Migraine-associated Vertigo And Vestibular Neuritis - Band Around My Head / Neck

Diagnosed with VN with possible MAV  in March 2015 and have progressed very very slowly, Life was liveable but not always great as still woke up in mornings with what can only be described as a hangover feeling which subsided as the day went on.

Suffered from what can be described as a feeling of a tight band running from my forehead across my head to the base of my neck but i just tried ti ignore it, however in the last few weeks i have stiff neck tingling nose and a head that feels totally full .........its like i have gone back 8 months and now i'm wondering if i have a problem in my neck as its always worse in the mornings anybody else struggle in the mornings with this?

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Trimethoprim :: Feeling Sick And Unable To Eat

12 hours ago I finished a course of 6 x 200 mg of Trimethoprim. Felt sick and was sick all the way through. Still feeling sick and unable to eat. Can anyone tell me when it will stop.

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Migraine With Cold And Nausea Feeling

For around the last 4 years been having migraine / nausea symptoms on and off , never been able to identify what exactly triggers it . It will usually happen in afternoons (3-6 ish) and will always start of as a mild headache at which point I try to take strong painkillers which never seem to do anything ,then around 15 -20mins later a migraine comes then i start feeling sick shortly after and will will be sick a lot 2 or 4 times then after that I will sometimes feel cold with nausea type feeling with for 1-3 hrs in bed . never been able to work out why this happens and been through it all really.

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Vestibular Neuritis - Vestibular Nerve On My Left Side With 80% Weakness

2 years ago I had gotten a bad ear infection after a trip to Disney from pool is what doctors believe.  It was misdiagnosed at first so it severely damaged my vestibular nerve on my left side with 80% weakness.  Of course this was all found out after the slew of mri's, mra's, various vestibular testing, color/hot water in ears etc.  6 months of testing and 2 rounds of vestibular therapy have not helped me at all.  I am on my 4th

specialist in NYC who finally put me on acetazolamide for the sick side effects of nausea and brain fog.  6 months into these pills and now my body is starting to become accustomed to them and are not working so well.  My symptoms are

1) Overall unsteadiness and dizziness (fall to the left)

I work in NYC so my commute walking is the worst, shopping too.

2) Brain Fog - how else to explain this just a horrible feeling in my head

constantly that very rarely feels better.

3) Nausea (without the pills I could just be laying in my bed and fell like

I am going to throw up)

4) Disgust and Depression over this whole mess I am only 51.

I am told by many doctors 95% of people recover, right side compensates for the left side over time.  This has not happened at all.  I also have never heard of anyone having it constantly for this long.  Can someone at least tell me they are the same?

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Vestibular Rehabilitation Training For Vestibular Neuritis Recovery?

Does anyone know if it is possible to over do the vestibular rehabilitation training for vestibular neuritis recovery?

I have mild vestibular neuritis and was prescribed, by a balance physiotherapist, a vestibular rehabilitation training program. This developed 13 months ago, and with the VRT, it did clear up. The symptoms came back recently and I've started VRT again. This time I'm having trouble recovering.

I do an intense program of 6-7 different exercises, 5 times per day, plus 40 minutes of walking or running per day. I do this everyday of the week without days off. Could I be over training and not allowing the brain to compensate?

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Pituitary :: Low T, Ultra Low LH And FSH, Vitamin In D Deficiency

Very healthy adult male, with these numbers:

LH: <0.2 (undetectable)
FSH: <0.2 (undetectable)
Vitamins D, 25-hydroxy: 27.4
T: 154

All of these are abnormally low. I feel fine, but I suffer from ED, low libido

Doctors 'note' on the bottom of the test results were:

Needs to see endocrinology specialist AASAP!

Ok, nobody likes to see ASAP! Written by a Physician... How worried should I be?

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Vertigo / Dizziness :: Foggy And Lightheaded With Headache

Ok I saw a million posts about these generalized symptoms so don't want to repeat the stories. However, after thousands of dollars and visit to every possible doctors in existence I still have these symptoms daily. Some days worse than others. Can someone please tell me how they were diagnosed and with what? Also did it ever go away alone and after how long?

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Mirtazapine :: Ultra High Doses Work?

Is there anybody who finds that ultra high doses of mirtazapine worked better for them? In the past I have taken mirtazapine in doses 30 mg and it had worked for a while but then I have changed my meds (bad for me). The second time I have taken mirt 45 mg without success It's the best drug I have ever taken, but it's not working anymore. I have taken many of the drugs, like SSRIs, bupropion and others, but none of them worked like mirtazapine in the past. How do you think, is there any possibility that ultra high doses like 60-90 mg would be work better for me?

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Neurological - Foggy And Blocked / Fatigue / Drowsiness?

Since this June I have been to so many places from my physician’s office to the ER and everywhere in-between. Nobody can find what's wrong with me. I’ve had two neurologists give up on me and one who (after running a bunch of tests) say I have anxious tendencies. I had every test possible ran on me and they all came back normal. Actually on paper I’m as healthy as can be. That's the problem, all my test results are perfect so people think there’s nothing wrong. It’s hard to explain what I feel like. My thoughts feel foggy and blocked, I’ve become very forgetful and academically I’m struggling. That is only the mental portion unfortunately. Physically I have muscle cramps, fatigue/drowsiness, disorientation, trembling, tingling, and clumsy-ness. I’ve had a spinal tap, loads of blood tests, two EEGs, MRIs, and been evaluated by six different doctors. Every blood test you could think of has been ran on me. Including heavy metals, vitamin b-12, Lymes, lupus, hormones, blood sugar… there are loads more but I can’t remember them all. I’m worried most about the cognitive aspect of my problem. Its very debilitating. Some days are better than others, and some are worse. Today was one of the bad days. I can’t  stay focused or have clear thoughts. When I talk I don’t make much sense. I say words that don’t fit into context, have a very hard time finding words, and as a result, can’t keep up a conversation very well. I try my hardest to overcome these problems but I don’t think its a matter of how much effort I put forth. Some days I just can not think straight. I even have problems understanding what people say to me. I understand the words, but the meaning of what’s said just doesn’t get through. Like I said, some days are better than others. The memory isn’t isolated to only short-term or the forming of new memories. I have a hard time remembering things that happened long ago as well as what happened five minutes ago. The things I remember are fragments and very inconsistent. I was stating to think that my problem could be low magnesium or something like that which was overlooked. From my understanding of a mangesium deficiency. It takes a long time for you to become deficient. This makes sense because this problem didn’t just stat overnight, I’ve actually been having this problem since February. I’ve been blowing off the symptoms as lack of sleep or just being tired but it built up to the point that I realized something was truly wrong. So magnesium might make sense, maybe. I’m just guessing at this point though.

So, what do you think? If you have any ideas what the problem could be please let me know. As I said before, I’ve had my heavy metals, Lymes, hormones, vitamin b-12, lupus, csf (spinal tap), and blood sugar checked. I’ve also had a complete metabolic panel ran, a complete hormonal panel, and complete nutritional panel checked. I think an allergist might be a good idea but I’m not sure. I guess its worth a shot.

 Here’s some info about me. I’m 17 years old, male, 5’9’’ and weigh 128 LBs. The problem is constant 24/7, never goes away.

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Allergies :: Difficulty To Speak

I have to force much effort to speak sometime because extra spit in my mouth like allergy and my word are out of order and missing.

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Autism :: 3 Years Old Child Can Only Speak HELLO

My son is aged 2.8years. when he was 1.5 years he could speak some words, some time last year January the house was changed. after the new one came the boy couldn't speak the words he used to speak and again you could find him seating some where looking as if he is stressed. When i arrive home from work he could come running to the door but this days he is not concerned at all. When i speak to him the words he used to he can't speak them again, You call him and he doesn't respond. I'm a worried Father, What do i do, i want him to remember what he used to do, to say. Where did we go wrong in bringing the boy up. He is turning three May 29th, he can only speak just one world "hello" he repeats that all the time. Is there a medication i can give him to change the situation?

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Migraine :: Migraine Attacks Are Back / Menopause

I never suffered from migraine attacks until I was in my mid-40's.

They seemed to be linked to the beginning of hormonal changes related to the start of menopause. I would get a pain over my left eye (usually, though right occasionally), with a feeling of nausea and sometimes slight numb feeling on the side of my face. I would turn quite a pale white colour, and also feel very tired, yawning a lot. I would take medication, migraleve tablets and lay down in a darkened room. Usually, I would recover within 24 hours, though I would feel 'worn out' for a few days after the attack.

Since I have discovered by self analysis, that citrus fruits, especially orange juice (which I no longer drink), chocolate and strong coffee all seem to be triggers, which I try to avoid.

For the last five years, I have been clear of migraines, but have now started to get them again. I have passed the menopause but have had a lot of stress in my life recently, so I wonder if this is the cause of the recurrence? My last attack was quite different from the others I have experienced, in that I was feeling fine (though had been really tired the day before for no apparent reason) when I suddenly developed black zigzag lines across my left eye (very frightening at first). These went on for about 10 minutes and then slowly I developed a severe migraine, though this was not over one particular eye, but both. I had feelings of nausea and also felt cold at times. I took Migraleve pink and yellow but the headache is still persisting the next day. I wonder why I developed these other symptoms of visual disturbance. Can stress really do this to your body?!

PS I know there is a family history of migraine.

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Classic Migraine Changed To Silent Migraine In 30's

I had classic migraines through my teenage years which stopped for a couple of years before continuing at on average one every couple of months with the odd instance of a back to back cluster of 3-10 at once. They were always the same 20 minute aura then axe in the head pain and repeated vomiting for 6 hours followed by a 24hr hangover.  Over the years I have tried all preventers with only Epilim and Topiramate working for 18 months. I built up tolerance to Epilim and Topiramate gave me side effects that ended in a blood disorder so cannot take either any more. Beta blockers and antidepressants never worked and Lisinopril was also a short lived waste of time. The only triptan that ever worked was Maxalt rizatriptan but again it lost its effect after 6 months. Something weird has now happened and I wonder if others have had this? I am now 36 and in the last 6 months my migraines have totally changed. I still get the aura but if I take Express Nurofen and an anti sickness tablet straight away or use a heat pack on the back of the neck no pain or sickness comes just 6 hours of extreme tiredness. I always used to throw up any tablets so this is a miracle however the frequency has stepped up to between 5 and 20 a month so it is really impacting on my life. I have had an MRI and all is normal. I have also tried supplements and alternative therapies with no success. Botox and nerve blockers are the next suggestion but will they treat this scenario if there is no pain? Will it stop the aura too and prevent the whole episode? Help!

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Lupus :: Not Able To Speak Due To High Blood Pressure - Blood Clot In Nerve

Now she's is going through speech therapy to bring it back to normal. I would like to find out any other possibility to treat her any part of the world for immediate cure

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Hormones :: Feeling Like Im Dying, Tired,headaches, Feeling Sick

I'm only 17 years old. I have felt the way i feel now for months. I am not pregnant before anyone suggests that!

I suffered from a disease/illness where my glands swelled up til they were huge and you could clearly see them. I had a fever all day, i would go cold and the hot, i had no energy at all and was generally sick! The doctor gave me some antibiotics and it cleared up.

Ever since then i have not been myself. I feel sick at some point during the day, i constantly have a weird feeling in my head, its not pain as such, but like a numbing feeling and irritation. I feel like im going to faint all the time, im weak and very tired, i also get chest pains from time to time & my breathing is rubbish, its hard to breath at times, i generally feel like im dying

I have had countless blood tests and all of them showed nothing!

This totally upset me because im frustrated, i just want it to be over!!

The doctor told me just to have lots of water and exercise.

My family were convinced that i suffer from anxiety and panic attacks!

As i had a panic attack due to the fact i felt so ill i thought i was dying!

It wasn't just happening to me for no reason the attack.

so they took me to the doctor where he told me my symptoms were that of anxiety and panic attacks so he gave me some tablets to take.

But i still feel the same!!

I do not believe that i have anxiety

I am sick if people believing that is what it is!!
.......

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Asthma :: Feeling Tired, No Energy, Constant Uncomfortable Feeling

I am slightly worried, but last thursday i was told i had asthma and i was given 2 inhalers, but since then my breathing has gotten worse, i suffer from chest pain and a "that's not right" feeling in my chest, and i am soooo fatigued and have no energy and now have lost my appetite :-(
and also feel sometimes light headed, I have been given a blood test but results aren't out yet and i hate waiting also i am really worried which make me worse and i have some back pain as well.

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Vestibular Neuritis - Getting Along

On nov 10th I was in Penn station in NYC with my 3.5 year old daughter and aunt and just had a wonderful day in NYC. I bent down to grab something from the stroller before boarding the train and when I stood up I felt like I was going to pass out and that my brain was floating and I was moving. My aunt freaked out and said we have to get on the train. We did and the spinning and horrible sensation of movement continued along with the train my brain was in overdrive. I then had a panic attack all hoping to just make it to the stop so we could get off the train. I had suffered a panic attack years before so I thought maybe this is some sort of panic disorder?? Got off the train and drove home still didn't feel right. The next morning I went to my dr and he said I had vertigo it would be for 2 weeks and gave me antivert to take. I had blood taken which all came back normal. I should preface that I had been to the dr the week before complaining of dizziness but it was attributed to a sinus infection he thought I had since I was starting to have a sore throat. I took levaquin an antibiotic 3 days before the incident in penn station. I know now for a fact that I was suffering from vestibular neuritis probably prior to the incident in penn station. I had gotten off an elliptical bike and felt very dizzy and heart racing but I attributed it to not cooling down. I also had about a week prior to the main incident a light headed feeling and chills each time I was eating. For me eating at the beginning would trigger a lot of feeling I was moving.

Well I took the antivert meds and tried to take care of my daughter since I'm a stay at home mom. Trying to stay awake on antivert was the worst thing I did and it put me into a severe depression like state. I have a mother who suffers from depression and I felt like I was in a hole I couldn't get out of. I called my dr and asked if I could have a perscription for xanax anything I felt like I was in a constant state of anxiety and panic along with the constant movement and unbalance and stress of what I was going to do to take care of my daughter. I finally decided to the ER where they finally gave me valium which def helped to calm me down and understand that this is a virus and not an anxiety disorder. I went to my ENT and got the vestibular neuritis. My ent told me he had suffered from a bout of this years ago and everything I was feeling was normal the panic the anxiety and was disappointed I had to go to the ER to obtain something to help me. He prescribed valium which I took at night the first 10 days. I was able to get a nanny for my daughter. I'm in week 4 and each day is different. I came down with a cold during week 3 which I think set things off again. I'm getting better from the cold. I suffer from TMJ and think it's made it hard because a lot of times before this illness I would wake up with a horrible headache from teeth grinding.

The mornings are the worst for me. I'm sensitive to light and feel very lightheaded and very out of it. The coughing has made my back and neck very sore. I just each morning hope I won't have the feeling of floating and just want to feel in control again.

I haven't driven since this happened. I haven't been able to take care of my daughter which is the worst of all.

I need advice on how to get back on my feet again I feel good some parts of the day and other parts I feel like I'm floating. I have been out of the house only a few times in 4 weeks. Always with my husband or a friend. This past Sunday we went out and I felt pretty good but I'm really afraid about going out alone.

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Physiotherapy For Vestibular Dysfunction?

After my ENT said my vertigo/dizziness was caused by BPPV, I was sent to see a physical therapist. The PT did a lot of testing and actually ruled out BPPV (which I suspected would happen), and said I most likely have a unilateral vestibular deficit. (I had a bad sinus infection a few months ago that took forever to get better which caused some ear issues, including diagnosed Eustachian Tube Dysfunction). She explained things very well (much better than my ENT ever did...) and has started me on some therapy exercises to help me get used to/help make the vertigo better.

Has anyone else gone through this type of physical therapy? Has it worked in helping you feel better (less dizzy/vertigo)?

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Vestibular Neuritis - Can Have Flu Vaccination?

My wife has had acute vestibular failure/vestibular neuritis/neuronitis for the last 13 weeks and wants to have the flu vaccination but is apprehensive in case it makes her illness worse. So, is it safe to be vaccinated? She is so ill with the vertigo etcetera and feels that a dose of flu would finish her off. She has asked her GP who says it is OK but the GP doesn't seem to know much about this illness.

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