Okay, first things first…who the heck has been praying for my patience? ‘Fess up! Whoever you are, I ❤ you and appreciate your kindness, but you can stop now. Please.
This has been a busy, chaotic, stress filled couple of weeks. So once again, I found myself neglecting my blog. This upsets me deeply, as I made a promise to myself when I started this, that I would keep up with it. I wasn’t going to toss it to the side like so many other projects I’ve started. I have a tendency to just shut down when I feel overwhelmed, then the guilt and other negative thoughts start to creep in, which makes me shut down more. When depression starts banging on the door, I don’t feel much like communicating with anyone. I’ll be honest; I’ve hardly looked at the WordPress app icon, let alone open it these last two weeks. The funny thing is, that’s probably when I should have been on the most. To connect with others on here, express the chaos that’s in my head, and read something that’s enjoyable to me, has been a tremendous help the last seven months. If I haven’t already mentioned, I’m a procrastinator at heart. This is something I want to change also. Starting now, I am going to post something every day. It may just be a picture or a couple of sentences, some days. I don’t want to bombard you with my posts, but I feel that making myself post something each day will get me into a better habit and my blog will never feel neglected again.
An update on the lab work I had done and the spinal cord stimulation trial:
My bone density scan hasn’t really changed since my last one, four years ago. It still shows osteopenia. I am thankful that it has not progressed to osteoporosis. All of my bloodwork came back normal. The 24 hour urine collection I had to do, could not be completed due to not having enough sample. I can’t help that I didn’t have to pee much that day, sheesh. So now I have to redo that test. Oh yes, the ever so fun, tinkle into a plastic ‘toilet hat’ and then pour it into a collection jug, every time for 24 hours. Grossed out, yet? Who comes up with these tests anyway?
I had my one time visit with the psych doctor for the stimulation trial (nice guy). He explained that the insurance company requires this visit because the trial and permanent placement is a very expensive procedure and they want to make sure that the pain doctor, psychologist and you all feel this is the right option. After hearing that and answering all the paper and oral questions, I had a different interpretation of why they require the visit. The procedure is expensive and insurance wants to make sure that they are not going to fork out all this money, if you are just going to turn around and take your life. I know that sounds grim, but that’s the way my mind processed the information, sorry.
Now that I’ve had that visit, the PA at the pain clinic has submitted a request for the trial. Of course, it has to be approved by insurance before I can schedule. More waiting. In the meantime, she wrote me another prescription for hydrocodone, which I’ve been having to take daily. My eleven year old doesn’t like this and “lectures” me, because apparently they learned the dangers of opioid use, at school. I’m all for him being educated in the matter, and I hope he never ever needs them, but spare me the talk. I wouldn’t take them if I didn’t need them.
Are you tired of my babbling yet? I really just wanted to say that I’m still here, sorry I’ve been slacking, and thanks for sticking with me. I hope you all are doing well. Until tomorrow, friends.