All week we had been watching the weather in the UK – the “Beast from the East” causing chaos, with drivers stranded, airports shut down, villages cut off…but all the time, the little north west corner of the British Isles seemed to miss the worst of the weather. Then Storm Emma started romping up the west side of the UK…but veered over to Ireland just before reaching the top of Wales.
We had to get up early, at 5.00 am to drive over to Lyon, but I’d actually woken at 2.30 and not got back to sleep. I was actually much perkier than I’d imagined I’d be. We set out to Lyon airport hoping that the plane would not be cancelled. It wasn’t even delayed!!
Wearing a double surgical mask and latex gloves, to protect from infection – as these days were the days when my white blood cell count would be at its lowest, and I would be most vulnerable to infection – I cut a slightly pathetic picture. We comandeered a wheelchair at the airport and Mr FD pushed me through. I’m very glad, as it was quite a trek to get to the correct terminal. We went through security (surprisingly there was no queue at all) – I caused some problems as I explained about the stent for chemo, and they wanted to see proof of this. It was in my handbag, which had already gone through the scanner, so people were running aroud to fetch it. Then I had to be scanned with a hand held scanner rather than go through the walk-through scanner. It all took a bit longer than usual, but we had plenty of time. As I was in a wheelchair we were allowed through passport control ahead of others (huzzah!) and soon got settled on the plane. I plugged in my earphones and listened to a podcast for the flight. At Manchester we waited until everyone had left the plane, and then climbed the steps into the terminal building. As I entered the bhuilding I slipped on some very wet rubbery matting, and fell down: luckily I went quite slowly, and nothing was hurt, but the cabin crew and pilot who were just behind were very helpful and sympathetic. Also luckily, a wheelchair had been left at the top of the steps and we were encouraged to use it – which meant priority going through border control!! Although we’d been so slow there weren’t many people left waiting anyway. Then we took the time to organise a wheelchair for the return journey, at Manchester airport. Later on, Mr FD contacted Lyon to organise assistance at that end too.
Mum had said she’d pay for car hire, so we went andpicked up the car, then drove to mum’s, in Liverpool. We had lunch, and then my sister arrived from Leicester (not held up by snow at all), and my brother from Stokesley (near Middlesborough) Despite the fact there was still a lot of snow on the east side of the country, he had encountered no problems with the trains getting over. It was lovely seeing them all! We sat and chatted all afternoon, as I had to take it easy, while Wonderful Mr FD went on a mission to buy, and then put in place, a new toilet seat for mum. We had dinner and then, as I’d been awake so early, suddenly fatigue hit me. I was in bed and asleep byabout 9.30, I think!
On Friday evening, we had hastily arranged a meet-up for lunch with my nephew Conor (Judy’s son) and my niece Rose (Mike’s daughter), her husband and baby, over in Manchester. So after relaxing all morning, while everyone else went out shopping for a disabled friend of mum’s, or taking things to the tip, or buying supplies of logs, we all set out for lunch.
Here we are at Croma Pizza, passing Billy the Baby round the table – except not to my end, as I had to stay away from babies (hotbeds of infection, apparently. And Billy was quite snuffly).
There were some, let’s say less traditional pizzas on the menu, but I decided to have
Baked garlic mushrooms, served with (quite a lot of) rocket and a slice of olive bread
Then I chose another starter for a main course, which was a chorizo and Bury black pudding bruschetta, with a goats’ cheese and beetroot side salad. It was very nice.
and with it, I drank a delicious Manchester craft beer, called “Manchester Skyline”
For dessert I chose a “Banoffi Mess” – basically Eton Mess, but made with bananas, meringue, ginger biscuits and cream, with toffee sauce. It was a bit of a disappointment – masses of cream, big chunks of meringue, two slices of banana and one crumb of ginger biscuit. It let down what was an excellent meal, and although I did mention it to the waiter no more was said about it.
Afterwards, Judy and mum went back to Liverpool, while Mike, Mr FD and I went to spend the afternoon with Rose, David and Billy.
Billy in his bouncy chair
I spent some of the time “resting my eyes” but it was lovely just chatting with them, and watching them play with Billy. I kept my mask and gloves on for the whole time, to avoid any infection. And then Mike, Mr FD & I set off for the Bill Bailey comedy gig – this was our Christmas present for Mike. We arrived quite early, but that was fine. I sat in my seat and “powered down” – that is to say, pulled my hat and hood over my eyes and just sat quietly with my eyes closed, relaxing and conserving energy.
Here we are, after my powering down, waiting for the show to start.
It was a very good show – Bill Bailey is a slightly surreal comic, but we thoroughly enjoyed the show. Here is a review of the show from The GuardianOurs was a little different, set in Manchester rather than Southend, but – ad libs aside – it was basically the same. We got home at about 11.30, and we went straight to bed.
On Sunday morning, mum went to church, but I decided it wasn’t worth expending more “spoons” than necessary, considering we had the Elbow gig in the evening. ( The “spoon theory” is a disability metaphor and neologism used to explain the reduced amount of energy available for activities of daily living and productive tasks that may result from disability or chronic illness. … A person who runs out of spoons has no choice but to rest until their spoons are replenished. from Wikipedia) So Judy, Mike & I looked at an old photo album, discussing who the various members of our family were, as Mike has spent quite a lot of time researching our family tree. Unfortunately, while we have great grandparents who were Irish, this is not enough to entitle us to an Irish passport. Mr FD played about with mum’s computer, organising our boiarding passes and assistance at Lyon airport for the journey home.
After lunch, Mr FD and I set off for the hotel in Manchester that we’d booked for Sunday night, about a mile away from Manchester Arena, where the gig was being held. For some reason, the Sat Nav didn’t want to work in Manchester city centre and we couldn’t find the hotel anywhere. We were just about to start a blazing row when Mr FD said “Look!” and there it was, in front of us. Getting to it was another kettle of fish, due to one way systems and taxi/bus lanes, so in the end we parked the car in a carpark and walked! Again, I saved my spoons, while Mr FD went to try to get the car to the hotel – another difficult time, but he finally made it.
We took the tram to Victoria Station, which is next door to the Arena, and Mr FD went to the Box Office, while I sat with a coffee in the station buffet. We grabbed a bite to eat at Greggs (I had a cheese and onion pasty.) and then headed to the Arena. You may remember the terrorist attack that took place in Manchester in May last year. I had imagined it taking place in a large plaza area outside the Arena, but when I saw how narrow the walkway and foyer area are, it is no surprise that the effects were so devastating. There was good security – only ticket holders being allowed up to the walkway, and then passing through X-ray machines at the entrance to the Arena itself.
Again, we were early, so I “powered down” until the support act, John Grant, came on. And then – huzzah! – the main event. Which was excellent! (Review from the Manchester Evening News)
Mr FD’s photo from during “Mirrorball”
After the show we left by a fairly quiet exit, and were lucky enough to be able to hail a taxi straight away. It was a 5/10 minute drive back to the hotel. We thought about going to the bar for a drink, buit they’d stopped serving – and really, that was a good thing, as I was dropping. Even though I was buzzing!!
The next day, we had a full Northern breakfast – sausage, bacon, fried bread, fried potatoes, mushrooms, tomato, black pudding, baked beans, fried egg (which I’m not allowed to have) – plus trimmings (toast-and-marmalade, juice, coffee) and then made our way to the airport, pausing at Asda for a few last minute purchases of the DVD of “Death of Stalin”, some magazines, Zantac indigestion tablets & Tiger Balm (cheaper in the UK!)
Mr FD wheeled me through the airport, on the pre-booked wheelchair, which gave us Fast Track through security and a designated seating area in the very crowded departure lounge. I bought some huge slabs of chocolate (CDM!)
Then we were given a heads-up to the departure gate, so we were there before everyone else, and a very nice gentleman then wheeled me to the plane, so we were in our seats and luggage stowed before the usual scrum. At Lyon, we waited until everyone had got off, then were met by a man with a wheelchair, who wheeled me swiftly through the terminal. When we reached the back of the queue for border control, a quick Excusez-moi! and we were fast tracked through Passport Control. Pausing only to pick up the hold luggage, the man insisted on wheeling me right to the car in the car park. And we headed home, arriving at 6.30 pm.
Today I’m a little fatigued, but not too bad. I slept until about 8.30, when the nurse arrived for my weekly blood test. I wonder if it will show my white blood cells are down?
It was the most amazing weekend. Mr FD was a complete star throughout, looking after me, organising everything and allowing me to just rest and to enjoy myself. Even if I have caught an infection (and I was very careful, using hand sanitiser after every bathroom visit, in between bathroom visits, after touching stuff…Etc etc. Plus my double mask protection and latex gloves in crowds & public places) it was worth it!! It did me the most enormous amount of good.
And thank you all so much for your positive messages of support – they have been very much appreciated.