2009 Achilles Walk for Hope & Possibility
*RSDSA at the 2009 Achilles Walk for Hope & Possibility in NYC*
*June 28, 2009 | Central Park
**Online Registration and Forms are now available!
*
* *
Walker and Virtual Walker Registration Available
*Click here for more
information
*
* Team **Co-captains: Jackie Drake and Marsha Tyszler*
Since RSDSA promotes public and professional awareness of CRPS, a neurologic
syndrome characterized by severe and persistent pain that can lead to
disability, we are charged with educating those afflicted with the syndrome,
their families, friends, insurance and healthcare providers about the
potentially-disabling pain it causes.
We have teams in the Achilles Walk for Hope & Possibility to promote
awareness and encourage support for people with CRPS and their family and
friends. Our participation highlights the disabling part of the syndrome and
offers hope to those who suffer from it.
You can participate in the walk and raise pledges, or put together a
corporate team. Perhaps your company has a matching funds arrangement for
not-for-profit fundraising events. Visit the website or contact us to get
started!
http://rsds.org/4/awareness/Achilles/2009/nyc.html
* *
*This E-alert was made possible by the contribution of the members of the
Reflex Sympathetic Dystrophy Syndrome Association (RSDSA). To learn more
about becoming a member of RSDSA, please click
here.
* *RSDSA Privacy
Policy
* *RSDSA Home
Page
*
RSDSA | 99 Cherry St. | Milford | CT | 06460
*June 28, 2009 | Central Park
**Online Registration and Forms are now available!
*
* *
Walker and Virtual Walker Registration Available
*Click here for more
information
*
* Team **Co-captains: Jackie Drake and Marsha Tyszler*
Since RSDSA promotes public and professional awareness of CRPS, a neurologic
syndrome characterized by severe and persistent pain that can lead to
disability, we are charged with educating those afflicted with the syndrome,
their families, friends, insurance and healthcare providers about the
potentially-disabling pain it causes.
We have teams in the Achilles Walk for Hope & Possibility to promote
awareness and encourage support for people with CRPS and their family and
friends. Our participation highlights the disabling part of the syndrome and
offers hope to those who suffer from it.
You can participate in the walk and raise pledges, or put together a
corporate team. Perhaps your company has a matching funds arrangement for
not-for-profit fundraising events. Visit the website or contact us to get
started!
http://rsds.org/4/awareness/Achilles/2009/nyc.html
* *
*This E-alert was made possible by the contribution of the members of the
Reflex Sympathetic Dystrophy Syndrome Association (RSDSA). To learn more
about becoming a member of RSDSA, please click
here.
* *RSDSA Privacy
Policy
* *RSDSA Home
Page
*
RSDSA | 99 Cherry St. | Milford | CT | 06460






I would like to join the Achilles walk and obtain donations. Please contact me at 949.784-.9394. I have had RSD since March 2006 and installed the spinal cord stimulator lat November. My attitude is positive, however, I still have my pain and down days. I would love to be around people like me because I feel alone and no one understands. I have great days and then my pain can get to a ten in a heart beat. I am requesting my vendors for donations so we can research this crazy disease and would love to obtain more information regarding it. I'm happy I still have my right leg after three Achilles tendon repair, but dissatisfied I incurred RSD/CRSP. It is a long story, I thought I started having seizures because I would shake and sweat in the middle of the night. I will share more later....I just do not want to re-hash everything right now and I feel it is my duty to walk next month and be with my kind. Therefore, please contact me..my girlfriend who has supported me through this whole ordeal will be walking with me and that makes me the happiest person on earth. We have been through the ringer....I'm from LOng Beach, Ca and she is from Phoenix, AX. She is the best, also known as my ROCK. I love Amy.
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