Monthly Archives: January 2017

My week in pictures

Monday

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First of two hospital visits, with a little bit of work afterwards.

Tuesday

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My phone is full of photos of books I want to read, I loved The Miniaturist.

Wednesday

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An innocent meeting with my PhD supervisor ended with me giving up my PhD as illness and time are not working in my favour. Still hurts.

Thursday

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No heating at work and for some reason I am not sweating like a pig.

Friday

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Post Friday Film night cuddles in mummy’s bed.

Saturday

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My mum and I survived Lulu’s 6th Birthday party.

Sunday

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Fairy lights behind my bed? What more could a girl ask for???

 

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But I can’t help falling in love with you

I love food, I mean everything about it. The history, the preparing, the reading, the eating. It is my passion, and often my reason for being, and it has been for as long as I can remember. I was making choux pastry at 10 years of age, churning my own butter at 11, at 13 I was making hand made filled chocolates, by 14 I had a subscription to US Gourmet magazine, at 16 I decided that I wanted to own my own catering company and live a life revolving around food for the rest of my life. And then life got in the way. A bit of family trauma, a bit of displacement, a violent boyfriend at uni and the diagnosis of coeliacs disease at a time when gluten free bread occasionally still came in tins!

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Picked up those lovely Goodhousekeeping ones on the left at church fete, complete bargain!

A catering company when I couldn’t taste anything seemed crazy so that idea faded away with sadness and instead I ended up working in the nightclub/bar/restaurant industry. It was hard work, fun, crazy, tiring and a complete buzz. My (ex) husband was extremely successful in his field of nightclubs – I think there is a still a plaque dedicated to him somewhere in the bowels of Fabric! – and we spent our spare time, and money, not clubbing but going to amazing restaurants and bars in the Uk and abroad. Foliage at the Mandarin Oriental remains the best food I have ever eaten, Chris Staines we love you!

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The ones I requested as Christmas gifts.

I started hosting dinner parties again. 14 people around a table that took up our whole living room in a our tiny basement flat in Notting Hill was not an uncommon event. 8 courses with a wine flight? I’m your gal. all prepared in a kitchen the size of a small wardrobe – the fridge lived in the hallway. Oh how I loved it. I have collected cookery books as long as  can remember, I never part with any of them, I read the recipes for pleasure, they relax me, always have. I was the odd 12 year old at the library borrowing cookery books and then taking them home to type out the recipes as I couldn’t afford to photo copy them and the internet didn’t exist then.

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Mixers and blenders and whisks, oh my

How could I let this passion slip away from me? I have no idea, it lights me up, makes me feel enthusiastic, it’s my measure of life. if I tire of cookery book I know I have tired of life and am feeling a bit depressed. It is my constant gauge of happiness, its amazing. And yet I never really ever write about it, why? I have no bloody idea so I shall start writing about here, in my tiny space in the internet, and I shall love very single minute of it.

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Fascinating facts about food. I have re read this three times, never gets boring.

Tired of looking at myself, wishing I was someone else

The true cost of chronic invisible illness. And I’m not talking about the strain on the NHS or the economy due to lost days at work.

I’m talking about the personal cost. I read a piece recently about a woman who had had her  Disability Claim denied because her assessing Dr decided that, after viewing her pictures on social media “the person depicted in most of these posts appears to be a young woman who is engaged in life activities, awake, smiling and alert. They do not appear to depict an individual who looks chronically ill”. He saw literally a snapshot of her life, he didn’t see the other 23 hrs and 55 mins of her day, the effort required to look happy, force yourself out of the house, to endure the ever constant pain and exhaustion is impossible to impart. Every day is a struggle, every single day.

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Ahhh when I went blind for a few months

My relationships have suffered, with my friends as, after a day at work, all I am capable of doing is getting myself home, getting my child to bed before I am literally on the floor with pain and exhaustion. So no more socialising for me unless it is in very short time frames, I have had to cancel plans so often that I just don’t make them any more. With my partner, a lot of the time, merely having my hand held hurts, I think you can see where I am going with this. He is a loving and patient man but why should he sacrifice his needs because I am ill?.

I was off work sick for a substantial amount of time and while my employer was very understanding I do realise that being a team member down impacts on the business and my colleagues, the anxiety of staying at home is real, it isn’t an opportunity to put your feet up and relax. I was due to start my Phd in January of 2016 but had to defer due to my newly diagnosed illness and I commenced in September instead. Today I saw my Supervisor and after discussions had to acknowledge that I am going to have defer this semester too and start again in the September of this year as I cannot keep up with the work required. I cried about this and I am not really a crier.

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Lots of lovely meds

I am not the mother I was or want to be. It was Lulu’s birthday last Friday and I promised her a trip to McDonalds after I got home from work and hospital (I’m in the middle of a 8 week treatment course). By the time I got home I was so exhausted and in so much pain  that I was shaking and couldn’t think straight so I lied to her and told her that McDonalds had flooded – this has actually happened before when it rains- and that we would go the next day but Saturday came and I couldn’t use the last of my energy driving there as we had to drive to a friend’s house for Lulu’s dinner, I am constantly having to make choices based on my energy and pain levels which is acceptable but of course as a parent, and friend and partner, these choices impact on others.

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Can never find a vein

I had a brain procedure sone on New Years Bank holiday Monday but my veins are so bad they couldn’t get the cannula in, after a number of goes they managed it but by the afternoon the bruise was enormous and black, I couldn’t keep it disgusted so Lu saw it and was clearly concerned, it looked awful. Why should my child have to see these things? She is 6 years of age, she shouldn’t think her mum is sick. Last ear I had Erythema Nodosum all over my arms and legs, big painful red swellings, I couldn’t have Lu on my lap or hold onto my arm because it hurt so much. How frightening for her that must have been? Not being able to cuddle mummy when ever you want because you will hurt her?

As a side issue my vanity has suffered greatly. Months of being bed ridden and increasing doses of steroids have left me overweight, bloated – hello moon face !- and spotty, thanks for the steroid endured adult acne. Lulu announced the other day that my tummy was so big it looked like I had a baby in it but that she knew I didn’t and that I was just very big – I’ve had to coach her endlessly on not using the word ‘fat’ as it is hurtful to people. She also added that her dad’s girlfriend had a very small tummy because she wasn’t big – thanks Lu, I just has t0 smile through gritted teeth and agree.

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Back in bed

I can no longer walk very far, before slowing to a snails pace as it is very painful but I walk as much as I can, you know cause its healthy and all that. I spoke with my GP about applying for a disabled badge for parking so I could park closer to the station so the walk would be sorter and the amount of pain I would have to endure would be lessened but apparently I don’t fall within the criteria, the ability to walk more than 50 metres means no badge. I can walk more than 50 meters, in agony, and pain that is so exacerbated that it remains with me most of the day. I am one of those people that fall into a grey area. The fact that I go to wok every day appears to mean that there is nothing wrong with me, that I need no other support or assistance. I go to work, because I have to, not because I necesarily feel well enough to do so, I have responsibilities, a child, a mortgage and it’s just me and my daughter.  So essentially unless I am entirely bed ridden I am not eligible for any assistance. The fact that a day at work (see feature photo of me on train home) means that the other 12 hours of the day are  written off is irrelevant. Cleaning my house is a painful exhausting  and very time consuming event, so I am caught in a Catch 22. At the moment I feel like I am merely existing, functioning, getting though one minute, one hour, one day at a time. Doing the practical and necessary things as far as I can and then there is nothing left for ‘me’. My Phd was for me and now that has had to be shelved.

This post isn’t about self pity, I don’t feel sorry for myself, I feel upset and frustrated and tired and old and frightened. I never thought that at 42 I would feel this way. Never.

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Getting dressed & putting on make up took all my energy that day

So the long and the short of it is just because I look ok, just because I go to work everyday, just because I smile does not mean in any way that I am actually ok. Invisible illness is real, it affects 1000s of people, trust me when I say that I do not feel good. I am trying my best, my absolute best, I cannot explain how hard I am trying.

 

 

You say goodbye and I say hello

Goodbye 2016, hello 2017. I am programmed to see the start of the year aligned with the academic one, so for me September brings the joy of new note books, plans and pens. The beginning of a new calendar year denotes a time to take things up, re consider, but never give anything up, its too hard, like saying that what I’ve been dong is wrong and of course I am never wrong so I couldn’t do that, just ask my ex husband.

I am back on a self imposed (read : the bank are making me) spending ban. I do not include Lucia in this, but its a big fat no to new clothes, make up, books (arghhh) and magazines for the next 3 months. Those uni fees won’t pay themselves.

 

And this coming year I am going to paint the house, pink, everywhere, I am very excited, as it Lucia. My Pinterest board has been crammed full of pink inspired pics for over a year and now I can start saving for pots of those gorgeous Farrow and Ball paints. I think I may paint the front door pink also. It is definitely my happy colour

I also desperately need new sofa, as the puppies have chewed a hole in the top on the cushion on the one that I have. I have been coveting a pink velvet one from sofa.com for a while but need to be sensible as a the puppy is still a puppy and it is expensive item of furniture. Worth every penny, but still in the scheme of things a luxury. Damn not being a dual income household anymore.

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I’ve been trying to sneak pink into M’s colour scheme at his house but he is resisting. Though that is the beauty of us not living together, I can have all the pink, grey, flamingo, fairy lights I want at my house and he can watch rugby on his massive tv on his massive sofa at his house.

I will also be knitting that cardigan I thought about last year and on New Years Eve instead of donning my glad rags and hitting the town I shall be ordering seeds for the veg patch. This gives me greater pleasure than I ever thought it would.