Feeling of falling

Posted , 11 users are following.

Hi all

I'm looking for some advise and opinions.

I'm a 27 year old female. Since the beginning of December I have been feeling very strange.

It all started when I was at work one day. I am a hairdresser who runs a very busy day to day column. On the 5th December I had my 1pm client in my chair and all of a sudden I came over very wierd like I was very dizzy and had a fluttery heart feeling, I started shaking and could not continue cutting my clients hair. At first I thought it might be sugar levels so all my colleagues came to my rescue with a can of coke. My client was very understanding. I drank the can of coke and thought I'd try and continue but this feeling of dizziness and fear of falling kept coming over me.

I was sent home after this. I went straight to my doctor on the Monday and she examined me and said I was fine I may of just been experiencing low blood pressure. I did state that this feeling came over me after I had eaten.

So I went back to work as normal on the Tuesday and still continued to have this feeling and felt like it was getting worse. My legs started to become weak and felt like I could not stand. I went back to the docs and because this feeling scared me so much I dint want to go back to work so I did have a few days off. He told me it was labrynthitis so he prescribed me some stemetil.

I went back into work and felt a little better and continued with the tablets. Although I did not feel 100%.

I saw another doctor and he did loads of balance checks and Co ordination tests and I was all good. He said this didn't look like an inner ear virus to him.

I am now still on stemetil, I have had blood tests for everything and they are all normal.

I am also waiting for a neurologist appointment to come through.

I really feel so down about this as I love my job so much I feel like it will end my career.

When I am standing behind my chair or to the side of my chair doing someone's hair, I literally feel like my legs are going to crumble on me. I'm leaning on the chair to support me I'm sitting on cutting stools to feel less like I'm going to fall.

Has anyone ever had this feeling?

Any help and advise will be much appreciated x

0 likes, 38 replies

38 Replies

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  • Posted

    Maybe see if Valium helps calm it down. Take it at night so you aren't tired during the day. Check w a dr first of course. Hope you feel better soon.
    • Posted

      Ok thankyou I will try. Do I purchase from a chemist? What does it do? X
    • Posted

      Dr has to prescribe it. Calms everything down. Shouldn't take it for long but if you tried it for a week to see if it helped it might be worthwhile. Again I wld discuss w a dr. Also yoga or exercise wld be helpful.
  • Posted

    I have all of what you said and more since Oct its very scary and very much out of my control and its all day and everyday. Smoking makes it all worse I hope you find an answer I'd love to know what's going on with me as well my Dr just says anxiety but I know it's more then that. I've had tons of labs and an EKG in the er alittle over two weeks ago was normal. I just want to say your not alone at all. Do you also at times get like a hot sensation come over you with the dizzies? I had a spell today got hot and very dizzy thought I was going to faint scared me.I also thought low blood sugar at first when this started happening its not that. I just pray everyday for god to lift this up off me.
    • Posted

      Hi Pamela

      Yes I do go all hot and sweaty but think it's because a get a panic feeling as I can't stand straight without leaning on something. It's so hard.

      Hope we find some answers soon I will keep pushing until I get an answer.x

    • Posted

      I'm pushing to with no luck but I'm not going to give up in this cause its taken my quality of life from me.
    • Posted

      I've had a rocking feeling every day all day for 18 mos. diagnosed as idiopathic mal de debarquement. But I wasn't on a cruise or anything. It's gotten better but I think hormones def play a role. I'm 39 so maybe peri menopause. What I will say is that I take Effexor for anxiety and amitriptyline. It has helped a great deal. Stress only makes things worse. Hope you get better.
    • Posted

      Hi Pamela,

      boy do I know this feeling!! It first started for me in June 2015. 8 months later and I'm afraid to tell you I'm still at the mercy of this illness. BUT I think had I accepted it for what it was at the start and took proper precautions then I would most likely be well now.

      So here's what you need to know:

      You are NOT dying.

      It is not any of the terrible things you think.

      It is a virus.

      It affects your inner ear and your vestibular system and is systematically infecting you.

      It is probably the Epstein Barr virus (get a blood test for this from GP). You probably have a mineral deficiency too (test for B12, vit D, magnesium and zinc). Mine was zinc.

      To beat it you need to take 6 weeks at least off work and go on COMPLETE rest. Spend as much time as you can lying quietly. Don't read, watch TV, cook, clean or wash your hair. Just lie there calmly. As much as you can. It is made worse by sensory over-load (certain lighting, movement, TV programmes and noise.) as you get better KEEP resting. Rest more than you need to.

      Showers can make it worse because of heat, standing etc.

      STOP taking the inner ear meds as these can stop symptoms but also stop your body's natural healing process meaning it goes on longer and can in some people never heal as a result of over using the meds. (This is fact not pseudo- science.)

      IF you must take something because perhaps you are leaving the house for a medical appointment then take cinnarizine. You can be prescribed it for the ear or you can buy it in chemist (it's brand name is sturgeon 15 and it is marketed as for travel sickness.)

      TAKE a good quality multi-vitamin, a daily berrocca effervescent, a daily odourless garlic capsule (natures antiviral can buy in health stores or amazon they don't make you smell), and take echinacea drops 3 times daily (takes these 2 weeks on then 1 week off to stop resistance building.) all of these things will help your body fight the virus.

      EAT as many veg as you can. Try to 'eat clean' no processed foods, refined sugars.

      REMEMBER you have a bad virus. A very bad virus. You might only feel it as dizzy spells and heart flutters now but trust me it gets a hell of a lot worse if you don't treat it with respect at this point.

      STOP drinking milk. You are likely to find the virus has made you lactose intolerent. I bet those heart symptoms come on worse after you have had a cup of tea or some cheese. Common with viruses that people become lactose intolerent for a few months. (Again a medical fact not theory.) on this note try taking a combined wind relief and antacid when these spells happen. You may find sometimes it is linked to acid reflux.

      TRY two tbsps of apple cider vinegar plus a tsp of ground cinnamon in a glass of water just before you eat a meal. This helps stabilise blood sugar which is a contributor to this feeling too. It is a thread of hypoglycemia. (Thank you virus!)

      Be WARNED I stopped trying to push through it too late. I like all of you was told initially there was nothing medically wrong with me except perhaps a very slight inner-ear or visual vertigo thing. I too was told it might be anxietey or panic attacks. Three months later I was HOSPITALISED with an ongoing infection!!!! 4 weeks after I started doing all the above my blood work showed the infection had finally cleared. I have been left with a horrible post viral syndrome, arthiritis for a month in my joints followed by fatigue issues and ongoing issues with the original symptoms (but only when I really over do it thankfully). I have an appointment with an infectious disease consultant this week who I know will be diagnosing me with CHRONIC FATIGUE SYNDROME. This is due to the length of time I have now had these issues. However as I have seen vast improvement since doing the above I am confident I will shift all symptoms eventually. But it is likely to take more than a year at least. BE WARNED AND TAKE NOTE TO LET YOUR BODY HEAL NOW!!! Please please please don't do what I would have done at the start and think that this must be different to what you have because it's not. I am part of a post viral group full of people who made that mistake a paid the price.

      De-stress and rest-up xx

    • Posted

      I'm in perimenopause but I don't think this is hormones in my case this is horrible and very intense and it don't fluctuate like hormone symptoms usually do on me or come and go
    • Posted

      I've been struggling for 18 months but, found that it does get better. What have you been doing for treatment? Assuming it has been diagnosed as vestibular neuritis or labyrinthitis or, have they simply said totally it's anxiety?
    • Posted

      I have no answers they say anxiety and not taking me seriously I've been to Dr many many times and given anxiety pills. I've begged and pleaded for my Dr to listen to me I'm at a loss. I cant see ent Dr without referral so I saw a new Dr in same office explained my symptoms she gave another anxiety pill they meds don't help and this is 24/7 with me at times it very bad and I just cry
    • Posted

      I know deep down its more then anxiety this hit me hard out of the blue and I've not been normal since. I get a pulling sensation at times I feel like im in an elevator how it makes you feel when its stopping I get bad spells like i get hotness come over me and i get very dizzy faint feeling and weak legs. Moving around and smoking makes this all worse how does one live like this and cry everyday cause terrified your dying and have no answers. Nothing is blurry or doubled in my vision no headaches nothing is spinning but I'm woozy inside my head all day long. Sometimes I'll feel like things moved in my vision and they don't or my head moves but doesn't weird hard to explain.
    • Posted

      Sounds like vestibular neuritis which is what I had.  The dizzy spells usually create the anxiety not vice versa, unless you have suffered from anxiety prior to this condition.  The place to start is with an ENT but, the best doctor for inner ear issues is a Neurotologist/Otologist.  Sorry to hear that your doctors can't see your need.  Look up the symptoms of vestibular neuritis and maybe you can take that with you to your doctor for discussion.  After showing that information I would ask why they think it is not that if they still won't refer you to a specialist. 
    • Posted

      Thanks terry how bad did you feel with vestibular neuritis? I'm laying here and I feel like I'm moving its bad tonight and don't know why I swear i get scared thinking its my heart causing it
    • Posted

      Terrible for months.  I was off work for over 2 months.  My head felt foggy and I could not concentrate. My vision was bouncy when I would walk. When I would turn my head things in my visual field would lag a few seconds behind. I had things that I would see in my peripheral vision but, nothing was really there. My head felt like it was moving separate from my body and with all of that came balance issues.  My head still feels like it's a little bouncy and being in large stores or wide open spaces can cause me to feel like I am unable to balance. 
    • Posted

      I feel those things too but I also have racing heart off and on out of nowhere palps feel like I have to take breathes at times this head thing is connected to my chest issues I'm sure of that. I get this adrenaline fear on my on its own. I was hooked to heart monitor they said heart normal rhythm and EKG was normal I just get scared not knowing what its from for sure
    • Posted

      Don't know if you are in the US or UK but, it would appear that your doctor would be wise to do the necessary tests to rule out another issue.  I would also ask them if it's anxiety why the pills are not relieving the symptoms.  Anxiety is a symptom of inner ear issues as well.  This forum is full of responses where doctors have attributed this to anxiety rather than understanding the inner ears symptoms producing the anxiety.
    • Posted

      Exactly what's going on with me the issue is what's causing the anxiety uncontrollable anxiety, I have noticed its all a bit better then when it started but not enough to make a difference.
    • Posted

      That could be the anxiety kicking in when you have those feelings in your head.  I've experienced some of that as well.
    • Posted

      I'm in the US as well.  I assume that your insurance requirements is what is keeping you from going to a specialist without a referral?  I might try another GP practice if you are not getting what you need from your current one.  The best information on vestibular issues is on a website Vestibular Disorders Association.  If you google that you should see the website it's also called VEDA.

      You shouldn't have to work this hard to find out what is wrong.

    • Posted

      Hi sarah,

      I found your post very interesting and helpful as I have been suffering with VN for 13 months and have tried many things to help aid my recovery.

      I note that you mention avoiding processed foods and refined sugars, these are two things I have not reemoved from my diet (although I eat very little processed food) as I have already removed so many other things (e.g caffiene, alcohol, chocolate, reduced salt intake, most dairy especially milk).  I was informed by my consultant that the reduction in salt wasn't neceassry for VN sufferers but was for anyone suffering with Menieres.  He did though tell me to avoid certain take-away meals such as Chinese and indian foods as they contain MSG (but I do occasionally have this).  I also try to keep my fluids up and drink plenty of water, ginger and camomile tea (with the occasional roobosh and decaf tea/coffee)

      I have just purchased some  echinacea but am reluctant to take this as I do suffer allergies e.g hay fever. Do you think this has helped you? Do you ever have the odd 'bad' thing or have you totally excluded the foods you know upset your condition?  I am desperate to get well again (as we all are) so will take any proven advice as you state that you are now beginning to feel the benfits of avoiding these things.

      Like you I had from the start tried to keep active and hence worked for the initial month of my illness before then getting signed off by my GP.  I think by not resting from the outset has hindered my recovery and my reluctance to give in to this thing by trying to do normal day to day stuff has probably not helped.  I was unfortunately dismissed by my employer in August due to my continued absence and all the stress and anxiety this caused has not helped my recovery but I have made some slight improvment since then. I do though wish the improvement could be more evident so will now try avoiding the things you have stated in your post.

      Also like you I have ME or CFS, I was diagnosed with this over 20 years ago but was mostly recovered until getting the VN, this I think has aggravated my CFS (and vice versa) but not to a great extent.  I have the awful rocking sensation 24/7 which is exacerbated by any sort of activity but I do press on (e.g I have spent 4 hours on the PC today).  I was also told that sleep is a vial ingredient to getting well so try to rest/sleep when i am able during the day.  unfortunately I have never been a good sleeper and this may all be due to the CFS?

      Anyway, any further help and advice would be much appreciated.  Terry (who I see has also posted) has been very good at giving me advice in the past and I am gareful for his help.

      Best wishes

      Laurence

    • Posted

      Epstein Barr can cause mono but it doesn't always present as mono. It is the virus (epstein barr) that causes different conditions (mono or in this case vestibular neuritis). That is what I'm saying, if you had mono you would rest, fluids etc. Because it is presenting as your symptoms and not typical virus you are more likely not to look after yourself which can result in complications.

      I had EXACTLY the same symptoms as you!! Hot flush, strange kind of dizzyness, feeling pulled when I walk, heart palpatations, adrenaline rushes, it all suddenly coming over in 'funny turns'. I had same fears as you that I was dying or suddenly developed anxietey for no reason (previously never had panic attack or anything). And mine came on suddenly like yours. I was happy and healthy previously. I ended up with CFS type syndrome because I did not realise that this was actually a nasty virus at the start. Google esptein barr and labyrinthitis/inner ear it will come up as a cause. Have you had any blood tests done? Do you have an ever so slightly elevated white blood count?

    • Posted

      I've had labs alot of labs done and its funny u mentioned slight elevated white blood count I'm always told that. But all other labs normal. I just want whatever the cause is to leave me alone it's horrible to live like this. I can be laying in bed and feel like I'm sinking in the bed or being pulled and Whoozy head never leave.
    • Posted

      Hi Laurence,

      really glad you found my post useful, I just want to do anything I can to help others start recovering from this debilitating illness.

      I couldn't comment on hayfever and echinacea I'm afraid, perhaps take an antihistimine tablet before you take it?

      Basically all my techniques have been based around helping the body to heal itself. Immune boosting supplements and plenty of easy to digest food full of vitamins. Yes I've certainly had the odd slip from the diet. It doesn't seem to do me any harm if it is say one meal once a week but the rest of the day and week have been healthy. Over Christmas I threw caution to the wind for a full week and indulged in everything naughty (but alcohol and caffeine). As a result I had my first ever new infection since starting the regime and had all my original symptoms come back for the first time since the very start! I found it real conclusive proof that for me at least, the diet and nutrition really works. I'm much healthier than I was before this illness so feel that once I'm better much good will have come from it. smile

      I found that removing stress from my life helped too as that certainly inflamed my symptoms similar to yourself. Don't stress the job, I know it is easier said than done but once your better you will find life has more fun in store for you.

      My CFS has been triggered by this illness, I did not have it prior to this and I am hoping it is more of an extended post viral syndrome as it is getting better. Rest really is the magic ingredient so make sure you are getting good quality rest. You don't need to be asleep, just quiet and not stimulated by tv etc.

      Final thing on diet- I have a green smoothie each day made with a nutribullet. This really helps get all the goodness in for definite each day.

      For anyone else who stumbles across this post - I want to be clear that I am sharing this info because it is what has worked for me when I had VN followed by a post viral syndrome (google it one often follows the other.) I had the EXACT symptoms described at the start of this thread and they gradually developed into even more profound symptoms over some months (unbalanced when walking, very sensitive to fluroscent lighting, moving traffic, noise.) I continued to work to the point where I was bed-ridden. I am a journalist by trade (was a deupty editor at a New York based international magazine) so after I had exhausted the help of doctors I applied my research skills to finding what had worked for others who RECOVERED from this.

      I interviewed people who had recovered, I spoke to functional medicine practitioners (GPs of 13 years who belive in getting to root issues not just treating symptoms.) My advice and regime are built from that and for me it has worked. I am not 100% recovered yet but I have gone from 15% at my worst to 85% at my best. I think time is probably the final component.

      Most people who do not recover in the first 6 months recover after 18 months.

      If you are only a month or so into this you may not think my story is a reflection of your own, I wouldn't have at the start, but I wish someone had told me to put into action the diet and supplements I have suggested back then because I fully believe I would be 100% recovered by now had I started the regime earlier. You know inner ear issues are caused by viruses. Start giving your body what it needs to heal the virus.

      Good luck in your recovery!

    • Posted

      I used to get sinking in bed feeling horrible isn't it! I used to find just as I was nodding off I would wake with a start because of it.

      The white blood slightly elevated is same as me and because it is so slight they tell you it might just be because you smoke or are stressed. They were testing me after some months for autoimmune issues and discovered I had some antibodies high (anticardiolipin IGG if you're interested). These combined with the white blood were proof that I had an active infection. They told me I just had to wait for it to pass. This was after three months of it being active. I started my research and discovered there are lots of ways to help your body fight a virus through vitamins, garlic, echinacea etc. I thought by that point it was worth a shot, I needed to feel I was actively doing something to get rid of these symptoms. It worked. 4 weeks after my regime my blood work showed normal white blood and the antibodies had gone down to normal too.

    • Posted

      Treat the cause (virus) not the symptoms. Before this I stupidly didn't even realise that you can have an active virus for this long that didn't show as flu like thing.

      Crazy the things you get!

    • Posted

      What scares me is my heart always seems to be palpitating or feeling like its beating fast for no reason. This scares me thinking its my heart causing all this. This off balance stuff is horrible and smoking brings it all on so much worse.i not to smoke much I'm only one to two a day.I have to find a new Dr cause mine wont even listen to me everything is anxiety. But whatever is going on is creating the anxiety not other way around
    • Posted

      I too found it impossible to get my first GP to understand that symptoms came first and anxiety was created by them being so unsettling! I gave up smoking in the end because the withdrawal symptoms were not as bad as how smoking made me feel with it.

      Try taking some 'bachs rescue remedy' in a cup of chamomile tea when heart sensations come on to help calm you. I used it for about a month and found it helped a little. It's not your heart. It will eventually get better xx

    • Posted

      Thanks Sara today is a bad day I'm just standing and feel like I'm swaying and that adrenaline fear coming on at the same time this I can't do its too much.
    • Posted

      Hi Sarah,

      Many trhanks for your detailed response it is very much appreciated.  When you say green smoothie are you talking about a vegetable smoothie.  I have started drinking fruit smoothies to help with any sugar cravings I may get by no longer eating so many cakes (I don't eat chocolate though).

      I do take a very strong fish oil supplement and a multivitamin, this has always been part of my daily routine.  I am finding that most of my dizziness is due to a lightheaded feeling and a feeling like I am about ot pass out, this has got worse over time but is different to what I experienced from the start of the illness.  Like you I also noticed that I began to develop new symptons over time so I am hoping by eating even more healthily some of these will start to ease.  I don't feel that the CFS is that bad as I do not get many symtoms associated with this but I do feel as though there is a virus contnually going around in my body.  I mentioned this to my consultant but he doesn't agree.

      Anyway, it is very encouragaing to hear that you have improved from 15 to 85%, I feel that I am at around 60% but have been stuck around this level for months.  Once again thanks for all your advice.

      Best wishes

      Laurence

    • Posted

      hi , where I can buy cinnarizine in Canada or USA?
    • Posted

      Hi Sarah,

      I want to thank you for your post and recommendations. I agree with Laurence, your recommendations are very helpful..., and not only for fighting the virus, but also rebuilding the body's strength and immune systems that could have been compromised due to other causes. 

      I read that some people are not sure if they have the virus...

      Yes one will not know if they have Epstein Barr unless specifically tested for it's antibodies. The CDC reports that about 90% of adults have the antibody, indicating that they got the virus at some point in their life. This is something that can pass through body fluids, for example, when accidentally using the same utensils, cups, through kissing, etc., so easy to acquire. If someone gets it in adult age first time (vs in childhood or adolescent years), they may experience more symptoms  and takes longer to heal. In terms of treatment/prevention, vaccines are being developed, but none available yet. Therefore it is important to strengthen the body's own immune system, to fight the virus. And of course if the virus have caused certain conditions, such as VN, specific treatment for that particular condition is also needed.

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