reach out to each other and stand up and be counted.
coming together as a PALS to show we are here and doing what ever it takes to keep on living.

this registry is a awareness tool.
There are 814 PALS in the registry who recently joined us.

ALS/MND Registry
This is a registry for Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease, or ALS) intended to help Persons with ALS (PALS) reach out to each other and stand up and be counted. It was originally started it as a mailing list by Bobby Brannigan, PALS and PatientsLikeMe community member, and it is now being maintained by PatientsLikeMe.
http://www.patientslikeme.com/registry

If you are a PALS, you can add your name by signing up for a PatientsLikeMe account and filling out your profile. If you have any questions email PatientsLikeMe at support@patientslikeme.com.
You can help by passing this info on to other PALS.

PatientsLikeMe members, want to see your name listed here? Just enable your Public Registry permission and fill out your first and last names!


ALS/MND Registry
http://www.patientslikeme.com/registry

and to keep from over posting things , news, pals stories, anything ALS/MND i post them all at
http://neurotalk.psychcentral.com/forumdisplay.php?f=6