Eustachian Tube Dysfunction For 2 Years!
I am a teenager,aged 15. I have been suffering from problems with my eustachian tube for 2 years now. I felt thumping,buzzing,vibrations come from within my ear-but at the same time I felt the symptoms to DEEPER into my ear. It has created some headaches and I have to pause between conversations to attempt to unblock my ear.
However,nowadays I cannot unblock my ear properly. The 'stuffed-up' feeling I get has gone even DEEPER. I got an okay in many audiometry tests (PTA tests) and I got a weird thing that sucked out all the mucus in my throat a good 2 TIMES.
The doctor says it will go within time. I've had for 2 YEARS already, It would be terrible to go on like this without being able to swallows properly! Yes,one of my symptoms is the inability to swallow properly without the pressure building up where my tube is at-it makes me go light-headed and faint sometimes.I've tried taking nasal sprays,but they were hell as the steroids made my adenoids act up and swell (but my adenoids are okay now).One point to add,I have only got a deficiency in Vitamin D and I have no thyroid deficiency.
A few questions:
1: Does any UK hospital or the NHS have a cure/treatment to this?
2: Is it normal for teenagers to have ETD for a long period of time such as 2 years?
3: Do home remedies work,like the Candle Ear treatment? I've tried steam treatment but it doesn't work.
Please give some suggestions, It's truly uncomfortable getting out into the cold or out into the hot with such a feeling of 'stuffiness'.
Chronic Eustachian Tube Dysfunction?
I have been reading the boards about ETD and all the other potential causes of my ear problems for the last 6 months and am still without a clue what is causing my particular issue.
The story is long and like so many others on these boards also very frustrating. In March I was diagnosed with and inner ear virus as I was dizzy, foggy headed and had a slight sensation of fullness in my left ear (all occurred less than 24 hours after a 3 hour flight). This lasted for 3 weeks at the end of the three weeks all symptoms subsided except for the constant need to "pop" my ears. This lasted 4 days and was gone.
For 3 weeks I was symptom free, I had to take another flight which went off without any problems. For days after the flight I had spells of dizziness and on day 7 after the flight hear came the ear fullness and need to "pop" my ears.
Went back to the ENT and was told I have ETD and will resolve....6 months, 4 ENT's and an Allergist later my ears still feel pressurized. I have mad improvement over the months and instead of having to "pop" my ear 1 million times a day I am down to maybe a half a dozen.
My major concerns are:
While driving my ears bother me the most I feel increased pressure instantly no matter if the windows are open or closed.
Also I have post nasal drip MD diagnosed with non allergic rhinitis, never had that prior to the dizziness and ear issues.
ENT and others say it will go away it just takes time, I have not read of anyone's ETD going away on this board and feel like I can not live with this forever!
What are your opinions: will it resolve over time are we stuck with this forever?
I have been on oral and nasal steroid no significant improvement, I am doing acupuncture and seeing a chiropractor. I am negative for any allergies and my MRI came back negative.
The next step is tubes which they say can help in 50% of case and may make it worse in the other 50%, as much as I want this to go away I can not even take the chance of making it worse.
Eustachian Tube Dysfunction :: Tinnitus And Excess Mucus
This started a week ago at night I started getting ringing sensation in both my ears which persisted that night and wouldn't let me sleep went to the Ent department and got diagnosed as eustachian tube blockage as I had popping of ears and had to constantly swallow so that the ears feel better had a Pure tone audiometry done which should no hearing loss then had a tympanometry which showed a bit increase in the middle ear pressure got prescribed with antihistamine and antibiotics any idea when the tinnitus goes it has decreased to an extent it doesn't disturb but if I close my ears I can hear it anyone experienced the same?
View 58 RepliesEustachian Tube Dysfunction Cause Vertigo That Lasts A Couple Of Hours?
I have recently been diagnosed with Meniere's disease because I had a few vertigo attacks, hearing loss, tinnitus, and ear fullness.
However, after much thought I am beginning to doubt that diagnosis. My ETD had been blocked for exactly the same time my symptoms appeared, I know that easily through the valsalva maneuver, my good ear is clear and bad one is blocked. Also, my bad ear does not pop properly after a flight. And my most severe symptoms happen within a few days after flying, which happened twice. I was vertigo free for 6 weeks in between the 2 flights. Another weird thing is I only get vertigo attacks in the morning right after I wake up, as if my horizontal sleeping position had something to do with it.
My questions:
1) Is it possible with ETD to get vertigo (room spinning) or severe dizziness attacks lasting up to a couple of hours?
2) Do any of you ETD sufferers sense that you get more dizzy after you get up from bed?
Eustachian Tube Dysfunction :: Information, Symptoms And Treatment / Cure
As far as I know, there is not ETD cure, yet. I am interested in finding one. I am a Caucasian 34 year old man living in Santa Clara, CA. I have a BA in Psychology and work in a Neuroscience Lab. I was diagnosed with ETD a year ago. I have been suffering from it for 17 years. 13 years ago I had a bought of Bulimia that lasted for about a year. I had Anorexia Nervosa as an adolescent. I was given the maximum dose of testosterone to boost me through puberty since Anorexia was preventing it. Soon after I abused alcohol, marijuana, tobacco, and various other drugs until 2005. I believe all these factors have contributed to my ETD. I was diagnosed with OCD and Generalized Anxiety Disorder two years ago and have been taking Effexor (Venlafaxine) to cope. An Ear, Nose, Throat doctor (currently called Head and Neck surgeon in US) prescribed me Flunisolide (corticosteroid) to reduce ETD inflammation. It seems to help a little, but it is certainly not a cure, even when used for a significant period of time (i.e. 3 weeks).
My ETD has been recently aggravated by my attempts to remove pimples and skin tags, which may be a symptom of OCD. Has anyone else experienced this situation? Numerous doctors say there is no connection between the skin abrasions and ETD, but they obviously don't have ETD.
Primarily, I am asking for information regarding ETD. I need to know the statistics of ETD so that I can develop a valid research proposal. Health organizations neglect to respond to my questions. It seems that most biological research is involved in diseases such as cancer and heart disease, which is great. But, as I am sure that anyone reading this knows, Eustachian Tube Dysfunction is a debilitating disease that hinders one's ability to live to their fullest potential. As I have recently graduated with a Bachelors degree. I am researching what my next step will be. I am strongly leaning towards statistics and data mining, since that is a much needed position in all research fields.
I am looking for information on the number of people with ETD worldwide and specific to certain regions. A timeline of ETD cases in these regions. Research groups, Academic and Professional, that are researching ETD. Research groups that are investigating ETD from the Neuroscience and/or Ear, Nose, Throat (Head and Neck surgery) perspective. Any other information is helpful as well, especially your own personal accounts of ETD. Please share your history, as much as you care to disclose, so that I can begin to develop an etiology of ETD.
I have read many of the other discussions on ETD and recognize that many of you are suffering and I certainly empathize with you all. I am still trying to decide if my anxiety disorders are the result of ETD, my ETD the result of my anxiety disorders, if they are mutually intertwined, and/or if something else is going on. I very much hope to hear from you so that we may begin to develop a cure for ETD so that we may not be hindered by this ruthless malfunction.
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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)?
Erectile Dysfunction :: Vitamins For ED?
So I've been having partial E.D and I looked up vitamins to help. I wanted to know if taking these all together were bad. If so which should I stop. Which will help. I got vitamin c 1000 mg, vitamin E 1000 IU, zinc 50 mg, magnesium, B1 250 mg, saw palmetto 900 mg and super b complex. Is that to much to do once a day?
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How do i can get back into the mood? Is it true a man can achieve an erection up to the level where the penis is heading towards to the person's head as shown in the blue films? Is blue films is one of the reason for this problem?
What medicines or changes that I need to do to get back into the mood & have frequent & quality erection?
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Wondering if anyone else has had this issue or has suggestions on how to treat it. (It sounds strange, but it's true and troubling.)
I took Adderall regularly from 2011-2013 and had no ED issues, but delayed ejaculation. Since then, I've switched to a different antidepressant medication, and when I restarted the Adderall, I had ED.
I would watch porn and masturbate for up to 30 minutes before I could get an erection. When I did, I would have some pre-ejaculate (which I never had before). Once I got an erection, because it took so much work, I didn't want to lose it! So I would put on a c*** ring and edge for up to an hour before ejaculating. Even if I only took the Adderall a few days a week, these side effects and the subsequent cycle continued daily. I've stopped the Adderall, but I still have to masturbate a flaccid penis for up to 15 minutes before it gets erect, and like before, there's eventually pre-ejeculate, I get very hard, then can masturbate normally and eventually ejaculate.
I feel like the aggressive type of masturbation I used to produce an erection when I was taking the Adderall has completely altered my penis' reaction to stimulation. Now, 15 minutes of stimulation + porn produces pre-ejaculate and then an erection. Stimulation from a partner does nothing to arouse me. I now have to go through this process to get an erection.
I've never had ED issues before, or any trouble getting an erection when masturbating or with a partner. Now, after all the aggressive masturbation caused by the Adderall-ED issues, my penis' response is so drastically different, I'm worried and don't know what to do?
Will an ED med get me back on track? Do I have to avoid masturbation and porn for an extended period of time and then my arousal cycle will return to normal? I feel like I've literally retrained my penis on how to respond to stimulation, and I need to retrain it back to normal, but not sure what to do.
Has anyone else experienced this or have suggestions?
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