Hello everyone & welcome to Climbing Out of Depression's donation page...With just 1-click you can securely donate to our non-profit charity.All proceeeds go to those who need our help.Here's what we do.... About Climbing Out of Depression:Climbing can provide some light in the dark for those who are grieving and who are suffering from depression or any other form of mental illness. It's not a cure but focussing on something enjoyable and all-encompassing can provide relief from the pain and anxiety that people experience. Climbing Out of Depression aims to reach individuals in need of support and provide an activity that creates structure, teaches new skills and team work and provides relief and distraction. Mission Statement: To provide a service to anyone suffering from any form of depression. To lease with councillors and other charities, hospitals, schools etc and offer climbing as an activity that is know to improve ones mental health. Offer heavily discounted or free sessions to those referred to us to learn to belay and climb with others in similar situations. We will aim to have a trained psychologist present at these sessions as well as the qualified instructor, to help, advice and support if necessary. Funding will pay for the organisation of these sessions, instructors, helpers and to pay the climbing walls.
!!! Aidez nous à financer une expérience humanitaire unique au Népal !!! Qui sommes nous ?Notre association étudiante Dauph'International Youth organise chaque année un voyage humanitaire pour venir en aide à des populations défavorisées et victimes de catastrophes naturelles. Notre équipe se compose de 20 étudiants de l'Université ParisDauphine à Londres. Notre ProjetCette année, nous avons la chance de partir pendant 3 semaines dans la région de Katmandu au Népal en mai 2019. Cette expérience unique se fera grâce à l'association Service Volontaire International. Notre programme sur le terrain se divise en deux principales activités :• Education pour des enfants à travers des cours d'anglais et des activités manuelles, de jeux, de découverte• Aide à la construction d'habitats et de propriétés publiques durables et résistants aux tremblements de terre.Notre but est de récolter la somme de 20 000£ pour financer le voyage de chaque étudiant. Comment nous aider ?En participant au financement de notre mission, vous nous aidez à avancer un peu plus dans le projet. Un autre type d'aide serait de partager notre projet afin qu'il touche le plus de personnes possibles. Nous contacter Pour plus d’informations sur notre mission humanitaire, n’hésitez pas à entrer en contact avec nous et à suivre l’évolution de notre mission à travers les réseaux sociaux. Nous sommes également à la recherche de sponsors si vous êtes intéressés, merci de nous contacter. Via notre page Facebook : https://www.facebook.com/dauphinternationalyouth/ Via notre compte Instagram : @dauphinternationalyouth Téléphone: +33 6 78 32 74 26 Merci d'avance !Avec ou sans expériences nous avons l’ambition et la volonté d’aider, d’échanger et de partager avec cette communauté. Ce projet contribuera à l’amélioration des conditions de vie du village et sera le début d’une longue histoire liant les étudiants de dauphine et le villageois. Ce projet ne pourra voir le jour que grâce à votre soutien, même modeste ... Nous vous tiendrons au courant de nos aventures qui, grâce à vous, pourront prendre vie !
We lost are pal James in April 2018 aged 29 after he battled for 2 years with a Grade 4 Glioblastoma. This type of tumour is the most aggressive of its kind, it infiltrates the brain and spreads very quickly. James was an incredibly selfless human being who dedicated his life to helping others. Despite his diagnosis he continued his charity work and was able to raise £30,000 for Brain Tumour Research. He was and still is a total inspiration and we would like to do our bit to carry on his legacy. The James Clifford Campling Trust has been set up by his wonderful family. Their aim is to provide fantastic experiences and allow brain tumour patients to fulfil their bucket list dreams (just like James). In May this year Alex and I climbed Ben Nevis in Scotland and in true Alex and Lucy style decided that if we could climb Nevis we could definitely scale Everest.....how hard could it be?? So a few months later we booked and paid for our trip. When we actually sat down to plan our trek we realised that this might be a tougher than we orginially thought, so we put on our hiking boots and hit the hills. James would have loved this challenge, so we climb in March 19 in memory of him! I know it's nearly Christmas but please help us raise some money for this wonderful trust....every penny will help us train and trek harder on those hills! All your donations are safe and secure and every penny will go to the trust. For more infomation please visit: jamescliffordcamplingtrust.co.uk or watch this lovely video on YouTube https://www.youtube.com/watch?v=v3_QBJq38YY Loves.....Lucy and Alex xxx
Hello everyone & welcome to this money pot!ENGLISH: I've been working on this CD for a couple years now and we are fast approaching the end of the recording, mixing, editing, mastering etc, etc and it's time to come up with real money to make this happen. My first CD "Current Residence" came out about 4 years ago. It was a totally different style of jazz and a very different type of musical situation I was living at that time. Our style and repertoire has evolved enormously since then and this new album is much more contemporary - inspired by gospel, rock, funk, fusion and even some New Orleans Second Line !!- for the purists out there, I did say "inspired by" :-) The working name is "Second Residence" - clever, don't you think? It features:Lionel Pellissier on DrumsStephane Mondesir on PianoSebastien Alquier on Basseand 2 or 3 surprise guest soloists and me on trombones and vocals... There's music by The Meters, The Crusaders, Charlie Hunter, Joe Zawinul, Leroy Jones, Donald Fagan, Stealer's Wheel, Duke Ellington and more... I think the CD is simply really cool ... I'm really excited about it and I hope that you will like it too! I need some help to bring it all together and finish the production, pressing, graphics, licensing... If you help me with a donation, think of it as pre-paying your CD. And you will be a "producer" !! With luck, I will be able to get everything finished and submitted to the pressing company at the beginning of October with a delivery date of mid-October. I'm heading to Japan on October 17 to give several promotional concerts and I really hope I will have the finished product with me. If you would like to help me out on this, I would appreciate it very much. You can donate as much or as little as you want of course - every contribution will help! I will offer a free CD as a gift for donations of 20 euros / 2 CDs for 40 euros... For huge donations - let's talk about giving a private concert in your home or town !! :-) in music,Michael Steinman FRANCAIS: Je travaille sur ce CD depuis deux ans maintenant et nous approchons rapidement de la fin de l'enregistrement, du mixage, du montage, du mastering, etc. Et il est temps de trouver de l'argent pour y arriver. Mon premier CD "Current Residence" est sorti il y a environ 4 ans. C'était un style de jazz totalement différent et un type de situation musicale très différent que je vivais à cette époque. Notre style et notre répertoire ont énormément évolué depuis et ce nouvel album est beaucoup plus contemporain - inspiré du gospel, du rock, du funk, de la fusion et même de la New Orleans Second Line !! - pour les puristes, j'ai dit "inspiré par" :-) Le nom de ce nouvel album est "Second Residence" - malin, vous ne pensez pas? Il comporte:Lionel Pellissier à la batterieStéphane Mondesir au pianoSébastien Alquier à la basseet 2 ou 3 solistes invités surprise et moi au trombone et au chant... Il y a de la musique par The Meters, The Crusaders, de Charlie Hunter, de Joe Zawinul, de Leroy Jones, de Donald Fagan, de Stealer's Wheel, de Duke Ellington et bien plus encore ... Je pense que le CD est tout simplement génial ... J'en suis vraiment ravi et j'espère que vous l'aimerez aussi! J'ai besoin d'aide pour tout rassembler et terminer la production, le pressage, les graphismes, les licences ... Si vous m'aidez avec un don, c'est comme vous pré-payez votre CD! Et vous serez un "producteur" en plus !! Avec un peu de chance, je serai en mesure de tout finir et de le soumettre à l'entreprise de pressage au début du mois d'octobre avec une date de livraison à la mi-octobre. Je vais au Japon le 17 octobre pour jouer plusieurs concerts promotionnels et j'espère vivement avoir le produit fini avec moi. Si vous souhaitez m'aider, je vous en serais très reconnaissant. Bien entendu, vous pouvez donner autant ou aussi peu que vous voulez, chaque contribution aidera! Je vais offrir un CD gratuit en cadeau pour des dons de 20 euros / 2 CD pour 40 euros ...
Welcome to the Winchester Great War Dead Fulflood & Weeke Project Men of the 1st Hampshires in Ploegsteert (Plugstreet) Wood, Flanders, during the winter of 1914-15 November 11, 2018 will mark the centenary of the Armistice that finally silenced the guns in the Great War. Up and down the country, in what will undoubtedly be deeply poignant commemorative services, communities will remember the hundreds of thousands of soldiers, sailors and airmen who died in a conflict that is still etched on our national psyche. Fulflood and Weeke in Winchester will be no exception. The churches of St. Paul and St. Matthew contain memorials to no fewer than 91 men from the parish who went off to war never to return and they will be remembered at services in November. Although these men died more than a century ago their stories are only now being retold thanks to the efforts of a local research group. Over the past three years the researchers have worked to build up a picture of the lives of the parish’s war dead – where they lived and worked, where they went to school, their families, and, of course, where they fought and died. The stories we have glimpsed have been moving and fascinating. Young men from the streets of Fulflood, Weeke and elsewhere in Winchester went to fight and die not only on the Western Front but also at Gallipoli, Mesopotamia (modern Iraq) and even Russia. Winchester, of course, was a garrison town so many joined those regiments based here – the Hampshire Regiment, the Rifle Brigade and the King’s Royal Rifle Corps. Others served in the Royal Navy and the fledgling air force. Men from Canada, Australia, New Zealand and East Africa with family connections in the parish, volunteered to fight for the “Mother Country” and their names are remembered on the memorials. One of these men had been on Captain Scott’s final expedition to Antarctica in 1912 and was to die in a German prisoner-of-war camp. Many schools where the men went to are still here. Several went as infants to Western School, then in Elm Rd, and onto St. Thomas School in Mews Lane, which was eventually amalgamated into Kings’ School. There, they are remembered on the St. Thomas School Memorial Board. Some went onto Peter Symond’s Grammar School, now the Sixth Form College, and they too have a memorial board. Some went to prep schools and onto public schools such as Winchester College where they are also remembered. Some schools they attended no longer exist, for example, St. Peter’s in Chesil Street - but their records do. The time has now come to make their stories accessible to all interested people and aspects of this will take money! With just 1-click you can donate to this cause on the Contribute button on the right side of this page. * The most expensive item will be to publish a book of their stories which we aim to have available by Remembrance Sunday, on the 11th November this year.* We also plan to have portable permanent exhibition boards which can be displayed in:* St. Mathew’s and St. Paul’s, the churches of the parish of Fulflood & Weeke.* Local schools* Hampshire Record Office & the Discovery Centre* Community halls* Relevant military museums & local military bases* Creation of a website with all the information on it which will have an element of interrogation for example, do any of the men live in your street?* We hope further that:* Teaching resources will be created in liaison with local schools. Many current pupils in Winchester, especially at Western, Westgate and Peter Symmond's, may live in houses that were once the homes of these men.* A programme of Public Lectures & Guided Tours will happen.Long-term, we also hope to tell the stories of all the men who went to fight in World Wars I & II but that is not part of the current project. Thank you for reading this page and we do hope that you find this a worthwhile cause to contribute to.You can further help if you think you are related to any of the men and even have relevant photographs. A
Hello and thanks for coming by. My name is Lexy, and the adorable pup by my side 24/7 is Jaxx. About three years ago I was diagnosed with a rare genetic condition, called Ehlers Danlos Syndrome. I have the most common type of Hypermobile EDS. It's a horrible, multi-systemic condition that wreaks havoc on the sufferer, and can affect any number of things throughout the body. For me, personally, I experience a lot of pain and joint subluxations (partial dislocations) and often, full dislocations. While living in the US I had sought treatment to find out why my neck was so constantly painful, why I had trouble supporting my head upright, and why I almost constantly had a headache, that was only relieved by laying down. While in the Us, I was also diagnosed with Postural orthostatic tachycardia syndrome, Chiari malformation and we still suspect Mast Cell activation syndrome. With few answers, and a need to return home and escape my troubled marriage, I left the US. Upon returning home, shortly before Christmas, I started slipping in and out of consciousness. It was so quick and successive that I was unable to tell anyone what was happening or reach out for help. My blood pressure was tanking but we did not know why. I sought answers from doctors, neurologists and neurosurgeon team at Queen's square, I was sent for a supine MRI upon which they told me that I did have Chiari but that it was ''not symptomatic'' because of it's size. Initially, I accepted these answers, why would they not be correct? But my condition declined further and after an incident with my University bed collapsing, I was left unable to lift my head from my pillow due to extreme pain and dizziness. I almost missed Christmas with my family as I was unable to travel for a two week period leading up to Christmas day. I was frustrated and desperate to know what was going on. I emailed a doctor in Spain, a specialist within our EDS community and found the price for a consultation. In between raising that money and sending my imaging off, I started falling unconscious when lowering my head down. I attended the A&E in Barnet, where I was discharged because they couldn't work out why this was happening. By the time I sent my images and received my report, my speech was impaired, fatigue was running rampant, and the period of time in which I can remain upright has greatly lessened (about two hours at a time without a break). My gait, breathing and eyesight are all impaired, sporadically too. I opened the report expecting a few levels of my neck needing to be fused, what I read was shocking. My neck is very unstable, I have little to no spinal fluid flow. I was diagnosed with Chiari malformation and recommended a decompression surgery for those symptoms and the csf flow, Cervical cranial instability and Antalo-axial instability. What this means for me is that I need my whole neck fused, hard. On the 8th of July I flew out, accompanied by my best friend, to Barcelona to have further imaging and meet with my surgeon. It was confirmed that I do need these surgeries urgently, or I will simply continue to decline at the rapid rate I have been. I have been given a rough estimate of 50,000 gbp, and understandable, this isn't change I can grab from the sofa cushions, I need help to save my life. That isn't easy to say. Things have deteriorated rapidly since the bed incident, slipping in and out of conciousness, I lost control of my bladder and my spo2 stats drop frequently to below 90. I am terrified of how far I can decline, and what my body can come back from. So please, if you have anything to spare, please consider helping. Frequently asked questions: - Why wont the NHS fund this - The NHS have a few reasons, the first is that they don't like operating on people with connective tissue issues, due to the potential complications and risks we pose. They also dispute, despite numerous success stories, that the surgery is beneficial. They don't have a surgeon qualified
Moussa*, jeune majeur isolé, est scolarisé dans un lycée professionnel de la Haute-Garonne. Sans aucune prise en charge du département, sans assistance des institutions qui devraient pourtant l’accompagner sur le chemin de l’autonomie, il a passé sa première année de CAP tant bien que mal, grâce à la solidarité qui s’est créée autour de lui. Pour finir son lycée, obtenir son diplôme et « vivre », tout simplement, Moussa a besoin d’aide. L’argent récolté permettra de payer ses fournitures scolaires, ses transports, et de lui acheter à manger les week-ends et pendant les périodes de stage en entreprise. Une partie de la cagnotte sera aussi reversée au lycée qui prend en charge son hébergement à l’internat pendant les semaines de cours. Le texte qui suit revient sur le parcours de Moussa, son exil depuis l’Afrique de l’Ouest et les épreuves qu’il a traversées. Notre solidarité est un des moyens qui permettra à Moussa d’écrire lui-même la suite de l’histoire. (*Prénom modifié)Moussa, le porteur de fardeauxAu paysUn jour, alors que sa mère est alitée, malade, on fait venir Moussa à son chevet, avec son grand frère. Sa mère lui dit : « toi, tu es Dounouba Sambo ». Le porteur de fardeaux. Son frère, lui, se fait appeler « élève Kambano », le jeune étudiant. « Elle disait des choses que je ne comprenais pas mais maintenant je me souviens de ce qu’elle voulait dire. » Moussa perd sa mère quand il a sept ans. Il vit avec ses trois frères, sa sœur et sa grand-mère, dans la maison de son père disparu. Moussa fait ce qu’il peut. Il va chercher du bois, porte l’eau, s’active « pour mettre les choses plus près de la maison ». Moussa grandit, apprend. Il a onze ans. Le collège est à quelques kilomètres. Pour aller en cours, il doit marcher du village jusque là bas. Souvent, il fait très chaud. La plupart des élèves sont à vélo mais lui est à pied. « Ça a bien marché au collège, sauf que j’étais tout le temps en retard. Mais vu que j’avais des bonnes notes, ils m’ont laissé. » Moussa continue et rejoint la ville pour aller au lycée. Il veut devenir comptable. Il s’accroche, va au bout de sa seconde, puis passe en première. Entre temps, la situation familiale s’est dégradée. Tant de dépenses s’accumulent, pour s’inscrire à l’école, payer les fournitures, l’uniforme… Son grand-frère vient d’obtenir son bac, il veut commencer la fac, mais le voilà bloqué. C’est le temps des grandes décisions. Élève Kambano dit qu’il veut partir pour aider sa famille. Moussa dit à son frère qu’il va partir à sa place. Ils discutent. Élève Kambano est en moins bonne santé que Dounouba Sambo. Alors, c’est Dounouba Sambo qui ira. « C’est là qu’a commencé mon voyage sans retour. » L’exilPendant l’été, pour tromper son attention, Moussa donne rendez-vous à son frère à la ville le dimanche. Et Moussa part le samedi, avant que son frère n’arrive. Il laisse juste une lettre pour lui annoncer son départ. « Dans la famille, tout le monde a pleuré. C’est là que j’ai su que j’existais pour eux. Moi aussi, j’ai pleuré jusqu’en Libye. » Ses frères l’appellent tous les jours, mais Moussa leur donne le moins de nouvelles possibles. Bamako. Ouagadougou. Agadez. À Agadez, le désert, comme une mer de sable. « Je savais pas que y avait le Sahara. » Pour traverser, il faut deux mille francs CFA, « pour avoir la bonne couverture, à manger, et tout ». Dounouba Sambo porte sa nouvelle charge : il travaille une semaine à Agadez pour les passeurs, tient la souche des billets, note les noms et prénoms de ceux et celles qui ont payé. Les passeurs n’ont pas fait l’école. « Je faisais ça pour passer. » Un jour, un convoi rempli à moitié part pour la Libye. « Il m’a mis dedans. » Le convoi arrive à Gadron, sur le territoire libyen. Les galères s’enchaînent. Le manque de nourriture. Le manque d’argent pour continuer le chemin. Moussa bosse en ville pour des passeurs qui tiennent sa vie entre leurs mains. Après trois semaines, un autre convoi part en direction de Tripoli, Moussa embarque dedans,
HOPE - Helping Other People Excel!Today we bring together over 100 children from the outskirt villages of Kampala to provide them with the basics of life; education, shelter, food, clothing and health care. With a few dedicated staff members, volunteers and donations we are able to provide a safe and nurturing environment for some of Kampala's most vulnerable youth. By donating today you can help provide the material and equipment needed to enrich our children's lives. While we provide a loving family environment we are lacking basic essentials for our facilities. Below is a just a few of the many items our building needs: 3 Doors - €2309 Windows - €650Concrete Flooring - €250Wall Plastering - €90 Our donation platform will be ongoing and once we have provided our facilities with these basic needs we hope to expand our schools and to assist as many children as possible. We at Hope, and our children THANK YOU!!!
🔈 Salut à tous! Ikea font des plaids à 2€ pièce. Avec la période de froid qui va arriver, ils peuvent représenter une bonne manière d'aider ceux qui passeront des nuits dehors (en en commandant quelques uns et en allant les distribuer, par exemple ) N'hésitez pas à partager l'info, ça pourrait aider quelques personnes n'ayant pas la chance d'avoir un toit pour l’hiver . Tous les dons comptent même les plus petits ! Virgil et Augustin Merci et bonne année à tous ! 😊
Bonjour à tous et à toutes cette cagnotte à pour but de sauver une cinquantaine de chiens qui sont livrés à eux même dans une zone néante cela fait presque une année qu’on essaye de faire quelque chose mais pour des bénévoles c’est très difficile voir même impossible ced chiens risques d’être massacrés car il y a un projet qui vas débuter très prochainement et comme toujours la commune ne vont que les éradiquer l’association comme chiens et chats vont opérer pour cette noble action afin de sauver ces chiens mais on a besoin d’aide car il y a pas assez de fonds pour effectuer cette action ces chien vont être vaccinés, stérilisés, deparasités et ils auront des tagues sur les oreilles svp main dans la main pour garantir une fin heureuse à ces chiens innocents qui ne méritent pas d’être massacrés
Hi,We are planning to take a group of vulnerable people with learning disabilities to Durban South Africa, to volunteer at The Genesis Project, which supports the local community which has been affected by Hiv/Aids. 49% of the families have lost 1 or both parents, and we will be able to volunteer at their youth club, hospice and day centre. The visit will be life changing, improve the education of those we support, broaden their understanding of the wider world, and enhance the commitment to social responsibility and 'looking after each other 'which underpins the values of People and Gardens. The cost for 10 people is approximately £18,000. This covers flights, accommodation, food, hire of mini bus and driver, plus internal UK. travel and accommodation on rout.We need to still raise £8,000. We will be having fundraising events locally to make this trip a reality. It will be hard work but a once in a lifetime experience fr some of those who we support. Please help if you can. Ken RadfordManagerPeople and Gardens CIC
TO CHANGE LANGUAGE pls go to the very bottom of the page Hi there! My name is Isabella Curran and I am 13 years old. Because life is sometimes weird and things unexpected happen, I became aware of many things... one of them is cancer. My mum was disgnosed with breast cancer and she had to undergo chemotherapy. One of her biggest fears besides other stuff about the treatment was that she would lose her hair. She always says: “If you look sick, you feel sick.” This is why I have decided to donate my hair towards a wig for a child who has lost his or her hair due to cancer. I want to help them regain their confidence and make them feel healthy, beautiful and good again. The charity I decided to send my hair to is Little Princess in the UK. At the same time, I would like to raise money for “Verein zur Krebsforschung in der Frauenheilkunde” (yeap, its a mouthful unless you speak German) in Innsbruck, Austria. It is a cancer research centre which is also part of the hospital where my mum did her chemotherapy. Against all odds, and because of one of their studies in which she participated in, my mum kept most of her hair. I can tell you, she looks great and feels so much better for it! The Verein zur Krebsforschung in der Frauenheilkunde is determined to develop a blood test that can detect malignant tumours at an early stage so people may not have to go through aggressive chemotherapy and lose their hair. They are also working on the development of anticancer drugs and new surgical methods in cooperation with other European and American cancer researchers. Unfortunately, public funding in Austria is insufficient so they have to rely on donations like most research institutions. I hope you can help me reach my goal to raise awareness of how early detection of cancer can help save lives and maybe, even remind yourself to listen to your body and do your check-ups regularly. Every penny helps in the global fight against cancer! With just 1-click you can help. * Give however much you want* All payments are 100% secure* Why Leetchi.com? It's easy & transparent!TO CHANGE LANGUAGE go to the very bottom of the page. Thank you!
Rachel Cracknell is only 24, but has complex medical issues, including a very rare subtype of Ehlers Danlos Syndrome, a faulty immune system due to a very rare autoimmune disease, bowel problems resulting in a colostomy, respiratory issues which mean a tracheostomy is likely in the near future, and epilepsy. Rachel has also had multiple strokes, leaving her wheelchair dependent and hoist dependent. Recently, further damage to her brain has left her unable to speak. With grip issues making writing painful and difficult, and no speech, Rachel is unable to communicate when out and about. Despite all this, Rachel is an intelligent, sociable and friendly person, completely aware of her situation and incredibly frustrated since she is reliant on others for all areas of personal care, but can no longer communicate her wishes and needs easily, let alone socialise with friends. I have known Rachel for four years now, and worked with her to raise money for charity in the past. She would do anything to help anyone, but is now left needing the help herself. The NHS locally do not provide speech assistance devices anymore.No-one should be left without a voice, but at only 24 years old and with so many other issues, this loss is especially cruel. This page is to help raise the money for an assessment, and then purchase of equipment. The target will be updated once we raise the assessment money, and have more idea of exactly what equipment is required. To kick start fundraising, I am asking for sponsorship for a challenge which will push my abilities to the limit. Like Rachel, I have Ehlers Danlos Syndrome, and various other health issues, and I am wheelchair dependent. I am going to attempt to try 28 different sports/physical activities during the month of February. I plan to try everything from ballroom dance to burlesque, and from wheelchair badminton to hand biking. I will keep a diary and record of my attempts.
The Long Term Plan. Welcome to 'Cycle of Violence' A trilogy of interlinking short films. Three patients, locked away from the world for their own safety, tell their stories. Murder, Love, Addiction, Redemption and Obsession all come into play in this feature length psychological thriller. The ProjectWhat we are up to this year! 'Killer Confessions'We are looking to film the first part of this feature as a stand alone short film. This short will then be released to film festivals and independent distributors in order to gain greater funding and recognition from both the film industry and viewing public. The Story When murder is not just a sin, but a disease. Meet Mark. Marks 27. Mark lives by himself. Mark is a serial killer. Haunted by the memory of his first victim, Mark is on a downward spiral of insanity. Will the appearance of a new love interest spell salvation or disaster? When your sharing your home with your first victim nothing is for certain. How can you help?We have already cast the film and shot a teaser trailer, but any project like this requires a budget. Funding is hard to come by and therefore we are turning to you, the viewing public. Any donation, of any size, is benefical. Your contributions go towards paying the actors/crew, renting locations and equipment, aiding distribution and advertising. We can not do it without your help, so therefore we are offering a series of insenstives. Donations* £2- A personalised thank you card!* £5- A mention in the credits of the film and a personalised thank you card* £10- All of the above, plus a signed photo from the film* £15- All of the above, plus a signed poster from the film* £20- All of the above, plus a personalised video thank you from the cast.* £50- Two free tickets to the films premiere, two glasses of presecco and all of the above.* £100- Four free tickets, a bottle of Presecco and a goody bag of merchandise* £200- Eight free tickets, two bottles of Presecco, a goody bag, invites to after party However ANY donation is welcome!! Any money we are left with or generate from this first short will be invested in to the next two shorts! Meet the Team Nicholas Benjamin/Alexander Wright (Lead Actor/Producer/Story Writer)Nicholas is an actor, writer, director, producer with over 17 years of experience. Over the years he has worked for ITV, Discovery Channel, The Welsh National Opera, many bollywood production companies and countless Independent Film Companies. His most recent music video hit 50,000 views in less than 48 hours, and he has already been signed on to two films for working title. He met David, on the set of an independent film 'Strong' in 2018, and over the course of many drinks the passion project 'Cycle of Violence' was born. Nicholas is passionate about giving young artists a spring board into the industry and believe's that projects like 'Cycle of Violence' can act as one of those spring boards. David Ingram (Director/Producer/Screenplay Writer)David is a writer and director. 'Killer Confessions' will be David's directorial debut outside of short student film projects. David Holds a HND in Creative Media Production and currently working completing his BA degree in Film Studies at Oxford Brookes University. He met Nicholas during his time on the set of 'Strong' in 2018, which led to the pair cultivating this film trilogy, specifically this first film. It is the aim of this film to act as a way to build the experience of all those involved and path the way for future work to be created. Jack Parker (Director of Photography/Camera Operator/Producer)Jack will be acting as the man behind the camera on the set of 'Killer Confessions' as well as a producer alongside David and Nicholas. Jack holds a HND in Creative Media Production and is currently working to complete a top-up degree course in Media Production at Southampton Solent. Jack and David met through the HND course they both studied on. Since then the pair have frequently collaborated on vari
Bonjour à tous,Cette cagnote leetchi a pour but de récolter de l'argent afin que nous puissions mener à bien notre campagne pour devenir le bureau des sports extrêmes à Neoma BS pour 2019-2020. Ainsi, cet argent nous permettrait de proposer des évènements de qualité cette année aux étudiants. Le bureau des sports extrêmes (BDX) organise de nombreux évènements majeurs de la vie associative néomienne, notamment le sémineige (semaine de ski), le sémisurf (semaine de surf), etc... et a pour objectif de participer à la translaponie en 2020, projet phare de ce bureau. Merci d'avance à tous pour votre générosité et votre soutien !
Our sweet baby Kjeld has fallen out off a 4 storey high window. He took down a barrier that was supposed to keep him away from going outside and keep out mosquitos. He has been in the hospital for 2 days now and he is in surgery, the total costs of this are already higher than 1300 Euros, we have some buffer to pay for all of this, but his surgery which was estimated at 700 Euros is just a bit too much. He is having his right femur head removed as it was shattered during the fall.Every little bit will help in this case, so if you can donate anything even if it's a dollar we will love you forever. Or even a share will go far!! A message acknowledging it and sending love, still, we’ll love you forever!Our other cat Thijsje really missed her little brother and he came home today, he has to stay in a puppy cage for at least 2 weeks and get a lot of care.When Thijsje spotted Kjeld I’ve actually heard the sweetest meow ever!
Sinds een paar jaar doe ik aan kunstschaatsen. Ik vind dit super leuk! Sinds afgelopen seizoen ben ik intensiever gaan trainen zodat ik kon deelnemen aan wedstrijden. Ik heb er nu een paar gedaan en vond dat een geweldige ervaring! Om mezelf verder te verbeteren en te ontwikkelen zou ik heel graag in de zomer aan een super intensief trainingskamp willen deelnemen. Dit trainingskamp vindt plaats in Estonia ( Estland ) en duurt in totaal 2 weken. Nu kost dat trainingskamp en alles wat erbij komt kijken (vliegtickets en verblijf) een hele hoop geld...Het zou een droom zijn die uitkomt om dit te kunnen doen! Maar daar heb ik wel wat hulp bij nodig...Zou jij een donatie willen doen, groot of klein zodat ik weer een stapje dichterbij mijn doel kom?Alvast hartstikke bedankt!
Our sweet little son Sirdi, the blessing of our family is diagnosed with Acute Lymphoblastic LeukemiaWe are a family from Albania and Sirdi is our only child, for whom we are able to give everything away in order to save him. He is only 3 years old and has a tough health situation to overcome.I beg to all of you reading this text to help our son survive. Any little help of yours, means a lot to us. We are financially unable to support all the expenses of treating this illness, but together with all your help we believe we can make the miracle happen. We will be grateful to everyone helping to see our baby recover the health and hope of living! Sirdi jonë i ëmbël, drita e syve, gëzimi i familjes është diagnostikuar me Leucemi Akute Limfoblastike. Jemi një familje e re dhe Sirdi është fëmija jonë i vetëm për të cilin jemi të gatshëm të japim gjithçka. Ai është vetëm 3 vjeç dhe ka përpara një luftë të vështirë dhe të gjatë me jetën.Ju lutemi të gjithëve të na ndihmoni qoftë dhe sado pak pasi çdo vlerë e vogël për ne do të thotë shumë. Mundësitë tona janë të pakta por me ndihmën tuaj mund t’ja dalim! Do të Ju jemi mirënjohës përjetë dhe lutemi që Sirdi një ditë t’jua shpërbleje të gjithëve. With gratitudeThe Pambuku Family! *For US Donors, if your donation gets denied the 1st time, please notify your financial institution to authorize the payment, otherwise it will be flagged as suspicious and denied again.
Macy, our sweet beloved 5 months old bernese mountaindog puppy, is born with a life threatening liver abnormality. It's diagnosed as a Portosystemic Intrahepatic Livershunt. The shunt is not normal operable because too many vessels are attached to it and it's too dangerous located in the liver, to have surgery on. In the next months, when there is no medical intervention, she will become seriously ill and cross the rainbow bridge before her first birthday... We want to save her, but we are in need of financial support. We want to let her have the last possible major life saving intravenous surgery on her liver, to shut the shunt. This is a very difficult and expensive surgery that can take place when Macy is 6 months old (because of the completed growth of her liver). The medical costs will reach at least 10.000 euro After the surgery she can have a normal life again!!! Macy means the world to us. After losing Max, our first bernese mountaindog, last June to cancer, we adopted Macy to lose the cloud of sadness that hung over our family... Saying goodbye to Max was so sudden, so heartbreaking... Saying goodbye to little bear Macy would be so devastating... She made us smile again after losing Max... We would be so grateful if you help us save Macy, every donation is very very welcome and we are thankful for every donation. You can follow our sweet Macy on Instagram: @max.and.macy.berners to stay informed about her well being and her daily puppy life. Please help us save our sweet little Macy !!!
when I was seven years old, I had cancer so my leg was amputated.now on my 25th I would like to continue working on a blade that is a sports prosthesis.in collaboration with ottobock and the Roessingh I want to make this prosthesis.I would really like to be able to run professionaly. my goal is to get as far as possible for the kika run and the nike run in Amsterdam.