Researchers at BC Cancer and SFU are conducting a new study exploring Canadian cancer survivors’ preferences for using (not using) cannabis. If you are a cancer survivor interested in participating, please visit https://cc-arcc.ca/cannabis-survivorship-study-2019/ for more information.
If you are free on Thursday, October 10th from 10 a.m.-11 a.m. MT, you may wish to attend this free webinar. Based on the description of the session, it is going to be time well spent. Register here.
Join patient partners and thought leaders in an engaging panel discussion on the value of patient and family partnerships. Learn first-hand about what works well for partnering with patients and families, what doesn’t and tips for collaborating on your system transformation and organizational quality improvement initiatives. This webinar features panelists who have a range of collaboration experience, including at organizational, health system and policy maker levels.
• Did you know that as an Albertan you now have access to your personal health record?
• Did you know access to personal health information and digital solutions could improve health care experiences and outcomes?
• Do you want to know how to become an active partner in shaping how technology will transform our health care system?
You’re invited to Partners in the Power of Information Sharing: Educate, Empower, Engage, presented by IMAGINE Citizens Collaborating for Health and the O’Brien Institute for Public Health.
This FREE day-long event is designed to inform citizens about the power of digital health, and provide engagement opportunities to shape Alberta’s rapidly expanding digital health landscape.
WHEN: October 3, 2019
WHERE: Red & White Club, Calgary
On September 17, we will recognize #WorldPatientSafetyDay with a viewing of a documentary "To Err is Human," alongside @Patient_Safety, Patients for Patient Safety Canada, @HSO_world & @CAEHealthcare.
— The Partnership (@CancerStratCA) September 13, 2019
In a recent article found in the Globe and Mail, the following was addressed. “One of my friends says she can do a video chat with her doctor, why isn’t this option more widely available?” If, like many others, you are wondering the same thing, you may wish to read the article here.
If you are interacting with patients, here is something important you might want to remember.
If you think you are patient-centred, patient engaged, patient partnered etc. you may want to check your privilege and power.
— Julie Drury (@SolidFooting) August 25, 2019
As you may be aware, more and more residents from the US are purchasing their prescription drugs from Canada, due to the lower prices. While this is increasing sales for pharmaceutical companies and their associates, there is a something more important that must be considered. Namely, what effect are the sales of Canadian medicine to our US neighbours having on Canada and we Canadians?
According to a number of professional groups, the outcome of these prescription sales may result in drug shortages Canada. This, in turn, can have negative repercussions on the healthcare of Canadians. As a letter sent by groups representing patients, health professionals, hospitals, and pharmacists to Health Minister Ginette Petitpas Taylor states, “‘The Canadian medicine supply is not sufficient to support both Canadian and U.S. consumers…The supply simply does not, and will not, exist within Canada to meet such demands.”of the potential for increasing drug shortages.'” Read more about this here.
What does PJ Paralysis mean?
- PJ Paralysis is a term used to describe the negative physical and psychological effects experienced by patients who spend lengthy periods of time being inactive, and in their pyjamas, while in hospital.
What is End PJ Paralysis?
- End PJ Paralysis is a global movement that aims to help people live the richest, fullest lives by reducing immobility, muscle deconditioning, and dependency, while at the same time protecting cognitive function, social interaction, and dignity.
How can you get Involved?
- Join the global online summit on July 10-12, 2019, and learn from and with others who are interested and involved in this movement.
Check out this website to find out more.
“‘I feel like I’m living in a bubble. Outside is everyone else’s world and inside is mine.'” https://aptnnews.ca/2019/07/05/freds-story-living-and-documenting-dementia/.