Category: Sarah

Illuminated Fragments (by )

Currently it is the Gloucester History Festival - happening very differently to previous year in the restrictions on numbers and the shift to more outside pre booked things and mostly online talks and interactive virtual tours. Even if I'd been well enough there is no way Cuddly Science/History could have done it's normal activities with sand pit digs and cloth puppets 0.o

I am seeing past events popping up on Facebook memories and they are awesome but do you know what? So is this year... there is a festival that had to completely start from scratch and reorganise some great stuff and they managed it and on their big year too! 10yrs of the Festival and 25yrs for the Heritage Open Days!

And it's not like I am completely devoid of involvement - back in the spring an art and archaeology project that I was very excited to be a part of obviously had to go on hold but now the exhibition is there for anyone who wanders over to see! They are asking people to pre book free tickets and wear face masks when in the building as well as doing track and trace.

It's at Llanthony Secunda Priory and called Illuminated Fragments. There were 15 of us lead by Jacqui Grange of Creative Solutions with access to the archaeological finds from the area thanks to Cotswold Archaeology, and tutorials on calligraphy as well as researching the history and stories of the area.

I really enjoyed the parts of it I managed to get to and the work produced is truly spectacular - it is only up until the 14th of Sept 2020. Including the Heritage Open Day.

So Many Things (by )

There is so much I want to write, some of it I have been sketching out but mainly I have been unable - this year has been wiped out by illness and I lost weeks to seizures and fevers and now have graves disease - I posted on Facebook and social media when I felt up to it - maybe I'll get around to rounding all that stuff up and maybe I won't. Once I started to feel better and started doing things again it rapidly became apparent that I was intact not well and resulted in an ambulance ride - to cut a long story short my immune system has gotten over excited and attacked among other things my thyroid leaving me with Greaves Disease, eye issues including five years premature ageing and so much medicine I rattle when I walk from all the pills - I am a prescription junky and it is going to take one or two years of treatment. Also I may have become diabetic in the same process.

I have wibbly wobbly nails showing in a similar way of tree rings when and just how sick I was - in times of extreme stress the amount of nail grown differs drastically. My skin is cracking and dry from all the hand washing - the kids have gone back too school for the first time in half a year but we are all just waiting for it to all be closed down again as we watch infection rates rise knowing that antibodies only last for about 3 months with cold type viruses which Carona is. I am not sure I can survive what I went through again but all we can do is make sure each of us is well rested and well fed - and yes that is at the exclusion of homework.

I am also feeling ashamed as I am simultaneously relieved to not be trying to educate or entertain the kids and missing them and worried that this time it will be one of them that comes down just so very sick - and that's before I add in my 70+ mum's health.

Adaption has been the key to my existence these last few months as I was well enough to really feel the bite of what had happened. I have new glasses and I can now see enough to do some work but my vision is still awful and I think that is it now - there is nothing that can make it better - I am worried about how long its taking to sort some of the medical stuff out as I don't want to make eye sight stuff even worse. My bones hurt and feel... fragile, my muscles cramp and it feels like someone is actively trying to push my eyes out, my heart hearts as in a physical pain. Time is seesawing around me being fast and slow at the same time and little blood fleck spots keep erupting on my skin as I've had some sort of reaction to one of the medicines and so on.

Once again I have almost died, but this time the world stopped with me, this time there are so many many others ill and dying and the drs just do not have capacity and yet they have gone out of their way to treat me and to see if Alaric could help others with his blood and to get physio to Jean and give me advice on Mary. Al's hair now sparkles with silver and is as thin as mine in places - oh yeah my hair is falling out - A; is just thinning/going bald but probably due to the stress - they say they had to watch me being carted off to hospital once again unsure of what the hell was going to happen.

I feel that last chance of having a child is vanishing over the hill not helped by people repeatedly telling me I am old enough for menopause and even suggesting that is what is wrong with me - Graves disease is often misdiagnosed as menopause as it can and in my case did shut down periods.

We have had financial ups and downs with jobs coming and going and furlough and redundancy and people not paying when they should and events being canceled and then all the jobs and offers of help until we find ourselves with just a few weeks in-between the lowest financial ebb and a peak so good we have bought a thing we have wanted for our entire adult lives and never managed - once we had enough before but we went to South Africa to see family and that was always going to be the important thing to do and it is awesome that we could do that and we have a house and we are so lucky but there was a point in all of this were once again we had an empty fridge and it was friends dropping food parcels... and thoughts of this financial security or mirage of it float and haunt us but we are in a good position that many of my friends can only dream of and that makes me angry and bizarrely feel guilty. Soon hopefully we can give back again - we should have done that before buying our shiny but I know how it goes - if we waited there would have been a crisis and then the money would have had to be spent on that.... Al has a fantastic job but we maybe using it to pay for health care and yay we can do that but grrr and what if of those who can't?

I spent money I didn't have on stuff from my dead friends Etsy shop for multiple reasons and all the stuff I ordered in Feb and March to make our garden good arrived in dribs and drabs and the garden now has nice things on beds of rubble including the table that arrived the last week of August but was still somehow worth it because I know not how many suns I will get to feel on my skin - especially as it decided to be allergic to sunlight for the beginning of the summer - and another friend died and I have now lost track of how much death there has been and how is still with us and I get scared to ask how people I've not seen for a while are.

Everything seems on a knife edge and I have friends and family on the front lines dealing with the general public trying to make people well and keep us all safe and worry about them.

So many things but were do I even begin?

I begin here and hope I can continue to tell of the muddle in thoughts and medicines and art and science and sunsets I love.

Protected: Llanthony Remains (by )

This content is password protected. To view it please enter your password below:

Moving Story Telling Cafe (by )

Over the last year or so I have been working very hard with two amazing story tellers to bring story telling to Gloucester and finally we have arrived - our first story telling session is on Thursday 21st November 2019 at The Cafe Rene - this was the first pub I ever went in around here back before we even moved to Gloucestershire. The pub has some amazing history including a well inside and is next to a glorious grave yard and ancient ruins. It is a fantastic venue.

This is the first of four nights though we hope to get it running on a permanent basis.

Gloucester Moving Story Cafe

Aural traditions such as singing and story telling are the basis of our modern literature and novel reading not to mention the theatre and even film. The tradition has held on by it's finger tips but now it is time for it to be once more!

Come and share with us 🙂

It is for grown ups only and sadly due to the antiquity of the building it is not wheel chair accessible though the other venues are.

Body Blob (by )

Again issue with doing lots of performance stuff is all the photos of me being fat - they are me doing things and I will myself use them but you know when good photographers still don't manage to make you look good! Well that... I am well aware that I have gained weight what with the miscarriages and just not caring with Dad's and others deaths.

We've been monitoring my weight weekly and everything I've tried results in 12 and a half stone :/ except that time I ate all the crap and I mean all of it from BBQ through to giant ice creams and I went down to 12 and 1/4 stone - the next week was period time complete with swollen painful legs and that was 12 and 3/4 stone but was then back to 12 and 1/2 stone the following week (it took about four days to loose the swollen feet and legs - something I have never before had outside of pregnancy and even then only really Jean's when I had all the blood clot issues).

The nurse for thyroid, diabetes and dietary stuff no longer exists as her role got axed at the drs - and I need to loose weight - I am literally carrying around half a me extra! As I should be 8 stone but the healthiest I've ever been was 10 stone when I was an outdoors pursuits instructor.

It's the mobility that really does me in with the weight or rather the lack of it and I am sick of it. Yesterday the venue we were at had no real food so I bought a chocolate bar but then felt so guilty about it I didn't eat it and instead ended up eating a really late dinner at home where I ate more cheesey type stuff than was sensible as I was REALLY hungry by this point.

I think I need to just follow what I did before with the nurse but am doing more work stuff now and I was so light headed, Passy outy and feeling like I was going to throw up that I just don't see how I can do that and be working at the same time :/

I have gamified my walking with Pokemon go and feel that if I can just shift some weight then my pelvis will improve and I'll be able to loose the crutch and maybe even go back to park runs or something - I have bought a load of medals ready to complete various challenges to help motivate me - they start with walking and ramp up so we shall see!

Please don't suggest the dieting groups like slimming world and weight watchers as they make me want to punch something and keep punching if I am completely honest! They are pretty much my definition of hell and I don't mean the food part of it - it's just a social dynamic thing - I have friends and family they worked really well for but they are not for me.

WordPress Themes

Creative Commons Attribution-NonCommercial-ShareAlike 2.0 UK: England & Wales
Creative Commons Attribution-NonCommercial-ShareAlike 2.0 UK: England & Wales