Except from Epilepsy Durham Region newsletter, July, 2013
Imagine that your four month old child begins having seizures. Then imagine that they receive a devastating diagnosis, whereby epilepsy is one of several very big problems on the horizon. Where do you go? What do you do? Who do you talk to? So many parents are faced with the incredible difficulty of raising a child that has a seizure disorder. They are faced with all of these questions, countless doctor’s appointments, intensive exercise and diet regimes, roadblocks in the school system and all they can ever hope for is that their child gets through the day with a “free pass” from their daily seizures.
This is everyday life for Holly and Barry with their now 14-year-old daughter Katy of Bowmanville, Ontario. Katy first started having seizures at just four months old. After seeking help from many medical professionals, a neuro-opthamologist was finally able to
The Ontario Public Drug Program has outlined changes to OHIP+ for children and youth. Please see the information below provided by the Ministry of Health and Long Term Care Drug and Devices Division.
Amendment to Ontario Regulation 201/96 made under
the Ontario Drug Benefit Act to make changes to
Ontario Drug Benefit Program coverage for children and
youth aged 24 years and under (OHIP+)
February 27, 2019
Further to recent announcements, the government is changing OHIP+ by focusing benefits on those without private plans. The changes come into effect on April 1, 2019.
The changes affect OHIP-insured children and youth 24 years of age
Did you know March is National Epilepsy Awareness Month? We are excited to see a wave of purple spreading across Durham Region during the month of March to help in our mission to raise epilepsy awareness, starting with proclamations from our council members across the municipalities in our community!
Exerpt from Canadian Epilepsy Allicance: http://www.canadianepilepsyalliance.org/canadian-epilepsy-alliance-statement-on-ken-jeongs-netflix-comedy-special/ on February 25th, 2019
CANADIAN EPILEPSY ALLIANCE Statement on Ken Jeong’s Netflix Comedy Special
Deirdre Floyd, President of Canadian Epilepsy Alliance: “I am somewhat mystified as to why forms of entertainment find it amusing to inaccurately portray first aid for seizures at all.”
For Immediate Release – February 25, 2019
Once again the Canadian Epilepsy Alliance is responding to another example of inaccurate information in relation to first aid for seizures on Netflix’s Special called “Ken’s