The Platform of Plasma Protein Users (PLUS) is a consortium of 7 patient organisations representing people living with treatable rare plasma related disorders.

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To those of say compensating #plasma donors is unethical and dangerous: Do you understand that patients in the world depend on #PDMPs coming largely from compensated donations? That regulatory authorities such as EMA have long deemed these products to be safe and effective?

PLUS has been promoting patient centredness and stakeholder collaboration around issues linked to the collection of #plasma and access to #PDMPs since 2010. Read our two first consensus statements here: https://bit.ly/3jeFZ96 (2010) and https://bit.ly/3xT088N (2011) !

28th June will be a very special day… do you know why?
#Neonatalscreening helps speed-up diagnosis and treatment of #rarediseases in newborns, it can even be life-saving! https://bit.ly/3zW6UfT
#InternationalNeonatalScreeningDay #INSD #ISNS #neonatal #Screen4Rare

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