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Table 3 Perceived healthcare system and provider level barriers to epilepsy care

From: Barriers to epilepsy care in Central Uganda, a qualitative interview and focus group study involving PLWE and their caregivers

Financial constraints

We don’t have any drugs, so they tell you to go and buy the drugs.” Respondent PR#5

Location issues

“The problem with transportation is that we come from far away. Sometimes we would love to come but lack of transport stops us”. Respondent PR#2

Health care provider issues

 Poor communication skills

“You can meet a care provider who is just too proud! She yelled back at me instead. Maybe she had been angered moments before, but if you are a care provider you don’t respond rudely to patients”. Respondent PR#3

Why should I go to a government hospital to queue up and tell me to buy the medicine”? Respondent PR#13

Lack of drugs

 Appointment difficulties

“When we went to hospital, we were told that the doctor who handles such conditions (epilepsy) comes on specific days in a week and yet you have to first make a booking. So hospital looked like a loose end, so we never went back”. Respondent CG#23

 Inadequate disease investigation

“What I am saying is what the doctor said; they need to first check me up and see what is on the brain”. Respondent PR#20