Walk on the Wild Side

Visitor Information

 

 

Visiting us today?
Find out our essential information here.

Opening times: 
Monday 5th & Tuesday 6th Dec:
9.30am – 4.00pm or dusk if earlier*
*Last admission 3.00pm

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Latest news

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Penguini's Now Open

Please be aware that the Café UmPhafa has now reopened as Penguini's Pizza and Pasta....

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Lost Madagascar Express Road Train reopens after devastating fire!

Sadly on 23rd December 2015 the Lost Madagascar Express Road Train and it's station...

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Christmas came early for our Elephants!

Over the past few weeks Colchester Zoo’s elephants have been enjoying a fantastic...

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Enjoy 15% off a Zoo Pass!

An offer not to be missed! 15% off Zoo Passes - join our family of Zoo Passholders! If...

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Colchester Zoo Autumn Magazine 2015

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Support Action for the Wild through Ebay!

Are you having a pre-Christmas clear out? Perhaps you’re planning to sell some...

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Colchester Zoo awarded best large attraction in Essex!

As part of the VisitEssex Tourism and Hospitality awards Colchester Zoo has proudly...

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Work continues on the Chimpanzee Lookout redevelopment!

Our chimp family tree has grown and grown and their home is growing too as work continues...

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Latest News

  • Penguini's Now Open

    Please be aware that the Café...

    Find out more
    01
  • Lost Madagascar Express Road Train reopens after devastating fire!

    Sadly on 23rd December 2015 the...

    Find out more
    01
  • Christmas came early for our Elephants!

    Over the past few weeks Colchester...

    Find out more
    01
  • Enjoy 15% off a Zoo Pass!

    An offer not to be missed! 15%...

    Find out more
    01
  • Colchester Zoo Autumn Magazine 2015

    Find out more
    01
  • Support Action for the Wild through Ebay!

    Are you having a pre-Christmas...

    Find out more
    01
  • Colchester Zoo awarded best large attraction in Essex!

    As part of the VisitEssex Tourism...

    Find out more
    01
  • Work continues on the Chimpanzee Lookout redevelopment!

    Our chimp family tree has grown...

    Find out more
    01

See and do

see and do

Upcoming Events


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Homepage Twitter

Join us for our next Christmas Starlight Night on the 17th December when Colchester Zoo remains open until 8.30pm!… https://t.co/2MpvdEw4mr
Looking for a new and exciting adventure for 2017!? Check out the internships at our reserve in South Africa!… https://t.co/oHpLCrMqEm
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The best day we have had in years and the staff were so helpful....


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Latest News

Michael Parmenters climb to raise money for daughter's memorial fund

My name is Michael Parmenter and I am an extremely lucky man. I am the daddy to a very special little Angel, my daughter Isobel, and I would like you to read my story about the reasons why I need your much needed sponsorship.

Michael and Izzy

Isobel was a beautiful, bright and cheeky little girl with the biggest brown eyes and a smile to match. She had an infectious laugh and lit the room up wherever she went. Isobel adored Peppa Pig and idolised Mr Tumble. She loved painting pictures and most importantly, stickering everything with her thousands of stickers. Her favourite animal was Elephants or “hufty’s” as she knew them as. Shortly after her first birthday, Isobel started to show signs of being sick. It was nothing out of the ordinary to begin with but then she rapidly deteriorated. She was admitted to hospital in March 2014 and from then on, my wife’s life, my life and more importantly, Isobel’s life, was changed forever. Isobel was transferred to a specialist unit where she endured so many horrendous tests for a 15 month old little girl. These ranged from numerous blood tests, endoscopies, colonoscopies, biopsies, x-rays, ultra sound scans and MRI scans. She ended up having to have a Nasal Gastric Tube to help provide her with much needed nourishment as she was unable to eat and eventually P.I.C. lines and a Hickman Line to help with all the medication, blood and platelet transfusions she required on a daily basis. Throughout this time, Isobel’s spirit never faltered and she continued each day with determined strength, a huge amount of courage and with a smile on her face. She was inspirational!

In August 2014, my wife and I were dealt the horrific blow of being informed Isobel had a rare cancer called Langerhans Cell Histiocytosis (LCH). Words fail to describe how my wife and I felt at being delivered this news. You don’t ever expect to hear those words as a parent, you think it happens to other people’s kids not yours. Things then became a whirlwind of various further tests and investigations to establish just how much this disease had spread. It was an incredibly hard, very scary and highly emotional time for us as a family but Isobel still continued to display such bravery and her cheekiness and lust for life carried us through the dark times, of which there were many. In the end Isobel was found to have LCH present in her gastric tract, skin, ears, liver, spleen and bone marrow and she was started on chemotherapy straight away. It was at this time that Isobel started collecting beads as part of the Beads of Courage scheme in hospital where she received a bead for every time she had medication or a procedure carried out. In that short time, Isobel received 1,314 beads!

Unfortunately the first two cycles of chemotherapy did not work and so she had to commence salvage chemotherapy. My wife and I were told that there was a chance Isobel would not make it but we wanted to give our little girl every chance to beat and survive this horrible disease. If anyone could do it, Isobel could! Unfortunately, Isobel picked up an infection and deteriorated rapidly which meant she had to be transferred to Paediatric Intensive Care. In the afternoon of the 5th October 2014, Isobel was placed on a ventilator. It was then that my wife and I had to make the worst decision ever of our lives, to turn off the ventilator. Isobel passed away that evening in her mummy’s arms with myself holding her hand aged only 22 months old. Heaven gained the most beautiful Angel that day. It was just over 10 months since she had started showing signs of being sick to losing her and we couldn’t believe how quick this disease had taken Isobel from us. The 5th October will forever be the worst day of our lives and no parent should ever have to experience the pain of losing their precious child.

LCH is a chronic disease. It is estimated 1 in 200,000 children become ill with LCH each year but it can affect adults too. Doctors and scientists do not know what causes LCH as it is not hereditary and it is not infectious and is currently treated with chemotherapy, radiation, steroids and in some cases, a bone marrow transplant. Most patients with LCH will survive but some may develop long-term side effects such as diabetes insipidus, stunted growth, bone defects, hearing loss, or neurological problems. The diagnosis is currently made by a specific tissue biopsy and prognosis depends on the extent of the disease and the types of organs affected. It is believed to be under-diagnosed as some patients may have no symptoms at all while others may have symptoms which are mistaken for other more common conditions.

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My wife and I are determined that we will not let our grief for Isobel destroy us and it’s hugely important to us that Isobel’s memory lives on. Colchester Zoo agreed for us to dedicate their new Butterfly Glade exhibit to Isobel which thousands of visitors now enjoy every day. We decided to channel our energy into something positive and started fundraising in Isobel’s memory which began in January 2015. We have made it our mission to spread much needed awareness about his disease amongst the public and health professionals and to raise much needed funds into vital research. We had never heard of this disease before and if by fundraising it saved one other person’s life, then Isobel’s legacy and our mission would have been fulfilled. During this time we have held numerous charity events and we are lucky enough to be supported by some wonderful friends and family who have undertaken some gruelling personal challenges, all inspired by Isobel. Due to our hard work and determination in fundraising, we were awarded the Pride of Essex Highly Commended Community Champions Award 2015 of which we are very proud of. As of November 2016, with the help and loyal support of our lovely friends, family and our supporters, I can proudly say we have raised just over £33,000.00 for HistioUK, the Children’s Cancer and Leukaemia Group and other Cancer related charities. In December 2015, we set up the Isobel Parmenter Memorial Fund, a special named fund which is part of the charity the Children’s Cancer and Leukaemia Group (CCLG). All the funds we raise through this fund go towards research into LCH as we hope one day there will be a simple test to diagnose it and a guaranteed cure for this vile disease. Which leads me to why I now need your support more than ever.

On the 21 September 2017 I am undertaking a challenge of a lifetime by climbing Mount Kilimanjaro in Tanzania, Africa on the Machame Trail to raise money for Isobel’s Memorial Fund. The mountain stands at 5,895m tall and over 7 days, I will be climbing through tropical rainforest and rocky terrain to reach the snow-capped summit. I am also likely to have to compete with altitude sickness along the way. I am just an ordinary man who has never done anything like this before and I’m not exactly the athletic type but I am training very hard each day to fulfil this ambition of mine, all for Isobel. I have already paid for all the necessary expenses so that every single penny raised through sponsorship, goes directly to Isobel’s fund. I feel incredibly lucky to be supported by Colchester Zoo and the CCLG in my adventure and I cannot thank them enough for their help. Please sponsor me via my designated sponsor page at http://uk.virginmoneygiving.com/MichaelParmenter  or by visiting Isobel’s memorial Fund Page at www.cclg.org.uk/Isobel-Parmenter-Memorial-Fund. You can also follow my progress on Facebook at The Isobel Parmenter Memorial Fund. Thank you.

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First Spider monkey baby born at Colchester Zoo in 8 years!

On 17th October 2016 a young female Spider monkey was born at Colchester Zoo. This bundle of joy was born to mum Cheekaboo and Dad Julius, this is the first spider monkey baby born at Colchester Zoo in 8 years, after Cheekaboo previously gave birth to twin boys, Chester and Charlie, who transferred to Dudley Zoo in 2014.

The group in which the baby was born was newly formed last year and is now made up of 6 females, including baby, and 1 male Julius, baby’s Dad!

Spider monkeys have a gestation period of 7-8 months. Their hands lack a proper thumb but this is compensated for by their tail, which is remarkably useful and has a bare underside at the tip to give it a good grip around branches. This tail is known as a prehensile tail!  The rest of their body is covered in glossy, black fur. 

This species is listed as ‘vulnerable’ the IUCN redlist with the population facing threats such as habitat loss.

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Colchester Zoo wins Raring2Go award!

We are honoured to be presented with two Raring2Go Awards! Colchester Zoo was voted the WINNER of this year’s Family Favourite Day Out, as well as runner up for the Readers Choice award! 

A huge thank you to all of those who voted! We are always developing Colchester Zoo with both our animals and visitors needs in mind and each and every visit made to Colchester Zoo not only supports the ongoing developments and animals in situ but also assists the zoos charity, Action for the Wild, help conservation projects worldwide.  

For the full list of winners click here.

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About Our
Animals

 

Our magnificent animals are waiting to be discovered. Learn more about the animals and see them up close and personal.

 

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