Wednesday, 10 September 2014

What is big, shiny, loud and can fit small children inside?



This is a picture of my euphonium…  What’s a euphonium?  Well I normally describe it as a small tuba or big trumpet, but it’s big, shiny and loud and small children could fit into it!  Most people have never heard of a euphonium and I’m not quite sure how I ended up playing it, but I’m very glad I did as it started my love for all things musical!  I also love singing and, together with Hannah, have been coming along to Little Hiccups since 2010 to run music sessions with the Thursday group.  Running sessions at Little Hiccups encouraged us to set up our own early years classes called Tiny Tempo which we've been running for nearly two years now (www.facebook.com/tinytempoleeds)

Even before they’re born, babies are listening to sounds or feeling vibrations and music can help babies and children to relax, to get excited, to bond with their parents and to communicate.  Every child is different and responds to and dislikes different sounds and sensory stimuli.  We plan sessions for Little Hiccups to incorporate all the senses and explore these likes and dislikes; from a hungry caterpillar session with tasters of different food to country garden sessions outside, complete with flute and euphonium duets (you haven’t heard this particular combination of instruments very often for a reason, but we like it…!)

We have loads of different percussion instruments and materials to feel and look at; shiny material with ribbons, animal fur, jangling tambourines and clock-like claves.  We try to have something for everyone and do whatever we can to include everyone and their personal preferences in each session. We even learnt every song from Frozen following a request from a child at Hannah House where we also work (and tried to pretend we didn’t love every second…!) At Little Hiccups, we try to include parents as much as possible and give simple ideas for things that you can do yourselves at home.  We think everyone can sing and enjoy music with their children, and try our hardest to make everyone feel comfortable with music, whatever their experience.

Little Hiccups is a very special and supportive group of people and we love our sessions there.  On a personal level, they have supported me through losing some of my eyesight a few years ago and being registered as visually impaired.  Having the continuity of the sessions there and the support of everyone to carry on with music really made a difference to me and is one of the reasons that I’m still working today.  I may not recognise anyone in the street but I can from the first note they sing!

Kathryn O'Doherty (Tiny Tempo)

Tuesday, 2 September 2014

The peoples march for the NHS



Below are the thoughts written by one of our families who are fighting to keep our NHS by joining the People’s March for the NHS which aims to highlight the rapid dismantling, privatisation and destruction of the NHS. First we had the Health & Social Care Act, then Section 75 and more recently Clause 119 of the Care Bill. The Government have legislated to open the NHS to the open market. The People’s March for the NHS believe every penny saved in the NHS should go back into improving and developing our NHS. They don't want to see private companies operating in the NHS under the heading of 'efficiency' when they know they are accountable to their share holders, who are only interested in maximum profit before patient health care. They encourage anyone to join them for a mile or two, or join them for ten or the full 300 miles, come to our rallies, just be part of the fightback.The March is still ongoing.

 Our family joined them in Leeds and they shared their thoughts below:

"On Friday 22nd August we joined the People’s March for the NHS. We (Mick, Helen and Rosy) marched from Headingley to Leeds City Centre. We joined the Darlington Mums who set out on a 300 mile march from Jarrow on 16th August and will arrive at the Houses of Parliament on the 6th September. The intention of the March is to publicise the creeping privatisation of the NHS which has accelerated since the passing of the Health and Social Care Act 2012. We decided to march in support of the NHS and against politicians and their mates picking it to pieces for profit. Our lives turned upside down in Sept/Oct 2011 when Emily (our youngest Daughter) started having infantile spasms and this has brought numerous stresses and strains. The idea of also having to worry how we would pay for the many medications Emily needs or that her care might be judged on how much profit can be made from it is frightening. You don’t know what you have got until it has gone. So please let the NHS focus on care and not cash."

For further information of the People’s March see link: www.999callfornhs.org.uk

Follow on Facebook: 999callforNHS
Follow on Twitter: #march4NHS



Wednesday, 16 July 2014

The Million Steps Fundraiser

The below was written by Rob Heckman for a Spanish publication. Rob is the son of Vince Heckman who is the very kind gentleman who bought an donated a Kangoo for Little Hiccups before even meeting us! It goes to show taht there are some truly amazing people in this world and I'll be honest - I meet a LOT through Little Hiccups. I think you'll agree that the article below is well worth a read! And many thanks to everyone who helped that day as we raised over the fantastic amount of £1200. You can read more of the Million Steps Challenge on our website at: http://www.littlehiccups.co.uk/millionsteps




"Social media is often portrayed as a negative aspect of the modern world. However some good can come from it. A year ago, we started to help out an anti-knife crime charity called Billy’s Wish that was organised by a close family friend whose son was tragically murdered. After working closely with the charity, our friend Paul Dove introduced us to another friend of his that had helped organise a day of football activities to fund raise for Billy’s Wish, Brendan O’Connor. We became very close friends and thanks to him we became aware of another charity named Little Hiccups which is based in Leeds and aims to help children with special needs and disabilities.

After hearing about this charity and what the mothers and children have been through, we felt the need to help out and support their cause. First of all we made a donation to the charity however after reading about a special needs buggy called a Kangoo, we decided that we would buy and donate a Kangoo buggy to Little Hiccups to give the children the opportunity to go places where no other buggy can go as the Kangoo buggy can be taken on terrains such as sand, woodland and even snow! It can be converted into a car seat and it also securely straps the child in so the mother can even travel down stairs putting the child at no risk.

After much talk with Brendan O’Connor, he informed us that a friend of his named Antony Newby was organising a fund raising event in Leeds that consisted in over 250 people running up 1,000,000 stairs. After much preparation, the day finally arrived and professional boxers such as China Clarke participated in the challenge along with everyone else. The target of a million stairs was completely smashed as the final tally that was counted was 1,219,786 stairs in around 6 hours! During this event, there was also the presentation of the donated Kangoo buggy to Little Hiccups. Former boxing world champion John H Stracey was kind enough to not only present the Kangoo buggy to the charity, but to also donate a signed photo collage of his career to help raise money for Little Hiccups.

After this chain of events helping out Billy’s Wish and Little Hiccups, us as a company have come to realise that there is a positive side from social media due to the fact that without it, we would have most likely never been introduced to Little Hiccups and therefore, we would have never been able to help out these two charities that our close to our hearts.

For any details on how to make a donation to either Billy’s wish or Little Hiccups, please follow the web addresses below.
http://www.littlehiccups.co.uk/
http://www.billyswish.co.uk/"

Written by Rob Heckman










Thursday, 27 February 2014

Fun at the beach



This picture for me says it all. Meet Jack (in orange), Jenna (in the rainbow) and Lindsay. I’m Katy and behind the camera. Jack is eight years old. Jenna is three and a half. The last time Jack was on the beach Jenna wasn’t even born. Accessing the beach before this day was ni-on impossible.

In the February half term a few parents from the Leeds based support group for families of children with disabilities Little Hiccups joined several other families for a leisurely stroll (and a few races) along Bridlington’s north beach. The difference between ourselves and the other families we met was that three of our children have complex health needs.  

National statistics back up what we as parents and carers already know. Children with complex disabilities (physical, sensory, behavioural, emotional etc etc) remain significantly less likely to participate in leisure and sporting activities than non-disabled children. Including strolling along the beach, country parks, historical sites, skiing, and family bike rides. The majority of things we as children probably took for granted. This is not to say that it is impossible for everyone, but have you ever tried carrying a bucket and spade, suction machine, feed pump, oxygen, emergency medication, changing items, food and drinks whilst manovering a 25kg child in a 25kg wheelchair with wheels as small as a computer chair on wet sand. Believe me it’s training for any solider!

Rather than accepting total defeat we at Little Hiccups searched for an all-terrain wheelchair and thankfully found the Kangoo.

What’s so special about this wheelchair?
This wheelchair is amazing!! It's versatile and practical (two things every parent loves). With various attachments it can be taken on the beach, parkland, forests, attaches to a bike as a trailer, converts to a car seat and even has ski's! It comes in a range of colours and even has wipe down material.

For all the family it’s fun! The last time Jenna and I raced in her wheelchair buggy was against my seven year old niece in Toulouse Airport killing time waiting for our plane. Apart from the odd holiday maker and piece of hand luggage the terrain was totally flat. I’ll admit now (hoping our rep doesn’t read this) I think that’s possibly where we broke the suspension. That was fun, and tiring for Ruby and I, Jenna not so much. Compare that to eleven year old Georgia and I racing Jack and Jenna across the bumpy sand, splashing in puddles, legs kicking, gasping against the sea air and their beautiful smiles show it’s no contest.

Exhausted for all the right reasons, walking back up the beech we met Tracey and James waiting patiently on the ramp. Lindsay, Jack and Georgia sped ahead chatting to the kind rep who drove the length of the country to let us play in the sand. Walking with Tracey pushing James in his own chair back up the ramp I didn’t need to ask them how accessible they thought the Kangoo was. I could see for myself every few steps Tracey, heaving, pushing and willing James’ chair up over the slippery cobbles whilst I one handed pushed Jenna in the Kangoo and filmed them struggling.

Once together we dissected test day two and I asked them what the day had been like:

‘’This is awesome’’ (Lindsay)

‘Sooo much easier than James chair’ (Georgia)

‘It’s so much comfier than my own chair, comfier than a car seat…’ (James)

‘How about compared to a sofa’ (me), ‘Yeah, just like the sofa’ (James).

‘I’ll get to do loads more now, can we take this on our holiday this year’ (James).

Why is this so important?
Recently I was chatting to a family member who visited a country park where we first tested the Kangoo. I asked if he’d had a nice time and what they’d enjoyed as a family.

“Nice place but there’s not much there,” he replied.

I might have been incredulous had I not been accustomed to such responses, for over the past three years since having my daughter I learnt that sometimes those who can see, see little. How was it possible, I asked myself, to walk for an hour through the woods and see nothing worthy of note? Linsay and I, parents of children with severe sight impairments search endlessly for things that interest Jack and Jenna through touch, smell and sound. Taking the two in the Kangoo wheelchairs into the woods to feel the delicate symmetry of a leaf, pass their hands lovingly about the smooth skin of a silver birch, or the rough, shaggy bark of a pine is priceless. Thinking of the spring to come and imagining taking them into the woods to experience the first signs of awakening nature after her winter’s sleep. To feel the cool wetter air, the smell of sweet, damp earth, hearing the birds in the trees, touching the velvety texture of a flower and discover its remarkable convolutions is unbelievably exciting.

As parents of children with disabilities/sensory impairments/additional needs we are compelled to be creative in the ways in which we teach our children. The Kangoo’s versatility and practicality overcomes a huge accessibility barrier.  We hope that giving family’s access to use these wheelchairs for day trips like ours, weekends and holidays will give something more than just a single moment in time, but enriches their lives and give their families life long memories (and if like us a hundred new photo’s to share with family and friends). 

Written by Katy Swinhoe



From the left that’s me with James, Lindsay, Georgia and Jenna in the middle and Tracy with Jack on the right.

Monday, 10 February 2014

Meet the Little Hiccups Chairperson - Noel (save us all!)


Noel with his family

So we have all been ask to do this blog thing so you guys can get to know the members of the committee a little better. Hi my name is Noel and I’m 32, I like ice cream and long walks on the beach….what…this is not that kind of blog!

Ok so I got involved with Little Hiccups originally for a number of reasons. I was sat at home one night and a dude with a charity can knocked at my door (not even hassling me on the street!!) as I was talking to him (and letting all the heat out of my house) he asked me if I gave money or time to any good causes, and it dawned on my….I didn’t!

Now at the time he obviously wanted me to hand over all my card details and save the pandas in Scotland or whatever it was (I had to hold back the Wife!) but when I was stood there in my dressing gown giving all the passers-by on Leeds Road a fantastic site I had an epiphany. I can help Little Hiccups!

Little Hiccups were formed by Linsay and Jenny, when they found little to no support for kids under 5 with special needs in Leeds. Freya is Jenny’s daughter and also my Goddaughter so there was my connection. Now at the time we created the committee Lindsay and Miriam ran Little Hiccups. Miriam is also a very close friend of mine so helping with Hiccups was an obvious decision…..sorry Scottish pandas!

When we created the first committee I joined to see Jen and Freya more and to help in any way I could. My primary role has been to help out on our monthly trips out….I’m normally the loud guy you all see when you first arrive with a big smile and two kids hanging off me. I also do the games at the annual balls we have at the Marriott. Give me a microphone and a room full of people and I’m in my element! We have a belter planned for this year…watch this space!!

Speaking of kids, Hiccups has given my two Sprogs a fantastic learning opportunity. They get involved helping me and the committee every trip and they have made some lovey new friends. It’s another reason I wanted to join. It helps them to see the world a different way. Not a lot of kids get to do that. I hope they see me helping and that somehow rubs off on them a little.

Two years on now I’m the committee Chairman. I think it just means Linsay gets to shout at me more when I say silly stuff. I have asked for a crown for our committee meetings but they have still not given me one.

I think that’s enough waffle from me. If you ever see me on an event and you want to chat just give me a prod, say hi, I don’t bite…unless I’m in my Zombie makeup but that’s a different story…

Written by Noel Davis-Atak