RSDSA
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Round Table Regarding Imaging Neuroinflammation Workshop
RSDSAofAmerica
6 views
Scientists, clinicians, people with CRPS and other pain syndromes discuss the workshop and next steps.
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Barby Ingle, President of the Power of Pain Foundation
RSDSAofAmerica
14 views
Ms. Ingle discusses her advocacy with people in chronic pain.
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Virginia Ladd, Pres. and Exec. Dir. of the American Autoimmune Related Diseases Association
RSDSAofAmerica
7 views
Virginia Ladd, RSD/CRPS, Neuroinflammation, Chronic Pain, MicroGlia, Emerging Science, Brain, Neuroimaging, Autoimmune
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Vincent Clark, PhD, Univ. NM. Dept. of Neurosciences
RSDSAofAmerica
13 views
Vincent Clark discusses Neuroimaging, Neuroinflammation and Neural Information Processing.
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Tony Wyss-Coray, Ph.D, Stanford Univ.
RSDSAofAmerica
3 views
Tony Wyss-Coray discusses Visualizing Neuroimflammation in Bioluminescent Transgenic Animals.
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Sandip Biswal, MD, Stanford Univ.
RSDSAofAmerica
6 views
Sandip Biswal discusses Molecular Imaging and Autoimmunity
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Roberto Perez, Ph.D, VU, University Medical Center, Amsterdam, NL
RSDSAofAmerica
5 views
Roberto Perez discusses Trauma Related NeuronaL Dysfunction (TREND) Knowledge Consortium and it's partnership with RSDSA.
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Richard Larson, MD, Ph.D, Vice President for Translational Research
RSDSAofAmerica
1 views
Richard Larson describes both regional and national roles that the University of New Mexico plays in basic, clinical, and community service research.
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Ralph James, Ph.D, Brookhaven National Laboratory
RSDSAofAmerica
3 views
Next Generation of SPECT/PET Imaging Tools
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Phillip Getson, DO, Drexel University, Philadelphia, PA
RSDSAofAmerica
5 views
Phillip Getson discusses Imaging the Spread of CRPS with Thermography.
About RSDSA
The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) was founded in 1984 to promote public and professional awareness of Complex Regional Pain Syndrome (CRPS), also known as Reflex Sympathetic Dystrophy (RSD).
Our mission is to promote public and professional awareness of CRPS and to educate those afflicted with the syndrome, their families, friends, insurance and healthcare providers on the disabling pain it causes. We encourage individuals with CRPS to offer each other emotional support within affiliate groups. And finally, we are committed to raising funds for research into the cause and cure of CRPS.
Please visit our website (www.rsds.org) for information on our other initiatives.
The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) was founded in 1984 to promote public and professional awareness of Complex Regional Pain Syndrome (CRPS), also known as Reflex Sympathetic Dystrophy (RSD).
Our mission is to promote...
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