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

$1,570 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

Surviving & Healing: Help Zariah's Medical Journey

Medical

Surviving & Healing: Help Zariah's Medical Journey
Hello everyone, My name is Zariah, and I am reaching out for urgent help as I navigate a lifelong medical battle. When I was just 12 years old, I was diagnosed with Alport Syndrome. This progressive genetic condition led to Chronic Kidney Disease, then kidney failure, and eventually, the incredible gift of a kidney transplant. For a long time, I was managing well—traveling from Nassau to Miami every three months for routine laboratory work and specialized checkups to keep my kidney safe. Unfortunately, my journey took a scary turn this past February. My body began experiencing transplant rejection. I was hospitalized in Miami from February all the way until April fighting to save my kidney. Because of this active rejection treatment, my medical routine has drastically changed. I now have to travel from Nassau to Miami every single month for critical treatments and doctor visits. Each trip costs roughly $325 for flights and $150 for lodging. On top of the physical and emotional toll, I am facing a major financial hurdle to keep my healthcare active. Because my recent illness forced me to put my university studies on hold, I am at immediate risk of losing coverage under my mother’s group health insurance, which requires me to be a student. To protect my transplanted kidney and continue my life-saving monthly treatments in Miami, I urgently need to transition to an independent medical insurance plan in my own name, which costs just over $400 a month. While I am incredibly blessed to have a supportive workplace that has stood by me, the cost of monthly international travel, temporary lodging, and taking over my own insurance premiums is more than myself with the help of my family can handle. My goal of $10,000 will create a vital 6-month safety net. It will directly cover: My monthly roundtrip flights and medical lodging in Miami. My monthly individual health insurance premiums so my coverage never lapses. A basic emergency buffer for food and transportation during unexpected hospital stays. Every single dollar goes directly toward keeping me alive, surviving, and healing. If you are unable to donate, please consider sharing my link on WhatsApp or Facebook with your friends and family. Thank you from the bottom of my heart for standing with me in this fight.

$370 raised Of $10,000

Lifetime Fund for Disabled Subhashini (49 Years)

Medical

Lifetime Fund for Disabled Subhashini (49 Years)
My sister, Subhashini, is 48 years old and has been severely disabled since birth. She has never been able to walk independently. Throughout her life, she could only take a few assisted steps, but now her condition has worsened to the point where she can barely move even with support. She is completely dependent on others for all daily activities, including bathing, dressing, washing, sitting, and moving from one place to another. As she is a woman, we must employ a female caregiver to assist with her personal needs. Unfortunately, due to the increasing cost of living, it has become extremely difficult to continue paying a caregiver's salary. Caregivers often leave for better-paying jobs, leaving our family in a desperate situation. Since childhood, my parents consulted numerous doctors hoping for treatment, but they were informed that her neurological condition could not be cured. She has an underdeveloped brain and lifelong neurological disabilities. My father, who cared for her for many years, passed away three years ago. My mother is now 75 years old and suffers from severe sciatica, largely caused by decades of lifting and caring for my sister. Despite her own health problems, she continues to help as much as she can. I am now the sole financial provider for our family. I support my wife and three children while also caring for my elderly mother, my disabled sister, and the caregiver. Every household expense, including food, medicines, and daily necessities, depends entirely on my income. Because of my caregiving responsibilities, I cannot work additional hours or night shifts to increase my earnings. My greatest concern is ensuring that my sister and mother continue to receive proper care throughout their lives. Therefore, I hope to establish a lifetime fund that will help cover: Monthly caregiver salary. Medical consultations, medicines, and regular health checkups. Weekly physiotherapy sessions to improve mobility and comfort. Mobility aids and assistive equipment, such as an advanced walking aid or, if funding permits, a robotic lower-limb exoskeleton. Occasional outings and recreational activities to improve my sister's mental well-being and quality of life. Essential support for my elderly mother's medical needs. This fund would provide long-term security and dignity for my sister, ensuring that she continues to receive proper care even as our family's circumstances become more challenging. I sincerely request your support in helping us create this lifetime fund. I am willing to provide medical records, photographs, videos, or any other proof required to verify our situation. Thank you for taking the time to read our story. Sharing it has given me hope, as I rarely have the opportunity to explain our family's struggles. Your kindness and support would make a lasting difference in my sister's life.

$0 raised Of $50,000

Family Needs Help

Medical

Family Needs Help
100 metres. That is the maximum distance I can walk before my body stops obeying me. Every step can become a frightening struggle: sudden dizziness, tremors in my hands and legs, and the feeling that the ground is disappearing beneath my feet. I was once an athlete and a swimmer. Today, even leaving my home is a major challenge. Progressive cerebellar ataxia is slowly taking away my mobility and independence. At the same time, I live with Type 1 diabetes, which requires constant monitoring and treatment. But this struggle is not mine alone. My wife, my 15-year-old son, and I all live with disabilities and Type 1 diabetes. Our small family depends on insulin pumps and continuous glucose monitoring systems to keep our blood sugar at safe levels. Sensors, infusion sets, catheters, and insulin reservoirs are not optional medical accessories for us. They are essential, life-sustaining supplies. We are currently living in Bucharest, Romania, after being forced to leave our home because of the war in Ukraine. We also carry the pain of being separated from my nearly 80-year-old mother. She is seriously ill, unable to travel, and remains alone across the border. Our days are organised around medical care. Because of my ataxia and tremors, even simple tasks are difficult. Yet we must constantly monitor glucose levels, replace pump supplies, and make sure that all three of us have what we need to avoid dangerous complications. Although insulin is provided free of charge in Romania, essential diabetes supplies are not covered for refugees. Our family needs approximately €1,000 every month for insulin-pump consumables and glucose-monitoring supplies. I can no longer work, and this amount is far beyond what we can afford on our own. We are not asking for luxury. We are asking for the medical supplies that allow us to stay safe, avoid life-threatening emergencies, and live with dignity despite disability and chronic illness. Every donation, no matter how small, helps provide essential treatment for me, my wife, and our son. If you cannot donate, please consider sharing our campaign with others. Thank you from the bottom of our hearts for seeing our family, supporting our fight, and helping us continue to live.

$0 raised Of $20,000