- Mar 1, 2018
- 871
- Tinnitus Since
- birth/ recent spike 2/2018
- Cause of Tinnitus
- Born with ETD, several acoustic traumas, most recently ETD
I am a life long T sufferer. I have habituated several times throughout my life. I grew up on a farm where I was exposed to loud noises since a very early age (read tractors, stock car races, machinery, power tools etc). I have no noticeable hearing loss. My T is around 15 khz and about 15 db at the moment. It could be high frequency hearing loss.
I had repeated tubes put into my ears since birth due to a Eustachian Tube defect. This was found at the Mayo Clinic in Rochester, MN. This has caused scarring on both ear drums. I was told that my Eustachian tube was narrower than normal, and I would have to live with it. So I did.
I have had many life experiences which could have caused or contributed to the T. I went to many concerts. I had an accident where I was without blood flow and oxygen to my brain for 7 minutes when I was 16. After I was resuscitated my T was quite profound. This has caused me some emotional and mental difficulties. I also developed a learning disability from this.
I have learned to overcome these barriers. I am 31 years old. I have a PhD in Cancer Economics and run a cancer prevention program in the USA. I feel I have a lot to offer this community when it comes to experiencing ETD, Tinnitus, PTSD, and Stress. Also understanding research, and research articles. You can PM me if you want to learn about my near death experience. I will also gladly answer any cancer questions. But I am not an oncologist or an MD. But I can tell you the cheapest way to reduce cancers across a large population
Oh my story...Well 8 weeks ago I finished a valium taper (down from 20mg) and lunesta (3 mg). I had to be clean for a new job opportunity (I wanted to move into an area of research that required TSCI) I woke up with severe neck pain, aural fullness, and screaming T and H. I was suicidal. Doctor ignored the drop in medications, gave me flexaril for my neck and told me to come back in a few weeks. I was not satisfied so I scheduled an appointment the very next day to meet with someone else. The second GP said I had visible fluid in both ears. She prescribed me anti-biotics (cefdenir) and told me to see an ENT. I saw an ENT a week later (insurance is good for me, I have 30 dollar co-pay and max out of pocket of 250) I had a hearing test (up to 8khz) which was normal. The ENT looked at my results and said "I bet you have fluid in your middle ear". Apparently there was an air-bone gap of around 10db. Bone being better. She was able to visibly see fluid behind the ear drum yet my tympanometry was normal.
This is very important. I had a normal tympanometry, but an air-bone gap. A less astute ENT could have missed the ETD diagnosis because I had a normal tympanometry. I did have very obvious effusion of fluid in both ears. She promptly prescribed a 12 day taper of prednisone (starting at 60 mg). I have been using flonase, allegra, pseduoephedrine, and mucinex daily. I am currently 5 weeks out from this most recent spike and have stepped back from the ledge. The H is gone. My god, I thought T was bad (and it is) but H did me in... I have an appointment on 3/30, a follow up with the ENT to look again at my ears. I have habituated many times, and I will habituate again. If you are curious about ETD or dealing with a life of T I can happily or unhappily depending on my T
help.
Sorry for the rant. The CDC is a mess and my T is screaming.
If something doesn't change in the next year, I am moving to T research
I was afraid to join because I thought that would make the T more real. But I am done playing tricks with my head...or am I...
I had repeated tubes put into my ears since birth due to a Eustachian Tube defect. This was found at the Mayo Clinic in Rochester, MN. This has caused scarring on both ear drums. I was told that my Eustachian tube was narrower than normal, and I would have to live with it. So I did.
I have had many life experiences which could have caused or contributed to the T. I went to many concerts. I had an accident where I was without blood flow and oxygen to my brain for 7 minutes when I was 16. After I was resuscitated my T was quite profound. This has caused me some emotional and mental difficulties. I also developed a learning disability from this.
I have learned to overcome these barriers. I am 31 years old. I have a PhD in Cancer Economics and run a cancer prevention program in the USA. I feel I have a lot to offer this community when it comes to experiencing ETD, Tinnitus, PTSD, and Stress. Also understanding research, and research articles. You can PM me if you want to learn about my near death experience. I will also gladly answer any cancer questions. But I am not an oncologist or an MD. But I can tell you the cheapest way to reduce cancers across a large population

Oh my story...Well 8 weeks ago I finished a valium taper (down from 20mg) and lunesta (3 mg). I had to be clean for a new job opportunity (I wanted to move into an area of research that required TSCI) I woke up with severe neck pain, aural fullness, and screaming T and H. I was suicidal. Doctor ignored the drop in medications, gave me flexaril for my neck and told me to come back in a few weeks. I was not satisfied so I scheduled an appointment the very next day to meet with someone else. The second GP said I had visible fluid in both ears. She prescribed me anti-biotics (cefdenir) and told me to see an ENT. I saw an ENT a week later (insurance is good for me, I have 30 dollar co-pay and max out of pocket of 250) I had a hearing test (up to 8khz) which was normal. The ENT looked at my results and said "I bet you have fluid in your middle ear". Apparently there was an air-bone gap of around 10db. Bone being better. She was able to visibly see fluid behind the ear drum yet my tympanometry was normal.
This is very important. I had a normal tympanometry, but an air-bone gap. A less astute ENT could have missed the ETD diagnosis because I had a normal tympanometry. I did have very obvious effusion of fluid in both ears. She promptly prescribed a 12 day taper of prednisone (starting at 60 mg). I have been using flonase, allegra, pseduoephedrine, and mucinex daily. I am currently 5 weeks out from this most recent spike and have stepped back from the ledge. The H is gone. My god, I thought T was bad (and it is) but H did me in... I have an appointment on 3/30, a follow up with the ENT to look again at my ears. I have habituated many times, and I will habituate again. If you are curious about ETD or dealing with a life of T I can happily or unhappily depending on my T

Sorry for the rant. The CDC is a mess and my T is screaming.
If something doesn't change in the next year, I am moving to T research

I was afraid to join because I thought that would make the T more real. But I am done playing tricks with my head...or am I...