Help Jannah fight Lymphatic Malformation

Hi, my name is Yassine and I am fundraising on behalf of family of Jannah.

Jannah, Our little angel, was diagnosed with a Lymphatic Malformation at the age of three weeks.

A Lymphatic Malformation is a benign tumor that might have a few cysts or thousands of cysts. They are most commonly found in the neck, although they can appear practically anywhere on the body and expand in size over time.

Lymphatic Malformations are still being researched to figure out what causes them. They think they're caused by'somatic mutations.' Somatic mutations are flaws in the genetic code that happen when it's copied from one cell to the next. This means that once an error occurs, it will appear in all cells derived from the original cell.A somatic mutation, despite affecting the genes, is not passed down from generation to generation since it only affects the portion of the body where the lymphatic abnormality occurs, not the germ cells that create new life. Change is the only way for somatic mutations to arise.They don't believe anything done by the parents before or during pregnancy causes a Lymphatic Malformation. ‏

We are fortunate to have a world-class medical system. We were assigned to a pediatrician with experience with this unusual disease, who followed Jannah every four weeks, organized treatment (Sclerotherapy), and connected us to one of the best plastic surgeons in the area when it came time for surgery. Thanks to Medicare and our public health-care system, we had no out-of-pocket payments.We truly have one of the world's top health-care systems. Unfortunately, there are children in other nations who suffer from Lymphatic Malformations who are less fortunate. They might not have access to doctors, pediatricians, or surgeons who are experienced.Alternatively, they may be unable to afford the medical assistance they require. This is where I ask you to open your hearts and join me in my effort to raise funds for families affected by this rare disease.

Jannah is an 18-month-old girl who was born with a Lymphatic Malformation.

Jannah's family is desperately trying to earn enough money so that when she becomes ten months old, she can have surgery to remove his Lymphatic Malformations.

Surgery and travel fees are about 15000 usd

Our combined efforts can have a significant impact on Jannah's life; let's work together to provide this newborn girl a better future.

Any amount you can contribute will be much appreciated.

to receive updates about Jannah's case : [email protected]

all updates on fb page : Save Jannah

ps: If the desired goal is reached

The extra money in the campaign will be transferred to treat similar cases or goals

Thank you for your support ‏