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, if your doctor recommended meds then this is likely to be good advice. ARVs are safe and effective. They work against HIV. If you have trouble with the first treatment your doctor should help with something else.

  2. Aristo

    I was diagnosed December 2012,I only took dbdrugs for a month.I stopped due to faith on God,so last yr I was sick 2months,wen I took some drug my body reacted n got rashes all over..
    what am I saying is DT if I should start taking dis drugs will I come to my normal body

  3. Darknight

    I am just been diagnosed with HIV+ and the more I read about the side effects it scares me more than the virus it self.The reason I wanted to take meds was so my family wont find out but with all these side effects it seems impossible.

  4. Robin Jakob

    I am sorry to heat about your diagnosis.

    Although people usually get some side effects when they start treatment these are usually mild and get better after the first few weeks. ARVs today are much better than older ones and have less side effects.

    Depending on where you are based there should also be several treatment options available. This means that if you find the side effects of one medication to much you can change to another.

    Being on treatment is a good thing and the only way to control the virus. Many people who have HIV and are on treatment can now expect to live as long as people who do not have HIV.

  5. Rebecca McDowall

    Hi Vincent,
    I am sorry to hear about the difficulties you are having accessing treatment. US residents should be able to access state provided treatment for HIV. If you contact GMHC they should be able to advise you on this. Stopping treatment can put you at risk of opportunistic infections if your CD4 count falls below 350 so it’s important to access support to get you back onto treatment.

  6. Vincent

    I was diagnosed in 1986…..started w/meds when cd4 drooped below 50. But now am in financial distress. Local charity…desert aids project…..let me down big time….and VA social services incompetent. Am just waiting for inevitable since I can’t afford meds and have stopped. V

  7. Simon Collins

    Thanks for posting about your experience. Even thought the drugs may not be perfect, they are now pretty good. They can only work though if you take them. Once you start treatment, good adherence is really important.

  8. Surverice

    A little heads up for those that have similar views on quality of life.
    If you can manage to take your meds. you will notice little to no quality of life issues.
    However, if you don’t (from personal experience). Your quality of life will degrade. I am legally blind as a result of HIV, and let me tell you my quality of life sucks now. I have seen people with many many worse issues due to lack of adherence . Atrophy/neuropathy is a big one, Pain, and immobility. Also the wasting of your body so you look appropriate for Halloween.
    It’s fine when you are in your 20s to say you don’t want to live xx amount of years. All kids never want to grow old, and normally old for them is 40. But once you get to your 30s, that all changes. and as you mature, you find you like your older self. Give yourself a chance for the future, just in case you change your mind about growing old/older, leave the option of having a full life on the table, by taking your meds.
    Most people get/got the disease from sex. See what not following the rules gets ya? Now you have a second chance for life, don’t blow it.

  9. Rebecca McDowall

    Hi RM,
    I’m very happy to hear that you have found a doctor who is able to help you deal with your diagnosis and all that comes with it. I wish you the best of luck with the future- please don’t hesitate to contact us if you have any further questions now, or in the future.

  10. Rm

    Rebecca, my count was 224 before it dropped back to 150.
    I sought out another specialist today. He was super informative explaining more to me in one hour than my other specialist did in all three visits!
    Definitely switching specialists!
    He is taking me off Atripla and also one of the antibiotics I was on, and putting me on a newer med, (do not remember the name), he felt as though one of the components in Atripla was causing my tiredness and side effects.
    He also prescribed a low dose anti depressant.
    This Dr. was so good, I feel really good about him!

    On another note he also did agree that the diagnosis was no reason to stop working, however he explained to me why I was feeling the way I was.

    I actually love my job and am up for promotion again and did not want to throw that away, I just could not get any answers before.

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