Below is an IR image of 3 beehives. The two to the left are two Paynes polystyrene hives, and the one on the right is a wooden hive. You can see the difference in surface temperature and hence heat loss.
These are the same beehives but from the front. Note that there is a relatively high temperature in the entrance of each polystyrene hive
A closer look at a polystyrene hive showing heat leakage from the gap between the brood box and the super, then a larger gap to the roof.
Monday, 1st March 2021. Lockdown. I paid for Elysium last Friday and have been told that she is ours.
Elysium is her current name, but neither of us really like it, so we are trying to decide on a new name. This may take us a while.
We organised a full survey and a river trial. Essentially she is sound with a good 10mm base plate, 6mm hull and 3mm cabin. The engine is a Lombardini LDW903 20hp 3 cylinder diesel, and it not considered a great engine.
She has a rather odd layout inside. A nice shower with a grim loo leading into a kitchen, bed and a lounge. This will change. I like the idea of a bed at the bow.
The gas hob and oven will be removed. I don’t trust myself with gas on a boat, if there is a leak the gas will make its way to the bilge. We will have a meths cooker and a microwave. Not sure what to use the gas lockers for.
The plan is to get her ready to move in April/May from near to Heathrow back to the Fens and to a marina near to Newmarket. Its going to be an interesting summer.
Elysium is being craned out of the water on the 3rd of March to be cleaned and the hull blacked, then an engine service and cam belt change. The engine bay is in a poor state and needs a good clean. Craned back into the water at the end of March.
I was diagnosed in early 2020 with Rheumatoid Arthritis, specifically psoriatic arthritis. At the time, I was not convinced of the diagnosis but the symptoms have been getting a lot worse now in early 2021 so I am convinced.
‘Bone pain’ – a deep ache seemingly from deep inside my limbs. Shoulders, arms, hands, legs and feet. Level varying from 1 – 5 out of 10. Especially bad in the mornings and evenings. Finding a comfortable position to sleep involves lots of wriggling to finally find that position with no pain. Its great for a few minutes and then it starts again. It takes me ages to sleep.
Specific pain – it began at the rear of my heels, I could not lay on my back because of heel pain, but now it has moved to fingers and toes. Level up to 7 / 10
Fatigue, exhaustion. All I could do was to lay down, too exhausted to read, watch Netflix, listen to the radio. Too tired to sleep.
Brain-fog – inability to think straight, to get the right words out. Clumsy. Easily upset. Depression, hiding.
So far I’ve tried hydroxychloroquine which seemed to enhance the symptoms, methotrexate tablets which made me rather sick and now methotrexate injections that wipe me out for 2 days and another 2 to recover. However, after 3 days of just starting steroids a lot of the aches have gone – steroids are not a long term solution.
How will I know that the medication is working ? I’m currently having biweekly blood tests showing two inflammatory markers and liver function indications. Hopefully the inflammatory markers will lower before the liver damage becomes significant. Its all a bit of a balance.
And the prognosis ? Well I hope to find a medication that will successfully blunt my immune system so that it stops attacking my joints and I can get back to some sort of normal life. There are a number of RA medications to try yet, all I need to do is to find one that works.
As a beekeeper, you end up with a lot of brood frames which need replacing, wax scrapings and mappings from when processing honey. Melting these down by heating up with water will not remove the impurities such as propolis, dead bees and other waste. An easy way to both remove the wax and as a first stage filter would be to heat the frames or whatever in a black box sealed under glass.
This was an unused double glazed roof light, the back sealed with a piece of wood and the inside lined with aluminium painted black. The box was tilted to point at the sun, and the bottom edge was lined with aluminium foil to collect the wax.
The wax/tin foil mix was was then heated with water to melt it into a more convenient shape and filter it some more. One trick is to put the dirty wax into an old pair of tights and heat up, the was will liquify and escape to float on the surface and the debris will remain behind. This is great, but some debris float to contaminate the wax. Using the same principle of a cafetière, I make this press to keep the debris on the botton whilst the wax cools. The filter was cnc cut out of aluminium plate
Hopefully this week, we will finalise the purchase of Elysium. I have a medium term plan to convert her to hybrid power using a 48v motor as well as the Lombardini 20HP diesel engine.
Elysium ( her name might change ) currently has a 12v system configured as below ( circuit drawn with kicad ) :
This is all fairly standard. However, Elysium’s 12v system needs upgrading and I have plans to convert Elysium to a hybrid diesel electric drive and will need a 48v high capacity supply for this. So, the questions is – should I install a 12v system for the short term or a ( complicated ) 48v system for the long term ?
Below is the proposed solution. I like Victron kit. The engine’s existing 12v alternator charges the cranking battery and the 12v/240v inverter feed one mains input to the quatro, the other being from shore power/generator. This has the minor advantage for being able to charge the 48v battery bank to its full capacity ( 14.4 bulk charge ).
The disadvantages are the unnecessary complexity, especially creating the 12v for the fridge, bilge pumps and comms radios. The design feels unsatisfying. In order to charge the 12v battery bank, both the quatro and the 12v charger will need to be running, with the power loss that entails.
The next image is a slight modification where we add a fictitious 48v input 12v 3 stage battery charger, I’m not sure these exist.
Of course the upgraded 12v only system is easier, it will just need replacing if I move to 48v propulsion :
I’m writing this during the winter early in 2021, during a pandemic. There are a lot of reasons to feel down, but that is not quite the answer.
*** If you are feeling depressed, please seek professional medical help. I’ve tried it and it works, eventually ***
I can think of a lot of reasons to be down
The expectation of friends, never being able to fulfil them
Feeling in pain for much of the time
Nausea and vomiting from migraines and RA medication
The impossibility of being in a job that I love, which happens to be killing me
Things I am avoiding doing
Worry about the future
Guilt about the past
Current political and social trends
Well I could go on, but all the above things don’t add up to depression for me, they create stress, frustration and often the energy to get on top of them but not depression.
My experience of depression is when everything, even small things seem insurmountable, there is no end in sight where things might improve, there is no point in trying and there is no hope.
I’m not feeling like that as I write this, but I have been there and I have friends who are there at the moment. I am hovering on the edge though. I can feel myself :
catastrophising – when you take any small irritation to the logical end, then further into fear and hate, and sometimes beyond. This is a bad place. It almost seems fun at the time, it really is not, and I am now very good at stopping myself
avoidance – not answering emails, phone calls. Hiding from friends and family because conversations will not go well.
Doom scrolling – read twitter, Facebook, BBC news. Find threads that you know will make you sad, but gleefully read all the bad stuff from trolls
finding things to buy on eBay or Amazon that you’ll probably never use
loop listening you music that takes you down
This is a great place to consider what would help to bring me back out. How can I help someone who is already down there.
I know this sounds a bit wishy-washy, but it works for me. I have a thought experiment. I’ve been given £100,000 and I have to spend it on other people. Which friends need it most ? What would they really like but cannot afford ?
Try to remember a time when you were really happy. Who you were with, what you were doing, see if these memories make you smile, or even cry.
If you feel brave, then think of the worse case scenario. If you job is *so* terrible, then just leave. Would that be so much worse ? Can you afford it ? Have a quick look at recruitment sites
Be with friends. Quiet friends who will give you space to talk. Friends who have been there and have survived
Avoid people who are consistently negative, they are dangerous when you are feeling down
I have had migraines on and off since my late 20s, my mother and sister both have migraines too. I wanted to blog a little about my migraine treatments over the last 30 years, the successes and the frustrations and what seems to be coming next. I am worried that once this is on the internet, a prospective employer would never hire me after reading this. So far, I have managed to do my job because have been blessed with understanding Employers and some really exceptional line managers.
Lets go back to the late 1980s. Working hard, two young children, taking turns with my partner to go clubbing in London. I noticed that my hangovers seemed to be getting worse, so that even a taste of alcohol would start off a day of debilitating headaches with sickness. It took me a while to realise these were migraines
Giving up alcohol seemed to help, but there is a huge list of possible migraine triggers.
Chocolate – gave up for 4 months, no effect
Caffeine in general – gave up for 3 months, no effect
dairy – vegan for a month, same migraines
citrus fruit – I’m pretty sure that orange juice invokes migraines
Migraine vs Headache
I get headaches as well as migraines. Sometimes a headache will morph into a migraine over time.
So what’s the difference ? For me, I classify a headache as pain without any other migraine effects, see below. The pain of a headache can be more than a migraine but somehow easier to cope with.
I used to worry that my migraines were not really bad. For instance with a low level migraine, I could still work, socialise like a real human being and laugh. I could find distraction in a low level migraine, usually involving concentration and appear ok, albeit a bit tired and grumpy. The downside was that concentration often leads to worse migraine outcomes.
I then found this paintable, and it made so much sense
So, with a headache you get
Whereas with a migraine I get
Intense sensitivity to smells
Awful taste in my mouth ( this is my biggest migraine indicator )
lack of concentration
emotionally clumsy and sensitive
Its usually better for me to be away from people. I can still work, but am horrible to be with.
Next blog post will be about the medications I have tried to help with migraines, but for now I’ll quickly give my experience of Candesarten
I was very sceptical about yet another daily drug to try in order to help my migraine symptoms, but as I had to stop sumatriptan injections I really had no choice. I started 8 mg around Christmas 2017 with little improvement in my migraines, then went up to 12mg in January. My migraines just stopped. No migraines for over a year but then they came back. It was a very nice year..
I first used slackware Linux in the early 90s, possibly, and have used Linux quite extensively since then.
The init/service management has changed a lot over that time, from editing /etc/rc.d now to systemd. I have struggled to keep up. So here is a terse set of commands to help me when I come to add or manage services on a Linux box that uses systemd
List all the systemd units ( no need to run as root )
Because I have a supressed immune system ( Methotrexate etc ), I was given the Astrazeneca Vaccine first injection today on the 12th of February 2021. The outside temperature was -1 C.
I parked at the Newmarket Racing Centre, where the Rookery Medical Practice have set up their local Vaccination Hub.
The Volunteers and Staff were wonderful. I was directed to a table to gel my hands, another table to confirm my name and then to a station to be injected. The injection was painless. Either the skill of the medics has improved, the needles have become finer or my sensitivity to pain is minimal. As I had driven to the vaccination, I was asked to wait for 15 minutes in the cafe before heading home. I was prepared with a warm cloak.
So, back to the staff and volunteers. They were working in a building with lots of ventilation, windows and doors fully open as it should be. The cafe seemed to be providing as much coffee as they could drink, there was donated chocolate and the cafe provided cups of hot water just so that the volunteers and staff could get the feeling back into their hands.
It was almost painless to use, much less painful that the sumatriptan injectors for migraines that I used to use. I did feel odd afterwards and was glad that I was in bed, the next day, Tuesday was nauseous and Wednesday was the usual migraine and generalised pain ( 4-6/10 ). Better by Friday I hope.
This is a 15mg injection, this should start to have an impact on my inflammatory markers ( ESR and CRP ) soon, but I have to keep an eye on liver breakdown protein to make sure that my liver does not take too much damage ( it can regenerate ? ). My Rheumatologist will increase the methotrexate injection amount as necessary. Blood tests every 2 weeks.