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If you or someone you know has ALS and is currently experiencing symptoms of COVID-19, please contact your healthcare provider immediately.  

With the recent assignation of COVID-19 as a pandemic by the World Health Organization, we are sharing pertinent information with the ALS community to understand the risks and impact of SARS-CoV2. Please note that per the CDC, this is a rapidly evolving situation, and the CDC will continue to share updates daily.

While there is currently no evidence to show that patients with ALS are uniquely sensitive to the virus, individuals with respiratory health issues, chronic medical conditions such as heart disease, diabetes or lung disease, and those who are elderly may be at a higher risk for experiencing COVID-19 severely.

Prevention & Management: 

In addition to following the CDC recommendations for the prevention and management of COVID-19, we recommend asking your ALS clinic care team whether they recommend an in person or tele-visit. You may also find the Les Turner ALS Foundation’s care recommendations for respiratory issues helpful.

The ALS Association has published  “ Tips to Help the ALS Community Plan Ahead During the COVID-19 Pandemic”  developed for people with ALS and their families, to help them advocate effectively with healthcare providers, healthcare facilities, emergency medical technicians and medical transport systems to ensure fair and appropriate treatment during the COVID crisis.

Information Related to Clinical Trials:

If you are currently participating in a clinical trial, contact your trial care team to determine if there are any changes to protocol or timeline.

In an Emergency Situation:

If you are in need of assistance from an emergency medical technician (EMT) please reference this document from I AM ALS for helpful information to provide to them and emergency room staff regarding additional precautions to take when caring for ALS patients.

The CDC and other health professionals are learning more about COVID-19 every day. While the possibility of contracting a contagious disease is scary, it is important to stay calm and follow recommended prevention and management strategies. Please continue to check the CDC’s website for the most up to date information about COVID-19 in the US.

Support Resources

Augie’s Quest, Team Gleason, Les Turner ALS Foundation, I AM ALS, LiveLikeLou, Hope Loves Company, The Joe Martin ALS Foundation, The Brigance Brigade Foundation and others across the ALS community are banding together to support ALS families during this time. We have compiled a list of resources that are providing assistance to families with ALS who are affected by COVID-19. 

Financial Assistance & Volunteer Support:

  • The Healthwell Foundation is offering a small grant to help people cover costs related to COVID-19 such as delivery of food, medications, transportation and telehealth visits. Check out the eligibility details here and call (800) 675-8416 to apply over the phone.
  • The Susie Foundation in Connecticut has introduced a Good Neighbors program that will connect families affected by ALS with volunteers who will run 1-2 critical errands for them per week. They are also repurposing their Flex Grant program to provide emergency funding to families who are struggling with unexpected expenses due to the spread of COVID-19. Learn more about their programs and how to apply here
  • The Les Turner ALS Foundation in the Chicagoland area is providing emergency relief funding. Learn more here
  • The LiveLikeLou Foundation has launched the Great LiveLikeLou Outdoor Clean-Up for ALS Families to match ALS Families with Phi Delts to offer volunteer support to ONLY 1) outdoor projects and chores, 2) no personal contact and 3) CDC-allowable interactions.  This is a “one-time” or “occasional” support for ALS Families so that the college students in particular can meet their families’ expectations for support.


  • Your ALS Guide is donating 5,000 FDA-approved surgical masks to people living with ALS, caregivers, and ALS professionals in the United States. People can request masks at Masks for the ALS Community and they will be mailed out within 48 hours.
  • Every 90 Minutes, Team Gleason and Evergreen Circuits are providing ventilator filters from Philips Respironics to ALS patients who are unable to get it through a DME supplier. Click here to apply
  • Team Gleason is continuing to provide all of its services to people living with ALS, with the exception of adventures which have been suspended. Learn about how they may be able to help you and apply for assistance here
  • Acknowledging that there may be a shortage of some supplies, Respiratory Quality Services researched ways to clean your breathing device accessories. You can read them here. Be sure to consult with your Respiratory Therapist on these guidelines.


  • The House Committee on Veterans’ Affairs has helpful information on COVID-19 resources for veterans with ALS here.

Virtual Engagement:

  • Hope Loves Company is going virtual! Check out their site for updates on online activities and their upcoming Pen Pal program for children, teens and adults. 
  • Team Gleason and The Center for Medicare Advocacy will be hosting a webinar to address benefits in the rapidly changing Medicare environment. Stay tuned for the scheduled date.
  • The Brigance Brigade Foundation (BBF) will soon launch the BBF Caregiver Club, which will be a virtual meetup of caregivers of people living with ALS (CALS). The Caregiver Club will encourage CALS to set aside time to practice self-care through guided activities such as art, journaling, meditation, and exercise. Email Amy Mullan at to learn more and sign up.

Good News:

Know of a resource to support people affected by COVID-19 that we missed? Email us at and we will include it once vetted.

ALS won’t stop and neither will Augie’s Quest

Augie’s Quest to Cure ALS
PO Box #9886
Denver, CO 80209

T: 949-506-1007

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