and this is why I don’t own blush

Oh hey. The thing is, I told myself if I started waiting tables again I’d schedule writing into my life in a structured way so that I don’t end up not writing for long chunks of time.

And then I didn’t do that, and here we are.

I was actually starting up a bit of an anxiety storm in myself over sleeping in today and not getting up early to write this post. However, I didn’t sleep well, I worked a busy night last night, I’m recovering from being sick, and I have work tonight. So I’m going to back off myself on this one.

Firstly, is anyone creeping on the saorza Instagram? I’m still slightly peeved that I can’t just be saorza thanks to that existing account, but that’s just me holding on to something I have no control over whatsoever. I was steadily posting on Instagram until I really started working, and then I fell off that horse, as well. But I’m going to do better.

I’m also going to get back on theme again, today! I keep veering off into mental health and anxiety/stress, etc. but I had a couple of kidney-related follows on the Insta and realized…maybe I should keep talking about the main issue at hand, here.

I’ve been relatively pain-free lately. I’m very, very, very grateful. After an ab workout Monday I was a bit tender in the left side, and I did have my UTI-like symptoms hit me hard about a week ago. However, there are some symptoms that haven’t acted up in a while, which is awesome.

My fatigue issues have been pretty chill. I think this is partially due to sleeping a bit later than I ever did before on a regular basis, thanks to a job that lets me do that.

My left arm hasn’t flared up in a while. That’s usually the sign that I’m about to be in pain up and down the left side of my body, but sometimes I’ll only feel weak and achey in the arm – which used to happen more frequently.

I also haven’t noticed a face rash in a bit. I am about to show you some VERY unflattering pictures from over the years of the recurring rash that led my doctor to believe that lupus could be a factor. I did have an elevated ANA last time I had a detailed blood panel, but the rheumatologist I last saw (and really like!) does not believe it’s lupus, and I trust her. BUT for the sake of sharing my weird ailments with you, here are some niiiiice pics.

These gorgeous pictures above were both taken in my college days…roughly around the spring of 2015. I know this because of what I’m wearing and also my horrifying eyebrows. I actually feel a little bad about subjecting you to these. BUT. What was up with that rash?! These were two different days, and the rash had been coming on and off for months before I started trying to record it. I wasn’t using any experimental skin care products or anything like that, and I never wear foundation. If anything, the rash would appear when the left side pain came out to play, or sometimes when I switched rooms with drastically different light or heat.

These two examples are from 2017. Again, so attractive. The one on the left captures the strange blank spot on my right cheek that the rash seemed to scoot around. Similar to the one on the right, where I had a yellowish mark in the middle of my left cheek. I remember that the picture on the right was after I stood up from laying on the floor, and the one on the left was after a shower. I wish you could see that I’m in a towel, not just hanging out naked. Not that there’s anything wrong with that.

I haven’t had such an intense-looking rash in a while, but I still get the red splash across my face from time to time, usually when I’m not feeling well. I never got any answers about why. Does anyone have any insight? Does this look familiar, or do the conditions sound like anything you’ve gone through? I’m curious and eager to find someone who might recognize what’s going on here! If it never comes back, all the better…but it’s been off and on for around 5 years so I’m anticipating she’ll be back the next time pain comes knocking.

In the meantime, I hope everyone is well and taking care of themselves this rainy May. I share lots of self-care related art and lists and whatnot on my Instagram, so if you feel that you’re lacking any of that, come visit me over there. 🙂 (@saorzanyc)

One thought on “and this is why I don’t own blush

  1. Wow, that rash is something! I can see why they suspected lupus.
    I’m so glad you haven’t had it in a long time and you have been doing so much better. I hope it continues. Continue to care for yourself first.
    I think this blog should be all about what you deal with, not just your trials with your kidney dysfunction, so please continue to discuss it all.
    I haven’t been on Instagram in quite a while, I’ll try and pop over there soon.
    xo

    Like

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