A student here looking at dementia in the community as part of my project.
I would be grateful if carers can give me some insight...
1. Before knowing Alzheimer's society existed, would you carers have known services available to carers?
2. Please name some services.
3. How did you know about services available to you?
4. Do you think that these services are adequate? If not, why?
5. How do carers like yourself see you and your loved one's prospects with government funding being changed?
Thank you. Your input is appreciated!
I would be grateful if carers can give me some insight...
1. Before knowing Alzheimer's society existed, would you carers have known services available to carers?
2. Please name some services.
3. How did you know about services available to you?
4. Do you think that these services are adequate? If not, why?
5. How do carers like yourself see you and your loved one's prospects with government funding being changed?
Thank you. Your input is appreciated!
