SPD vs. A Pandemic World

I thought it would be fun to write a post from the perspective of living in this pandemic world as someone who has SPD. If you have some of your own perspective on how the pandemic has affected you or someone you know with SPD, I’d love to chat about it! Either drop a comment on this post or feel free to email me.

**First, let me establish that I DO NOT have the coronavirus.**

**Second, I wanted to personally thank all of the first responders, healthcare workers and other essential workers (yes, I’m also talking to YOU teachers, nannies, grocery store employees, ETC…). You all are ROCKSTARS and our world wouldn’t function without you. **


Wash Wash Wash Your Hands

For me personally, washing my hands (and showers whenever I actually take one hahaha) is one of my least favorite daily activities haha. I choose to do it only when its absolutely necessary. So, the moment my hubby told me about what was happening with Covid-19 and that we are going to have to be extra careful, I was like, “NOOOOOOO that means I have to wash my hands more!” I know it doesn’t sound trivial, but seriously…washing my hands sucks.

⤅When I get to work, I wash my hands.

⤅When I come back inside from playing with my nanny kids, I wash my hands.

⤅When I go to the restroom, I wash my hands (obviously).

⤅When I get in my car after being in the store or gas station, I wash my hands (with sanitizer).

⤅When I get home from work, I wash my hands.

That’s a TON of washing hands! Eekers! :p

Soap and hand sanitizer feel so slimy and soft…yuck to the yuck! Not only does the soap hurt, but the entire process hurts as well. The water, the towel to dry off and the feeling afterwards all cause different feelings of pain. I can’t stand the way my hands feel after being washed, mainly because I don’t like the soft feeling that is left over. Even a few minutes after, I can still feel the pain from the water and the towel.

🙊 Speak No Evil 🙊

The one thing I knew when it came to my mask of choice is that I wanted to make sure unicorns were on it. Before I had this sweet, handmade mask (second pic), I decided to use my unicorn scarf. Might as well try to bring a little magic into people’s days right?

Thanks Stasia for my unicorn mask!

Yes, the pictures are full of squinty smiles, but to be honest, wearing a mask is irritating and painful. I totally feel for the healthcare workers out there (especially those who have SPD) who have to wear masks all day…you guys really are having go through the ringer. I’m so lucky to not have to wear a mask at my job. (I’m a nanny for an amazing family.) When I go to the store, I try to get in and get out asap so I can take off the mask.

To describe the pain a little more- since the mask isn’t giving me any deep pressure (good thing cause I wouldn’t be able to breathe hahaha), I can feel the fabric rubbing across every inch of my skin like a burn or sting. After I take it off I have to rub my face to try to reset the nerves…it doesn’t fully help but it takes some of the pain away. My ears don’t really hurt except when I put the mask on and take it off because the straps don’t move once on.


**If you have any questions for me about other things that might be bothering me during this pandemic, please leave a comment and I’d be happy to respond! :D**


Some food for thought: I urge you to not jump to conclusions if you hear someone (at any age) complain about things bothering them or causing pain. Yes, a mask and washing your hands seem harmless, but to someone with SPD, they are causes for more pain. Let’s change our habits of saying, “Oh, that doesn’t hurt” or “How can that hurt” into encouragements, “I’m sorry it hurts” or “Is there anything I can do to help ease your pain?”

The Princess Chronicle vol. 6


Today’s chronicle is filled with some coolio stuff! I hope everyone is staying healthy and safe while the Covid-19 Pandemic is happening!

Make sure to check out my next post where I will talk about how this pandemic affects someone living with SPD.


Peanut Butter Podcast

What an adorable name for a podcast, eh?! My friend Stasia invited me to be a guest on her show! The best part is that it was specifically for me talk about SPD!

When I asked her how I should describe her podcast for my bloggers- this is what she said,

Stasia interviews neat people about neat things for the benefit of all mankind.

How magical is that?!

I’d love for you to not only check out the episode that I’m on, but also make sure to listen to the other episodes she’s done-it’ll be a blast!

OH! I almost forgot to mention that Stasia is actually the artist who designed two blog logos! She’s just a magical, creative bean isn’t she?

Thank you SO much Stasia for interviewing and letting me spread the awareness about SPD and thanks for always making me laugh. ❤


What You Missed Last Time

I found this fun, little test to see if I have SPD. 😀 I recorded my answers and included a link for YOU to go do it. Even if you don’t have SPD, you should still go and see if you learn something new about yourself. If you do take the test, I would love for you to share what you got by leaving a comment!


Journal Entry

Within the past year, it came to my attention that my sensory processing disorder DOES affect my mouth. Now I’m not a picky eater and textures don’t bother me when it comes to food, so I always wrote off my mouth for not being affected by SPD.

One day I was reading through this SPD Facebook group that I follow. A post caught my attention when someone mentioned that their was kid having a really difficult time with brushing their teeth. I felt like a light switch in my brain turned on immediately.

So here’s the thing…I HATE brushing my teeth. It’s not that it hurts necessarily, but I always gag and even sometimes puke (TMI? haha…sorry). I never knew why and have tried all sorts of different toothpastes, which never helped.

Seeing this post helped me realize that the issue with brushing my teeth is most likely a symptom of my SPD. Unfortunately, the knowledge doesn’t really take away my problem, but it has allowed me to have grace towards myself through the frustration. Sometimes knowledge can make a difference when you have a struggle.

I’m A List Person


If you’re new to the The REAL Princess & The Pea story, welcome! I hope you were able to learn something new, felt understood and I also hope you know that you aren’t alone.

I enjoy writing lists, so I thought for our newcomers, I’d write one to explain some of the reasons why I write this blog!

  • First and foremost, I don’t want ANYONE to ever feel like they are alone in this struggle of living with SPD. SPD is still not super well known to most people, so it can feel isolating. I want this blog to be a place where you can come and get advice, perspective and comfort.
  • To bring awareness to others about SPD.
  • I love to write and when I find time, I really enjoy telling my story with SPD. (It also helps to clear space in my brain for other things in my life like writing music!) 😀
  • To help educate others about SPD…and honestly I’m learning too!