Research Article

Internet Usage by Patients with Multiple Sclerosis: Implications to Participatory Medicine and Personalized Healthcare

Table 2

Participants' attitudes about information and the internet: number and percentage of patients that agree with attitude statements.

Attitude statementGIU- (%) General Internet UsersMSIU- (%) MS-Internet UsersP

It is easier to find information on MS in the Internet than in books13 (93)53 (88) .99
It is easier to ask the physician than to search the Internet15 (94)33 (56).005
Information in books is more reliable than information in the Internet5 (38)18 (33).75
People with other diseases find more information than people with MS2 (25)12 (21) .99
Information about MS helps me cope with the disease7 (47)46 (78).02
Information about MS frightens me5 (31)22 (37).69
I search for more information when the disease worsens6 (40)40 (69).04
I would be happy to read about how other patients cope with MS5 (33)39 (66).04
I would be happy to make contact with my medical team through the Internet6 (43)41 (68).07
I feel part of the decision making in my treatment9 (69)48 (84).24
The medical team encourages me to look for information about MS1 (8)14 (25).27
The medical team is happy to discuss with me new information I found6 (50)30 (59).75