Help Save Iman's Life – Lung Transplant Fund

Medical

Help Save Iman's Life – Lung Transplant Fund
Save Iman's Life – Give Her a Second Chance to Breathe Iman is a young woman from Lebanon who is courageously battling severe hereditary progressive lung disease that has left her fighting for every breath. Today, she depends on continuous oxygen therapy, and her condition continues to worsen despite ongoing medical treatment. After careful medical evaluation, doctors have determined that a lung transplant is Iman's only chance to survive. Her family is doing everything possible to save her life, but the financial burden is overwhelming. The estimated cost of the transplant, hospitalization, and essential medical care is $300,000—an amount far beyond what her family can afford. Today, we are asking for your help. Your donation will directly support Iman's journey toward a life-saving lung transplant and the medical care she needs before and after surgery. Every contribution, no matter the size, brings her one step closer to breathing freely again. If you are unable to donate, please share Iman's story with your family, friends, and community. Your support can reach someone who may be able to help. Together, we can give Iman the hope of a second chance and the breath of life she deserves. Every donation matters. Every share brings hope. Every breath is priceless. Thank you for standing with Iman and giving her a chance to live. # أنقذوا حياة إيمان – امنحوها فرصة ثانية للتنفس إيمان شابة لبنانية تكافح بشجاعة مرض التليّف الرئوي الوراثي الشديد، وهو مرض رئوي تقدّمي أدى إلى تضرر رئتيها بشكل كبير وجعل كل نفس تأخذه معركة حقيقية. واليوم، تعتمد إيمان على جهاز الأكسجين بشكل مستمر، بينما تستمر حالتها الصحية بالتدهور رغم جميع العلاجات التي تلقتها. بعد تقييم طبي دقيق، أكد الأطباء أن زراعة الرئة هي الأمل الوحيد لإنقاذ حياة إيمان. تبذل عائلتها كل ما في وسعها لتأمين العلاج، لكن التكلفة تفوق إمكانياتها بالكامل. تبلغ الكلفة التقديرية لعملية زراعة الرئة، إضافة إلى الاستشفاء والرعاية الطبية اللازمة، 300,000 دولار أمريكي، وهو مبلغ يستحيل على العائلة تأمينه بمفردها. اليوم، نتوجه إليكم بطلب المساعدة. سيُستخدم كل تبرع لدعم رحلة إيمان نحو زراعة الرئة، بما يشمل تكاليف العملية، والاستشفاء، والفحوصات الطبية، والعلاج والرعاية اللازمة قبل العملية وبعدها. مهما كانت قيمة مساهمتكم، فهي تقرّب إيمان خطوة إضافية من فرصة جديدة للحياة والتنفس من جديد. وإذا لم تتمكنوا من التبرع، فإن مشاركة قصة إيمان مع عائلتكم وأصدقائكم ومجتمعكم قد تصل إلى شخص يستطيع أن يصنع الفرق. معًا، يمكننا أن نمنح إيمان الأمل بفرصة ثانية، وأن نعيد إليها نعمة التنفس التي تستحقها. كل تبرع يصنع فرقًا. كل مشاركة تنشر الأمل. وكل نفس يستحق أن يُنقذ. شكرًا لكم على وقوفكم إلى جانب إيمان، ومنحها فرصة للحياة.

$1,985 raised Of $300,000

Help Jad Fight Duchenne Muscular Dystrophy (DMD)

Medical

Help Jad Fight Duchenne Muscular Dystrophy (DMD)
My name is Mohamad, and I am a Palestinian refugee living in Lebanon. Today, I am reaching out with hope in my heart to ask for your support for my beloved son, Jad, who has been diagnosed with Duchenne Muscular Dystrophy (DMD)—a rare, progressive genetic disorder that causes muscles to weaken over time. DMD is a devastating disease. Without effective treatment, children gradually lose their ability to walk, become dependent on wheelchairs, and eventually face life-threatening complications affecting their heart and lungs. As parents, there is nothing more painful than watching your child lose the strength to do the simple things every child should enjoy. Despite this diagnosis, Jad is a bright, loving, and courageous boy who continues to smile, dream, and enjoy life. Our greatest wish is to give him the opportunity to remain mobile, independent, and active for as long as possible. Today, there is hope through gene therapy, an innovative treatment designed to address the underlying cause of Duchenne Muscular Dystrophy. This therapy offers children like Jad the possibility of slowing the progression of the disease and preserving their muscle function, giving them precious years of mobility, independence, and a better quality of life. The treatment is currently available in specialized medical centers such as Sidra Medicine in Qatar and Medcare Hospital in the United Arab Emirates. However, the cost of the therapy and the associated medical care is approximately USD 3,000,000, an amount that is far beyond what our family could ever afford. That is why we are asking for your help. Your contribution to this campaign will help us work toward giving Jad access to this life-changing gene therapy, as well as cover the medical evaluations, rehabilitation, medications, travel, and specialized care required throughout his treatment journey. Every donation—large or small—brings Jad one step closer to receiving the care he desperately needs. More importantly, your generosity gives him the chance to continue walking, playing, learning, and living with dignity and independence for as long as possible. If you are unable to donate, sharing Jad's story with your family, friends, and community would mean the world to us. Together, we can reach more people who may be able to help. We are fully prepared to provide all medical reports, genetic test results, diagnostic documents, and any additional information needed to verify Jad's condition and treatment requirements. From the bottom of our hearts, thank you for taking the time to read our story. Thank you for your kindness, your compassion, and your belief that every child deserves the chance to live a fuller, healthier life. Your support is more than a donation—it is hope.

$21,316 raised Of $3,000,000

No home, cancer is stealing my father in Gaza

Medical

No home, cancer is stealing my father in Gaza
We once had a warm home and engineering dreams that I was studying hard to reach. Today, my home and books are rubble. We live in a fragile tent, and hunger is our constant companion, leaving us to sleep on empty stomachs. Yet, losing our home and pausing my education isn't our deepest pain. It is my father—our pillar of strength—who is now fighting a brutal battle against cancer. With no medicine or healthcare available, we watch his weakened body fade away daily, completely helpless to afford even a single dose to ease his agony. We refuse to give up, but we cannot do this alone. Your donation is a meal to quiet our hunger, a life-saving medicine for my father, and a step toward getting me back to my studies. Please be our lifeline in this darkness. كنا نملك بيتاً دافئاً وأحلاماً هندسية أدرس لأجلها. اليوم، تحول بيتي وكتبي إلى ركام، وأصبحنا نعيش في خيمة لا تقي برداً ولا حراً، حيث يرافقنا الجوع في كل ليلة وننام على بطون خاوية. لكن الوجع الأكبر ليس خسارة الجدران ولا توقف دراستي؛ بل هو والدي، سندنا وقوتنا، الذي يصارع اليوم مرض السرطان بجسد أنهكه النزوح والجوع. نراه يذبل أمام أعيننا يوماً بعد يوم، وعجزنا يمزقنا لأننا لا نملك ثمن جرعة دواء واحدة تخفف عنه هذا العذاب في ظل انعدام الرعاية الطبية. نحن لا نستسلم، لكننا نحتاجكم. تبرعكم اليوم ليس مجرد مال، بل هو لقمة تسد جوعنا، وجرعة دواء قد تنقذ حياة والدي، وأمل يعيدني يوماً إلى مقاعد الدراسة. كونوا لنا سنداً في هذه الظلمة.

$0 raised Of $30,000

Help Kevin take steps through intensive therapy

Medical

Help Kevin take steps through intensive therapy
Help Kevin Take Steps Toward Independence Kevin is a courageous and determined young boy from Lebanon living with spastic quadriplegic cerebral palsy. Every movement he makes requires tremendous effort, yet he faces each day with a smile, incredible determination, and hope. Kevin dreams of becoming more independent, standing taller, walking with greater confidence, and participating more fully in school and everyday life. With the right intensive rehabilitation, these goals are within reach. About Kevin Kevin is a loving 8-year-old little boy who enjoys spending time with his older brother (12 years) and younger sister (4 years). He attends school with the support of a shadow teacher and works incredibly hard every day to keep up with his classmates despite the physical challenges he faces. His family celebrates every milestone, no matter how small, because every new movement has been achieved through years of therapy, perseverance, and determination. Medical Background Kevin was born prematurely at 30 weeks of pregnancy and spent 45 days in the Neonatal Intensive Care Unit (NICU). He later suffered a brain injury known as periventricular leukomalacia (PVL), which resulted in spastic quadriplegic cerebral palsy. His condition affects all four limbs and his trunk, causing: Severe muscle stiffness and spasticity Weakness and poor motor control Balance and coordination difficulties Delayed gross motor development Difficulty standing and walking independently The need for continuous rehabilitation and specialized orthopedic equipment Kevin's medical team at American University of Beirut medical center (AUBMC) recommends: Physical therapy: (12/Month), occupational therapy (4/Month), speech therapy (4/Month) Adaptive equipment: wheelchair/adaptive stroller, standing frame, gait trainer, custom seating, orthotics. Medical care: orthopedic follow-up, imaging and operations. Home modifications: safe seating in bathroom and during shower (full bathroom modification), ramps and assistive equipments beside his bed. Travel & logistics: Equipped car compatible for wheelchair for transportation. Although Kevin has made meaningful progress over the years through regular therapy, he has now reached a stage where intensive rehabilitation is essential to continue improving his mobility, strength, balance, and independence. His rehabilitation specialists have recommended an intensive therapy program in Egypt, where he can receive several hours of specialized therapy each day over a period of 4 to 6 months. This program offers an opportunity that is currently unavailable to him in Lebanon. The program includes: Physical therapy 4 to 5 hours per day, 6 days per week. Occupational therapy 2 hours per day, 3 days per week. Speech therapy 1 hour per day twice per week. In addition to hydrotherapy (Plan to be discussed in details later on) Why We Need Your Help As Kevin's parents, we both work full-time and dedicate everything we can to his care. However, despite our best efforts, the financial burden has become overwhelming. Kevin's father works hard, but his employment is not stable, making it difficult to meet the growing medical expenses. Alongside Kevin, we are also raising his brother and sister while trying to provide them with a stable and loving home. The cost of intensive therapy abroad, accommodation, transportation, and the specialized equipment Kevin requires is simply beyond our family's financial means. What Kevin Needs Your support will help provide: Intensive physical therapy for 4–6 months. Occupational therapy and rehabilitation assessments. Accommodation in Egypt for Kevin and his caregiver during treatment. Daily living expenses throughout the rehabilitation period. Flights and local transportation. New AFOs and KAFOs as he grows. A gait trainer/walker. Wheelchair replacement or modifications when needed. Medical evaluations and follow-up care. Educational support: the need of a shadow teacher and assistive equipments during school Home modifications to make Kevin's life easier How Your Donation Helps Every donation, no matter the amount, will go directly toward Kevin's rehabilitation and medical needs. We are committed to being fully transparent and will regularly share updates, progress reports, and receipts whenever possible so every donor can see the impact of their generosity. How You Can Help Donate: Every contribution brings Kevin one step closer to greater independence. Share: Sharing Kevin's story with your family, friends, and community is just as valuable as donating. Connect: If you know organizations, therapists, foundations, or individuals who support children with cerebral palsy, we would be grateful for your introduction. Thank You Your kindness gives Kevin something priceless: hope. Every therapy session, every new piece of equipment, and every step forward is possible because compassionate people choose to help. Thank you for believing in Kevin and for helping him build a future filled with greater mobility, confidence, and independence. Contact number : +961 3 698291 (Rami Bark, Kevin's father) IBAN: LB50003900000002252110250006 Email: albouna.jenny@hotmail.com Wish: 30758428-03

$1,540 raised Of $40,000

Thalasemiya medical

Medical

Thalasemiya medical
Thalassemia is a group of inherited blood disorders in which the body produces less hemoglobin than normal. Hemoglobin is the protein in red blood cells that carries oxygen from the lungs to the rest of the body. Reduced hemoglobin production can lead to anemia and other health complications. There are two main types: Alpha thalassemia: Caused by changes in the genes responsible for making alpha-globin chains. Beta thalassemia: Caused by changes in the genes responsible for making beta-globin chains. Symptoms vary depending on the severity of the condition and may include: Fatigue and weakness Pale or yellowish skin Shortness of breath Slow growth in children Bone changes, especially in the face Enlarged spleen Dark urine (in some cases) Severity ranges from: Thalassemia trait (minor): Usually causes no symptoms or only mild anemia. Thalassemia intermedia: Causes moderate anemia and may require occasional treatment. Thalassemia major: A severe form that often requires regular blood transfusions and ongoing medical care. Diagnosis may involve: Complete blood count (CBC) Blood smear Hemoglobin electrophoresis or other specialized hemoglobin testing Genetic testing to identify the specific gene changes Treatment depends on the severity and may include: Regular blood transfusions for severe cases Iron chelation therapy to remove excess iron that can build up from transfusions Folic acid supplementation in some patients Management of complications In selected cases, a stem cell (bone marrow) transplant, which can potentially cure the disease Some eligible patients may also benefit from newer gene-based therapies, depending on the specific type of thalassemia and local availability Because thalassemia is inherited, genetic counseling and carrier screening can help individuals and families understand their risk of passing the condition to their children. With appropriate treatment and regular follow-up, many people with thalassemia can live long, active lives.

$0 raised Of $2,500