Signatures 908 total
Page: « ‹ 1, 2, 3, 4, 5, 6, 7, ... 19 › »
-
151
Name: Fsfs on Aug 12, 2008Comments:Flag
-
152
Name: Tammy Ma on Aug 12, 2008Comments:Flag
-
153
Name: Reta Clark on Aug 12, 2008Comments: Please consider the funding for this drug it is of value to the whole society. When we know we can make a difference it doesn't make sense not to. This is our YOUTH and future's we are working for.Flag
-
154
Name: Sarah Mourtizen on Aug 12, 2008Comments:Flag
-
155
Name: Anonymous on Aug 12, 2008Comments:Flag
-
156
Name: Lisa Green on Aug 12, 2008Comments:Flag
-
157
Name: Roland Semprie on Aug 12, 2008Comments:Flag
-
158
Name: Shannon Drage on Aug 12, 2008Comments:Flag
-
159
Name: Piper Gara on Aug 12, 2008Comments: It is unforgivable that this treatment is not covered in Ontario!Flag
-
160
Name: Glynis Gilman on Aug 12, 2008Comments:Flag
-
161
Name: Patricia Otero on Aug 12, 2008Comments:Flag
-
162
Name: Oona Tiplady on Aug 12, 2008Comments:Flag
-
163
Name: Matthew Levy on Aug 12, 2008Comments:Flag
-
164
Name: Anil Sayani on Aug 12, 2008Comments:Flag
-
165
Name: Anne De Silva on Aug 12, 2008Comments:Flag
-
166
Name: Kerry Sharpe on Aug 12, 2008Comments:Flag
-
167
Name: Marie Ibell on Aug 12, 2008Comments: A remarkable individual Simon is the victim of a government that would appear to be more concerned with votes over life. As a group with a rare disease they are rare in the number of votes. Hopefully the Ontario government is rare in its discriminatory approach .Flag
-
168
Name: Louise Winter on Aug 12, 2008Comments:Flag
-
169
Name: Patricia Noel on Aug 12, 2008Comments:Flag
-
170
Name: Christine Kiss on Aug 12, 2008Comments:Flag
-
171
Name: Lou Douillard on Aug 12, 2008Comments:Flag
-
172
Name: Tracy Johns on Aug 12, 2008Comments:Flag
-
173
Name: Tami Tate on Aug 12, 2008Comments:Flag
-
174
Name: Lucas Riedl on Aug 12, 2008Comments:Flag
-
175
Name: Rita Gara on Aug 12, 2008Comments:Flag
-
176
Name: Brad Stevenson on Aug 12, 2008Comments:Flag
-
177
Name: Suzanne Neumann on Aug 12, 2008Comments:Flag
-
178
Name: Lauren Karst on Aug 12, 2008Comments:Flag
-
179
Name: Rebecca Richardson on Aug 12, 2008Comments:Flag
-
180
Name: Nicholas Schubert on Aug 12, 2008Comments:Flag
-
181
Name: Jane Scurfield on Aug 12, 2008Comments:Flag
-
182
Name: Derek Dolsen on Aug 12, 2008Comments:Flag
-
183
Name: Kat Watson on Aug 12, 2008Comments:Flag
-
184
Name: Andrew Moll on Aug 12, 2008Comments:Flag
-
185
Name: Tracey MacLeod on Aug 12, 2008Comments:Flag
-
186
Name: Anonymous on Aug 12, 2008Comments:Flag
-
187
Name: Maureen Miller on Aug 12, 2008Comments:Flag
-
188
Name: Maureen Miller on Aug 12, 2008Comments:Flag
-
189
Name: Malcolm Adams on Aug 12, 2008Comments:Flag
-
190
Name: Anonymous on Aug 12, 2008Comments:Flag
-
191
Name: Anonymous on Aug 12, 2008Comments:Flag
-
192
Name: Danuta Pascore on Aug 12, 2008Comments: Please provide funding for the approved treatment for people with Hunter Syndrome (MPS II).Flag
-
193
Name: Gerry Barranda M.D. on Aug 12, 2008Comments:Flag
-
194
Name: Julie French on Aug 12, 2008Comments: how evil and devastating our government has become... I am an RCA and let me tell you that these poor victims of this disease demand just as much care as everyone else.Flag
-
195
Name: Cameron Gilbert on Aug 12, 2008Comments: Hopefully we can achieve this goal with the help of all our friends working together.Flag
-
196
Name: Peter Weber on Aug 12, 2008Comments: I am very much in support of this petitionFlag
-
197
Name: Lea Harper on Aug 12, 2008Comments:Flag
-
198
Name: Lesley Kroch on Aug 12, 2008Comments:Flag
-
199
Name: Russell Wong on Aug 12, 2008Comments:Flag
-
200
Name: Chris Davis Sr on Aug 12, 2008Comments:Flag