Sunday, 5 April 2009

Robin Watson adds to his comments on Mr Broomhead's photo


My name is Robin Watson and I was a patient at The Marguerite Hepton Memorial Hospital between 1941 and 1948. I was born on 11th December, 1936, in

Leeds. So
I must have been about five when admitted from Leeds General Infirmary.

In about 1943/44 I was sent home for about 9 months and then went back after
the T.B. hips flared up again. After a long time of immobilisation (standard treatment) and operations, I finally had a career of nearly thirty years in the nursing profession. A case of prisoner turned warder!!



The next photo is a mystery to me, it wasn’t taken on a visiting day, because we
would have had more space between the beds and our lockers would have been there. Furthermore, since we were church-mouse poor, there wasn’t a camera in the family. Perhaps a nurse took it, and gave it to me. It would be nice if someone new came along and shed some light on the matter.


As it is rather difficult to join in an established conversation half-way, I thought I would throw in random memories as they occur. Perhaps the first thing to mention is the names that I remember. Patients: Kenneth Inkpin, Michael Hawkesworth, Michael Grainger, John Taylor, John England, Geoffrey Gresty and Malcolm Dawson. Remembered because we all went on to Potternewton Mansion Special School after MHMH. Although the boys and girls were kept apart, I did know Delia Shaw on the girls ward because we were pen pals. [Note from Jane; Some of these must be in the photo of the ward posted on March 26th. Does anyone recognise themselves?]

Does anyone else remember having a pen pal
in the hospital? Other individuals include those already mentioned; Matron Downs, Miss M.A.Budd (Headteacher), Mr. R. Broomhead, Mr. A.B. Pain and Mr. Clarke (Consultants)

The book prize in this photo is entitled "How to see Nature" by Frances Pitt, who broadcast on the Home Service. The first line reads "The best way to see nature, is on one's feet". It wasn’t until years later that I saw the humour of that; at the time I was learning to walk again wearing a leather spica on one side and a steel caliper on the other side!!

Thursday, 26 March 2009

Robin's photo of the Big Boys Ward veranda

A view from the admin block end of the verandah, looking toward the main road. At the far back can be seen the houses on the opposiite side of the road, I think they were bungalows.


To the right is the avenue of chestnut trees which was the main drive. At the far left can be seen a corner of the baby ward. It looks as though there are about ten beds on the verandah, and most of the patients appear to be in bi-lateral abduction frames (frog splints), already described previously. I am one of the patient's in that row, not sure which!! and the year is about 1946.

Oh, for perfect recall.


I don't have any ideas about the man on crutches, but he seems involved with the younger lads with what appears to be embroidery. I remember we were taught knitting, sewing, embroidery and, I think, rug making. Looking at the shadows of the beds on the verandah, I wonder whether it i san evening session with a voluntary worker, and the crutches are incidental. I would be about ten years of age at the time, so I can't identify myself - unlike the girls who look individual. Perhaps it is the 'pudding basin' haircuts we all had.

Robin Watson comments on Mr Broomhead's celebration

My name is Robin Watson and I was a patient at the MHMH, Thorpe Arch from 1941 to 1948, with T.B. hips. As I am still re-reading all of the comments and memories from other patients, I will just add a little information about the photograph posted by Fred Dubber. The person sitting on the left with a bald head and spectacles, is, I feel sure, Arthur Bernard Pain, my consultant surgeon for about ten years. I lost touch with him after he discharged me in about 1955, but I did read later, that he had been made the Dean of the Faculty of Medicine at Leeds University.

Tuesday, 27 January 2009

Mr Broomhead's obituary

I came across this obituary at the Wellcome Trust Library some time ago. Fred and I thought it would make an interesting companion to the photo he posted a few days ago. It's from the British Medical Journal (Vol 288, 14 April 1984, p. 1170). The fact that his specialism was arthritis of the hip is relevant to Florence's experience.

"Mr R. Broomhead, formerly a consultant orthopaedic surgeon in Leeds, died on 3 February aged 81.

Reginald Broomhead was born in Beeston, Nottinghamshire, and was educated at Ackworth School before studying medicine in Leeds, graduating in 1925. He obtained the MRCS, LRCP in 1926 and the FRCS in 1927. At the Leeds General Infirmary he was house surgeon to Lord Moynihan. Attracted to orthopaedic surgery, he visited the clinics of Sir Robert Jones in Liverpool and Smith-Petersen in America to gain experience before becoming consultant orthopaedic surgeon to the Leeds General Infirmary at the age of 29. There followed appointments as visiting consultant to many hospitals over a wide area of the West Riding of Yorkshire. From 1946 he helped to develop the orthopaedic services at the Royal Bath Hospital in Harrogate. Always fond of children, he greatly enjoyed working at the Marguerite Hepton long stay hospital at Thorp Arch. In 1955 he left the Infirmary to go to St James’s Hospital, Leeds, where he worked until his retirement in 1967. In addition to his many hospital commitments he found time for a busy private consulting practice.

Mr Broomhead was largely instrumental in forming the Yorkshire Association for the Disabled, which, with minimal resources, opened St George’s House in 1952 for the young with chronic disabilities. For many years he was chairman and guiding spirit in this venture. Arthritis of the hip was his main surgical interest. After the war he travelled widely to study developing techniques and was one of the first to use the Smith-Petersen cup in Britain. Helped by engineering friends, he developed many new instruments, some of which are still listed in today’s catalogues.

Of his many other interests, the main one was cricket. It gave him great pleasure to be made a life member of the Yorkshire county cricket club, to which he gave his professional services for many years. He loved golf and was a regular player with a low handicap until recent years. He had a lifelong interest in music, playing several instruments; up to 1970 he regularly attended musical soirées in Leeds. He was a freemason and master at two lodges and achieved high mark in the order.

Doctors who were resident with Mr Broomhead still remember his kindness and consideration; to his postgraduate assistants his help was unstinted. His understanding and compassion for patients was a model for medical students. After retirement, he lived at Kipperford, where he developed a fine garden. He is survived by his wife Phyllis, a son, and two daughters. - JMF"

I wonder if the celebration in Fred and Andrea's photo was for his retirement??? If this jogs anyone's memory, do get into touch please.

Friday, 23 January 2009

Mr Broomhead's celebration??

Picture courtesy of Yorkshire Post Newspapers.

The other evening I was discussing Florence's sad experiences with Mr Broomhead with my wife Andrea. She said the name rang a bell and she was sure her late mother worked, as a housekeeper, for him in the late 1940s. Further she remembered a photograph her mother had been given by him and after much hunting around the photo came to light. It was taken by the Yorkshire Post or at least has a YP stamp on its reverse but is sadly not date marked.
The photo shows a celebration of some kind taken, it is thought, in Mr Broomhead's garden at his home in Adle, Leeds. Andrea's mother is seen standing at the very left of the picture. The questions are: does anyone recognise Mr Broomhead in the picture and what was the occasion, one obviously of sufficient importance to attract the Yorkshire Post. If you can answer either question or have anything to add please contact us via the blog email address.

Saturday, 17 January 2009

One last comment from Jane about Mr Broomhead's fusions

I was under Mr Broomhead, who performed a spinal fusion on me. I remember my parents telling me later on that the spinal fusion that I had was quite a new operation at the time, though I’m not sure about this – it might be worth checking it out historically. In my case, it worked very well – though the scar is a bit messy – and I wasn’t lame afterwards, like Florence, just a bit limited in what I could do. Maybe spinal fusions were easier to manage - after all, if you can't bend where the fusion is, you can bend a bit further up or down! So whilst I wasn't very supple, I could walk pretty well, play games (some better than others) and especially swim.

It might be useful to know, Florence, whether you arrived at MHH with rheumatic fever? Could you say a bit more about that when you have time?

Friday, 16 January 2009

Carole Reeves on conflciting surgeons' diagnoses

This is part of Carole's reply to Jane's query about putting up Florence's views on this. Jane had wondered whether this was rivalry between an experimental surgeon (Mr B) prepared to take risks, and a more conservative one (Mr P)who wasn't:

"As far as necessary or unnecessary surgery is concerned, I would have to do the research to determine whether these procedures were considered useful by the orthopaedic or rheumatology profession at the time and also in retrospect. She could have been part of a trial to operate or not operate, hence the selection procedure that she perceived to be biased towards private and non-private patients. But this is only guesswork on my part without seeking out the contemporary papers.

Basically, surgeons want to operate and physicians prefer to use 'conservative' management. Nowadays, it's unlikely that children with juvenile arthritis (I'm assuming this is what Florence had although she mentions rheumatic fever, which is a different thing, and the surgery carried on these patients was on the mitral valve in the heart, which is damaged by the bacteria causing rheumatic fever) would have surgery because the disease burns itself out and the management is always conservative - maybe with sparing use of steroids to reduce inflammation in severe cases. Also, they generally come under the care of rheumatologists (physicians) and not surgeons.

Hip fusion (arthrodesis) was a common procedure at the time for children with hip damage from inflammation or TB (both of which damaged the bone and cartilage of the hip ball and socket) and seemed to offer a means of restoring some degree of mobility and to reduce pain in the days prior to hip replacement. A number of our [Craig-y-Nos] TB children did have this procedure done, one of whom - Peter Wagstaff - went on to have quite severe spinal damage and now walks (with difficulty) with two sticks. So, I think possibly it was a case of therapeutic balance - balancing the long-term side effects of the operation with the effects of immobility and pain from joint damage. There could also have been personal rivalry between Broomhead and Pain (what a god awful name for a surgeon), which might be difficult to uncover without serious research."

Thursday, 15 January 2009

Comments on Florence's posting

Florence's memories give lots of food for thought! Is it right that you also went to a special school after hospital - as several of us did – Fred also had this experience, and a friend of his from the hospital days. I didn’t, though I don't know why. Maybe because there wasn't a suitable one near enough to where I lived (Pontefract), or maybe because my parents thought it would be best for me to go straight to mainstream school.

In fact I went to a local primary school – at the beginning wheeled there in a wheel-chair by my mother, then later I walked. That was quite difficult as I was different from the other kids. Not only couldn't run as fast, but I was still wearing a spika at the time, which because it prevented me from bending at the hip meant that if I fell I couldn't pick myself up on my own. Some people would help, others just stood over me and laughed. Probably they were embarrassed too, but it was very humiliating. To this day I’ve always been touchy about people coming to help me if I fall down in public, which has tended to happen from time to time, and more frequently since I had my hip replacement. I know they mean well, but I would ideally like to become completely invisible until I've been able to pick myself up and resume my imitation of being normal!

Often, like you, this makes me angry. And I think I was also a pretty unhappy teenager, too. You do a lot of comparing yourself with other people at that age, don't you, and I also think that because we had to learn to do lots of physical things rather deliberately we might have done more comparing than most. I moved awkwardly, and I hated my image in the mirror. Once the new free forms of dance (jive,cha cha, salsa and so on) came in and you didn't have to do the formal steps of fox-trot and waltz I really began to love dancing, but I was always too inhibited to trust myself and the rhythm of the music. As a wonderful Caribbean dance tune has it 'I feel it in mi waist' - but then my head gets in the way!

I found what you said about your family's reactions to your being in hospital really really interesing. I didn’t realise that sisters and brothers weren’t allowed to visit, though in fact several people mention it in their memories. It must have been very tricky on both sides, for them having to make space for a strange child who was supposed to be their sister, and for you having to find a space in the family.

I was my parents’ only child when I became ill, and they decided not to have any more while I was in hospital. They thought if I came home and found another child, I might assume I’d been replaced with a better model. Good psychology, I think now, though at the time I pestered my mother to have a brother or sister – preferably an older one!! By then I was 8, with my Mum coming up to 40 and probably not keen to start childbearing again. I wonder whether she might even have been quite relieved to be able to put off having another child – they’d had a lot of trouble having me.

There's a lot to say about the differences of opinion between surgeons, so I'll leave that till tomorrow.

Wednesday, 14 January 2009

Jane replies to Florence

Florence, I've contacted Carole about whether we can put such frank views up on the website, and her view is that of course we can. This is what she says:

"It's perfectly alright to put this up on the blog as it is. We have done the same with our [Craig-y-Nos] participants. It is, after all, Florence's experience and how she feels about it. That is historically acceptable and ethical. One of our ex-patients has written about being sexually abused by a ward sister whom she names and this is on the blog. The ward sister is still alive. One of our community workers - an ex-nurse herself, has attempted to make contact with her but without response so far. She hasn't sued us anyway! I wouldn't anonymise anything on a blog because the function of a blog such as yours and ours is to give a voice to the previously anonymous and to open up dialogue between others with similar experiences."

This is really helpful, and is what I personally think should happen. It also makes clear that none of us feel be inhibited about writing as we feel.

Florence Gill feels she suffered from surgeons' disagreeing diagnoses

Happy New Year! Let's hope it brings many new correspondents to the blog. The Wellcome Trust Foundation brochure Highlights is now out, which might bring in new people.

Here's the first posting of the year. Florence actually wrote towards the end of November, so I apologise for delay in posting her very interesting message. It became part of an interesting correspondence with Carole Reeves, so I decided to save it up and post the whole sequence.Here's part one!

"It’s some time since I last wrote to you about the Marguerite Hepton Hospital. I have written quite a lot in the rough and have been rewriting it to make it more legible. It takes me some time as my hand goes into cramps.

Cynthia says you were particularly interested in how you cope as a lame person and how you feel about one’s appearance. In hospital it didn’t enter my head as we only had mirrors for the head and shoulders. In the outside world you soon begin to know what it feels like to be different. Not school because most of us were in the same boat, but in the street and going out to work. Being made fun of, some copying your walk. People making remarks in your hearing as though we are deaf or unfeeling or a freak.

I didn’t take it lying down, if I could give them a slap I did, and I also developed quite a nasty bitter tongue and used it. I think I was rather an unhappy teenager. One boy used to follow me home and make fun of me. I did cry sometimes, but in a rage. I notice now when I am in a wheelchair people don’t look at you, it’s as if they don’t want to see you. I feel mad and angry even now as there was no need for the operation as I later found out.

When I recovered from the rheumatic fever I was put under Mr Broomhead and Mr Pain. Mr Pain told my parents to take me home to rest but Mr Broomhead had me put on the Thomas frame and sent to Thorpe Arch. He then told my parents if I had this hip fusion then I could go home sooner. No mention was made of the fact that this op would cripple one and cause damage to the lower spine, but he knew it would because when he asked his students what would be the outcome if the op went ahead one student said spinal damage. The doctors discussed this round my bed and I heard it. They think children don’t understand but I did.

I’ve already said we went to the LGI for operations at that time, and Mr Broomhead was ill, so nothing happened for a while, and then they sent me down to theatre and Mr Pain was operating and when he came out to see who was next he came to me and looked at my case notes, threw them down on my trolley and told the nurse I didn’t need an operation and to send me home. I would just like to say when he came out his apron was all bloody.

Much later, Mr Broomhead came back and I went down to theatre again. Two nurses came with the mask they put over my nose and began pouring the ether on and telling me to count to a hundred. I thought if I held my breath it wouldn’t work so I did, but I took the off my nose and threw it across the room. I fought, kicked and struggled but went down fighting until I knew no more.

The ending to this part of the story came with the forming of the NHS. I’ve more or less been having check-ups at the LGI since I was fourteen, and I saw a new specialist and he told me these hip operations were no longer needed and should not have been done in the first place. I was enraged and up to a point still am.

One other thing that makes a different to one on arrival home after five years was how one’s sisters and brothers react to you. When I got taken away I had two sisters and a brother, and one born while I was away. They were never allowed to visit so they didn’t really know me and for many years I felt an outsider apart from my brother; he was only eight on my homecoming but he was very welcoming.

There were quite a few private patients and they never seemed to have operations so I have to think we were guinea-pigs. My close friend Hetty Bryan felt the same way to me. We were in touch occasionally until her death some time ago.

I’m not too sure about this article being put on the computer. What do you think? Have you had anyone saying anything similar?

Tuesday, 16 December 2008

Season's Greetings


Dear all of you,
This is just to let you know that the blog has not died - I've just been stuck with a string of deadlines. One of them was for a little article about the blog to go in the Wellcome Trust's brochure, which is called Highlights. Carole Reeves, who is the Wellcome Trust's Outreach officer, and has been very helpful to me over the blog, invited me to do it. Apparently the brochure is distributed all over the world, so we hope it will bring in a new flurry of contributions to the blog. Carole has just sent me a copy of the brochure, just out. It's beautifully produced, and there we are on one of the centre pages. I'm hoping that, like last year's brochure, it will soon be possible to see it on the Wellcome Trust website, though it isn't there yet. I'll let you know when it is so you can go and see it.

Have a very happy Christmas holiday break, and I wish you all the very best for 2009, despite the gloomy outlook.

The Christmassy photo is courtesy of Fred!

Tuesday, 9 September 2008

Harry Dodgson is reminded of plaster beds


It is amazing how the posts bring back deeply buried memories.

Jane's post about the plaster cast making brought this all back to me. For a long time I had a posterior plaster but after my operation I had a full plaster from my shoulders to my hips. I remember the plaster sores which were very painful and had a terrible smell. After a while the plaster was removed in order to treat these sores but as soon they healed I had a new cast.
I recall when I was told I could learn to walk, however I first had to get accustomed to being in a vertical position. I was placed in a frame, made of wood I think, which enable me to be upright without falling over. After a while in this frame I must have been taught to walk although I don't recall that part of it.

After I was discharged and attended school, the headmaster, who knew I had had a long spell in hospital, did not know how to treat me and so came to discuss this with my father who told him to treat me the same as any other pupil.

When the patients were having lessons in hospital they had to write with pencils of course. Pen and ink was not possible. The result was of course that I did not know how to use a pen and ink. We had to use those awful pens with steel nibs and so I always had school books covered in ink blots which always got me into hot water. The headmaster had a short fuse and often threw the wooden blackboard eraser at an offending pupil. He was a good shot however as he never hit anyone.

Friday, 29 August 2008

Geoff Smith comments after spotting the blog & contacting us by email

I started training as an Orthopaedic Nurse at Huddersfield Royal Infirmary, as part of that training you were seconded to MHH, cant remember how long 2 or 4 months. I think only 2 or 3 groups were seconded, and then they were sent to a hospital in Sheffield. At this time (1971) it was not beneficial for nurses from a training point of view.


The staff were very friendly, and a lovely community atmosphere. The hospital had some lovely grounds, but not used. Nothing was locked up and you could go an raid the hospital fridge if you were hungry.


Gerry (Gerald Appleyard) was one of the Charge Nurses and that's how I got to know him.The Matron was called Weddall and her brother worked nights there. He used to make the porridge for breakfast. He had it cooking all through the night. He had a Ford Zephyr car and would go into Boston Spa and get us fish and chips.


Ward 3 was for older boys and Ward 4 younger ones.


Very few Orthopaedic Patients, some babies from Meanwood Hospital who had severe mental disability and stayed in cots all day, they were fed, washed. They had repeated epileptic fits and just awaited the inevitable. Most of their parents never visited.


There was a portacabin on the grass as you went into the grounds, this was

for admin staff.

Monday, 25 August 2008

Edward Green, at MMH 09/56 to 03/57. At aged 14, he was the oldest patient!

I came across your blog re. the above hospital. I was a patient from September 1956 to March 1957. I had an orthopaedic problem with my knee. I have lots of happy memories from my stay.

Aged 9 I took a really hard bang on my knee from a roundabout in a children’s playground. In the following 5 years the knee would repeatedly lock and I was back and forwards to Leeds General Infirmary to see an orthopedic specialist.

He eventually admitted me to MH Hospital for 2 weeks observation in September 1956, so that if it locked he would have a "reliable" witness. I thought "Great, 2 weeks off school”, as my Mam and I drove down the lane leading to the hospital in an Ambulance car. I saw all the kids on the veranda doing school work, and my bubble burst! I was 14 years and 2 months old, the next oldest boy was just 12.

MH. Hospital at that time was a probationary training hospital for nurses having to do a 2 year course then going onto larger hospitals, like Leeds General Infirmarly and Pinderfields [in Wakefield]. They started at age 16 then moved on at age 18.

Up to that time I had rarely come into contact with girls and couldn’t understand why I seemed to get more attention than the other kids. There where about 20 boys on ward 2, as it was known then, and I was the only one not confined to bed. I was amazed to find out some of the kids had been in hospital for years, being treated for TB, Polio and Perthe's disease. I became scared in case I caught one of the diseases until I was assured this could not happen.

I spent most of my time picking things up off the floor that had fallen off the other kids’ beds and passing comics, toys and any other item from bed to bed. On the day the orthopaedic specialist visited I was confined to bed. All our case-notes lay at the base of the bed. I picked mine up and tried to read it but couldn’t understand it, until I turned a page, and written across the full page in large letters were the words "TRUTH DOUBTFUL". I felt my face redden and quickly threw the case-notes back on the bed. I suddenly felt so alone and afraid. When the consultant came to me Sister told him I had been very active and very helpful on the ward - in other words there’s nothing wrong with him!

Two days before I would be discharged I was bouncing on my bed when my knee "locked". Ii screamed for Sister, she and 2 nurses came dashing from the office and witnessed my knee locked with a pea sized piece of cartilage protruding from the side of my knee-cap. The outcome was I had an operation, 12 pieces of shattered cartilage were removed (along with "that" page from my case-notes). I spent the next 6 weeks in a plaster cast, groin to ankle, but was still fully mobile, doing all kinds of jobs helping the nurses hand out and collect bed-pans and bottles. One job I enjoyed was rolling up the dozens of bandages on a small mangle like machine after they had been washed - they where used to strap all the kids’ legs into their frames and splints. Thirteen years ago, aged 53, I had a total knee replacement.

Christmas was a great time, with a doctor dressed as Santa handing out presents to us kids. The Registrar was a Mr. Yeomans, the Physio was Miss Anne Berry. I can only remember one nurse who I had a school-boy crush on, Margaret Brett, and Mary the cleaning lady. I have enjoyed writing about my 6 months in M H Hospital and many other memories have come flooding back. I do hope you have enjoyed my small contribution.

Sunday, 24 August 2008

Making plaster beds – a film about how they did it

Since the blog has gone a bit quiet, I though this might be a good time to share my rather curious experience of watching this film, last year before we started the blog. I thought it might interest especially those of us with TB spines, who spent much of our time at MHMH on plaster beds. I've mentioned my memories of this a couple of times (28 April 08, and again on 9 July when I promised to come back to it in more detail). So here it is.

It all started when I went to the internet to check some facts about how spinal TB was treated, including the use of plaster beds. I googled “tuberculosis of the spine”, and came across a reference to a film held at the Wellcome Library in London, called “A demonstration by diagram and illustration of preparing anterior and posterior shells in the treatment of tuberculosis of the spine in children”. So I decided to follow it up.

Because the film is very old, you have to view it with a member of the library staff in a special viewing room. So last July I made my first visit to the library – I’ve been a few times since then, and it’s a fascinating place with lots of interesting medical history documents, objects and pictures. My appointment was with Angela Saward, Wellcome’s curator of moving images, and I went with her to view the film in a special viewing room. She made sure I was comfortable and in a position to take notes, and offered to stop the film if I needed time to write, which I did at a couple of points. In fact, I was rather glad to have her there and that the viewing was set up in this rather academic way – it kept me fairly detached from what I was watching, rather than projecting myself into it more personally, as I might have done had I seen it on my own.

It’s a black and white silent film, quite grainy and faded in places, so the only sound effects were the whirring of the projection, and my own hasty scribblings. It was made in 1936 at Abergate Sanatorium, Manchester, and donated to the Wellcome Library by the British Medical Association Film Archive. Angela thought it might have been a training film to spread best practice at a time when there was no centralized training system.

It shows the making of two plaster beds on a small boy – an “anterior shell”, for him to lie on his front – and a “posterior shell”, for lying on his back. As the film progresses, the different stages of the process are illustrated with diagrams at the bottom of the film. I’ve tried to reproduce some of these to illustrate the stages. My drawing skills are not very sophisticated, but I hope the diagrams will help make the process clear.

The posterior bed they made in the film went up over the child’s head, as though for patients who had upper spinal problems, like some of you who have contributed to the blog. For this, the boy was placed face down on a frame, with a crossbar passing roughly under the stomach, to “ensure a degree of hyperextension of the spine” it said; in other words to keep it stretched and not curving inwards. His legs were bent and the shins and feet were raised by another pair of crossbars, one over the knees and one under the ankles – so that the finished bed would keep his legs slightly bent. (See diagram 1).



Diagram 1: Patient lying face down for making of
"posterior shell"




Next he was rubbed all over with Vaseline, and his head wrapped in a cloth. Then they laid strips of bandage-cloth impregnated with wet Plaster of Paris on the child’s body in a carefully designed pattern, slightly overlapping and patted down till they all melded into a single piece (see Diagram 2 below).

Diagram 2: Patient lying face down for making of "posterior shell". The numbers show the order in which the strips were placed, and the arrows the direction of the strips


In the film, the first strip went from the bottom of the child’s torso (leaving the behind clear) right up the centre of the back and over the head, and was carefully tucked in to follow the curve of the neck (1). Next came side slabs (2). Then a curved slab was placed round each shoulder just touching onto the central one (3), and another went across all three (sorry, I omitted this from the diagram, and I don’t want to re-scan it). For the legs, a single strip was placed along the back of each leg, from the groin right down to the ankle (4). Then bandages soaked in plaster of Paris were rolled back and forth crossways to this slab, moving from thigh to ankle and creating a curved shell (5). As the different sections were applied, they were smoothed and slathered down very firmly until they form a continuous whole, with seam-lines down them which looked like those on a certain design of dress, or the taped joins of the ‘liberty bodices’ I remember wearing later on.

Finally, presumably when the plaster had dried enough to keep its shape, you saw the whole shell being removed, and placed on a wooden frame. The final frames show the child lying on his back in the plaster bed on the frame.

The process for the anterior bed – made on the front of the body for lying in face down – was pretty similar, except that the child’s legs were straight, and there weren’t any crossbars to maintain the correct position of the spine. In this one, the leg slabs went to just above the knee, with no further bandaging to and fro.

As to how it all relates to what I remember, this is quite a difficult question. Angela asked me if we had been as compliant as this child, who kept so still I thought they must have used a doll – which Angela doubted – or that he was anaesthetized. Both processes, but particularly the one for the ‘posterior bed’, looked extremely uncomfortable, so perhaps anaesthetization was used. Yet I don’t remember any such discomfort, and I was certainly conscious throughout. What I do remember vividly was the feel of the plaster slabs, warm, wet, sticky and smelly, and the slapping and smoothing involved in their application. I imagine the Vaseline-ing must have been a strange sensation, too, though I don’t remember that either. I wonder how they cleaned it off us afterwards – we must have had to have some sort of bed bath, I suppose.

I mentioned this film to Cynthia Coultas when we had a long talk on the phone not long ago. It seems that by the time Cynthia was involved in this process at Thorpe Arch, they used single sheets, rather than strips, laying them over the whole back, or front. Apparently, each patient had an anterior and a posterior bed made, because we had to be turned frequently to prevent bed sores. Funnily enough, I have no memory of being turned, yet from what Cynthia says it must have been quite a frequent process.

So watching the film jogged my memory, but also left me with a whole series of questions. For instance, I wonder what happened to our muscles over so many years of lying flat, and what kind of preparatory physiotherapy we were given before the magic moment when we actually stood up to walk. Without any at all our legs would surely have crumpled under us!

I wonder, too, why I didn’t ask more questions about this all once I’d come out. I suppose at that age children take an awful lot for granted, and don’t question something which, though it appears peculiar with hindsight, was our ‘normality’. Then, coming home, it must have all faded into the background as I moved forward into a new ‘normal life’. I did tend to explain my inability to perform certain physical activities in terms of my having been in hospital – for instance, I always found it very difficult to sit on the ground cross-legged, but really without analysing it too much at all.

Does any of this jog memories for anyone else? Does it contradict your memories, or help fill them in? Or does it jog other memories altogether? Perhaps Cynthia will have a look at this, too, and fill in details from the nursing point of view. Please comment and add details, questions, differences of view, and so on.

Friday, 8 August 2008

Cynthia Coultas gives a nurse’s perspective on visiting limitations, and other aspects of nursing children in the

Rowland’s memories certainly back up the importance of parental input and the reason for modern day thinking and the changes to the care of children in hospital. Hence the development of programmes such as those at Great Ormond Street and others.
Like all the other things involved with caring for the sick, visiting is a multifaceted problem. There were unexpected problems when unlimited visiting was instituted, which it took time to sort out. By the time this happened I had moved on to the general hospital, but the principles are the same. On the first day we were all prepared for welcoming extra people to occupy the patients. Brilliant, we would have more time to get on with individual treatments.

As the doors opened, a flood of people surged forward to the bedsides of their loved ones. With them arrived shopping bags, wheelers and arms full of gifts. By 10 am. coffees and teas were being drunk from flasks, and by lunch time sandwiches were being enjoyed by patients and visitors alike regardless of diets! A dangerous situation for diabetics, etc. and nurses had no idea whether patients were eating or just hiding problems behind the aura of fruitfulness provided by their families. This trend continued until the last buses were due to depart and those with cars dawdled even longer.

After a few weeks of this type of scenario, patients, staff and visitors were all complaining of fatigue. Patients were exhausted and suffering from constipation and other associated digestive upsets, staff were unable to perform personal care without embarrassing the patients as they explained what they wanted the patients to do to cooperate, and visitors were finding financial implications on a long term basis.

Also needing addressing was where all these people were to sit. Inevitably the beds seemed the obvious place. Plenty of room for two or three. As bed clothes were pulled tight, wounds groaned under the pressure and wound healing was being delayed. Added to all this of course was the added risk of infections carried in unknowingly by the visitors. I will mention MRSA and then say no more.

Again my point is that there is no easy answer to any one problem and sometimes the tug on the heart strings is the lesser of many evils.
In general, I suppose we can’t overlook what things were like at the time. 1950 was a very early post- war situation, and it is always difficult to put oneself in the mind set of an earlier period and what was happening generally to children. Money was short for everyone so food as well as clothing and everything else had to be completly eaten or worn out before it was thrown away or even still passed down to 'little Johnny'. I remember my father saying that if I didn't eat what was before me it would be returned at the next meal. That was no idle threat! 'Make do and mend', was the quote of the day for making clothing last longer, etc.

Drugs then were very minimal and basic (no broad spectrum antibiotics for example) hence lots of fresh air and rest! TB itself was also something that doctors were learning about, and without the appropriate drugs to help in the treatment they were fighting a very difficult battle.

The point Fred made about the staff being young and inexperienced is also valid. Again this doesn't or shouldn't happen today because the training separates the nurses from the wards until they have gained some knowledge. On the other side of the coin nursing is a very practical work and full knowledge can only be gained at the bedside in order that the intangible can become intuitive. We were taught about diseases and what to look for in a patient who were unwell.

Today nurses are taught about health and have some idea if a patient admitted for a cataract operation is at the time of admission developing a further problem. Not to take over the Dr's position but to know when to call for his attention.

Monday, 4 August 2008

...and Jane responds again

This added bit about your later visit to the hospital is also very interesting - it always struck me as curious that such a little place as Thorpe Arch incorporated a children's hospital, a munitions factory, then a prison and the British Library (which I think is still there). I wonder how much of that was due to re-using buildings that already exist.

I was surprised to hear that you had to be quite so assertive about staying with your son when he had his operation - I thought by then it was almost commonplace for parents to be allowed to be with their children, but obviously it all took longer than I thought, or at least did so in some places. I've read quite a lot of stuff on how Great Ormond Street hospital led the change, but of course that was up 'at the sharp end' of medical practice.

I would have liked to be able to 'walk the place' as an adult, as you did, not only lay ghosts – more to conjure up a few, especially as I have such vague memories of the actual physical aspect of the hospital. So I was sorry it wasn't there any more when we finally got around to going (in about 2005, I think). At the same time, I can understand your feelings about obliterating it. A similar hospital at Craig-y-Nos (I've mentioned their blogspot a number of times, since it inspired ours) was housed in a castle, which is now a luxury hotel, and rumoured to have at least one ghost of a child. Presumably new-build houses won’t have any at all.

Sunday, 3 August 2008

Rowland replies – with his experience of the hospital as a patient’s parent in the late 1960s

It may be of interest to know that between Sept 1969 and January 1973 I served as a young prison officer at the Thorpe Arch prison directly opposite MHH. My middle son David who was born in Malta in 1968 with Telepes (club Foot) was actually operated on at MHH to correct the deformity. The Paediatric surgeon that carried out the operation, Professor Silk, an American on secondment to Leeds Infirmary, opened up the MHH obsolete operating theatre solely for that one operation.

I have to say at that time it was a totally different hospital from what I remembered but even so the visiting arrangements were by today's standards still harsh and unfeeling towards both the patient and the parents. After my experiences of MHH both my wife and myself made it quite clear that one of us would be staying with our child throughout and one of us did for almost a week until he was finally discharged.

My return to MHH was with mixed feelings hoping to make some sense of what happened to me there. Of course in 1973 it had changed considerably from what I remembered in 1950 and to be perfectly truthful it didn't hold the terrors that I thought it might. I was allowed to wander the grounds and hospital and as I did so I laid to rest some of the fears that I had. Personally speaking I am glad that the hospital was eventually pulled down and some better use made of the grounds. That may sound ungrateful especially of all the good things that came out of MHH and of the hundreds of children myself and my son included that benefited so greatly from its existence but I don't mean it to. It's just the way I feel.

Saturday, 2 August 2008

Jane responds to Rowland and Fred

Thanks for sharing these memories - it must have been quite difficult getting them down on paper in order, and you're the first one to have done it so frankly! Like Fred, I find they remind me of some negative memories, too, especially of being left at the hospital by my parents. I'd been transferred from a hospital in Wales, and had spent about a month at home, encased in a plaster cast. I remember lying on a sofa in the front room downstairs. Looking back, I can't imagine how my mother coped; she told me that in the first days when I got home, I regressed to a sort of baby-ish state when I wouldn't let her out of my sight for fear she'd disappear, I suppose. She even had to negotiate to go to the loo. So I felt desperately homesick when I got to Thorpe Arch, and I remember being told off because I wouldn't stop crying.

I don't get the nightmares you write about, but I was a very fearful child for quite a long time. do remember a lot of harsh treatment from some of the nurses. I still remember how one night a nurse took away the rag doll I slept with to punish me for being naughty - don't remember what I'd done - and gave it to the girl in the next bed. This doll was made for me by my Granny, and I think it was like a safety blanket to a smaller child. I cried and cried till in the end this girl got fed up and gave it back to me for a bit of peace. The nurse came to see whether I'd fallen asleep crying, I suppose, saw me with the doll, and took it away again... That kind of thing seemed like pure malice to me.


However, Fred had these second thoughts after responding to your email, which fit well with what I want to say here: "Maybe it's too easy to judge the MHH nurses by today's standards. Some of their actions would probably have been considered far less shocking fifty years ago, and were probably based on their own childhood experiences. Fred remembers his parents threatening to serve up uneaten food at the next meal time. My own parents' reaction to my pickiness was to take the plate away from me when they'd finished eating: "Oh!, so you don't want any more", till I got so hungry I ate pretty well everything that was put in front of me, with a few exceptions, like slimy mushrooms and tapioca (as I think I've said before). As their contributions to the blog show, many of the nurses were trainees and probably only in their teens with little knowledge of how to deal with awkward, stressed children in an alien environment.

I think the once a fortnight limit on visiting was the rule, actually - as you'll see from the other messages. What really used to bug us, though, was that the visit day would sometimes be postponed a week if it coincided with some apparently arbitrary date, like the 1st Saturday of the month. Then we had to wait three weeks.

I've done a bit of research into the way the rules on visiting changed, as child psychologists became aware of the damage early, sudden separation from parents could do to children. In 1956, under the Labour government of the time, the Ministry of Health set up a committee which took evidence from a huge range of people - doctors and nurses, of course, but also parents of children like us and child psychiatrists. They issued a report in 1959, called the Platt report, discussing the whole thing, and recommending more frequent visiting - though they recommended that it should be carefully managed in long-stay hospitals, where it was also important to create some semblance of a normal life for children, including school and independent play time.

Some of the evidence they considered came from letters in reaction to a series of BBC programmes. Only the scripts are left, and I've been able to see some of them in the BBC's Written Archives. They were broadcast by Woman's Hour, and some were outside broadcasts to village halls, to conduct a sort of panel discussion with local people, a bit like Any Questions nowadays, I suppose. Many ordinary people, but especially doctors and nursing sisters, were against more visiting, which they thought would disturb the ward routine and upset the children when the parents left. But the research showed that children settled better if they saw their parents more - couldn't we just have told them that!

After that, they began to bring in new policies and nowadays, of course, we have daily visiting and parents allowed to stay with their kids. I'm sure these would have created other problems for our parents - my home was in Pontefract, so the journey for my Mum was a long one, too, as she had no car, though I remember kind friends giving her lifts in their cars.

Thursday, 31 July 2008

Fred responds to Rowland Jagger's account.

Rowland was a patient during the time I spent at MHH, 1950 to 1952 and we are of the same age. He has awakened in me memories that I had long since forgotten or perhaps I had managed to shut them out where he has struggled. I found reading his account to be both heartrending and disturbing. I don't believe my life was scarred by the experience but it has had a lasting impact on me. I find it easy to withdraw into myself and am content with my own company. I am almost compulsively independent and find it extremely difficult to ask others for assistance, I need to be in control. Oddly enough I feel very comfortable being this way, confident that whatever life throws at me I can deal with and there have been challenges to face as is the case for everyone. I believe this resilience stems from the time at MHH.

Hospital antiseptic I remember as ether, but I've always liked the smell, can't say the same for the boiled cabbage but I don't mind the smell of methylated spirits even now. I cannot remember protesting too much against being strapped down in my frame but I do remember, when I first arrived, hoping that they weren't going to strap me down in one of those things.

Yes I have memories of unkindness, sometimes being subjected to mental cruelty but in my case it had the effect of hardening me up, if I kept my head down and didn't make a fuss, withdrawal I suppose, I could get by without becoming the centre of some nurses anger.

Looking back I remember the good times more readily than the bad, maybe my "conditioning" was more effective than Rowland's e.g. I cannot leave food on a plate and will eat most of what is in front of me even if I don't like the taste and maybe I began to believe I was "too big to cry". I suspect Rowland's will was probably more resistant than mine and he remembers the struggle more because of it.

I wonder how Rowland feels about the medical profession today, I have had to return to hospital for major surgery on a couple of occasions, admittedly they don't keep you in quite so long these days, but I had few fears of the surgery and only warm memories of the way I was treated by all the medical staff attending me. Even today I attend outpatient clinics and almost look forward to them, certainly without any trepidation.

Finally I wonder if Rowland had the same disorder I had, Perthes disease. It is a condition affecting the hip joint and my treatment was exactly as described by him down to regular x-rays and hip manipulation. I was completely cured, physically anyway, by my hospital stay. Length of stay was dependent upon how far the joint had worn before diagnosis and how quickly the hip ball joint recovered, in his case considerably quicker than mine. I am not entirely sure complete mobility would have been restored with TB and await someone more knowledgeable to correct me.