Yes with the same percentage! All depending by qEEG and MRI resultDo you know if he helped some people with T already?
Yes with the same percentage! All depending by qEEG and MRI resultDo you know if he helped some people with T already?
I hope!!!! I had live for 7 years happy with mild T. it sound like a win at national lottery. My quality of life is 0!! Dont forget the psychological rules... The mind could done the remaining 30%So basically he can help you if you fall under the criteria to go from severe T to mild T?
I keep my fingers corssed for you. Hope you already got some realif just by know that it might be something out there working for you.I hope!!!! I had live for 7 years happy with mild T. it sound like a win at national lottery. My quality of life is 0!! Dont forget the psychological rules... The mind could done the remaining 30%
So, they say your problems come mainly from neurovascular conflict (tinnitus, hearing loss, h/s) and that is what they treat? What about your past neurovascular decompression surgery? I did a different job? Or didn't succeed as it should? I mean they mainly treat neurovascular tinnitus, not acoustic trauma ones? And what about your case? Did they manage to tell what is causing your tinnitus?This surgery have a series of requirements that can be showed thank to Loreta qEEG. I have this requirements: bilateral hearing loss, neurovascular conflict with sure nerves overactivation, chronicity, drug resistant and not maskerable. The percentage of success with this requirements is of 50 to 70% of relief. The same target is for my trigeminal nevralgia and facial spasm because there is a multiple conflict on the Mri scan between the bloodvessel and nerves 7 and 8. The risk are minor of 1% see it on www.sonimodul.ch click on "The concept"
A big hug from Solothurn
When i go back in Italy i will send you a message where explain better my situation. It is not easySo, they say your problems come mainly from neurovascular conflict (tinnitus, hearing loss, h/s) and that is what they treat? What about your past neurovascular decompression surgery? I did a different job? Or didn't succeed as it should? I mean they mainly treat neurovascular tinnitus, not acoustic trauma ones? And what about your case? Did they manage to tell what is causing your tinnitus?
It is all a blare to me, I don't understand what Loreta qEEG exam shows.
Thanks Ivan, enjoy your staying there, all the best! How long before you return? Are you planning on visiting the clinic again?
This is a very sad possibility because the surgeons in 2008 had used the SPONGOSTAN that is a reabsorbible material. In fact on various MRI scan during the time, this material is not visible!!! This is the worst thing that could have happened to me. Remember that mvd surgery must performed exclusively with TEFLON or IVALON and not SPONGOSTAN!!!!@Viking,
Did the first surgery (mvd) fail? Perhaps the tephlon is displaced after time?
There are not reasons like food drink or smoke in improving/worsening of my tinnitus. It is defibitely due to nerve damage. When i developed tinnitus in 2006 i was living the most happy time of my life. I had a work, university studies, girlfriend, motorbike group... it is not related to stress or anxiety or others psycological causes.ivan you must remember in 2-3 days of partial silence the last year what happened before these happy hours.
What you eat how many hours you slept if you smoked or not cigs everything to try reproduce the silence.
My suggestion before any surgery is to stop completely smoking i know it is very hard but improvement from stopping smoking comes after several weeks not in 3 or 4 days.
If you cut off smoking and benzos and you don't see any improvement after 3 months then you can say that
these are not the cause but iam sure that you will see difference.
Also you must remember what was the cause of initial T. It was a stressful event like university exams lack of sleep etc ?
I see. So there is a possibility of surgery materials failure. This is why you've been much better after surgery and then you got much worse! Can you tell us (or via pm) where did you do the mvd and how much did it cots you please?This is a very sad possibility because the surgeons in 2008 had used the SPONGOSTAN that is a reabsorbible material. In fact on various MRI scan during the time, this material is not visible!!! This is the worst thing that could have happened to me. Remember that mvd surgery must performed exclusively with TEFLON or IVALON and not SPONGOSTAN!!!!
hold on!
Best wishes
The mvd surgery have not a cost in italy. It is all covered by the national care system. The same for surgery out of italy exclusion for private clinic (hifu). The problem is how "surgeon hands" can choose and if they want risk it.I see. So there is a possibility of surgery materials failure. This is why you've been much better after surgery and then you got much worse! Can you tell us (or via pm) where did you do the mvd and how much did it cots you please?
Thank you for your advice. I haven't decided yet cause it is not clean what is the problem with my T.In my mind, writing some email with De Ridder i would go in Belgium and italy cover this type of surgery excluding cost of travel, food and others extras.
You must not go alone. My advice is always to travel with a parent or friend because the head surgery is serious.
Best wishes
Is he in New Zealand or Belgium
If you cut off smoking and benzos and you don't see any improvement after 3 months then you can say that
these are not the cause but iam sure that you will see difference.
They speak about it in this thread ... https://www.tinnitustalk.com/thread...ditory-cortex-implantation-for-tinnitus.8377/This never ends! Another opinion. What now my friend?
Its like Tinnitus suddenly has options, therapies to choose from... What can I say? I give up!
What is this procedure like?
The above case study actually states:They speak about it in this thread ... https://www.tinnitustalk.com/thread...ditory-cortex-implantation-for-tinnitus.8377/
seems like it uses the timeframe 5 years ! ... please just give a pill or zap the bloody thing out of the universe ... 5 years ...
With the dual stimulation his pure tone tinnitus remains abolished after 5 years of stimulation
Have you been thereLoreta qEEG in brain tinnitus Beligian clinic
Dear Cristian,I spoke with @Viking and other friends about the price for consultation with dr Jeanmonond, price is 2200 CHF...
What I have noticed is that he has done qEEG and talked psychologically and had neurological examination. I did not see he has done some other examination with highly sophisticated devices.
Loreta qEEG in brain tinnitus Beligian clinic is 140 euro.
I do not understand. If we accept that Daniels price is reasonable, and it cost so much and it is MINIMAL s @dan say, so dr daniel does not earn severely on patients how come consultation with him cost 2200 euro, and in brain clinic same tests are ca with hearing test 300 euro.
Why is different? 2200 € or 300 € ? Can you tell me? (pointing out price we pay for only speaking with Daniel Jeanmonod? Is it possible he charges just to speak and get his opinion without grantee 10 times more than in other hospital and he claim to work on minimal price)
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