Q and A

Question

How long will I live if I stop taking my medication?

Hi,

I decided that at the beginning of December that I would stop taking my meds for good. I’m in my late 20s and had HIV now for about 2 and a half years. I started meds not long after I found out I was infected.

I went from being negative, to positive and on meds in the space of a year. In Nov my CD4 was just under 500 and my viral load was undetectable for the 1st time. At times I stopped my meds, had to change them and wasnt great at taking them.

Unrelated to HIV my health wasn’t great last year was in a bad accident and wreaked my body. I’ve never been at ease with being on meds hence why I wasn’t great with them in the past but I’ve thought long about this and wont change my mind.

I dont want to live to be old because I wont have a good quality of life so id rather let hiv take me when im young. How long, I know you cant just say oh 1 year 2 years etc to me, but in general terms can I expect to live for?

And what kind of illnesses would I expect to get from the HIV?

I’ve had Hodgkin lymphoma in the past would that be likely to return?

Many thanks.

Answer

I am sorry to hear about the difficulties you are going through. I can appreciate it must be extremely hard for you to deal with so much at such a young age. Do you have anybody close to you who is supporting you through all this? Do any of your friends or family know about your HIV status, and have you spoken to anyone about the feelings you are grappling with?

To answer your direct question first, how long someone lives without ART will vary a lot. It might be as little as a few years or it might be much longer. If your CD4 count ever went very low, then HIV is likely to progress more quickly. If your CD4 count has always been high, then it would take longer. Maybe 5 to 8 years on average.

Letting HIV progress without ART would not be an easy or reliable way to end your life. Most to the complications of late stage HIV are very difficult and unpredictable. You can easily research this by looking at the early days before there was ART.

It sounds like you have had a lot of difficult things to deal with and HIV is only one of these. Without commenting on what you decide, the way you are writing sounds very close to someone with depression, which is an illness in itself and this is something that needs its own discussion with your doctor.

Without realising it, depression can take hold after a serious life threatening illness or traumatic event. It is common then to focus on something that seems certain and even better, like an earlier death, when time with a counsellor or advisor might help you see that other options are available, but which you just can’t see by yourself. Again, this is not a comment on the things you say, just something to think about.

Many people find it hard coping with an HIV diagnosis, let alone being diagnosed at such an early age and having to start treatment so soon after. Some people come to terms with it soon after, however, many more people take a long time. You are therefore not alone in feeling this way.

Although you were diagnosed just over 2 and a half years ago, it is still early days. It may take you some time to learn to cope with living with HIV and all that entails. With the right treatment, care and support, most people find that they begin to move on with their lives.

You mention that you don’t want to live to be old because you may not have a good quality of life. The reality is, you can live to be old and have a good quality of life, even with an HIV diagnosis.

The medication we now have available to treat HIV is very effective in enabling people to lead healthy and fulfilling lives. Some of the people I know who were diagnosed in their 20s and 30s are now becoming parents and grandparents.

You asked about how long you can expect to live. Modern HIV treatment (ART) now means that life expectancy for an HIV positive person is the same as an HIV negative person. This means you potentially have a lot of time work through the things that re difficult and to have time to enjoy life.

You mention that you were not adhering very well to your medication. Are there any particular issues that you were concerned with? Was it side effects, or was it just having to take pills? Did you speak to anyone at the hospital about finding it hard to adhere?

A good health advisor could talk about newer HIV meds that might be much easier to take.

Without knowing the details of your other complications, if you have responded well to treatment for Hodgkins lymphoma, you have already been very lucky. The chance of long term remission are similar as if you were HIV negative people. This is about 70% survival at five years, which in oncology is seen as similar to a cure rate.

Your other question was about whether the Hodgkins lymphoma is likely to return. As your CD4 count drops, as it will do when off treatment, this is likely to increase the risk that the Hodgkins could return.

Stopping treatment will mean your CD4 count and viral load are likely to quickly return to levels before you started treatment. If this has always been high, then if the break will help you for psychological reasons, the risks are relatively low. However, if your CD4 cont ever dropped below 350, and definitely if it went much lower, stopping treatment is much more risky.  The risk for Hodgkins to relapse is likely to be higher when you are not on HIV meds, compared to being  on treatment.

You said your CD4 count is about 500 and an undetectable viral load. These are a good indication that the medication was working really well. And that you are healthy.

The BHIVA (British HIV Association) guidelines recommend everyone should starting treatment even at high CD4 counts.

As you are based in the UK, you may find it useful, in the first instance, to chat with one of us over the phone. The i-Base treatment phoneline is 0808 800 6013. It is free from landlines and most UK mobile networks.

Other organisations you might find useful to contact are:

  • Positively UK – They support people living with HIV . They also have a mentoring service which you may find useful.  A mentor will be assigned to you and you can see them regularly over a period of time until you are ready to move on.
  • Body and Soul – they provide support to families living with HIV and have a service specifically for young HIV positive people like yourself.

Note: This answered was updated in April 2023, December 2021 and January 2017 from a question posted in January 2012. The answer was updated to reflect changes in treatment guidelines.

605 comments

  1. Simon Collins

    Hi Tilly, thanks for adding your experience – there will be newer meds – one of which might be dolutegravir, perhaps by next year. See:
    http://i-base.info/htb/30642

  2. Tilly

    Wow Kayla. I really feel the same way you do. Iife happens to the best of us. All we need is to get up and keep going. I started on meds but I stopped taking them cause they were too much for me. 6pills a day! I’m just grateful I’ve always been healthy and stil am healthy with my cd4 at 530. And praying one day Il get a better option in treatment. Maybe injections and one day pills that have less side effects. I eat healthy and exercise a lot and laugh more. Thank you all for your support and input.

  3. Simon Collins

    Hi Dave – once you have become undetectable, an hour either side of the time is fine.

  4. Dave

    I’m Dave.
    I really don’t understand when they say, take your drugs on time. I take mine around10pm and sometimes 11pm and I haven’t skipped taking my drugs. Does my inability to maintain a certain time affect my treatment?

  5. Simon Collins

    Hi Danny, please get back in touch with your doctor. If you have been off treatment for two years, your CD4 count could already be very low. This would put you at high risk of serious health problems. Your doctor will be pleased to see you again and will monitor you quickly. You can also talk bout some of the reasons why you decided to stop treatment, in case these issues can be resolved in the future. Don’t be scared, but please realise how important this is for your health.

  6. Danny

    I need urgent advice. I stopped taking my drugs for the past two yrs and now am always having feverish most in the evening and little headache. Will I still break down with the sickness bcos am scared.

  7. Simon Collins

    Hi Emeka.

    The only thing you need to do every day is to make sure you take your meds.

    Everything else is optional. There are lots of reasons to have a nutritious balanced diet – but this is the same as for HIV negative people. Fresh vegetables are probably more important than fruit, both both provide fibre.

    Eating five portions of fruit and vegetables a day is a good target.

    This UK site gives lots of examples for what counts to your five-a-day:
    http://www.nhs.uk/livewell/5aday/Pages/5ADAYhome.aspx

    Once your viral load is undetectable, you have a bit more flexibility with the timing. This means that a few hours earlier or later that the time you are aiming for is likely to be fine.

  8. emeka

    must I take fruit everyday with or without my medicine as a HIV patient?? secondly what happened if I don’t take my drugs on time

  9. Simon Collins

    Hi Kayla, thank you for sharing your experiences. You are doing so well to come through this as a strong person. Som any other women share similar experience and go on the lead happy and full lives – including with partners and having families. HIV stigma is difficult but it doesn’t mean you can’t find a partner. Try to connect with other positive people who can be a good part of your support newtwork. Being on treatment means that your partners are protected and this might reduce stigma. See this link if you haven;t heard about the PARTNER study yet:
    http://i-base.info/qa-on-the-partner-study

  10. Kayla

    im Kayla

    my first boyfriend gave me HIV the very day he took my viginity at 21 years, im only 22 and i started with my medication about a month ago, already i feel alone and scared that my life now depends on a pill that i have to hide all the time. He had a higher cd4 count, he didnt need medication…he just ran out on me and went back to his ex-girlfriend. i love myself im beautiful and intelligent but one thing that i can say to people out there is that, life does not owe us anything… hiv happens to most of us, we did not apply for it. like in my case i stayed a virgin thinking i would meet the right guy but i met someone who cheated on me over 20 time with different women, when i found out it was already too late. such is life…. i take my medication with pride. i am still the same person, i just met up with hiv.

    im scared and all that, i might never meet someone again because then i would have to explain my status and hope that they do not reject me after that. my greatest fear is that i will wake up one day feeling tired of medication. or that the ARV industry will run out of the medication….

    im not hoping to give anyone hope, all i want to say is that, life happens to all of us. one way or the other we will die and hiv might not even be what kills us. i just want to live my life and see what tomorrow holds. maybe i sound like im strong but im not, im scared like most people i just choose to know that no one is immortal and noone should be…. i did not choose life, life chose me and so did hiv. so i choose not to over stress or blame myself over things that i feel i can not change.

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