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# NameComments
701 Paul Ferrara
702 Dorothy Mary Hatfield
703 Judie Rollins
704 Kathie Stephens
705 Julia Mtei
706 Jonathan ClementThis proven treatment should be available
707 Lalit VarmaI request both provincial government and federal government to consider this petition and help not only Simon Ibell but also other patients suffering from MPS-II.
708 Grant Connor
709 Alan Wilmott
710 TamiERT makes a big difference in our MPS childrens lives. Without it my children would not be alive and having a normal life. Driving, going to school, dating, and being normal young adults. Shame on Ontario drug plan for not covering this wonderful treatment. You want to see what a difference ERT can make...... visit my caringbridge page at www.caringbridge.com/ca/slawson
711 Mahdi
712 Amanda
713 jen diana
714 AnonymousElaprase is the ONLY treatment available to patients dx with MPS II. It's so important that patients start treatment ASAP, every day they wait more damage is occuring to the body. My son has been on this treatment for 2 years now and has shown remarkable improvement.
715 Leslie Phillips
716 Melinda Van Rheenen
717 Anonymous
718 Keith & Teresa Middleton
719 Jessa JenningsI moved here from BC, and am shocked that the ON government wouldn't step up their game and follow suit. I want to take pride in my new province.
720 Karin Adams
721 Blair Hurst
722 Blair Hurst
723 Kate Ayotte
724 Michael Root
725 Anonymous
726 Anonymous
727 Scott MalcolmThe fact that our government could be so obtuse, ignorant and shortsighted is equal parts enraging and terrifying. This is a needed and noble fight. I will help any way I can.
728 Peter
729 ROLAND
730 James Clapp
731 Helen Grogan
732 Kimberly Orr
733 Adam O'NeillPlease provide the funding Ontario.
734 Jeff Bridge
735 Stephen Anderson-MacdonaldMy Permanent Address and Contact Info: 2979 Cedar Hill Road Victoria, BC, V8T3H8 250-294-1648 (alternate: 612-353-4667)
736 kevin ansley
737 Heather Auden
738 Heather Auden
739 Anonymous
740 Erika Heller
741 Jean-Jacques Dugoua
742 Jane Frisby
743 Jacob Dowhy
744 Gerry Ayotte
745 Anonymous
746 Anonymousplease continue the research to help the children with this desease!!
747 James MacIver
748 Lynn DurocherWhat a shame. And we are in 2008.....ok
749 Wanda Rozwadowska
750 AnonymousQuality of life is important. I hope the Ontario government realizes that sooner than later for the young MPS II patients.