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Amyotrophic Lateral Sclerosis (ALS), is a disease that progressively attacks motor nerve cells in the brain and spinal cord, that tell muscles what to do - from walking to breathing. However, most often, cognitive abilities remain intact. The ALS Association estimates that every 90 minutes someone is diagnosed with ALS, and passes away from it. This makes ALS particularly devastating with complex, rapidly changing care needs. Life expectancy after diagnosis is typically 2-4 years, and in the later stages of the illness, patients require significant carer support. Research Grid Founder and CEO, Amber Michelle H., recently shared her expertise and insights on ALS, a condition that she researched as a neuroscientist in her early career, with Essence Magazine. The article, by Ebony Flake, explores the challenges of caring for a loved one with ALS and the resources and support required for long-term care. In the interview, Dr Hill highlighted: 💡 The extraordinary resilience of people and families living with ALS 💡 Why rare conditions like ALS need greater attention 💡 The many ways you can lend a helping hand 💡 The importance of disability education and awareness The impact of rare diseases, like ALS on families and communities is far-reaching. At R.grid, we are proud to support over 7,000 diverse communities worldwide in their efforts to engage in research, raise awareness, and improve the lives of patients affected by rare diseases. Read and share the full article: https://lnkd.in/ekR9sekq #rarediseases #ALS #MND #LouGehrigdisease #alsawareness

The Unbreakable Spirit: A Caregiver's Testimony And Expert Guide For Supporting A Loved One | Essence

The Unbreakable Spirit: A Caregiver's Testimony And Expert Guide For Supporting A Loved One | Essence

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