Prednisone for meniere's disease

Common Questions and Answers about Prednisone for meniere's disease


230948 tn?1235847929 The best test for diagnosing this is called the ElectroCochleagram and is a very specialized test that is only done here in major Vestibular Clinics or specialist in <span style = 'background-color: #dae8f4'>meniere's</span> Disease. The time honored treatment for <span style = 'background-color: #dae8f4'>meniere's</span> is a VERY low sodium diet, like 2 gram a day. This often means even buying low sodium bread. My best friend developed meniere's about 5 years ago and she is often as miserable as you describe. Her best results have come from rigid adherence to the diet.
Avatar f tn Thank you for writing about your autoimmune disease of the inner ear. This diagnosis has been mentioned to me as I have "issues" going on with my right ear (I am deaf in the left). What were/are your symptoms of AIED? Was there a test to diagnosis?
209591 tn?1267418314 the CDC [Centers for Disease Control], the Infectious Disease Society of America (IDSA), and most MDs believe it is a short, non-serious ailment that goes away either on its own or with a couple weeks of antibiotics. There is a competing view, held by LLMDs, many of whom are members of a different organization, International Lyme and Associated Disease Society (ILADS).
Avatar n tn That would cause a conductive loss, which means it could be surgically correctable. If you are dizzy, etc., its probably viral and maybe <span style = 'background-color: #dae8f4'>meniere's</span> disease. Have you had episodes of ringing in your ears, vertigo, etc. in the past? It can come and go for years, and each time zap a little more hearing. The vertigo can be quite severe which is a telltale sign. If this was the start of meniere's you may see some recovery with the steroids but could have future episodes.
212059 tn?1292942129 Started out at 80mg p/day (taking it for Sudden Severe Hearing Loss related to my <span style = 'background-color: #dae8f4'>meniere's</span> Disease) Have tapered down to 40mg per day since the PVC's started, two weeks into my treatment. Went to the ER with chest discomfort last weekend but no heart attack. Seeing a Cardiologist on Monday. Can't WAIT to get off the prednisone!!
Avatar m tn Please also search Ménière's disease it is said that u should get tested for tumors as well because they can produce similar symptoms to Ménière's disease and good luck!
1920497 tn?1322605527 The ENT doctor I saw put me on a high dose of <span style = 'background-color: #dae8f4'>prednisone</span> for three weeks and then weaned me off the drug. I took it to bring down inflammation in my left inner ear, where the meniere's started. I suppose it helped, but I'm very glad to be off the prednisone; it's a horrible drug to have to use with awful side effects. The doctor also told me to keep my salt intake to under 2,000 mgs. a day. Anyway, I do hope you guys will be able to answer my two questions.
Avatar n tn In the meantime, I'm considering asking my GP to give me another trial of <span style = 'background-color: #dae8f4'>prednisone</span>. I am otherwise healthy. Looking for any insight into how to handle this problem.
Avatar n tn I know very little about it, but I believe there is thought to be some possible overlap between <span style = 'background-color: #dae8f4'>meniere's</span> disease and migraines. meniere's disease causes episodes of ear fullness, tinnitus, and fluctuating hearing loss, but also vertigo, at least the typical meniere's. The etiology (cause) of meniere's is uncertain, and thinking has changed about it recently. Also, I think there are many variants of meniere's and migraine, which can make diagnosis tricky. You might investigate this connection.
Avatar f tn I have been suffering from anxiety for six months now after being diagnosed with Ménière's disease. During that time have had many symptoms that have come and gone but the one that keeps lingering even as my anxiety has lessened is achey legs and twitchy tight calf muscles. This discomfort is almost constant and seems to be getting worst - although my increased worry about it could be playing a role in how I am perceiving the pain.
Avatar m tn I'm not saying you have <span style = 'background-color: #dae8f4'>meniere's</span> for sure or that food will help, but I saw your post and thought I'd mention my experience in hopes that it would help you. Maybe you just have simple allergies. But I know the torture of ear problems. So if this helps, great. If not, keep trying to find answers. If it is meniere's, they use diuretics to drain the fluid from the inner ear and my doctor also used a low dose BP medicine to open up the capillaries to maximize blood flow to the ear.
787406 tn?1339206783 I also have Raynauds and Livedo reticularis, mitral valve prolapse and 3 minor leaky heart valves, hypoglycemia, hypothyroidism after thyroid cancer last year, Tinnitus, meniere's disease, bi-positional vertigo. I am looking for a reason for the eye things, does anyone know what this is? My Neurologist thinks it might be seizures but she is sending me to another neurologist for a second opinion.
Avatar n tn Got in somewhere else. Thinks it may be <span style = 'background-color: #dae8f4'>meniere's</span> Disease. If not better in 1 week, will do MRI to make sure it isn't Acoustic Neuroma (benign tumor), MS, or something more serious. I say, better to find out as soon as possible what you are dealing with. What if it is a stroke or something that needs immediate attention?
Avatar n tn I am desperate for help. I am 49 year old female with a history of <span style = 'background-color: #dae8f4'>meniere's</span> Disease and Fibromyalgia. In June 2006 I developed an excruciating postural headache, nausea, vomiting, blurred vision, which lasted for 42 days, at which time I received high doses of prednisone. There is no history of trauma or accident. I'm told this is Spontaneous Intracranial Hypotension. The prednisone relieved the headache, although I still have daily headaches but not nearly as intense as the initial.
Avatar n tn Eventually, after MRI, Spinal Tap, x-ray, and blood tests, I was diagnosed with viral meningitis, resulting in nerve damages to my ear and a mild case of Bell's Palsey. They put me on <span style = 'background-color: #dae8f4'>prednisone</span> for the nerve damage to my ear. Unfortunately, I'm having a lot of serious side effects from the prednisone...i'm feeling worse than before. While this may not be your condition whatsoever, as i'm only a patient, maybe you can discuss it with your doctor re vestibular labyrinthitis: http://www.
Avatar n tn Grave's Disease, Hashimoto's Thyroiditis, <span style = 'background-color: #dae8f4'>meniere's</span> Syndrome, Thyroid Eye Disease, and Polycystic Ovary (PCOS). I was in a wheelchair in excruciating pain to the point life seemed a burden. Simply getting out of bed was something I dreaded beyond belief as it felt like stepping onto broken glass for my feet to touch the floor. Every joint in my body was inflamed and I was holding onto 50 pounds of water due to swelling and inflammation.
1139187 tn?1355710247 a disorder of the inner ear characterized by recurrent dizziness, deafness, and tinnitus. In 80 to 85 percent of cases, only one ear is affected. Damage caused by certain drugs, including aspirin and certain antibiotics Hearing loss Trauma or injury resulting from a blast or explosion Temporomandibular joint syndrome or TMJ: pain and other symptoms affecting the head, jaw, and face.
Avatar m tn That's 1 symptom why chiarians get missed diagnosed with <span style = 'background-color: #dae8f4'>meniere's</span> disease. I had to take Dramamine several times daily for 7 weeks b4 my surgery (Dramamine is Anivert over the counter). I was having severe vertigo issues along with hearing loss in right ear. I received injections of steroids thru my eardrum into my middle ear, but I went into the most severe vertigo attack EVER after the 1st injection. The room started spinning at least 100 mph......
Avatar n tn Not too long after completing it I had what came to be termed (after seeing an ENT and a hearing specialist) two <span style = 'background-color: #dae8f4'>meniere's</span> Disease-like episodes; in which for 24-48 hours, I effectively lost hearing in one ear. The sensation was as if my hearing had 'closed in on itself', leaving only a very small frequency left. Both times it cleared up on it's own and I had only minimal long-term loss.
293157 tn?1285877039 There are a lot of causes of severe vertigo from <span style = 'background-color: #dae8f4'>meniere's</span> Disease to a lesion in the brainstem. ALL of them make you feel cruddy. What you are describing with feeling completely wrung out and disoriented are well known result of vertigo. Even after the attack is over you can have problems with visual tracking or dealing with visually busy environments. Also, I get the hissing sound in my head for days after a bout of vertigo. Mine sounds like white noise or rushing water.
Avatar f tn I work in a pathology lab and after throwing up all over the ER waiting room, I had a CT scan done which was fine, the next day I went to an ENT doctor, had hearing tests which I was told were fine and that it might be <span style = 'background-color: #dae8f4'>meniere's</span> disease, an ear disorder. He did say I had nystagmus (eye jerking) and I was put on prednisone which caused me to have a manic response, but did help with the symptoms greatly.
Avatar m tn It got to the point in December that I had to set up to sleep because I could not breath laying down. Also, my ears started ringing. Cut forward to today, I have been tested for Lyme, disease, parasites, Celiac, H. Pylori, thryoid and adrenla gland problems, and they have all come back negative. Some doctor say they think I have acid reflux and some say that I don't. I have not been on acid reflux medicne since last year and don't know if I should start back on it.
5121236 tn?1363899782 At first I thought I did have an attack of <span style = 'background-color: #dae8f4'>meniere's</span> Disease but my symptoms didn't quite fit most people's experiences. My vertigo was slight and it came on after 2 days of my hearing loss. I've had ringing in my ears before, but never with vertigo. As I read about more about other hearing problems, mine fit the SSHL. My ENT had an audiologist MD do a full hearing exam and it showed my eardrums to be OK, no wax, but it did show nerve damage.
Avatar f tn While the test may not be 100% specific for Lyme disease, it does appear useful for monitoring patients with chronic, persistent Lyme disease who are receiving immune supplements." I don't know what immune supplements means but if it means the Betaseron that you're taking, if you are, then there might be a good reason for doing the CD 57. About Betaseron----- are you saying you're taking that medicine? It a pretty hefty drug and I hope you bypass all the side effects.
Avatar n tn I am almost certain that what most of you have is either Labyrinthitis or <span style = 'background-color: #dae8f4'>meniere's</span> disease. Labyrinthitis usually follows a cold or flu and is caused by a viral infection of the inner ear.
Avatar n tn My ear both are affected less hearing ability checked with ENT doctors, they told me inside of the ears have a small hole. So need treatment.So I want to know what are the treatment me to solve the problems.I have 49 years old and have controlled sugar complaint. Please answer me the details.
13556457 tn?1430481345 I woke up 1 morning with right ear stuffiness & thought I had fluid in ear too. My PCP gave me prednisone to dry up any fluid which of course did not work. I went to ENT by the 3rd day & had steroid injections through my ear drum into middle ear (OUCH!!!) in an attempt to save hearing & he also ordered MRI which showed Chiari. I had significant low tone hearing loss & it sounded like a helicopter or some big machine was stuck in my ear which was Tinnitus.
427784 tn?1224973122 Hashi's is short for Hashimoto's thyroiditis. It's an autoimmune disease that's the most common cause of hypothyroidism in the developed world. Whether you have it can be determined by a blood test to check for the antibodies that your body produces if you have Hashi's. It's a very good idea to always get the results of all the tests your doctor runs. You can call your doctor and either get the results verbally or ask for a copy.