Post Operation
Hi
everyone
The
first post-operation reports from Dad himself are
that he had a very difficult night after the
operation and yesterday he was in excruciating pain,
which he described as the worst pain he’s ever
experienced. One can’t help but wonder if he
has, in fact, been in comparable agony immediately
after the accident but of that, he fortunately has no
memory.
The
bone graft operation which Steve performed entailed
taking a 5cm wide piece of bone from Dad’s pelvis,
cutting it into strips and inserting it into Dad’s
leg, along with a metal plate and 4 screws to provide
additional support. During the accident, Dad
lost a significant area of bone from his leg.
It was a compound fracture with many breaks from his
shin downwards. The hospital in Tours had
previously told us that this complex break, with
missing bone along with many fragmented pieces of
bone, was in a particularly tricky location because
it was near his ankle, which meant his long term
prospects of how this would affect his leg’s
stability and balance were questionable. Dad
has fortunately, thankfully, been in superlatively
good hands, having Steve as his surgeon, giving him
the best opportunity for the best recovery
possible.
Dad
now, sadly, has to ride out the pain and count the
days until the cast comes off, with some very
intensive physiotherapy ahead to regain his mobility
as quickly as is realistically possible. He is
being encouraged to try to stand and move around his
bed a little with the use of a zimmer frame, but he
is still extremely weak and his muscles have wasted
away so much that this is very hard for him to begin
to do. This is not helped by the fact that he
is still struggling to eat anything other than tiny
quantities, so he has very limited energy intake at
the moment too.
No
doubt, things will start to improve gradually but in
the meantime, Dad has to endure the pain and
discomfort from this latest procedure. The pain
he had yesterday has subsided a little today so each
new day should see the pain
dwindling.
We’ll
let you know when we have more news.
P.S. We’ve just heard that Dad won’t be back in
the UK for at least 6 weeks. He will begin his
rehabilitation in a specialist centre somewhere Paris
in order to allow him to return to the hospital he’s
currently in so that they can do post-op check-ups
themselves on his leg on two separate occasions,
before Dad returns to the UK. This is
disappointing in the sense that Dad will still be so
far away, but it’s much better that it is the
operating hospital who assesses Dad’s leg’s progress
in two and six weeks’ time.
Love
Nat
xxx
The Operation

Hi everyone
We
know everyone will be anxiously waiting to hear how
Dad’s operation went
yesterday.
The
operation didn’t take place until very late in the
day, due to other patients’ emergencies taking
priority. From what I know, the operation went
well, with bone being taken from Dad’s pelvis to
replace the bone which was lost from his leg during
the accident. As predicted by Steve, Dad’s
surgeon, Dad is in a great deal of debilitating pain
and discomfort, for which he is having morphine.
It is expected to be several days before the
pain really starts to subside, so we’re hoping that
he’ll spend as much of that time as possible
asleep.
We’ll
of course keep you posted when there’s more
news.
Love
Nat
xxx
The Operation
Hi
everyone
Dad
did not have the operation today because he has an
infection which needs to be under control before
undergoing surgery. The operation will go ahead
tomorrow (Tuesday) instead.
He
has had a challenging day today emotionally and was
particularly overwhelmed when he received a parcel of
goodies, very kindly sent by some friends in
America.
Because
his operation was originally scheduled for today,
there were no visitors planned, but there are a
couple of very kind nurses and a doctor who looked
after him whilst he was in the Intensive Care unit,
who have been visiting him regularly and who came to
see him today too, a gesture which he also founds
very touching. Preparations have also been
underway for the operation, so this has helped to
fill his day, although he was disappointed that due
to these he missed a visit from Steve Hansen, his
surgeon. Once tomorrow’s operation is behind
him, Dad will be counting the days to having the cast
removed and being able to really get his physio
underway with full steam ahead! Needless to say
that he will then start to feel far more positive as
he sees the results of this and his physical strength
returns. Simultaneously, I’m sure his emotional
fragility will melt away and he will start to feel
far more upbeat. Although he tries to stay
positive, it’s frustrating beyond measure for him to
be so immobile but his darkest days ARE behind him
and he will also be happier when he is ready to be
transferred to a UK hospital, nearer to family and
friends (and a local M&S food hall perhaps
too!).
Things
are improving a little on the food front – he did
actually have some hospital soup, which he quite
liked!!!!
That’s
all for now, really as none of us are there to report
personally, but please do keep your messages coming
as I’m now able to email them all to him on a regular
basis.
Love
Nat
xxxx
friday and Saturday
Just a quick Blog from
yesterday and todays visit.
I arrived
a 2pm yesterday afternoon, Dad looks quite well
however he is still very weak, we had an interesting
time trying to get him from Bed to Chair and vise
versa, even managed to put my own back out trying to
lift him!!
Anyway, I arrived with a bit of Chinese, rice, pork,
chicken etc, he had some but only small portions for
Dad as he really is not very hungry as his stomach
has shrunk so much over the past 3 Months.
Spent the afternoon chatting and then both has a
quick snooze before Natalie phoned and woke us both
up.
Popped and found some Roast chicken and rice, dad
only had a very small taste again, as he was feeling
quite squeesey and nauseas. I stayed until around 9
pm and then returned to my humble accommodation.
Returned today at 2PM with some little delights,
quiche lorraine and a little salmon st Jacque and
carrot salad followed by sorbet. Still no appetite,
Dad ate small bits but still felt sick. I paid to get
the TV on and were both pleased to watch a football
match, Man U V Everton and then we watched the Rugby
at the Stade de France, just up the road from here,
shame we could not both go!! Popped out again as Dad
needed Creme Caramel, mints and water. I also bought
him a small Baguette and ham toms and fromage. Not
easy to buy Ham around here, being the Muslim part of
Paris! However good old Lidl came up with the goods.
Got back made a small sandwich, however before we
even got started, Dad was very sick, too much acid
and he needed to get it all up. Once we cleaned up
the mess, he felt a little better and eat a little
more bread and a creme caramel.
Now watching programme about Ferraris.
That's all folks
.Max and Barrie
Natalie wednesday

Hi everyone
The first part of today's update was dictated by Dad
and the second is my more detailed overview of
how Dad is.
"I've moved from Intensive Care to the 3rd floor
where the atmosphere is much more relaxed, however
the staff levels are also a lot smaller so if you
want anything done, it's a half hour wait at best.
They do try but they have too much to do.
I'm thrilled to have a visit from my daughter,
Natalie, who is writing this blog for me. The next
big op is on the 27th, so if that goes well we might
be getting somewhere!
Greetings to all and thanks for your messages.
Barrie"
Today's visit was, by chance, so perfectly
synchronised with Dad finally leaving Intensive Care
which meant that rather than me being able to see him
for only two hours or less, I was incredibly
fortunate to be his first visitor to be able to stay
from 1pm to 7pm (I wasn't able to stay later because
of the Eurostar's current timetable disruption!)
Dad was already sitting in the armchair when I
arrived and stayed there for the longest time so far,
to about 4.30pm. Although I saw Dad just a
couple of weeks ago, I have to say I was still really
taken aback by how thin and drawn he has become. It's
hard to conceive how someone as physically strong as
Dad could suddenly become so seemingly vulnerable and
frail. Until recently the considerable swelling which
Dad suffered from his oedemas masked this very
deceptively.
Dad continues to have regular bouts of being overcome
with emotion but fortunately he doesn't try to
suppress this as he completely understands that this
is a process he must just go along with at the moment
in order to mentally heal and to avoid long term
psychological problems.
Despite all this, we soaked up each other's company,
with Dad having many stories to tell about a
diversity of subjects and, intermittently, Dad
listened keenly to 10 pages of your latest messages
that I'd printed from the blog pages! He really is so
touched by the astounding level of support from you
all, so thank you so very much.
Poor Dad certainly isn't embracing the concept of
hospital food, but this may be because his tastebuds
are distorting flavours because it's so long since
he's eaten properly. Having said that, another
M&S raspberry jelly went down well, along with
some of their shortbread biscuits and a few grapes!
Whist Dad is doing really well with his recovery, he
is inevitably finding it unimaginably frustrating
that his complete lack of strength and mobility have
stripped him of the simplest level of independence.
This though, is bound to be a powerful driving
force for him throughout his physical rehabilitation
via physiotherapy. He hopes to be able
start this as soon as it is practical after next
week's orthopaedic reconstructive surgery to his leg.
All in all, it was really lovely to have an intensive
block of time with Dad today and I felt very close to
him. None of us forget how lucky we are to still have
him with us and it's something that stays in the
forefront of our minds, in particular during visits.
I am really looking forward to Dad's further and
ongoing progress, but just wish we had a magic wand
to make it all happen without the emotional and
physical battles that still lie ahead for him! There
is no doubt in my mind that Dad will be just fine,
generally, in time. He's doing brilliantly and I'm
very, very proud of him!
It was a long visit with a lot of insight into Dad's
current situation, so I'm afraid I've gassed on a
bit. I hope someone out there is still awake!!!!!
Thanks once again to you all for the mountain of
support and especially too, to René who so kindly
regularly gives his time and fills in the gaps by
visiting Dad when we can't be there.
Dad is now looking forward to Max's visit on Friday.
Love
Nat
xxx
Fabulous news
Tuesday 21 October - this is an
important date as Barrie is out of intensive care
after more than three months
He is now in the orthopedic ward on 3rd floor in room
324
Visiting hours are much easier between 1pm and 8pm
His general health has improved a lot, he still has
urologic issues to be taken care of and of course
next will be the leg operation on 27 October when the
surgeon Steve Hansen will do a bone graft and put
plates to strenghen the lower leg
Natalie will be in Paris on 22nd, so more detailed
news to come
Maite
Dictated By Barrie
Barrie the Blogger
Rene
Ligonet at visiting time
For some unknown
reasons I was alllowed to sleep til 10.30 this
morning with the brilliant sunllight completly hidden
behind the solid rollerblind
I thought
the clock had stopped
Once cleaned up, I was hoisted with hydraulic lift
into my morning chair from where I dictate this
message
Sitting alone in the room, I started to analyse the
state of my physical condition
I arrived at the shock decision I was very very weak
as I had to take a knife to open a plastic top bottle
of water
Two ladies from the physio department came to help me
with my breathing technique .... 60 years of asthma
has taught me most of what I need to know and they
were surprised to find my lungs pretty clear (a month
ago in Tours I had a serious asthma attack which even
the hospital had difficulties in clearing)
The love of my life is typing this for you and will
be transmitting asap
Love to all
Barrie
PS for Malcolm
As much as I would like to come to Xmas lunch in my
old 80's suit, the chances are slim but if you want
to book 2 places provisionall, you can do so
BTW I have not seen a computer since 14 July
------------------
Maitie first visit friday a message from Barrie
Today I had my first go at getting out of bed without hydrolic lift, just 3 nurses and a zimmer frame, it was bloody hard
I can't believe that in 3 months, my good leg has withered so much, it would not support my new super light body, 75kgs
Free from all attachments from the medical machines (at last) I hope to get moved to a different floor shortly
Special greetings to Stan and Jean-Pierre who I understand read this blog daily
Many thanks to John McDonald for his touching message
Thoughts of being only 75kgs once the plaster is off means that my 10 years old Savile Row suit might fit
So if you see some overdress smarty pants in the BRDC lounge, it might just be me
Greetings to all
Barrie
------------------
Wednesday
He told me that they are thinking of moving him out of intensive care now he is better.
The beds are at a premium in intensive care and he may soon be in the orthopedic department (on 3rd floor)
Barrie continues to have regular visits from his friend Rene and his wife Ha at lunchtime and a few more visitors in the evening
I will be in Paris from Friday, so more detailed reports will be available at the weekend.
Until then, thank you all for your support and keep sending messages
Maite.
------------------
Monday
The doctors are doing tests to find out the cause.
I had a chat today with Dr Lazare who is very pleased with Barrie
They have now removed the tubes for the dialysis, so slowly he has less and less tubes attached to him and is looking less like a cosmonaute....
I am returning to London Monday night but will be back in Paris on Friday lunchtime.
Our friend Rene will visit Barrie tomorrow and on Wednesday Alexis will pay a visit
So hopefully he will not be too lonely
Maite
------------------
Message from Barrie
After a peaceful night, I woke with a massive asthma attack which took the charming young nurse Elise Cassini over 2 hours to get under control, leaving me tired but breathing
Sorry there is no more exciting news from France sunny capital
I am now marking time till 27th when my surgeon will complete the final procedure
Greetings to all
Barrie.
------------------
Sunday
Sorry I didn't write last night but Alexis Barichella came with me to the last visit and he then took me for a meal, so came back late
He will go an see Barrie on Wednesday night and will go also the following week
Barrie was better yesterday, not so down as the previous day. I think he was quite shocked by all his emotions and told the doctor about it in the evening who said it was quite normal and that it would help to release some of the pressure he felt inside.
Last night Barrie has a slight fever but not sure why. They were going to investigate
He still has a hard time eating the hospital food but my ice cream goes down well as well as nice muscat grape and pear.
I will go and visit early this evening so that I can be at Gare du Nord at 19,45
Will do report for blog this evening on train
XX
MT.
Message from Barrie
Really bad day yesterday Saturday 11, I had 2 bouts of uncontrollable emotions, one brought about by asthmatic problems and seeing my darling, the second provoked by an extremely touching email by my daughter Natalie.
The doctors said it was quite normal reaction to all my traumas
To top all of that fully asleep at 11am the one awkard nurse decided to wake me to change all the sheets by switching the light on, then did exactly the same at 4am
Fortunately nurses like her are few and far between
Love to all from Barrie
saturday
He was very down which is quite unlike him but quite understandable under the circumstances.
On top of that, his breathing was not very good which means he gets stressed and the stess makes his breathing worst, so a real vicious circle.
I told him how well he has been doing and that he should not be discouraged.
Easy to say for me but for him progress is too slow and he would like to be able to get up and do his exercises.
I realise he is bound to have days like that but it is very upsetting.
I hope tomorrow will be a better day and that watching the GP will have cheered him up a little bit.
Maite
thursday evening
All is calm, Barrie eat some lunch, no too much, this is my fault as I found him a Sorbet, this he has been asking for since he regained conciseness!! So lunch visit all went very well, we had a bit of a laugh and there were no mysterious stories today. He was sitting upright in his chair again, however this does becomes a little uncomfortable after a few hours, so then we request to get him back to bed.
Having returned tonight, he had retaken the horizontal position and seemed fine again. He eat some soup, however main course was not very nice, he tried a bit, had a few veg and pushed the rest to one side, there was no way I would have eaten it!! Luckily for him I found another Sorbet delight, Raspberry and coconut, needless to say, he eat the lot!!
I left him in good form and he is now looking forward to seeing MT tomorrow.
Hopefully Paul has had the pics and will stick them up on the Blog.
Signing off,
Max
Much the same news for this evening, to
thursday lunch
Wednesday with Max
Just left another good visit, Barrie a little tired today but in good form, they gave him a little sedative last night to help him sleep, he much prefered to be sleeping all night rather than staring at the ceiling and watching the clock tick!
Took him a nice fresh melon, raspberries and figs , all from the local market. He eat a bit of each and liked very much. He had a cup of tea, no milk and then we had a look at the menu and put in our order for tonight to see how he does with some real food. So we have ordered, Soup of the day, steak hache, veg and compote for desert, not that he needs any more deserts, he has loads of fruit and M&S goodies left.
So all in all no problems, his mind fully ok, no wondering off anywhere. We had good chat about the usual, cars , Paris etc. Spoke to Steve, who had some positive thinks to say. Even that possible may be able to come home a few weeks after next Op, which has now been confirmed to be the 27th OCT, on the Eurostar!!!!
That would be amazing !!
Steve is making enquires today, ref Hospitals in London and will let us know in due course, anyway one step at a time, we have plenty of time to arrange the transfer and UK hospital. Dad has asked me to come and pick him up in our New Audi !!
That's it for now.
I am now on the bus off to Port St Ouen, see If I can find that Art Deco dining room table, not sure how i will get it back!!
Max
------------------
Tuesday with max
Hi Gang, having arrived at the hospital, feeling more than a little apprehensive, I was met by Steve Hansen and we had a chance to chat for 10 mins before seeing Dad. He was really please with his progress and explained that his kidneys had started to work again and hopefully this would be the last of the dialysis machine!! Fingers Crossed.
I was then pleasantly surprised to see Dad sitting upright in his bedside chair and I good form! We chatted quite normally about various things and I managed to stay until 3.15.
Dad managed to eat not only a Raspberry Jelly but also a Creme Caramel, I was very jealous, as they both looked so good!!
After an hour or so he was becoming a little uncomfortable and wanted to get back into his bed, so we arranged for this too be done. Whilst drinking some water in his bed, he managed to have a minor coughing fit and blew his Valve off in his throat! That instantly left him speechless. Simple Fix though, just plugged the valve back in and he could speak straight away again, this could be very useful later on!!
Dad was on the case the whole of the 2 hour visit, not once did he wander off to Never never land and I left feeling in a far better state to when I arrived.
He has now sent me away with a shopping list! Melon and sorbet for dinner tonight.
Let's see how he does with that.
That's all for now.
Max
Monday with Natalie
Sorry
about the delay in doing this – it was started ages
ago, but too many interruptions today! Here’s
the latest update…..
Hi
everyone
I
visited Dad in Paris yesterday, with great excitement
about being able to chat with him for the first time
since the accident. Initially, Dad wasn’t
making any noise when he spoke but then I realised
that the device which allows him to speak isn’t a
permanent fixture and I needed to ask the nurses to
fit it for him so that his words formed sounds.
It really was music to my ears to be able to hear Dad
talk. Under the circumstances, he was in
amazingly good spirits, although he is inevitably
getting pretty fed up with his
situation.
I
asked Dad if he fancied anything to eat and the
nurses moved him into the armchair so he was in a
better, more upright, position for this. Dad
has been eating very, very, little, so I brought with
me a few goodies, including some organic apple and
strawberry purées which come packaged in a soft pouch
so they’re easy for Dad to hold, eat and control for
himself how much he sucks out of the pouch. I
also brought a Marks & Spencer raspberry jelly,
which I was hoping he’d find refreshing and
reasonably easy to digest. Fortunately, he did
and polished off the whole pot, so I think this is
probably the largest amount of “real food” he’s eaten
so far! With hindsight and with Dad still being
a little bit shaky, I concluded that jelly perhaps
wasn’t the most practical food to expect poor Dad to
be able to keep on the spoon without a bit of
help!!!! Not wanting to rob him of small
opportunities to do things for himself independently,
I left him, in the main, to do a splendid job of
eating this himself!
Before
I knew it, the first visit was over but the first
thing we did on the evening visit was to launch an
attack on the next item on the menu which was an
M&S crème caramel! It was very encouraging
to see Dad beginning to eat - under my bad influence,
all sweet things! This visit was spent mostly
lip-reading because although Dad did still have the
speech device attached to his throat, it wasn’t
working. About two-thirds of the way through
the visit, an attending nurse noticed that it had
detached from a tube to which it needed to be
connected, which is why Dad hadn’t been making any
sound when he tried to talk (I’m sure there are a few
people who are probably now frantically trying to
find a supplier of these devices (minus the essential
tube) for me!). So we had about 5-10 minutes of
relief with spoken conversation (whenever Dad could
fit a word in edgeways, of course) before Dad’s
breathing became so laboured that the nurses had to
replace the device with the ventilator. So we
were back to lip-reading again!!! I was also
able to give Dad a bit of a moisturising session and
hand massage and noticed a massive difference in the
size of his now thin hands, compared how swollen they
were from the odoemae on my last visit just before he
left Tours for Paris.
All
in all, for me personally, it was a really worthwhile
trip, even if I could only be there for the day.
Dad was in a really “soft and gentle” kind of
mood and seemingly less fed up, for the second
visit. Although he became increasingly tired,
it was lovely to have had both of the visiting hours
with him being awake and communicative the whole
time.
It’s
anticipated that Dad may come off the ventilator
towards the end of this week. Steve Hansen is
going to perform Dad’s second leg operation when he
returns from holiday and hopefully Dad will then be
able to be moved out of Intensive Care and onto
Steve’s orthopaedic ward. In addition to
marking Dad’s progress and a new stage in his
recovery, this will also mean more generous visiting
hours.
Max
has arrived in Paris today, staying until Thursday
and then Marie-Thérèse will be there on Friday for
the weekend.
Love
Nat
xxx
Barries Blog
Barrie dictating paul the Chef typing. this is the first outgoing message i have been able to send you since the accident it is with your good wishes and encouragement and support of my wife family and friends-Thank you all that was why I was able to pull back from the brink I would like to extend special thanks to the cobra club for the help in my rescue we will have to meet at silverstone sometime next year.
I expect I have another 3-4 months before i am completely out iof the woods so thumbs up for now Barrie from Paris
friday Paul in paris
Barrie was a little drowsy as he had had some kind of injection he was sure he was about to be moved for a operation but I think it was just the drugs playing with his mind a little. Today he is on dialysis currently every four days the plan seems to be to get the dialysis to every five days then six etc .and gradually the kidneys will kick in and things will return to normal.
he was otherwise in good form and the plan is while i am here is for Barrie to write his own blog entry that may be tonight but I think most likely to be tomorrow while he is not on dialysis and sitting in his chair!
Barrie was starting to get quite lively before I left a definite sparkle in the eye so looking forward to the next visit.
Paul more later......
Thursday great news !
So the 1st of October is a date to remember !
He is now encouraged to sit everyday for about one hour and when I called this morning he was sitting down and the doctor took the phone to him so that I actually managed to speak to him
This was great. He was in the middle of a small asthma attack but still managed to speak for a few minutes
He is back on dialysis this evening
I am hoping for more good news every day
Thanks again to everyone for all your messages of support
All the best to all
Maite
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