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.