Dear BAFF family! As each year around Thanksgiving, the Baltic-American Freedom Foundation family and friends join their efforts to support a good cause and those in need. For this year's BAFF Charity Campaign we have chosen to support the NPO Minutes of Silence (MTÜ Vaikuseminutid) in Estonia. The goal is to increase the well being and brainpower of Estonian children. We make short awareness exercises accessible and applicable to the Estonian education system as well as for families. WHO predicts that mental health problems will be the main cause of incapacity for work in the world by the year 2030. Smartphone dependency and focusing problems are likely to increase as well. Studies show that the skill to direct and maintain attention improves the ability to cope with anxiety, stress and negative emotions.The mission of the NPO Minutes of Stillness is to support the development of focusing and self-management skills based on the science-based method of mindfulness. The exercises for the development of focus and calm help children, young people and adults escape from mental distractions, destructive emotions, and stress. It promotes the skill of self-management and focusing on what is important.The NPO Minutes of Stillness has provided training to over 4,00 teachers and parents and to about 45,000 children. The income from training fees covers only a part of the cost of their operations. They need additional support for further expansion and development.Your donation will help to create audio exercises and training videos and provide even more effective support to parents and educational institutions. By donating you also help promote the message! http://vaikuseminutid.ee The recommended donation amount is 25 euros, but more significant donations to support this cause are very much encouraged as we aim to raise a record of 2500 euros this year from BAFF family and friends. With just 1-click you can support this great organization!Please follow the “Contribute” button on the right and do not postpone it to later!Be sure that all payments are 100% secureThe amount donated will be transferred directly from Leetchi platform to NPO Minues of Silence bank account that will then be available for them to use. Thank you!
Hello everyone & welcome to an online donation for EmilyOn Saturday 2nd November Ballyfore and Clogherinkoe GAA will play in a fundraising challenge match to raise money for Emily. As part of the event there will be a raffle and Auction but also on the night our good friends Kevin "Boots" Corcoran and Darryl Brereton will part with their much loved and famous beards! We would kindly ask that you donate to this worthy cause Thank you!
Raising a funding campaign as I came across the story of Marc Alexander, 18 month baby boy born in Haiti and diagnosed bilaterally deaf (both ears). Long story short, Haiti does not have the proper medical infrastructure and the government support to help this little boy get a cochlear implant surgery that would give him the ability to hear and speak. The longer he waits to get the implant, the more irreversible speech and development delay will occur. This would cost USD 30,000 including a trip abroad to get the surgery done (I myself have done research for my daughter and no kidding, it really cost that much). I spoke to his mother who didn't know what to do and who to turn to, and I felt the need to help them. As a French national and a Hong Kong resident , and as a mother of a 6 months deaf baby myself, my family is fortunate enough to have access to the best-in-class health support, excellent medical care and infrastructure ...and this is all (or almost) FREE!! We tend to forget how lucky we are. This little boy does not share our luck.Please take some time to read his story, DONATE and SHARE THIS POST to help him get access to a cochlear implant surgery, this amazing, life changing technology that will give him back the gift of hearing and speech.Carine Story of Marc Alexandre: Hello everyone. We are Kamaïa and Darlin Jeanty, parents of 18 months old Marc-Alexandre. We live Haiti, one of the most under-developed country in the world.We suspected the deafness of our son when he was 2 months and a half, as he was not reacting to sound. Due to lack of medical resources and infrastructure in Haiti, we were unable to obtain a diagnosis right away. When Marc-Alexandre turned 12 months old, we had been recommended to have him checked out in Republic Dominican. Without a second of hesitation, we took out all of our savings and bought a flight for the 3 of us to go meet an ENT specialist there. The results were devastating: Marc-Alexandre was diagnosed bilaterally deaf (both ears). We were not sure what to do or where to turn. We do not know if he would ever say, "I love you Mommy and Daddy." We have prayed for a happy, productive life for Marc-Alexander, and we want him to go to school and someday graduate from university to pursue a career and a life that he chooses.The ENT was adamant that our son needed cochlear implants; Implanting Marc will give him access to sound which will provide him with the only chance of age-appropriate speech and language development. This will provide him the opportunity to a better education and independent employment as an adult in the future. If not implanted, it may lead to permanent changes in the auditory cortex in the brain which may make it impossible to benefit from a cochlear implant or any form of hearing restoration surgery in the future. The cochlear implant bypasses the damaged portions of the ear and directly stimulates the auditory nerve. The signals are generated by the implant and are sent passed the auditory nerve to the brain where the signals are recognised as sounds. However, the cochlear implants will cost USD$30,000 as we do not have insurance and there is no government social subsidy or help of any kind. We are raising money to pay for medical expenses including surgery, cochlear implant device, and a trip abroad for the surgery.Marc is growing up and as his parents; we know we have to do something. The only future for our son is to hear with cochlear implants. Just like everyone else, we want to give him the best possible future there is.Life is so precious and this innocent boy who deserves the right to live normally. In advance, we extend our heartfelt thanks for your incredible moral and financial support. Thank you for helping us change the life of our child. Kamaïa and Darlin Jeanty
Hello everyone! This summer my brother Max has been diagnosed with lung carcinoma complicated by pulmonary embolism. It was very unexpected because Max even has no bad habits.The situation looks even worse as Max and his wife are expecting a baby to be born in early 2020. The oncologist prescribed chemo/immunotherapy as soon as possible without delay - for the duration of one year. The cost is 5 000 EUR per treatment (every 3 weeks). He needs approximately 18 treatments for the year. He's chance of survival depends so much on this treatment. Our family appreciate so much any help you can give us.
Nous sommes 6 étudiants en 3ème année d’école de Commerce (NEOMA Business School) et nous avons pour projet de venir en aide à une association en faisant un appel d'aide auprès des entreprises et des particuliers. Notre équipe avons donc choisi d’aider l’association : Un Rêve pour Arthur. But du projet: - Participation au financement d'équipements pour aider Arthur dans sa croissance: Fauteuil adapté, poussette adaptée.-Participation au financement des thérapies d'Arthur (12 000€/an). Ces éléments sont un réel soutient au bon développement d'Arthur. En quoi consiste cette association ? Un Rêve pour Arthur a été mis en place par Julie Moulin, maman d’un petit garçon, Arthur 7 ans atteint d’une grave maladie neurologique due à une mutation génétique très rare: CDKL5. Arthur a un important retard de développement psychomoteur et subit quotidiennement d’intenses crises d’épilepsie. En 2012, il a été diagnostiqué sur Arthur une Myoclonie (épilepsie infantile), cette maladie s’est avérée pharmaco résistante. Cette maladie située dans le lobe occipital a entrainé la perte de la vue chez Arthur. Le syndrome de West (spasme intense) s’est ajouté quelques mois après. Arthur devient donc hypotonique. Il ne voit pas, ne communique pas, et ne tient pas sa tête. Durant sa première année de vie, Arthur a passé une centaine de jours au CHU de Rouen. En mars 2013, son pronostic vital a été engagé pendant plusieurs jours. Cette maman pleine de courage a créé cette association dans l’espoir de faire face aux frais liés à la pathologie d’Arthur (thérapies à l’étranger, équipements…). Julie souhaite également faire connaître cette maladie rare. C’est pour cela qu’elle apporte son soutient aux familles vivant ce combat tous les jours ! C’est pour cette histoire et pour ce combat, que notre équipe avons décidé de nous engager ! Nous faisons appel à votre générosité et votre gentillesse pour venir en aide à cette famille et nous aider dans notre projet. Nous espérons que vous ressentirez l’émotion et le dévouement que de notre équipe avons mis dans ce projet. Pourquoi pas en faire partie avec nous ? Le site internet de l’Association pour plus de détails: www.unrevepourarthur.fr La Page Facebook: https://m.facebook.com/unrevepourarthur/
Hello everyone & welcome Sri Lanka is a country with numerous medical difficulties where there is a lack of contribution from government to improve healthcare facilities. Vision 2025Empowering Apeksha hospital to be one of the best in South East Asia. MissionWith the Generous Contributions of the General Public Equipping Apeksha hospital with all the advanced technological equipment to take care of the most deserving ones in our society. If you could contribute even a single penny would be the most welcome. Very much love.
It is with sadness that we, family and friends, write this about SALOHINIAINA MANOHISOA Estelle Evan (S'telle Ny Aina ). S'telle Ny Aina is a loving nurse from Madagascar. She's a devoted wife and mother of two. Since she entered the health care profession, she dedicated herself to her fellows well-being. Taking care of people and seeing patients smile during their hardest time was a pure joy. She has been an Operation Smile Madagascar volunteer for more than five years. With Operation Smile, she participated to many medical missions as a Post-Anesthetic Care Unit nurse (PACU nurse). In 2018, S'telle Ny Aina was diagnosed with an End stage Chronic Kidney Disease . She is currently undergoing dialysis three times per week which is very costly in Madagascar. But even under the dialysis her condition isn't improving. Her doctor suggested that kidney transplant is the only way to save her. Transplants surgery is a surgical procedure that still cannot be done in Madagascar.So we, Family and friends have contacted some hospitals in India for the procedure (Apollo Hospital). As of now, we collected just enough for some aspects of her treatments in India (the surgery) . But we still need your help for her pre and post-operative treatments, accommodation and flights to India, etc... S'telle Ny Aina still has her hope high. She believes that her job in this world is not done yet. We friends and family would like to fight together with her and not let down her two small childrenWe would be most grateful for any financial helps and support to give S'telle Ny Aina a chance to live.Please keep her in your prayers
Billie braucht einen Autistenhund - und ihr könnt helfen!Billie ist Autistin, Aspergerautistin oder hochfunktionale Autistin, wie immer man es auch nennen will.Billie hat jetzt schon einen Hund, George Michael - er hilft er jetzt bereits sehr im Alltag, aber er soll eine echte Ausbildung bekommen und dann wirklich verlässlich zur Seite stehen können. Billie wirkt nach außen komplett normal, aber sie dennoch komplett anders gestrickt als die meisten Menschen. Sie hört und sieht viel mehr und besser als normale Menschen, dh die Welt ist für sie immer sehr laut und grell. So lustig Billie auch ist, so schwer ist es manchmal für sie, andere Menschen zu verstehen, die meisten sozialen Regeln muss sich Billie beibringen, und wenn sie Fehler macht, dann nagt das sehr an ihrem Selbstwert. George wird dann für Billie:. Erkennen, wenn ihr die Umwelt zu viel wird und sie von zu starken Umwelteinflüssen abschirmen (indem er ihre Aufmerksamkeit auf sich lenkt). Erkennnen, wenn sie einen "Sensory Overload" bekommen, dh, wenn ihr Gehirn von den vielen Sinneseindrücken übervoll wird und nicht mehr mit der Informationsverarbeitung nachkommt. Er warnt sie dann und leitet sie aus der Situation heraus.. Er hilft er beim Einschlafen. Er senkt ihre Nervosität . Er hilft ihr bei der Bewätigung sozialer Ängste. Er ist ein Brückenbauer zwischen ihr und anderen Menschen. Er ist immer für sie da und sie für ihn. Ein Autismushund kostet wegen der umfassenden Ausbildung bis zu 30.000 euro. Da wir unseren eigenen Hund ausbilden wollen, wird es billiger - aber noch immer sehr teuer. Abhängig davon, wie schnell George lernt, wird es 10.000-20.000 euro kosten.Die Krankenkassen zahlen nichts dazu - wie bei den meisten Therapien für Probleme, die AutistInnen haben. Wir sind zwar als Familie in der glücklichen Lage finanziell nicht in einer angespannten Situation zu sein, da wir aber schon so sehr hohe Zusatzkosten aufgrund des Autismus haben (Einzelunterricht, wenn Billie wegen ihrer Ängste nicht die Schule besuchen kann, Psycho- und Physiotherapien, Betreuungsperson, Hörschutz, Sehschutz, Gewichtsdecke, etc etc) sprengen die Kosten für die Hundeausbildung wirklich unsere finanziellen Möglichkeiten. Es wäre sehr toll, wenn ihr mithelfen könntet, dass Billie mehr Freiheit & Lebensglück bekommt, indem sie einen Autistenhund an ihre Seite bekommt. Jede Spende, egal wie klein/groß ist willkommen :) DANKE! ---- Billie is autistic, she is Asperger's or high-functioning autistic, however you wanna call it.Billie already has a dog - called George Michael - he already helps her a lot with her daily routines, but he needs to be properly trained so he can be a real realiable assistance for Billie whereever she goes. Billie will look totally "normal" for other people, but still she is completely different to your average Joe and Jane. Her hearing and visual abilities are way beyond regular human standards - which means this world we live in is constantly too loud, to bright, too colorful and generally to wild and exhausting for her. Billie is a very fun person, but it is incredibly hard for her to get to understand how other humans work, operate, socialize etc. She has to teach herself pretty much anything in the context of social interaction and especially in terms of language - reading between the lines, so complicated! Billie suffers a lot when she makes mistakes and usually other humans are not very forgiving regarding her misinterpreting standard human behavior. George will be there for Billie to:. Notice when Billie is getting overwhelmed and then distract her by concentrating her attention on himself.. Notice when she is going into "Sensory Overload", when her brain is overflown by too much sensory input and fails to digest and filter all the information. He warns her and leads her out of the stressful situation. . He helps her fall asleep.. He lowers her anxiousness. . He helps her deal with social phobias.. He connects between her and other people. He is always here for her and vice versa. Ein Autismushund kostet wegen der umfassenden Ausbildung bis zu 30.000 euro. Da wir unseren eigenen Hund ausbilden wollen, wird es billiger - aber noch immer sehr teuer. Abhängig davon, wie schnell George lernt, wird es 10.000-20.000 euro kosten.Die Krankenkassen zahlen nichts dazu - wie bei den meisten Therapien für Probleme, die AutistInnen haben. Wir sind zwar als Familie in der glücklichen Lage finanziell nicht in einer angespannten Situation zu sein, da wir aber schon so sehr hohe Zusatzkosten aufgrund des Autismus haben (Einzelunterricht, wenn Billie wegen ihrer Ängste nicht die Schule besuchen kann, Psycho- und Physiotherapien, Betreuungsperson, Hörschutz, Sehschutz, Gewichtsdecke, etc etc) sprengen die Kosten für die Hundeausbildung wirklich unsere finanziellen Möglichkeiten. Es wäre sehr toll, wenn ihr mithelfen könntet, dass Billie mehr Freiheit & Lebensglück bekommt, indem sie einen Autistenhund an ihre Seite bekommt. Jede Spende, egal wie klein/groß ist willkommen :) DANKE!
Hello everyone, This pot is created to help Rayyona fight with leucosis. Rayyna is a small girl of 2 years old from Uzbekistan. She urgently needs lifesaving bone marrow transplantation in Memorial Hospital, Turkey. This procedure can save her life, but it can be done only in Turkey as this treatment is not yet available in Uzbekistan. Please help small Rayyona to stay alive and to win leucosis. We trust it can be done together with a small effort of every kind heart. Your help of 5 - 20 - 30 euro is very important for Rayyona to fight leucosis and live a long healthy life. WeThank you!
Hello everyone & welcome to this money pot!Unfortunately our veteran community is suffering an epidemic of untreated PTSD and related mental health issues due to chronic lack of government post service support. This lack of support means that we have a massive amount of ruined lives within our veterans community and a disturbing rate of suicides also. The Minds At War team work tirelessley to prevent suicides and give much needed support and therapy to those that are most in need. We provide a safety net where possible for those that come under our radar and need your help to keep our service operational and expanding.Our team is currently totally volunteer based and we need funds urgently to be able to operate and expand our first responder helpline, travel across the country in every day emergency situations, pay for therapists for ongoing support, and other general running costs. Please give generously whatever you can afford and you will be helping us immensely to change lives and save lives. - Thank you in advance Minds At War
Hello everyone & welcome to this money pot!With just 1-click you can help an individual in need cover medical expenses and get back on their feet* Give however much you want* All payments are 100% secure* Why Leetchi.com? It's easy & transparent!Thank you!I am trying to raise funds for my dear friend Rose. She has been selfless all throughout her life and helped others in need. Working long hours and often volunteering in her spare time.She needs urgent medical care and cannot raise the funds herself. Please any small amount helps to get her on her feet again. God bless
Hello everyone & welcome to this money pot!So far, two of my young friends/classmates succumbed to leukemia, he was 17 and she did not live to reach 30. Both were happy, sporty, active persons from good families. After their deaths I felt like 'Why them, why not me?'. But I could not change the unchangeable. Many years have past, and I keep watching young people, young sportsmen battle with this disease and lose. I have no clue what could cause this, probably food, probably 'medicine', I really don't know. Till this point I did not know what I could do for them, but for now, I will start this fundraising, and try to donate continously, and personally. I won't go to foundations where I do not see the path of the money, I will aim the family of the next young guy or girl with what you gather here [+ what I can afford from my salary]. And hopefully the next, and the next [because we cannot assume this evil thing will stop]. This could and should be documented, probably via a blog. We will find out. Thank you for reading!
Our Dad, only 63. received the devastating news last October 2015 that he had an extremely rare and aggressive type of bladder cancer, small cell mixed transitional cell carcinoma. Less than 1% of all bladder cancers are this rare type.The main cause of bladder cancer is smoking, Dad has never smoked and prior to diagnosis led a fit and healthy lifestyle.After undergoing three cycles of the standard chemotherapy we were told that this cancer has a slim chance of being treated with the drugs available on the NHS.In a desperate bid to save our Dad's life, we have found a specialist onchology doctor in London who has given us hope.Dad's biopsy of the tumor has been sent to America where the molecular status of the cancer cell can be examined with the aim to find a target drug the cancer cells respond to.In the meantime Dad is battling gruelling rounds of chemotherapy to control the spread of the cancer while we await news on which drugs will be the right tonic.These privately funded drugs are extremely expensive. We have put our total life savings into the treatment so far and have already spent up to £50,000.00 on the chemotherapy drugs, biopsy, blood tess, research, train fares, CT Scans, specialist fees.We are reaching out from the bottom of our hearts for help with these vital funds. Any donations will mean so much to us and our small family and if you are struggling to donate then please just raise awareness.Dad has a positive attitude and knows he can fight this with the right treatment. He is so kind and generous and nothing is too much trouble for him. He puts everyone else before himself and he's finding it difficult now he's the one in the spotlight. Dad is a massive animal lover and has always donated to animal charities. We would like to return the kindness and love he has given to us over our lives.We do not want to lose our Dad and and know this can be treated. He is being supported all the way by our dear mum and loving wife Ret. Please help our small family to achieve this. This research may also hellp bladder cancer patients in the future who are unfortunate to have this rare type.We will keep all supporters updated n treatment and how things are going.Thank you from the bottom of our hearts,Daughters Kelly, Karla and loving wife Ret
Hello everyone & welcome to this money pot!My Uncle is a mentally and physically strong man in his fifties, actively helping my grandparents while I have to work in a remote location. Yet, he is facing a heart operation now, and I want to provide him with the best possible doctor and best operation methodology in our country, which means a greater chance of success, a shorter recovery phase than usual and a quicker re-enlistment to work. It is important for him to get this threatment as soon as possible, because his condition can worsen every day. What can I provide in exchange? Hopefully a signed family photo with the recovering patient in the center, and a dedicated thank you email from Him + reports of Our (You and We) success. (Plus copies of forthcoming medical papers, if you like. Just to be sure, just for evidence.) Probably more. Probably my software development services on a discounted price [details later].
¡Hola a todos y bienvenidos a este bote de dinero!el niño Daniel Ciofani ozuna, tiene retraso motor y de desarrollo causado por daño cerebral al nacer, ha perdido la audición en ambas partes y no es autónomoPor favor, quién puede ayudar con su tratamiento y su comida ya que su madre debe estar al cuidado del niño y su padre no puede encontrar un trabajo. DIOS lo recompensará il bambino Daniel Ciofani ozuna, ha un ritardo motorio y di sviluppo causato da un danno cerebrale alla nascita che ha perso l'udito in entrambe le parti e non è autonomoDIO ti ricompenseràPer favore, chi può aiutarti con il tuo trattamento e il tuo cibo poiché tua madre deve prendersi cura del bambino y tuo padre non riesce a trovare un lavoro.
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