Episode Transcript
Available transcripts are automatically generated. Complete accuracy is not guaranteed.
(00:01):
Welcome to the Parents Guide to Advocacy.
I'm your host, Ashley Hinkle.
My mission is to equip, empower, and support parents to become fierce advocates for their children's unique educational needs.
Our goal as a community is to be resourced and resilient parents continually growing to be the safe place our children need.
(00:24):
We will navigate the challenges of raising neurodivergent kids, highlight the joyful moments, and celebrate the successes our families experience when we see the spark in our children's eyes from learning something new.
If ending the feelings of overwhelm, guilt, and frustration to embrace courage, perseverance, and empowerment, Sounds good to you? Then let's go.
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Hey friend.
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I'm not sure about you.
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But I get into seasons where I just feel 100% burned out.
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Our family and I'm sure many of you can relate.
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Is juggling intensive educational services.
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Play therapy visits, social calendars, and that doesn't include school work in the adults therapy schedules.
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Sometimes I wish life would slow down.
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Maybe then it would be easier to be present.
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And reorient my perspective to what truly matters.
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But I'm learning that carving small amounts of personal time.
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To relax, learn and focus on personal growth can be possible.
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Even in chaotic seasons.
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I've had to get creative with our plans and ask for help.
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Both are things that I'm currently working on.
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I took a big step this week and letting go of my usual responsibilities for 48 hours and attending the apraxia kids national conference in Pittsburgh.
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It was my first time staying in a hotel alone.
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And I was feeling lonely and scared without my tribe.
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Even though my kids were driving me a little bit crazy.
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I started missing them before I backed out of the driveway.
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Several times I wanted to turn the car around and go back home.
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But I knew deep down I needed this.
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I needed it for me to face uncertainty and fear.
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My kids needed it to learn that they are safe with other people.
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And that mom will always come back.
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The separation anxiety was real though.
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I called my husband and told him I can't sleep.
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I feel like a homesick kid at summer camp.
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I did eventually sleep though.
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And even though the distance was difficult, traveling on my own to speak at a Praxia kids.
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Helped build my confidence and remembering that I can do hard things.
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It also showed me that there's one strategy that allows parents to recharge.
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And learn at the same time.
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And that is attending a conference based on your child's neurodivergence.
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A professional conference in your field.
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I may check a similar box, but there's something about connecting with other parents.
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Educators and service providers related to a loved one's wiring.
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That is really refreshing.
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You are connecting with people facing similar struggles and successes.
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These people may be farther along in the journey than you are.
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So they may share information with you that helps you feel more equipped to handle the unique circumstances you're facing.
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The added bonuses.
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That you realize you aren't alone.
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Your family.
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Isn't the only one experiencing a version of raising differently, wired children or having.
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A differently wired partner.
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At the apraxia kids conference, I felt recharged and I learned new strategies to use with my family after talking to a husband and wife team.
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Presenting on screen for you therapy for kids.
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With childhood apraxia of speech.
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As you all know.
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My son has CAS.
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In six months ago, we received a diagnosis of autism and ADHD.
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Around the same time.
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My husband received the same diagnosis.
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I went into connect with another couple in a similar situation.
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But I've not found anyone living in similar circumstances.
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Meeting another wife that is raising children with extra needs.
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And has learned how to communicate better with her husband.
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With ASD.
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I was like a breath of fresh year.
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Finally someone who understands.
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Hearing her husband's input on navigating family life was also really insightful and helpful when I reflected on how I communicate with my husband.
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Just her saying when emotions rise, wait 24 hours before talking about it, it will help decrease the defensiveness.
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That resonated so deeply.
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There's a lot of defensiveness in my house and it can be overwhelming.
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I've been waiting before talking.
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About different things, but definitely not 24 hours.
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That tip was specific and from someone who knows what works.
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They even transparently shared.
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How ASD can be difficult on marriages.
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Being able to speak freely with others that can offer support was like a lifeline.
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They shared their contact information and told me to contact them.
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And pass their info onto my husband too.
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I felt so hopeful about my family's situation after connecting with that couple.
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I'm realizing that people at neurodivergent affirming conferences.
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Are eager to learn and help others.
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They are passionate about their child and how they're uniquely wired.
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There is an instant camaderie.
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Once kids stories start being shared.
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You notice that there's a community of people around these challenges that you can become a part of.
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One conversation leads to another and parents advocates, speech therapists, teachers.
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Are all collaborating.
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Strategies for developing strong IDPs or shared how to advocate to insurance companies when to stop over-servicing your child.
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And how to support your child socially.
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We're just a few of the conversations that happened around conference tables.
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It's a reminder that the world is bigger than we think.
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Tunnel vision is easy in our small corner of life and traveling to a conference helps to regain perspective.
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Another interesting reminder.
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Is that there are always more resources than we know.
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Going to a conference and just listening to sessions and impromptu conversations.
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Around the tables.
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We'll leave you full of information.
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Once a few people in a parents advocacy session.
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Found out that I was a professional advocate, a small line formed.
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I was able to talk with them about their child's unique situation at school, how the school is handling it and how they could respond.
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We were having informal assessment in IEP conversations over lunch.
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It felt good to help someone else and see that is truly meaningful to them.
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I was able to trade contact info.
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With another advocate that happens to live in the same Metro areas.
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I do.
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One fun thing about conferences is that people are usually looking to connect in network.
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They also want to meet people who are like them, or it could help them in some way.
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After a fluxing on how refreshing connecting with others about similar passions was.
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I realized we could also get more involved with local organizations that build community for individuals and families experiencing neurodivergence.
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This is especially good.
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If you aren't able to travel right now.
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Some churches now have special education ministries with events like respite nights for parents.
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Small community groups, monthly dinners, and other social opportunities.
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We all need a supportive community around us, especially when we are leading families with extra needs.
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If there aren't any support groups or opportunities.
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For neurodivergent learners in your area.
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Try looking for online communities.
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This journey can be isolating at times.
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And it can be completely different with more teammates by your side.
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My family and I tried this path alone for way too long.
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COVID hit when Luke was 20 months old and we had a newborn.
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We were physically cut off from our social network for Uh, until we could get them vaccinated.
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Time passed.
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And we started to resume a semblance of a normal life.
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But about a year after that.
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We realized that we hadn't had any help with our kids.
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Except for the occasional visit from Grammy and almost five years.
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We also threw another sweet baby into the mix.
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We had gone it alone.
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And this just took a toll on our mental health and our marriage.
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I can zoom out now and see how I would have done so much differently in hindsight.
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These experiences grew us, whether we wanted it to happen that way or not.
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Problems just seem to be piling up.
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Surrounding me at every turn.
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Once I decided to grow, instead of having to know why in the midst of this difficult season, I was able to start recharging and actually retaining my learning.
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I had to make mental space to recharge and learn.
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My mind was too crowded to take on anything else for over a year.
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But the shift happened when I chose to grow in this dark place.
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Rather than spend any more time wondering why it was happening.
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Once I made space for growth.
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I researched autism and ADHD.
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And started noticing how it impacted my family uniquely.
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I also submitted an application to speak.
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At the apraxia kids conference and was accepted.
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So this conference I just returned from, I was actually a speaker at.
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These are things I couldn't have imagined doing two years ago.
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But everyone around me was challenging me to grow.
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Public speaking has been my worst fear from as early as I can remember.
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And in this season of growth.
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I noticed that some things like advocating for our kids are too important not to talk about.
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Even though trying new things can scare us to death.
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When we look back.
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It reminds us that we can do hard things.
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I don't know the details of your situation.
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I can't imagine how difficult, exhausting and overwhelming your journey is.
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But I know that you love your kid.
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I know because you're listening to this podcast, trying to figure out how to advocate for their needs.
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As we wrap up.
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I hope you're able to reflect and think about ways to take breaks with the goal of recharging.
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Then I hope you have resources that are helpful for your own style of learning.
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Whether it be podcasts, books, courses, or conferences.
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When we are knowledgeable and equipped.
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We are more resilient.
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As we become more resilient.
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We are better leaders for our families.
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Being committed to personal growth will improve our quality of life and will ultimately be a huge benefit for our kids.
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I also encourage you to find a supportive community to walk with you through this challenging and beautiful season of parenthood.
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Until next time, my friends.
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Ash.
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Hey there, before you go.
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Please go on iTunes and leave me a review.
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It will help more parents become resourced and resilient advocates for their children.
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Also, if you feel overwhelmed and unfamiliar with what services are available for your child and what to ask for in an IEP meeting, then visit my website, sparkeducationadvocacy.
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org.
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If you are ready to become your child's best advocate in IEP meetings and in social life experiences, I provide parent coaching.
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And IEP representation, both virtually and in person.
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I will help you break down the special education system and IEP documents in a relatable way so it's less complicated and more manageable.
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Together, we will defeat the inner voices of guilt, overwhelm, and frustration.
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You will be equipped with the knowledge and communication skills necessary to hold school staff accountable for meeting our children's educational needs.
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I'll also share the key questions and phrases I use in IEP meetings to get things done.
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If you're ready to take your seat as your child's expert at the IEP table, go to my website, ClarkEducationAdvocacy.
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org, and fill out the contact form.