I’m trying to exercise some patience and be more receptive to change. Part of my therapy is trying to break out of old patterns and identify bad habits. I’m thinking a little extra proofreading is in order for this post as this is my first time using the voice feature to blog. I’m trying to get myself what break I can in my off time. Prednisone is helping with the swelling joints but now I’ve entered night time and the steroid is starting to wear off. Gentle little prickles of pain are becoming gradually more noticeable. I thought of taking the steroid in the afternoon or something but I have to sleep at some point, right?
This voice blogging is kind of weird but not terrible. Actually I rather like it now that I’m starting to get used to it. However punctuation and things like that are a little more Awkward. I’ll go through this later and see what I missed to be sure.
I’m in the process of wrangling myself a sooner appointment with my rheumatologist. I don’t believe the Arava which I’ve taken for several months is doing me any good. My guess is the next thing to try is methotrexate but my doctor may have something else strange up his sleeve. We shall see I guess. I’ll probably start getting some relief soon as I have another Humira shot on Friday. If it’s anything like what it was before I stopped using it I’ll be in good shape.
Work goes well but I’m worried about how long I’ll be able to stand up to the physical nature of my job. I know my inflammation will only get worse as the cold gets more intense. At least that’s how it happened last year. On the other hand I wasn’t on DMARDS last year.
Anyhow, gearing up for Christmas and immediately regretting jumping back to typing this post on my android. Thinking a bath with some Epsom salt is in order. I want off the prednisone but right now I’m thinking that I should keep it up until I get seen again. Pls Pray for Thom.
In spite of pain and stuff it’s been a wonderful day. My man got me strawberry pancakes this morning and the rest of the day was quite pleasant.
I have today off from work as well as tomorrow. This fortunately coincided perfectly with today being Humira day. I haven’t noticed much in the way of ill effects, outside of one thing. After the first round I woke up the following day feeling REALLY strange. I can’t really describe it beyond that.
I just got home from about a two and a half hour bus trek to acquire this week’s Humira Pen from the Rheumatologist’s fridge. Did my shot on the left side of my belly with no trouble. It did sting a bit, but that’s only noteworthy because generally speaking I barely feel it.
I’m feeling some definite relief from my current meds (Arava and Humira ). I’ve not needed prednisone since I was in Alaska. Since I started the injections I haven’t been taking ibuprofen at all which is great for me, one less thing stressing my liver. I’ve been watching the news about obamacare with some nervous agitation. My plan appears to be safe for now but my premium is probably going up. I’m glad my plan is as good as it is. It’s so worth it not having an HMO.
As I mentioned, I haven’t noticed any real issue with the Humira, though it could take a long time to really kick in. I dunno, I’m pretty resilient when it comes to putting up with medications and side effects as a general rule. A few meds have really rubbed me the wrong way but most I used without issue. I’m not really worried, as long as I stay vigilant with blood work I’m all good.
The thing that concerns me now is avoiding getting sick or infected. The drugs I take for RA are immune suppressants so there is an increased risk for fungal and or opportunistic infections. I’ve already gotten a flu shot and am going to ask my Doctor about the pneumonia vaccine. Last year I wasn’t on anything for RA and I got a respiratory infection that lasted six weeks and made me miss my Sister’s wedding.
Anyhow, not hurting too badly and enjoying life today. I’m not trying to be paranoid about getting sick, just being realistic and taking precautions.
Chance favors the prepared mind and all.