I was informed in 1993 that I only had five years to live.

Naima is among the longest surviving MND patients in the world.

November 26th 2024.

I was informed in 1993 that I only had five years to live.
Naima Chakkour, a vibrant and active woman, was enjoying a holiday at Hotel Le Mirage in Morocco when her life took an unexpected turn. She received a devastating diagnosis of Motor Neurone Disease (MND), an incurable illness that would slowly deteriorate her muscles and ultimately lead to paralysis. Despite the grim news, Naima chose to keep her diagnosis to herself, determined to continue living her life as normally as possible. She couldn't bear the thought of burdening her loved ones or facing their reactions to her terminal illness.

As a mother of four, Naima's first thought was for her children. When the doctor told her she had only five years to live, she couldn't help but think of her youngest child, who was only four at the time, and her oldest, who was nine. She was determined to stay strong for them and not let her illness define her.

Before her diagnosis, Naima was an active runner and a busy mom, always on her feet. She had grown up in a small fishing town in Morocco and had moved to London after getting married. But as she entered her thirties, she began to experience weakness in her hands, which eventually made simple tasks like tying her son's shoelaces impossible. After numerous visits to the doctor, she received the devastating diagnosis of MND in 1993.

Naima's MND was initially easy to hide, but as her symptoms progressed, it became more challenging to conceal. She had to adjust her wardrobe to cover up her weakened muscles and drooping neck. She even used makeup to draw less attention to her thinning lips. However, there were times when she couldn't hide her illness, like when she was stopped by doormen at a posh party who mistook her slurred speech for drunkenness.

Naima had always been self-reliant and didn't like showing vulnerability or asking for help. So when she finally decided to share her diagnosis with her friends and family, it was a difficult and emotional experience. Most of the reactions were of shock and sadness, with many expressing disbelief that someone so young could have such a terminal illness.

But Naima's journey became even more challenging when her husband unexpectedly left her and their children in 2005. Although their marriage had been distant before her diagnosis, his decision to abandon them still felt like a betrayal. Naima was left feeling alone and ashamed, but she found strength in her older brothers and close friend who supported her through this difficult time.

Today, Naima describes living with a terminal illness as being in an "anteroom" between life and death. She dreams of running when she sleeps and listens to her favorite songs when her mind wanders during the day. But the fear of the future and how her illness will ultimately end looms over her constantly. She has lost everything, but her mind remains her only solace. Despite the obstacles and dark thoughts, Naima continues to defy the odds and live with MND for decades, showing incredible resilience and determination.
Naima Chakkour was a woman who lived life to the fullest, always on the move and busy with her four children. But when she received the devastating news of her Motor Neurone Disease (MND) diagnosis, she chose to keep it to herself, not wanting to burden her loved ones. She continued to carry on with her daily life, trying to ignore the "smell of death" that seemed to follow her.

At the age of 64, Naima found out that she only had five years left to live. The first thought that came to her mind was her children - their faces popping up in front of her. She couldn't bear the thought of leaving them behind. Before her diagnosis, Naima was an active runner, traveler, and busy mom, always on her feet. She had moved from her small fishing town in Morocco to London after getting married and by her thirties, she had already begun to lose strength in her hands.

After multiple visits to the doctor, Naima was diagnosed with MND in 1993. She felt lost in a "huge, dark cloud" and suffered in silence, crying herself to sleep at night. At first, she was able to hide her symptoms by padding her shoulders and changing her wardrobe, but as her condition worsened, it became impossible to hide. She was forced to open up about her diagnosis, which was a difficult thing for her to do as someone who prided themselves on being self-reliant and not showing vulnerability.

The reactions from her friends and family were mostly shock and sadness. They couldn't believe that someone so young and full of life could be facing a terminal illness. In 2005, Naima took her children on a holiday, but when they returned home, they found their father had left them. Her husband had grown distant before her diagnosis, but his decision to leave still felt like a betrayal.

Alone and ashamed, Naima found strength in her two older brothers, Abdeslam and Ahmed, and her close friend Habiba. They supported her through this difficult time and helped her to move forward. Today, Naima describes living with a terminal illness as being in a place between life and death. She dreams of running when she sleeps and imagines driving across London with her favorite songs blaring during the day.

Despite losing everything, Naima still holds onto her mind and fears the future and how her life will end. The biggest obstacle she faces is the constant dark thoughts that haunt her. But Naima continues to defy the odds, living with MND for decades and cherishing every moment she has with her loved ones. She is a true inspiration, showing strength and resilience in the face of adversity.

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