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Social care remains vital in face of government cuts

HIV con­tin­ues to be one of the most impor­tant com­mu­ni­ca­ble dis­eases in the UK with many thou­sands of peo­ple still being diag­nosed every year. There is still much stig­ma around HIV and a diag­no­sis can be trau­mat­ic which is why social care remains so vital.

Lat­est data from the Health Pro­tec­tion Agency shows that more than 6,000 peo­ple were diag­nosed with HIV in the UK in 2011. This is a slight decrease on the year before and con­tin­ues a down­ward trend from a peak of 7,820 in 2005. There are rough­ly 100,000 peo­ple liv­ing with HIV in the UK today with about a quar­ter of them undi­ag­nosed.

Social care has pro­vid­ed vital sup­port for those liv­ing with HIV since the start of the epi­dem­ic 30 years ago. Then it was intro­duced to help those who were ter­mi­nal­ly ill. Nowa­days, thanks to bet­ter diag­no­sis and treat­ment, very few peo­ple in the UK are dying from HIV.

Social care needs are chang­ing too. “Those who were diag­nosed in the ear­ly years of the HIV epi­dem­ic may remain quite phys­i­cal­ly impaired because of the dam­age their body has under­gone through HIV and chal­leng­ing ear­ly treat­ment regimes. Oth­ers may need emo­tion­al sup­port because of stig­ma, shock of diag­no­sis, chal­lenges around dis­clo­sure and social iso­la­tion,” says Yusef Azad, direc­tor of pol­i­cy and cam­paigns at NAT (Nation­al Aids Trust).

“We are now also see­ing sig­nif­i­cant num­bers of peo­ple with HIV with­in the immi­gra­tion process. These may be either asy­lum seek­ers or oth­er migrants who may well not be in work and who may be poor or des­ti­tute. So there is a lot of pover­ty and social need among peo­ple with HIV which is why social care remains real­ly impor­tant.

Social care has pro­vid­ed vital sup­port for those liv­ing with HIV since the start of the epi­dem­ic 30 years ago

“Up until 2010, the major­i­ty of sup­port in Eng­land was fund­ed via the Aids Sup­port Grant, a ring-fenced fund specif­i­cal­ly for HIV social care. How­ev­er, cuts to local coun­cil bud­gets, a dri­ve to reduce bureau­cra­cy and a move away from con­di­tion-spe­cif­ic care have dra­mat­i­cal­ly changed the land­scape for HIV social care.”

In 2010, the Gov­ern­ment announced an end to the Aids Sup­port Grant and coun­cils were instead expect­ed to iden­ti­fy their own pri­or­i­ties from a cen­tral­ly pooled bud­get. Through con­cert­ed cam­paign­ing by NAT and oth­ers a bud­get line specif­i­cal­ly linked to HIV social care needs was, how­ev­er, retained with­in the pooled bud­get, cal­cu­lat­ed on the basis of the num­ber of peo­ple with HIV in the local area, albeit that this mon­ey is no longer ring-fenced.

NAT under­took a sur­vey in 2011 of local coun­cils in Eng­land to estab­lish how they were pro­vid­ing care for peo­ple liv­ing with HIV. They found that the num­ber of local coun­cils spend­ing all their HIV/Aids sup­port allo­ca­tion direct­ly on social care for those with HIV had dropped from 86 per cent in 2008 to less than 61 per cent.

How­ev­er, more than a quar­ter of coun­cils sup­ple­ment­ed their HIV-spe­cif­ic fund­ing with addi­tion­al mon­ey to pay for the social care they pro­vid­ed for peo­ple with HIV. And a wide range of ser­vices are still being pro­vid­ed.