Sickle Cell Awareness Group of Ontario (SCAGO)

Let your voice be heard

Hospital Experience Reporting Portal

Let your voice be heard

Hospital Experience Reporting Portal

Let your voice be heard

Hospital Experience Reporting Portal

To ensure that peers with Sickle Cell Disease (SCD) continue to receive optimal care when interacting with the Ontario healthcare system, the portal is established by the Sickle Cell Awareness Group of Ontario to support patients in documenting the quality of care they receive, whether optimal or sub-optimal.

01

Information Collected

Kindly note that the information collected on this portal will be used to advance advocacy and education in improving the quality of care delivered to peers with SCD in Ontario. Personal identifying information provided, such as your name and contact details, will be used to contact you should you need us to advocate on your behalf with the hospital.

02

How your Information is Used

Your information will not be shared with any hospital or third-party institution without your explicit consent.

03

Submitting Responses

Please respond to as many of the following questions as possible for your most recent hospital experience. Please do not hesitate to return and complete the questionnaire for any future hospital visits.

To ensure that peers with Sickle Cell Disease (SCD) continue to receive optimal care when interacting with the Ontario healthcare system, the portal is established by the Sickle Cell Awareness Group of Ontario to support patients in documenting the quality of care they receive, whether optimal or sub-optimal.

01

Information Collected

Kindly note that the information collected on this portal will be used to advance advocacy and education in improving the quality of care delivered to peers with SCD in Ontario. Personal identifying information provided, such as your name and contact details, will be used to contact you should you need us to advocate on your behalf with the hospital.

02

How your Information is Used

Your information will not be shared with any hospital or third-party institution without your explicit consent.

03

Submitting Responses

Please respond to as many of the following questions as possible for your most recent hospital experience. Please do not hesitate to return and complete the questionnaire for any future hospital visits.

To ensure that peers with Sickle Cell Disease (SCD) continue to receive optimal care when interacting with the Ontario healthcare system, the portal is established by the Sickle Cell Awareness Group of Ontario to support patients in documenting the quality of care they receive, whether optimal or sub-optimal.

01

Information Collected

Kindly note that the information collected on this portal will be used to advance advocacy and education in improving the quality of care delivered to peers with SCD in Ontario. Personal identifying information provided, such as your name and contact details, will be used to contact you should you need us to advocate on your behalf with the hospital.

02

How your Information is Used

Your information will not be shared with any hospital or third-party institution without your explicit consent.

03

Submitting Responses

Please respond to as many of the following questions as possible for your most recent hospital experience. Please do not hesitate to return and complete the questionnaire for any future hospital visits.