I'm a rehab nurse and grad student in public health who's researching the health care and self-care needs of people with SCIs. I'd be eternally grateful to hear what you all have to say about the questions I listed below. Feel free to answer any or all. Thank you so much!
1. If/when you were in inpatient rehab, who taught you the most about bowel/bladder and skin care? Nurses? Patient Care staff? Therapy? What worked or didn't work?
2. In your community, do you have accessible sources of nursing/skilled care to help with health issues? Do you use them?
3. If you don't have accessible sources, what would you suggest for your community? What would help?
4. Do you have local support groups and advocacy groups that are actively promoting disability issues?
1. If/when you were in inpatient rehab, who taught you the most about bowel/bladder and skin care? Nurses? Patient Care staff? Therapy? What worked or didn't work?
2. In your community, do you have accessible sources of nursing/skilled care to help with health issues? Do you use them?
3. If you don't have accessible sources, what would you suggest for your community? What would help?
4. Do you have local support groups and advocacy groups that are actively promoting disability issues?
Looking for feedback
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