The ALS March of Faces

Misson and activities:

To raise public awareness of ALS, Amyotrophic Lateral Sclerosis, aka Motor Neuron Disease or Lou Gehrig's Disease. To help raise funds for ALS research, communication devices and family assistance

Our organization works at the national level.

Our organization is mainly run, controlled and represented by disabled people.

We have expertise, or are interested in cooperating with other organizations, in the areas of:

Accessible public transportation.
Assistive devices.
Awareness raising.
Coalition building and networking.
Computers and disability.
Education and vocational training.
Employment.
Independent Living Skills Training.
International development and disability.
Legal aid.
Legislation.
Media work.
Peer support.
Personal assistance.
Recreation and travel.
Research.
Self-advocacy.
Travel.

Contact us:

This entry added: Thursday 10th September 1998. (record #108) Changed: Tuesday 29th March 2005. Link checked Tuesday 3rd December 2024.