Please use this forum for any general discussions about Lou Gehrig disease, and inquiries or questions you may have regarding ALS/MND.

ALS Tips, Tricks, and Gadgets you have found useful for people affected by ALS/MND. Post items that you have invented, adapted, found or made usable for PALS.

Please place your stories of hope, and reasons to look forward to the future in this forum. Much of what we read about ALS is sad and depressing, this forum is not the place for those threads.

Have symptoms? Not sure if you have ALS, or what ALS is? Would you like to ask a general question about ALS symptoms? Please post all related questions to this forum.

This forum was created to give individuals with ALS an opportunity to meet and discuss topics of interest. Individuals recently diagnosed with ALS can feel free to ask other members questions they may have.

ALS/MND Caregivers are welcome to share experiences, answer questions, discuss topics of interest and provide help to people affected by motor neuron disease.

Post your event information for all to see. Feel free to post your questions and thoughts about an ALS fundraising event.

Post and read about interesting ALS related research news. Keep everyone updated, post your updates about Lou Gehrig's disease and ALS research news.

Healthcare professionals can meet and discuss current issues or gain insight and knowledge from other individuals affect by Lou Gehrig's disease.

A place for CALS to remember their beloved PALS. Please use this forum to inform us of a loved one's passing.

This forum is for ALS related equipment sales. Any items that are no longer needed may be of great use to others affected by ALS.