hello, i am lyric, though you may call me bubba/papa/papa lyric/mister.
i am 21 and use he/him pronouns
this is an exclusively SFW caregiver blog, dedicated to the care of SFW regressors, whether they be age regressors/dreamers, pet regressors/dreamers, syskids or permakids!
my ask box is open permanently, though i do take frequent breaks from answering requests
please do not DM me if you are under 18, though you are free to interact and send asks
I BLOCK NSFW ACCOUNTS UPON INTERACTION, DO NOT INTERACT WITH ME IF YOU ARE A K!NK FOCUSED BLOG
i interact from @tinybardblue , which is my regression blog
below the cut you will find a list of rules for my requests, and what fandoms/media i will do
RULES FOR REQUESTS
- i am more likely to accept your request if you say ‘please’ and ‘thank you’. kindness costs nothing
- i will NOT do anything from nsfw-centric media, though i will do requests from media that happens to have NSFW parts/scenes
- if you are unsure whether i take requests from your chosen media, don’t be afraid to ask! the worst i can say is no :]
- you may claim an anon tag if you so wish!
FANDOMS I DO
- the witcher
- hannibal
- dungeons and dragons
- baldur’s gate 3
- general sfw concepts
- all sfw media, even if i am unfamiliar (i will not do headcanons for media i am unfamiliar with)
a flag for caregivers who are nerds or nerds who are caregivers. whether
the nerd label is self assigned and a source of pride or was forced onto one
who is reclaiming the term any nerd caregiver can use! meant to match my
nerdre flag here.
this flag is f2u! if using please credit kate somewhere on the post, in the tags,
or on your profile. reposting is fine but please give credits and do not claim as
your own ! public use and repost without credit is not allowed. please feel free
to tag kate in edits╱creations; she'd love to see!
idk if this is controversial but as a caregiver I feel like we are not allowed to be silly or stupid nearly enough, yes we take on a very important caretaker role and that is something to take seriously, but just like any parenting there are many different ways to do it!
I don’t give my kids rules unless they explicitly ask for it and even then, they don’t have to be taken so seriously, if my kiddo stays up past their bedtime they WILL get a long drawn out explanation of WHY it isn’t a good idea. however they will never be taught they are being bad. and shoot, if they wanna go out for ice cream to have that talk? who am I to say no.
I feel like we have to start treating littles with some more respect and like they’re learning (cause they are!) instead of taking everything so seriously, have some fun with the dynamic and role you take for your little, because at the end of the day this is a coping mechanism and not something that should be used as a power trip.
idk, saw something that made me a little sad because for me parenting is fun, not a chore
a flag for autistic caregivers╱caregivers who are autistic. perhap's one's
autism affects or informs one's carerspace, though any autistic caregiver
can use and interpret as desired!
this flag is f2u! if using please credit Us somewhere on the post, in the tags,
or on your profile. please ask before reposting! use without credit and repost
without permission is not allowed. please feel free to tag Us in edits╱creatio
⸺ns; We'd love to see!
For caregivers who live with disabilities, but still pour love, safety, and care into their littles. Their way of caregiving may look different — maybe slower, maybe with adaptations, maybe with boundaries — but it is no less strong, gentle, or valid.
A disabled caregiver shows that care doesn’t come from perfection, but from presence. Whether through words, cuddles, or creative adjustments, they give comfort in their own unique way. Disability doesn’t diminish their role — it enriches it, proving that love adapts, endures, and thrives.
🧸This identity can include neurodivergent regressors, system littles, or anyone who doesn’t experience regression in a linear or “standard” way
🖤 Reblogs > likes
🔁 Credit appreciated but not required
P.S: This isn't meant to offend or romanticise or put all disabled people into a box. I know that living with a disability is very hard and isn't always what the media makes it out to be, so I am deeply sorry if I did offend anyone.
I know I can’t always be there, and I know I must worry you sometimes. But I promise taking care of you is one of the highlights of my day. You’re a good kid. Thank you for your kindness and patience. I hope we can still have fun together, regardless of what happens.
❤️🩹 - 🍼🧸🍼 - 🍼🧸🍼 - 🍼🧸🍼 - ❤️🩹
Headcanons Below 🖍️
⭐️ Good days and Bad days will always look different, but regardless they’ll do their best to keep things cozy and fun.
⭐️ Bring them their cane when it’s too far away.
⭐️ Going to the doctors office together, you get to sit in the waiting room playing with toys, while they go back for their check up.
⭐️ On good days, they’ll take you to the movies. Something fun for the both of you, but low energy enough to not risk a flare up. We can bring our blankets and plushies, and even sneak in some snacks, shhhh-
⭐️ However, when they’re not feeling good, and they can’t do much. You’re always welcome to spend time in their room: We can color, watch a movie, listen to an audiobook, or have naptime. Just keep things low energy for their sake.
⭐️ Letting you decorate their pill organizer and cane. They got stickers and you have your creativity.
⭐️ Reminding them to make their medicine and fill their water bottle, and then asking you to do the same.
⭐️ Helping them in the kitchen, cooking comfort foods, and eating together to make sure we’ve both eaten. Even if it’s something simple.
⭐️ Helping them restock their bedside cart with essentials, and getting a snack of your choice in return. And maybe a gold star.
⭐️ Setting up a cozy chair next to their bed for you. So they can read to you, watching shows with you, and just hold your hand and listen to you talk about anything.
⭐️ But on very bad days, when you can’t visit, you make get well soon cards and drawing. Bringing them over when you can. And seeing their face light up knowing they were being thought of.
⭐️ Having window time, just cracking the window for fresh air and listening to nature together. A small moment, but a very important one.
⭐️ Holding their hand wherever you go to keep them steady in your own way.
⭐️ Walking slower than normal to make things easier for them. It just means you get to spend more time together.
⭐️ On bad days, just laying around and watching the celling projector together. Maybe some music in the background.
⭐️ Though after too much inside time, they take you on a little adventure, maybe the mall, the grocery store, or just anywhere to feel less isolated. Even for a few minutes.
⭐️ But the most important thing, get well soon hugs. With your cozy hugs, just maybe it’ll make things a little easier.
“You made this for me? Oh my goodness, I- I don’t know what to say. Thank you, thank you so much.”
“I’ll be okay, you go play, I’ll be here if you need me.”
“Remember to drink your water okay? Do you need any snacks?”
“It’s just a check up, I’ll be out soon.”
“Thank you for being here bubba, i really appreciate it.”
Hey sweetheart, it’s getting close to bedtime now. You don’t have to be productive anymore and you don’t have to hold everything together. I’m here with you, and this part of the day is just about getting you cozy and safe.
Let’s slow things down together. Go ahead and change one small thing in your space to make it softer. We can dim a lamp, turn off the big light, or switch on a little night light. It does not need to be dark if that feels scary, just gentle enough to tell your body it is okay to rest.
Take a few sips of water or a warm drink for me. That’s it, nice and easy. You’re doing a good job taking care of yourself.
If it helps, pick something comforting to hold. Bring your stuffie, blanket, or pillow close. I’ve got you, and it’s okay to let your body relax into that comfort.
Let’s do a small check in. You do not need big words. Are you tired, or are you overwhelmed? If you’re overwhelmed, you can sigh or cry a little here with me. If you’re tired, we’ll tuck you in gently.
Now we do our bedtime basics together. Let’s brush your teeth slowly, then change into your cozy pajamas. No rushing. Each step helps your body understand that it is safe to sleep.
Go ahead and lay down now. I’m right here, smoothing your hair and making sure you’re comfortable. You did enough today, and tomorrow can wait. If your thoughts get loud, we’ll bring them back down together by noticing the warmth of your blankets, the quiet of the room, and your steady breathing.
Sleepy time is coming now, little one. You are safe and cared for. Miss Blair is very proud of you for winding down tonight 🌙🤍
