Building support systems for people living with HIV

Support systems are relied on when things aren’t going well or when one is not feeling too great. We all need support and encouragement every now and then, for it is such a tough road to walk alone. Take Emeka for instance, when the doctor told him that he has HIV. He was dumbfounded and dead inside. Throughout that week he was unable to sleep and eat, depression, gruesome fear and anxiety gripped him, for weeks he was torn between confusion of what happens next and whether or not he’s going to tell anyone, not to mention what their reaction would be.

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Emeka’s story is one of the many other stories of how lonely people living with HIV could get when the news hits. Like Emeka many of them they are more worried about how the world will treat or accept them once they know of their status than how to a live healthy life. It is a fact that getting support from family, friends, partners and colleagues can make a huge difference for persons living with HIV (PLWHIV). The society needs to understand that we can be the support system they need. So when someone tells them of their status they are not asking for pity, rather support. Research has shown that non-communicable diseases are becoming a growing problem in people with HIV as they live longer on successful antiretroviral treatment. It is also documented that some antiretroviral drugs may increase the risk of heart diseases and diabetes while HIV itself increases the risk of some cancers.

Tayyib Oladimeji Abdulkareem, a health advocate and the convener of The Wellbeing Initiative, explains that these things happen because of the alterations that the infection causes to the body. He opines that for specific diseases, the pathological pathway to disease onset would be followed through research works bearing in mind that the infection affects the immune system and other body organs.

Getting help from others has been proven to be the first step towards getting through a crisis. It is liberating, fulfilling and helps us all heal or conquer what beats us down faster. Question is how do people living with HIV go about getting this help when all they get in return is stigma from others and resentment from themselves?

Hart Kingsley Akabuike, the Head, HIV Counselling and Testing (HCT) Unit, 82 Division Military Hospital, Enugu, Nigeria, agrees that stigma can emanate from self or people. In recent years the struggle of people living with HIV coming to the public with their status has reduced but not as much as United Nations project 90 90 90 is hoping for. There’s still this rejection that comes if one discloses their HIV status when applying for work. The employer tends to withdraw the offer or quickly comes up with an excuse that the position is already filled. Then there’s the learning environment; such a place is for information but unfortunately it is another breeding ground for stigma and discrimination. At the top of the cherry is the name calling and verbal abuse by healthcare professionals, right inside working space. You hear this typically in local parlance,

“whether na me say make you go get HIV.” Now imagine if clinics, hospital environment that ought to be safe spaces are crawling with judgmental eyes and mouths, how does one blame people living with HIV for not asking for help?

Support comes in many forms and places. Example is motivating a friend or family member who is living with HIV by way of encouraging them to stay on treatment, practice safe sex and positively reminding them that they can still live a healthy life and achieve their dreams. It is on record that 1.1 million persons living with HIV are currently on treatment in Nigeria. Now families of these persons could be their major support system because there’s no substitute for family and good friends to support and encourage the person. Having someone listen to your concerns helps everyone feel supported and understood, which in turn encourages one to look at things (life inclusive) differently. Psychotherapists believe that helping someone with HIV can be stressful but very rewarding too, because aside the emotional support, one might be helping them figure out how to work through the medical system. Truth is around one in three persons living with HIV have symptoms of depression at some point in their lives. Like Emeka, it could take weeks, months even years to survive the shock of learning that one is HIV-positive. When the reality sets in we begin healing and acceptance process which is also another journey that no one should walk alone. Fatimah, a mother of two was in shock for two years within which her husband passed on. It wasn’t until years later that she was able to tell her story. She recounted how everything seemed bleak and unsafe, how she would be wishing for death. It is not surprising as many go through shock, grief, anger, sadness and fear when diagnosed with HIV just as in the case of Emeka and Fatimah even though there’s now anti-retroviral treatment (ARV) which can help one live long but the knowledge of the virus in one’s system is just uncanny. Psychologists believe that this feeling does go away with time which is why they advocate for information and support, enhanced support, HIV specialists and psychotherapies and specialized psychological and mental health intervention. Social and mental support is such an important factor in developing and maintaining healthy lifestyle and mental wellbeing behaviours.

It is important that we consciously lend our support to love ones as it is a scary thing not being able to confide in anyone of your deepest fears or worries for the fear of been judged or discriminated against. If we remember everyday that we could lose someone at any moment, we would love them more fiercely and without fear not because there is nothing to lose, but everything to gain.

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Ekene Odigwe, an OAP and human rights ambassador, wrote via email

The post Building support systems for people living with HIV appeared first on The Sun Nigeria.

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