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Boy Ãåéá óáò. Åßìáé ï ¢êçò.

Äéáãíþóèçêá ùò ïñïèåôéêüò ðñéí áðü 4 ÷ñüíéá.
Ôþñá åßìáé ðïëý êáëÜ óôçí õãåßá ìïõ. Äåí Ý÷ù ðñïâëÞìáôá õãåßáò.
Äåí íéþèù ÷Üëéá øõ÷ïëïãéêÜ ðëÝïí, üðùò óôéò áñ÷Ýò âÝâáéá üôáí ôï Ýìáèá.
¸êáíá 8 áðüðåéñåò áõôïêôïíßáò áëëÜ äåí Ýöõãá.
Áõôü ìÜëëïí óçìáßíåé üôé äåí Ýöôáóå ç þñá ìïõ áêüìá.

¸ìáèá ìÝóá áðü áõôÞ ôçí åìðåéñßá üôé ðñÝðåé íá ìÜèù íá æù ìå áõôü.
ÐñÝðåé íá ìÜèù íá áãáðÜù ôïí åáõôü ìïõ ðåñéóóüôåñï.
ÐëÝïí ôï ìüíï ðñüâëçìá ðïõ áíôéìåôùðßæù åßíáé üôé åßìáé ìüíïò ìïõ ÷ùñßò ó÷Ýóç åäþ êáé 3 ÷ñüíéá.

Äåí Ý÷ù ó÷Ýóç áõôü ôïí êáéñü, ãéáôß öïâÜìáé áêüìá êáé íá îåêéíÞóù êÜôé.
Ãéá ôïõò Üëëïõò ôï íá åßìáé ïñïèåôéêüò èåùñåßôáé üôé åßíáé ðïëý êáêü êáé áõôü ìå ôñïìÜæåé éäéáßôåñá.
Èá Þèåëá âÝâáéá íá æÞóù êé åãþ êáíïíéêÜ üðùò üëïé ïé Üëëïé Üíèñùðïé, Ý÷ïíôáò ìéá ó÷Ýóç êáé êÜíïíôáò ôåëéêÜ ïéêïãÝíåéá.
ÁëëÜ ðùò èá ãßíåé áõôü; Ðïéá ãõíáßêá èá ìå äå÷ôåß;

Åõêáéñßåò åß÷á ðïëëÝò ìÝ÷ñé óÞìåñá áëëÜ äåí ôüëìçóá ðïôÝ íá ðñï÷ùñÞóù ãéáôß öïâÞèçêá íá ðù üôé åßìáé ïñïèåôéêüò.
Ôþñá åßìáé ìüíïò êáé åßíáé ôï ìüíï ðïõ ìå óôåíá÷ùñåß êáé ðïõ äåí èÝëù íá óõíå÷éóôåß.
ÌáêÜñé íá åßìáé êáëÜ óôï ìÝëëïí êáé èá äù ôé èá êÜíù ðáñáêÜôù.
Åëðßæù íá âñù ôï èÜññïò íá ôï ðù êÜðïéá óôéãìÞ.
ÈÝëù íá ðéóôåýù üôé êáíåßò äåí ðÜåé ÷áìÝíïò.




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Lancet

Ðñüóöáôåò äçìïóéåýóåéò óôï ðåñéïäéêü The Lancet HIV

Optimised second-line regimens in the public health approach

Globally, most people receive antiretroviral therapy (ART) in programmes that follow the WHO-recommended public health approach, using a small number of standard regimens and simplified monitoring.1 A single standard regimen—dolutegravir (an integrase strand transfer inhibitor [INSTI]) with tenofovir disoproxil fumarate and lamivudine (both nucleoside reverse transcriptase inhibitors, [NRTIs])—is currently taken by the large majority of people on ART in these programmes, including those on second-line therapy (following previous failure of a non-NRTI regimen).

Prioritising HIV drug resistance testing according to risk

Tenofovir–lamivudine–dolutegravir (TLD) is recommended as an initial treatment regimen and a preferred optimised regimen for people living with HIV without a history of previous viral non-suppression, referred to as TLD in first-line therapy (TLD-1). For people living with HIV with persistent viral non-suppression, TLD largely replaced protease inhibitor-based regimens following efavirenz-based initial regimens, referred to as TLD in second-line therapy (TLD-2), as it is at least as effective, better tolerated, and more affordable.

Ending paediatric AIDS: time to close implementation gaps

WHO's global health sector strategies on HIV, conceived to guide the health sector in implementing strategically focused responses to achieve the goals of ending AIDS by 2030, target a reduction in the number of children aged 0–14 years newly infected with HIV from 150 000 in 2022 to 20 000 in 2025 and 15 000 in 2030.1 To track progress toward these targets, accurate estimations of the number of annual infections in children in each country is crucial. However, in many low-income and middle-income countries, where the burden of paediatric HIV is the highest, children are not systematically tested for HIV in programmes for the prevention of vertical transmission (PVT).

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