4 Mar, 2015

Why Social Workers Make the Best Reproductive Justice Activists

By |2021-08-19T18:42:44-04:00March 4th, 2015|Categories: Public Health & Social Work|Tags: , |0 Comments

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March is one of my favorite months of the year. There’s a lot happening during March for us to raise our voices about, including Women’s History Month, National Day of Appreciation for Abortion Providers (3/10th), National Women and Girls HIV & AIDS Awareness Day (3/10th), and National Native HIV Awareness Day  (3/21st) (among others).

My favorite thing about March is that it’s all about the social worker. March is National Social Work Month, and this year’s theme is “Social Work Paves the Way for Change”. From individual counseling to managing an evaluation project or grant process, social workers make a difference in the lives of individuals, families, schools, organizations and communities.

What’s so great about this year’s Social Work Month is that I’ve been invited to be a co-presenter for a 3-part webinar series focusing on two of favorite topics: social work and reproductive justice. This series, sponsored by Social Workers for Reproductive Justice with support of The Abortion Conversation Project , will focus on not only how social workers are change agents in the lives of many, but how social workers are often in the forefront of many social justice movements. While this series is meant to be educational and empowering for any professional social worker or student social worker (as well as anyone interested in going into the field), this series will also touch on how the personal views of social workers can often get in the way of our clients’ right to self determination, and what we can do to make sure we remain unbiased in our interaction with our clients and the resources we provide.

Social work was a natural progression for me before I could see how it would relate to my ongoing work as a college student activist, and I am grateful that I’ve been able to combine reproductive justice with social work, in addition to the program evaluation work that I do.

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10 Dec, 2014

What Do You Do When Self Care Isn’t An Option?

By |2021-08-19T18:42:13-04:00December 10th, 2014|Categories: Self & Community Care|Tags: |0 Comments

“Caring for myself is not self-indulgence. it is self-preservation and that is an act of political warfare.” ~ Audre Lorde

Today is International Human Rights Day. First commemorated in 1950, International Human Rights Day brings attention to the Universal Declaration of Human Rights as the common standard of achievement for all nations.  The 2014 theme, “Human Rights 365”, celebrates the fundamental principle that everyone is entitled to the full range of human rights at all times, that human rights belong equally to each of us, and these rights bind us together as a global community.

Given the pain, frustration, and unrest that have resulted in protests in recent weeks around the United States to bring awareness to the increase of policing tactics against communities of color, the constant attacks on women’s reproductive access, continuous news about hate crimes against members of the LGBTQ community, the debates surrounding immigration rights, and countless other stressors on marginalized communities, the state of basic human rights around the world is nothing short of dismal.

As social workers, counselors, and therapists, we are receptacles of our clients’ trauma. We encourage clients to work through a traumatic experience by giving voice to it, but what ends up hopefully being a cathartic release for our clients, leaves us literally holding our clients’ trauma in our hands.

As teachers, agency or nonprofit workers, or community activists, the well-being of our communities is a priority for us. We conduct needs assessments and speak to our students and community members about what needs to change within the school system, agency, or community. What ends up being a positive way for community members to voice their concerns can leave us drained because what needs to change—often at a systemic and policy level—can feel daunting.

When your communities are constantly under attacked, when there seems to be no end in sight, and when your fundamental rights are being taken away, what do you do when self care isn’t an option for you?

When times get tough, I rely on self care activities and rituals that I’ve developed for myself. I mention self care, especially to service providers and activists, because I believe that you can’t raise your voice for others if you’re not able to care for yourself.

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3 Dec, 2014

Who Are The People Behind The Numbers?

By |2021-08-19T18:41:54-04:00December 3rd, 2014|Categories: Research & Evaluation|Tags: , |0 Comments

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(Photo credit: Kaiser Family Foundation)

“Statistics are real people with the tears wiped away. When statistical data are presented, they seem sanitized and tend to distance the reader from the actual problem at hand.”  ~ Dr. B. Lee Green 

Let’s take a look at this graph, taken from the policy fact sheet “Sexual Health of Adolescents and Young Adults in the United States”, developed by the Kaiser Family Foundation.

This fact sheet provides key data on sexual activity, contraceptive use, pregnancy, prevalence of sexually transmitted infections (STIs), and access to reproductive health services among teenagers and young adults in the United States.

The chart above is taken from this fact sheet, and the data and information is listed in the 2013 Kaiser Women’s Health Survey. To list some statistics:

**70% of women 19 to 24 rated confidentiality about use of health care such as family planning or mental health services as “important”; however, the majority of girls and women were not aware that insurers may send an explanation of benefits (EOB) that documents use of medical services that have been used to the principal policy holder, who may be a parent.

**Today, 21 states and DC have policies that explicitly allow minors to consent to contraceptive services, 25 allow consent in certain circumstances, and 4 have no explicit policy;

**38 states require some level of parental involvement in a minor’s decision to have an abortion, up from 18 states in 1991. 21 states require that teens obtain parental consent for the procedure, 12 require parental notification, and 5 require both.

Of course, the correlation makes sense: the older a woman is, the higher likelihood she is aware of what a EOB is and how health insurance companies many send them by mail to her home. In fact:

One of the earliest [Affordable care Act] provisions that took effect in September 2010 was the extensions of dependent coverage to young people up to age 26, who had the highest uninsured rate of any age group at the time the law was passed. In 2013, over four in ten (45%) women ages 18 to 25 reported that they were covered on a parent’s plan as a dependent. because that are adult children, the extension of coverage has raised concerns about their ability to maintain privacy regarding the use of sensitive health services such as reproductive and sexual health care and mental health. (Kaiser Family Foundation, 2013)

I also find it interesting that the younger a woman is, the higher she is to rate confidentiality when seeking various health care services. Also the fact that only 21 states and DC allow minors complete consent to access contraceptives and that most states require some level of parental involvement in a young person’s decision to have an abortion is worth looking into, especially in states that allow young people to access contraception without parental consent.

But we’re not here to talk about completely about the statistics. And we’re not here to provide a full-on critique of policy fact sheet.

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1 Oct, 2014

10 Common Mistakes that Keep Respondents from Completing Your Survey

By |2021-08-19T18:39:34-04:00October 1st, 2014|Categories: Research & Evaluation|Tags: , |0 Comments

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Developing survey questions is harder than it looks. Asking questions is easy, but asking direct, unbiased, and valid questions is more of an art form. There’s a lot that goes into it, including flow, how the questions tie into what your program evaluation wants to answer, and keeping your respondents engage enough to complete the survey.

Here are 10 common mistakes and my tips for avoiding them:

Not knowing your target audience: Understanding who your audience is can help you craft survey questions that are pertinent to them. Avoid using words or phrases that your respondents may not know the meaning of. Instead, use words and phrases that are tailored to your target audience. Are your surveying nurses, social workers, or teachers? It’s ok to use words or phrases that are most common to those target audiences. On the other hand, if you’re not sure if your audience will understand what you mean by “reproductive justice”, it’s best to gather insights from the program coordinator or workshop facilitator to see if this term has been discussed.

Not explaining WHY: Believe it or not, most respondents are willing to help you if you share the value in completing your survey. When a respondent knows what’s in it for them, there is likelihood that the survey gets completed. If respondents know that their responses can aid in determining pay raises or in the restructuring of an under-performing program’s activities you’re more likely to complete it. If an incentive (i.e. a gift card to the respondent’s favorite retail store, coffee shop, or to wherever Visa is accepted) is included when a respondent completes your survey, indicate that on your survey at the very beginning before respondents begin.

Including extensive demographic questions: When you ask too many demographic questions, it can result in taking up a lot of room that could have been used for other questions. Before you add in questions to gather information on a respondent’s income level, religion, socio-economical status, etc., consider if it’s appropriate and relevant to the overall survey and the basis of the evaluation. Also, unless the rest of your survey depends on these answers, consider leaving demographic questions for the end of the survey as they tend to be the more uninteresting parts of a survey for respondents to complete.

Asking too many questions: Tying into the second point, asking too many questions can be the downfall of your survey. There are a variety of question types—open-ended, multiple choice, Likert or interval (very satisfied, satisfied, neutral, dissatisfied, very dissatisfied), ratio (“How many days do you spend studying?”), and dichotomous (true/false, yes/no, agree/disagree)—but it’s more about the intent behind the question. My recommendation is to create a survey that can have up to 15 questions. Keep in mind that engagement levels wane, especially during an online survey where there are more distractions (i.e., social media, videos, online shopping, etc.) (more…)

25 Aug, 2014

Sound Off: One in Three U.S. Teens Are Unaware That HIV is a Sexually Transmitted Infection, Survey Reports

By |2021-08-19T18:37:49-04:00August 25th, 2014|Categories: Equity & Justice|Tags: , |0 Comments

(Image courtesy)

A recent report released by the MAC AIDS Fund, reports that U.S. teens can benefit from more education on HIV. The survey, conducted by Kelton Research between May 22-June 5, 2014, surveyed 1,039 American teens ages 12-17 on their views on HIV stigma, transmission, and prevention.

Some of the highlights from the report include:

* 9 out of 10 (88%) believe they are not at risk for contracting HIV. Also, one-third (33%) were not aware that HIV is a sexually transmitted infection.

* 50% of respondents are afraid of contracting HIV and would be nervous if they were to get an HIV positive diagnosis (93%), around the same percentage as if they were to get a positive pregnancy test (94%) or have to engage in first-time sexual activity (91%)

*While the belief that their risk of contracting HIV is low, the respondents were far more likely to believe they are at greater risk for developing cancer (38%), diabetes (33%), heart disease (28%) or obesity (22%) during their lifetime.

*While most believed that using a condom (71%), abstaining from sex (58%), or getting testing for HIV regularly can prevent the spread of HIV (55%), most did not know that HIV prevention also includes reducing the amount of sexual partners (47%), not using alcohol or drugs (33%) or talking with others about prevent HIV prevention (29%).

*While teens feel they can benefit from more education on HIV and AIDS and are open to having more discussions on prevention and transmission (59%), 45% admit that having these conversations makes them uncomfortable.

*Teens would feel ashamed (53%), scared (69%), and feel that others would be afraid of them (50%) if they were to be diagnosed with HIV. Also, if they were to meet someone with HIV, 24% wouldn’t want to share food or drink with that person, touch them (31%), or treat them as a normal person (51%).

Nicole’s take: Other than age, we don’t know much else about the survey respondents. Where’s the rest of the information? Can we at least get a breakdown of the data based on age range? I understand that not all quantitative data collection is solid, but I feel that we’re missing some valuable information by not including other factors. It would have also been great to see how the beliefs of the respondents break down based on geographic region, gender, race and ethnicity, urban versus suburban or rural location, grade level, or age of onset of sexual activity. That would have also been interesting to know if the students who reported receiving sex education from schools (56%) or from family members (38%) were receiving abstinence-only education or comprehensive sex education. (more…)

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