Showing posts with label Congenital heart condition. Show all posts
Showing posts with label Congenital heart condition. Show all posts

Wednesday, 17 September 2014

The Ups and Downs of Living with Half a Heart

As part of our Handmade Hearts series, LHM’s young members talk about life with half a heart. To learn more about Handmade Hearts, click here. 


Carys (18, DILV) describes the ups and downs of growing up with half a heart, her aspirations for the future and how LHM has helped her on her journey.image
"I was born in 1996 with Double Inlet Left Ventricle, Hypoplastic right ventricle, hypoplastic aortic arch and Transposition of the Great Arteries. At four days old I had my first of four open heart surgical procedures at the Birmingham Children’s Hospital, where I received care until I was 16. This was when Surgeon Mr Bill Braun crafted my ‘handmade’ heart. 
My first three operations were as planned – my Fontan circulation was completed in 2001 and I was lucky that all of my first three ops went well and I recovered pretty quickly.  However, at age eight I went into hospital for a cardiac catheter for a partial fenestration closure, only for Dr Wright to find a large blood clot in my pulmonary artery.  A two night stay turned into over two weeks and full-blown open heart surgery.  I wasn’t impressed – although skating up and down the ward on my drip stand a few days post-op nearly made up for it. Looking back I was so lucky that the catheter happened when it did – if that clot had broken up it could all have been very different!"
Click here to read it in full.

Monday, 8 September 2014

Transition Event


At the end of August, Suzie represented the charity at a cross London event organised by the GOS, Brompton and Evelina/St Thomas’s team to help their patients  beginning the move from Children’s to Adult services.
Transition is for some a worrying time. Making the move from the team that have looked after you since you were born to a completely new team can be very daunting for the young adults as well as their parents. The Transition Event was created to help young people understand what moving from one service to another is all about and to explore issues about living with a congenital heart condition. Many of the units also hold their own transition events where their young patients can find out more about their own unit and meet the adult cardiac team who will be looking after them. 
This was a new event, hosted by the British Heart Foundation, where lots of the national charities as well as the charities that work at the three London hospitals were invited to let young people know about the services they provide. I was there to talk about the Zipper Zone Youth group which young LHM members from the age of 10 upwards can join. I had copies of our newsletter and our new Youth stand which one of our youth members, Luke, helped us create following his work on an art project.  It was great to meet the teenager and some young adults and chat to them about the challenges that they face. Some of them gave me their details and will be joining the youth group which is great.
There were also lots of other organisations there highlighting different services and support. Prospects – careers advise, Beat Bullying and Changing faces helping people talk about their scars.
Thank you to the teams that invited us to attend it was a great opportunity to talk about what we do.

Monday, 18 August 2014

Film Review: #MyStoryTheirStory

One of our young members, Lucy, is also part of the press team for meet@teenheart and went along to the #MyStoryTheirStory premiere down at The British Film Institute at the end of July. She's written a great review about what she thought about the films, and the day in general.


A few weeks ago, I was headed back to London, where I was shown the two new films made by the British Heart Foundation. Here is my review of the day.


We entered the BFI Southbank Cinema. This cinema had a restaurant and seemed to have a lot of historical value, shown by the pictures on the walls, its information service and gift shop. When we entered the theatre, there were photographers and many young heart patients, and representatives from other heart charities. Also, there was someone dressed up as an elephant, greeting everyone at the door. This was clever, it tied into the films we watched, but I won’t spoil it too much!    

We enjoyed the films, and afterwards some of the crew, cast, writers and the direction sat on stage for a question and answer session. They let us in on the whole experience of making a movie. You could tell that there was a lot of work put into these films, and a lot of passion also. It all began 2 years ago when some heart patients were sharing their stories and came up with a script that was interpreted into these films. The actors were cast, some of which were heart patients and some were not. One boy, who was not a heart patient, said that being part of the film helped him learn a lot about heart conditions and how they affect the person’s entire life. It was great to see all the things that the people part of the film had learned along the way, it was a great experience for them to have. Everyone involved made the films as great as they were, and set them approachable for anyone to learn from them. 

After the question and answer session was over, we all joined together in the lobby for some drinks and food. There was also a photo booth for us all to enjoy.

Overall it was a great day, with learning experiences, funny moments and a fantastic time for all. If you would like to see these movies, or become involved with the meet@teenheart events, stay tuned on the YHeart Website- www.yheart.net

Monday, 4 August 2014

Year 7 & 8 Booklet

We're currently working on a new booklet for our education series about what to expect in Year 7 and 8 at Secondary School.

We really need some of our young members (ideally those of you who are in those years or just finished them, but if you're a little older that's ok too!) to have a read through the booklet that we've written so far and let us know if there's anything we've missed or any changes that we need to make.

Now, reading something that isn't for school might not sound like the greatest thing (especially with it being the summer holidays) BUT by helping us with these booklets you can help to ensure that younger members (like those who are starting secondary school soon!) feel happy about moving up to secondary school. Plus you guys have first hand knowledge of what it's like so you're the best people to give advice!

If you want to be part of it, you (or your parents) just have to email Laura and say you want to help with the booklet :)

Wednesday, 23 July 2014

Keeping Safe in the Sun

How great is it that the school holidays have started with such awesome weather?! I think everyone loves it when it's sunny and warm (maybe not so much when you're trying to go to sleep and it's REALLY hot, but in the days it's nice to have summer here!) The warmer weather may suit you if you have half a working heart but it is VERY important that you don't become dehydrated. Dehydration means that there is less blood circulating around your body and this effects the way your heart works, and how your kidneys work. It also can make the blood stickier so this means that there is a greater risk of getting blood clots.

Make sure that you have plenty to drink throughout the day (even if you don't feel thirsty!) and especially if you are on diuretics - if you aren't sure what medication you're on, talk to your parents. It's a great idea to carry of bottle of water with you wherever you go to make sure you keep hydrated.

Try and stay in the shade during the hottest parts of the day (normally between 11am and 3pm) so that you don't get sunburn. Keep an eye out too for signs of heat exhaustion - feeling dizzy, fainting, headaches, shivers and goosebumps - and tell your parents if you have any of these, normally a good drink and staying in the shade should help. Try and have catch up rests in the shade too so that you can reinvigorate yourselves! 

For more information about keeping safe in the sun look at our Travel and Trips Booklet.

Monday, 7 July 2014

meet@teenheart

The British Heart Foundation’s meet@teenheart programme offers 13-19 year olds in the UK who have heart conditions an opportunity to meet other young people like them, gain confidence, learn new skills and have fun.

They've got a great new events programme. These events will focus on providing young heart patients with increased confidence, communication and problem solving skills as well as building up their determination and resilience. Over the coming year they will be delivering three exciting one day events and a residential experience. The three one day events will run the same programme so you will only be eligible to attend the one closest to where you live :    

One day events...
· 13 August – Bristol -Register interest by 16 July
· 29 November – Manchester -Register interest by 1 October
· 21 February – Glasgow- Register interest by 4 January
Residential event...The Stunner is back for 2014!
· 21-22 August – Birmingham -Register interest by 16th July

You can register your interest now to join BHF for a creative adventure (combined with fun outdoor activity sessions on the residential). Register here: www.surveymonkey.com/s/BHFEvents

The events are totally free to attend and BHF will reimburse reasonable travel to and from the event.

If you have any questions, you can get in touch with Amanda Kenn: kenna@bhf.org.uk 

Monday, 23 June 2014

Ella's Story

At 9 years old, Ella has already had three rounds of open heart surgery.
The proud mum of a nine-year-old girl born with only half a heart has spoken of her daughter’s bravery in the face of three major operations Dawn Woodcock and her family have already seen ‘little smiler’ Ella overcome three heart operations after being born with a rare cardiac condition.
Mrs Woodcock was told at Ella’s 20-week scan, half-way into her pregnancy, that her unborn daughter had hypoplastic left heart syndrome – or only half a heart. She had her first life-saving open-heart surgery at London’s Great Ormond Street Children’s Hospital at six days old, a second at six months and a third aged four. In the long-term she could even face the prospect of a heart transplant.
Until then, 46-year-old Mrs Woodcock, her RAF logistics sergeant husband Martin and Ella’s 16-year-old sister Chloe mark every day as a triumph. And they have agreed to tell their story to mark Children’s Heart Week, a national awareness campaign for children with congenital heart disease. It is being backed by the Birmingham-based Little Hearts Matter charity, celebrating 20 years since its launch.
Ella – one of only 200 children a year diagnosed with hypoplastic left heart syndrome in the UK – attends the Horncastle St Lawrence Special School for children with moderate learning difficulties. Her proud mum said: “We take every day as it comes, one at a time, because we simply don’t know whatthe future holds. The family adapts to exactly how Ella’s feeling because, with only half a heart, she gets very tired very quickly. But she’s a very happy child and has smiled through everything, even at the nurses straight after surgery. We know there isn’t a cure, but she’s someone who adapts to her needs and just comes out smiling. Ella may require a heart transplant, but that’s in the long-term. The school is fantastic and we can’t say enough about Little Hearts Matter because, through them, we’ve also met some very close friends.”
Little Hearts Matters’ chief executive Suzie Hutchinson said: “Twenty years ago children with complex single ventricle heart conditions could only be offered experimental surgery to give them a chance of life. This charity evolved at that time because of the stress, fear and lack of understanding such complex diagnosis created. Parents handed their precious children over to surgeons not knowing if they would survive the treatment. We are taking the opportunity of Children’s Heart Week to celebrate the amazing children and families. Thanks to improvements in surgery, they now have a greater chance of survival. We hope to highlight the challenges they face every day as they learn how to balance living within the disability that having only half a working heart creates. Little Hearts Matter works to support, inform and empower children, young people and their families as they learn to cope with the roller-coaster life that comes when you live with only half a heart. Many will face a heart transplant as they move into their adult life. However, today, there are young people in their late ‘teens and early adulthood thanks to the innovative surgery that has been developed over the last 20 years.
Story taken from Lincolnshire Echo.

Wednesday, 18 June 2014

Hannah's Story

Hannah is one of our youth council members, as well as the first young trustee member with a heart condition for Little Hearts Matter. Here's a bit of her story:
When I was born, actually about 6 hours after, I was diagnosed with having Half a Heart. There is a list as long as your arm but I won't bore you.This is me at 15 months old, just after my first major open heart surgery. 
 
I was lucky that my array of conditions balanced my condition out for a lot longer than most children born with Half A Heart. But it was a very trying time for my mum and dad, and I'm really not sure how they got through the first few months to be honest. This is me at my second op when I was 9.
When we became members of Little Hearts Matter, everything became a lot more bearable and for the first time I met kids with the same condition as me and mum and dad could speak to parents with similar problems.
This charity has basically helped me become who I am today, yet many people are still not aware of Congenital Heart Disease and the life time effects.
Half a Heart, Not Half a Life!!!!

Monday, 16 June 2014

LHM Spring 2014 Newsletter

Little Hearts Matters's spring 2014 newsletter is now available here! It features an article explaining what an MRI scan involves, advice on the dreaded DLA, an article on Education and what schools need to know, family stories and lots more. Make sure to head to page 19 for the Youth News!

Monday, 9 June 2014

Supporting Pupils at School with Medical Conditions

The Department of Education has developed new guidance on how to support children with long term medical conditions in school. 
This is a big piece of work that has been supported by the Medical Conditions in Schools Alliance, a collection of some twenty charities that are all concerned with how children are looked after in school. 
Little Hearts Matter is part of the alliance and is delighted that new guidance has taken major steps forward to put children’s medical needs firmly within their education plan. 
We hope that it will help parents as they work to raise the needs of their children with teachers and local education authorities. To read the new guidance click here.

Wednesday, 4 June 2014

We Got Mail!

So I (Laura) always love to get mail (messages, pictures, jokes... anything!) from the young members of Little Hearts Matter because it really brightens up my day :) I always put a little note in the youth newsletter to ask people to get in touch because I love hearing from them. After the most recent newsletter came out, I had a great message and photo from one of our young members called Mia. This is what she had to say:

Hi, Laura! My name is Mia, and I have just got the LHM newsletter today, and I decided to write to you........and I can't ride a bike either!
Anyway, I was just writing to you about my Operation. I am the only person in my school who has half a heart, but my best friend understands me though. I am really lucky that I am still alive!!!! So thank you and everyone at LHM for Everything.

From,
Mia :-)  ♥

Those cupcakes look delicious! I wonder if I'll ever get cupcakes sent to me...

Monday, 2 June 2014

Hypoplastic Left Heart Syndrome

What is Hypoplastic Left Heart Syndrom (HLHS)? This 3D medical animation explains more about the condition, as well as information taken from the Little Hearts Matter website.

hypoplastic-left-heart-syndrome
Hypoplastic Left Heart Syndrome is a congenital heart condition (a problem that a baby is born with). It is made up of a collection of problems on the left side of the heart. Usually, the pumping chamber (Left Ventricle) is small (Hypoplastic) and the Mitral and/or the Aortic valve may be narrow, blocked or not formed at all. The body artery (Aorta) is often small (Hypoplastic) and there is a hole (Atrial Septal Defect) between the two collecting chambers.
The blood’s journey through the heart is very different from normal. The blue (deoxygenated) blood flows into the right collecting chamber (Right Atrium), through the valve (Tricuspid) into the right pumping chamber (Right Ventricle). From there it is pumped up to the lungs where the blood receives oxygen. The red oxygen-filled blood then flows from the lungs into the collecting chamber (Left Atrium) in the left side of the heart, but it will be unable to then pass into the left pumping chamber (Left Ventricle). As the valve will be blocked, it therefore passes through the hole between the two collecting chambers into the right side, where it mixes with the blue blood and follows the normal path to the lungs.
Whilst the Ductus Arteriosus is still open (patent), the blood will pass from the lung artery into the body artery and then around the body. When the duct closes, the baby will no longer have oxygen flowing to their body. Gradually they become sicker and die.
Hypoplastic Left Heart Syndrome is a fairly rare problem that occurs in approximately 1 in 5000 babies and accounts for 1% of all congenital heart disorders.
Follow the links below for possible treatments for this condition: -

Monday, 26 May 2014

Young Ambassador

In May, Ben and his Mum Louise were guest speakers at a Cardiac Conference in Birmingham. 
They were taking part in an ethics debate where doctors and nurses were learning more about information giving and care planning for children and young adults with complex congenital heart disease.
Both of them used their personal journey to describe the different times when they had felt anxious or stressed and to talk more about how individual care is so important. 
Well done both of you for bringing such an informed and mature voice to the debate.
Ben with his Mum Louise

Ben with Little Hearts Matter Chief Executive, Suzie

Saturday, 17 May 2014

Heart Selfie

Some of our young members came up with the idea of doing a "heart selfie" (a selfie with a heart!) to raise awareness during Children's Heart Week last week, and were asking their friends to do the same.

Here's some pictures of people who got involved:

Friday, 16 May 2014

Feel Good Friday - Special Edition!

This Feel Good Friday is a little something different, to mark the fact that we're coming to the end of Children's Heart Week. We've collected some of the wonderful little hearts moments that our young members have shared about their heart journey! Rachel talks about her sister, Sophie, who has Hypoplastic Left Heart Syndrome (HLHS). Evie has HLHS too and talks about her life with the condition, and Carys who also has HLHS has shared some brilliant pictures of her heart journey.

Rachel's Little Hearts Moment

Sophie is my role model. Before she was born, Sophie was diagnosed with a very serious heart problem called Hypoplastic Left Heart Syndrome (what a mouthful!). In short, Sophie has half a heart. 
By the time Sophie went to school, she had completed three stages of open heart surgery. As she got older, she got stronger and today she seems just like everybody else- happy, bubbly and full of energy. 
But having half a heart has its struggles. Sophie is part of the first generation in the UK to survive- parents and families just like ours are faced with a unique set of challenges and an uncertain future.This is where Little Hearts Matter comes in. Little Hearts Matter is a UK run charity, and a gift to families like mine. They offer ongoing support, allow families to access the latest information, and give Sophie the opportunity to meet other children with her condition. Without them, we would be lost. 

Evie's Little Hearts Moment

When I was born, I was very ill and was diagnosed with a life-threatening heart condition called Hypoplastic Left Heart Syndrome. In other words, I only had and still have half a working heart. 
After three lots of open heart surgery before I was four, I began to grow like a normal baby and with the care and support of my brilliant Mum & Dad, I have been able to enjoy most things that children do as they grow up.
However, what has made it more bearable is the support, love and advice that Little Hearts Matter has provided me and my family.
Little Hearts Matter is a UK run charity, small yet perfectly formed, and offers ongoing support to families like my own, holds their hands as their children go through surgery and then begin to thrive, as well as provides all important information to help them make the best decisions. However, more importantly Little Hearts Matter has given me the opportunity to meet and become special friends with people facing the exact same challenges I face. Without them, I'd live in a very lonely place.



Carys's Little Hearts Moment

Photo: 'a picture that sums up your heart journey' #littleheartsmoment #chdawareness
Embedded image permalink




So, that's a few Little Hearts Moments that some of our young members have shared with us! Make sure to share your story and use #littleheartsmoment!

If you'd like to support Little Hearts Matter, you can donate by texting LHMO14 £2 (or the amount you wish to donate) to 70070.

Remember, half a heart - not half a life.

22 Year Old with HLHS Lives Life to the Full

Woman born with half of a heart lives every day to the fullest, unsure of tomorrow (Article from WCPO)
Doctors told Tri-State parents that their baby girl wouldn't live long because she was born with a heart defect. But 22 years later those doctors stand corrected.
Meghan Roswick lives with half of a heart due to a life-or-death decision her parents made more than two decades ago. "I was born with a congenital heart defect called hypo-plastic left heart syndrome," Roswick said. "Which means I was born with virtually half a heart."
Patty and Rick Roswick, Roswick's mom and dad, consulted the doctor when their daughter was born in danger. "We asked the doctor what he would do and he said honestly if it was his child, he would give her morphine and let her die," Patty Roswick said. The Roswicks found a new doctor who was willing to perform experimental surgery to reroute Meghan's blood circulation. The procedure would force the right side of her heart to do the work of the left. "First surgery I was 11 days old, second surgery at six months, third surgery at 13 months, then heart failure again and had surprise fourth surgery," Meghan Roswick said. 
From that point she began pushing the envelope every chance she got by taking up various sports. "I started gymnastics, and my mom was on the phone with the surgeon, saying, 'Is this good? She's ramming herself into the vault, falling really hard on the bars. Is this OK?'" Meghan Roswick said. "(The) surgeon said, 'Yep, it's fine. That's why we do this.'" Her adventures didn't stop with gymnastics. She's pushed herself to the next level ever since. "It gives me kind of a rush," Meghan Roswick said.
"We made a decision that we weren't going to limit her, nor say, 'Meghan, don't do that,'" Patty Roswick said. Roswick took up skateboarding three weeks ago. She skied over the winter. She has the symbol for adrenaline tattooed* on her neck. "I always just wanted to live, to feel adrenaline pumping through my veins, to prove those doctors wrong," Meghan Roswick said. "Who said I would never have a good quality of life?" Roswick makes each day a new adventure, but she's not in the clear yet. Within the next few days, she is scheduled to undergo tests to see if she needs more surgery. "It's really scary, especially getting older because you don't know," she said. "The oldest people with it (hypo-plastic left heart syndrome) are not much more than 10 years older than me, so sometimes I think to myself, I only have 10 more years."
Most of Meghan Roswick's time goes to things that don't make her worry. "The time we have on this planet is short," she said. "We never know when our time is up and I want to do as much as I can, jampack my life with a bunch of experiences and adventures."
You can keep up to date with what Meghan's doing via her Facebook page.

*There are things for you to consider when you have a single ventricle heart condition if you’re thinking about piercings and tattoos. All tattoos and piercings carry some risk and most cardiologists and health professionals recommend you avoid tattoos and piercing altogether. Any procedure which breaks the skin carries a risk of introducing bugs into the blood stream. These bugs can settle on the heart causing endocarditis. The most important thing to know is that good hygiene is vital. Keep the area clean with a skin disinfectant containing alcohol or chlorhexidine before and after the procedure, until the wound is healed.
Remember, the decision to get a piercing or tattoo is yours, and if you choose to proceed, this list will help you make the procedure as safe as possible:
  • Visit a reputable place that follows rigorous hygiene guidelines
  • Make sure pre-packed sterilised needles are used only once and then thrown away
  • Ensure left over ink is thrown away
  • If the piercing becomes red and sore, you should remove the ring/stud and seek medical attention
  • If you need to remove the ring/stud because of infection, you should not replace it until the infection is completely cleared

Saturday, 10 May 2014

Take a Little Hearts Moments with our Thunderclap

As you may know, Children’s Heart Week will be taking place from May 12-18th this year. To celebrate, Little Hearts Matter (and now us!) are asking you to join a Thunderclap and take a #LittleHeartsMoment to raise awareness for children and families affected by single ventricle heart disease. 

We’re asking you to join here by pressing support on Facebook, Twitter or both. That’s all you have to do! Then, on 18th May at 12:00pm a message will be posted from your account saying: 
“I’m taking a #littleheartsmoment for children with only half a heart. Because Little Hearts Matter.http://thndr.it/1f3xxV5”
Simple. And it would be even better if you could then ask your friends to do the same!
Find out more about Thunderclap through Little Hearts Matter's blog here

Monday, 31 March 2014

Cardiac MRI Scans

Many children and young adults now undergo MRI scanning as one of their cardiac tests. At our Open Day on Saturday Simon McGuirk, a Radiologist, showed us a film that the Birmingham Children's Hospital team have created to explain a bit more about the test so that children and young people will worry less when they have their MRI appointment.
If you are looking for more information about going into hospital or an outpatient test visit your hospitals website, they may have films that will help you and your children prepare for your next visit.

Wednesday, 26 March 2014

Mother's Day

Add a Little Heart to your profile picture and let your friends know you're proud to know, love or be a #heartmum caring for a child with half a heart this Mother's Day. Follow the link and press "Add to Facebook/Twitter" and join us to say THANK YOU to all the LHM #heartmums working so hard to care for their children this Mother's Day. http://twibbon.com/support/heartmum

Tuesday, 25 March 2014

Some Musings from Andrew...

One of our young members, Andrew has written this blog piece about the Open Day on Saturday, living with half a heart, and why you should smile if you have half a heart :) Oh, and something about guinea pigs...

Hey everyone! I'm Andrew and I have Hypoplastic Left Heart Syndrome (HLHS). It was lovely seeing lots of you at the Open Day and I'm sure you’ll agree that it was a great day! :)

I'm a people watcher. I'm not a massively sociable person. I’d happily have a conversation with someone, but also, I’d be just as content sitting in the corner in my own little world (Yay for being introverted!). And as I was sitting in the corner, watching on on the morning’s happenings I just loved how everyone was smiling and happy! I'm sure if you put 50 young people who didn't have heart conditions in a room together they wouldn't be as outgoing and chatty as we all were on Saturday, but because we have this common ‘thing’ that unites us, I feel like we’re all great friends without knowing much about the other person! I guess it just made me happy! :’) (cue emotional music...).

As much as Little Hearts Matter being around for 20 years is a long time and an amazing achievement, in the grand scheme of things, 20 years isn't that long. The surgery that many of us went through when we were born is still relatively new, so as I stand here, an 18 year old guy, I feel really old! When I was born, Dr Norwood, who came up with the Norwood procedure, (aptly named...) came over to the UK to perform the surgery on me and teach the medical team in London how to do the surgery, so I think I was the second survivor of HLHS from London because of Dr Norwood. That is a weird thought. What also is weird, is that I've never met Dr Norwood since, so I've never been able to meet, let alone say thank you (and give a big hug) to the guy who saved my life... But I guess that’s why doctors and nurses do an incredibly amazing, fantastic job. They save the lives of regular people like you and me everyday and don’t always get the recognition that they deserve.

I'm going to be honest and say that there are times when I go “man, having half a heart really sucks!” Being the one that’s left out at school, or not being able to go somewhere because I'm too tired or whatever it may be, I can’t deny that fact that there are times when I just wish I had a whole heart! There are also times when the thought about having half a heart really excites me! The relatively new surgery that we went through when we were born has now been perfected on us and is a fairly routine procedure in specialist cardiology centres and is saving lives daily! Because of you and what you've been through, lives are being saved! You are amazing! It’s not just the doctors and the nurses that are the unsung heroes. Because of what you've bravely been through all of your life, children now have the chance of life!! That’s the exciting bit!!  We are ground-breakers, not guinea pigs! You are special, unique and the best version of you that there will ever be, so don’t let anyone tell you that you’re not good enough!!

If that’s not a reason to smile, then nothing is! I'm sure that every smile at the open day brought hope to a family who are just about to go through what we've already come through. So when the going gets tough, just remember that what you've been through and whatever you go through in the rest of your life, is giving another child the chance to live.


Phew! That was deep and meaningful! So to lighten the mood, here’s a picture of a dancing kung-fu* guinea pig. Adios.


*Andrew emailed a dancing guinea pig... But Youth Leader Laura has a stupid laptop that didn't want to show the image and she couldn't find a dancing one but she did manage to find a kung-fu one so...