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. Rebecca McDowall

    Hi RM,
    I’m sorry to hear that you don’t feel you got the care you needed from your doctor. Although he is right that HIV shouldn’t stop you from working so long as you are feeling well it sounds like you would have benefited from more support to help deal with the stress you are experiencing since your diagnosis.

    It is important to find a doctor that you feel comfortable and confident with, and it does sound like you would benefit from some psychological support.

    You said your CD4 count went down to 150, what was it before this? It is very normal for CD4 counts to go up and down a bit and unless this was a large drop (50 counts or more) from your previous result it is unlikely this is something to be worried about. If this is a big drop you should have this test re-run to make sure it is a true result and not a lab error. You can read about CD4 count fluctuations here.

    You should tell your doctor about the symptoms you are experiencing. Numbness in the feet can be caused by something called peripheral neuropathy, which can be a side effect of HIV itself or some HIV drugs. The general run down could be a symptom of an infection or might be caused by stress or sleep disturbance. You might find it helpful to keep a diary of these symptoms so that your doctor can assess how these are affecting your life.

  2. Rm

    Rebecca I was but now my numbers are declining again I have my partners support and a few close friends. I do not want to work anymore as a lot of people are gossiping about me already sometimes I feel lost. I live in central fl. I also do not understand why I am feeling so run down, my legs are cramping all the time my feet are numb I don’t know what’s going on and can’t seem to get answers

  3. Rm

    I asked my doctor if he would fill out FMLA paperwork for me so I could take time off work as I have been really tired and I have a high stress job with long hours and he absolutely refused and put in my file aids was no reason to stop working. he also told me that my counts were good and when I finally got a copy of my bloodwork I found out my cd4 count went down to 150! I am seeing a new doctor this week I don’t need a doctor who lies to me also I found out they were supposed to recommend a physchiatrist for me when I was first diagnosed then the cd4 count was 54 , and they never told me. Thoughts?

  4. Rebecca McDowall

    Hi Rm,
    I’m very sorry to hear how confused and upset you are feeling. Finding out you have HIV is never easy, and it’s very normal to feel like this. It’ important to get some support to help you deal with your diagnosis. Do you have any support? If you let me know where you live I can try to suggest a local organisation. There are also online support forums which can provide support. Try looking at poz.com for an example.

    It sounds like you are already doing very well and progressing on treatment. Can you tell me a bit more about the things that are worrying and confusing you?

  5. Rm

    I am so confused, recently diagnosed, had aids and now HIV , but sometimes I don’t know if it Is worth the fight

  6. Christian Guy

    Don’t give-up , I found out I was positive 2 years ago, I am on Atripla which I adjusted to very well. It’s not the end, but just a great reason to fight strong. God bless u

  7. Lebo

    Dont give up, I recently found out and its not easy but am more determined than ever to fight and live, its not going to be easy, but u are stronger than you think. Best of luck.

  8. Simon Collins

    Hi Stephen

    It sound like your doctor is giving you a good option. Kidney damage is often measured using something called eGFR. Very mild damage is when this has fallen to between 60 and 90 mL/min. This concern increases when eGFR falls below 60. Progressive damage is graded by bands of 45-60; 30-45 with severe kidney impairment being less than 30. Some clinics follow slightly different grades with mild impairment defined as between 50-80 and moderate as 30-50 ml/min. Without knowing your value it is difficult to comment on this aspect of your health. However, several studies have reported a good chance that your kidney function could improve after switching away from tenofovir.

    I also wondered whether you were on a third drug, or perhaps mixed up tenofovir with Truvada, which would be more normal. Truvada is the 2-in-1 combination that includes tenofovir plus FTC.

    Studies looking at darunavir monotherapy (including MONET and MONOI) have showed pretty good results. You actually take darunavir with a separate boosting dose of ritonavir, but it is still called monotherapy because only the darunavir is acting on your HIV. An early rport on these studies at this link, but both have I think reported good results for over two years now.
    http://i-base.info/htb/5966

    The decision to not use ‘nukes’ (ie tenofovir, 3TC, abacavir or FTC) has probably been suggested to minimise the risk of further kidney damage. It very unlikely that your viral load will rebound on darunavir/ritonavir monotherapy, but if it did you could easily add the raltegravir back in to your combination.

  9. Stephen

    I am on HIV treatment – tenofovir and raltegravir and have been told I have chronic kidney problems. I have an undetectable viral load. I have been given the offer to switch to darunavir and I’m worried about going on to this mono drug and its effectivness. Please could you give some advise as the switch is due to take place while I am overseas and I am unsure even after the discussion with my clinic doctor and the pharmacy, thanks Stephen

  10. Chris

    I can recommend MyHIV forums where you will find a great deal of support and get to “meet” others with similar difficulties etc.

    http://www.myhiv.org.uk you will need to register to use the forums, but it is well worth a go.

    take good care

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