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

8 D
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

8 D

117%
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

69 D

10%
Improving Mental Health for the Poor in Cambodia

Improving Mental Health for the Poor in Cambodia

This page is to donate money to Prof. Alex Wood to help some of the poorest people in Cambodia to get better mental health care. The money is planned to be used as part of an ongoing project to improve the treatment of mental health in the region, or to be donated to a hospital which gives good healthcare to the poorest people for free (or at a cost affordable to them).Best value charitable donation - no middle menA key challange with giving to charity is knowing how much actually gets to where it is needed. Alex is able to personally take the money to where it is needed and use or give the money directly to the hospitals. No middle men, no employees, no advertising, none of the normal worries about the efficiency of charities.Our Mental Health ProjectImproving mental health services is a key health challenge for developing countries across South East Asia. Cambodia faces particular challenges following a genocide and series of wars in the 1970s and 1980s. During this period health care and university services were nearly entirely destroyed, including through a particular targeting of medical practitioners and academics for execution during the Pol Pot era. In the last two decades, Cambodia has made impressive efforts to rebuild its health and educations systems, including through the establishment of a basic infrastructure of hospitals, medical education universities, and aspirations to conduct international quality research. This has led to notable improvements in physical health as seen, for example, in arrested and declining HIV rates. However, mental health needs have been nearly entirely neglected, and the Cambodian population is largely without access to even rudimentary psychiatric or psychological treatments in both primary and secondary care, leading to several problems.First, rates of untreated mental illness are very high, with associated suffering and stigmatisation. Globally, the World Health Organisation (WHO) estimates that depression alone causes more suffering than that generated by all physical disorders combined. This suffering may be expected to be exceptionally high in Cambodia as almost no one in the older generation will have avoided witnessing or experiencing highly traumatic events, and the younger generation will have been born and parented in the recent aftermath of the trauma.Second, mental health conditions are often miss-diagnosed as physical, leading to inappropriate treatment that both wastes resources and risks harming the patient through unnecessary treatment, which in many cases exacerbates the mental health condition.Third, the treatment of chronic physical health conditions is complicated through a lack of assessment or treatment of co-morbid mental health conditions, resulting in the physical health conditions being more difficult and expensive to treat, as well as causing a considerably worse prognosis for the patient. For example, key challenges of HIV programmes include; (a) missed appointments, (b) patients dropping out of the system, (c) the need to locate patients that have so disengaged, (d) lack of adherence to treatment leading to both the emergence of opportunistic infections and HIV medication failure, (e) the need to use newer, more expensive medication due to first line medication failure, and (f) erratic medication compliance risking the emergence of drug resistance at the population level with international implications. Much of these problems emerge from patient disengagement and non-compliance, a key predictor of which in other countries is untreated simple mental health conditions such as depression. Adding a mental health assessment and treatment protocol may both reduce these problems and lead to a net financial saving for the programme.The implementation of an evidence based mental health programme is not currently possible due to the near total lack of research on how to assess or treat mental health in Cambodia, and there is no current mechanism to disseminate new p

£90

101 D

9%
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

131 D

0%
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

39 D

13%
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!

£1,015

256 D

Help the heart of my father Mario Pernía keep beating!

Help the heart of my father Mario Pernía keep beating!

Help the heart of my father Mario Pernía keep beating!  My father, Mario Arecio Pernía, needs the urgent implantation of a new pacemaker since his current one is about to stop working. His doctor told him that he needs to replace his pacemaker within the next 30 days. My Dad lives in Venezuela and was diagnosed with hypertensive heart disease (HHD) 12 years ago. Due to this condition he has been the holder of a pacemaker type DDDR since 2005. The life span of this particular pacemaker is about 10 years, which means his machine has been overdue for replacement for about 2 years. Due to the weakness of the current machine my father is showing signs of dizziness and severe impaired locomotion. My father is a 75 years old retired career officer of the Finance Department of the Venezuelan National Assembly (VNA). In the middle of the Venezuelan political and humanitarian crisis the government decided to shut down the budget and the health insurance of the VNA members for political retaliation. As a consequence, today my father cannot afford the cost of the new pacemaker and the implantation surgery. The cost of the new DDDR pacemaker and its surgical implantation is USD 3,292.0 (€ 2,770.0). The surgical procedure will be led by Dr. Elías Najas (MD-ID/MSAS: 22848)  in the "POLICLINICA METROPOLITANA C. A." (http://www.pcm.com.ve) in Caracas, Venezuela.  Please help me raise the money for my father's surgery by sharing and donating. Every cent counts! Thank you so much for helping! Click to make a contribution.* Give however much you want.* All payments are secureThank you!

€895

24 D

32%
Help Elena Moeseeva

Help Elena Moeseeva

Всем привет. Есть одна молодая девушка, Elena Moeseeva.Она борется с раком лимфатической системы уже больше двух лет. Мы, её друзья, пытаемся собрать средства для её дальнейшего лечения, и вынуждены обратиться с просьбой о помощи. Ей срочно нужно собрать сумму в 35 000 долларов США, для того чтобы начать лечение в Китае. Если у вас есть желание и возможность помочь финансово, вы можете связаться с ней напрямую или сделать пожертвование здесь. Если вы можете помочь советом или словами поддержки будем очень благодарны! Любая сумма приветствуется! Больше информации о болезни и ситуации вы можете найти в группах поддержки:https://www.facebook.com/groups/elenamoeseevahelp/permalink/1965992440344534/https://vk.com/elenamoeseevahelphttps://www.instagram.com/elena_moeseeva/ Спасибо большое за ваше понимание. --- We're raising funds for Elena Moeseeva, a young girl who has been fighting cancer for more than two years. She needs to be sent to China for a CAR T therapy ASAP. The cost of the treatment is 35 000 us dollars. More info is in the official support group:https://www.facebook.com/groups/elenamoeseevahelp/permalink/1965992440344534/https://vk.com/elenamoeseevahelphttps://www.instagram.com/elena_moeseeva/ Please donate if you can or spread the word. Every contribution is welcome. Reposts are welcome. Any message of support is welcome. Thanks!

€575

100 D

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

8 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

98 D

3%
Medica Afghanistan's medical emergency fund

Medica Afghanistan's medical emergency fund

Welcome to Medica Afghanistan's medical emergency fund !Violence against women and girls is still pervasive in our country and it hinders peace and development for all Afghan people. At Medica Afghanistan, we have been committed to end this violence since 2002. Despite struggling with an increasingly insecure environment, our team successfully supports 2,000 women every year with psychosocial counselling and legal aid. We also work with key people in politics and society to raise their awareness and build their capacity, and advocate for local and national policies to strengthen the rights of women. All of the women served by Medica Afghanistan are especially vulnerable – many of them being widows who have been traumatized by violence and face extreme poverty with no means of economic support. Some of them need urgent medical support.  While we don’t provide medical services ourselves, we cooperate with hospitals where we refer our clients for examination and treatment. To continue offering this support in 2017, we still need funding. Every donation counts - even a small donation of 20 – 50 Euro can provide them with the medical attention they need to cope and recover from their pain and hardship. * One of our clients, a 25 year old woman, was suffering from goiter, a condition which causes an abnormal enlargement of the thyroid. As a result of this, she had difficulties in breathing and swallowing, oftentimes leaving her coughing at length and breathless. She would often jolt from sleep and was always nervous about not being able to do something very basic, that is, to breathe. As she was very poor and not able to support her treatment’s expenses, we supported her through her surgery after which, her nervousness, palpitation, shortness of breath and fatigue disappeared.“Now I feel better. I can easily communicate in society and I don’t feel ashamed. Before that I felt that everybody paid attention to my illness.”  The cost of her treatment was approximately US$300. * Another client was suffering from severe prolapsed uterus, a condition which causes the uterus to weaken and sag into the vagina. Provided she was client to another services of Medica Afghanistan, yet again we helped her for her treatment, because due to her tight economic condition she was not paying serious attention to her health situation. We urgently referred her for medical examination and a hysterectomy was performed on her. To support her, we helped to pay her laboratory tests and medicine at a private hospital, which amounted to approx. USD$120. * Another client, a survivor of violence, was suffering from severe back pain as a result of beatings. We referred her to a Japanese clinic for physiotherapy to manage her symptoms. After six sessions of physiotherapy, she no longer has pain in her back and is happy to be able to return back to her normal life and live free of pain. To support her, we helped to pay her physiotherapy sessions which amounted to approx. USD$40.We have also supported many other clients from funding their CT scan examinations to surgery and finally, ensuring they receive physiotherapy treatment so that they can completely recover post-treatment.Currently, we are seeking urgent funding for a number of our clients. One of our clients who is only 23 years old is suffering from congenital heart disease, which is defect in the heart structure. She has been treated at the French Medical Institute for Children in Kabul, Afghanistan. However, the doctors have recommended that she undergo further examination and treatment in India, where there are facilities and specialists to look into her specific condition.  We are currently looking for 1500 $ of funding of her trip to India so that she can obtain the initial treatment that she urgently needs to fully recover and return back to her normal life once again. Any contribution at all is valuable. Most survivors of violence who are brave enough to leave their homes and approach us for assistance

€435

100 D

8%
MR & MISS FIGHT 4 LYME DISEASE TREATMENT

MR & MISS FIGHT 4 LYME DISEASE TREATMENT

welcome to our money pot my names Lauren & my partner is called Andy and we are both fighting lyme disease caused by the infectious bacterium borrelia burgdorferi. we are kindly asking for your help for much needed funding for private treatment as the NHS can't help us. we got funded by a charity called lyme aid uk as we couldn't afford to have the private tests done for Lyme disease,and our blood tests was sent to germany labs.the NHS testing for Lyme disease is less than 50% sensitivity and missed we had Lyme, like they are missing loads of people .our germany tests are 95% sensitivity and they are top specialist laboratorys in tick borne diseases. both myself and partners test results from germany come back possitive for lyme disease! the NHS have now refused to treat our Lyme disease or except our private results. Leaving us to get sicker and worried for what the future may bring,with no ways of getting any help without paying out for it our selfs. sadly this is a very big problem for many lyme patients trying to get help in the UK as the NHS testing is missing many people and not helping if they test private for this potentially deadly disease . we think it's now chronic lyme disease due to many symtoms we display.this can be fatal if not treated and left.we both have many other diseases and we have suspected co infections that come with lyme disease making us very sick.lyme disease infects the whole body through the blood to tissue to organ joints bone marrow and brain nothing escapes it and it comes with a very long list of mind blowing horrible dibilitating symptoms.This is a small range of what we suffer to give you a rough idea- Chronic fatigue Migrating chronic body pains/tenderness/tendinitis Pins & needles Numbness over body Swelling joints Terrible Memory issues/mood swingsSpeech problems Insonimia Depression/ anxiety Tingling, throbbing sensations all over body, itching crawling under skin ,cold dripping sensations in head and eyes these are so bizarre to explain! Bruises come and goSkin Rashes Servere Migraines/headaches Sickness Heart palpitations Bowel issues Eye irritation Cramps Tinnitus Extream Dizzyness &Unsteadness on feet.Sensitivity to lights/ noise /touch A feeling of drunkness and spaced out losing track of conversations Burning insides random parts of body Breathing issues/wheezing /coughingFlu symptoms on and off Total exhaustion doing the smallest of things and the list goes on!    we have been left with know choice but to try and raise some funds  for private treatment and really hope and pray you can kindly help us with a small donation to go to a private clinic, normally this does cost thousands for private Lyme disease treatment but we have found a place that's cheaper to start with, it may not be a cure but it is a good starting point to try and get into some kind of remission . we have three wonderful children and they also show some signs.This is a great concern for us and we now need to get them tested.The private clinic we plan to go to is a few hours away from home and this is going to cost us all £600 to see a private doctor there, to start treatment for myself and partner and get some answers /clinical dignosses for our three children. we can't afford to pay for us all to go, so your help and support is much neededAny small donations from a few pence to pounds would be very welcomed by my family.  Thank you for taking the time to read our appealand a BIG BIG Thank you if you did kindly donate to our money pot xxxx PLEASE FOLLOW OUR LINK BELOW TO OUR OUR FACEBOOK PAGE PLEASE FOLLOW AND SHARETHERES LOTS OF INFORMATION ON LYME DISEASE 💚💚 Or if the link doesn't work find us on facebook search -Fighting 4 Lyme disease treatment  https://www.facebook.com/pg/lhan1981/about/ More info at Www.lymediseaseuk.com    Click to make a contribution.* Give however much you want.* All payments are secureThank you!

£60

63 D

10%
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.

€50

357 D

0%
Help Ania fight off the cancer

Help Ania fight off the cancer

"Hope sees the invisible, feels the intangible and achieves the impossible."I have decided to create this Money Pot to help my friend Ania, who is battling cancer metastasis. Ania is 40-year-old mum of two (13 and 3), loving wife and a good friend. But life wasn't too gracious for her. In 2014 she lost her mother due to cancer. Month after her mum's funeral Ania was diagnosed with malignant breast cancer. She underwent chemotherapy, then mastectomy of right breast and radiotherapy with hormone therapy.In July 2015 cancer was defeated. She couldn't have been much happier. But her happiness had lasted for about one year only. In November 2016 she was told about metastasis to bones (left hip, pelvis on the right side, ribs on both sides, spine). And her battle with cancer had started again...Ania is very determined to fight it off, because she has very important reasons to live. Unfortunately conventional medicine is not able to help her, only to ease the pain with some strong drugs. But... There is a chance to cure Ania with intravenous infusions of vitamin C. Unfortunately 6-month treatment costs about £9,000 (one year costs £18,000!). It's not covered by NHS. To get this kind of treatment she has to travel abroad. It's very expensive, but it's the only hope for her and her family.Hope is the last thing to be lost. We can't lose it. If we lose hope, we lose everything. That's why Ania needs your help. Without this money she is not able to undergo the treatment which may save her life.Please remember one thing, helping Ania you are giving her sons hope that they will still have their mum...Every penny counts. Give however much you want.Thank you!If you wish to contact Ania, you can find her on Facebook: Anna Piżewska. With love,Edythe

£35

100 D

0%
Back to top