ALStogether
A centralized community for pALS to connect, share, and support each other.
The headquarters for all affected by ALS
With a fast-moving, devastating disease like ALS, we have to live, adapt, and share at the speed of ALS. Unfortunately, existing groups and resources are scattered, making it difficult to connect in real-time.
We brought this problem to the executive team at Salesforce, stating that the ALS world needs tools to move faster.
Their response? Go.
So we pooled our experts and built a patient community for those living with ALS in Slack called ALStogether.
For those who don’t know Slack — Slack is an incredible platform to chat and connect. Slack has allowed us to create a digital headquarters for ALS that can be accessed anywhere.
Imagine you have a question about adaptive equipment, or just learned about a new clinical trial- you can open Slack and talk to your fellow pALS.
With dedicated channels for various topics and interests, from genetic variants to veterans to financial tips, you can find your answers within our platform.
Our goal is to have everyone living with ALS across the globe in this community, and eventually we'll open this up to families, caregivers, advocates, ALS organizations, and providers.
We brought this problem to the executive team at Salesforce, stating that the ALS world needs tools to move faster.
Their response? Go.
So we pooled our experts and built a patient community for those living with ALS in Slack called ALStogether.
For those who don’t know Slack — Slack is an incredible platform to chat and connect. Slack has allowed us to create a digital headquarters for ALS that can be accessed anywhere.
Imagine you have a question about adaptive equipment, or just learned about a new clinical trial- you can open Slack and talk to your fellow pALS.
With dedicated channels for various topics and interests, from genetic variants to veterans to financial tips, you can find your answers within our platform.
Our goal is to have everyone living with ALS across the globe in this community, and eventually we'll open this up to families, caregivers, advocates, ALS organizations, and providers.
