Prevention, Education and Testing at Triad Health Project in Greensboro, I see firsthand what a difference it makes for teens to have access to confidential health care. All the teens I counsel have two things in common: they are scared, and they are ignorant of their risks. They’re scared to go to Mom and Dad for fear of being judged, or thrown out of their homes. Many don’t know how STDs are transmitted.

In my first six months on the job, a 17-year-old boy tested positive for Gonorrhea, and a 15-year-old girl tested positive for Chlamydia. Both shared that without confidential testing and treatment, they would not have known where to turn. I scheduled appointments for treatment at the health department, counseled them on how to use condoms correctly and how to prevent STDs. I encouraged them to wait until they were older and in a monogamous relationship before having sex.

This week, a mother came with her daughter to get test results. The daughter had come for confidential testing three weeks prior by herself, concerned about HIV and STD risks.  Admittedly, I was surprised to see a mother and daughter for test results, so after giving the daughter good news that she was not infected, I asked them what prompted them to come together. The mother said, “I can’t always be around, and I don’t always know what my daughter is doing. I came to support her, but sometimes she won’t tell me everything she does because I’m her mother and I worry. I also don’t know all the facts about HIV like you do. I don’t feel as comfortable talking about sex and STDs. She doesn’t want to listen to her mother all the time.  But, Mr. Varner, she came on her own, and she listened to you. You didn’t judge her. You helped her. You tested her, educated her and gave her condoms.” The daughter added, “If my mom were to give me condoms, I’d be too embarrassed to take them. But taking them from you seemed easier. When you told me how proud you were that I came to get tested on my own, I got the strength to talk with my mom, and that’s why I wanted her here. I wanted her support. I feel more comfortable talking with her now. But, if I had to go to my mom first, instead of being able to come to you first, I would have been too afraid.”

If state legislators pass the new parental consent bill into law, they are not only taking away the choices and voices of our young people, they are taking away the voices and helping hands of the medical professionals, behavioral health professionals and health educators in our state.
That, finally, would be something broken that would need fixing for years to come.

___

Tuesday, May 14, 2013

An Open Letter to the NC General Assembly: Stop HB 693

Guest columnist Julie Nielsen Lindsey, M.D., responds to NC House Bill 693, which would require notarized parental consent for teens who seek a doctor's care for testing, prevention, or treatment related to STDs, pregnancy, mental illness, and substance abuse.

Dr. Lindsey practices family 
medicine at Cary Healthcare 
Associates in Cary, NC.
As family medicine physician who works with teenagers and as a parent of preteens,  I reject the notion that HB 693 would improve communication in families. Rather, HB 693 would undermine the helpful relationship teenagers have with their physicians and expose teens to increased health risks and pregnancy. HB 693 will also adversely affect physicians who work with teens and fundamentally undermine the therapeutic relationship between teenagers and their medical providers.

As a physician to teens, I strive to be an objective, non-judgmental, caring adult resource whom teenagers can consult about very personal health care needs, including sexual health and mental health. I can assure you that neither I nor any medical colleague I know advocates teen sexual activity, however offering confidentiality opens the door for teens to address sexual and mental health concerns. While we encourage teens to discuss all health matters with their parents including sexual health, we know that sexuality is a difficult topic for teens to discuss with parents, even supportive parents. I am most concerned with how this bill will harm teens in troubled homes. How will HB 693 affect the girl who is raped by her father or her mother’s boyfriend and becomes pregnant or contracts an STD? How will HB 693 affect teens who are depressed and having PTSD due to emotional abuse and neglect by a parent with substance abuse? These are not rare exceptions. Sadly, we see these troubling situations all too often in healthcare settings. If HB 693 passes, teenagers in both supportive homes and troubled homes will be less likely to seek medical care for sexual and mental health care needs, and as a result more teenagers will get pregnant, get STDs, spread STDs, have severe pelvic infections, and there will be more suicides and untreated mental health conditions. 

 In addition to harming teenagers, HB 693 will intrude on physicians’ clinical judgment and professional ethics. Ever since medical school, physicians have been taught to respect teens’ confidentiality in regards to sexual health and mental health, as these are sensitive personal issues fraught with challenges for teenagers. HB 693 would impose a fundamental change in how medicine is practiced, without a full understanding of the harms and without endorsement of the medical community. Such a fundamental change in medical care should originate within the medical community after careful research on benefits and harms.

Furthermore, HB 693 will increase legal liability and confusion for physicians who work with teens. If HB 693 passes, I will not be able to offer my teenage patients STD testing, prescribe birth control or conduct mental health evaluations without first consulting a parent. If it is my clinical judgment that these are needed services and a teen won’t discuss this with their parent, I will either incur liability for offering the service or I will neglect my medical duty by denying the teen the service. To add confusion, HB 693 will not apply to facilities which receive Federal Title X funding or to patients with Medicaid. So before addressing a teen’s concerns, a physician will need to verify what kind of insurance a teen has, and then alter what medical services are offered. There seems to be an element of discrimination, as some teens will be offered more rights and services than other teens, simply based bureaucratic concerns.

Since I work in a private practice, with mostly commercially insured patients, I will be unduly limited in the scope of care that I can offer teenagers compared to what is offered in a federally funded clinic or hospital system. Simply put, teenagers would not have the right to confidential healthcare in my practice, and they will go elsewhere. This will be a boon for facilities that receive Federal Funds. Teens are smart, and they will preferentially seek out health care where they are afforded the confidentiality they need.

 As a family physician, I love working with families, and I cherish the opportunities I have to improve communication between teens and parents. I try to walk that fine line between encouraging teens to delay the onset of sexual activity but still educating them about sexual health, and I always encourage teens to talk with their parents. Typically, parents choose a health care provider whom they trust, and that doctor is an extension of the support the parent offers the teen. There is no adversarial relationship between physicians’ and parents as some proponents of this bill suggest. Rather physicians, parents, and teens typically collaborate in a helpful way. HB 693 would undermine the positive relationship that teenagers have with the family’s health care provider, and teens will get delayed and fragmented care in settings more removed from their family.  

Lastly, I speak as a parent of preteens. Like many parents, I too am uncomfortable by the thought of teenagers having sex, and I am distressed by the highly sexualized and violent content that my children get exposed to through the media and at school. While we as parents prepare our kids the best we can and instill good values, we know that much of our teenagers’ lives are beyond our control. We can hope and pray that our children make good healthy choices, but as they get older we must let go and support rather than control. Offering a teen a confidential relationship with a healthcare provider is a loving way to extend a positive influence in areas where our parental influence is waning. As my children get older, I will take great comfort in leaving the exam room, knowing that my child can freely share any health concern. It is a risky world out there, and all the more teens need access to quality and confidential health care to support them through this challenging time of life and manage the risks. Please, let’s not make life any more difficult for teenagers or for the doctors who serve them. House Bill 693 fundamentally undermines healthcare for teens in North Carolina.




Tuesday, May 7, 2013

Fact Sheet: Protect the Health and Safety of Youth – Oppose HB 693


House Bill 693 would prevent minors from receiving medical treatment for sexually transmitted infections, mental health problems, pregnancy prevention and substance abuse without prior consent from their parents.

These are all serious medical issues that require time-sensitive and appropriate care. If left untreated, all of these conditions may lead to life-threatening situations.

Most youth will at some point talk to their parents about these concerns, but if they cannot or will not for whatever reason, it is still essential that they receive appropriate care. Sexually transmitted infections, mental health issues and substance abuse problems can lead to death if they are not treated in a timely nature.

Adolescents will be less likely to get tested and treated for STDs if they have to get parental consent.

  •  A survey of adolescents at two pediatrics practices in North Carolina found that 92% would undergo STD testing if their parents “definitely would not” find out about the test whereas only 35% would undergo STD testing if their parents “definitely would” find out about the test.[1] 

There are compelling public health arguments for promoting STD testing among youth.

  • Early diagnosis and treatment are the best hope for preventing new HIV cases. UNC-based research finds early, uninterrupted treatment with anti-retroviral medications reduces new HIV cases by up to 96%.[2]
  •  In North Carolina, adolescents aged 15-19 make up the second highest rate of chlamydia and gonorrhea infection, and 23% of new HIV cases in our state are among people under age 24. [3] 
  • Over 50% of youths aged 13-24 with HIV do not know they are infected. [4]

Increased STD rates in our youth lead to increased public health costs.

  • Average lifetime medical costs to treat a person with HIV ranges from $567,000-618,900 with higher costs resulting when HIV is diagnosed late in the disease progression.[5]

Recognizing the time-sensitive nature of these medical issues, every state in the U.S. allows teenagers to seek confidential care for the diagnosis and treatment of sexually transmitted infections. 18 of these states allow, but do not require, a physician to inform a minor’s parents that he or she is seeking or receiving STI services when the doctor deems it in the minor’s best interests.[6]

With a parental consent requirement, many adolescents will forgo testing and medical treatment leading to greater STD transmission to their peers and greater economic costs to society.

Sometimes, parents are the reason why a young person needs to seek medical care. In cases where the minor is emotionally, physically or sexually abused by the parent, it is critical that the he or she have the ability to access care without the consent of the parent perpetrator. Each year, there are nearly 70,000 reports of abuse and neglect – it’s critical that all of these youth have access to health services.

Public health policies should always encourage adolescents to seek timely, professional health care—not impede access to confidential care. This is why the American Academy of Pediatrics and the American College of Obstetricians and Gynecologists oppose mandatory parental consent laws.



[1] Carol Ford & Dana Best, Confidentiality and Adolescents’ Willingness to Consent to Sexually Transmitted Disease Testing, Archives of Pediatrics & Adolescent Medicine, Vol. 55, Sept. 2001, 1072.
[2] Cohen et al., Prevention of HIV-1 infection with Early Antiretroviral Therapy, N. Eng. J. Med.,365(6):493-505, available at www.nejm.org/doi/full/10.1056/NEJMoa1105243#t=articleTop.
[3] North Carolina HIV/STD Quarterly Surveillance Report: Vol. 2012, No. 2, Communicable Disease Surveillance Unit. 
[4] Ibid. 
[5] Schackman, et al., The Lifetime Cost of Current Human Immunodeficiency Virus Care in the United States, Med. Care., 2006 Nov.; 44(11):990-7.
[6] State Policies in Brief, Overview of Minors’ Consent Laws, Guttmacher Institute, February 2011.

Monday, May 6, 2013

ADAP Stories: Thomas

Hometown: Pinehurst, NC
Occupation: Transportation Specialist and Peer Educator

I am a native of Pinehurst and now reside in Roseboro, NC. I am employed with Commwell Health as an HIV Peer Educator.

I have been HIV positive for 15 years.

I am very grateful to the ADAP program. It has really helped my cost of medicine, which is really expensive.

Friday, April 26, 2013

ADAP Stories: Stephanie



Hometown: Fayetteville

Profession: Aspiring business woman; B.A. Mass Communications from Fayetteville State University 

Q: What has the North Carolina AIDS Drug Assistance Program meant to you?

A: ADAP has been important to me because my medicine is my lifeline. I can’t take a test at home to know my viral load and CD4 count, but because I know my meds are consistent, I also know my health is stable, and I can remain undetectable. 

Losing ADAP for those who don’t have any other access to their medication would be like losing hope all together. If we lose the money funding ADAP people will die. 

For the infection rates to be going up and the money funding programs like ADAP to be going down is just a contradiction in itself. 

We deserve to live like anyone else. When you take away the funding that helps us to live what does that say about how you run your state? It says that obviously you don’t care about the people living here. 

It is sad that people have to be put in the situation personally to understand it. God forbid they have a family member or someone they love become infected, but most of the time that’s what it takes for people to truly understand how important programs like ADAP are. It’s sad that we have to fight to live. 

We need to do something about this epidemic now so this isn’t still affecting our children and grandchildren. It should be a human right to have reasonable access to health resources. North Carolina can’t be neglected anymore. We’re in the top 10 states infected. Don’t ignore my state.

Why voting rights?


NCAAN Votes

The NC AIDS Action Network fights for the rights of people living with HIV/AIDS, their loved ones, and those at risk for acquiring HIV. As part of this mission, we work on making sure that North Carolina’s state policies advance those rights. And when it comes to influencing policy, our votes are our power.
Voting is the first and most basic way we participate in our government. If we want to keep building power for the communities most affected by HIV in North Carolina, we need to keep voting convenient.
Three quarters of our Action Team voters went to the polls in the last election. More than three-quarters of those voters cast their ballots early. Those votes made a difference. When we ask legislators to support programs that make a difference in the lives of people living with HIV and those at risk, it helps to have those leaders know that our members - and others most affected by HIV - vote.
 Attacks on Voting Rights
In the last month, North Carolina legislators have introduced bills that would require photo ID to cast a ballot, cut back early voting, end Sunday voting and same-day registration, and severely limit voting rights for students, people who have completed a felony sentence, and others.
These bills would hit especially hard for many of the groups of voters most affected by HIV, such as young, low-income, African-American, Latino, and transgender voters. For example, African-American voters are more likely to vote early, more likely to vote on Sunday, and more likely to not already have a government-issued photo ID. They are also 10 times more likely than white North Carolinians to be living with HIV.
Bottom line - if these bills pass, it will be harder for the people who are most affected by HIV in this state to vote in the next election. And that means we’ll have fewer voters who are fighting to protect funding for HIV medications, access to healthcare, anti-discrimination laws, and other issues that we care about.
If you’d like more information on these bills, Democracy North Carolina has good information on bills affecting voting rights in NC, who would be most affected if those bills become law, and the impacts of the voter ID bill
If you'd like to take action to keep voting accessible and convenient in North Carolina, you please send an email to our legislative leadership now.

Friday, April 19, 2013

Harm Reduction Victories in Raleigh


We just got some great news from our friends at the North Carolina Harm Reduction Coalition! Here's the email:
_____

You Advocated, Your House Members Listened! NC Republicans Introduce Needlestick Prevention Bill to Improve Law Enforcement and Community Health
Dear NCHRC Members,

We wanted to share this exciting news with you! The same week that the Good Samaritan/Naloxone Access bill was signed into law, Republican legislators introduced more harm reduction legislation - House Bill 850 (HB850),  "Possession of Needles, Tell Law Officer."  HB850 aims to decriminalize the possession of syringes and other sharps if a person declares them to a law enforcement officer prior to search. Current law criminalizing syringes or other sharps intended for drug use provides incentives for people to not tell the officer of their possession when being searched by an officer and leads to high incidents of needle-sticks among law enforcement. Currently, one in three officers will get stuck by a syringe or "sharp" during their careers and 28% will suffer multiple sticks. In an effort to encourage honest conversation between a person carrying a syringe and law enforcement and reduce injury and disease exposure, HB850 would decriminalize the possession of syringes and other "sharps" if they are declared to an officer prior to search. The bill applies to syringes and other sharp objects on the suspects' person, in pockets, in a vehicle, or on the premises.

HB850 is being introduced by a team of Republican legislators. Current primary sponsors are Rep McNeill and Rep Faircloth, both retired law enforcement officers, and Representative Hardister, and Dollar. The bill currently has 15 co-sponsors from both parties and will soon be debated in committee. This is an important step towards protecting law enforcement from needle-sticks and potential exposure to blood-borne disease, as well as improving community health.
 
What's next?

1.) Call the primary sponsors to voice your support of this important legislation and to thank them for standing up for law enforcement and community health!

Rep Faircloth 919-733-5877
Rep McNeill 919-715-4946
Rep Hardister 919-733-5191
Rep Dollar 919-715-0795
 
Please send an email to NCHRC if you have done this by sending an email torobert.bb.childs@gmail.com

2.) Join the conversation on our social media
Twitter:  http://www.twitter.com/NCHarmReduction
Facebook Group: http://www.facebook.com/group.php?gid=49624519007   

In solidarity,

Robert Childs
NCHRC Executive Director

and

Tessie Castillo
NCHRC Program Coordinator

Monday, April 15, 2013

ADAP Stories: Michelle W


Hometown: Winton-Salem
Occupation: HIV/AIDS Advocate

What has the North Carolina AIDS Drug Assistance Program meant to you?

I’ve been on ADAP since 2008, and it has meant life support for me and my children.  It has enabled me to be here today; it has been a huge financial support and a source of stability and encouragement. 

When I was first diagnosed I had no hope. I was one of those who thought life was over the next day. I had no idea where I was going to be able to find financial or medical support. 

Once I was introduced to ADAP I realized there was hope. It gave me courage to go out and help others and teach others about these resources.

It gave my kids great hope as well; it let them know help was on the way. A sick parent can’t raise a child, but ADAP gave my kids a foundation to know that their mom was going to be okay. 

It’s important to preserve ADAP because our state will end up spending more money burying those who die because they don’t have access to medicine and providing foster care for the orphans left behind than they would on ADAP itself. 

We need to save lives, not take them. ADAP saves lives. 

Interview by Blaire Benson

This is one of a series of interviews highlighting the impact that the AIDS Drug Assistance Program has on the lives of people in North Carolina. If you would like to share your story, contact Claire at claire@ncaan.org

To take action to save the AIDS Drug Assistance Program from proposed budget cuts, send an email to your legislators now.


Thursday, April 11, 2013

ADAP Stories: Glen

Glen gets ready to deliver postcards in support of ADAP
to Senator Austin Allran.
Hometown: Newton

Q: How has the North Carolina AIDS Drug Assistance Program affected you?


A: I am a person with HIV who lives in Newton NC. I work at a job that does not provide any health insurance and pays around ten bucks an hour. 

 
My doctor has me on three medications that are used to control my illness. Together, they cost over three thousand dollars a month if I were to purchase them at Wal-Mart or Walgreens. That is three times my take home pay. I can barely afford aspirin.
 
ADAP gets me these drugs at no charge which allows me to keep a full time job and pay my taxes. Without these drugs I would surely lose my strength, then get sick with weird illnesses which in turn would lead to very expensive treatments, at taxpayer expense, that would not prevent my inevitable death.  ADAP is a bargain.


This is one of a series of interviews highlighting the impact that the AIDS Drug Assistance Program has on the lives of people in North Carolina. If you would like to share your story, contact Claire at claire@ncaan.org

To take action to save the AIDS Drug Assistance Program from proposed budget cuts, send an email to your legislators now.

Tuesday, April 9, 2013

ADAP Stories: Jerry

Jerry shared his story during HIV/AIDS Advocacy Day. 

Hometown:
Asheville

Occupation: Disabled veteran

Q: How did the North Carolina AIDS Drug Assistance Program affect your life?

A: I was diagnosed with HIV June of last year. After having many major surgeries, I was did not accept the diagnosis when they told me I had HIV. I refused to take any drugs because of denial.

At that point in time, things got so bad that I tried to commit suicide. I tried on January 7 of 2013. At that time, I accepted that I had HIV and went to my county health department, which introduced me to the Ryan White program, which would fund me with meds for my recovery.

I thought that I had a death sentence, but they told me I could get my level down to where it’s undetectable, which is a God-blessed thing. With them supplying my meds, I am able to have my levels down to undetectable.

That brings me to what I am doing today. I feel it was a God-sent thing for me to have HIV so that I can come down to advocate to for those in Western NC who are not able to come. I tell my legislators that funding does not need to be cut, it needs to be increased. I would like to tell my grandkids that I was part of bringing HIV to an end.

Now, I get my meds through the federal government, because I am a veteran. Because I am a veteran, I am honored that my healthcare is taken care of, but there are people out there that have low income that are not veterans. I’ve been given the outlet to help people with this soon-to-be-ending disease. 

Q: You came all the way from Asheville today. Did you come to the conference today with a group?

I came with WNCAP. They are doing such a great job in the western North Carolina area. More funding is needed to reach out to the street levels where AIDS is running rampant and to touch people that are not coming to be tested, who don’t know that they have HIV.

I am also part of Varick Chapel AME Zion Church. We are using our church ministry to reach out to people in the community to be tested for HIV/AIDS. Dec. the 7th, 2012 was our first health fair, and seven people were tested for HIV. This year, we’re looking to test 20. That’s the community level. Members know people. The high risk people. The church knows the people in the community. 

This is one of a series of interviews highlighting the impact that the AIDS Drug Assistance Program has on the lives of people in North Carolina. If you would like to share your story, contact Claire at claire@ncaan.org

To take action to save the AIDS Drug Assistance Program from proposed budget cuts, send an email to your legislators now.

ADAP Stories: Brian

Hometown: Charlotte

Occupation: Public Health Strategist
A

Q: How has the North Carolina AIDS Drug Assistance Program affected you?

A: ADAP has allowed me to share experiences with people that are not only infected, but also affected by HIV/AIDS in North Carolina. It’s been a gateway for me to be an advocate and trailblazer toward an AIDS free-generation. ADAP saves lives, and it changes lives. The landscape of people living with HIV and their life experience is completely different because of ADAP. 



Interview by Blaire Benson

This is one of a series of interviews highlighting the impact that the AIDS Drug Assistance Program has on the lives of people in North Carolina. If you would like to share your story, contact Claire at claire@ncaan.org

To take action to save the AIDS Drug Assistance Program from proposed budget cuts, send an email to your legislators now.

ADAP Stories: Michelle


Hometown: Asheville

Occupation: Disabled. Volunteers as CNA advocate for the Western North Carolina AIDS Project

Q: How has the North Carolina AIDS Drug Assistance Program affected your life?

A: ADAP has drastically changed my life. If it had not been for ADAP and my case management with Western North Carolina AIDS Project I would not be a success story today.

When I was diagnosed, I was moving down a very unhealthy path. I could not afford my HIV medication; I had very little income; and I was living a very unhealthy lifestyle centered on alcohol and drugs. ADAP has healed me. I was able to get medication not only for treating HIV, but for my other illnesses (high blood pressure, high cholesterol, diabetes, etc.) as well. 

As my health began to improve I became more hopeful about my life. I lost 85 pounds and have kept it off for over three years now. I no longer have to take any medication other than my HIV medication. I’m now sober and healthy. Being healthy has allowed me to create a much more stable life for myself.  I’ve had the same address for the last seven years. That is a huge success for me. 

When you don’t have your basic needs taken care of you don’t care about the medication, so creating an overall healthy and stable lifestyle is a very important part of ensuring that people take their medication. ADAP has helped me rise above the stigma of being HIV positive. I was at death’s door—literally. Now I am healed—in so many ways. My new healthy lifestyle is sustainable because I know I will be able to continue my medication through ADAP. 

ADAP has also changed the lives of people I love. My sister passed away from AIDS. When she was diagnosed the HIV virus in her body had already advanced to AIDS. Before she passed, she had four children—none of which contracted HIV from her because ADAP provided medicine to my sister while she was pregnant. ADAP is the reason my nieces and nephews are negative. They give me hope, and ADAP gives me hope.  

Interview by Blaire Benson

This is one of a series of interviews highlighting the impact that the AIDS Drug Assistance Program has on the lives of people in North Carolina. If you would like to share your story, contact Claire at claire@ncaan.org

To take action to save the AIDS Drug Assistance Program from proposed budget cuts, send an email to your legislators now.