vivdunstan: Photo of some of my books (books)
Finally going through the Edinburgh Book Festival programme, and disappointed as the proportion of streamed talks diminishes even further for yet another year. Luckily I am finding some gems, including Robert Macfarlane and Hallie Rubenhold. But it is pretty poor representation on accessibility grounds.

I used to attend the Edinburgh Book Festival in person, though usually then only attending one or two talks. But those days are past, as my neurological disease progresses, and streaming that took off as Covid started was a huge help to housebound me. And now that’s in major decline.

P.S. Streaming tickets now bought, for the above two talks, plus those with VE Schwab and RF Kuang. I will probably watch them belatedly on catch-up in bed.
vivdunstan: Part of own photo taken in local university botanic gardens. Tree trunks rise atmospherically, throwing shadows from the sun on the ground. (Default)
I often deal with imposter syndrome in my academic work. Not least as my progressive neurological illness affects me more and more. But going into the weekend feeling confident about things I'm working on. And excited for the next stages. A very encouraging state of affairs considering everything!
vivdunstan: Photo of me from Melrose Grammar School plus NHS thanks (nhs)
Could happily have done without one of my appalling choking fits while eating at dinner. They're becoming more frequent. Especially likely when I'm extra confused or overloaded cognitively. But can happen at any time. I'll have to mention them to the rheumatologist next time I speak to her, along with the extremely frequent now forgetfulness and losing things. My neurological disease is progressing more and more with time. But since I've lived with it for 30 years, and we managed to slow it down a lot, I'm grateful to be coping as well as I am.
vivdunstan: Photo of some of my books (books)
Setting up a new Kindle Paperwhite to replace my rapidly dying old one. Main priority is change font and layout to be friendly for my progressive neuro illness challenged brain. I can read small print in eye tests, but for extended reading find large print vastly better. Big before/after difference!

Brain damage from my progressive neuro disease is why I struggle so much with normal print books now. When I did my PhD on historic Scottish reading habits I was phenomenally envious of many readers I studied and the books they read! Empathised with those who no longer could through age or disability.

vivdunstan: Arms of King James V of Scotland with a unicorn among thistles. Above the unicorn is the blue and white saltire flag, below the unicorn the red and gold lion rampant (scotland)
Back to Gaelic study, and restarting from the beginning with Moray Watson's books. Hoping to get a bit more of the vocabulary to stick this time, despite my severe memory problems from my progressive neurological disease! Which really really doesn't help, and eg stops me using things like Duolingo. Also conversational teaching doesn't suit me. On plus much grammar has stuck over the years. I'm surprised how much has stuck. But I need to make a more conscious effort re learning new vocabulary. And increasingly so as my neurological disease progresses. I love Gaelic and its sounds. And was given a Gaelic middle name at birth. Will persevere!
vivdunstan: Photo from our wedding in Langholm (wedding)
Another 3-card past/present/future spread, using the Urban Crow oracle deck. And musings on how these might relate to my current circumstances.

Gifts / Commitment / Play. Generally the guidebook for the cards suggests viewing them non literally, more symbolic/metaphorically. But in this case I'm just going to go for the literal approach.

It's my birthday imminently, and I've already started getting some treats. Today I got an almost birthday present for self, that I would have asked for as a present, but it was selling out so quickly on a limited print run, so I ordered it anyway. It's a book about Commodore 64 SID music composer Rob Hubbard, famed for legendary 1980s British computer music such as "Monty on the Run". There are still some copies left to buy, but it is selling well, and won't be reprinted.

Looking simply at the Commitment card I'm reminded of our upcoming 30th wedding anniversary. I have been extremely lucky with my choice of husband, and despite my ill health it's been a happy 30 years together. It hardly seems any time, certainly not that long! To be fair I still feel 21! But we will be remembering the day 30 years ago in September when we eloped, aged 22 and 23.

And Play, well I need to still make an effort to have fun. I am severely disabled from my progressive neurological disease, and largely bedbound now. Happy working on academic research projects and journal papers. But I need to have fun too. That's important.

vivdunstan: (lord of the rings)
I'm continuing my reread of The Fellowship of the Ring. And the party have just got through Moria. But I was struggling hugely to visualise in my mind the different rooms and levels that the party were going through, especially later on in their time in Moria. But I can remember a time when I could visualise them clearly. For many years. So this seems to be something I've lost since, or can't do now anyway. It's not that I'm not remembering the Peter Jackson movie version. But my image of the journey through Moria was memorably different from the movie I saw in 2001. I remember clearly having "thoughts" about the film's depiction of Moria, and how different it was from how I imagined it looked ever since I'd started reading the book for the first time as a young child. But now I can't really visualise any geography at all as I read.

Relatively recently I tried an aphantasia online test. And scored highly. Which would fit with my struggles to visualise things in my mind now. Including faces. Even very close family! But I'm now wondering after this LOTR rereading experience if it's something that I've developed more in recent years. Perhaps as a result of my progressive neurological illness.

When I was young I could visualise things, and draw from images in my mind. However when my neurological illness started in 1994 at age 22 I quickly noticed my ability to think abstractly diminishing. Rather a big problem for a computer science PhD student needing to program. I quickly lost the ability to program effectively in lots of languages. Though at the time I just coped as best as I could. It's more distressing looking back.

So yup, I wonder if visualisation is another loss with time, perhaps due to my long term illness. It's partly also why I dreaded designing cover art for my latest IFComp game. But hey, got there!

Curiouser and curiouser anyway. I am enjoying my LOTR reread despite this. Next up Lothlorien.
vivdunstan: Part of own photo taken in local university botanic gardens. Tree trunks rise atmospherically, throwing shadows from the sun on the ground. (Default)
I'm trying to remember to make time for this each week. To randomly draw a simple past/present/future 3-card spread of the Urban Crow oracle cards which I got recently. And find very easy to work with/interpret.

As usual, I'm using them as a tool to reflect on my situation and circumstances. And think about where I am and what I want to do. I am not using them in a predictive kind of way.

Here is today's spread. With thoughts/comments after the picture.



The middle card, Freedom, was lovely to see. I am currently newly in a better patch in between my recurring rollercoaster of post Covid vaccine neurological autoimmune disease flares. I've had these flares 9 times now, after every Covid vaccine (I get, and need, a lot of Covid vaccines because I am severely immunosuppressed). Each time I am even more ill for up to 3 months, with phenomenally increased sedation, headaches, arm and leg loss of control, and increased bladder incontinence. Many people wouldn't put up with this. But I'm not willing to sacrifice my much needed Covid vaccine protection. And I know I am generating good antibodies from each one.

So I'm in a better patch, for the next couple of months. After that I will get my 10th Covid vaccine, and be iller again for another 3 months. I will just cope. Plus my neurological disease is still progressing, and leaves me severely disabled, even in the better patches. But that progression is slow. And that's partly why I'm still here 30 years into living with this illness!

So yes, this is a time of relative freedom for me, and I want to make the most of it. Maybe get more things done, including the academic journal papers and research projects I am working on sporadically. And maybe get out more with Martin, to have fun.

The left card, reflecting the past, is Anomaly, which can be a problem, or something out of the ordinary, or other interpretations. It's making me think of my latest Covid vaccine flare more than my long-term neurological disease. A devastating neurological flare which has run from early May to early August. And it does tie in with Freedom.

The rightmost card, reflecting looking ahead, is Caching. Which again fits nicely with where I am. I want, in this short better patch, to make new valuable memories, and get things done I can look back on in future. So I want to make the most of this time, in a way I can look back on happily when I'm much iller again.

An interesting draw anyway, and some nice things to think about.

Meanwhile re Freedom, today is the start of the Glasgow Worldcon, and I have digital streaming access thanks to my attending ticket. I won't be watching much live, but hope to see one talk later today. And catch up on even more in the coming weeks and months. I also have Oxonmoot to look forward to in a few weeks. Again with a digital ticket. And ditto for the Edinburgh Book Festival. Streaming has been transformational for me.
vivdunstan: Photo of me from Melrose Grammar School plus NHS thanks (nhs)
So phenomenally sedated at the moment - this has been going on for many weeks in the latest bout, but recurring for many years, if not decades. It's like I've taken a strong tranquilliser. And as if there's a curtain shutting down in my brain. I finally struggle up for dinner, very sleepy, then back to bed after. Thank goodness I don't have much to do! I do have a game to finish off for IFComp in the next few weeks. But that is final polishing. I started coding early for very good reason ... But yup, could do without this.

And yes, we know why this happens to me, with my progressive neurological disease and also recurring post Covid vaccine neuro flares. Throwing more treatment at it doesn't seem to help. It's just where I am, and it's getting worse. But hey, lucky to be here after 30 years of this. Just don't want to sleep all the time ...
vivdunstan: Photo of some of my books (books)
Compared to last year's 60 books finished reading this year has not got off to a good start. We're approaching the end of January, and I've just finished my second book of the year. However I anticipated problems, as my reading slumped dramatically in late 2023 after Covid vaccine number 8 and yet another long neurological illness flare. Plus there is ongoing disease progression. So I set my 2024 Goodreads reading goal as just 25 books. I wonder if I will make it!

So far I've finished illustrated poem Wenceslas by Carol Ann Duffy, which was nice, especially the illustrations, but unbalanced in retelling the traditional Christmas carol story. And today I finished The Children of Hurin by JRR Tolkien, collecting the various strands of their story in a single version. That was um something. I don't think I will reread it, but glad that I did read it if just once. Even if I skipped the Silmarillion-esque intro. Rating 3/5. Ditto for the poem.
vivdunstan: Photo of me from Melrose Grammar School plus NHS thanks (nhs)
This year marks 10 years since I had a summer of gruelling chemotherapy infusions in Ninewells Hospital. I finally demanded the strongest treatment that my consultant had ruled out for the previous 14 years for various reasons, and he agreed. I’ll be sharing some memories of that time in the coming year. It stabilised my life-threatening neurological condition, allowing me to lower my daily drug cocktail. But my disease is still progressing a decade on, but more slowly than it would have done without that treatment. I’d have that chemotherapy treatment again without hesitation if I needed it a second time. But I am glad it is behind me.

Profile

vivdunstan: Part of own photo taken in local university botanic gardens. Tree trunks rise atmospherically, throwing shadows from the sun on the ground. (Default)
vivdunstan

July 2025

S M T W T F S
   1 234 5
6789101112
13141516171819
20212223242526
2728293031  

Syndicate

RSS Atom

Most Popular Tags

Style Credit

Expand Cut Tags

No cut tags
Page generated Jul. 6th, 2025 05:32 am
Powered by Dreamwidth Studios