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We believe in a brighter future for those affected. Have you or a family member recently. Been diagnosed with MPS or a related. We are here to help and can. Provide you with information and. Support to help you through. We Are Here To Help.
Watch our video to see how the National MPS Society is changing lives. Have you or your child recently been diagnosed with MPS or ML, or is your child undergoing diagnostic testing? We are here to help and can connect you with the information you need. Give to the National MPS Society. Support those affected by MPS and ML. The National MPS Society funds research that may lead to treat.
My Brother or Sister has MPS. My Brother or Sister has MPS. Links and Books for Siblings. I Know or Care for Someone with MPS. About the MPS and Related Diseases. To value, nurture and support those affected by Mucopolysaccharide and related diseases. When MPS keeps pushing me down I just keep moving. My Brother or Sister has MPS.
How can we help? Lysosomal Acid Lipase Deficiency. A PAUSE to changes to the NICE drug evaluation process. What Vimizim means to Sam. What Vimizim means to Gracie.