ALS Heroes is about honoring the heroes amongst us who have stared devastation in the face only to say “you do not define me!” They have chosen to claim their own destiny and have dedicated their lives to overcoming our common adversary, ALS. The mission of the Laljii ALS Foundation is to bring awareness and innovation to finding a cure for ALS.
“So many thousands of lives are impacted by this ruthless disease, and it is time to give them a voice and a reason to fight,” said Dr. Shelena Lalji. “Join the fight for a cure now to make a significant difference — to give hope.”
“This is a disease that has a lot of potential to be treated if given the right attention and the right awareness,” shared Zoe. “Although we may feel that our efforts alone are insignificant, we have the ability to make a huge impact by merely raising awareness and educating others about this disease.”
The foundation provides financial support, information and hope to families dealing with ALS.
ALS stands for Amyotrophic Lateral Sclerosis and is a progressive neurodegenerative disease that affects two out of every 100,000 people each year. It attacks both the upper and lower motor neurons of the body, slowly robbing the body’s ability to walk, talk, move and breathe on its own and eventually paralyzes those affected by it. You may remember this disease from the 2014 ice bucket challenge or as the disease Stephen Hawking had. The life expectancy is two to five years, depending on the disease’s progression, and scientists have been researching fervently for the last 70 years to find a cure.
Since the disease hits everyone differently, it has been difficult to solidify any sort of root cause, and for this reason, there is no known cause, essentially no treatment and no cure for ALS. So how can we even begin to understand such a complex and mysterious disease – a disease which essentially traps people inside their own bodies? What is the mystery behind the disease?
In reality, very little is known about what ALS does inside the body. ALS is merely a name to describe a collection of symptoms that coincide with no concrete known pathology. This is why it is time to come together as a community in the face of such a devastating disease to raise awareness and provide hope and support to suffering patients and their families.
Dr. Ayeez Lalji has such an immense will to live – not just to survive through this, but to thrive, make a difference and leave his mark on the world. Dr. Ayeez Lalji was diagnosed with ALS a few months ago, and since then, has been a beacon of relentless strength, resilience, faith and positivity. He has been nothing short of a warrior through this unbearable hardship and a true inspiration to anyone whose life he touches. Every day presents new challenges and new reasons to give up hope, but regardless he keeps on fighting, pushing himself to his absolute breaking point, and then some, to fight this battle nobly with grace, humility and gratitude. Every time I look at him, I see this flame in his eyes which never dies no matter how bad things get. In fact, it grows stronger day by day. Despite all that he has lost, he remains grateful for the functions he still has and continues to live life courageously every day. He epitomizes strength and “smiling through the pain” better than anyone.
Dr. Shelena Lalji, has been another hero in this story. She has spent literally thousands of hours searching, consulting, researching and creating therapies and protocols with the knowledge and information she has gained from hundreds of worldwide experts and studies. She believes, “The cure is out there; we just have to find it!” In addition to doing countless hours of research, she has managed to be the primary caretaker for Dr. Lalji and their 2 children Zoe and Zade, doctor to her patients and the ultimate multi-tasker.
Through this journey, the Lalji family has learned what it really means to never give up and fight with everything you’ve got. Together, they have acquired such a beautiful mission through this, which is to support and generate hope for other ALS patients and their families around the world and show them that ALS does not define them. The Lalji Foundation will start a movement. Like Martin Luther King, Jr. once said, “I have a dream.” The Lalji Foundation has a dream that ALS patients around the world will wake up one day and will be able to walk again, talk again, move again and breathe again – to take back what this disease has stolen from them.
The Lalji Foundation encourages everyone in the community to join us in raising awareness. If you or anyone you know has been affected by ALS or any other neurodegenerative disease, please share your stories with us, and join our mission to find a cure.
What is ALS?
ALS (Lou Gerhig’s Disease) is a progressive neurodegenerative disease that attacks both the upper and lower motor neurons of the body, slowly robbing the body’s ability to walk, talk, move and breathe on its own and eventually paralyzes those affected by it. The life expectancy is 2-5 years, depending on the disease’s progression, and it affects about 2 out of every 100,000 people.
Scientific Advisory Board
We have brought together many of the world’s most insightful clinicians, scientists and key opinion leaders on ALS to be a part of our scientific advisory board. These doctors are dedicated to tackling ALS from all angles and defeating this disease once and for all.