On the other hand, I've had a couple pretty decent weeks M.E. wise, which is wonderful! Milder flu symptoms and less weakness. I've been doing a few outings per week, short stuff less than an hour. I've also been able to fit in a little art (printmaking).
Here's a photo of me and Tegan (I'm starting to show my age) from an outing about a week ago down the road to see the ice on Lake Superior. We walked out just a little, there were a LOT of people out ice fishing, but I could tell that it wouldn't be safe too much longer.
And of course I'm still doing my daily PhD writing and editing session each a.m. from 1/2 hour to 2 hours. Progress is slow.
And given the 6 week relapse I suffered this winter (and slow progress), we've applied for another medical leave, despite the fact that I've used up the four that are allowed. I very much doubt they'll give it to me. I have found the university very unaccommodating for the most part…while the professors have been great, the policies are discriminating.
Basically if you are ill to the point of being disabled (unable to work), I don't recommend doing something like this. I would quit today if I weren't so close. As well, if you are too ill to work, it's a lot of money and precious energy to spend with almost no outcome (I'm as ill as when I started thus won't be able to work when I'm done). Also, the time I've spent reading and writing could have gone toward healing and social, I have so little energy to go towards living life, and I've spent 6 years of it like this, alone with my books and paper, writing something maybe 3 people will ever read.
Anyways, these are the small details and frustrations of my daily life. With the little bit better health the last two weeks, though, I am coping emotionally better with the day to day, not just constantly wishing it would end. It's amazing how years of being ill can really weigh one's psyche down; also, how when my immune system crashes, usually so does my mood and vice versa. Also sun….its crazy, but my mood is always better on sunny days (like today).
I am waiting to hear back on my most recent WBC, to see if my immune system is showing a little bit of improvement since the relapse, it usually does.
So I'm reading a book called "A Tale for the Time Being". It's good, although I'm not completely wowed yet. However, I keep finding these little jewels in the narratives, and this one (below) especially hit me. It speaks to blogging. Blogging is such an interesting phenomenon. Why do I keep doing it? what need is it filling for me or anyone else? While in the past, it has connected me to people who face similar health challenges, I find myself reading other blogs less and less. Anyways, I thought this quote was pessimistic, but also insightful:
"It made me sad when I caught myself pretending that everybody out there in cyber-space cared about what I thought, when really nobody gives a shit. And when I multiplied that sad feeling by all the millions of people in their lonely little rooms, furiously writing and posting to their lonely little pages that nobody has time to read because they're all so busy writing and posting, it kind of broke my heart" (excerpt from "A Tale for the Time Being by Ruth Ozeki).
Lovely photos! I am glad to hear you've had some good moments recently, that is music to my ears! I have too, still my fair share of bad but I can't complain about that. I also did your poll in the sidebar, I'm interested to hear the results of that.
ReplyDeleteTake care
Hayley-Eszti
I read A Tale for the Time Being this winter too. I enjoyed it. An interesting story and very introspective characters!
ReplyDeleteHi UpNorth, Love your photos, thanks. I read several blogs but yours is the only ME related one I've frequently put in a comment. So I would imagine that there are many out there that also read your blog regularly and never comment. I especially like your blog because you get down to the nitty gritty of living this M,E. life and how hard it is to include any of the normal living stuff of life. I was one of the cemmentators that encouraged you to continue on with your PhD, but I can understand with this recent post what you are up against, using up so much of your good time on your research. Still, you've come so far I just hope you are able to continue. I've lived almost 20 years with this disease and like you mentioned find that I'm entering a new relationship with it. I used to visualize myself healthy, travelling about, seeing friends - given up on that ! Tho sometimes I get into a day dreamy mood and imagine myself in Rome or Paris, ha ha. I looked up the book your reading, go it on my Kindle. I don't have OI, I do have severe neuropathy. Well, sure hope that this slight lift to your, relatively speaking, decent weeks have continued. from Leah
ReplyDeletedid I mess that up, hope it went thru, from Leah
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