Support for caregivers from government and social institutions |
10(22.7) |
17(38.6) |
5(11.4) |
10(22.7) |
2(4.5) |
Quality of medical care for your 22q11DS child |
1(2.3) |
14(31.8) |
7(15.9) |
20(45.4) |
2(4.5) |
Access to specialists (neurologist, geneticist, genetic clinic, psychologist |
9(20.5) |
20(45.4) |
2(4.5) |
12(27.3) |
1(2.3) |
Access to medications for 22q11DS children |
19(43.2) |
15(34.1) |
7(15.9) |
2(4.5) |
1(2.3) |
Access to and financial help with rehabilitation for 22q11DS children |
2(4.5) |
7(15.9) |
11(25) |
14(31.8) |
10(22.7) |
Access to information on 22q11DS
|
14(31.8) |
16(36.4) |
3(6.8) |
9(20.5) |
2(4.5) |
Support for 22q11DS children and caregivers from healthcare professionals |
9(20.5) |
16(36.4) |
8(18.2) |
10(22.7) |
1(2.3) |
Physicians’ knowledge about 22q11DS
|
17(38.6) |
19(43.2) |
2(4.5) |
6(13.6) |
0(0) |
Physicians’ practical information about 22q11DS(how to provide care for your 22q11DS child; how to perform various tasks) |
14(31.8) |
14(31.8) |
11(25) |
5(11.4) |
0(0) |
Physician’s/neurologist’s/geneticist’s communication skills |
5(11.4) |
13(29.5) |
4(9.1) |
21(47.7) |
1(2.3) |
Support caregivers receive from physicians |
9(20.5) |
13(29.5) |
12(27.3) |
9(20.5) |
1(2.3) |
Physicians’ empathy |
5(11.4) |
12(27.3) |
7(15.9) |
18(40.9) |
2(4.5) |
Drug and healthcare expenses |
7(15.9) |
5(11.4) |
15(34.1) |
7(15.9) |
10(22.7) |
Adaption of home to the child’s needs |
21(47.7) |
12(27.3) |
5(11.4) |
2(4.5) |
4(9.1) |
Lack of access specialised care equipment |
16(36.4) |
13(29.5) |
10(22.7) |
3(6.8) |
2(4.5) |
Drug reimbursement or purchase of drugs |
16(36.4) |
13(29.5) |
9(20.5) |
2(4.5) |
4(9.1) |
Contact with genetic clinic |
3(6.8) |
6(13.6) |
10(22.7) |
24(54.5) |
1(2.3) |
Contact with psychological clinic |
3(6.8) |
8(18.2) |
16(36.4) |
14(31.8) |
3(6.8) |
Contacts with the healthcare system |
1(2.3) |
3(6.8) |
21(47.7) |
10(22.7) |
9(20.5) |