Freedom?

So apparently we’re out of lockdown and most restrictions disappear on the 19th, or two weeks today. In the same press conference, the Government predicted that cases will rise to about 50,000 per day by the end of the month. I think this is completely bonkers.

But what I’m most concerned about is the removal of the work from home guidance. Personally I like working from home, but, ignoring that, I’ve only had one vaccine dose so far. So I’m definitely not getting on a train before I’ve had two doses. And even after that… I just can’t see myself commuting regularly. Commuting is horrible and while there may exist pleasant offices, my employer’s is not one of them. My ‘office’ at home is a hundred times nicer than an open plan office.

I don’t know whether my employer will start pushing for me to come back to the office, but he was starting to talk about it when we did salary review a few weeks ago.

I re-arranged my ‘office’ over the weekend so I feel ready to start interviewing again. I’ve been getting inundated by recruiters lately, so I went back through the last few days’ email. I found and replied to six that looked potentially promising.

Phsyio

The physio trip was interesting. He spent a lot of time poking my ankles and said he was confused. Apparently, when I’m standing up normally, I tend quite strongly towards supination (underpronation). He said that usually when people are like this, their ankles lack the mobility to overpronate so that’s not their issue. But with me, the movement is there, and I have a strong callous on the inside of my big toe which suggests I am overpronating. He seemed to think it was a bit unusual.

He did all the poking and pressing based diagnostic tests for a neuroma, but couldn’t get any of them to be positive. This matches my experience with the podiatrist years ago – he did all the tests, they were negative, and then goes “well, I still think you have a neuroma”. The physio was less sure. It’s not really that important unless someone is proposing cutting into me, though maybe at some point I should go to the GP and see if I can get some imaging done on it.

Anyway, the outcome is that he wants me to 1) Stretch my calves a lot, because he thought they were resisting even at a neutral foot angle. He said the lack of movement in the calf could be compensated for by my metatarsals and my ankle (i.e. pronation). And 2) get some insoles to support my foot more. He put me on a pair of insoles and seemed to think that everything aligned better when I was stood. I was a bit worried he was going to try to sell me some ridiculously expensive insoles, but he actually just gave me the name of some and said “you can buy these online for about £10”. So I have.

I’m still getting numbness though. Even after having a few very easy weeks, which in previous flareups was always enough to settle it down.