The Princess Chronicle vol. 2

Welcome to The Princess Chronicle!


Thanks to everyone who messaged me about how they loved the format of my little newspaper-style post; I think it definitely helps break up the flow from those longer blog posts. If you have any ideas of what else I could add to The Princess Chronicle, drop a comment or message me!


Bi-Weekly Journal Entry

Positive: The hunky and I went camping this past weekend at Chain O Lakes near the Wisconsin border. It was so fun, relaxing and invigorating. My SPD didn’t flare up too bad either, so that made it even better. I made sure to bring some compression socks, which helps my SPD in the evenings when it gets colder.

Real Talk: Now I love roughing it in a tent and sleeping on the ground, but the whole Princess and The Pea thing is legit. I can feel every rock, pebble and bump in the ground. Thankfully I have to take medicine to sleep, because I know I would’ve been up all night feeling the “pea” under my sleeping bag. I love to camp, so it’s totally worth it.


The vast majority of health professionals just want to help, so describing your challenges as accurately as possible is really the best approach. Plus, advocating for yourself is important…

-Some great advice from the Love, Your Brain blog

What You Missed Last Week

My hunky, Jon, took time to answer some questions about what it’s like to live with someone who has SPD. He did such a great job and it’s been really cool to see the responses to this. It’s also been neat to hear how his post has already helped others with their relationships. If you missed it, go check it out and if there is another question you’d like answered, make sure to comment on the post so we can do another round!


What To Look Forward To

Next week, I’ll be talking about how hard it is to rate my pain when people inquire about it (especially doctors). I sure am glad that I’m not Pinocchio, because sometimes I have to lie about my pain in order to really have them diagnose the problem…hmmm interesting eh? Make sure to check back next week for more!

If you aren’t a blog person, head over to Twitter and follow me there! I will post little blips from the blog, inspiring quotes, and other fun things.


The Princess Chronicle vol. 1

Welcome to The Princess Chronicle!


Every other week, I will be doing a newsletter-style of post. It will be a fun post filled with lots of goodies: quotes from my readings about SPD, journal entries about my current week, a recap of the previous week’s post, a quick write up about the upcoming week’s post, and who knows what else will get rotated in. I wanted to keep the momentum going with the blog, but then not overwhelm you with long blog posts about sensitive topics. Here’s what I’m thinking it will look like:


Bi-Weekly Journal Entry

Positive: This past weekend I was able to try a Huggaroo pouch, which I enjoyed immensely. (In the future, I will write a review about it with full details, but I just wanted to mention it as my positive for the week). The deep pressure that it provided, really helped me feel safe and pretty comfortable overall!

Real Talk: Our apartment gets extremely hot since we are on the top floor of an old, badly insulated house. So, we have to have the window units as well as two fans blowing to keep it comfortable. To be honest, I can’t stand the fans because it makes any hair on my body move and brings me an annoying pain. BUT, if we don’t have them on, then I’m sweating, which I hate even more. **ouch**


If we feel overwhelmed, our nervous systems drive us to defend against overstimulation and preserve the self.

Too Loud, Too Bright, Too Fast, Too Tight by Sharon Heller

What You Missed Last Week

I answered some of the main questions that I get after people find out that I have SPD. A takeaway from the post that I want to highlight is: “People tend to think that if someone does something that’s against “social norms” that it’s ok to immediately judge them instead of asking the WHY question and putting forth effort to try to understand.


What To Look Forward To

Next week’s post is going to be a really great one! My hunky, Jon, agreed to answering some questions about what it’s like to live with someone who has SPD. If you have a question you’d like answered by Jon, drop a comment below or feel free to shoot me an email!

If you aren’t a blog person, head over to Twitter and follow me there, where I will post little blips of the blog.