Video of a Partial Seizure // close-up of eyes

This is a partial seizure Raelynn had a couple days before Christmas. Skip ahead to 01:48 if you just want to see it.

But keep watching to hear about Raelynn’s roller coaster adventure the days leading up to Christmas!


Partial seizures are also called focal seizures. They happen in one part of the brain.

Raelynn has been having more of these kinds of seizures lately. As you can see, they’re a lot different from her tonic clonic seizures. Tonic clonic seizures are very loud and convulsive, while partial seizures are basically silent. Her partial seizures are also often much shorter in duration than her tonic clonic seizures. While her tonic clonic seizures are usually between three and five minutes long, her partial seizures can often just be a few seconds long. So by the time we notice her having one, and get out a phone to record, she’s often already done having it. So it’s pretty rare that we’re able to record one. But Abby was able to this partial seizure because it was quite a bit longer than her normal ones.

Sometimes taking care of a child like Raelynn is a roller coaster ride. We were able to avoid a hospital stay this Christmas, but I can remember many other holidays when we couldn’t. But that’s ok! We’ve learned to always be flexible and no matter where we are, or how Raelynn is doing, to always have hope.

Visit Raelynn’s website to learn even more!

👇 AND PLEASE SUBSCRIBE if you find this content helpful.…

The links below show a few seizures Raelynn has had throughout the years:

▶️ 17 months old:
▶️ 18 months old:
▶️ 21 months old:
▶️ 2 years old:
▶️ Almost 3 years old:
▶️ 6 years old:
▶️ 8 years old:

A few playlists you may find helpful:
⏩ Seizures:…
⏩ Tobii Dynavox:…
⏩ Assistive Equipment:…
⏩ Medical Procedures:…
⏩ Living Life with Disabilities:…


Raelynn has epileptic encephalopathy, global developmental delay, cerebral palsy, cortical vision impairment, and I could go on and on. In fact, I’ll go on a little more. Raelynn is quadriplegic. She has a gastro-jejunal (GJ) tube through which she “eats” all of her food. She has a vagus nerve stimulator (vns), and is currently getting intravenous immunoglobulin (ivig) treatments to hopefully help with her seizures. She regularly wears a shaker vest, uses a nebulizer, and a cough assist machine to help her breath better, especially when she seems extra susceptible to aspirating on her oral secretions.

Raelynn’s been to the doctor more times than the rest of our family combined!

In this whole situation, if we were looking for hope in our circumstances, we honestly wouldn’t find much. Raelynn will probably always be in a wheelchair. She’ll probably always be fed via a food pump. She’ll probably never talk. And she has virtually no chance of getting better.

I can’t tell you how many times people have told me, “God can heal her.” I’ve actually come to find it a little funny when people say that (and I’m a pastor!). I know that God CAN heal her, and I know that God will heal her in eternity, but the point of life is not that we wouldn’t have difficult circumstances.

God is using Raelynn exactly as she is right now. I see how much I’m a better person because of Raelynn. I see the ways God has changed my family, the things He’s taught us, the people He’s put us in connection with, all because of Raelynn’s problems. When I see how much God uses her disabilities, I see that God takes the bad things, the hard things, the hopeless circumstances of our lives and brings beauty, goodness, and hope from them all.

That’s what this channel’s about.

We post videos of Raelynn’s life, seizures, and other disabilities to this channel three days a week (Monday, Wednesday, Friday).

If this sounds like something you could benefit from, please consider subscribing! Your subscription will help us keep making videos of Raelynn’s life and assistive technologies! ❤️…

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