Fighting Lou Gehrig's Disease on Every Front!

Our Mission: To lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig’s disease and their families to live fuller lives by providing them with compassionate care and support.

Monday, September 13, 2010

Heath Care Reform Webinar this Week

The ALS Association Advocacy Department would like to invite people with ALS
and their family members and caregivers to join us for an informative
webinar about the new health care reform law enacted earlier this year. The
webinar will provide a general overview of health care reform and will
include a slide presentation by the Advocacy Department.

This is an opportunity for you to begin to learn how some of the key
elements of health reform will impact people with ALS and their families as
the law is implemented over the coming months and years. It also is an
opportunity for you to ask questions you may have about health care reform.

WHEN: Thursday, September 16 at 12:00pm ET

WHAT: Health Care Reform: What it Means for People with ALS and their
Families

HOW to Access the Webinar Presentation:

To join the webinar and view the presentation on your computer, go to:

https://alsa.webex.com/alsa/j.php?ED=139908717

&UID=1130829407&PW=NMjdjYzNlYzc3&RT=MiM0



Space is limited to the first 200 participants so please plan to login early
to secure your spot.



To join the audio conference:

Call-in toll-free number (US/Canada): 866-699-3239

Meeting Number: 821 586 154

Meeting Password: TopicCall2010

If you have any questions, please contact the Advocacy Department at
advocacy@alsa-national.org. We look forward to you joining us for this
webinar.

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