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Join the GM1 Patient Network to accelerate treatment for GM1 Gangliosidosis!

The health information of those impacted by GM1 Gangliosidosis is essential to advancing medical research and for drug developers working to translate research to the clinic and to treat patients.

Help build momentum by joining this shared network!  Patient advocacy organizations and clinicians, and the GM1 community at large can help build a comprehensive database of de-identified data.  This data is an extremely valuable tool for understanding the patient population and to help plan clinical trials.  Furthermore, patients can receive useful information regarding clinical trials as they become available.

Promising research is advancing and this network will help amplify patient voices and help advance the drug development process.  Please provide as much information as possible to move research forward from bench to bedside!

Research is advancing on multiple fronts globally. We must contribute in any way possible to bring these treatments forward. In every second that goes by, the world could be closer to an end of GM1 and to the end of conditions like GM1. Innocent children who have the incredible misfortune of receiving disease-causing genes could have a chance at life.   Please help now!

 

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Join the GM1 Patient Network to accelerate treatment for GM1 Gangliosidosis!

The health information of those impacted by GM1 Gangliosidosis is essential to advancing medical research and for drug developers working to translate research to the clinic and to treat patients.

Help build momentum by joining this shared network!  Patient advocacy organizations and clinicians, and the GM1 community at large can help build a comprehensive database of de-identified data.  This data is an extremely valuable tool for understanding the patient population and to help plan clinical trials.  Furthermore, patients can receive useful information regarding clinical trials as they become available.

Promising research is advancing and this network will help amplify patient voices and help advance the drug development process.  Please provide as much information as possible to move research forward from bench to bedside!

Research is advancing on multiple fronts globally. We must contribute in any way possible to bring these treatments forward. In every second that goes by, the world could be closer to an end of GM1 and to the end of conditions like GM1. Innocent children who have the incredible misfortune of receiving disease-causing genes could have a chance at life.   Please help now!

 

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Join the GM1 Patient Network to accelerate treatment for GM1 Gangliosidosis!

The health information of those impacted by GM1 Gangliosidosis is essential to advancing medical research and for drug developers working to translate research to the clinic and to treat patients.

Help build momentum by joining this shared network!  Patient advocacy organizations and clinicians, and the GM1 community at large can help build a comprehensive database of de-identified data.  This data is an extremely valuable tool for understanding the patient population and to help plan clinical trials.  Furthermore, patients can receive useful information regarding clinical trials as they become available.

Promising research is advancing and this network will help amplify patient voices and help advance the drug development process.  Please provide as much information as possible to move research forward from bench to bedside!

Research is advancing on multiple fronts globally. We must contribute in any way possible to bring these treatments forward. In every second that goes by, the world could be closer to an end of GM1 and to the end of conditions like GM1. Innocent children who have the incredible misfortune of receiving disease-causing genes could have a chance at life.   Please help now!

 

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