Imad is 14 years old. He can no longer move his legs and is increasingly struggling to use his hands. His disease remains undiagnosed. We are raising funds for a specialized medical evaluation, genetic testing, and stable housing.
No one has been able to name Imad's disease. Without a diagnosis, no proper care plan is possible.
Imad can no longer move his legs and now has difficulty using his hands.
The family faces severe financial hardship and risks losing their rented apartment.
Imad is 14 years old and lives in Meknès, Morocco. He is a curious and endearing teenager, passionate about manga and video games. His mobility has decreased over the years, but his world remains vast: stories he devours, worlds he explores from his wheelchair.
From a very young age, Imad struggled to walk. His loved ones noticed his movements required more effort than other children's.
Over the years, walking became increasingly difficult, until it became impossible.
Imad can no longer move his legs and has difficulty using his hands.
Several children in his family have shown similar symptoms and sadly passed away around the age of 18 to 20.
An evaluation by specialist doctors, accompanied by appropriate genetic and DNA testing, is the only path to try to identify what Imad suffers from. A name for the disease would allow his family and doctors to understand what is happening, organize appropriate care, and inform other family members who may be affected.
Toward what truly matches his condition.
Years of uncertainty for Imad and his family.
Other relatives affected by similar symptoms.
These tests have a cost that the family cannot afford.
Imad's family is in great financial difficulty and risks losing their rented apartment. A stable and accessible home is the basic condition for caring for Imad daily.
Consultations with specialists able to examine Imad's condition.
The analyses needed to try to identify the cause of his disease.
Helping the family keep their rented apartment.
Daily support that makes Imad's life more comfortable.
No. His disease is not diagnosed to date. This is precisely the purpose of this campaign: to enable a specialized evaluation and genetic testing.
We cannot confirm this. Several children in the family have shown similar symptoms, but only a medical evaluation can determine if there is a genetic cause.
Donations are collected on the official campaign page and are intended for the medical evaluation, genetic testing, and housing stability for the family.
Yes. The donation page is accessible to international donors.
Share this page and Imad's video. Visibility helps as much as donations.
If you can't donate, sharing can make all the difference.
For any questions about the campaign, visit the official collection page or contact us by phone.
Every donation, big or small, brings Imad closer to a diagnosis and appropriate care.
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