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 has been updated to August 31 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

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left

81
contributors

£1,175
collected

117%
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 has been updated to August 31 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

£1,175

5 D

117%
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

£1,250.20

97 D

250%
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

66 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

€630

91 D

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

128 D

0%
Tous pour Newtøn

Tous pour Newtøn

Bonjour les ami(e)s des BBS ,je me présente pour ceux/celles qui ne me connaitraient pas : je m'appelle Newtøn, j ai 5 mois et je suis atteint de ce que l on appelle Non Union du Processus Anconé (dysplasie du coude gauche).J ai une maman qui souhaite le meilleur pour moi et qui a pris rendez vous avec le Dr Ragetly au CHV de Frégis pour le 22 septembre a 10h.Comme ma sœur Naphtaline, maman , les chats et moi vivons dans l'Ariège , cela sous entend TGV et hôtel durant 5 jours.Je vais subir scanner , arthroscopie et chirurgie mais je n ai même pas peur , je suis un battant et j ai confiance. La suite m embête plus , a savoir immobilisation pendant 1 mois puis  rééducation (kiné ,ostéo et hydrothérapie.)Hélas tout cela a un coût et je ne voudrais pas que maman décide de braquer une banque a cause de moi ...je me vois mal lui porter des oranges en clopinant lolBref je fais appel a votre bon cœur , sans obligation bien sur et en rappelant que ce sont les petits ruisseaux qui font les grandes rivières donc il n y a pas de petits dons et chaque euro compte.Merci de m avoir lu et de ce que vous pourrez faire pour m aider .Signé : Newtøn Hello White Swiss Sheperds friends, I introduce myself to those who do not know me: my name is Newtøn, I am 5 months old and I am suffering from what is called Ununited Anconeal Process (dysplasia of the left elbow).I have a mom who wishes the best for me and who made an appointment with Dr. Ragetly at the CHV of Frégis for September 22 at 10am.As my sister Naphtaline, Mom, the cats and I live in Ariège, this underpins train and hotel for 5 days.I'm going to undergo scanning, arthroscopy and surgery but I'm not even scared, I'm a fighter and I have trust. The following is what bothers me the most :, immobilization for 1 month then rehabilitation (physiotherapy, osteo and hydrotherapy).Alas all this has a cost and I would not want mum decides to steal a bank because of me ... I do not see myself limping to bring her oranges lol In short I appeal to your good heart, without obligation of course and remembering that it is the small streams that make the great rivers so there are no small gifts and every euro counts.Thank you for reading and what you can do to help me. Signed : Newtøn

€903.18

22 D

De corazón a corazón

De corazón a corazón

CAMPAÑA SOLIDARIA DE CORAZÓN A CORAZÓN Familia grande de amigos y amigas: Nuestro querido GONZALO CARDOZO ALCALÁ, reconocido escultor boliviano, a vuelto a ingresar a Terapia Intensiva, con múltiples diagnosticos complejos. Necesitamos estabilizarlo para trasladarlo a la ciudad de Cochabamba, donde se debe someter de forma urgente a una cirugía de RECAMBIO DE VÁLVULA AÓRTICA. Esta cirugía cardÍaca implica una especializada atención médica y una erogación económica importante (alrededor de Bs. 100.000.- equivalente a 13.000 euros). A todos los amigos y personas de bien, les invitamos a sumarse a esta campaña solidaria para la recaudación de fondos monetarios destinados a su recuperación. POR EL CORAZÓN DE GONZALO UNAMOS NUESTROS CORAZONES, GRACIAS!  SOLIDARITY CAMPAIGN FOR GONZALO Our dear friend GONZALO CARDOZO ALCALA, renowned Bolivian sculptor needs our help. He must be urgently transferred to the city of Cochabamba to undergo a valve replacement surgery. This cardiac surgery involves specialized medical care and significant economic expenditures (about 100,000 Bs. corresponding to 13,000 Euros). To all friends, we invite you to participate in this solidarity campaign to raise funds. ALL OUR HEARTS TOGETHER FOR THE RECOVERY OF GONZALO   CAMPAGNE DE SOLIDARITE POUR GONZALO Notre cher ami GONZALO CARDOZO ALCALA, renommé sculpteur bolivien a besoin de notre collaboration. Il doit être transféré à la ville de Cochabamba en toute urgence afin de se soumettre à une intervention chirurgicale de remplacement valvulaire. Cette chirurgie cardiaque implique des soins médicaux spécialisés et une dépense économique importante (environ Bolivianos 100.000 égal à 13.000 Euros). À tous les amis, nous vous invitons à participer à cette campagne de solidarité pour collecter des fonds. TOUS NOS COEURS ENSEMBLE POUR LA RÉCUPÉRATION DE GONZALO  SOLIDARITÄTSKAMPAGNE FÜR GONZALO Unser lieber Freund GONZALO CARDOZO ALCALA, renommierte bolivianische Bildhauer braucht unsere Hilfe. Er muss dringend in die Stadt Cochabamba verlegt werden um eine Herzklappenersatz-OP zu unterziehen. Diese Herzchirurgie beinhaltet spezialisierte medizinische Versorgung und einen großen wirtschaftlichen Aufwand (etwa 100.000 Bolivianos circa 13.000 Euro). An alle Freunde, laden wir Sie in dieser Solidaritätskampagne zu beteiligen.  ALLE UNSERE HERZEN GEMEINSAM FÜR GONZALO

€1,745

36 D

13%
Indispensable Urielle

Indispensable Urielle

Cette cagnotte est organisée par la famille Delierre, Lucie et Nature et progrès pour venir en aide à Laurent Lafourcade et à sa famille qui viennent de subir un gros coup dur. Voici l'histoire : Nous, les Delierre et Lucie (ainsi que son conjoint Antoine), avons passé le mois de décembre 2016 en wwoofing chez Laurent Lafourcade. Laurent est un jeune agriculteur idéaliste et engagé.Il travaille sans produits chimiques et surtout se fait aider par Urielle pour mettre en forme son petit près, "le lou pradot" en basque. Il veut que sa vie, son travail aient un sens et il fait pas mal de sacrifices pour y parvenir. Urielle est le nom de sa jument de trait. Elle est de race trait breton, 800kg toute en puissance qui réagit au murmure de Laurent tout au bout de ses longues rênes. Laurent convaincu de sa mission, nous fait découvrir à Lucie et à moi le travail de la terre avec Urielle. Nous passons des moments inoubliables où nous ne savons plus vraiment qui aide qui, et apprenant rapidement à mettre notre orgueil dans notre poche,nous découvrons que dans le champs, c'est elle la patronne et qu'elle sait très bien ce qu'elle fait. A nous de la gêner le moins possible ... "le dernier jour, nous avons construit un rond de longe avec Antoine. M'etant initiée a l'ethologie dans une vie antérieure, j'ai voulu essayer avec Urielle, qui, sans me connaitre beaucoup, m'a enormément donné" (Lucie) Quel exercice de communion fantastique. Nous avons vu pendant le mois une Urielle forte, déterminée, généreuse et un peu gourmande, c'est vrai ! Le deuxième jour, elle me connaissait à peine, mais elle a consenti à travailler avec moi dans son sillage, en autonomie, sans mépris pour le débutant. Elle m'a emmené en promenade sur des chemins difficiles où je me suis senti voler tant sa course était douce, même au galop. C'est vrai, elle aimait sa poignée d'orge après le travail. Vous l'aurez remarqué, elle est à présent au temps passé. Jeudi dernier, elle a fait une petite fugue pour un peu d'orge en plus, mais n'a pas su raison garder. Laurent l'a retrouvé au petit matin avec le nez dans le stock d'orge. Sans doute un brin de malice au fond de l'oeil pour le larcin commis, elle était déjà en sueur et gonflée. L'orge, en grande quantité, est extrêmement énergétique et fermente dans l'estomac du cheval. Le vétérinaire n'a rien pu faire et malheureusement elle a succombé à l'overdose. Laurent et sa famille sont évidement effondrés. Laurent l'a accompagné jusqu'à son dernier souffle qu'elle est venue expirer sur le pas de leur porte, comme pour finir auprès de sa famille, des gens qu'elle aime. Urielle était bien plus qu'une jument. Elle ne sera pas remplacée facilement, mais Laurent doit continuer à travailler et dans les meilleures conditions possibles. Cette cagnotte est pour lui, pour qu'il puisse continuer à avancer. Il voudrait former 2 poulains pour qu'ils se tiennent compagnie l'un l'autre. Le défi que relève Laurent est compliqué, il ne roule pas sur l'or, mais c'est un homme généreux. Je vous propose de le soutenir, non pas parce qu'il le mérite, mais parce que la générosité partagée est plus forte que toutes les méritocraties.   Merci pour eux !

€930

21 D

23%
Recover the brain cavity

Recover the brain cavity

Urgent – Important – Heart express! Dear all, my young dear brother SUMAN KRISHNAN aged 36, married and father of 2 young girls (age of 2years old and 1month old) had a bike accident on 22/06/2017 near Mamallapuram (Tamil Nadu-India) he falls pretty hard and get directly unconscious, transport to hospital in Chennai ( Tamil Nadu-India) where they find out a big clot of blood in his brain and directly have to take him as emergency for an extreme operation, 2 days later they find one more big clot of blood in his brain so they made 2nd operation. Operation in that kind of stage happened in one of the biggest expensive hospital in Chennai. The ambulance takes him to hospital in Chengalpattu (Tamil Nadu-India) but the doctors said they don't have all the equipments to save him, it was life or death, in this situation the only person in the ambulance it was my mum, as mum to save her son she leaves the choice to the ambulance Thats how we save his life. From now onwards my family had to pay 600 000 rupees (9250 euros ) only for the first 4days. When my family finds out it's lots of money they changed the hospital on the 26th juin where they charge 3000 rupees (45 euros) par day. The doctors say it can take few months to recover and then he needs one more operation. The 3rd operation will be to recover the brain cavity that will cost around 300 000 rupees (4600 euros). As per as we feel completely useless to see my brother in the hands of god choice, we also feel pretty devastated with all expenses. We need around 1 300 000 rupees (20 000 euros)Me and My family already collect 650 000 rupees (10 000 euros).We need more 650 000 rupees (10 000 euros) and we need the friends support for that! So I come through the Social Media for once as to take his word: SocialSo today, as a human, as a brother who wants to see again his brother healthy, as a son to help my parents, as all i can, i send hearty request to you all dear friends and family for any financial help to release my family from a over debt. I believe friends of my friends will be my friends, and heart will speak as an echo to help a life, a family life.We enquire all of you who would like to contribute to help us to get this amount. To help us you can send any amount you can by Western Union to: Krishnan SugumarFranceMobile number: 0033 666 171 962Email: sugukrishnan11@gmail.com We can show you all hospital reports and if someone feel also you can see a video about his actual status, but this video can hurt sensitivity. But we would like to share with you all the information to show you all the actual situation. We ll share with you all the hospitals bills and the updating after that.Your sincerely and heartilySugu

€560

5 D

2%
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

95 D

3%
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