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

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£1,275.20
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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

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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

€630

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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!

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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

9 D

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

€6,626

38 D

94%
Tony's Surgery

Tony's Surgery

Welcome to Tony's money pot ! Tony Macedo is a Brazilian, 29 years old, from Paraiba, and his heart burns to do missions for his church. During his life he has engaged in lots of missionary projects and evangelising in place such as, Cacimba de Dentro, Joao Pessoa, Dublin, Jordan, Newcastle, London and Portugal.In his most recent mission he went to Portugal to work with children, with 'Beach Missions Portugal'. During the presentation drama with these children he suffered a really serious injury, breaking his femur (thigh) in two places, last 14th July.Unfortunately he does not have any confirmation when he can have the surgery because he has no possible finances to pay for this expensive surgery.During these days he is in serious pain and suffering, while he waits on a 'public waiting list' in Portugal, and there is no telling when he might get the attention he so desperately needs.This is where We can help Our brother. 1. Through your generous financial contribution, enabling Tony to have his surgery as soon as possible. 2. By sharing this website link in your social media with your friends and local communities, such as workplaces, church, and schools. 3. And lastly and most importantly, by Praying for our brother Tony.Prayer targets:To collect enough money for the surgery.To ease Tony's suffering while he waits for surgery.For may God help Tony pass through this moment of sufering and pain. Click to make a contribution to help our brother Tony. * Give however much you want.* All payments are secureBlessed is the one who considers the poor!In the day of trouble the LORD delivers him. Psalm 41:1 Thank you brothers and sisters.

€3,435

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22%
Fundraising for Kaleigh's DIPG Brain Tumour Treatment

Fundraising for Kaleigh's DIPG Brain Tumour Treatment

Office Raffle - Fundraising for 7 Year Old Kaleigh Lau's Brain Tumour TreatmentThis website is for people who would like to contribute to the office raffle through electronic contributions. Cash payments / paper raffle tickets are also possible. Please contact Urmi Bharne via kaleigh.raffle@yahoo.com Fundraising background: Last year my friend's 7 year old daughter, Kaleigh Lau, was sadly diagnosed with a rare, aggressive, inoperable DIPG brain tumour. After many struggles, her parents have recently moved to Mexico for specialist pioneering treatment which is having positive initial results. Kaleigh's Campaign: Kaleigh's campaign was covered in the Evening Standard newspaper (see links below). The campaign also received support from Kaleigh’s MP and various celebrities (see Twitter feed / articles below). Office Raffle: To fundraise for Kaleigh's treament costs we have arranged an office raffle with 40+ wonderful prizes all donated by national chains and local businesses. Tickets are £2 each. Once an electronic donation is complete, I will contact you via email with your ticket numbers. The prize draw is planned for Saturday August 19th 2017.   Prizes: Information about prizes is in my covering email / yammer message. However please contact kaleigh.raffle@yahoo.com if you would like information about them!  Thank you so much so for your support! It means the world! Urmi Bharne Kaleigh's campaign: http://kaleigh.ethanet.co.uk/ Facebook: https://www.facebook.com/Kaleighstrust/Twitter: https://twitter.com/Kaleighstrust Evening Standard newspaper:Oct 2016 article: http://www.standard.co.uk/news/health/stars-back-brain-tumour-funding-after-girl-6-given-two-years-to-live-a3380176.html April 2017 article regarding new treatment: See article below Femail/Daily Mail Online treatment progress: http://www.dailymail.co.uk/femail/article-4570944/Terminally-ill-British-miracle-recovery.html

£526

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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.

€2,174.43

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10%
Help pour la reconstruction de la voiture de Nicolas

Help pour la reconstruction de la voiture de Nicolas

Bonjour,Vous l'avez suivi à Tours le week-end du 27 mai, Nicolas a beaucoup abimé la Sub lorsqu'il a percuté le mur après ces jolies battle !Le week-end suivant, tout le monde était très surpris de le voir sur le circuit Paul Ricard.Là encore une belle 12ème place en qualif, suivi d'un beau top 8 serré, malgré la déception, et surtout la semaine passée avec peu de sommeil et des réparations à la va-vite. Après tous ces efforts, la sub reste très abimée et le chassis a rebougé lors de la compétition du Castellet, ce qui explique, entre autre, son absence ce week-end à l'Anneau du Rhin.Nicolas fait tout, tout seul depuis le début, avec l'aide précieuse d'amis passionnés, que nous remercions au passage. Cela veut dire la fabrication du moteur, la fibre de verre, la peinture, l'organisation pour les déplacements, les trajets, le changement des pneus et les réparations de dernière minute lors des compets, c'est dire si la motivation est grande.  Mais là, les dégats sont trop importants et il devient difficile de poursuivre sans aide car la caisse a besoin d'être remplacée, et y mettre un arceau soudé devient nécessaire.L'argent récolté sera utilisé pour l'achat d'une caisse nue, poser l'arceau et remplacer les amortisseurs, jantes et autres pièces cassées...   Nous faisons appel à votre générosité, à votre solidarité pour l'aider à poursuivre les compétitions de Drift !A bientôt sur la piste

€550.01

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18%
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

159 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

223 D

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