Tag Archives: Over the Wall camp

Going that extra mile – 7Y2D COVID-19 Diaries Week 37

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There is no question that the last 9 months have had a huge impact on the mental wellbeing of all in the UK and worldwide. The rapid change to our usual routines left many feeling extremely discombobulated and the uncertainty of knowing when we can get back to anything that even vaguely resembles our old “normal” can lead to a sense of a loss of control, which itself can drive anxiety levels sky-high.

As we’ve all adapted to a life that is a great deal more home- and family-based than many of us are used to, so have many organisations similarly changed how they work in order to continue providing their services in whatever way they can. The benefits from doing 4 weeks of Stagecoach on Zoom were absolutely tangible for G and M, and it was encouraging to hear them giggling their way through the 3 hours of classes on a Friday evening. They’re delighted to be able to be back to “real life” classes this week and seeing some old familiar faces, both teachers and friends.

One organisation that has definitely gone the extra mile is Over The Wall. I’ve written numerous times about the amazing impact their camps have had on G and M over the last few years and this year was no different. It would have been so easy for them to simply shrug their shoulders when it became clear that camps couldn’t be held as normal, but instead they rolled up their sleeves and worked hard to produce the fantastic online “Camp in the Cloud” sessions for all who had applied for camp places. The week-long activities broke up the mundane experience of life in lockdown and challenged both children in a different way that they very much needed. That opportunity to connect with other young people who really understood how they might be feeling once again proved invaluable. Some might think that this charity’s determination to still deliver their regular offering as best they could despite the circumstances is going the extra mile, and I wouldn’t disagree, but I’m actually speaking about that something more they’ve now gone on to do.

Following the resounding success of their online camps, OTW has gone that one step further and continued to hold cabin chat sessions via Zoom on a monthly basis. G and M were both keen to participate and that hour or so at the start of each month has been a real lifeline for them. Cabin chat was open to anyone who had attended the virtual camps no matter where they are based and so both children have found themselves in groups with others from across the UK. It has been an hour to chat, laugh, accept and set challenges and just generally share how the last few months have and are affecting them. They’ve both made new friends and once again the boost to their mental wellbeing has been evident immediately. The planned chats have now finished, but we’ve all got our fingers tightly crossed that they will start again in the New Year.

Of course, none of these things could happen without the dedicated team of staff and volunteers at Over The Wall and we can’t thank them enough for going that extra mile and once again supporting G and M as best they can. Over The Wall have announced today that they are planning to continue with the virtual camps next year and beyond, even once the residential camps are able to start up again, which is quite simply the best news ever.

CitC Take 2 – 7Y2D COVID-19 Diaries Week 23

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With the start of the new school term being just a week or so away now, the last few days have been a great end to the extended break from school for G as she has eagerly followed in M’s footsteps and taken part in this week’s Midlands Siblings Camp in the Cloud. She has been waiting patiently for camp to start and firmly put M in his place last week when he offered to help her explore the virtual campground and point out where cabin chat challenges would be set and so on.

Being the ages they are, both children had the same set of challenges, which you might have thought would make this second week less attractive, but in fact the exact opposite has been true. A couple of the craft activities set had proved challenging for M as he found some of the finer details frustrating with his dyspraxia and he spent much of his time browsing the virtual campsite and taking part in the online activities, rather than completing the practical ones.

G, however, has tackled the crafts with relish and with perseverance; and, having discovered that watching the online videos was key, created a beautiful origami crane mobile, a working robotic hand and whizzed her way through the clues for the “locked box” challenge. She has loved joining in the nightly cabin chats and has come more out of her shell as the week has gone on. Her blue team has connected via Instagram, and if the amount of notifications buzzing through to her phone is any indication, they’re a chatty and engaged lot!

With Storm Francis hitting us hard with rain and wind this week and wiping out our new-in-lockdown 16ft trampoline by taking down one of the trees in our paddock, this week’s Camp in the Cloud has been a welcome distraction. Even better, M has re-engaged with some of the free-flow activities he didn’t complete during his week of camp, which has kept them both quiet and occupied with something other than the inevitable screens. In a summer that hasn’t quite been what we were hoping it would be, Over The Wall has kept us all sane and given both children some much-needed smiles on some otherwise grey days.

Camp in the Cloud – 7Y2D COVID-19 Diaries Week 20

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Since their first camps in 2016, G and M have looked forward to the start of every year to find out if they have got a place at their choice of Over The Wall camps. The initial outcome of this year’s applications saw both children on the waiting lists for their respective choices and, in M’s case in particular, with fingers tightly crossed that they might be lucky enough to make it to the actual camp when the time came about.

Like so many other activities, the coronavirus pandemic understandably shut down the Over The Wall camps this year, something that we all understood although it did leave the children somewhat disappointed. However, no sooner had we been advised that camp wouldn’t be happening this year, than an email was sent telling us that they were looking into a virtual alternative and to keep an eye out for future updates to be sent. It didn’t take long for the final details to reach me and both children eagerly signed up to the first ever Camp in the Cloud.

M was first up with the online South Health Challenges Camp and about 2 weeks before the start of camp his Camp in the Cloud box arrived on our doorstep. He did a grand reveal and shared opening his box with my Mum and Aunt over Face Time on the Saturday afternoon. Hidden inside was a padlocked box, sealed envelopes labelled for each day, face paints, a stationery set and, most importantly, his team t-shirt revealing he’s risen to the heady heights of being a green boy. The box also included a pot of M-friendly hot chocolate for cabin chat. The note on the container reminded him he could make it with the dairy-free milk alternative of his choice – a small thing that showed just how much OTW focuses on the finer details for each and every camper in their care. They also followed that up with an email just before camp began to remind me to check the ingredients to make sure I was confident that it was safe for M to drink.

The week of Camp in the Cloud came at a perfect time for M. It was a good start to his so-say summer holidays and proved to be a great distraction from the sad news of losing Grandpa the weekend before. The daily challenges gave him a focused activity to try his hand at and he loved being able to explore the virtual campsite, searching for the hidden Newman’s sauce bottles and participating in all his favourite camp activities in one way or another. The highlight of each day was most definitely the camp chat via Zoom, which gave him around 45 minutes to meet his team mates, accept, or set, team challenges and just chat in a face-to-face context, something he hasn’t really been able to do since lockdown began.

I was intrigued to see what M’s response to the week would be and it couldn’t have been more positive. Whilst he commented that it obviously wasn’t as good as going to camp itself, he loved being part of it and having something different to do after so many weeks of the same old, same old. Being able to dip in and out of the online platform during the day worked perfectly for my usually active child and the evening cabin chats really made it feel like camp. M was so impressed with the camp that he even contacted OTW himself to suggest that Camp in the Cloud is something they could continue to do in the future. He loves going to camp and always feels the bitter disappointment when he isn’t successful in getting a place. M believes that being able to offer Camp in the Cloud to those children who aren’t able to go the physical camp would be a great alternative and would reach out to offer the fantastic OTW experience to even more campers than they usually can. Whether they consider doing that, we simply don’t know, but anything we can do to help make it a reality we will.

Now we’re onto the countdown for G’s Midlands siblings camp at the end of the month – and she just can’t wait!

Heading North for the Bank Holiday

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No sooner had we arrived back from London, than G and M disappeared off to South Wales with my Mum and my Aunt for the week leading up to the August bank holiday, leaving Mike and me at home to work, wash clothes and start to sort out what was needed for our bank holiday adventure in Manchester. We travelled to South Wales on Friday evening to pick the children up and spent the night there before heading off to Manchester the following morning. We decided to try and avoid as much holiday traffic as possible, so wended our way across mid- and North Wales to reach our final destination and that decision proved to be the best one we could have made as we saw very little traffic at all. We reached Manchester, and one false start later – who knew there’d be so many Premier Inn hotels in the Salford area? – had arrived and were ready to start our visit.

Sunday was dedicated to the IWM North (that’s the Imperial War Museum for the uninitiated) to support G’s GCSE History studies about the rise of Hitler in the inter-war years and the Cold War period, and proved to be an excellent exhibit to visit. Their audio-visual short films shown every hour were a great addition to everything that was on display and there was a nice mix of interactive elements for the children to do as well. The sections covering the time periods of most interest to us were, perhaps, not as in depth as we would have liked, but overall we enjoyed the time spent there. G and I also took some time to walk around their special exhibit about the Yemen crisis, although M had definitely had his fill of all things history about that point and abandoned the galleries for the cafe with Mike. It was fascinating to see G’s reaction to the photos and displays about this more recent crisis and she was keen to express her thoughts about the responses of politicians and their excuses for not doing what they knew was needed.

Originally we hadn’t planned to do anything for the rest of the day as we weren’t sure how long we would spend at the IWM, so over our lunch, we investigated and discussed where to head next. M was keen to do something “fun as a family” and so was delighted to learn that we could visit EscapeHunt Manchester and try our hand at one of their themed escape rooms. We were lucky to get a booking for their “The Last Vikings” challenge and had just enough time to walk our way from Mediacity across the city to the escape rooms. It’s the first time we’ve attempted an escape room as a family, but is definitely something we will try our hand at again. We had lots of fun, although we failed at the final hurdle and were in the midst of solving the last clue when our time ran out.

Our decision to go to Manchester were twofold, the first being the IWM North, but our second was perhaps the more exciting, especially for G and M. This was the day for their indoor skydive in aid of Over The Wall and despite a somewhat grumpy start from our youngest, we arrived at iFly Manchester with 2 very excited children. Unfortunately, I wasn’t able to participate due to a shoulder injury I sustained at the start of the year, but Mike was keen to try his hand too, so we had booked them a family session which allowed them to split 10 minutes “flight time” between them. I was impressed at what appears to be the natural skydiving skills of my husband and children and the smiles on their faces said it all. Mike and M are both keen to go back and do it again, but G is less convinced, though glad she gave it a try in the first place. All in all, it was a fantastic bank holiday weekend and we were back home for a rest before school went back the following week.

20 years of #mischiefandmagic

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A lot can happen in 20 years.

In the years since our wedding in December 1999, our family has doubled in size and we’ve moved schools, houses and jobs at a rate that has to be seen to be believed. We’ve survived illness and loss within both our families and our friends, and continue to do so on a daily basis thanks to some long-term diagnoses that have oft-times caught us when we were least expecting them. Chronic illness has become a much bigger part of our lives that we could ever have imagined, but with that has also come some amazing friendships, connections and opportunities that we never even dreamed would happen and that, in many ways, I wouldn’t change for the world.

One such relationship that we have all absolutely come to value is the one with the charity, Over The Wall. They have been a phenomenal support to G and M since both first attended their camps in 2016 and are, in an almost unbelievable stroke of serendipity, also celebrating 20 years since they were first launched by UK businessman Joe Woods following in Paul Newman’s footsteps and the development of the Hole in the Wall Gang camps in Connecticut USA in the late 1980s.

So what are we doing to make this a year of note?

As far as our anniversary goes, I’m hoping that Mike and I might manage a night out somewhere special, though celebrating the week before Christmas can make that difficult as we negotiate the huge numbers of office Christmas parties that we inevitably encounter when trying to book a table anywhere without a lot of forward planning.

And, of course, it will come as no surprise that we are also working hard to raise awareness and funds to support Over The Wall’s ambitious plans to take a record-breaking 1,000 children to camp this year. Mike started the year in style with a sponsored polar dip on New Year’s Day and we’ve turned our hands to a few other things – some old, some new – to see just how much we can raise. We followed the “sparking joy” fashion and adopted a Marie Kondo approach to clearing out our wardrobes, committed to giving a regular amount each month and even stood in the entrance of our local Tesco superstore a couple of weeks ago to collect what we could and spread the word about the camps too.

We’ve taken OTW with us wherever we’ve travelled, sporting branded t-shirts, hoodies and bandanas with aplomb and almost quite literally went “over the wall” with them during our visit to Berlin.

G and M have obviously been a big part of many of our efforts, but are now launching an appeal of their own. Their yearning to do something truly spectacular has unfortunately been somewhat hampered by not yet being quite old enough to participate in the activity of their choice, but they have instead picked the next best option in their eyes and will be taking part in a sponsored indoor skydive at the end of this month.

How can you help?

Well, it goes without saying that any sponsorship you can give would be very gratefully received by G, M and OTW, especially if you can help them meet their fundraising target of £200 – scaled back somewhat from M’s original suggestion of £20,000 – by visiting their fundraising page here.

If you’re not able to donate, but live near a Tesco store in one of the following areas*, OTW is one of their Bags of Help Centenary Grants recipients until the end of August and by adding your blue token to their box, and encouraging friends, family and fellow shoppers to do the same, you will help them receive a significant grant that will be genuinely life-changing. Remember “Every Little Helps”, even if that’s by a blue token!

Finally, sharing the OTW message of #mischiefandmagic with friends and across your social media channels will not only help the charity reach even more of the estimated 50,000 children and young people living with serious health challenges across the UK, but sharing our fundraising page will hopefully bring even more cash donations pouring in to help them achieve their goals not only this year, but in the future too.

Thank you!

*OTW is currently starring in stores across: Perth & Kinross, Angus, Stirling, Fife, Clackmannanshire, South Ayrshire, East Ayrshire, Dumfries & Galloway, Scottish Borders, East Lothian, Midlothian, Somerset (inc Bristol), Wiltshire and Swindon.

Welcome to 2019

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It feels a little strange to be putting fingers to the keyboard and sharing news with you all once again. Since the last time I wrote, we’ve celebrated Christmas, seen in the New Year, made some big decisions about future plans and the children have headed back to school. Mike kicked off the New Year in style – something I’ll share more about in my next post – as part of our family commitment for 2019.

To be honest I was glad to see the back of 2018, which had challenged us all from almost the beginning of the year, thanks to a nasty bout of Aussie ‘flu and…well…everything else that then followed on from that. Don’t get me wrong, it wasn’t all bad and there were also lots of highlights from our year to celebrate too. Unfortunately and almost unbelievably, 2018 finished in much the same way it started with the sad news that one of my Godmothers passed away just before Christmas and 2019 obviously didn’t get the memo that it needed to improve on our experiences and kicked off with further news of ill-health for both friends and family.

However, I’ve learned some important lessons in 2018 and will be taking them forward into our New Year. I have some wonderful freefrom finds to share amongst other news and I’ve no doubt there will be discoveries and adventures to write about as 2019 unfurls.

Here’s to a year of discovery and wonder for us all.

Finishing the summer in style

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With Christmas now just 6 weeks away – eek, where has this year gone?! – it’s hard to believe that I still haven’t finished telling the tales of our busy summer. You’d have thought our fairly last-minute plans to fly out to Canada for 2 weeks would have been more than enough to keep us all occupied, but we had even more adventures squeezed in to the final 10 days of the summer holidays before school started back.

We had the return journey from hell with a disrupted flight thanks to a group of rowdy French exchange students, who got into arguments and near fist fights with both the airline crew and other passengers, just rows away from the seats we were sitting in. I have never been so upset on a flight and am just grateful that the children were more entertained by the films they chose to watch, than scared by the events going on around them. This behaviour continued in the Dublin airport terminal and didn’t help the stress of a delayed flight back, which meant we missed our onward flight home by mere minutes. Mike and I were tired, grumpy and so fed up by all we experienced, that we complained long and hard, which fortunately secured us a later flight home, though it was 12 hours later than originally planned, and a hotel room for the day, which gave us the chance to catch up on some much-needed sleep, something that had been impossible on the plane.

We were both back at work the following day, whilst G and M went to my Mum’s for the last 2 days of the week. We rushed through the washing and then found ourselves packing once again for a weekend in Liverpool to see the Terracotta Warriors exhibition that we had missed when we visited back in April and what was, perhaps, the highlight of M’s summer holiday – a week at Over The Wall. Our weekend in Liverpool was a great success, especially as we managed a return trip to both of the fabulous freefrom restaurants we had discovered on our previous visit, something both children were desperate to do. The morning spent at the World Museum was well worth it and we all enjoyed seeing the amazing Terracotta Warriors that were on display. It’s hard to believe that it’s been 17 years since Mike and I first saw them in Xi’an, China and fantastic to introduce G and M to this incredible ancient tribute to China’s first emperor. They also insisted we explored every other part of the museum we could and given the rather miserable weather, it was a great way to entertain them whilst away from home.

From Liverpool, we headed back South, dropping M off at the Midlands OTW Health Challenges camp for what we had no doubt would be an amazing week for him again. I cannot begin to describe the incredible benefits that M gets from OTW and why this charity deserves all the support and praise we can possibly give it. Once again the camp chefs outdid our expectations and created meals for M that went beyond our wildest dreams – and yet again apparently put my attempts to shame. This year, however, I can take great solace in the fact that M shared with the chef that I put my recipes on this blog and he not only took a look at them, but also used them to help cook treats for M whilst he was at camp. Just as with his stay at the South HC camp 2 years ago, M was exhausted after a week of unbelievable fun and challenge and just about managed to survive the very final bit of our seemingly endless summer adventures.

OTW’s Midlands camp is based just minutes away from the National Memorial Arboretum near Lichfield, Staffordshire and it seemed a shame to be so close and not stop there for a relatively quick visit. The NMA is somewhere I’ve long considered visiting and we chose a beautiful day to make the trip. Both children were about studying the World Wars at school and with 2018 marking the centenary of the Armistice, it seemed fitting to spend some time walking the grounds and exploring the many memorials that are found here. It was a remarkable and moving place to visit and I’m glad we made the effort to, despite M’s reluctance and overwhelming tiredness from a week away from home.

#NEAW2018: D is for Donate

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May 21: D is for Donate

There’s nothing I hate more than spotting a charity canvasser on the street and I’ll happily confess that I instantly become one of those individuals who speed up and drop my eyes down to avoid drawing too much attention to myself if I can help it. It’s not that I’m not prepared to donate to charity – oh how ironic this post would be if I was – but I am definitely not a fan of being pressured to sign up to an ongoing commitment to any one charity whilst out and about doing other things. Part of my problem is that I hate to say no to people and always end up feeling very disingenuous as well as guilty when I come up with a reason why I don’t want to set up a regular donation on the spot.

A cash donation can help, of course it can, but these days I don’t really know what charity to suggest when it comes specifically to making a financial contribution to support those diagnosed with EGID. There are no charities in the UK currently working on research into gastro conditions and few investing time and energy into supporting families living with the consequences of this challenging diagnosis. As long as gastrointestinal disease remains the “poor” cousin to so many other life-impacting conditions, there is little chance of much progress when it comes to finding ways to improve the day-to-day life of those living with it.

However, donation is about much more than just the money. Your time, your care and your support can make an incredible difference to a family living with chronic illness and the impact should never be underestimated. When someone takes 5 minutes to ask how M is doing, and, even more importantly, asking how G and the rest of the family are too, that effort is priceless. At the moment, we seem to be a state of status quo with M’s health which is fantastic, but there is also a sense of overwhelming ennui when it comes to our ongoing relationship with our local hospital and M’s gastro consultant. Taking the time to talk to me about life apart from M’s EGID makes a big difference and should never be seen as inconsequential. We teach M constantly that there is so much more to life than his illness and it’s important that we hold on to that truth and don’t get bogged down in the mundane.

There are, of course, a million and one charities who need financial support and it’s a challenge to choose the cause that’s not only closest to our hearts, but needs that money the most. This year we’re not actively fundraising as part of NEAW, mostly because I only changed jobs a month ago and haven’t found the time to be more organised, but thanks to M’s bold cheek, we have a small fundraiser planned for the end of June. Last year, he asked the founder of their Saturday dance school if this year’s end of year concert could be a fundraiser for the amazing Over The Wall charity and he and G are now working hard on their presentation to introduce the evening. M is thrilled to be attending an OTW Health Challenges camp again this summer and we continue to be extremely grateful for the care, support and opportunities they have given both children. Both OTW and my new role with our local air ambulance have shown me so clearly that whilst the money is important and enables both charities to continue doing their fantastic work, volunteering with them has equal value. At work our volunteers are an integral part of our workforce and the truth is, quite simply, that their daily contribution to the running of the charity cannot and should not ever be underestimated.

#FFFA18: The Shortlist

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It’s really only been a couple of weeks since I was a third-time judge at this year’s FFFA and the exciting news is that the shortlist for the Awards has already been published. I absolutely love scanning through the shortlist, even for those categories where I’ve been involved in the judging, because I find it so encouraging to discover a plethora of products, many of which I’ve never heard of before, which will make such a difference to those living with a variety of food allergies. As well as those I’ve already identified as particular highlights for me on the day, I was excited to see La Crèmerie’s rice yoghurt detailed on the Milk Product Alternatives list. I actually discovered this rice yoghurt during my visit to the Foodmatters Live conference back in November and whilst I have yet to try this with M, I know it’s something that could be a real game-changer for him and I’d love to see this do well in the overall Awards.

What has been even better for me this year than list after list of amazing foods, is the final named category: the FreeFrom Hero Award. Back in December I was asked if there was anyone I would like to nominate for this special category and it’s been really encouraging to us as a family to see our 2 nominees appear on the final shortlist. You can only imagine my delight this week as I received copies of the emails that have been sent to tell our very own heroes of their success. When you look at the list I’ve no doubt that you’ll immediately be able to identify one of the nominations I made, that of Steve Whitaker and Jason Conners, the cooks at Over The Wall. Ultimately I don’t know whether either of our suggestions will be the winners of the category, but I wanted to share my reasons for nominating this fantastic pair for special recognition at FFFA18:

Your reason for nominating them: M’s rare gastro condition, complex food allergies, restricted diet and associated problems has meant that he has never been able to stay away from home except with his Grandma. At nearly 12, he has never stayed away on a school camp or even had a sleepover with friends. In 2016, he was offered a place on the South Health Challenges Camp run by charity, Over The Wall, which meant he would be able to stay away from home for a week, fully looked after by an amazing group of volunteers who cheerfully give their time to support these children, who suffer with life-changing illnesses.

In preparation for the week, I spoke to OTW several times to discuss M’s dietary needs and at least 2 months before camp, I was sent a sample menu of the food that the chefs were planning to cook for him based on his extremely limited diet (just 5 foods plus 1 oil and sugar), which was truly amazing and that M loved the sound of. We touched base the week before camp to just check whether there were any changes and when we arrived at camp, the staff took time to meet with me to discuss all of his needs.

M ate like a king the entire week he was away and reluctantly told me that “Sorry Mummy, but their food was even better than yours!”. He was kept safe, had no allergic reactions because of their incredible awareness of the care that needed to be taken, was able to make friends with others facing similar health challenges, tried out so many experiences he’d never been able to have before and just felt like a child as his health problems firmly took a back seat to the more important job of him just having fun. As Mum, I felt confident that they knew what they needed to do to support him and have subsequently seen just how amazing their care can be when they called whilst G was away on sibling camp because they were concerned that she wasn’t eating the GF/DF food they were preparing for her.

We are hoping that he will be able to go to OTW camp again this year, but are just so grateful that he even had that opportunity to experience it once. These chefs (and all staff to be honest!) really deserve recognition for making M’s first experience of being away from home such a positive one.

The results will be announced on Twitter, on the evening of April 17th (@FFFoodAwards) and I’m hoping that we might once again be able to be there to recognise the hard work and incredible dedication of all those shortlisted finalists as well as celebrating the success stories of the worthy winners.

Charity Cut

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Whenever I write my blog, I am always conscious of not wanting to focus on any one emotion more than another, particularly when life seems pretty bleak to us. Yes, sometimes things feel overwhelming, but I know that in the grand scale of things life could be so much worse and I’m truly grateful that it isn’t. However, this is one occasion when I’m not going to apologise for shouting from the rooftops about just how fantastic both my children are in my eyes. They’ve both had brilliant end of year school reports and Stagecoach reports, which is a real testament to how hard they’ve worked this year, but this post is about something so much more than that and something of which Mike and I are incredibly proud.

In May, as part of National Eosinophil Awareness Week, M wrote to his Headteacher to ask if he could hold a “Dress as your Hero” day at school. Unbeknownst to me, M was invited to speak at one of the whole school assemblies about why he was running this fundraiser and took this opportunity completely in his stride. Both his class teacher and the Head have told me that he spoke confidently and with great articulation, able to clearly explain who Over The Wall are, what they do and the importance of these camps to him and to G. The school responded in amazing fashion and M’s hopes of raising around £100 proved to be a woeful underestimate of the final total.

Back at the start of the year, I wrote about our family’s New Year Resolutions  and mentioned that G had set herself a resolution that would be revealed in the fullness of time. It’s a real privilege to now share that resolution with you all. My gorgeous girlie decided that she wanted to cut her beautiful long hair before we travel abroad this summer and was keen to do it for charity if at all possible. So, for the past 7 months as G has been growing her hair as long as she could get it, she has been researching just how she could support a charity by doing so.

Two weeks ago, G faced her charity cut and had over 10 inches cut off to benefit 2 amazing charities. The 10-inch plait has been sent to the Little Princess Trust, who will use it to make real hair wigs for children across the UK who have lost their hair due to intensive medical treatments. Not content to leave it at that, G decided to join M in his fundraising efforts for OTW and asked family and friends for any sponsorship they were willing to give her to support her in her efforts. Regardless of any lingering nerves or uncertainties, G was excited to see her final look and I’ll be honest enough to say that we now have a teenage daughter that looks stunning and even more grown up than she did before. She really is rocking her new style:

Working together with this shared purpose, G and M have succeeded in raising more than a phenomenal £760  for Over The Wall, the charity that provides free camps for children with serious health challenges, their siblings and their families. As you’ll have read more than once on here, G and M have both benefited hugely from attending the Over The Wall camps and as a family we have chosen to support the work of this charity in every way we can. This really is a proud Mummy moment for me, seeing G and M be determined to raise awareness and financial support so that OTW can keep creating the magic they do every day at camp.

We are, of course, more than happy to keep collecting for this fantastic cause and you can add to the hard work of both children over the last couple of months by donating via our Virgin Giving website here. Thank you