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.

Saturday, December 31, 2011

A WONDERFUL POSTING FROM DOWN UNDER! HAPPY NEW YEAR TO ALL!

Happy New Year from Down Under!

This has been an amazing year for me.  I have had the privilege of becoming officially involved with Parkinson’s Australia, and hopefully through my radio and other interviews, and involvement in workplace education, I am helping to change the perception of Early Onset Parkinson’s and Dystonia.  So many people see both conditions as a freak of nature – the lack of knowledge, particularly about Dystonia, continues to worry me.  However, we WILL get the message across that Dysto-dudes and dudettes are not under a death sentence – Dystonia and Parky are just THERE in our lives and we cope really, really bloody well!

I am particularly chuffed that I am managing to cope alone at present, with my husband being in Afghanistan serving his country with the Royal Australian Navy. I am immensely proud of him – and of myself, for living my Dysto-life the best possible way while he is absent.

There is no way that I could ever be as sane (?) as I am without my beautiful Rogers.  She continues to inspire, enlighten and most of all make me laugh hysterically.  Thank you Rog – you are awesome.  And also Bailey, my Dysto-daughter – the two of you have given me so many gifts this year, with your fabulous laughter and understanding.

To all out there struggling with the challenges Dystonia and Parkinson’s presents, I can only say this; I am with you all the way on the frustration, the pain and the ceaseless explaining you do to strangers.  But there WILL be a cure – and I just know that it won’t be 20 or 30 years from now.  With hope and strength for 2012 and beyond from the Dysto-Wonder Down Under, 

Kate S-C xxx


2 comments:

  1. Great post, so encouraging!! I too have Dystonia with early onset parkinsonism and believe a cure is not too far. www.questofthenocturnalbaker.blogspot.com

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  2. I love BEAT DYSTONIA. It seems to be the only group that has no politics and I always feel better after reading anything on here and on the Facebook page. Thank you.

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