HOW TO DONATE to BEAT DYSTONIA (501)(C)(3)

www.cftexas.org/beatdystonia (for donations online)

BEAT DYSTONIA is housed by the stellar Communities Foundation of Texas. Communities Foundation of Texas traces its roots back to 1953. Since that year, more than $1 billion in grants have been made by the Dallas-based foundation. It has grown along with North Texas to become one of the largest community foundations in the nation.

For more information on how to donate to BEAT DYSTONIA, here is the main page:

http://www.cftexas.org/NetCommunity/Page.aspx?pid=183

WE NEED YOUR SUPPORT. Thanks!

WE ARE ALL PRO BONO. 1% overhead for clerical costs.

Email: beatdystonia@me.com
Twitter: @beatdystonia and @auntrogers
My Space: Beat Dystonia

If you have any questions, please call 323.251.1021

Please check out ASEA. A portion goes to the BEAT DYSTONIA fund.
http://www.teamasea.com/beatdystonia

ALL QUESTIONS WELCOME! It has helped me greatly!
Talk to your doctors before taking it since we are all on different medications.



Dystonia is an orphan disorder that needs more money for research.

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Los Angeles, New York, Dallas/Fort Worth, United States
I am the founder of BEAT DYSTONIA (501)(c)(3) and work daily on awareness, fundraising and personal advocacy. You are not alone and do not hesitate to post or reach out. I'm here and focused on our collective wellness.

Wednesday, December 16, 2009

ADVOCACY CONFERENCE CALL hosted by BEAT DYSTONIA



A great way to kick off the new year!

All are invited to participate, listen, share on a conference call that I will
moderate along with the wonderful Renee LeVerrier.

It will be very open and hopefully, inspirational.

Details are:

Sunday, January 3rd, 2010
12pm PST, 2pm Central, 3 pm East

RSVP to beatdystonia@me.com

I will send out an agenda in advance so people can see what we will be talking
about and feel free to make suggestions after reading the agenda and I will do my best to incorporate them.

Once we are closer to the date, I will send out a call-in number with a passcode.

The only cost involved are your long distance charges.

No one should feel alone with this wacky disorder, so I would love to get folks that I already know via phone, email and some in person together so we can all feel a sense of community and support. And I hope some new people will join, as well. All welcome.

Love,
Rogers


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