Friday, October 26, 2012

Popple-Ox



I noticed this morning that my hands are covered in little blisters. This isn’t really a good thing – they’re annoying, painful and itchy, but when I saw them I had a moment of reflective thankfulness. A few years ago I had these blisters constantly. They’d go through cycles of appearing, then popping and bleeding, then just as they were starting to clear, new ones would appear. I had a couple of years where I couldn’t make fists, because every time I did my knuckles would split open and bleed some more.

It’s been a while since I’ve had this problem. In the last few years, they’ve appeared a few times when I’ve had particularly bad systemic flares, but it’s been a long time since they’ve been an everyday problem. So much so that when I first felt them on my hand this morning, it took me a while to recognise what they were. I realised I haven’t had them once in the time since my Raynaud’s first appeared, as I couldn’t work out whether wearing gloves would be helpful or harmful to them (my hands were cold so I decided to risk it.)

I’m hoping this flare up will pass soon as I’m not enjoying my hands being itchy and gross, but I’m so thankful that I don’t deal with this everyday anymore, I can deal with it for a few days.

I just looked up the proper name for this rash as I couldn’t remember it: pompholyx. I was thinking something that sounded like Popple-Ox. I don't think I was that far off, but I'm not sure my dermatologist would agree!

Thanks for reading!
Little Miss Autoimmune

Monday, October 15, 2012

Better the Monster you know...



On Thursday, I had an appointment with my new Rheumatologist. The result? Apparently I now don’t have a diagnosis of lupus.

This was a bit of a surprise for me. It was quite confusing, as it almost seemed the doctor was implying that I’d diagnosed myself with it. I knew very well that I hadn’t, but I did start to doubt myself. Had I totally misunderstood what my previous doctor and nurse had been saying? Eventually she explained that yes, I had been told I had lupus, but that was based on some of my blood tests being positive, but others done later (which are more specific to SLE) came back negative. 

We went round in circles for a while, as I tried to understand what was going on. Basically, though I don’t have drug-induced lupus, which is curable, there is still a possiblity that one of my medications could be causing an ANA-type reaction, which would explain my symptoms and blood results without the lupus diagnosis. Well, it would explain them, if most of the symptoms hadn’t started years before first taking this (or in some cases any) medication. So after discussing this for a while, the doctor decided that actually I do meet quite a number of criteria for lupus, though still not enough for it to make a clear-cut diagnosis. She said they haven’t ruled out lupus, so essentially I don’t NOT have lupus, but we can’t call it lupus yet either.

I was quite upset when I left the office, but I wasn’t entirely sure why. Shouldn’t I be happy that I potentially don’t have a rather horrible disease? Well, happy might be pushing it. The name lupus doesn’t actually change anything. I have the same symptoms either way, and my treatment options (or lack of) are the same. So why was I so upset?

I kept going over one particular part of conversation in my head. For several years, I’ve had reoccurring symptoms where it seems like I have a urinary tract infection. Every time this happens, my lab tests come back abnormal but showing no infection. A couple of weeks ago this happened again, and the GP I saw said it was most likely down to the lupus. This didn’t really change anything, as it didn’t provide a solution, but it at least provided an explanation for symptoms that had been a mystery for years. I asked the rheumatologist about this, and she said “well, inflammation in the urinary tract could cause those symptoms and produce those lab results, and that is something you might expect to see in lupus, but we don’t want to call it lupus because then we might not investigate and miss something else.”

Something else.

For years, being sick with symptoms that didn’t have an explanation was kind of like having a dark shape in my room at night. Maybe, when the light was turned on, it would be nothing. Or maybe it would be a monster. At the end of last year, when I was told I had lupus it was like the light had been turned on, and there was indeed a monster in the room. But at least now I could see it, and if I could see it then I could control it and maybe it wasn’t such a big monster as I’d originally thought.

I realised the reason I was so upset after this appointment was I felt like the light had been turned out again. It was back to being just a shape in the room, which was maybe a monster I knew, or maybe “something else.” “Something else” really is quite frightening. “Something else” potentially puts more than one monster in my room. “Something else” makes me feel powerless especially when it doesn’t really feel like anyone is investigating to see what it might be.

Despite the anxiety that this produces in me, I don’t really think there is something else. I’m fairly certain that what I have is lupus, even if a clear-cut diagnosis can’t be made. So for the moment, the other monster in my room probably is just made up of fear, and anxiety monsters can be pretty damned scary if you let them.

I’m going to do my best not to let this one be.

Thanks for reading
Little Miss Autoimmune.