Conference Day 4

Always at a conference there are one or two things that really stand out for you, and I'd been waiting for this to happen.  My curiosity had been spiked by a talk to be given by Prof Tony Holland about Vagus Nerve Stimulation, something I'd never heard of before.  What happens is that something similar to a pacemaker is inserted just beneath the skin on the chest.  It is designed to release electric impulses which stimulate the vagus nerve in the brain.  This type of treatment is used for patients with epilepsy and, during trials, it was noticed that patients lost weight.  So a trial was set up for 3 adults with PWS.

Presentation of this talk started with a brief introduction from Prof Holland and then each person with PWS spoke about their experiences, and then the parent spoke about the noticeable differences in behaviours, weight loss, appetite suppression etc.  The results were interesting.  Sadly, there was no weight loss, but there were noticeable changes in behaviours cited by both those with PWS and their families.  There was a very noticeable decrease in anxiety and stress, and also a decrease in the interest in food.  Tests were carried out at the beginning of the trial showing a timed session of "all you can eat" and done again after some months of treatment.  In the second "all you can eat" session, the interest in food, and consumption, was lower, although there was no overall weight loss.

What interested me most was hearing from the very articulate three adults who had undergone this treatment.  Each spoke highly of their increased confidence and lessened stress and all recommended this to anyone with PWS!  One lass said that without this measure of self-esteem, she would never have been able to get through what was the happiest day of her life - her marriage!

What more could you ask!

Conference Day 3

What can I tell you about today?  One of the most interesting issues in PWS which has turned up again and again, is this conference is about "delayed gastric emptying".  In other words, the contents of the stomach,  in the general population, take around about an hour to go through and into the intestines,  but take much longer in PWS, taking one hour 40 minutes.  So what does this mean?  It seems it could explain the gastric reflux that some suffer more than others, and the slower emptying of the stomach can cause a build-up of food which, if a person goes on an eating binge, can contribute to gastric necrosis (where the walls of the stomach are extended so much they thin out and can burst).  Also, the slower emptying can build up in the gut causing chronic constipation which is something  many people with PWS suffer from.  After listening to a few speakers who all mentioned this issue, but in different contexts, it all started to make a lot more sense.

Also very interesting was work done by Dan Driscoll et al on the nutritional phases that our guys go through, from birth to adulthood.  They did some tests with children who all had the same amount of calorific intake with no change and noted that the weight tended to suddenly increase at around 8 yrs of age.  They measured the amount of Ghrelin in the system (an appetite increasing hormone in the stomach) and found it was present in increased amounts which coincided with the sudden weight gain although appetite and calories had not been increased.  The inference is that obesity begins before the appetite increases, ie Ghrelin is probably involved in the increase of body fat, but not the hyperphagia.

I listened to an excellent talk by Jan Forster about insomnia, and her second talk about the need for routine. More of this on the blog later.

There was a blip in the catering front at lunch-time where catering had been done for far fewer than there actually were.  We were milling around outside waiting for sandwiches to come and without fail, everyone commented on how it must feel to have PWS!

Then there was the celebration dinner - held in a huge marquee with dancing and dancers (from a special dancing troup of wonderfully talented dancers with Downs' Syndrome) and everyone enjoying themselves.  Parents I spoke to all said the same thing, how wonderful it is to meet parents from all around the world.  Not only that, there are plenty of opportunities to speak to the professionals as many of them stay longer than just their two day conference and speak at the parents' conference too.  The pictures tell the story...

Conference, Day 2

Fitzwilliam College, Cambridge

Pictures are of the grounds of Fitzwilliam College in Cambridge.  It's one of the newer colleges so the buildings are more modern than the older ones.  The weather, as you can see, is fine and hot.  It has been this way for many days now with temperatures reaching 30C.  Thankfully, two of the main rooms where the conference is being held, have airconditioning...

Entrance to Fitzwilliam College

Day 2 saw the completion of the Scientific Programme and the Caregivers' Programme.  I was interested in reading some of the posters.  There was one from Israel about pre-natal diagnoses of PWS and whether there are vital 'clues' in utero that might indicate the presence of PWS.  These came mainly from various measurements of the foetus when compared with a normal growth rate.  There are differences in growth, head circumference etc and so now it may seem possible that in the near future pre-natal tests can  in the done in the first few weeks of pregnancy.  I learned that since this has been put into practice for Down Syndrome, the percentage of DS births has diminished considerably.  It is surely an ethical dilemma.

A long-term follow=up study has been done on patients previously presenting with psychotic illnesses, looking at the recurrence of any further incidences and at the general health of the individuals since their partiuclar episode.  Of 20 patients, mostly with the UPD (uniparental disomy) diagnosis, only two had experienced a recurring eposide.  Of these two, one was UPD and the other was PWSDel (deletion).  The majority of patients were taking psychotic medicine, and ten out of 18 were taking more than one type. The conclusion was that relatively few people had more than one psychotic illness; that after regaining their health they maintained it, and that medication played an important role in helping maintain this balance.  This was a study done by Prof Tony Holland et al.

Quite a lot of information is now being gathered as to the often adverse affects of anaesthetic on those with PWS.  Having come through whatever operation it was, there are now some worrying anecdotal stories of patients displaying odd and different behaviours.  Talking to other parents, I found other cases of this happening.  The patient can present with hallucinations, confusion, poor sleep, violence, bizzare behaviour and so on.  It is suspected that these are triggered by their response to the anaesthetic.

I was interested in a poster looking at the amount of depression suffered by parents of children with PWS, particularly the mothers. thirty-nine completed the survey, of which 8 were fathers,  The results showed that 36% showed mild to moderate depression and severe depression was not found.  Personally, I found this rather comforting - it must mean that the support, information, and knowledge that is available today is much better and more helpful than it was some 30 years ago when many of us faced the complete unknown.

(Some views around Cambridge)

Conference: Day 1

From our Japanese children

The first day of the conference started with the Scientific presentations and, alongside this was the Caregiver Conference.  I am simply not able to report on everything (but there will be a report on the conference at a later date), so this blog will just be me talking about the things I have heard and seen.

Although the Scientific conference is always the first place you look to for any new developments, my first interest is always to do with how we can best manage and care for those with the syndrome.  Today I sat in on two of the scientific presentations that interested me, and the rest of the day was with the Caregivers.  The presentation "Can Oxytocin Help in Prader-Willi Syndrome" was of interest to me because of the studies being done to see whether oxytocin, in the form of a nasal spray, will help to modify "behavioural temper tantrums, perseveration, obsessive compulsive behaviours, manipulative conduct, sudden aggression and abnormal food seeking".  Thirty-one participants enrolled in the trial conducted at the University of Sydney, Australia.  Eight participants completed the trial with a lower dose; 17 participants completed with a higher dose.  The age ranged between 12 and 30 years and participants were selected because they had difficult or challenging behaviours.

Behaviours were evaluated daily by a primary caregiver:  hyperphagia, temper outbursts, skinpicking, obsessive and compulsive behaviours and under-reaction to pain.  At the end of each phase the carers also completed questionnaires about the individuals' general behaviours, sleep patterns, social skills and emotional liability.

After all the clinical trials were completed, the answer to the question, "Can Oxytocin help in Prader-Willi Syndrome" was, (and I quote) "No."

Apparently there were no differences noted in any of the above behaviours.

I guess this is disappointing since we all hope for something that will help those with PWS to be less ruled by their behaviours and become happier people, fitting into society.

After that, I sat and listened to part of the Caregivers Conference where a lovely young man called Aneil who lives in a residential setting here in the UK spoke with his caregiver about his life.  These are some of thing things he told us:

• Know and understand me.  
• Don't label me, I am individual.  
• Listen to me and advocate for me.  
• Prioritise the things that are important TO me and be realistic about what is important FOR me.

Somehow it always helps the balance of things to actually hear from the people we are always talking about!

.... More tomorrow!

Linda

Genetic Subtypes in PWS

When I first knew anything at all about PWS, there was nothing mentioned about genetic subtypes.  Either you had PW, or you didn't.  The thing was, in those days (some 30 years ago now) PWS was diagnosed clinically by the characteristics that presented themselves.  And, of course, often these characteristics were not very apparent in the small baby or growing child.  Often diagnosis was made in hindsight once the person had reached his or her teenage years and was presenting with obesity, non-stop eating habits, and challenging behaviours.

Making a genetic diagnosis was difficult and blood samples had to be sent away so that results were often weeks and months later.  Even then, the diagnosis would come back as a "yes" because a deletion on the 15th chromosome had been found, or "no", because the deletion had not been found.  And, as we know today, just because there is no obvious deletion it doesn't mean the diagnosis of PWS is incorrect.  A maternal disomy diagnosis (where the developing embryo has picked up two pieces of its mother's chromosome, instead of a bit from its father's) won't show up as a deletion.  And certainly the third diagnosis of imprinting, won't show up as a deletion either.

Scientists began to realise there was something more to diagnosis than just looking for a deletion and the breakthrough of different subtypes was made some 15 or more years ago.  What does this mean?  To the scientists and researchers, it is quite a significant breakthrough genetically.  To behavioural specialists, psychiatrists, psychologists and those who manage the behaviours, it is also a significant breakthrough and much work has been done on looking at the three types as individual groups, ie, those with the Deletion (also known as the Type I deletion), those with Maternal Disomy (also known as Type II), and those with the Imprinting.  To understand the theory behind all this, have a look at the article by Merlin Butler and Susie Cassidy.

Studies around the world have been done to try to identify different types of behaviour, and characteristics -  such as a pretty unique ability to complete jigsaw puzzles  (for those with the Deletion), a lighter skin pigmentation (for those with Maternal disomy), similarities with autistic-like behaviours (for the Imprinting),  a higher IQ for the Maternal Disomy group (often leading to more challenging behaviours) and many others.  But the main thing to realise about all of this is that your child is unique.  He, or she, will have many attributes gained from his or her upbringing, siblings, family environment that will make him/her quite different from any other child with, or without PWS.

We know that if it weren't for the scientists, researchers, and medical teams around the world, there would be no gains made in the strides taken to understand the syndrome, but we must also never forget that if it weren't for the parents' concern and love for their child, we would never understand the person behind the label of PWS.

A Special Story

Michela, a young woman with Prader-Willi syndrome. is getting married in October this year to Roberto. It all began by chance at the New Year’s Eve party on 31 December, 2007 when, in celebrating the coming of the new year, they met. Michela and Roberto did not know each other until then, but they both belonged to the same sports club where Michela practiced swimming, and Robert tennis-table, but for various reasons neither had seen the other.

"A party where,” says Roberto, “we were one of 20 athletes from the club among friends and others; one of those lucky chances.  Most of these guys at the party were from the PHB POL Bergamo non-profit organization where both Michela and I do competitive sports.”

While there he was enjoying singing and dancing, “then, I saw Michela and, believe it or not, we were sitting at the same tavolata but we had not even introduced.  There she was sitting all alone while the others were having fun, so I said at once, ‘you can’t not have fun!’”

“Then I went over to her and asked her to dance, and after a few attempts I managed to convince her and that was the start to our wonderful story.  We went with some friends to have breakfast in the morning and later, I jokingly told her not to go home and say that had found a boyfriend, but really it was so!”

“Then we began to go out; I knew her parents, both lovely people who welcomed me immediately.  We were all going carefully and slowly; Michela met my parents (she has a soft spot for my dad), so our story went on.

“Hand in hand together we faced all the difficulties we had to encounter (difficulty dealing mainly with the food, but also the fact that, however, I could not leave her alone) and thanks to her and my parents, we have every time  tackled every difficulty , resolving them without drama but with the understanding that we would always have to resolve them.

After three and a half years of engagement where Roberto and Michela  continued to get to know each other, share the same sport, do the same activities with the same enjoyment, they began their life together.

Roberto, who works as a surveyor, has renovated the apartment according to their needs where they have lived for one-and-a-half years already, in their made-to-measure apartment

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Michela is a multi-champion of Italian swimming and table-tennis and competes to have fun while Roberto says, "I really like to share all the emotions she feels and be close to her in every moment of her life and be able to make her happy.  For me it is my real victory in my life, and I know that the day has come that is the beginning of a life unique and special just like Michela is.”

Happy Mother's Day!

This Sunday (at least Downunder) it's Mother's Day.  A commercial gimmick, yes, and one that normally I don't worry too much about, as a mother.  But I always recognised it for my mother and loved the fact that she had a special day.  And, of course, there's Father's Day, and, bless him, he never really minded another pair of socks, or a plastic-handled screwdriver.

In a way, it's really more important for the children than it is for the parents - and it gives them something to think about!

So every year I get a card and a box of chocolate-coated almonds from my daughter - the one with PWS. In spite of, or probably because of, her disability around food, it's the one thing she loves to share and buy for others.  Fortuitously, all these gifts have arrived uneaten.  So far.  But it's the card I love best.  It usually says the same thing, but it still makes me a little teary when reading it:

"MUM!!
Happy Mother's Day.   It may not seem like this to you in the 28 years you've had to put up with me.  I know it hasn't been easy and we've had a few really troubled times.  But every second of the Day you've been there for us kids, especially me.  There has never been a second that you've wanted to Give up on me or the other two.  Mum Ure the BEST and I couldn't have asked for a better Mum.  Words cannot express how much you mean to me, your love and support unfaulting.  I couldn't have had a Better Mum than you.  Thanks Mum.
Love for ever"

I'm pretty sure my daughter is not unique in her effusion for her mother.  There does seem to be a really strong bond between the child with PWS and his or her parent(s).  Usually it's the mother who holds that bond, for some reason.  Often the two parents are played off against each other and, with the limited understanding of the child, it becomes "love you/hate you" when simmering point is reached.  But, no matter what the situation (and I see, this year, my daughter has lifted the level to "really troubled times"... with good reason...), there is this undying love expressed in a way that only they can.

The "troubled times", although extremely difficult, have to be assigned to the syndrome and, if possible, not to the child.  Hard as it is to let the issue go, if you can eventually see past the trouble and recognise the vulnerable child underneath (no matter what their age), then this is your reward.

So, to all the mothers around the world, no matter what the day, "happy mother's day" to you!