Special Needs Child Bedtime Routine // treatments, therapies, and meds

Raelynn has many disabilities, so this is a special needs child bedtime routine. Raelynn's bedtime routine includes her breathing treatments, some therapy, and of course her meds.

AFFILIATE LINKS

CBD: https://usamedicalshop.com/#a_aid=sunshine
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Fun stuff Raelynn uses:
✔️ Galaxy Projector: https://amzn.to/3yQyR8x
✔️ Towel Warmer: https://amzn.to/3uIQioa
✔️ Travel Pillow: https://amzn.to/3pbsgRv

Must-have medical gadgets/supplies:
✔️ Fingertip Pulse Ox: https://amzn.to/3i92oEr
✔️ Forehead Thermometer: https://amzn.to/2SIQlD3
✔️ Oil Sheets: https://amzn.to/3uGceAk

Helpful accessibility things:
✔️ Wheelchair hook: https://amzn.to/3fFFkve
✔️ Gooseneck Tablet Holder: https://amzn.to/2SPYOEF

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✔️ TubeBuddy: https://www.tubebuddy.com/sunshinebaby

Website: https://sunshinebaby.tv
Instagram: https://instagram.com/sunshinebaby_tv
Tiktok: http://tiktok.com/@sunshinebabytv
Subscribe: https://www.youtube.com/channel/UCZn7hETm79vEeavluBxGrnQ?sub_confirmation=1

00:00 Intro
00:25 Breathing Treatments
02:04 Meds & Food
05:40 Hand Splints
07:18 We're Not Perfect
07:41 Goodnight!
ABOUT RAELYNN'S YOUTUBE CHANNEL

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! ❤️
https://www.youtube.com/channel/UCZn7hETm79vEeavluBxGrnQ?sub_confirmation=1

#specialneeds #bedtime #routine

https://sunshinebaby.tv

Видео Special Needs Child Bedtime Routine // treatments, therapies, and meds канала SunshineBaby