Welcome.

I always thought of blogs as being narcissistic, business related, or as my sister's, a way of keeping in touch or memorializing.

But, by necessity, I am learning a lot about myself. I find I need to get my thoughts out, and it helps me to know that someone else will read them. So I have created this little space for myself, to express the things I have trouble saying (be it emotional or physical trouble), to share what I'm going through, and what I'm learning through it.

I absolutely welcome comments. It's nice to know how people relate to what I'm saying.
To send me a private message, please e-mail me: flylittlewordsfly@gmail.com
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Showing posts with label Acceptance and Awareness. Show all posts
Showing posts with label Acceptance and Awareness. Show all posts

Monday, 12 May 2014

This one is a real cold

About a month ago, I wrote about the cold symptoms that turned out not to be a cold at all, but an overstimulation of my immune system and about how it's really important that I learn to actually feel the oncoming of a cold, so I can make adjustments to my meds to avoid the escalation I experienced a couple of months ago (http://flylittlewordsfly.blogspot.ca/2014/04/the-cold-thats-not-cold.html).

Today I'm writing because I am awfully proud of myself, and I want to share that. Last week, I felt it. Before the big symptoms hit. When it was just the teensiest shift in how I was feeling - a touch more congestion, and the vaguest sensation of a tickle in my throat. I asked for support in making the decision not to start up my immune meds again, cancelled my appointments, and settled in to wait and see.

Today, I feel like absolute crap. My sinuses are clogged, my throat is ugh, my ears are popping, I'm sneezing and coughing... you know... the classic cold. All of which as you know makes my regular symptoms that much stronger. And now I'm waiting and seeing again, hoping that by not starting up my immune meds again, I will not go into that cycle of overstimulation that ends with me on the couch for two months.

It's not pleasant in my body right now. It sucks to be feeling this way again. And yet I'm less frightened than last time. Because I know. Or rather, because I knew. I sensed something brewing and was prepared for this. I can also sense that it's not depleting my energy reserves - not yet, anyway, and I'm confident I'll be able to tell if that starts to happen.

Friday, 25 April 2014

Distance, Effort and Mind

I had this thought the other day. I was sitting in the car, watching my son and his friend run to the lake, and as they got smaller, it struck me... things seem a lot farther than they used to. I lived in a house in University that was farther from the lake than I was at that moment, and I walked to the lake all the time. I walked all over campus. Heck, I used to walk to work when I lived downtown.

I wanted to go down to the lake. I wanted to sit on the bench at the boardwalk and take it in. And it was just too damn far. And that was ok, because if I'm honest with myself, it had already been a busy day and I had already done a fair bit of walking. And so I started thinking instead.

Friday, 11 April 2014

The Cold That's Not a Cold

I had a great phone session with my doctor in California. He suspects these colds I'm having are not all colds - that the symptoms are actually due to over-stimulation of my immune system due to a combination of the viruses that hit me and the meds I take to stimulate my immune system, and of course, also due to the nature of ME. Oh yeah, and to those pesky mycotoxins in my sinuses.

You see, part of what causes the fatigue and neuro-immune dysfunction has something to do with the production of cytokines being not quite right. There are already too many. So when I get sick and my body starts producing more, then there's a really big overload. Which leads to greater fatigue, brain fog, and more viral symptoms. Apparently this cytokine thing also affects cortisol? And together they make sleep really tough to come by. So add a layer of lack of sleep to all that. Oh yeah! And then when I take my immune-stimulating meds, even more cytokines get produced, and I end up a big gooey mess. I'm sure there's a lot more to it than that, but that's my understanding at the moment.

Saturday, 22 March 2014

The Chronic aspect of Chronic Illness

I hope one day I can get off this see-saw.

I've been re-reading some of my older entries, and been quite surprised at how long I've been off work, how little has changed, and at the same time how much has changed. Some really strong themes going on, still... and probably forever.

In any case, I've been re-reading them because I've had a really rough month. I wanted to check, and yes, it's true, I've been in and out of my parents house now for about 18 months. I've been unable to function independently for over a year, and I don't like it.

I'm turning 40 this year. This is not what I thought I'd be doing at 40. I'm in the process of grieving again. My optimism is still intact, for sure, in a more cautious and tempered way, though. The events of the last couple of years are most definitely taking their toll.

I'd love to know if it's a common experience... I'm sure there are stages that people go through as the years of being chronically ill pass... Maybe one day I will feel up to looking it up. It would help me to know that others who are as affected by their illness go through similar patterns.

Friday, 17 January 2014

Landing

It's been about a month now that I'm home. It still feels like a new experience. I'm most definitely still in a period of adjustment and reorientation, and I am more at peace with that than ever before.

My kitchen has yet to back up to the point I have to call in for reinforcements. A day at most of unwashed dishes. We've done the laundry - once (it's a good thing we both have plenty of underpants). We mopped the floor in the entryway once. I've had a few showers. My son is having regular showers. We're both sleeping well. We're both eating well. My fridge is not full of rotting food.