500 miles PKU

You've heard the one about walking 500 miles, well in 2017 I will be running 500 miles and hopefully more, including the Barcelona marathon in March, to raise funds for The National Society for Phenylketonuria (NSPKU) that help families coping with children diagnosed with PKU.PKU is a rare genetic condition that causes an amino acid called phenylalanine to build up in the body. Our bodies normally break down protein in foods like meat and fish into amino acids, which are the "building blocks" of protein. These amino acids are then used to make our own proteins.Any amino acids that aren't needed are broken down further and removed from the body. People with PKU can't break down the amino acid phenylalanine, which then builds up in the blood and brain. In short it means that people with PKU have to have a very restricted diet with very few "exchanges" of protein. That means no meat, fish, bread, dairy products and a host of other daily food items we take for granted.My nephew Christy (pictured) was diagnosed days after his birth with PKU. Thankfully, he is a happy and healthy boy thanks to the family support network around him that know about and can help him deal with the condition as he grows older.Funds raised through this project will go helping families that aren't so fortunate and aiding research into advancements in how to treat the condition.Thank you so much to anyone who can donate anything. I will be thinking of you on the roads and treadmills for the next 12 months.Kieran

217 D
left

35
contributors

£1,275.20
collected

255%

Siblings against poverty and exclusion - sponsor our 20km run!

This year, we will be running the 20k de Bruxelles for another amazing cause: fighting social exclusion and poverty, and helping people in difficulty to get back on their feet.   All the money we collect will be donated to Les Petits Riens, a Brussels-based social-economy enterprise that helps reinsert socially excluded people (mainly victims of homelessness, but not only) into society through work and activities aiming to reduce their feelings of isolation and helping them regain autonomy. This is achieved through a homeless shelter, a home for young people in difficulties, a service that offers medical and psychological support, help in the search for individual living accomodations and 2nd-hand shops which fund their running costs, but also employ and offer training to people in need (reinsertion through work). For those in Brussels, you can also donate clothes and furniture - click here for more information. If you also believe in a more just society, where all are treated with respect and dignity, then please help us help them by donating to our cause and motivate us to run the distance!  HELP US MAKE A DIFFERENCE (and train HARDER)- DONATE!   See you at the finish line on the 28th May!  Celia & Oscar

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12
contributors

€650
collected

500 miles PKU

500 miles PKU

You've heard the one about walking 500 miles, well in 2017 I will be running 500 miles and hopefully more, including the Barcelona marathon in March, to raise funds for The National Society for Phenylketonuria (NSPKU) that help families coping with children diagnosed with PKU.PKU is a rare genetic condition that causes an amino acid called phenylalanine to build up in the body. Our bodies normally break down protein in foods like meat and fish into amino acids, which are the "building blocks" of protein. These amino acids are then used to make our own proteins.Any amino acids that aren't needed are broken down further and removed from the body. People with PKU can't break down the amino acid phenylalanine, which then builds up in the blood and brain. In short it means that people with PKU have to have a very restricted diet with very few "exchanges" of protein. That means no meat, fish, bread, dairy products and a host of other daily food items we take for granted.My nephew Christy (pictured) was diagnosed days after his birth with PKU. Thankfully, he is a happy and healthy boy thanks to the family support network around him that know about and can help him deal with the condition as he grows older.Funds raised through this project will go helping families that aren't so fortunate and aiding research into advancements in how to treat the condition.Thank you so much to anyone who can donate anything. I will be thinking of you on the roads and treadmills for the next 12 months.Kieran

£1,275.20

217 D

255%
Hera's IVDD Surgery and Recovery

Hera's IVDD Surgery and Recovery

VERSION FRANCAISE CI-APRESENGLISH VERSIONOur adorable 4-year-old dachshund Hera's hind legs were suddenly paralyzed on Sunday the 5th of February. After rushing to a veterinary clinic, she was diagnozed with intervertebral disc disease (IVDD) type 4 (paralysis, but still sensation in hind legs). We were unaware of this genetical disorder until the day of these events, and 25 % of all dachshund are victims of it, normally between ages of 4 and 6. We had the choice of either going for the disc surgery immediately (with 80 % probability of Hera being able to walk again), or going for heavy medication forcing her to stay immobile for 8 to 12 weeks, and with 30 % probability of being to walk again. This option also meant a great risk of the condition returning later in her life. The chances of recovery depend on the delay of the surgery (up to a maximum of 48 hours); the more waiting time, the less is the chance of walking again...We chose the surgery option, because we cannot live without this little creature, who fills our lives with lots of love and hugs since 4 years. We wanted to give her the best possible chances to live a normal life again.The purpose of this money pot is to finance the operation cost (2000 €), and the recovery cost which is estimated to be between 10 and 15 days (250 € per day). The payment will be divided into several parts, which gives us time to raise and save the necessary money.All sums of contribution will be greatly appreciated.We thank you in advance with all of our hearts.Elodie & SimonInstagram: https://www.instagram.com/hera_dachshund_ivdd/ VERSION FRANCAISEAmis amoureux des animaux nous appelons à votre gentillesse et bienveillance.Notre adorable teckel Héra de 4 ans s'est retrouvée du jour au lendemain (le dimanche 5 février) paralysée des pattes arrières. Après avoir couru le plus rapidement possible chez une clinique vétérinaire ouverte, le verdict est tombé : Héra a une hernie discale de type 4 (paralysie mais sensation dans les pattes arrières toujours existente). Cette maladie génétique, que nous ne connaissions pas précedamment, touche 25 % des teckels entre leur 4ème et 6ème année.Nous avions le choix soit de l'opérer immédiatement avec 80 % de probabilité qu'elle puisse remarcher par la suite soit de passer à la médication lourde et une immobilisation totale de 8 à 12 semaines qui lui donnait 30 % de chances de remarcher (et un risque d'aggravation). Le pourcentage de chance que l'animal puisse remarcher depend de la rapidité d'action (jusqu'à 48h)... plus le temps passe, plus les chances de récupération de mobilité s'attenuent.Nous avons fait le choix de l'opérer car ne nous pouvons pas vivre sans ce petit être qui nous partage nos vies en nous couvrant d'amour et de calins depuis plus de 4 ans. Nous voulons lui donner toutes les chances possible de retrouver une vie "normale".Le but de cette collecte va servir à financer le coût de l'opération (2000 €) et de la réhabilitation estimée entre 10 et 15 jours (250 € / jour). Le paiment va être divisé en plusieurs fois ce qui nous laisse du temps de collecter et économiser au maximum sur les prochains mois.Toute participation sera grandement appréciée.Nous vons remercions par avance de tout notre coeur.Elodie & SimonInstagram: https://www.instagram.com/hera_dachshund_ivdd/

€670

65 D

Help Save Yamina

Help Save Yamina

Help Save Yamina (Version en français sous le texte en anglais)Our little two-year-old daughter, Yamina, has a malformation of the bile duct (common bile duct cyst), and the only cure is surgery, until then, her life is at risk. We need your financial support to pay for the surgery. Surgery should be performed early in order to limit the development of fibrosis / cirrhosis or hepatic complications of the cyst, such as pancreatitis or cholangitis (biliary tract infection). The surgery involves removing of all the dilated, and likely cancerous, bile duct, and reconstructing the bile duct using an intestinal loop to reach the liver.Today we live with the fear that the disease worsens, which is likely to happen since after childhood the cyst can easily degenerate into a carcinoma. Yamina follows a strict diet (no dairy products, little or no fat, no chicken, no eggs) to prevent a possible worsening of her condition, knowing that she already had pancreatitis.As you can see in the attachments, the cost of the operation and hospitalization amount to 10,387€ (See quote attached). My husband and I are from low-income families and are employees with average incomes. Unfortunately, we do not now have the means to pay for the surgery's fees.I resumed my work few months ago because we have to pay for her care. I have to leave my daughter with her aunt, when I would have preferred to stay close to her. The professor we consulted told us that we should not wait too long to avoid complications due to this malformation (fibrosis, cirrhosis, pancreatitis, cancer). This is why we come to you today; we put our hopes in you to help us save our daughter and allow our family to resume a normal life.Thank you for your contribution, however much you can give. Rest assured that all payments made through the collection platform are secure.To donate: https://www.leetchi.com/c/solidarity-yaminaYou can contact us with any queries you may have at the following email address: helpsaveyamina@gmail.com.With our gratitude.Yamina's mumNotre petite fille de 2 ans, Yamina,  présente une malformation des voies biliaires (kyste du cholédoque) et le seul remède pour une guérison totale est la chirurgie.La chirurgie doit être précoce afin de limiter le développement d’une fibrose/cirrhose hépatique ou des complications du kyste, comme une pancréatite ou une cholangite (infection des voies biliaires). La chirurgie comporte l’exérèse de toute la voie biliaire principale dilatée susceptible de cancériser, suivie d’une reconstruction de la voie biliaire par une anse intestinale montée vers le foie.Aujourd'hui nous vivons avec la peur que la maladie de notre enfant s’aggrave, car après l’enfance, le kyste peut dégénérez vers un carcinome. Yamina est sous régime alimentaire (pas de produit laitiers, pas de gras ou peu, pas de poulet, pas d’œufs) afin d’éviter toute aggravation de son état sachant qu’elle a déjà fait une pancréatite.Comme vous pouvez le voir dans les PJ, les frais de l'opération et de l'hospitalisation s'élève à 10 387€. Mon mari et moi sommes issus de familles modestes et sommes des salariés avec des revenus moyens, et malheureusement nous n'avons aujourd'hui pas les moyens de payer de tels frais. J'ai repris mon travail depuis plusieurs mois puisque je l'avais mis de côté pour être près de ma fille. Maintenant, je dois la  laisser avec sa tante, car nous devons financer ses soins.Le professeur que nous avons consulté nous a expliqué qu’il ne fallait pas trop tarder pour éviter les complications dues à cette malformation (fibrose, cirrhose, pancréatite, cancérisation)C'est pour cela que nous venons vers vous aujourd'hui, que nous mettons nos espoirs en vous pour nous aider à sauver notre fille et permettre à notre petite famille de reprendre une vie normale.Merci pour votre contribution, quelle qu'elle soit. Sachez aussi que tous les payements fait à travers la plateforme de collecte sont sécurisés. Vous pouvez nous contacter à l'adresse mail: helpsaveyamin

€1,260

23 D

12%
Let's help Waren :)

Let's help Waren :)

Welcome to this money pot ![English version]Let me introduce you to Waren:Waren lives in Siargao island, in the east of The Philippines. The inhabitants of the island had always earned their leaving from fishing. However, with the rise of the tourism the best way to earn a living now is giving surf lessons.I want you to meet Waren because he is the best person I’ve ever met. Waren is a surf instructor (a really good one!) and he uses all the money he earns to support his family (parents and brothers). Each surf lesson costs 10€/hour. The breakdown is as follows: 4€ goes for the surfboard rental shop; from the 6€ remaining, 3€ are used for the motorbike's rental to bring the boards and the student to the surfing beaches. Hopefully he gives one or two classes every day, so all that remains for him are 3€-6€ per day to support all his family. That’s why I’m asking for your help: Help me making Waren’s life easier. Let’s buy him the only thing he is lacking to do perfectly his job: a motorbike. With that, he would be able to earn double that what he does now and so, give his family a better life. He already has unlimited amounts of motivation, happiness, energy and patience Waren is such a good guy that makes you feel bad. He makes you want to be like him: always helping others and willing to share everything he has. “My mum is the only treasure I have” he told me in a random conversation, “That’s why I do that for her. I’m happy giving everything to my family. They raised me when I was a child and they had nothing at that time”. In another random talk I found out he has never had a present “I don’t know how to open a present, my parents could never buy me a present” he said between smiles. Because Waren is a happy boy, with the biggest heart you can imagine. Let’s give altogether the first present Waren has ever received, the 6th of july, on his 29th birthday. Let’s give him the tool that will help him buy double portion of food to his family. Any contribution is welcome. Thank you so much for your help! --  [Español]Dejadme que os presente a Waren:Waren vive en la isla de Siargao, al este de Filipinas. Los habitantes de esta isla han vivido siempre de la pesca, pero con el auge del turismo la mejor manera de ganarse la vida ahora es dando clases de surf.Quiero que conozcáis a Waren porque es la mejor persona que he conocido jamás. Waren es instructor de surf (el mejor!), y con el dinero que gana mantiene a toda su familia (a toda, padres y hermanos). Cada clase de surf cuesta 10€/hora. 4€ van directos al alquiler de la tabla; con esto le quedan 6€ para él, de los cuales 3€ van al alquiler de la moto para llevar las tablas y al estudiante a las playas donde se hace surf. Teniendo en cuenta que hace una o con suerte dos clases al día, tiene 3€ o 6€ al día para mantener a toda su familia. Aquí es donde os pido vuestra ayuda: Ayudadme a hacerle la vida un poco más fácil a Waren. Regalémosle entre todos lo único que le falta para poder hacer bien del todo su trabajo: una moto. Con esto, podrá ganar el doble de lo que gana ahora y así darle una vida mejor a toda su familia. Ya que las ganas, la alegría, la energía y la paciencia le sobran. Waren es tan bueno que te hace sentir mal. Te hace querer ser como él, ayudando siempre a los demás con una sonrisa y sólo pensando en compartir lo poco que tiene.“Mi madre es el único tesoro que tengo” me dijo de la manera más natural del mundo, “por eso hago esto por ella. Soy feliz dándoselo todo a mi familia, ellos me cuidaron cuando era pequeño y ellos no tenían nada”. Entre conversaciones casuales descubrí que nunca había tenido un regalo “no sé cómo se abre un regalo, mis padres nunca pudieron darme uno” me dijo entre sonrisas. Ya que Waren es un chico feliz, con el corazón más grande que puedas imaginar. Hagámosle entre todos el primer regalo de su vida, el 6 de julio, para su 29o cumpleaños. Regalémosle la herramienta que le permitirá comprar el doble de verduras y de pescado para su famili

€830

9 D

83%
Solidarity for Victoria

Solidarity for Victoria

Welcome to Solidarity for Victoria  ,a human help money pot !We are the parents of Victoria.Victoria is affected from many years from  with Borderline Personality Disorder (BPD) with Major depressive disorder and Panic attackNow she is 35, and she has not been able to have a life as the others girls.. Who is affected by it  tend to be extremely sensitive. Some describe it as feeling like an exposed nerve ending. Small things can trigger intense reactions. And once upset, you have a hard time calming down. It’s easy to understand how this emotional volatility and inability to self-soothe leads to relationship turmoil and impulsive—even reckless—behavior. There is often an extreme fear of abandonment, frequent dangerous behavior, a feeling of emptiness, and self-harm. When you’re in the throes of overwhelming emotion, you’re unable to think straight and stay grounded. You may say hurtful things or act out in dangerous or inappropriate ways that make you feel guilty and ashamed later on. BPD is related to lower functioning and disability, even when socioeconomic status, medical conditions, and all psychiatric disorders were controlled .It’s a painful cycle that can feel impossible to escape. But it’s not.There are several treatments that are most often used to manage BPD:1. Dialectical behavior therapy (DBT) focuses on the concept of mindfulness, or paying attention to the present emotion. DBT teaches skills to control intense emotions, reduce self-destructive behavior, manage distress, and improve relationships. It seeks a balance between accepting and changing behaviors. This proactive, problem-solving approach was designed specifically to treat BPD. Treatment includes individual therapy sessions . DBT is the most studied treatment for BPD and the one shown to be most effective.2. Mentalization-based therapy (MBT) 3. Transference-focused therapy (TFP) 4. Good Psychiatric Management: GPM provides mental health professionals an easy-to-adopt “tool box” for patients with severe personality disorders.5. Medications can cure BPD and can help treat other conditions that often accompany BPD such as depression, impulsivity, and anxiety, SUICIDAL ideation . Often patients are treated with several medications.6. Self-Care activities include: regular exercise, good sleep habits, a nutritious diet, taking medications as prescribed, and healthy stress management. Donate to funding better therapies and, ultimately, cures...and to find better life. we are in difficulty now, after years of therapies and medicines to really high costsYour donation will help real Victoria who live through this!With the help of Charity  we can help her with her mental illness and for suicide preventionCharities where your money will be put to good use. So we can  sustained the programs for her healthy and recover . God bless you all  Click to make a contribution.* Give however much you want.* All payments are secureThank you!

0

248 D

0%
LadyBird Project

LadyBird Project

HELLO ! HELLO !  Welcome to LadyBird Project Money Pot ! Everything started in October 2013, since then, every week-end I am baking delicious Homade Cakes and Tapas for the partiers and gourmets gone out in the Vieux-Lille, Wasemmes and around.Next step, raise funds to develop the Website and the Mobile App for everyone to discover and appreciate my new recipes, but also, aquire better equipment to succeed the cooking formation needed to develop the concept.The project isn't only about offering local, fresh food. It's also creating bonds between producers, local business owners and you, the customer! Less distance and intermediary for more transparency because ecology and conscious consumption are not a fashion but a reality that concerns all of us! The project is inspired by fundamental values like passion, solidarity and green development. Ladybird really wants to support and develop partnerships with cultural and charity events in France and abroad.To support the project, suscribe and like my facebook page MYLADYBIRDONLINE where you can find informations, pictures, events and more! THANK YOU !------------------------------------------------------------------------------------------------------------------Voici la cagnotte pour soutenir LadyBird ! Pour l'histoire, depuis Octobre 2013, j'élabore de délicieuses créations sucrées et salées distribuées aux fêtards et gourmets du Vieux-Lille, Wasemmes et ses alentours. Prochaine étape, lever des fonds pour développer le Site Web et l'App Mobile pour que tout le monde puisse découvrir et apprécier mes créations culinaires mais également acquérir du meilleur matériel pour me former et obtenir un jour le titre d'Artisan. Le projet n'est pas seulement de vous proposer des Tapas et Desserts "Fait-Maison" avec des produits locaux. C'est avant tout créer des liens entre producteurs, commerçants locaux et vous, les consommateurs ! Moins de distance et d'intermédiaires pour plus de transparence sont nécessaires car l'écologie, la consommation consciente ne sont pas un efffet de mode mais une réalité qui nous concerne tous! . Le projet se veut inspiré par des valeurs fondamentales telles que la passion, le partage et le développement durable. LadyBird a également pour vocation de soutenir et développer ses partenariats avec les évènements culturels et associatifs en France comme à l'étranger.Pour soutenir le projet, likez et abonnez vous à ma page facebook MYLADYBIRDONLINE sur laquelle vous retrouverez les infos, photos,évènements de LadyBird et bien plus! Vous pouvez aussi contribuer à la cagnotte Leetchi . Chaque subvention, quelque soit le montant permettra d'investir pour développer le concept avec et pour vous. Cette outil vous permet également de payer en ligne suite à une commande* ou pour acheter vos places** lors des LadyBird's Events!Merci de votre intérêt!LadyBird

€160

126 D

1%
SOULAGER BRACHA

SOULAGER BRACHA

Bonjour à tous, c'est l'histoire d'une petit fille Bracha qui a 12 mois aujourd'hui , et qui est née avec un syndrome rarissime qui s'appelle Aicardi.Elle est née avec une seule moitié du cerveau (l'autre partie "rongée" en fin de grossesse).Depuis le jour de sa naissance, sa vie est une véritable épreuve. Elle fait des crises d'épilepsie jusqu'à 100 crises par jour, oui je dis bien 100  crises d'épilepsie par jour. Elle reçoit plusieurs doses de cannabis médicalisées afin de l'aider dans son calvaires et sa souffrance. Je précise que les doses qu'elle reçoit ne sont pas remboursé hélas. Un des autres médicaments, malheureusement, lui a fait perdre la vue. C'est terrible mais c'est vrai! Cette enfant en plus d'être paralysé en grande majorité et en plus presque aveugle Du côté de son corps, toute la partie gauche est paralysé Elle a une hypotonie au niveau du cou et le reste du corps et n'a plus de corps calleux ce qui explique qu'elle ne peut tenir ni sa tête ni son dos seul. Elle a donc besoin d'équipements fait sur mesure spécialement pour elle et qui hélas ne sont pas pris en charge ni par la koupa ni par aucune association. C'est une enfant qui ne dort que très peu car à cause de cette moitié de cerveau rongee et qui est envahi par de l'eau lui provoque comme de l'électricité dans la tête et la fait terriblement souffrir. Aujourd'hui je vous raconte tout cela car elle a un besoin urgent d'équipements pour alléger toute ces souffrances terrifiantes. Elle a besoin d'une chaise adaptée pour la maison, pour pouvoir enfin être assise et sur élevé , une poussette médicalisée adaptée à son corps où elle sera en sécurité et qui lui permettra de sortir et s'aérer et aussi un équipement pour la douche pour pouvoir se laver décemment et en toute sécurité. A part cela elle a besoin de soins médicaux particuliers, méthode MEDEK, pour lequel il n'y a  pas non plus de prise en charge par la koupaholim (300 shekels pour 30 minutes).Bracha en a besoin le plus vite possible car son corps n'est pas en mouvement, ses muscles sont extrêmement faibles et cela fragilise encore plus ses os qui ne peuvent se développer. Malheureusement il n'y a pas de traitement pour Bracha, mais il y a une autre solution: " LA SOULAGER"  dans son combat. Nous avons estimé l'achat de ces 3 équipements vitaux à 7000 euros, sans compter les soins médicaux. Je vous en supplie ne la laissons pas. Cette petite est dans un état que personne ne pourrait imaginer. Si chacun d'entre nous donne 5 euros alors dans quelques heures nous pourrons annoncer à cette maman que grâce à vous tous, son bébé bénéficiera enfin du minimum vital pour continuer la vie qui lui a été destinée mais avec une souffrance physique diminuée. Svp ne restez insensible, ne restez pas sans rien faire. Donnez je vous en supplie même 1 euros mais ne l'oubliez pas. Svp Ne fermer pas ce post sans avoir donné même 1 euros Merci à vous tous. Je voudrai juste rajouter juste une chose kol akavod au parents qui malgré la situation inimaginable, impensable, ils sont là ils lâchent rien et avancent pas à pas

€6,426

94 D

91%
Roberta's Recovery

Roberta's Recovery

Help support Roberta's recovery!In February my fiancée Roberta suffered a brain haemorrhage from a burst aneurysm, 4 months before our wedding. She was taken to a local hospital in her home town where they operated to stop the bleeding. She was then transferred to a hospital in Rome where they slowly brought her out of an induced coma. For a few days things were looking very positive; Roberta was able to confirm that she could understand those around her and was able to mouth words. Unfortunately, a week later there was a complication and Roberta suffered an ischaemic stroke, damaging a large part of the left side of her brain. She remained in a coma for some weeks. Doctors at the time said that she may not be able to wake from the coma but Roberta is strong and managed to wake from the coma. Although alert, as yet, she has not yet found a way to communicate and has significant movement issues. It is hoped Roberta can shortly be transferred to a specialist rehabilitation clinic. We do not know what the future holds for Roberta but with her strength and passion for life we are optimistic that she will make significant improvements over the coming months and years. This page has been set up to raise funds to to enable Roberta to access the best treatment and rehabilitation available to aid in her recovery process. Nel mese di febbraio la mia fidanzata Roberta ha subito un'emorragia cerebrale da un aneurisma, 4 mesi prima del nostro matrimonio. Era stata portata in un ospedale locale nella sua città di origine dove operavano per fermare il sanguinamento. Fu trasferita in un ospedale di Roma dove lentamente l'ha portata fuori da un coma indotto. Per qualche giorno le cose stavano cercando molto positive; Roberta riuscì a confermare che poteva capire chi era intorno a lei e riuscì a parlare di bocca. Purtroppo, una settimana dopo c'era una complicazione e Roberta subì un ictus ischemico, danneggiando gran parte del lato sinistro del suo cervello. Rimase in coma per alcune settimane. I dottori allora affermavano che potrebbe non essere in grado di svegliarsi dal coma ma Roberta è forte e riuscita a svegliarsi dal coma. Anche se attenta, ancora non ha ancora trovato un modo per comunicare e ha importanti problemi di movimento. Si spera che Roberta possa essere subito trasferita in una clinica di riabilitazione specialistica. Non sappiamo quale sia il futuro per Roberta ma con la sua forza e la sua passione per la vita siamo ottimisti che farà notevoli miglioramenti nei prossimi mesi e anni. Questa pagina è stata creata per raccogliere fondi per consentire a Roberta di accedere ai migliori trattamenti e riabilitazione disponibili per aiutare nel processo di recupero.

€2,133

79 D

10%
UNIFORM PROJECT : helping 5 women of one of the poorest slum of Pune ,India

UNIFORM PROJECT : helping 5 women of one of the poorest slum of Pune ,India

Bienvenue dans cette cagnotte!Sil vous plait aidez moi à aider 5 femmes indiennes d'un bidon ville de Pune à monter leur propre confection d'uniformes d'écoles indiennes. Depuis Février 2017, au sein de l'organisation DEEP GRIHA SOCIETY, une ONG indienne de Pune, j'ai appris à 5 femmes à coudre ces uniformes d'enfants. Aujourd'hui ces femmes continuent à s'entrainer avec des tissus de récuperation et de vieilles machines à pied. Elles se sont engagées à continuer à travaill ensemble dans le but de créer leurs propres ressources économiques au sein de leur bidon ville très pauvre oū elles habitent. Le departement IGP de Deep Griha s'est engagé à les former et les soutenir dans l'organisation, le lancement de la production et l'obtention de la qualitè professionnelle requise. Mais Deep Griha n'a aucun budget pour ce nouveau projet . C'est pourquoi,  Ces 5 femmes , courageuses et persévérentes ont besoin de votre aide pour honorer leur première commande qui habillera les enfants pauvres parrainés et ceux de l'école en milieu rural de Deep Griha Academy. Les besoins financiers sont pour :* l'aménagement de la salle du centre de Deep Griha dans le bidon ville de Bibvewadi : conformité électrique, placards de protection, fenêtres* l'Achat des machines à coudre, table de coupe, fer et table à repasser, accessoires de confection...* l'Achat des fournitures nécessaires pour produire les uniformes: tissus, mercerie, matériels...Chaque donation compte!  Par exemple le budget des 3 premières machines nécessaires est 532 euros, mais savez vous qu'avec 2 euros , on peut acheter le tissu nécessaire pour confectionner une chemise de garcon? alors cliquez pour faire une donation!donnez ce que vous voulez et soyez rassuré, le paiement est sécurisé du fond du coeur je vous remercieau nom de ces femmes admirables , soyez béniPascale pascaledeforge@live.comwhatsapps : 0033638332823 Welcome to this money pot !Please HELP me to help 5 underprivileded indian women to set up their own SCHOOL UNIFORMS TAILORING business! From February 2017, Within DEEP GRIHA SOCIETY NGO,  I have taught them how to stitch children uniforms , Today they are practicing with rubbish fabrics and non-electrical old machines . They are committed to continue  to work together in order to create a sustainable livelihood in their very poor slum community.  DGS Income Generation Program is committed to train and support them in organizing and professinal quality production launching. Deep Griha has no fund for this brand new IGP project, so These courageous women need your help for delivering their first order that will benefit DEEP GRIHA SCHOOL sponsored and rural poor CHILDREN. Financial needs are for :THE SPACE REMODEL : In Deep Griha BIBVEWADI SLUM CENTER : electricity wiring, cabinets and windowsTHE MACHINES : semi-professional sewing and overlock machines, cutting table, ironing table, ironCUTTING AND STITCHING ACCESSORIES : Scissors, needles, bobines,pins...THE UNIFORM SUPPLIES : Fabrics, canevas paper, threads, dry goods... Every gift is welcome , for example, the first machines needed cotation is 532 euros but do you know that with 2 euros they can buy the fabric for one shirt ? so  Click to make a contribution and * Give however much you want.* All payments are secureThank you so much ,for these lovely women, Be blessed,Pascalepascaledeforge@live.com whatsapp : 0033638332823

€580

211 D

Saving A Single Mother

Saving A Single Mother

Suheir Halawani, 50, is a mother of four. Not more than 11 years ago, Suheir was a married woman in a perfectly healthy state who had moved with her children to Lebanon from Ghana, where they were all born.That very year, 2005, she began experiencing numbness in her left first toe. Thinking that it could possibly be due to an unnoticed bump during rush times, or perhaps due to the difference in climate from Ghana, Suheir dismissed the idea by taking over-the-counter medication. Nonetheless, the numbness only increased as time went on, until it stretched across her entire left leg. She had already begun seeking medical attention and performing numerous tests at the time, only to be told something along the lines of "Your case is strange, we have never seen this before." Her tests showed absolutely no sign of deficiencies nor anything she should worry about. At least that's what the doctors said.About one year later, Suheir was virtually paralyzed. She could not feel nor control her lower half. It was not until one doctor who used cortisone treatment on her that she was gradually able to feel and walk on her legs normally. It was a dream come true. This dream lasted for a good four years. After that, her health plummeted once more. This time, it was due to marital problems. Since she has a nervous issue, anytime she gets worried or angry, her legs would turn as stiff as stone. She then went back for even more tests. In fact, she had spinal fluid extracted twice as well as a sample from her lips in one of the best medical centers in Lebanon, all in vain. Unfortunately, every doctor's calming promises were eventually broken. "You will walk out of this hospital, trust me," they said. In 2013, Suheir got divorced, and was cut from the monthly income her ex husband sent to her and the children, who were taken back to Ghana.Within a month, she was back at her mother's house with none of her children, and zero financial income. Needless to say, both her mental and physical health deteriorated after that.Perhaps I should mention that Suheir also has only one kidney, as she lost the other in a childhood accident. She therefore needs periodic bowel checkups, which she hasn't had for over 3 years now.I also didn't mention that I am Suheir's 16 year old, and last son. During the one month that I see my mother in every year, I have seen her giving up too many times, and hate to think that she is helpless. My only dream is to know that my mother is healthy, able to walk, and that she is reunited once more with my siblings and I. Thank you.  Please click to make a contribution, and be ensured that every single penny raised from this fundraiser will go solely to the treatment of my mother in the University of Ulm, Germany.* Give however much you want.* All payments are completely secure.Thank you!

€659.50

215 D

3%
Access to Art school for Skye

Access to Art school for Skye

ENGLISH:Welcome,my friend!Let me explain to you my situation:I'm a young student who is working on their dream of becoming illustrator and author of comics since I am four.Unfortunately I'm not rich enough to pay the art schools,and my parents neither.I am doing all the little jobs I am able to do to raise enough money and yet it's not enough.This is why I decided to open this pot as a free contribution.I am doing a lot of fanart and "free" comissions/requests on Tumblr and Deviantart.I do a lot of portraits too....So if you can and want to support me in my dream and hard work do not hesitate no more!Even one little $ can change anything!* You can give however much you want and can.* All payments are secure.Thank you so much!* My professional Website: Skye Illustration* You can also send art request and follow me: On Tumblr or Patreon FRENCH:Bienvenue, mon ami!Laissez-moi vous expliquer ma situation:Je suis un jeune étudiant qui travaille sur son rêve de devenir illustrateur et auteur de bandes dessinées depuis mes 4 ans.Malheureusement je ne suis pas assez riche pour payer une école d'art et mes parents non plus.Je fais tous les petits emplois que je peux trouver pour amasser assez d'argent et pourtant ce n'est pas assez.C'est pourquoi j'ai décidé d'ouvrir ce pot comme une contribution libre.Je fais beaucoup de fanart et commandes sur Tumblr et Deviantart.Je fais beaucoup de portraits également...Donc si vous pouvez et voulez me soutenir dans mon rêve et travail acharné n'hésitez plus. Même un petit euro peut changer beaucoup! * Vous pouvez donner autant que vous voulez et pouvez.* Tous les paiements sont sécurisés.Merci mille fois!* Mon site pro: Skye Illustration* Vous pouvez aussi m'envoyer des commandes et me suivre : sur Tumblr ou Patreon

€500

279 D