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.