Resuming driving

Posted , 5 users are following.

Hi everyone, I just wondered if people have resumed driving and if so when they did so? 

I not had a severe attack or nystagmus in 8 weeks. I feel unbalanced still at times and some days are better than others. 

I’ve already had to leave my dream nursing job as it would be too stressful to carry on using public transport, plus the stress of the job and have had to go to another job Just a 17 minute train journey away and only do 2 long days days a week. I did my driving to make life easier for my daughter and myself as her school is 1.5 miles across town which I can rarely walk without suffering for it later on. So I’m keen to get back to driving and would love some people’s experiences. 

Thanks, Sarah 😊

0 likes, 13 replies

13 Replies

  • Posted

    Hi Sarah.  I am 37, been diagnosed for 4 years, and I still drive.  I get my vertigo attacks about every 2 months and they last from 4-48 hours.   When I’m not having an attack, I still have daily dizziness but not bad enough to quit my job yet or stop driving.  I do occasionally lay down at work though for 30 minutes which helps a lot.   I do not drive on the highway or any long distances.   Just locally around my town.  I have gotten attacks twice while driving but have been able to focus my eyes and concentrate enough to get home and immediately crawl into bed.   I have heard that sometimes the state will revoke people’s licenses who have vertigo so I pray that my doctor never reports me bc I am a single mom and have to take my kids to school and go to work.
    • Posted

      Thanks for you response. 

      Are you on any medication at all then? 

      4 years is a long time to go without having a long period of not driving. Good for you though, it’s good to hear not everyone is having to stop driving. 

      Sarah 

    • Posted

      I am on a daily 25mg diuretic, but that’s it.   I eat a very low sodium diet, which has been hard to adjust to, but it’s getting easier.   I do not drink alcohol or caffeine anymore, but have not seen any improvement by cutting those out.
  • Posted

    Hi Sarah,

    I have to say I'm quite shocked that people are actually driving when they have MD.  In the UK dizziness (i.e. MD) is on the list of notifiable problems you have to let the DVLA know about so if you don't and you still drive it would make your insurance invalid.  So there is that aspect to think about.  Plus of course there is the possibility of having an attack that causes an accident to people other than yourself.  I have had MD for over ten years and I would categorically not get behind the wheel of a car - a dangerous weapon in the hands of someone who is not fit to drive.  I have been in the car as a passenger and had attacks that make my world flip upside down and been heartily glad that I was not driving.  I would most definitely have crashed and they were entirely out of the blue.  Luckily I rarely get an attack like that and mostly feel one coming on so can do something about it.  But the worst one I had was the first and it was in the car.  I'd never had one like it before so just because you normally have ones where you can cope and get home doesn't mean to say you won't have a sudden onset bad one.  YOU SHOULD NOT DRIVE WITH MD.  You are not insured.

    Sorry about being so blunt but I feel strongly about this and so would you if you imagined yourself with one of your nearest and dearest killed in an accident caused by an MD attack either to you or by some other driver.  Put yourself in that position and think very carefully about what you are doing.  One and a half miles is not too far to walk or cycle for your daughter.  Nor for you.  (I actually don't ride a bike either where I might fall off into traffic)  So please don't drive.

    • Posted

      Actually the DVLA states that once you have been symptom free for 3 months you can resume driving, which is possible for some as other discussions on this forum show.

      It is too far for me to walk everyday as I have balance issues currently. And you’re not aware if my child has health issues of their own. With the condition we have I would assume you wouldn’t be so judgemental or take things at face value. Also the fact I have no choice but to work 12.5 hour shifts twice a week and I’m laid up after those. I would get the full story before judging others.  

      I will go by what the dvla say and make my own judgements. 

  • Posted

    You are right to say the DVLA is not totally prohibitive on this issue. The question is if an attack starts whilst driving would you be able to stop safely?

    When I first had the disease and was having acute attacks I stopped driving voluntarily for about a month. As the effectiveness of Betahistine improved and attacks ceased I resumed. I had discussions with my GP and consultant. Both said to inform DVLA and insurers.  I waited until I had been free of symptoms for about 5 months and then completed the form on the DVLA website indicating the medication I was taking and that I was symptom free. They cleared me to continue driving. My insurers were very relaxed and said if DVLA were happy so were they.

    So - if you are on betahistine get the dose up to a level where you are completely controlled, stay on that for 5 to 6 months then wean off. If symptoms start to return go straight back on max dose and increase further if necessary. This strategy worked brilliantly for me. My max was 64mg tds and I have permission to go higher if needed!

    An afterthought - have you been checked for BPPV - I got a touch of that too about 2 years after first diagnosis.

    It was succesfully managed with 3 Epley manouevres and has not reappeared. Touch wood.

    • Posted

      Thanks for your response.

      I ceased driving voluntarily just over 2 months ago as I knew it was not safe. 

      I have since been attack free, however do still get minor spins occasionally and do not always feel balanced therefore I still don’t drive. 

      The 16mg TDS I have been taking has prevented any minor attacks and I have been free of nystagmus the entire time with only twice having had what I call internal spins. I am not confident in driving again yet so I won’t be resuming. 

      I’m very frustrated currently as I don’t have another appointment until the end of September with ent and my gp isn’t happy to change dosage, although she has written to my specialist for advice on the meantime. I am hoping she will hear from them soon. 

      I would not resume driving until I was confident that I am 100% able to do so safely as I would never put others at risk. 

      Thank you for sharing your experience 

      Sarah 

    • Posted

      So I’ve spoken to my gp and she’s refused to authorise me to up my betahistine dose because the BNF states 16mg TDS is max for maintenance dose. But as I tried to explain to her I’m not looking for maintenance I’m looking for the dose that stops symptoms and the wean back down but she’s refused point blank to agree to it or prescribe me a diuretic. 

      Feel pretty lost now 🤔

    • Posted

      Find a new gp.  smile.  My diuretic is the only thing that can keep my vertigo attacks under control. 
    • Posted

      I have gotten in contact with a specialist I used to work with while a student and he is going to help me out. 

      I’ve been trying to get a diuretic for ages but this gp isn’t having any of it 😓

    • Posted

      I just remembered that you can buy diuretics over-the-counter.  There’s one called The Water Pill.  It’s probably just as good as the prescription stuff.  
    • Posted

      You need to see the right consultant, preferably an Aural Physiologist (although they are pretty thin on the ground - the only one I know of outside of the London area is semi-retired and works in the Portsmouth catchment area). Next best is an ENT who is up to date on high dose betahistine.

      Changing your GP is unlikely to help because ythey all run scared of stepping outside the rules unless a consultant says its OK!

      Keep trying.

    • Posted

      Very true! 

      I’m hoping just to get a diuretic from the gp. 

      I’ve suffered with swollen feet, hands etc since being pregnant 11 years ago. Hopefully this one may do something along those lines. I don’t expect miracles from my gp as being a healthcare professional I know where their limitations lie. 

      Just someone trying something would be enough for me 

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