We have had over 400 signings and messages so far supporting Darby Rimmer MND Foundation Rob Burrow CBE Ed Slater Marcus Stewart, partners and Geoff Burrow - Open letter to the Mirocals consortium. See all the messages here and perhaps add your voice?
united2endmnd.org/2024/04/30/wou…
#united2endmnd
Please show your support for letter sent to MND Association King's MND Centre Neuroscience Institute SussexNeuro QM Neuroscience last Monday by Darby Rimmer MND Foundation Geoff Burrow Rob Burrow CBE Ed Slater on TRANSPARENCY on #Mirocals trial here united2endmnd.org/support-miroca… MotorNeuroneDisease Challenging MND Dodd1e5 Gr4nd S7am Team #MND
Last week Patients United2EndMND supporters Darby Rimmer MND Foundation Steph Houghton MBE Rob Burrow CBE Geoff Burrow Ed Slater & Jo, Marcus & Louise Stewart asked vital questions of 4 UK #Mirocals Consortium members. Pls go to united2endmnd.org/support-miroca… to read & sign to support our plea for transparency
Huge thanks Darby Rimmer MND Foundation Steph Houghton MBE Rob Burrow CBE Geoff Burrow Jo & Ed Slater Marcus & Louise Stewart for sending open letter requesting TRANSPARENCY on commercial contracts for #Mirocals to involved scientists & MND Association To show support please see united2endmnd.org/support-miroca…
MND Association it says something when your highest profile patients feel compelled to write an open letter. Patients want and deserve treatment with Proleukin. We have been BEGGING for 16 months. MIROCALS Consortium must answer patients and take action Darby Rimmer MND Foundation Rob Burrow CBE
Huge thanks Peter Ash #Corrie for supporting Darby Rimmer MND Foundation Rob Burrow CBE Geoff Burrow Ed Slater Marcus & Louise Stewart letter to MND Association Neuroscience Institute King's MND Centre BSMS Clinical Neuroscience QM Neuroscience asking for TRANSPARENCY on #Mirocals trial.
Pls support @ united2endmnd.org/support-miroca…
#mirocals trial ended nearly 2 yrs ago & we still await results! Typical survival once diagnosed with #mnd is just 2yrs! Something wrong here? If touched by #mnd please support Darby Rimmer MND Foundation Rob Burrow CBE Ed Slater & Marcus’s OPEN letter to the consortium. BW Lee
#united2endmnd
Richard Evans MND Association Some may think a little harsh, but if you could engage with this ASAP it would be a fantastic start united2endmnd.org/support-miroca… We look forward to working with you. Good luck! Darby Rimmer MND Foundation Rob Burrow CBE Geoff Burrow Ed Slater
razadu Darby Rimmer MND Foundation Rob Burrow CBE Ed Slater Here is the iltoo announcement of the mirocals consortium agreement in May 2023
iltoopharma.com/wp-content/upl…
Lee Millard Darby Rimmer MND Foundation Rob Burrow CBE Ed Slater Lee Millard I have one question: Mirocals is a trial conducted by Iltoo, right? And Iltoo is a French company or am I wrong there? So I was wondering if you are working together with French ALS advocates. I know UK is not part of EU, but if different ALS advocacies from Europe
Tanya Curry Daniel Boffey It's also vital Patients United2EndMND MotorNeuroneDisease challenge 'accepted ways' of accessing new treatments & demand transparency required of a taxpayer/charity funded trial like #Mirocals , especially when our lead charity is a member of Consortium. MND Association King's MND Centre SussexNeuro
David Kilgannon Please see this patient advocacy website that has a whole menu section on MIROCALS it may explain things more clearly. In essence patients are not been spoken to at all by ILTOO Pharma & on a limited level by the consortium. It really beggars belief! united2endmnd.org/mirocals/