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  • Jailbreak 2019 - Friday 25th to Sunday 27th

    Published 11/05/20, by Admin

    The Wallys

    Multiple Award Challenges

    9 x Loyalty Card – 2 miles each: Petrol Stations and Fast Food Restaurants.

    19 x Advocate – 2 miles each: Little Miracles logo in challenge submission photo.

    2 x Public Service – 10 miles each: Photo with Fireman & Ferry Worker

    6 x Tourist – 10 miles each: O2 Arena, War Graves, Hourglass & Dunkirk Beach, NATO Building, Dover Port & Victorian Lighthouse, Cliffs of Dover.

    5 x International – 50 miles each: France, Belgium, Holland, Luxemburg, Germany.

    5 Miles Challenges

    Random Encounter: Statue Street Performer

    10 Mile Challenges

    Video Advocate: Girl signed ‘please support Little Miracles’ on video

    White Collar: Man dressed in suit

    Two for Flinching: Man dressed in yellow jacket

    Name Envy: Best team name. Additional 5 miles for Wally’s being accurate (jamie forgetting passport).

    50 Mile Challenges

    Tactical: Last to leave Peterborough

    Desperate Times: Jamie sleeping on bench

    Long Haul: On a Ferry

    Sweet Talk: Blagged showers and accommodation via Facebook

    One for The Grandkids: Jamie getting searched for at border

    100 Mile Challenges

    Vlogger: Most video submissions

     


    Mad Girls

    Multiple Award Challenges

    1 x Loyalty Card – 2 miles each: Service Station

    8 x Advocate – 2 miles each: Little Miracles logo in challenge submission photo.

    6 x Tourist – 10 miles each: Edinburgh Castle, The Kelpies, State, Mountain Memorial, Loch Lomond.

    5 Miles Challenges

    Grass, as far as the eye can see: Grassy hillside photo

    10 Mile Challenges

    Happy to Help: Shop worker with tongue out

    Keep the Day Job: Kicked out of car for singing

    ROYGBIV: Picture of rainbow

    We have a Moment: Having a go on a toy car ride

    25 mile challenges

    Absolute Unit: Picture next to the tallest person

    Getting Involved: Picture in Loch Lomond frame

    50 Mile Challenges

    International: Scotland.

    Stand Out: Best fancy dress effort, superheroes with capes and oriented shirts.

    100 Mile Challenges

    Musou Mode: Dressed in martial arts gear and completed a sequence

    Captured the Moment: Best picture – image of the Scottish Highlands.

    Awwww: picture with cutest animal

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  • Why you need a Max Card & how to get one

    Published 11/05/20, by Admin

    Max cards … what are they and what do they do?

    Max cards are the UK’s top discount card for families of children with additional needs, disabilities and/or life-limiting conditions or illnesses. One card covers a family of four.

    There are hudreds of places across the UK where you can use these cards and discounts vary from place to place. They can be used at all Merlin attractions where you can get significant discounts and some places are free!

    Some places offer discounts for the whole family, others just for the disabled child.

    For a list of all attractions, information and discounts available, please visit www.mymaxcard.co.uk.

    Even better news….

    Little Miracles are an authorised stockist of Max Cards and can be purchased from us for £5. You can either collect from our Peterborough Branch or we can post for an additional £1.55.

    Little Miracles require proof of additional need/disability via DLA or Diagnosis letter. These can be sent to admin@littlemiraclescharity.org.uk.

    To request a card from us, please fill out this form.

    Once the form has been received, an invoice will be sent out to you. Your card will only be sent once proof and payment has been received.

    Have you been anywhere and used your max card? Did you get great discount? Please let us know if there is anywhere you recommend so we can share with our families.

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  • Personal Story of Planning Addict​​​​​​​

    Published 11/05/20, by Admin

    Throughout my life I have been a planner - I have tried every diary going, and when they have not been perfect I have made my own. When I found out I was expecting my first child it was no different. I read books, I planned everything, I knew what parenting techniques I wanted to use, what equipment I wanted to buy and I organised everything in advance.

    I planned that I wanted our babies gender to be a surprise. It didn’t matter providing they were healthy.

    I never planned to be in 5% of babies born needing additional support at birth.

    I never planned to hear that my child’s condition was considered "incompatible with life."

    I never expected to be told that my child would be unable to eat, unable to drink, unable to walk, talk and at some points breathe for himself.

    I never expected to be that mum.

    The news that my son had Downs Syndrome (caused by having an additional 21st chromosome) and other associated complex medical conditions was never something that I planned to hear. But every day in the UK a mum will give birth to a baby with Downs Syndrome and back in 2007 that mum was me. For parents who are given the news whilst pregnant between 88% and 92% (depending on what data you read) will go on to have a termination.

    Before having my child I knew very little about Downs Syndrome, I was a young mum and had always associated it with being something that happened to older mums. For us, the Downs Syndrome was minor in comparison to his other medical conditions but that news changed my life forever.

    We had two very different experiences as we had two consultants tell us the news (both thinking they were the first.) One was very gentle and mild and the other very direct and to the point.

    Both gave me, at 35 weeks pregnant, the option to terminate the pregnancy.

    I was given the choice 2 weeks before my son was born whether or not he had the right to live or die. I have always been pro-choice and have always felt that women should have the choice over what happens to their body but I cannot help but feel let down by the way my options were presented and the information I was given.

    I was led to believe that my son's quality of life would make it not worth living. I was given a lot of incorrect and out of date information and being a planner I went and read everything that I could about Downs Syndrome and his particular health conditions. But when you have medical professionals telling you what is right for your child and your body you believe them.

    I understand why I was given all the negatives but I wish I had been told that I had other options as well.

    My son has complex health needs, is severely disabled and has Downs Syndrome. He is also fun-loving, sometimes naughty, always cheeky, he loves to sing, he loves animals (especially cows) and babies. He has amazing empathy - his hearing loss often means that he struggles to keep up with conversations but he can read a room better than anyone else I know and gives amazing hugs to anyone who needs them.

    If I could give any advice to 2007 me, or anyone else in the same position it would be to read and educate yourself. Meet other people in the same situation especially other parents. Your journey will be harder. It will not be what you planned for but it will be amazing you will find a whole new family of people there to support and guide you - they will become your best friends. Sometimes you will cry - but you will also laugh more than you ever have before and you will receive more love than you ever imagined.

    Whilst I may understand why I was given the option to terminate my pregnancy I wish it hadn’t been the first option I was given and I wish that I had been told about the positives alongside the negatives.

    If I could give advice to anyone who has to deliver the news “your child has Down's Syndrome” I would like to ask them to be honest and explain the hard times but also that it is not all-consuming and that whilst things won’t be what I planned for that there are also many positives and offer to link them to other parents like those at Little Miracles.

    My son has Downs Syndrome, and I am ok with that, he is an amazing young man who deserves to be celebrated his life does not have less value just because he has an extra chromosome. I like to think of him as being a bit like one of the X-Men - genetically enhanced to love and accept others. For anyone who has been given this or similar news please speak a parent of a child with the same condition. Speak to Little Miracles. Get help and support and make up your own mind - termination may be an option but its not your only option and you can educate and plan what you want to happen.

    For anyone else reading this thank you for reading my story. To support a family like mine it costs under £20 - could you donate £20 to help a family in the same position know their options?

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  • Linx Printing Technologies Bank-Holiday Challenge Supports Local Charity, Little Miracles

    Published 11/05/20, by Admin

    Linx Printing Technologies Ltd (based in Saint Ives) have organised and completed a large fundraising event for their Charity of the Year partner, Little Miracles (based in Peterborough). Little Miracles provides support to families that have children (aged 0-25) with additional needs, disabilities and life limiting conditions.

    Linx staff spent six months preparing the fundraising event – a personal challenge for six cyclists (all Linx employees) who cycled 372 miles over four days (with over a 17,600ft climb) starting on the morning of 24th May and finishing on the evening of 27th May. The cycling event is the latest of a series of fundraising events organised by Linx for Little Miracles; this cycling event and a car wash has raised £1950 excluding GiftAid (which when claimed could raise as much as £2437).

    Additional information and the route that was taken can be found at https://www.justgiving.com/fundraising/cyclemay2019.
    (the figures included above are the actual amounts, not the ones on the justgiving page)

    Sean Robson, Business Development Officer at Little Miracles said “The money raised is enough to provide a whole year of weekly two-hour sensory sessions at Little Miracles Peterborough’s playcentre, The Spinney in Westwood. I’d like to thank the cyclists for their fantastic efforts, the event organisers for working out the logistics, all individuals and companies who supported the event, and of course everyone who donated. It is not too late to get involved – simply visit justgiving.com/fundraising/cyclemay2019.”

    Linx staff provided their own food, bikes and accommodation to increase the amount raised for Little Miracles. Linx the company sponsored the fuel for support vehicles as well as time for staff to prepare for the event. Perry’s provided a minibus for cyclists to drive to the starting point in Scotland and a van for volunteers to travel in; all free of charge. Print Solutions provided vinyl signs to go on the support vehicles.

    There are too many supporting companies to list but guesthouses that put the cyclists and supporting volunteers up for reduced fees and let them use their garages.

    Below quotes were posted on Linx’s Facebook page for the event.
    • “We made it. 28hrs20mins, 372 miles later and over 17,600ft climb over the last 4 days”
    • “Everyone is glad to have finished and it’s been a real challenge”
    • “Time to hit the showers and rest those weary legs!”
    • “An awesome effort in pretty gruelling conditions”
    • “the next 16miles was challenging but the views rewarding with fleeting showers”
    • “shoes full of water and soaked to the bone”
    • “The first glass of Pepsi didn’t taste sweet”
    • “I didn’t do the views justice in the advertising for this event: stunning!”
    • “tomorrow could be a washout!”
    • “11 miles and 50 mins in, X crashed into a parked car! Don’t worry the car is fine!”

    Little Miracles and friends want to wish the key people for this event a massive thank you for taking on this challenge and helping us raise vital funds that keep the charity running!

    Paul Gregory – Senior Electronics Engineer at Linx (main organiser and cyclist)
    Lisa Hunter – Marketing Communications Manager at Linx (arranged with Little Miracles to have representatives come in and talk to Linx’s staff, main point of contact for Little Miracles
    Jorn Frank (he came over from Linx’s German office just to take part in the challenge), Jamie Shelley, Tom Manwaring, Neal Gregory, Slawomir Kozubal – Cyclists
    Stuart Hardy, Dan Barnes and Malgorzata Gorecka-Kozubal – drove the support vehicles and provided most of the catering and bike mechanics

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  • May Half Term in Peterborough...

    Published 11/05/20, by Admin

    188 families came in just four days of being open to our fun-filled May Half term.

    Tuesday, we held a Teddy Bears Picnic. The rain did not stop the fun as we sang and danced away!

    Wednesday, Serenity Loves hosted a pamper day for the children at The Spinney. Children had face painting, nail painting, and hair braiding and platting.

    Thursday, we headed to Wildwoods in Peterborough who kindly donated us their cinema room for three private showing (with lots of free popcorn). We watched Incredibles 2, Fantastic Beasts: The Crimes of Grindelwald, and Aqua Man.

    Friday, we had meercats and snakes in the garden as the Party Animals’ came to The Spinney to show and teach groups of families about different exotic animals.

     

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  • A Summer to Remember!

    Published 11/05/20, by Admin

    AND YOU CAN MAKE A DIFFERENCE!

    Did you know last year Peterborough branch had 2,021 people attend our playscheme???

    In order to make this happen again this year we need to raise £11,387!!! This seems like a massive amount but if everyone on our facebook page donated £2 we can make this happen straight away, please consider making a donation as every penny counts! Would you notice a £2 donation? Could you donate more or hold a fundraiser for us?

    As a result of attending 86.4% reporting feeling less isolated, 70.4% felt they had made progress to towards a developmental milestone and 87.7% reported an improvement in their wellbeing. All of this via having opportunities to play! Please make a small donation in order to make this happen again and lets aim for a bigger and better year!

    Fundraising ideas for schools, churches, and youth sports teams

    Thermometer By ABC Fundraising®

    DONATE NOW

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  • Peterborough January – March 2019 Timetable

    Published 11/05/20, by Admin

    If you are looking for fun, inclusive and enjoyable activities for the family, then come to The Spinney! We released our new 2019 timetable which includes term time activities that are available from January to March. Booking is not required for most activities, if you have any questions give us a call on 01733 262226 or email us at admin@littlemiraclescharity.org.uk

    We can recommend activities to suit each child based on their age and ability in order for them to get the best engagement and interaction out of each of their visits to The Spinney!

    Check out our new timetable below for more information on daily schedules and activities!

    Monday

    Home Education (5 years and over) 10:00 to 12:00
    Childcare available for siblings
    Lunch 12:00
    Gymnastics 13:00 to 15:00
    Phoenix Gym, Maxwell Road, PE2 7JE – No booking is required, pay £3 on arrival
    Scouts 17:00 to 20:00
    Contact the 58th Ravensthorpe and Westwood scout group – Call Jacquie Smith 07525345760

    Tuesday – Open Access

    Tiny Tots Group (0-4 years) 10:00 to 12:00
    Lunch 12:00
    Coffee, Cake and Chat 13:00 to 15:00
    Let’s Cook! 16:00 to 17:00
    Dinner 17:00 to 18:00 – Slow Cooker Surprise

    Wednesday

    Home Education (5 years and over) 10:00 to 12:00
    Childcare available for siblings
    Lunch 12:00
    Mad Science Club 13:00 to 15:00
    Practice experiments while learning about science
    Gaming Club 16:00 to 17:00
    Dinner 16:30 – Stir Fry
    Ballet 17:30 to 18:30

    Thursday

    Sensory Messy Play 10:00 to 12:00
    Lunch 12:00
    Sensory Stories – 13:00 to 15:00
    Seriously Sensory Session – 16:00 to 17:00
    Dinner 17:00 – Hunters Chicken
    Youth Club (11-25 years) 19:00 to 21:00

    Friday

    Express Yourself 10:00 to 12:00
    Lunch 12:00
    Freeplay 13:00 to 15:00
    Dinner and Movie Club 16:00 to 18:00

    Saturday – Open Access

    Free Play 10:00 – 13:00

    Information and Referrals

    Counselling – clinicalteam@littlemiraclescharity.org.uk
    Caravan Holiday – caravan@littlemiraclescharity.org.uk
    Family Support – familysupport@littlemiraclescharity.org.uk

    Feel free to contact us for any enquiries that you may have via these contact options below:

    Call – 01733 262226
    Email – admin@littlemiraclescharity.org.uk
    Address – The Spinney, Hartwell Way, Peterborough, Cambridgeshire, PE3 7LE
    Facebook – /TheLittleMiraclesCentre
    Twitter – @littlemiraclesp
    Instagram – little.miraclescharity

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  • Sibson Airfield Parachute Jump- 29th July 2019

    Published 11/05/20, by Admin

    Have you got a bucket list? If so I wonder if jumping out of a plane is on their? Many of us have it as a pie in the sky type item that we think we will do it one day and then put it to the back of our minds. However skydiving is easier than you think to achieve, will conquer your fears and make you feel amazing! Add in the adrenalin of jumping at 13,000 feet and the perfect calmness and how beautiful the world is as you float back down why would you not want to?

    If nothing else think of the selfies!

    You have the opportunity to experience this whilst also enabling local disabled children to have a summer they will never forget.

    On the 29th July we are working Sibson airfield UK who are affiliated to the British Parachute Association. All instructors are highly trained and very experienced to ensure you experience a safe, enjoyable time. On the day you will undergo a training session designed to keep you safe before boarding an aircraft that reaches around 13,000 feet in a parachute designed for two people. You will fall at around 120 mph descending to 5,000 feet before your instructor opens the parachute. It’ll then take around 6 minutes to reach the ground.

    Even more exciting is if you raise £300 then we will pay for the jump for you! So what are you waiting for complete the details in this link for more details and to have a once in a life time experience.

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  • Building a Strong Relationship Whilst Caring for Your Child

    Published 11/05/20, by Admin

    By: Tammy C. Forester

    All couples face adversity of some kind at some point in their marriage. With divorce rates on the rise, and some scary statistics for divorce rates for couples with disabled children it seems like it is harder today than ever to create a successful relationship. In a fast-paced modern world finding time to work on a relationship may seem like a difficult task in and of itself. For couples raising a child with a disability, it can be even harder to find time for each other. The child takes priority and it takes a lot of time and resources to care for the child’s needs. This often leads to increased stress within the family as well. It is important to find ways to work together and nurture your relationship even under the hardest of circumstances. Remember that your child needs both of you, and it helps if you are working together as a team instead of being separated.

    Research has found that most failed relationships are caused by a lack of communication. Especially in times of difficulties, it is important to keep the lines of communication open. At times it may seem easier to retreat into your own world and just not discuss your emotions, feelings, worries, or fears, but it is also a highly destructive practice. When frustrations build up and emotions run high, it is a recipe for destruction within a family. Keeping things to yourself does not protect anyone but instead may separate you from those around you who love you. As a couple, you are a team in all aspects of life, and it is important to communicate and work together to find solutions to problems that arise. Working together in stressful situations can help bring you closer together as a family and a couple.

    Even though things may get rough and at times it may seem impossible to deal with and accomplish everything that needs to be done and deal with the pressures of life, it is still extremely important to try to find some time to spend alone with your partner. Even little things like calling home to check in, saying I love you, being there for each other in times of trouble, or just encouraging each other can make a big difference. If you can find time to get away for a few minutes just to talk to one another or spend time together that would help a lot. Keeping an intimate relationship with your partner and offering encouragement and support will help keep the relationship strong and allow you to deal with problems that arise.

    It is also important for couples to realise that they are partners in life and in the care of their children. When a problem arises whether it be finances or a new diagnosis to face, they need to communicate and work out a solution together. Cooperation is the key in all of this. No one person can do everything. Both parties play a role in their relationship and the care of their children. If something goes wrong or a problems arise it may seem easier to place blame than to work together to find a solution. When couples blame each other, they only add to the problem and may be jeopardizing the structure of their relationship and trust. It is important to find ways to share responsibility and work together to overcome adversity.

    Couples should also find and take advantage of resources and support services available to them within the community as well as with family and friends. Raising a child with a disability is a difficult task and at times families may need help and support. There is no shame in asking for help when you need it. Whether it be with household tasks, babysitting, financial assistance, counselling services, or whatever the need may be, having a strong support system is important in dealing with stressful situations. Don’t be afraid to seek out help when necessary.

    I know that it seems hard to find time to look after your relationship whilst balancing the needs of caring for your child but it is an investment that will keep you working as a team and better able to juggle everything going on in life. Your children need you to be healthy and strong in order to be able to care for them. If things get hard and you feel like you can’t handle everything seek out professional help. If you need to, seek out family counselling or support groups – we can help you! Raising a child with a disability is a huge responsibility and everyone needs help sometimes. Remember that your children are depending on you and working together as a team can provide a sense of stability within the home while allowing you to grow closer and stronger than ever as a couple.

    Marriage is difficult even under the best of circumstances, and having a child with a disability can limit the time and resources available to families and couples. It is important to stand by each other and help each other to grow and overcome obstacles that come your way. It takes communication, effort, and determination to help couples survive even the most difficult of circumstances, and sometimes ultimately things do not work out but you still need all of the above and to work as a team to get what is best for your child.

    We are here to help you, if you need to talk to someone please get in contact on either 01733 262226 or admin@littlemiraclesharity.org.uk to chat to one of our support team.

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  • Self-Care Is Not About You

    Published 11/05/20, by Admin

    By Andrew McCallum

    If I were to ask you, “What does self-care mean to you?”, does your mind immediately wander to bubble baths, a couple of glasses of wine, massages, long lazy lunches, a day at the spa…? Or do your eyes glaze over wistfully as you think, “I wish!” As much as those luxuries would be welcome in most of our lives, we know they aren’t realistic and achievable – except, perhaps, as an extra-special treat.

     

    The term ‘self-care’ suggests it is about ‘self’. But in context of caring, it is anything but.

     

    As a carer or parent, you’re on-call 24/7. The responsibility is enormous and the stakes are high. But what happens when the carer or parent becomes sick or incapable of providing the care? This is every carer’s worst nightmare.

     

    Think of yourself as a cup.

     

    Sometimes, you feel your cup is empty. Your resources have been drained and you feel you’ve nothing left to give. That’s when the guilt kicks in – when you realise you’re not Superman or Wonder Woman, but feel you ought to be.

     

    On the other hand, sometimes you feel your cup is full and running over; not with the milk of human kindness, but with stress and worry and chaos and challenges and that ‘just-one-more-thing’ you suddenly find yourself having to cope with.

     

    So, what do we really mean when we talk about self-care? And how can we achieve it with everything else that’s going on?

     

    Self-care is about keeping enough space in your cup so you can deal with the tough stuff that inevitably comes along when you’re a carer, without that cup being overwhelmed and running over.

     

    Self-care is about finding small ways creating that little bit of extra space that will make you a little more resilient, a little bit stronger for the person you are caring for.

     

    Self-care is not about you. It’s about the person you’re looking after.

     

    Of course, it sounds really simple – and it isn’t simple.

     

    But the first step is. The first step is just to give yourself permission. The first step is to say to yourself, “Okay, if I don’t have space in my cup, then I’m not going to be as much use as I want to be and need to be to… [the name of the person you’re caring for].”

     

    So, actually, doing things to create that space is not selfish. What you’re doing is creating space to be able to care for the people you care for.

     

    One of the best ways to do that is to have people around you. It’s important to have people who can help look after you, listen to you offload, provide another perspective, share their experience and knowledge with you, and maybe even help you shoulder some of the workload.

     

    Keep in touch with your friends. Even just a five-minute natter on the phone can make all the difference.

     

    Find a network you can join. Ask other carers or parents to find out if there’s a carers group in your area. Many groups and charities, like Little Miracles, have family support workers or volunteers who organise and support carers groups and other activities that help create the space you need.

     

    If you have internet access, join carers networks on social media. In times of stress, it can be tremendously liberating and reassuring to know you’re not alone. A friendly supportive tweet can make all the difference – to other carers as well as to yourself.  Sometimes ev well-timed med cat video from Youtube can make all the difference!

     

    Mindfulness is another great way of expanding that space within you. ‘Mindfulness’ is just a fancy name for paying more attention to the present moment, to your own thoughts and feelings, and to the world around you. When you’re a carer, you can easily find yourself rushing through life without stopping to notice much. Mindfulness is about pausing, just for a minute or so, and reconnecting with yourself.

     

    Take a five-minute walk outside and stand in the sun (or rain!). Stop. Close your eyes. Breathe deeply. Focus on your senses. What can you feel? What can you hear? What can you smell?

     

    Sit down for five minutes. Listen – really listen – to a favourite track from a favourite album.

     

    Have a potter in the garden. Tend a pot plant.

     

    Have a quick snuggle on the settee.

     

    There is no right or wrong way to mindfulness. It’s about what works for you and the opportunities that come your way in your life as a carer.

     

    Stop and think about your day. Where is there space? Where are there opportunities for some ‘you’ time?

     

    Are you still at the ‘guilt phase’, perhaps? Then get over it! Taking some time to build your resilience pays dividends to the person you’re caring for.

     

    However you do it, just do it! Please, please… take care!  – and if you’re not sure how or need a bit of a nudge then please give us a call on 01733 262226.

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  • Disneyland Paris - 2017

    Published 11/05/20, by Admin

    On Sunday 22 October, 106 excited children made their way to Disney Paris, thanks to the local charity, Little Miracles.

     If you’re yet to hear about the wonderful cause, Little Miracles supports families that have children with additional needs, disabilities and life-limiting conditions. They offer everything from fun free play sessions at their centre (The Spinney – based at Hartwell Way, Peterborough), home education, outdoor days and activities ( such as their recent trip to Disney), counselling services, OT therapy and behavioural therapy for families in need. The list goes on! Just like everyone else, the children of Little Miracles need a place to play, laugh and create friendships. The charity provides this whilst the families are able to access the advice, support and care that they deserve.

    Those that attended the trip to Disney had an amazing time, as highlighted by numerous parents. Eloise Veale mentioned, “My daughter Hayley told me, “It was the best day ever. Everyone at the park made all the children with disabilities feel welcome and excepted. I can hand-on-heart say that we wouldn’t have experienced such a magical trip without Little Miracles.” Lou Merritt added, “My son, Charlie, very rarely shows his emotions. Even he said that it was the best day of his life. Little Miracles made everything so stress-free with the hours spent on making sure everyone’s individual needs were seen to.”

     

    The event organiser, Emily Sibthorpe, said “Highlights included the Parade and Fireworks, but to be honest it was all so amazing and magical. Everyone had a great time and we’ve already decided to go again next year. We hope to make this an annual event.”

     

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  • Meet Scarlett AKA Mini Dream Maker!

    Published 11/05/20, by Admin

    Hello Everyone 😃

    My name is Scarlett and I am 7 years old, soon to be 8! I have decided raise money for the Little Miracles Disabled Children’s Charity.

    I myself have Microcephaly, a learning disability and Hyper-mobility and have received such great support from Little Miracles. From seeing the success of this years Children In Need 2017 and the films of the charity that were playing on the news, it touched me and made me understand just how in need the children of the charity are, they need big smiles as well as support! So here goes…

    I will be doing lots of different events to raise money for the charity and I would be to grateful if you could follow me on my adventures and sponsor what you can! Events will be posted as and when and I will have a continuous Just giving page as well as sponsorship forms.

    Thank you all so much for supporting me on my exciting journey! Let’s get Fundraising!! 😃🌈

    To support Scarlett in her fundraising mission please like her Facebook page

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