If You Are New to the Autism World, These 3 Resources Helped Me
It’s been five months since my youngest son, Julian, was diagnosed with autism. The doctor’s decision didn’t come as much of a surprise. Julian has several autistic characteristics, including being nonverbal.
Even though I wasn’t shocked to hear the diagnosis, I still felt a rush of panic throughout my body. So many thoughts ran through my mind in that instant. How am I going to fix this? Should I have been more aggressive with his early intervention plan? What do I do now?
The doctor offered little help in terms of an action plan for Julian. He gave me a few pamphlets and tried to send me on my way. Luckily, in anticipation of the results, I already had a few questions prepared. But it wasn’t enough. After the appointment, I felt more lost than ever.
I didn’t know where to start getting help for my little guy. The doctor gave me a list of ABA therapy providers, so I began making calls. I wasted three days talking to different agencies. I was beyond frustrated.
By chance, someone in one of my mommy-Facebook groups directed me to a local organization that could help. This mom, who lives across the country, saved me a great deal of time and frustration. So in an effort to pay it forward, I want to let other moms know what organizations have helped me along my journey.
1. The Autism Society of America (ASA).
My Facebook-mom-friend directed me to the ASA. I looked up my local chapter online. (You can find your local chapter here). They offered a free “Autism 101” course for parents new to the world of autism.
I learned the “ins and outs” of autism in my area. She gave me helpful information, resources and insider advice. I left her office with a plan — a roadmap. I was no longer lost. I felt empowered.
2. Julian’s ABA provider.
Once Julian started ABA services, a team from the agency came out to meet with me. They have their own wealth of knowledge about private insurances and Medicaid. They were able to navigate through roadblocks and connect me with an organization that would help me if I needed it.
3. Medicaid advocacy groups.
These organizations help parents acquire services for their little ones. Individual states have their own groups. Local ASA chapters can provide information about groups in your state. In Virginia, I’ve been working with Moms in Motion. I remember hearing about them from the ASA coordinator, but I never thought I’d need them…until Julian was denied for a service I requested.
Our ABA therapist put me in contact with a MiM service facilitator. I feel like I have my own lawyer when I talk to my MiM rep. He not only helps me find resources I never knew were there, he has no problem fighting the battles I’m not comfortable fighting.
I’m still a newcomer to the autism community, but I feel much more knowledgable than I did a few months ago. My journey so far has certainly been bumpier than described here, but these three resources helped me tremendously.
What organizations helped you? Where did you find the most help?
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