We are looking to raise €20,000 to start the life saving cancer treatment in Germany for Dainora

We are raising money to help our good friend Dainora Berzina in her brave fight against cancer. Unfortunately, Dainora has a very aggressive form in triple negative breast cancer. She was diagnosed in 2016. Despite two years of chemotherapy, a masectomy and radiotherapy the cancer has now spread to her lungs, bones, liver and skin and became inflammatory. As of March, 2018 Doctors are claiming that her cancer is incurable. Dainora is not willing to accept this prognosis and we know that she can overcome this disease. Through investigating what options are available out there miracles do happen. One place that has a success rate higher than most is the Hallwang Clinic in Germany that offers next generation immunotherapy. Many cases of "miracles" have occurred and we want to give Dainora the best chance possible to beat this disease. This treatment, unfortunately, doesn't come cheap. That's why we have set up this page. We are looking to raise the €20,000 to get Dainora started on the treatment she needs to beat this. Time is also of the essence. Doctors have given Dainora 5 months to live. We refuse to accept this and there is plenty of fight left in Dainora. Let's give her the chance to beat this disease. Thank you for taking the time to read our page, any donations towards Dainoras treatment would be gratefully received by us. Family and Friends of Dainora

305
contributors

€10,219
collected

51%

Sophias treatment.

Sophia had her first seizure at 5 weeks old and was diagnosed with epilepsy at 6 weeks old. She has had so many blood tests, a lumbar puncture, MRI, ECG, EEG scans and more. On her 6 week birthday we saw our baby girl being sedated so she could have an MRI scan to check there was no brain damage. Thankfully there isn't. At 4 months we were in hospital for 2 weeks due to the number of seizures she was having, resulting in her being too tired and weak to feed. We left hospital with Sophia being so weak she could no longer hold her head up unaided, she was so unhappy and spent most of the days sleeping. At 9 months we got Sophia's genetic results back and unfortunately she has a refractory genetic epilepsy with a mutation of the SCN8A gene resulting in delayed development. We have been told she may never walk or talk. She has just turned 1 and is still unable to sit unaided, walking and talking is still unknown.  We want Sophia to have the best chance possible at having some sort of 'normal' life and need to give her care and treatment to push her and help her development. This isn't cheap, we have already spent nearly £2,000 on treatment and need her to have more. If you have read this and want to help we appreciate every single penny donated to help Sophia to develop as much as possible. Thank you,Anna and Marcus X Click to make a contribution.* Give however much you want.* All payments are secureThank you!

69
contributors

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left

480%
We are looking to raise €20,000 to start the life saving cancer treatment in Germany for Dainora

We are looking to raise €20,000 to start the life saving cancer treatment in Germany for Dainora

We are raising money to help our good friend Dainora Berzina in her brave fight against cancer. Unfortunately, Dainora has a very aggressive form in triple negative breast cancer. She was diagnosed in 2016. Despite two years of chemotherapy, a masectomy and radiotherapy the cancer has now spread to her lungs, bones, liver and skin and became inflammatory. As of March, 2018 Doctors are claiming that her cancer is incurable. Dainora is not willing to accept this prognosis and we know that she can overcome this disease. Through investigating what options are available out there miracles do happen. One place that has a success rate higher than most is the Hallwang Clinic in Germany that offers next generation immunotherapy. Many cases of "miracles" have occurred and we want to give Dainora the best chance possible to beat this disease. This treatment, unfortunately, doesn't come cheap. That's why we have set up this page. We are looking to raise the €20,000 to get Dainora started on the treatment she needs to beat this. Time is also of the essence. Doctors have given Dainora 5 months to live. We refuse to accept this and there is plenty of fight left in Dainora. Let's give her the chance to beat this disease. Thank you for taking the time to read our page, any donations towards Dainoras treatment would be gratefully received by us. Family and Friends of Dainora

305

€10,219

51%
A grands pas pour Naila

A grands pas pour Naila

Salamou alaikoum, bonjour à tous Moi c'est Naila, certains d'entre vous qui me liront me connaissent déjà un peu et pour les autres je vais vous resumer mon parcours: je suis une ancienne grande prematurée ( né à 6 mois de grossesse!  1kg155 pour 37 cm)Cette naissance prématurée a eu des consequences sur ma santé: je suis aujourd'hui infirme moteur cerebral, mes jambes sont atteintes de spasticité je marche en equin (sur la pointe des pieds) ce qui me déséquilibre et donc je tombe souvent (multiples traumatismes craniens et genous qui s'abiment ). Mes muscles se retrecissant au fur et à mesure que je grandis, j'ai  besoin de faire des séances de kiné regulièrement et de façon intensive pour reduire au maximum cette spasticité.C'est pour cette raison qu'en Aout dernier, j'ai été en réeducation intensive à Barcelone pour y suivre le programme Essentis ( voir methode essentis sur google, et photos ci dessous). Ce sont vos dons et vos invocations qui m'ont permis de realiser cela. Les résultats ont été probants et incha ALLAH, nous espérons mes parents et moi repartir labas pour entretenir les progrès que j'ai fait. Aujourd'hui, j'ai besoin de vous une nouvelle fois, car une opération chirurgicale existe qui va me permettre de diminuer ma spasticité: la myoténofasciotomie.Plusieurs amies à ma maman dont les enfants ont subi cette opération, ont eu des resultats très encourageants et notamment le probleme du pied en équin, plus d'équilibre... En quelques mots ce traitement consiste à réaliser des opérations sous-cutanées (fermées), en intervenant sur les fibres musculaires lorsqu’elles sont lésées pathologiquement, limitant les mouvements. De cette manière, il est possible d’éliminer toutes les fibres malades qui résident dans toute la zone des tissus mous,en sauvant un maximum de structures saines et sans devoir faire appel à l’immobilisation postopératoire. Cette méthode améliore également les mouvements, diminue voire élimine la douleur, rétablit les fonctions et les structures de l’appareil moteur, restaure l’équilibre du corps, augmente et consolide la masse musculaire.J'ai rencontré le dr Nazarov (medecin russe à l'initiative de ce traitement qui ne se fait pas en France) en consultation au siège de l'association "un sourire pour l'espoir" à Evry  et il a jugé que cette opération serait très benefique à mon developpement et résoudrait beaucoup de problemes liés à mes muscles. Nous avons donc rendez-vous le 10 Juillet 2018 à la polyclinique de Barcelone.Cette intervention chirurgicale à un cout: 4700€ sans compter le frais de transports et de sejour .Je fais appel à votre générosité.Et un grand merci à toutes les personnes qui me seront solidaires quelle que soit leur participation.  Merci, Baraka ALLAHou fikoum Pour me suivre au quotidien: https://agrandspaspournaila.wordpress.com/ sur facebook : des grands pas pour naila  http://paypal.me/agrandspaspournaila L'association A GRANDS PAS POUR NAILA a été créée, voici la parrution au JO: ( pour avoir un recu fiscal n hésitez pas à me demander par mail )  Photos du sejour à Essentis, en réeducation intensive, en Aout 2017

138

€4,265

77%
SFE doit rester sur free

SFE doit rester sur free

Aidez le Marcus Kreiss, le fondateur de souvenirs from earth, à maintenir sa chaîne sur free. Avec seulement 1 click aidez SOUVENIRS FROM EARTH à rester sur free pendant un an.Free est le seul opérateur qui nous charge des frais techniques (via des tiers) pour la livraison de notre stream, et plus precisement pour connecter un câble...pour nous free n'est pas free du tout. Free en revanche touche 5euro par abonné pour son service de TV par box et SFE, rien pour nous. Et même si notre chaîne ressemble fortement à un service public (FIP), on ne reçoit rien de la redevance audiovisuelle, ni aucune autre aide publique, pourtant on peut nous considerer comme le plus important centre d'art en France avec 2 million de visites par mois. On doit très vite trouver 3000e pour retablir notre diffusion sur free, interrompue depuis 10 jours. La chaîne se finance en grande partie grâce aux ventes des dessins et peintures de son fondateur. La publicité est difficile à trouver et ne couvre pas tous les frais. Aujourd’hui, dans une phase un peu difficile et face à cette dépense somme toute injustifiée,  on propose aux abonnés de free ( et nos fans sur les autres réseaux) de s'activer. Perdre les 500 000 abonnés qui regardent SFE via free mettrait la survie économique de la chaîne en danger. SFE vaut quoi pour vous? Donnez ce que vous voulez.  Dites nous merci pour 10 ans de service premium gratuit et sans pub. Chaque donateur recevra un mail de remerciement et une proposition de figurer sur une liste de donateurs sur la chaîne. Les grands "donateurs" (100e et plus) recevront un cadeau, normalement sous la forme d'un dessin. Depuis 11 ans SFE est un ovni qui vous ouvre une fenêtre vers un monde parallèle, cet espace de liberté complètement indépendant doit continuer à exister! Allez, soyez fous, payez vous une chaîne TV artistique! regardez SFE en direct sur Orange 221, Bouygues 217, free (211, suspendu) appli android/appstore SFETV, et sur le site SFE.TV

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€957

the fun fund

the fun fund

Welcome to this money pot !So, as we all know Anneliese and Mia are really going through it at the moment.IM sure I don't need to describe what's been going on as Im only really inviting people who know Anneliese to contribute.However, if you have friends on FB or outside FB who want to contribute to this worthy cause please feel free to invite them.We all have or know someone who has passed from Cancer......my dad, my mum in law, my godfather, the list is quite large....It's a shit, cruel, thoughtless, brutal disease and while none of us can magically rustle up a cure, we can try and make some really good memories for Mia to carry through to her future. So although this has been titled The Fun Fund, there are aspects of this that attract costs that aren't the fun bit. Getting to Ed Sheeran for a start! Anneliese is going to need a wheelchair for this excursion, which I know she has, but she needs to get there and stay at least the night before and night after or she'll be shattered......She is a single mum, with a pacemaker, terminal cancer and a 12 year old daughter who needs some fantastic memories. Wouldn't it be great if WE can help achieve that?? I know times are tough for most people but please donate what you can. Even being as ill as she is, she's still got a kick arse attitude and a wicked sense of humour......let's give her a few more things to smile about.LoveEm x  Click to make a contribution.* Give however much you want.* All payments are secureThank you!

13

£1,015

Ali's Recovery Fund

Ali's Recovery Fund

Dear Friends,Ali Ergul is my 50 years old uncle, living in the village of Tunceli in East Anatolia (Turkey). Ali was born with the genetic disease known as Marfan Syndrome that result in several deformities to his body. In addition he lost sight in his right eye 5 years ago.For over 30 years he worked in the construction industry and has, with that work, sustained his wife and two girls (both still in school age). In 2000 his doctor instructed him to discontinue to work, however this was not possible for him given he was his family's only bread winner. As a consequence he still worked until this past winter (2017) but will not be able to continue that this year due to his deteriorating health.  While he does receive a minimal pension from these years at work, he had to undergo several surgeries in the last year (eyes and stomach) for which he took on a 20,000 Turkish Lira  loan (this equals 4,060€ / 5,022$) from a bank that he is unable to pay off due to his now lost source of income. After interest payments, which the bank deducts directly from his pension, he has barely 500 Turkish Lira/month (this equals 100€ / 125$) to sustain his family.  With this project we are hoping to lessen his financial struggles and enable his family to survive without him being forced to go back to work or his daugthers to leave school. All the contributions will go directly to Ali and his family to help to:* pay of this high interest rate loan* purchase some farm animals (chicken & cow) to create a sustainable food source* cover necessary medical bills (follow-up eye surgery & dental implant as he has only 10 teeth left)We really appreciate any contributions and can assure you that they are 100% secure through this platform. If you have any questions about Ali, please reach out to us.  Thank you!

3

€650

15%
Elise's Surgery

Elise's Surgery

Hello, My name is Elise, I am 23 years old trans woman. I live in France. I create this money pot for helping me to the most important thing of my life, a surgery. The sexual reasignment surgery. I don’t like to ask money to people, I’m a woman who likes to do everything by herself. I always manage by myself whatever the problem and his difficulty. But today its about a very high amount, 15.000€ ! I calculated the time I need for have it, more of ten years. I can’t wait so much for my surgery, I need it as soon as possible. And the surgery is already scheduled for 2020. That’s a very short time for fund this amout it’s that why I need your help today, because I don’t have the time for have the amount. I need the surgery because I feel uncomfortable with my birth sex, when I take a shower I see me as a man due to it, I want to feel like a woman. I hate to see myself as a man, the society doing it enough. Of course I work, I work a lot, I work every nights except the sundays for having a little rest. And I have a hard work. But even if I work like this I can’t live decently. Because like everybody I also have lot of things to pay… Please help me to finally feel alive as a woman. Thank you very much if you help me and if you can't contribute, can you share the money pot, please ? That's can help me anyway.  Thanks you very much. Elise ____ Bonjour, Je m'appelle Elise, j'ai 23 ans et je suis une femme trans. Je vis en France. J'ai crée ce pot commum pour m'aider à payer les frais de mon opération génitale. Je n'aime pas demander de l'argent aux gens, je suis une femme qui aime tout faire par elle-même. Je gère toujours par moi-même les problèmes quelque soit le problème et sa difficulté. Mais aujourd'hui, il s'agit d'un montant très élevé, 15.000 € ! J'ai calculé le temps dont j'aurais besoin pour l'avoir, plus de dix ans. Je ne peux pas attendre autant ! J'en ai besoin le plus tôt possible. Et la chirurgie est déjà prévue pour 2020. C'est un temps très court pour financer ce montant, c'est pourquoi j'ai besoin de votre aide aujourd'hui, car je n'ai pas le temps d'avoir le montant. Alors, aidez-moi s'il vous plaît ! J'ai besoin de cette chirurgie parce que je me sens mal à l'aise avec mon sexe de naissance, quand je prends une douche, je me vois en tant qu'homme à cause de ça, je veux me sentir comme une femme. Je déteste me voir en tant qu'homme, la société le fait assez. Bien sûr, je travaille, je travaille beaucoup, je travaille toutes les nuits sauf les dimanches pour avoir un peu de repos. Et j'ai un travail difficile. Mais même si je travaille autant, je ne peux pas vivre décemment. Parce que comme tout le monde, j'ai aussi beaucoup de choses à payer ... Alors, aidez-moi à devenir une vraie femme. J'en ai besoin. S'il vous plaît. S'il vous plaît aidez-moi à me sentir enfin vivante, merci beaucoup si vous m'aidez et si vous ne pouvez pas contribuez, pouvez-vous partagez la cagnotte, s'il vous plaît ? Celapeut quand même m'aider ! Merci beaucoup ! Elise.

1

€50

0%
For the treatment of Veronica

For the treatment of Veronica

Hello everyone!Our daughter Veronika has a difficult post-vaccination complication (BCG osteitis). Tuberculosis vaccine from the vaccine destroyed the bone tissue of the leg and damaged 2 vertebrae.When she was 5 years old, she was operated after an anti-tuberculosis therapy in one of the orthopedic clinics in Germany. Unfortunately, the zone of growth was affected and now, when the girl physically develops especially quickly, one leg became much longer. This greatly worsens the formation of the whole organism.The operated leg should be lengthened. And for this, again to do the operation. And again in Germany. The operation will cost 26,000 euros, which must be paid into the account in advance. But this is by preliminary calculation - the final cost can be more. In addition, the self-stretching will take 3-4 months, and this time the doctors strongly advise us to be near the clinic. Therefore, for this period we will move the whole family to Germany. Unfortunately, we did not have any money - everything that we had, we spent on therapy and the first operation. In total, this amounted to about 70 000 Euros. Now Veronica can only count on your help. Before the operation, two and a half months remained. If you can, help her with the feasible amount. And we will pray for our daughter. And for you. Full Story:https://www.facebook.com/notes/help-veronika/%D0%B8%D1%81%D1%82%D0%BE%D1%80%D0%B8%D1%8F/172641459950735/ Conclusion of doctors with Ukrainian translation:https://www.facebook.com/media/set/?set=a.171924790022402.1073741830.166985703849644&type=1&l=836448ed9ePre- Calculus cost of treatment:https://www.facebook.com/media/set/?set=a.171924536689094.1073741829.166985703849644&type=1&l=d3328f4842 Total cost calculation:https://docs.google.com/spreadsheets/d/1NEqpej2Rv6XNDjZVoukCUfdkuXxj1R7diFXhrSRfBZg/edit#gid=0

1

€50

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