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Hi, I had my surgery a little over two weeks ago via the transmastoid approach on my L ear. I was wondering if you had any insight into the recovery process. Some of my symptoms are gone (the heartbeat in my ear, and my vision moving with my heartbeat), but the valsalva-induced dizziness is still there. Do you think this is related to the inflammation still going on, or do you think the surgery was unsuccessful? It's hard for my brain to wrap around the idea of some symptoms gone and others still being there, it seems it would an an all-or-nothing thing. I guess I am just a little disheartened, and am looking to hear others recovery process. Thank you!
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Hi. My son has just been diagnosed potentially with Superior Canal Dehiscence from a CT scan. We are in Orangeville Ontario so it would help to get info on the Doctor in London. Thanks!

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Hello - I sure could use some help. We believe after reading these posts that my 80 year old father may have SCD. He lives near London Ontario but we don't know where to begin with finding a doctor that can diagnose and treat him if this is indeed the disorder. Can you tell me the doctor(s) you have seen?
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I have just been diagnosed with SCDS. It took 2 years of many doctors and tests to finally have our local ENT supspect SCDS,.. he referred me to London , Ont. immediately. Dr. Lorne Parnes is a specialist and a Pioneer in this condition and in surgically repairing it. I am scheduled for surgery in August and although the thought is scary I am hoping to have relief from my symptoms which have taken over my life...I believe he will be going in behind my ear to repair this. If anyone that has had this surgery done by him could enlighten me on what to expect post surgery and how long it takes to feel "normal" again I would appreciate it...

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hi there! could you provide me with more info? 

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I hope all went well with surgery:)I know how frustrating it can be,i have had all the symptoms all of my life:)when they finaly diagnosed it as scd two years ago.my doctor has suggested having surgery because of the severity,a bit nervous but by going by what everyone who has had it done everything should be ok.:):)
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Who was your doctor? My husband has SCDS. thank you 

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I've been diagnosed with bilateral superior canal dehiscence and am now considering surgery but am very afraid of post-op pain/nausea and worse symptoms for months. Was your surgery in the UK?
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good afternoon....i have been diagnosed with the same problem. please tell me about the surgery, recovery and results
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Important. I have bilateral dehiscence that was discovered by Doctor Lloyd Minor at Johns Hopkins. I am very curious to know why your not a candidate for surgery to repair the dehiscence just because you have other issues such as menieres' disease. May i ask what doctor or hospital told you this.
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May I ask how long it took from the time you Submitted your application to be seen by Dr. Minor & the date you first saw him?
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Please send me your Doctor info. I am interested in looking into this more for my wife.
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Hi. I recently saw your post here. i live in ontario as well and was looking for a specialist who could help me. I have the superior semicircular canal dehiscence. I previously had surgery to fix it, but it was unsuccessful as after a few months I was feeling worse than before. I would appreciate any guidance you could provide. - Thank you. S.S
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Please tell me where to find a doctor, I have had 4 CT's from different doctors and none of them show the dehesience. Are all the CT's "reformatted"? Please explain this to me.
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Who was your doctor? I have had 4 CT's for SCD but they are all normal. I did find out though that it depends on the thiness of the slice to be able to see it. I keep getting reffered to neurologist who sends me back to yet another ENT. In the meantime I am steadily going downhill. Please Help!
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