Tuesday, 4 April 2017

I love April




Glamis Village in April
James MacIntosh Patrick



I love April. 

It was Mother’s birthday month and I associate it with the big bouquet we made for her with the flowers of the garden, mainly with irises and apple blossoms. She had a fondness for irises and she nursed and raised the plants, exchanging rhizomes with friends and collectors near our house: they came in all sorts of hues from the simple, straight, blue ones to the fat gorgeous golden yellow others, going through browns, pinks, whites, slightly striped, zebra, cut out, bearded petals. It seemed that the variations were infinite. We kept to the simple dark purple ones that were swathed in the frothy apple blossoms, a candid white tinged with a blush of pink rose. We would have devastated the orchard so we were left two or three trees which gave each year a crop of acid apples that never matured and which we used in the early autumn as prime elements to our desperate experiences to make cider.

Life is to be compared with April according to William Cowper: "It is a sort of April-weather life that we lead in this world.  A little sunshine is generally the prelude to a storm." And nowadays more than ever I do think so. What little joys we have are soon drowned by a shower of sorrows.


Spring in Eckdale
James MacIntosh Patrick


Elder Girl is still in hospital. I have been told by our doctor that she does not want to get up by herself, to stand up, to walk. Her food is processed and rolled and she eats it with a spoon. She speaks when she is spoken to and she passes the day sitting in an armchair. “An ideal patient”, said Matron over the phone. She never complains and she never moves.”  Our doctor was enthusiastic about the notion of our joining her in hospital and was highly surprised when I refused, telling him we were not ill and asking him to hasten her return home. “She will be a weight upon you”, he said, eyeing me dubiously. “And she will need continuous care with nurses at least twice a day, special implements like an electric armchair, another chair in which she will spend her days, people to transfer her from bed to chair and from chair to bed. “That sort of things.” “All right”, I answered, let’s get the help we need and have her back with us in her own home and environment.” “She is aging, you know”, he said. ”She is an old lady according to her pathology. She is aging fast.” I bit my lips thinking that his prescription of antidepressants, anxiolytics and sleeping pills maintained her surely in a state of half dozing that could easily pass for early senescence. He is glad to have slotted Elder Girl into her proper little square: at long last, she is under the thumb of the medical profession and made to behave as a proper Down Syndrome person.

I feel guilty to have let her out of my sight. I should have passed over our doctor’s injunction to let her go to the main hospital in Périgueux alone. From there she was dispatched to this wretched country hospital where I cannot go and see her regularly to keep her in the world of the living. Guilty. Guilty.

In order to keep my mind busy, I thought about poetry. No, I will not talk about “April, the cruellest of months” and about T.S. Eliot. I tried to lift up my spirits with the thought that this month is the promise of gold and blue days.

April, 1885
Wanton with long delay the gay spring leaping cometh;
 The blackthorn starreth now his bough on the eve of May:
 All day in the sweet box-tree the bee for pleasure hummeth:
The cuckoo sends afloat his note on the air all day;

Now dewy nights again and rain in gentle shower
At root of tree and flower have quenched the winter's drouth.
 On high the hot sun smiles, and banks of cloud uptower
In bulging heads that crowd for miles the dazzling south.

Robert Bridges, The Shorter Poems (1896).

Have you noted the internal rhymes within lines (delay/gay, now/bough, et cetera), the combination of end rhymes and internal rhymes across three lines (cometh/starreth/hummeth, shower/flower/uptower), and the internal rhymes across lines (smiles/miles, cloud/crowd)?


The Cornish April
Adrian Paul Allinson


The garden is sadly neglected but while going through it to open the gate for the cleaning lady’s car, I noticed how much the daffodils are on the wane, that tulips are perking up, that violets smile through blades of new grass, and that pâquerettes, these small, short-stemmed, wild daisies that are in full bloom for Easter (thus their name, as Easter is Pâques in French) are already dotting the whole grounds with the help of primroses and cowslips. April is a time of arrivals and departures.

In the Valley

On this first evening of April
Things look wintry still:
 Not a leaf on the tree,
 Not a cloud in the sky,
 Only a young moon high above the clear green west
And a few stars by and by.

Yet Spring inhabits round like a spirit.
 I am sure of it
By the swoon on the sense,
 By the dazzle on the eye,
 By the long, long sigh that traverses my breast
And yet no reason why.

O lovely Quiet, am I never to be blest?
 Time, even now you haste.
 Between the lamb's bleat and the ewe's reply
A star has come into the sky.

Sylvia Townsend Warner, Time Importuned (1928).

Here, "the dazzling south" of Bridges in the former poem meets "the dazzle on the eye" of Warner. And, coincidentally, Warner employs the same technique of end rhymes and internal rhymes across three lines used by Bridges:  sky/high/by; eye/sigh/why.


April in Epping
Lucien Pissaro


April's mutability is embodied in the trees:  their branches are still mostly bare, but, from a distance, they seem to be enveloped in a yellow-green haze.  Mutability and promise.  “Nature ‘s first green is gold” says Robert Frost.
April

Exactly:  where the winter was
The spring has come:  I see her now
In the fields, and as she goes
The flowers spring, nobody knows how.

C. H. Sisson, What and Who (Carcanet Press 1994).


April Sunshine
Victor Elford


But however much I want to glorify spring, I cannot prevent myself from worry for Elder Girl and melancholy for the time “when we were young” (with A.A. Milne) and when we were roughly and rudely pruning the apple trees with laughter to please Mother on her birth day.

Wet Evening in April

The birds sang in the wet trees
And as I listened to them it was a hundred years from now
And I was dead and someone else was listening to them.
But I was glad I had recorded for him the melancholy.

Patrick Kavanagh, Collected Poems 



Time has gone by. Mother is dead. Elder Girl is aging. I am too.


Glamis Village
James MacIntosh Patrick

Thursday, 16 March 2017

Flaming orange Pre-Raphaelite colour and black Malevitch square





Once upon a time ... I blogged regularly - almost daily. Once upon a time ... I could see properly. Once upon a time ... there was a Little Family. Once upon a time...

I see that it has been almost six months since I wrote an entry to this blog. I would like to resume this activity to rule at least one thing from my list of "Once upon a time". So let me explain briefly why I stopped and what has happened since November.

You may remember that my Elder Girl was diagnosed epileptic last October. In November, our doctor thought that she needed to have her treatment adapted to her condition under medical care, while I would have some respite by myself. The Girls were sent to the nearest cottage hospital for two weeks and I stayed at home.

It proved disastrous for all of us.




Was it relief, after looking after them for so long? I stayed in bed in the completely closed house, in the dark, and slept. I do not remember much. I know that I went to visit them and found Elder Girl sitting down on the floor of her bedroom with a mattress equally on the floor. It was a very dark Sunday in early December and I could not talk with the doctor or the nurse in charge of the ward. I planned to come back on the morrow. I went home and then I cannot remember anything.

Some time must have elapsed. One evening, there was loud banging on the kitchen door. I stumbled there and found the Head of the cleaning lady Agency with a Cleaning Lady. The Head seems to have decided to call the doctor in charge (ours was on holiday). I remember vaguely that I went back to bed and that I heard both Ladies doing the washing-up as our dishwasher had broken down a few weeks before. The doctor in charge came and probably made me an injection (I found the syringe later on my bedside table) and called for an ambulance.



I remember vaguely being carted from the house, telling the people around me which door should be closed last. I have no memory of the road to the main hospital, in Périgueux. I remember the lights when I arrived even more vividly because I was seeing a deep orange light in my left eye. I remember that I told this to one doctor, adding that it was gorgeously Pre-Raphaelite, and he wore a puzzled face. I remember that I waited a long time in a corridor, and then a box room, that there were analyses made and a scan test. I remember that I talked quite normally and fluently and did not understand why people seemed so eager around me. I remember there was a tight pain in my chest and then a sensation of gurgling water near my heart. I remember I was happy and at peace with myself.



Then there is a blank.

I awoke in a hospital room. I tore away the drip from my left arm and the contraption-like, ridiculous stockings into which my legs were encased. I went to the loo and a nurse came and severely reprimanded me, which I did not understand. Then there must have been a doctor and other tests. When I awoke again, the drip was there, in my left arm. I was attached to a monitoring machine. I could not move. I could not see with my left eye but black or darkness.

Little by little, I gathered that I had had a pulmonary embolism and what I thought was a severe migraine. It was nearing Christmas. I had no news from my Girls. I planned to have them with me on Christmas Day but was dissuaded of it. Christmas came and went. I had septicaemia with very high temperature. I could not read. I did not understand why it took so long to discharge me. I hated every day in hospital. I hated every night.

I had The Girls on the phone. They sounded very far away in their own private worlds and did not really understand me.

There was this disturbing black veil over the left downside of my left eye with bright flashes. The migraine was painful but did not want to explode and go away. I was given strong painkillers but with no effect.



New Year's Day came and went. The main doctor in charge of the service where I had been transferred came back from his holidays. Things and exams were brisker. At long last I had a brain scan. And the doctor's conclusions.

I would probably never recover the eyesight of my left eye as I had had a stroke. It was no migraine and it had happened when I was seeing this gorgeous orange Pre -Raphaelite light the night when I arrived. I had also had a heart attack. I would probably have to be careful all life long and take a heavy treatment. It had been a close brush with death. There could be others.

He was ready to send me back home but I did not feel equal to leading my old life with The Girls yet and I said so. He seemed surprised. I told him that I had been in touch with the cottage hospital where The Girls were and that I was awaited there.

Thus I was discharged and arrived at the cottage hospital on a sunny January day.



The Girls were grim at best, apathetic at worst. I was appalled at the way they were dressed. I was appalled because they did not show any sign of joy at our being reunited. I was appalled because Elder Girl did not walk anymore.  She was on the floor and was walking on all fours. She did not want to eat. I understood from the hospital doctor that she would not sleep. They were little animals.

That first evening, I said that we would have dinner all together in my room. I had to feed them, spoonful after spoonful. The whole meal. By the end of the day, which is eight o'clock pm in French hospitals, I had seen that there was a hard job before me if they were to behave normally again.

We spent a month in that cottage hospital. We could not go out because it was too cold. I was allowed to go to an ophthalmologist, and another time at home to have some cleaning-up done, trees severely pruned and the new dishwasher delivered. It was awfully cold as I guessed all fuel had been used. I emailed The Girls' financial guardian to ask for some more to be delivered before we would come back and the boiler seen to.

While we were at the cottage hospital, it was decided that we would receive help: a nurse every morning to help the girls wash and dress, and every evening to help them go to bed. Meals would be delivered while I was not able to cook. Daily help from the Cleaning Ladies Agency would be provided, as well as driving help to go shopping as I cannot drive anymore. It seemed all miraculously too good to be true.

I enquired again and again to make sure that all these wonderful provisions would be there when we left the hospital. I was assured that everything was ready.

When we arrived at home in the first fortnight of February, no fuel had been delivered: it was icy cold inside the house. There was nothing in the fridge and only two meals had been delivered: for The Girls only. I have no recognised existence to be granted this facility. Nurses would not come morning and evening: they were over-busied. The number of hours dedicated for help to The Girls was (and still is) the same as before: four hours a week. The situation was the same as the one we had when we were all healthy.



The Girls have been traumatized by their extended stay in hospital. Elder Girl has been driven to the emergencies in Périgueux hospital twice since then. She relapsed to non-eating, non-walking, non-getting up. She is now in hospital somewhere at the other end of the département and I have both no news and no means to go there: I cannot drive and there are no trains or buses.

I am slowly drowning back into deep depression. I mostly stay in my bed, in the dark, reading and "webbing" the days and nights.

Once upon a time there was a Little Family... Then, there was Flaming orange Pre-Raphaelite colour. Then there was a black Malevitch square.









Friday, 4 November 2016

Despair








Once I had a voice. And I screamed.

NOW

I have no more time to myself.

Idepend on the help I shall, may or might get - or not.

My life is now fully busy with The Girls.

Elder Girl is unmanageable because of her pathologies and because she hates me as I ask her to do things she does not want to do. The Younger follows the example of The Elder.

We have no hours.

They claimed for breakfast at eight this morning and went back to sleep in my arms until half past twelve. I was lucky they remembered they already had their breakfast otherwise we would have taken another one. I washed and dressed The Elder. I supervised and helped The Younger. I cooked their lunch. I made the beds while they were having lunch. I wrote the shopping list. I drank a protein liquid, and tried to e-mail the finance advisor and the Head of the Agency in order to have a planning for November. I was interrupted many times and yet nobody was ready when the Shopping Lady arrived.


No shopping for me as I had no time to wash and dress ... and eat. I am feeling like collapsing every time I move.


I tried to find a book in a card box but the box almost all fell down on my foot that is now swollen and blue, and I have no idea where the book is but a good idea where there is a spider nest.







I wish The Girls were elsewhere but far away from me. I wish I were in my own life with my own things, my own flat, my own friends, music, museums, conferences, exhibitions, books, studies - my life.


I wish I had new books - I mean books I would have never read: dove grey Persephones, green (or not) Viragos, yellow Grey Ladies, those wonderful although never seen Golden Age Mystery books from the British Library, the Fox books and magazines, Mrs Thirkell (those I have not...).


I even wish I had Margery Sharp, Ms Hocking, and all these undervalued women writers, and Daphne Du Maurier (for whom my foot is swollen).


And I wish I had a great, good, strong bottle of whisky or other alcool, and get drunk.


I am told I must assume the consequences of my former decisions and stop crying over myself (and spilt milk).


NOW

I have no voice any more.




Monday, 31 October 2016

In need of a word of comfort



I have started writing about what happened to The Little Family during the last month but I cannot end the post. Feelings are too raw and I am overtired.

Elder Girl had to be dashed to hospital after a fit where she convulsed and badly hurt her head and scalp. She had a scan, an electro-encephalogram, various tests, was examined by various doctors and a neurologist, and diagnosed epileptic, which is often the case when DownS persons are ageing and heading towards the end of their lives.

I shall not write about life at home. I shall do this another time. Later. Life is difficult, bleak. I do not know how to cope. I do not have the means to cope and help is distilled drop after drop when I shriek for it.

I am tired of advice from people who do not know what I am going through and what The Girls are going through. Fortunately, I have a few kind friends on Facebook who have helped me go through last week ordeal. Others are only living in their own intellectual sphere without understand.

If you read this, would you please be kind enough to wave, say hello, show that  you are here. No more. I feel alone and lonely. I try to be brave but I am NOT brave at all. I am frightened.

Thank you.

Monday, 3 October 2016

Some news from The Little Family




It has been a long time since I posted my last words on all my blogs. I think the middle of July is the last date for "Sketches and Vignettes from la Dordogne", when I talked about a play at the Avignon theatre festival. And it was even sooner than this for "Lights and Shades".
I have not left off blogging. I simply had no time. I have not much time left for blogging, writing, reading, or for myself.
Elder Girl has turned 57 on the 21st of July. I know that when she was born, and later still, she was not expected to live so long. Now, people suffering from Down Syndrome have a life expectancy of an average of 60 years. When she was born, it was at best 30 years. Therefore she has surprised everybody by outliving the supposed limit of her life. Congratulations must be addressed to her parents who took care of her when she was a baby, a child and a young lady. She had breathing difficulties that were remedied to. She overcame all childish illnesses. She was made, and kept, fit. She was attended to. She was taught to drink, eat, stand upright, walk, move, read, write, count. She was given friends. She was given social relationships. She was taught a job, helping to take care of little children in a kindergarten. She has had a full life - as much as her family was able to give her and as much as she could take in.
The counterpart was all the sacrifices that were made for her. Her patents gave most of their lives to her and for her and her well-being. They both died of cancer but mostly of exhaustion from having supported her as they did. Collateral consequences were then for those who have had to support her until now.
But she has been a grand lady.
Shortly after her birthday, I was awoken by a thud on the floor of her bedroom. It had already happened that she slid from an unperfectly made bed while having a nightmare. So, I was not that surprised. However, I was not prepared for what was waiting for me. She was lying on the floor, convulsing, thrashing legs and arms, eyes rolling, scum around the mouth and tongue protruding. I briefly thought of Mother dying in my arms almost the same way, and remembered as a reflex more than as a real thought what was advised for epilepsy crises. I cannot remember how long it lasted. It seemed hours but it was certainly more a matter of minutes. Then, I put her back to bed, and rang up the doctor. 
To be qualified as epilepsy, there should be other crises. There have been none. But some days, there are small electric jolts that last a fraction of second. After each she does not remember what she was saying and doing. There have been fainting fits - one of which was vicious as she banged her head on the corner of a shelf and cut her scalp. She now forgets things: she forgets the time, she forgets what she reads, she forgets to read, she forgets the days, she forgets words. She plays endlessly with her blue pencils - blue only - and never goes anywhere without less than three or four of them in her hand. She lives according a sequence of events whatever the hour. Therefore she woke up one day at two pm, took half an hour to be ready to get up, then had breakfast, wished she had her time for hugging, took her shower, got prepared and clothed, was ready by five o'clock, did not want to listen to her radio programme as in her mind it was not the proper time, but was infinitely surprised that we had no lunch and were closing the shutters when night came. She did not understand it was dinner time, TV time and bed time. She thought she was somewhat cheated of her day.
She forgets where she is and asks to come home, hears her mother, arrived one day saying "Mother is back", took me once for her mother's sister (one of her aunts), does not remember where things are in the house, gets glassy eyes, falls asleep in front of TV, sleeps a lot, cannot go up some stair steps. And I might go on and on.
Getting an appointment for a cerebral scanner test and an appointment on the same day with a neurologist at the nearest hospital in Périgueux is a "tour de force". Considering that she is not a productive person but one suffering from a mental handicap, receiving a State allowance, and being 57, our Western Liberal society is not very much interested in her. She does not produce anything and she does not consume much. What is the point of keeping her living? So tests and appointments are forever pushed back in time. There are more "important" people to see to before her.
Life at home revolves around her now and we live at her own pace. Not much time to read. No time to write or blog.

Anyway, I would be glad if you ever had experiences like mine of any advice you could give and share. Many thanks for your support and help.



Friday, 15 July 2016

For whom the bell tolls





Renoir - Le Moulin de la Galette



Time flies. Soon after France lost the final of the European football Championship, it was National Day and the yearly enjoyment in the Tour de France with its drugged cyclists - as usual. It was a cold 14 July, with clouds and bitter wind but the military parade on the Champs Elysées went on as usual, followed by the same stilted interview of the President by carefully chosen journalists, and the French went on with their holiday life. 

The days when France almost stops in her yearly summer siesta were beginning, although they have not the wholehearted and childish joyous unconsciousness of the 1960s and 1970s. At least, to compensate the ever growing "no more holidays at the seaside", there is the barbecue and the plancha, the discount supermarkets where you can buy at reduced price meat, ready-made salads and  ice-creams, and goods you may turn into junk food. 

After the barbecue, there is always the possibility of the local ball (perhaps) and the fireworks (surely). Then, refreshed by such festivities, the French retire for the night and for a well-earned sleep. Another Fête nationale of which the initial meaning has long been lost. 


Corot - Feu d'artifice



But it was not to be yesterday. At eleven o'clock at night, while the fireworks were in full swing in the whole country, a lorry made its way on the Promenade des Anglais in Nice. It was another terrorist attack for all we know that left eighty-four dead (among them ten children and youths), two hundred and two people suffering from injuries (among whom fifty-two people in critical condition) Several were children and families as it was a popular and all-age attraction. 

The country is shocked. The President went for another speech. Emergency state has been proclaimed for three more months. The lorry driver was killed by the police during the shooting following the attack, and then was said to be Tunisian with French roots. Condolences and sympathy come from around the Earth, expressed by Heads of States, friends or total strangers. Debates are flaming: should the French stop the arrival of migrants? Should migrants be called refugees? Should France expatriate all foreigners, following the example of some fanatic Brexit proponents (including in a rash moment the new, non-elected, Prime Minister). What about the gun control (and there, a look towards the USA)? Are the terrorists French and bred on French soil? Are all Muslims terrorists? Are all French racists?

More generally and to sum up all interrogations, is the country going to the dogs?

I have no answer. Nobody has any answer. We have no global view of the entire situation, which is worldwide, political, economic, perhaps religious (if religion is not used as a tool), long-standing, part of the fall of the colonial Empires, of the resurgence of tribal wars, of new wars created by greedy countries for economic reasons in the 1980s and 1990s, for pious reasons including Western ideas of democracy and Human Rights covering starker money-bound reasons in the 2000s. Public opinions are manipulated. The peoples are lied to. Extremes are rising up their ugly and venomous heads. Reason is forgotten. Law is violated. The people are pitted against each other.


Otto Dix - La Guerre


Slowly, very slowly, the tension is growing, and as a wheel that gets idler and rolls faster and faster, we are heading towards another world war. The demographic regulation needs it. The economic regulation needs it. The financial and industrial groups and individuals wish it.

On Sunday night, I was watching the Avignon Festival's flagship show: "Les Damnés", a play adapted from the film by Visconti, 'The Damned", about the rise of Nazism and Hitler with the complicity of the industrial and financial élite festering like a hotbed of vices. A modernist staging that might have shocked "gentle people" by its crudeness that never bordered coarseness, where the Comédie française found back its vocation of beacon of culture. There was a sound in it of what is happening now that tolled like a death knell.

Visconti - Film "Les Damnés"




Avignon - 2016 - Cour du Palais des Papes - Comédie  française - "Les Damnés"





Saturday, 9 July 2016

July: The Little Family is back (for better or for worse)! Good news / bad news ?








Some news from The Little Family who is now firmly rooted in July, warmth, sunshine, early mornings (when possible), sometimes late nights if there is something from the summer music and theatre festivals on TV, fruits, vegetables like courgettes, aubergines, tomatoes, peaches, apricots, nectarines, soon melons... 

And soon the Great House Scouring Party on the 21st of July, the day Anne-Fleur celebrates her birthday. As you know she will be 57 and cannot remember it because she sees such discrepancy "between her age and what she feels inside" - so she told me.

Add to this the Fête nationale (we never call it Bastille Day in France) on the 14th, Anne-Fleur's saint day on the 26th (Sainte Anne), and you may imagine what an eventful month we are living!

And we already went - no, this is not true - I went through three events this week: one good, one less good, and another that does not concern us/me directly, but that I wish to mention.

***





 There has been a leak for months in the loo. It was nothing important, nevertheless the noise was irritating and we were wasting water. The plumber had been ready to intervene since February but the finance administrator had given no green light for laziness, carelessness, and slackness. In the end all these were remedied and the plumber came at the beginning of the week. It took him ten minutes and a piece of black plastic to mend the leak. He has been working for us for some time now as he is the famous boiler man as well. In fact, he is the boss of a little enterprise nearby; he comes from time to time to do an odd job and overlook what his employees have been doing.

So, this job done, he stayed for a few moments, on the little terrace of the kitchen, talking to me. And then came the genuine kind word that was THE revelation for me! "Do you remember the first time I went? You were really ill then. You looked... You looked... Well, you looked badly ill. Now, you look..." Trailing voice. I get an appraising glance. "You look normal."

YES! For a non-professional like Dr Quack or social workers or, even, the Socializing/Shopping Lady, I look normal. I told this to a friend who said that there had never been a moment that I was not normal. If I was disabled, it was by illness, stress and strain. If I still was slightly disabled, it was as a consequence of the stress and strain. But at no time I was or am mentally handicapped or disabled.

Hooray! I am normal!

***






 BUT... Why is there always a "but"?

The Socializing/Shopping Lady is not as interested as she was before by The Little Family. She thinks that we are difficult patients. We do not want to "socialize". We spend our time in books, classical music, magazines, quiet occupations that we may lead alone, and this is definitely not normal. We should be going out more. Why don't I create some "social link" with The Girls going shopping with them? Why don't we go to the gym together? Why don't we have activities outside the house together? 

I told her that we had always found our happiness in reading, writing, listening to music, not in moving much, and not in doing the activities offered by the associations of The Village. That we were Townees. That we liked quiet. And that, plainly speaking, I was very, very happy to be left in perfect solitude, three hours a week, at home, while she was taking The Girls shopping. She watched me with a look of incomprehension, commiseration, and disdain. I was saying that I could be happy without The Girls. This is heretic when you are a parent or a sibling of handicapped people. They must be the Light of your Life. 

Therefore, she leaves us more and more into other hands: she is on holidays, she cannot come for such or such reasons, she is not available, etc. It seems that after some unpleasant fluctuations, we have a rather permanent Stand-In Lady who started this afternoon. As I did not know who and how she would be, I decided to go shopping with The Girls to test our Substitute Lady.

She was nice to The Girls, polite with me, and helped me, although she was clearly dejected not to  decide to which supermarket we were going, not to have to push the trolley (Anne-Fleur's task), not to make the menus (I had made them and then the shopping list accordingly), not to choose what to buy (ditto the shopping list plus the calculator to keep an eye over the spending). 

Coming back, while she was driving, she asked me: "But who is the mentally handicapped person? YOU are the one, aren't you?" I was utterly dismayed. 

Boom! Live with Down Syndrome people and YOU are the mentally handicapped one! Now I have to think very, very hard at what the plumber said. And I have to use the méthode Coué: "Je suis normale, je suis normale, je suis normale..."

No, truly: I am laughing.

***





The third event happened on Thursday night.

There were semi-finals in the European Football Cup and France was playing Germany. France won the World Football Cup in 1998 with a team that was called "Black, Blanc, Beur", which means that there were Black, of Arab origin, and White players. This had a very positive, if not lasting, effect on French society. We understood that we could be united, together, do something, and win. There was no question of skin colour or creed anymore. We were together.

Since then, there was the financial and economic crisis, the rise of the Extreme Right (Front National), the Arab Spring, DAESH, ISIS, Syria, Iraq, terrorism, attacks, racism again. Meanwhile the French team behaved like spoiled children, money came in, new generations came, and we did not even play one match in the World Cup on South Africa, on a whim. The French players went to the stadium but refused to get off the bus. We left the competition far, far before the semi-finals, at the very beginning of the competition! It has now taken years to build another team and we were not too sure of it!

Slowly, this year that France is host to the European Championship, the new French team went up, up up, match after match. Until we played Germany yesterday. It was in Marseilles, which is a difficult town with lots of problems with racism and violence. We were not too confident in a French victory and we were already congratulating ourselves that we had been so far! 

And we won!

I am not much interested in sports, even less in football. The Girls do not understand the game. We watched a film against racism on another channel. When it was over, I turned to Channel 1 and we saw the French players being applauded and applauding the supporters in the stadium. I understood that we had won. It was confirmed: 2 for France and 0 for Germany. But what was beautiful was this new "Black, Blanc, Beur" team and the usually oh so racist public sharing a moment of collusion and of joy. Tomorrow - that is Saturday evening - France will play Portugal in the final. We may well lose. I hope not. It would be wonderful to live another complicity moment between the team and the country. This would soothe the rise of racism, the horror of the difference, the fear of the refugee, the idea of a Frexit. I long for another time like the one that followed the victory of 1998.




And I want to thank England. There were different teams representing the UK, England represented England. While the English were playing in Marseilles, and after, as they left the competition rather early, English supporters created and built a "synthetic" stadium in one of the multiracial, difficult, and violent suburbs of Marseilles. This will allow youths of different origins to come and play together. 

 The UK voted for Brexit. But who says that all British are racists? Thank you, England. Thank you, UK. This is the way we like you.