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Testimonials

The Accelerated Cure Project repository is being assembled to address a significant obstacle in the search for a cure for Multiple Sclerosis and related demyelinating diseases -- the lack of sufficient numbers of biological samples and associated data from people with MS.

Many scientists have voiced their support for the repository and have identified it as a resource that will change the way research is conducted. Here is a selection of these comments:


"A rigorously collected bank of MS biological samples (including serum, peripheral blood cells, material for RNA/DNA extraction and CSF when available) on a clinically well-characterized MS patient population and matched control populations, would represent a precious resource to the MS research community. Individual researchers in the field of MS immunology and neurobiology continue to be faced with the ongoing challenge of acquiring high qualtiy samples to be applied to their specific laboratory systems.

The lack of a central resource has required many labs to generate their own samples. This has proven to be a demanding task which has, at times, limited labs from engaging in otherwise promising research. Moreover, generating samples in individual labs, using disparate protocols, has made it difficult to compare results across projects - an issue that is recognized as increasingly important with the growing appreciation of the subtleties of sample acquisition/processing/storage and the need for a uniform and validated approach. "

Amit Bar-Or, MD, FRCP(C), Montreal Neurological Institute


"I am delighted to provide you with my strongest support for the highly ambitious research initiative proposed by the Accelerated Cure Project. The project represents the largest and most comprehensive ascertainment of historical, epidemiological, genetic, and clinical data on multiple sclerosis to date. The protocol has been carefully and expertly formulated and refined.

"...scientists need a large collection of specimens from a variety of patients with detailed information about those patient's experiences with this disease. Only then will we be able to sort out the complex interaction between people and their environment that leads to the development of MS."

Elliot Frohman, MD, PhD, University of Texas Southwestern Medical Center


"The approach taken by the Accelerated Cure Project is a long overdue effort to collect the vital information and specimens from people, necessary for research such as mine to be fruitul. A concerted effort to expand this project will undoubtedly lead to benefits not just for patients with MS, but for science in general."

Ben Greenberg, MD, MHS, Johns Hopkins


"I believe your aims and project have great significance, and will provide an invaluable and very much needed resource to our community. Such a resource can immensely facilitate the progress in research, because it takes away the burden of field work, data and specimen collection for the always tightly funded and always competing investigators."

Bernadette Kalman, MD, University Hospital, State University of New York


"A definitive study regarding the role of mitochondrial DNA variants in MS is greatly needed. My lab is prepared to conduct such a study. However, the limiting factor in our ability to do so is the availability of sufficient numbers of DNA samples from clinically well-characterized MS patients and appropriately matched controls. The availability of large numbers of such samples through the repository established by the Accelerated Cure Project for Multiple Sclerosis would have a direct and immediate impact on my work by making it possible to perform a definitive study to address the critical question regarding the role that mitochondrial genetic variants play in MS. Because of the large numbers of samples and detailed clinical and epidemiological data accompanying them, studies that were previously impossible now could be performed."

David Simon, MD, PhD, Beth Israel Deaconess Medical Center

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