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Table 5.21 continued<br />

Author<br />

Year<br />

Reference<br />

Country<br />

Clarke et al<br />

2008<br />

[1]<br />

Canada<br />

Material<br />

Analysis method<br />

The first 30 blogs from each perspective;<br />

“Aspies” and parents/<br />

caretakers, by selected from a<br />

Google search using the term<br />

Asperger blogs during one day<br />

Qualitative content analysis<br />

of 2 x 30 blogs<br />

Emerging themes were noted<br />

after rereading the summaries<br />

of the blogs<br />

Majority of bloggers were females<br />

and older than 20 years old, al-<br />

though gender /age information<br />

were lacking in one third from<br />

each groups<br />

Informants Results Summary Study quality<br />

Comments<br />

Blogs written by self identified<br />

people with Asperger’s syndrome<br />

and parents/caretakers of people<br />

with AS<br />

346 Autismspektrumtillstånd – diAgnostik och insAtser,<br />

KAPITEL 5 • sysTEmATIsK LITTErATurövErsIKT –<br />

347<br />

vårdens orgAnisAtion och pAtientens delAktighet<br />

Major repeated<br />

frames by:<br />

A. “Aspies”<br />

• Self-pride and<br />

acceptance<br />

• Role of Internet for<br />

maintaining a positive<br />

identity<br />

• Important people<br />

with AS<br />

• Disabling environment<br />

• Opposition to con-<br />

ventional language<br />

B. Parents/caretakers<br />

• Acceptance of dom-<br />

inant definitions and<br />

terms<br />

• Treatment<br />

• Minority opinion<br />

• Opposition to<br />

medicalisation<br />

The majority of parents<br />

argues for early diagnosis,<br />

greater access to<br />

treatment, to elimination<br />

of the disorder, and to<br />

special schools and educational<br />

programmes<br />

pAtientens delAktighet vid Ast<br />

The “Aspies” and the parents/<br />

caretakers views are frequently<br />

oppositional to one another<br />

The Aspies argues against a<br />

pathologising and medicalising<br />

perspective, whereas the parents<br />

and caretakers accept the medical<br />

definition, seek assistance and cure<br />

for their children<br />

Aspies have only experienced their<br />

own realities. As children they have<br />

little or no awareness of normative<br />

expectations<br />

A theoretical, methodological,<br />

substantive and practical discus-<br />

sion can increase the understanding<br />

of the “Aspies”<br />

The confusing and difficult protective<br />

role of parents to children with ASD<br />

aiming to socialize, love nurture and<br />

protect is discussed<br />

Moderate<br />

A preliminary and<br />

exploratory study<br />

No random samples<br />

Socioeconomic data<br />

is lacking<br />

Ethic discussion<br />

included<br />

The table continues on the next page

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