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# NameComments
651 Jimmy Ngoc Luong
652 Nicole LandellsLife is a precious gift!
653 Patricia Slike
654 Jacob M HoeppnerI strongly urge the Ontario government to provide funding for this rare disease affecting Simon and others. If funding can be approved for sex change procedures, surely MPS II is much more important and of greater urgency!
655 Robert Kennedy
656 Graeme FraserWay to go Simon! The work you are doing is invaluable for those Canadians suffering from a rare disease. Our country desperately needs to create a policy that recognizes the unique nature of rare disorders such as Hunter Syndrome and an established national fund that provides patients access to life saving therapies.
657 Clete PurcellMy nephew, Trey Purcell, also has Hunter Syndrome. He participates in elaprase therapy once a week. In my view, the therapy has had a positive impact on Trey. It is absurd to me that the Ontario Government will not follow BC's lead on this issue.
658 Scott
659 Graem Millala
660 Robert S. Stevenson
661 Lindsay Ellen RoweLOVE YOU SIMON!
662 Anonymous
663 Anonymous
664 Anonymous
665 Rosalee Floyd
666 Anonymous
667 mano de silva
668 Amelie Mercier
669 Joseph WitalisIt is criminal that our government ignores the needs of people with Hunter's Syndrome and other rare disorders. Even with the relatively high cost of treatments, the population is so small that the total expenditure for all people with rare disorders across Canada would amount to about $200 million, about 2% of the total health care budget. For that small amount, people with these conditions can return to productive (read: "taxpaying") lives and add to society.
670 Laura Brick
671 Nicole Bentley
672 Jeffery Marques
673 Liza K Austin
674 Harris & Nancy Lusher
675 Sean Neeb
676 yolette vincentelli
677 Trish Hislop
678 Warren A. SpiresIt is a disgrace that the Ontario Government needs to be petitioned to provide this essential medical care for Simon Ibell and a hand full of Ontario residents who desperately need this treatment. The Ontario Government must step up now.
679 Donna Seaman
680 Dr. Adam Spires
681 Elizabeth MulhollandPlease fund this. It's only a small number of patients, but means everything to their life chances. Thank you.
682 Heather CardThe Ontario Government funds so many non-life supporting ventures that it is criminal that they are not funding the cost for MPS II patients.
683 Drew Rowe
684 Robert Orr
685 Kimberly Orr
686 Sonia LaneseI have an 11 yr. old boy with Hunters. I strongly urge the Ontario Gov't to fund this one and only treatment for Hunter Syndrome . This is a small price to pay for just a handful of Hunter patients here in Ontario. Make it happen because LIFE is PRECIOUS!!!! Give our children a fighting chance!!!
687 Lorna Read
688 krista burketti am the mother of a 17 month old with hunter syndrome who is getting these treatments. i have lost 4 family members to this before this treatment was avalible and the thought of someone not being able to get this treatment just makes me sick!
689 Bill Buckingham
690 Carla Embleton
691 Norma ChristouThe Ontario Government needs to support this treatment for Canada's patients dealing with this disease.Why is it that from province to province there is not a consistent treatment policy ???Blessings to Simon and his journey !
692 Rob Keen
693 Jan CheznowskiI encourage the Government of Ontario to fund treatment for Hunter Syndrome immediately, if not sooner, for the child, Szymon Cajmer !!! Please act !!!
694 Ruben Janssen
695 Kim LachanceThe people who have such a rare condition need your help. Please fund this therapy for the few who need it, God will bless you for it.
696 Tim Lachance
697 Julia Paisley
698 victoria grahamall are to be equal under the law and to have a free, full, and abundant life. the govmt' denies safety and oppresses the disabled like hitler did.
699 lyn creelman
700 Oly SandorGood luck man!