Let Hope Grow is a dedicated non-profit organization with a focus on enhancing the resources and care options available to those diagnosed with ALS and their caregivers. Through our own personal journey, we’ve witnessed firsthand the barriers families face while navigating an ALS diagnosis.
Our mission is to enhance the well-being of both caregivers and diagnosed individuals by providing tools, resources, financial assistance, respite opportunities, and meaningful connections. We believe that when caregivers are supported at a higher level, the care they provide can truly make a greater impact.
Based in the Greater Harrisburg Area | Serving Families & Caregivers Nationwide
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Learn About
ALS Progression
Click Through the Timeline to Learn More About ALS – Meet Pete
Defining ALS
Amyotrophic lateral sclerosis (ALS) is a progressive neurological disease that affects the nerve cells in the brain and spinal cord that control muscle movement. Over time, these nerves stop working properly, causing muscles to weaken and eventually making everyday activities like walking, speaking, and breathing more difficult.
While ALS does not affect a person’s ability to think or feel, it changes how the body responds, which is why support, care, and continued research are so important.
Our Mission
Welcome to Let Hope Grow. Our mission is to support individuals living with ALS and the caregivers who walk this journey alongside them. This organization was inspired by our family’s experience following a loved one’s diagnosis with ALS in April 2015. What began as a slow progression quickly accelerated, and within a year, the disease took away the ability to walk, speak, and smile.
Stepping into the role of caregiver was unexpected, but the experience profoundly changed our lives and became the foundation for the support and connection Let Hope Grow provides today.
Our Vision
Our vision is to build a nationwide community where hope grows stronger than fear, and no ALS family navigates the journey without support, dignity, and compassion.
Our Goals
Our primary goal is to connect caregivers and those diagnosed with ALS to meaningful resources, financial assistance, new avenues of care, and community during a time that can be isolating. Behind our overarching mission and goal, we do have plans to expand the way we provide for you and your family.
Als-ready vacation home
Increase our donations and impact to create an ALS-ready vacation home. This home would allow caregivers and families to enjoy time together in a fully accessible environment, without the financial burden of modifying a temporary vacation space.
Als-specific respite
Establish a trusted respite care location where caregivers and families can take a break while knowing their loved ones are supported by professionals experienced in ALS care.
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We’re here to support
families, caregivers, and individuals
diagnosed with ALS in any way we’re able, financially, emotionally, and practically.
Obtaining sustainable food options (financially & donation)
Rent and/or Mortgage Support
Support Resources
Connecting Your Care Network
Obtaining Medical Devices
Providing Empathy
& Connection
And So Much More
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More About Our Story
Proudly Created & Led by
Lura Sawyer
As someone who has experienced the firsthand progression and effects of ALS, I am on a mission to ensure those who feel left behind, isolated, or trapped, have our agency as a resource. I invite you to connect with me and get connected with our vast network of resourceful and supportive connections.
I know that together, we can make a difference and improve the quality of life and care for everyone affected by an ALS diagnosis and their families.