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Grow Your Advocacy Chops!

Caregiver Resolutions Advocacy The Arc Amplified

New Year Resolutions for the Busy Parent-Caregiver:

Grow Your Advocacy Chops!

A sentiment often shared by parents of children with disabilities is their wish to get more involved in advocacy efforts. It is obvious they possess unique experiences and an understanding of social and political issues that impact their kids and their families. Parents and caregivers have important stories to share and wonderful ideas to improve policies to better serve their kids and communities.

It is abundantly clear that parents of kids with disabilities are ready to step up as community change-makers. They possess the knowledge, the experience, the skills, the passion and the pragmatism.

What they do not often possess is time.

Parents are busy. All parents are busy. It is often part of the gig of becoming a parent.

But, parents of kids with disabilities are off-the-charts busy. We all know this.

Parents of kids with disabilities do all the regular parenting stuff…

And then, second-shift parenting begins, during which parents transform into a caregiver, a nurse, a teacher, a therapist, a pharmacist, a personal assistant, and more…

And all of this is in addition to whatever type of outside employment parents may hold, and whatever parenting or caregiving is required for their other children or family members.

THE RESULT: Many parents of kids with disabilities want to get involved in advocacy, but they do not see how that can be done.

THE ANSWER: Incrementally.

Small steps, my friends.

It is easy to feel overwhelmed when considering how to become involved in advocacy. There are so many policies that need attention. There are so many issues that need dedicated champions to push for change. That is obvious. However, it is impossible for one person to advocate, with any degree of commitment, on *all* the issues. And, that, too, is okay.

Your involvement in advocacy, at any level, on whatever issue, or issues, are most important to you, is absolutely worth it. Your presence makes change happen.

So, for those parents and caregivers who want to step up their advocacy game in 2022, here is a RESOLUTION for you:

Commit to 20 minutes of dedicated advocacy once per week.

Put it on your calendar and treat it as an appointment that you must keep.

That is it. Start there — with that first incremental step — and see where your year takes you….

Use that 20 minutes to read — without distraction — books and articles about what it means to be an advocate, or how to engage in the advocacy process.

Use that 20 minutes to write — without distraction — about your personal advocacy goals. Advocacy can occur at all levels of government. Do you want to advocate for increased accessibility at local playgrounds? Do you want to advocate in the local school district for increased inclusion of kids with disabilities in general education? Is there a state law that really needs to change? Is there a national advocacy group that you dream of joining? Whatever it is, write those goals down on paper, and tape that piece of paper to your bathroom mirror. Look at it every morning when you are brushing your teeth. Think about those goals in the shower. Keep thinking about them.

Use that 20 minutes each week to study issues that are important to you.

Use that 20 minutes to reach out to other family caregivers who are also working on those same issues.

Use that 20 minutes to learn about your state legislative district and those who serve your community. Then, send them an email sharing the story of your family and the issues that are important to you.

Each week, take your next incremental step forward into advocacy during that 20-minute appointment with yourself.

Change occurs over time. Change happens slowly — often, more slowly than we would like. But, change happens when people get involved. And, even 20 minutes of your time can be part of driving that change.

And who knows? Maybe your 20 minutes will incrementally turn into 30 minutes, and then an hour each week…

And then, soon, you will look back and realize just how much change was brought about by that first 20-minute, incremental step.

There is no better time than the present to take a first step.

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Whitney Stohr is a Parent to Parent Coordinator at The Arc of Snohomish County. She is passionate about advocating for medically complex children and children with disabilities and their families. She is a mom and medical caregiver herself, who is energized by working closely with other parent/family caregivers. She lives with her three-year-old son Malachi and husband Jason in Lynnwood. Connect with her on Instagram @rollin.w.spinabifida. Contact: whitney@arcsno.org.

READ-ALOUD: Can I Join Your Club?

Read Aloud Can I join Your Club The Arc Amplified

READ-ALOUD: Can I Join Your Club?

Duck wants to join a club. But he can’t ROAR like Lion or TRUMPET like Elephant. What’s a duck to do?

Duck starts his own club – and everyone is welcome! Because when it comes to making friends, being yourself is all that counts!

Do you want to join a club where everyone’s welcome?

 

Join Whitney Stohr a Parent to Parent Coordinator at The Arc of Snohomish County, as she reads: Can I Join Your Club?, written by John Kelly and illustrated by Steph Laberis (published 2017 by Little Tiger Press Ltd., UK, and Kane Miller Publishing, USA).

New Year Resolutions for the Busy Parent-Caregiver: Taking Back Control of Your Schedule

Resolutions for the Busy Caregiver Scheduling The Arc Amplified 1 1

New Year Resolutions for the Busy Parent-Caregiver:

Taking Back Control of Your Schedule

A lesson learned in caregiving: It is a marathon, not a sprint!

When a parent or family caregiver first learns of their child’s diagnosis, life can quickly turn hectic… in many cases, it becomes hectic to the point of unmanageable. There is so much to do! There are endless stacks of paperwork to complete, people to call, therapies to schedule, services to connect… It is a process of learning how to navigate within a new world.

Yes, those first years following a diagnosis are challenging.

Those first years are chaotic and busy. You may try endlessly to do *all* the things because you want to give your child the best start at life. You say “yes” to everything. You take every opening at your child’s therapy center. You are already nodding your head before you even consider your already full calendar. And you run, and run, and run…

And then, one day, a few years down the road, you stop running. Life calms down just enough for you to look around and see the chaos and feel overwhelmed by it all. That is the point at which family caregivers may come to realize that caregiving is a marathon, not a sprint, and long-term sustainability is the goal.

Caregiving responsibilities do not go away if a primary caregiver runs out of steam. Saying “yes” to everything, creating a calendar so full you forget to leave room to breathe, completely running yourself into the ground… that serves no one. And it is not sustainable when long-term caregiving is part of your future.

Raise your hand if you have been there…

(*With a sheepish grin, I slowly raise both hands, high into the air, nodding in acknowledgement*

Yes, I have been there.)

So, for family caregivers out there who are still looking for a New Year’s Resolution, here is one idea:

“In 2022, I resolve to take back control of my family’s schedule.”

What it means to “take back control” will look different for every family and for every caregiver. Set your own parameters. But, here are a few suggestions:

  • I will prioritize the activities that matter most to my family.
  • I will schedule time to take care of my own health and wellbeing.
  • I will leave time in my schedule to pursue my personal interests, hobbies and educational or work goals.
  • I will only say “yes” to therapy and appointment times that work for my family and that meet our priorities.
  • I will safeguard the right of my children to enjoy unscheduled playtime.
  • I will set aside time to concentrate on my relationships with my spouse or partner, my extended family and friends, and my kids.
  • I will protect and value my time and will not overbook myself or my family.
  • I will step back from activities that only bring stress and anxiety and that no longer serve our priority needs.

Remember: Caregiving is a tough job. It is hard work, and you are doing amazing.

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Whitney Stohr is a Parent to Parent Coordinator at The Arc of Snohomish County. She is passionate about advocating for medically complex children and children with disabilities and their families. She is a mom and medical caregiver herself, who is energized by working closely with other parent/family caregivers. She lives with her three-year-old son Malachi and husband Jason in Lynnwood. Connect with her on Instagram @rollin.w.spinabifida. Contact: whitney@arcsno.org.

Raise Your Voice: 2022 Legislative Advocacy Days

2022 Arc Advocacy Days The Arc Amplified

Raise Your Voice: 2022 Legislative Advocacy Days

The start of the 2022 state legislative session is just around the corner. Now is the time to re-engage in advocacy!

Each year, The Arc of Washington State organizes a series of ADVOCACY DAYS to provide opportunities for the disability community to engage in the legislative process, inform their elected officials on issues that impact our community, and drive policy change at the state level.

Due to COVID-19, legislative meetings, as well as The Arc Advocacy Days, have transitioned to a virtual platform. This will remain in effect during the 2022 session.

This is a good thing! While it is always nice to meet and talk with legislators face-to-face, a virtual option increases accessibility and allows disability advocates from across the state to participate in the activity that happens in Olympia.

The Arc of Washington State invites individuals with intellectual and developmental disabilities (IDD), their families, friends and service providers to participate in one or more of the planned Advocacy Days.

Participation is easy! Register using the links below, and you will receive information by email about joining the meeting.

Advocacy Day Calendar

January 12th

January 19th — Topic: Housing Accessibility — REGISTER HERE

January 26th — Topic: Civil Rights / Nothing About Us, Without Us — REGISTER HERE

February 2nd — Topic: Employment & Day Services — REGISTER HERE

February 9th — Topic: Barriers to Transportation — REGISTER HERE

February 16th — Topic: Caregiving of Children & Adults — REGISTER HERE

February 23rd —Topic: Meeting All Needs in Education — REGISTER HERE

March 2nd — Topic: Healthcare for People with IDD — REGISTER HERE

Before each meeting, consider a situation you have experienced in your life that highlights policy needs or service gaps, related either to your disability or to your role as a parent or caregiver. Come ready to share that story! (Click here to learn more about the legislative priorities of community groups and coalitions within the wider disability community in our state.)

How to Get Involved in Advocacy! Thanks to the gift of modern technology, you can engage in advocacy efforts without ever leaving your home. Here are a few steps you can take right now, and in the weeks and months ahead:

  • Watch this pre-Legislative Session video, by The Arc of Washington State, to learn more about the upcoming Advocacy Days and issues important to the IDD community: be/TQRTBKZ37ec.

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Whitney Stohr is a Parent to Parent Coordinator at The Arc of Snohomish County. She is passionate about advocating for medically complex children and children with disabilities and their families. She is a mom and medical caregiver herself, who is energized by working closely with other parent/family caregivers. She lives with her three-year-old son Malachi and husband Jason in Lynnwood. Connect with her on Instagram @rollin.w.spinabifida. Contact: whitney@arcsno.org.

New Year Resolutions for the Busy Parent-Caregiver: Commit to Taking a Walk

Resolutions for Busy Caregiver Walking The Arc Amplified 1

New Year Resolutions for the Busy Parent-Caregiver:

Commit to Taking a Walk

A new year is here!

I hope this year brings with it a sense of renewed hope, new goals and new adventures with a side of fun and family memories to each of you, your partners, your children and your family as a whole. I hope that you ask and accept help when offered. I hope that you carve out time for yourself, to try new things, explore new interests, and meet personal goals.

As a busy parent (or kinship) caregiver, finding that time to prioritize your needs, and commit to self-care, can be challenging. Family caregivers are BUSY — with a capital B – U – S – Y! Making yourself a top priority is much easier said than done.

But, also: We must take care of ourselves!

So, say it with me: In 2022, I will prioritize my needs!

Self-care is essential. But, that does not mean that self-care must be something huge! Self-care can be simple moments scattered throughout your day. It can be five minutes of deep breathing, stretching or Sun Salutations. It can be carving out time alone to simply sit down and think, read or journal. (Click here for more on self-care)

This year, commit to a Self-Care Resolution.

Again, it can be something very simple. For example, commit to taking a walk outside — even if only for 10-15 minutes, 2-3 times each week.

There are many health benefits associated with the physical activity of walking. But, moreover, consider how even a short walk outdoors, in the fresh air, might impact your mood, your headspace, and your energy levels.

If walking works for you… If you feel that added benefit… Then perhaps, set a goal for 2022 to walk a certain amount of time, or a certain number of days each week — either alone or with a friend.

It is simple and achievable.

And that is the gold standard for the busy parent-caregiver!

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Whitney Stohr is a Parent to Parent Coordinator at The Arc of Snohomish County. She is passionate about advocating for medically complex children and children with disabilities and their families. She is a mom and medical caregiver herself, who is energized by working closely with other parent/family caregivers. She lives with her three-year-old son Malachi and husband Jason in Lynnwood. Connect with her on Instagram @rollin.w.spinabifida. Contact: whitney@arcsno.org.

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