vertigo back advice needed please

Posted , 6 users are following.

After having several colds for the last two months and quite high stress levels I have developed vertigo. (Balance not right I have had this before 12 months ago it lasted 6 months) This time I have been told 2 other people at work have also been diagnosed with labythrititus. So maybe a virus. I have had it now a week and at first kept really active trying all the balance practice exercises. But I started to get really bad headaches which were completely disabling given cocodamol and most recently advised to take aspirin by Gp. I don't want this to last and don't know whether to rest or keep moving. I am seeing my own Gp on Monday. What should I ask? I was wondering about asking for a blood test. To see if it's viral. But if it is then what. I'm not sure it does me any good to know this or not. The Gp s I've seen so far have not really been that concerned. I saw one for vertigo snd they gave me betahistine and I saw another about head aches out of hours as it was really really bad. He gave me Co coda mol . And I spoke to one on the phone when Co coda mol was not working. She said take asprin. I have noticed that I feel more unbalanced with the headaches. I want to get to the bottom of this but I don't know what to do and terrified secretly that this might last a while. Hence me talking to you guys on this forum. I hope I might wake up and it's gone but incase it's not what action can I take? Any help advice gratefully received smile

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  • Posted

    Or if anyone can suggest what I ask my Gp. That would help
    • Posted

      I definitely agree with Gillian and Gilly flower. My GP told me I had to have this for 3 months for him to even consider referring me and then when he did I had another 2 month wait to see ENT!!!
    • Posted

      Exactly!!  They dint damn well care.  You have to tell white lies these days i'mmafraid!
    • Posted

      My Gp didn't even send my referral of straight away when he said he was going to , even though I have been seen now and been told It's bppv , ( they can tell by the movement of my eyes ) and seeing a audiologist , my GP still wants me to go down the mental health route , now I do agree I'm anxious , but it's unavoidable when your dizzy all the time , I wouldn't wish it on anyone , just my GP for a couple hours so he knows what it's like , so I don't have to explain anymore 
    • Posted

      Having had vertigo before for 6 months once I know this condition is a battle. I defy anyone to not feel anxious stressed hopeless. Make sure your doctor puts you in touch with a specialist which can get to the bottom of yours. I am sure you wouldn't feel half as stressed if your world would stay put. So keep strong and make sure you get the right treatment. Wishing you well and thanks for replying to my post
    • Posted

      Yes the anxiety is a side effect, which needs hammering into gp's brains, A SIDE EFFECT, not the cause!  I did accept CBT (via my .vestibular therapy physio, not gp directly , although she had to get the gp to,do the referral , the NHS system!!) as i wanted to talk to,someone who understands.  she was good and talked about this condition as a 'Silent illness', which was good to hear.  she used the Mindfullness technique which I do recommend to anyone who feels not just anxious,bt misunderstood.  If your gp,keeps pushing on it,,say you would   be happy to,see a CognitiveBehaviour Therapist as it's the popular 'thing' at the moment so you may as well take advantage of it.!!
    • Posted

      Your right , it is a silent illness , I said to my GP , that I don't mind accepting any help with the anxiety side of it , as long as it's understood that's it's the bppv that started the anxiety , not the other way round , but he just won't have it , 
    • Posted

      Dont worry when you get to see the counsellor ,,you can work that out with hi  or her, amd make sure you get them To agree,with you that the caus  is the physical problem, ie vestublar,,or whatever ,and the anxiety is the effect of  dealing  with it etc.  reason being. That when they do their report after you've had so many sessions (I Got eight), you want them to be writing that in plain speech so your gp  gets told in no uncertain terms! rEmember all that goes in your record and you don t want them having you down as having an an anxiety problem that  causes vertigo!
    • Posted

      Hi Gilly Flower,

      I developed labriynthitis at the end of December and am slowly starting to improve - working half days and doinglotsof exercises - seeing physio.

      Had it 20 years ago - bad - and had major trouble with anxiety.  This time, I'm trying to keep things in perspective and the anxiety is less of an issue.

      Are you sure you have BPPV?  If so, it is not viral.  check it out online.  One of my colleagues at the clinic where I work was flat on her back for 3 or 4 days with BPPV.  Went to the doctor and then to physio.  They did the epley manouver a few times and "poof" it was gone.  BPPV is caused by crystals in your ear being in the wrong place and the epley manouver moves them to their proper place.  it's easy and can be done at home - first thing my doc and the physio did.  I had really hoped that that was my problem versus a virus because there seems to be good treatment for it.  The epley manoever can be done at home - it's very simple.  They have ENTs doing it online.  check it out!!!!

      Best,

      Linda

    • Posted

      Hi Linda , yes they seem sure now it's bppv , was told Wednesday it can be severe and stubborn , sometime s , i had it like this in 1998 , lasted 18 months , but didn't have any treatment 
    • Posted

      Ha!! Yes I'm the same. Of course I wouldn't wish this on anybody but maybe a few in the medical profession who I've seen!! It's hard to explain it to someone who has absolutely no idea of what it feels like.

      I'm glad you mentioned the eye movement for BPPV as I worry when I'm really bad if I've got that. At the beginning a young Dr attempted to do the Epley on me but I'm sure he didn't do it right. Now I'm being told I haven't got crystals but vestibular neuritis.

      As for the anxiety, I can't believe your Dr would send you to mental health. That makes me so annoyed. I've been told I'm quite an anxious person but having this has made my anxiety go through the roof. it's anxiety to get better. But saying that, I did go for counselling but only went for 3 sessions as they couldn't understand what being dizzy was like!!!

    • Posted

      When they do the manerver  s , my eyes sort of jerk , and sometimes I can feel that happening 
    • Posted

      When mine was done my head wasn't held. I was just instructed where to move my head. But now I think about it he just talked me through the Brandt daroff exercise. As I felt really dizzy he just said I'd proved positive for BPPV. Didn't even look at my eyes!! A month later I had to return and another ENT did the dix hallpike test and said no you don't have crystals. So maybe he was looking at my eyes?
  • Posted

    Ask you gp,to be referred to an ENT (to start with.)  Your gp will know very little  about this conditon as we have all learned on here!! So really there's not much point asking him or her a lot of queations as they don't have the answers!  But what you can do,is bang on about that it,is affecting you sooo badly that it is affecting your job and having too much,time off etc etc.  that will get him into,gear to,ge you the referral,,okay.,? dont waste you time with gp's on this, take it from one who's learned the hard way!
    • Posted

      You are absolutely right!!!! thank you. I know from my own experience last time that all the Gps are floundering in a field they don't really understand or comprehend. I will ask for a referral. Last time I was refered to ent specialist was given a mri and told I had damage to my inner ear. Told to do exercises. I think the exercises are the key. I know they will help with persistence. But if this is viral? Should I ask for a blood test? As I am having headaches this time would a neurologist be better?
    • Posted

      By the way thank you for your help and your reply it is very kind of you and I am very grateful. Solidarity is one of the best forms of help when you have vertigo. So thank you
    • Posted

      The problem with,proving the viral,connection is hard. there are different viruses, and unless they do a blood test for a specific one, they could easily just say "no not  viral, go away'!  there are theories now that the epstein Barr virus is a cause of vertigo symptoms as it can lay dormant and you would t even know you've,got it.  and there are lots of strains so even an EBV blood test won't  necessarily show,up that you have it.   But anything can trigger a virus to emerge, another illness, stress, am accident.   I Feel mine is viral,induced and so i  treat ,myself as if Imhave one and try to,keep as healthy as possible diet wise and use supplements etc.

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