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: http://www.doh.wa.gov/YouandYourFamily/InfantsandChildren/HealthandSafety/GeneticServices/DownSyndrome
And read more about the programs at the Arc of Whatcom County here: http://arcwhatcom.org/
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 http://arcwhatcom.org
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
How I Became a Crunchy Pro-Vaxing Mom
We know that there are risks with every parenting decision we make, but we have to make them rationally and based on sound science. Since every country and every major medical and scientific body on earth supports vaccines and there is lots of evidence that the benefits of vaccines far outweigh the risk, immunizing myself and our children and advocating that the husband also gets up-to-date on his vaccines is one of the wisest health choices we have made.
So, how can I be crunchy and pro-vax? Simple. Because we do what we know is best for our health, based on sound science. Living healthy, i.e. being crunchy, makes sense to us. So does vaccination.
While I was running the Facebook page Informed Parents of Vaccinated Children, I became aware of the Immunity Community. In the Immunity Community, parents learn to use their social networks, both online and off, to advocate in a positive and non-adversarial way for immunization. We are taught to spread the word about the benefits and how to talk to parents who are concerned about the risks. I was thrilled to find this group and advocated strongly for them to come to Bellingham. Now I am part of the Immunity Community and I could not be happier. We got our program written up in the Bellingham Herald, on the front page, which was thrilling. Other parents are making a huge different at their children’s preschools, by sharing information in a positive manner. We are making a difference. And it is very exciting to be spreading the word that you can live in healthy, crunchy Bellingham, WA and also be fully immunized.
** As summer winds down, kids and their families across Washington State are gearing up for the start of a new school year. With a new year upon us, it is a good time to make sure you and your family are up-to-date on all the required vaccines for school entry. Vaccines are free in Washington State for all children under 19. For help finding a vaccination clinic visit: http://parenthelp123.org/resources/resource-finder or call 1-800-322-2588.
Curious how protected your children’s school is from vaccine-preventable diseases? Check-out http://www.schooldigger.com/WAImmunization/ to see your school’s vaccination and exemption rates.