| # | Name | Comments |
|---|
| 851 | Anonymous | I am from Ballarat in Australia. I have a son with MPS II and a nephew also with this disease. Our government has just approved funding for this treatment and already I have seen improvment in my nephew after 4 sessions. My son begins his treatment in the new year and it cant come a moment too soon.
The Government of Canada MUST approve this drug as quality of life is essential. I will be hoping and praying this happens for to have a drug that can assist with quality of life and yet is out of reach is one of the cruelest tricks one can do. |
| 852 | Anonymous | |
| 853 | Anonymous | |
| 854 | Ryan Jennings | This is provincial discrimination. As Canadians, we must object to the provincial resident of one province receiving superior care when compared to another. These are not Canadian ideals we hold in high esteem. |
| 855 | tasha oropeza | |
| 856 | Kelly Nicholson | |
| 857 | Jackie Chenier | |
| 858 | yvette harrison | |
| 859 | Rebecca Gingrich |
| 860 | Anonymous | What will it take for the ON Government of fund Hunter Syndrome suffers. It seems unthinkable to alway a child and their families to suffer in this way when there is a know treatment. |
| 861 | Libby Pust | My 2 yr old son has Hunters and receives treatment here in Ireland... try and stop me from petitioning for ERT in Ontario |
| 862 | Andrew Downey | |
| 863 | Anonymous | |
| 864 | paolo | |
| 865 | Bryan Blue | |
| 866 | Celeste Wagner | |
| 867 | jessica croft | my son suffers from this same disease therefore i can totally sympathise. i would be devasted if he could not recieve treatment, which thankfully he does. |
| 868 | Anonymous | |
| 869 | Darrell Gee | |
| 870 | Marc Rigaux | |
| 871 | Andrew Thompson | |
| 872 | Tom Keller | |
| 873 | Angela Moha | Please, Please approve he funding for this treatment!!!! It is so important. |
| 874 | tina hotchkiss | |
| 875 | Alicia VanMetre | |
| 876 | Joseph Witalis | Come on, Mr. Caplan and Mr. McGuinty - stop being so afraid of precedent that you sacrifice young lives. |
| 877 | Alison Galvin | So unfair that its not been provided for in Ontairo. This is such an important thing and makes lives easier for families all around. It is funded in Ireland and the UK as well as BC and Alberta. Sort it out ! |
| 878 | Anonymous | |
| 879 | Gary and Coena Riddell | I strongly agree that every human being is entitled the same opportunity for whatever treatments are out there to provide them a good quality of life. |
| 880 | Anonymous | |
| 881 | rachelle luebbing |
| 882 | Ryan Green | |
| 883 | Marianne Stevulak | |
| 884 | alicia todd | |
| 885 | Pamela Tate |
| 886 | Jordanna Mora | |
| 887 | Doug Blair | Wishing you all the best, Simon. |
| 888 | Paulette Harris | Patients with a rare disease deserve the same standard of care as everyone else. |
| 889 | Rhiannon Woodcock | |
| 890 | Jonathan Huyda | |
| 891 | Ashkaughn |
| 892 | trina | |
| 893 | kirk brown | |
| 894 | roberta halpenny | |
| 895 | Jennifer Bateman | |
| 896 | katelynn oneill | |
| 897 | Alycia Garcia | |
| 898 | sheelagh anderson | |
| 899 | Anonymous | |
| 900 | Jocelyn Elias | |