community resources | WithinReach WA
Home  >  Tag Archives: community resources

community resources

A Visit from KIND (Kids In Need of Defense)

Written by Meryl Safar, WithinReach Specialist, AmeriCorps

WithinReach Intercultural Competency Committee works to bring in guest organizations to inform our staff about their work, and how they’re making an impact in the community we all live in. Often times, these organizations give us insights into what our own clients might be facing. This helps us as a staff to better empathize with situations our clients might be in and to be able to refer them to the right services.

Last month we had the pleasure of hosting Kids in Need of Defense (KIND) at our Healthy Connections Team Meeting. Our presenters were Melody Young, Pro Bono Coordinating Attorney and Ellen Reed, Social Services Coordinator, who shared the organization’s origin and how they work to provide legal services for unaccompanied children. The legal classification of an unaccompanied child is someone that is under the age of 18 who has no immigration documentation, and has no parent or legal guardian that can provide care and physical custody at the time of the child’s arrival to the United States. Their work is crucial because in Washington State where no one, including children, has the right to legal representation in immigration court unlike other courts of law.

Legally unaccompanied children are not unaccompanied by choice. They are frequently escaping complex and varying situations of violence, neglect, and persecution in their home countries. Founded 10 years ago in part by celebrity Angelina Jolie and backed by Seattle’s own Microsoft, KIND has now grown into a nationwide organization. With field offices in multiple urban communities (Atlanta, Baltimore, Boston, Houston, L.A, Newark, New York City, San Fran, Seattle, WA DC), KIND has been able to connect with 14,542 referred children as of April, 2017. 477 legal professionals and associations function as partners in supporting the mission of KIND.

KIND actively works at all levels of the immigration system. They are directly involved in policy development and intentional lobbying for immigration reform. KIND representatives advocate on behalf of the children they serve to ensure equity in legal treatment. Furthermore, they protect unaccompanied children so that those children have access to the healthy futures they deserve. In order to achieve these goals KIND attorneys, alongside numerous volunteers and partners, work one-on-one with children to help navigate a multifaceted legal system.

Specifics for Seattle Field Office: KIND accepts referrals for children between the ages of 0-18. However, the majority their referrals are for children between 16-18 years old. Primary underlying cause of forced un-accompaniment for Seattle referrals is gang violence, domestic violence, violence against children living on the street and persecution.  

Referral Guidelines for KIND: Clients must live in King County or have supporting adults that work in the Seattle area. Clients also must be under 18 years old and meet the 200% of the federal poverty guideline income level. Cases are prioritized by level of urgency such as if a child is in removal proceedings.

How to refer someone to KIND: Call to start the referral process at (206) 359-2366. In the voicemail include the name of caller, name of child, reason for calling, country of residence, phone number, upcoming court dates, and name of referral agency (if applicable).

Volunteering with KIND: With their service to many unaccompanied children from South America, KIND works with bilingual volunteers to help translate between attorney and child. Here at WithinReach, one of our Bilingual Specialists on our Healthy Connections Team, Bradley Mills, volunteers for KIND as an Assistant to the Case legal interpreter. During his time at KIND, he has assisted many children with interpreting complicated legal lingo and providing translating support to attorneys, children and their families and caretakers. As a volunteer, he follows specific cases and interprets whatever phone calls or documents may arise along the way. Bradley, and volunteers like him, call families with the attorney present and asks for further information while navigating family situations. When going over complex legal documents with children, volunteers and attorneys try to bring normalcy to the child’s life by connecting with them about friends, hobbies, school, and family.

Bradley Mills with Ellen Reed, Social Services Coordinator and Melody Young, Pro Bono Coordinating Attorney 

 “It is hard to ask children to step up when they just want to be a kid.” -Bradley Mills


Referral statistics:

  • 75% of referrals, in the Seattle branch, come from Central American Countries such as El Salvador, Guatemala, and Honduras
  • Primary languages spoken: Spanish and Indigenous languages
  • 60% Of children arriving in the U.S. have no one to represent them in immigration court
  • Children without representation are five times more likely to be deported

In order to best provide holistic and sustainable support, KIND works to understand the child’s journey and incorporates the children’s personal stories into their work. An unaccompanied child faces barriers such as gender-based violence, deprivation, and often trauma. All of the barriers continue throughout the legal process, and are not restricted to the child’s journey to the United States. The deportation system for young children and people that do not have representation is incredibly limiting. Limitations such as language, legal vocabulary, background knowledge of the U.S legal systems, knowledge of what your status and requirements are, and fear of deportation are just a few of the barriers at play. Combine these barriers with the struggles of being a child in a foreign country, the children have an intensely arduous journey to physical, emotional, and social well-being. Every child deserves the opportunity to flourish without these barriers, and KIND works towards reducing the difficulties that these children face when confronting immigration court in the U.S.  

These statistics were provided to WithinReach staff at our December presentation from KIND and their 2017 Corporate Volunteer Fact Sheet. For more information about KIND and the work that they do, please visit  or contact the KIND Seattle office at


Have experience with this topic that you’d like to share? Complete our Google Form Here!


Tags: AmeriCorps. Healthy Connections   community resources   ICC   Intercultural Competency   Kids In Need of Defense   KIND   

A continued conversation with Jessika Houston, Arc of Whatcom County

At WithinReach, we get to engage with families who are on a wide spectrum of places in their journey with a diagnosis of a special health or developmental need. Sometimes a family is just learning of a diagnosis prenatally, and sometimes they have many years of experience. The Arc of Washington and its nine regional chapters are excellent resources for families who are looking to connect around developmental disabilities, wherever they are on their journey.

We spoke with Jessika Houston, Down syndrome Outreach and Young Adult Self-Advocacy Coordinator at the Arc of Whatcom County to learn more about how she works with individuals and families with developmental disabilities:

“Down syndrome Outreach is a program that exists for individuals with Down syndrome, their family members, friends and caregivers from birth through life. We provide resources, information, advocacy support, and connect families and individuals in our community to support one another on their journey. There are annual support events specific to Down syndrome Outreach (DsO), such as the Buddy Walk in October and the Spring Fling in May.

On World Down syndrome Day (which is March 21), our community helps to bring awareness to their schools and work places about Down syndrome. The goal is to focus on honoring and appreciating our differences, all of them, and therefore encouraging the celebration of our differences and bringing support to all ages. In Whatcom County, there is a vision of change and inclusion for future generations. This has really determined the focus of an aspect of the work I do with DsO, which is to support new families.

When I started at The Arc I heard from our community the need to strengthen the supports for new families with a diagnosis of Down syndrome. There are many misconceptions and stereotypes about people with disabilities, and as Down syndrome is a chromosomal condition, we are able to learn of the diagnosis in the prenatal and postnatal stages.

The opportunity to provide support and resources at the time of diagnosis is one that historically has been missed in the Down syndrome community worldwide. In addition, many families have experienced negative interactions when receiving the diagnosis, with a lack of support and resources.

If families receive the diagnosis and then are told to seek out their own resources, they are vulnerable to inaccurate and prejudicial information. This does not fully engage and support this new family. Despite the challenges, countless families and self-advocates have been propelled from their experiences and helped to create policy which has shifted the dynamic in which families receive support.

In June 2016 in Washington State, the Down syndrome Information Act was passed in legislature. The law came forth because self-advocates spoke out about the impact on their families, and their vision of necessary support to new families.

The 2016 Down syndrome Information Act states: Medical Professionals are to provide materials to families at time of birth or pre-natal stages in delivering a likelihood of a diagnosis. Medical professionals affected by this bill are: midwife, osteopathic physician and surgeon & osteopathic physician’s assistant, physician & physician assistant, nurse, genetic counselor, hospitals, birthing centers & anyone/place in above categories that provide a parent with a prenatal or postnatal diagnosis. The WA State Department of Health has been working in response to this Law, and I have had the chance to connect with them in detail to discuss how we can ensure it is accessible and followed through by medical professionals in Washington State.

This past March, we held a statewide webinar regarding this issue. I am so grateful for the opportunity to be a part of something that we can now utilize as a resource supporting new families across the state. It has been incredible to see different communities and organizations from all over Washington come together to connect about these important issues to empower families and improve systems of care and support.

Before this law was passed, connecting with medical professionals and providing resources to them about this condition, is something I worked to bring to our local community. I have had the chance to present to various meetings with obstetricians, nurses, and midwives, and will continue this work as practitioners become more familiar with this new law. The main message I hope to convey to medical professionals is that the support, resources, and language that is used to give the diagnosis greatly impacts how the family will view their child and how they will utilize the resources available to them.

Through this work I have learned that by opening up our perspectives and working to be a resource, we are able to create systems of support that will sustain through time. They will persevere, find strength and challenges in new and unexpected ways and help transform thinking that includes all abilities and backgrounds.”

You can find more information about this work at the Department of Health here:

And read more about the programs at the Arc of Whatcom County here:


Tags: Advocacy   care   community resources   Developmental support   diagnosis   Disability   Down syndrome   Down syndrome Information Act states   Down syndrome Outreach   education programs   empower   families   improve systems   intellectual & developmental disabilities   Medical Professionals   support   The Arc   Washington state   Whatcom County   Young Adult   

Family and Professional Connections: Promoting Self Advocacy at the Arc of Whatcom County

Through our work with special health and developmental resources, WithinReach has had the great pleasure to partner with agencies such as the Arc of Washington. The Arc is part of a national network dedicated to advocacy, community building, and resource referral for individuals with developmental disabilities and their families. Washington has nine chapters in King, Snohomish, Whatcom, Cowlitz, Grays Harbor, Kitsap/Jefferson, Spokane, Benton/Franklin, and Clark counties.

Part of the advocacy work that the Arc does is to support the perspective and rights of self-advocates, who are individuals with disabilities. To hear more about this important work, we reached out to Jessika Houston, Down syndrome Outreach and Young Adult Self-Advocacy Coordinator at the Arc of Whatcom County. Jessika was gracious to share with us her personal connection to this work, and what it means to her to be in this role:

“My work at The Arc directly relates to my personal life, as I am the sister of a young adult with Down syndrome, Mike. Mike has truly been one of the largest sources of inspiration for me and the path I have taken. I could not be more grateful for him in my life, for all that he has taught me and my family. From him I have learned persistence, patience, compassion, acceptance, resilience, will and grace, and the beauty of living in the moment. When I think of the strengths of living in a neurodiverse family, it comes back to those qualities in him that he has the ability to teach everyone that crosses his path. With him, there have always been moments that we wish we could just capture and visit any time we wanted – the moments that make you love life and trust exactly where you are.

And, in thinking of the challenges – those same qualities can come through, in a different light. The moments when Mike is so frustrated, trying to find the way to articulate what he needs or wants, and seems so tired and overwhelmed with…persisting, having patience…when acceptance of the situation cannot happen and the will takes over…those times are when you wish the moment would just end. There are also challenges that come from those that may not know about Down syndrome and how to engage someone with a disability. Yet, it is the moments of challenge that seem to inspire me the most.

After he was born, I found myself asking questions like: Why are people so afraid of what is different? How can I help? How can I learn about other perspectives? How can I be a resource to my family, my brother, my community?

I first learned of The Arc when I worked as a Living Skills Specialist for a supported living agency in Bellingham. My brother, without knowing it, inspired me to work there so I could learn more about what life as an adult can look like, how to advocate with and for someone, learn about independent living, how to help navigate the supports in someone’s life and discover what resources exist in the community.

In the Young Adult Self Advocates program, we talk about our visions, our goals and aspirations, and acknowledge the challenges and barriers that might exist. Self-Advocates are involved in community awareness projects, as well as focus on their individual skill building. They are also passionate about advocating in legislation for their individual needs, which also reflects needs in our community such as employment, housing, recreation, caregiver wages, among others. They aim to “Be Proud. Be Strong. Be Heard.

If you are interested in learning more about the Arc of Whatcom County and the Young Adult Self Advocate program, visit

Tags: Advocacy   community   community resources   Developmental support   Disability   Down syndrome   education programs   Independent living   intellectual & developmental disabilities   Resources   Special Health Care Needs   The Arc   Whatcom County   Young Adult   

Tis’ the Season!

“Never doubt that a small group of thoughtful and committed citizens can change the world; indeed, it’s the only thing that ever has.” This quote by the late cultural anthropologist Margaret Mead is truly apropos to a recent partnership that WithinReach and many others have been involved in!

Less than a month ago, one of our Community Partnership Associates at WithinReach, Jefferson Rose, was contacted by Ellie Marsh, President of the Western Washington Chapter of the National Association of Hispanic Nurses (WW-NAHN), about a school in the Edmonds School District that had several dozen children that were either unvaccinated or under-vaccinated due to lack of access to a medical home. These children needed a number of required vaccinations by January 4th in order to continue attending school.

Jefferson passed along this information to the Immunization and Healthy Connections Teams at WithinReach, which quickly mobilized to see what we could do to get these children vaccinated and connected to health insurance. Through our relationship with the Snohomish Health District we connected the health department and WW-NAHN together, and this is where the magic truly happened!

I’m excited to report that the WW-NAHN, in conjunction with Spruce Elementary School, WithinReach, Snohomish Health District, and the University of Washington School Of Nursing, hosted an immunization clinic for these families on Wednesday, December 16, 2015.

All vaccines were provided for free by the Snohomish Health District, six nursing students from the UW were on hand to give all of the injections to children, and WithinReach’s multi-lingual in-person assisters – Maricruz and Irina — were on hand to sign families up for health insurance, and provide other community resources for families!

As a result of all of these efforts, we learned that nearly half of the students that were previously identified as out of compliance with their immunizations were able to show proof of the required immunizations, and the other half received all the vaccinations necessary to stay in school.

Thank you to all the amazing partners who rallied together to protect kids from vaccine-preventable diseases and get them signed up for health insurance.



Tags: community resources   immunizations   Partnership   School   Snohomish Health District   Spruce Elementary School   University of Washington School Of Nursing   vaccines   Western Washington Chapter of the National Association of Hispanic Nurses   WW-NAHN   

Search Blog