Mask options

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toy

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We have a 5 year old foster son who has severe autism. He is developmentally 18 months. He is also nonverbal. we want to take him to Disney before he goes back home. Due to some trauma (held down and force fed) and his autism, he freaks out over a mask. Any suggestions for different types of masks or tips for getting him to wear one? We aren’t trying to get around him wearing one. He loves Mickey Mouse and may never get this opportunity again.
 
I would check on Etsy. There are masks that have the adjustable ear straps that are thinner, which are much more comfortable. It is a struggle in that situation because you can't just "get over" that feeling of being held down. I hope he is able to cope and find a mask that works for him so that he can enjoy WDW.
 
I have relatives/Friends who were foster care providers. Thank you for providing an important service. I assume you have contacted the agency and gotten clearance for him to go with you. If not, that would be a first step.

As for masks, the best advice is to have a bunch of different types to try. Both different materials and different styles - some people like the ones with pleats, others like the more formed types. Some prefer the disposable ‘surgical’ types pleated masks. Be aware of smells - some have an odor and some of the cloth ones hold the odor of laundry detergent after washing. Using scent free products and airing out help.
Have the masks available for him to see, touch and smell. Also wearing a mask yourself to model.

This link to Harvard Health has a great list of hints.
Also, people have posted they got suggestions from professionals like OT or teachers working with their child.

My youngest daughter is not autistic, but does have many sensory issues. We thought the Disney ones made from soft material similar to T-shirt material would be great, but she did not like those at all. Some people find those are their child’s favorite masks, so you never know.
We found some others from Kohls and some I made myself that she really likes and wears without any issue.

Some people don’t like the feeling of the straps and find ‘ear savers’ help with the felling on their ears. These pictures show some things people found helpful.
Buttons sewn onto a favorite cap to ‘receive‘ the ear straps.

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Ear saver that goes behind the neck. I’ve seen crocheted or knitted ones and some made of cloth. I don’t know if anyone on Etsy is selling them right now, but I have seen them there.

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There are masks that have "cages" build inside (or you can get inserts) that make the mask stick out a bit around the mouth and nose. I did a search on Amazon for "mask frames for cloth masks" and got a lot of options. Perhaps that would make the masks feel less suffocating?

My older daughter is a foster mom, and we had discussed taking her 3 foster kids to Disney. Sadly, they got placed with a "kinship" person before we could make that happen. OP, I hope you get to make some wonderful memories (or just have a great time) for your foster child.
 
Thank you all so much for the suggestions. I will look for the "cage" versions. I think that will help with the feeling of suffocation. Since we just decided this weekend to go, I will talk to the school about trying some out on him. He has out patient OT and in school OT. I will talk to both.
 
My son who has SPD will willingly wear disposable paper ones but the only fabric ones he finds comfortable are the Bloch brand. They are the softest ones I've ever found for sure.

Also, there are mask lanyards to keep them from getting lost and some of those have a toggle so you can tighten it around the back of the head a bit so that it's held on by that instead of his ears.

I recognize that neither of those is anywhere near sufficing, but maybe all of the above together.
 
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