Feeling like shit today. Woke up after sleeping 10-11 hours, ate breakfast, and then went to take a nap for another couple of hours. So, why am I so exhausted and feeling like I got run over by a steamroller?
Well, yesterday my husband was driving home from work when a tire fell off his car. I had to go pick him up and once I got there, we had to wait for the tow truck to come get the broken down car. It was supposed to be about an hour before the tow truck arrived, instead it was almost three hours. Three hours of sitting in the cold (we did turn on the heat in my car occasionally, but didn’t want to run it the entire time we were waiting). Three hours of sitting in a position that is not good for my back, neck, and joints. Three hours of my joints stiffening due to the cold and being cramped in the car.
I knew today I would feel rough after all that and expected my CFS/ME and Ehlers Danlos to flare up. As usual, I was correct, but I wish I wasn’t. Those who don’t have chronic illness and chronic pain have no idea how easy it is for normal, annoying life events to set us back for days. I think it is something you have to experience to truly understand.
I’m feeling rough tonight, maybe because last night I went to a little Christmas-themed park and got really cold, which often tends to aggravate my CFS, Fibromyalgia, and Ehlers Danlos joint issues. I had a great time though and wanted to share a few fun pics of the night.
Here is me getting cozy with the Gingerbread Man:
Who doesn’t love a big fire pit when it’s cold out?
Here is some crazy guy climbing the giant Christmas tree (I’m guessing he wasn’t supposed to be doing that):
Is it just me, or are these trees a bit spooky?
Pretty lights on the water:
I want to begin this post by sharing a horrible dream I had last night. I was sitting in row G of a live outdoor show (my dreams are pretty specific sometimes), when someone behind me threw up all over my head. It was disgusting! I still remember the smell and feel of the vomit as it trickled down my face and hair. Ick! By the way, how do you “smell” things in a dream? I don’t know, but I sure did!
Ok, now that I got that off my chest, on to the main topic of this post. I am frustrated with doctors. Why? Because time and time again, I have had to fight to get testing that I feel is important, because many doctors tend to think I am just being a hypochondriac or overly anxious when I tell them I suspect a particular diagnosis.
However, time and time again, I have been proven RIGHT when I finally got the testing. C Diff, MRSA, medication allergies, asthma, CFS, fibromyalgia, costochondritis, pancreatitis, Aspergers, bipolar…all of these are conditions I highly suspected long before I actually got diagnosed, and yet, I had to fight to even get them checked out because doctors thought I was just being paranoid.
The most recent testing I am fighting for is Ehlers Danlos (EDS). I meet the major and most of the minor criteria for the condition, but have been fighting to even get a referral for testing. EDS is often comorbid with high-functioning autism, so that is what first made me interested in the condition. I am positive I score at least 6 or 7 out of 9 on the Beighton Score (higher on the Brighton Score).
I guess I can sum up this post in one sentence: Why is it so damn hard to get a simple test done???
Hi everyone! First off, I want to say that I changed the theme (appearance) of my blog slightly. I don’t know if you all will notice or not, especially if you read most of my posts on WordPress’s reader function, but for those who actually visit my blog address, I hope you like the changes. I thought it was a bit more visually appealing, especially for sharing art and poetry, which I like to do.
Yesterday was the first day since my wisdom tooth surgery I was able to get out and have some fun. We didn’t do anything major, just went out to eat (still having to eat soft foods, so we opted for pasta), and did some Halloween shopping at Goodwill, where I decided to try on a couple “spooky” accessories:
It was fun just playing around and being goofy after being sick at home for so long. The surgery pain is much better, although I’m pretty sure that this whole ordeal has brought on a flare-up of TMJ (a jaw joint disorder), which I have had issues with in the past. It still hurts to open my mouth very wide, talk much, chew anything, or smile big.