

Caregiver Support Group
Saturday, December 16
9:30 a.m. – 10:30 a.m.
VIRTUAL & IN-PERSON
Register here! After registering, you will receive a confirmation email containing the virtual meeting link.
If you would like to attend in person at our Pittsburgh office (416 Lincoln Ave. in Millvale) please contact Ryan Tappe at ryan.tappe@als.org.
2024 Support Group Registration
Living with ALS Support Group
Saturday, December 16
11:00 a.m. – 12:00 p.m.
VIRTUAL & IN-PERSON
Register here! After registering, you will receive a confirmation email containing the virtual meeting link.
If you would like to attend in person at our Pittsburgh office (416 Lincoln Ave. in Millvale) please contact Ryan Tappe at ryan.tappe@als.org.
2024 Support Group Registration
Life After ALS Support Group
VIRTUAL & IN-PERSON
If you are interested in joining our Life After ALS Support Group please contact Ryan Tappe at ryan.tappe@als.org or Jill Kerr at jill.kerr@als.org.
More Options for Virtual Support Groups:
We want to make care services programs and resources accessible to everyone impacted by ALS no matter where they live. If you are unable to make it to your local ALS support group, we offer other opportunities for you to connect with our ALS community virtually every month.
Click the support group you would like to join below to register. After you register, you will receive an email confirmation with the virtual meeting link.
Living with ALS Support Group: December 12| 1:00-2:00 p.m. EST
ALS Support Group: December 12 | 6:00-7:30 p.m. EST
Caregivers Support Group: December 14| 6:30-7:30 p.m. EST
Newly Diagnosed Support Group: December 21| 1:00-2:00 p.m. EST
Caregiver Support Group (for Men): December 21 | 2 p.m. EST
Caregivers Support Group: No group in December | 1:00-2:00 p.m. EST
Caregiver Support Group (for women): January 4 | 2 p.m. EST
ALS Support Group: January TBD | 6:30-8:00 p.m. EST

Care Services Webinars
LEARN MORE: Archived Care Services Webinars
Webinar Feedback Survey
We value your feedback! Please answer a few questions about your experience with our webinars here.
MORE WEBINAR RESOURCES

Resources & Support
Start YOUR journey today: myalsjourney.org

My ALS Journey™ is a new interactive tool designed to help guide you to necessary resources, advice, and support, if and when you need them. By sharing your specific symptoms as you go, you will be able to stay informed of the latest treatment options and prepare for conversations with your care team.

Join the ALS Registry
The National ALS Registry is perhaps the single largest ALS research project ever created and is designed to identify ALS cases from throughout the entire United States. Most important, the Registry is collecting critical information about the disease that will improve care for people living with ALS and help us learn what causes the disease, how it can be treated and even prevented.
ALS Focus Survey Request
We are measuring the experiences of people with ALS and their caregivers who have sought health insurance coverage of ALS care, services, treatments, equipment, and supplies. Researching these experiences through ALS Focus surveys shows The ALS Association which tools will best support advocacy for stronger coverage of ALS care.
If you know someone with ALS or a current caregiver, please let them know that we want to hear from them at www.alsfocus.org
Local ALS Research Study Participation
The ALS Association would like to share information with you about research studies occurring in the Pittsburgh area.
For information about current or upcoming studies contact Jill Kerr. jill.kerr@als.org

Sign Up for Care Matters
With an ALS diagnosis, there are decisions to make, symptoms to manage, treatment options to evaluate, and adjustments to almost every detail of your daily routine.
Stay up-to-date by subscribing to our quarterly e-newsletter, Care Matters. You’ll receive the latest information about ALS care, disease management and resources to help you navigate your ALS journey.
Together, we will reach our goal of making ALS a livable disease. Sign up TODAY!
View previous issues of Care Matters here.
Sign Up for Research Matters
Our global research collaborations continue to make great strides in the fight against ALS. Stay up-to-date by subscribing to our monthly e-newsletter, Research Matters, delivered to your inbox the last Thursday of each month. You’ll receive information about the latest ALS research discoveries, key advances in technology and new treatment approaches taking place in clinical trials.
Together, we will create a world without ALS. Sign up TODAY!
View previous issues of Research Matters here.
GET MORE FROM THE ALS ASSOCIATION
Sign up for ALS Association Email! Get the latest ALS news, be inspired to take action, and learn more about how you can create a world without ALS.
Subscribe to The ALS Association Blog
Read about national initiatives & news and local stories from our ALS community.
Subscribe or read our latest blog now!
2023 Mission Impact Report


Connect with Jill:
412-707-3340 jill.kerr@als.org
Connect with Kristin:
412-632-4297 kristin.keefe@als.org


Connect with Brittany:
412-651-2313 brittany.mccall@als.org
Connect with Kate:
412-295-1221 kaitlyn.karlovits@als.org


Connect with April:
412-480-5268 april.smith@als.org
Connect with Ryan:
412-239-8057 ryan.tappe@als.org


We are proud to offer our local ALS Community a full range of services and resources to guide and assist you as you on your ALS journey.

