Hi everybody,
let me introduce myself.. I`m 36 , come from Slovenia.
I have been having T for like 10 years now. I didnt really notice it as it didnt bother me at all. It was very quiet (1/10).At the beginning I thought that those sounds were normal, that everyboy have it
I think my T was noice induced ~ as a teen I was going to loud heavy metal 3-4 times per month without any ear protection..you know young and careless..sigh
I had a spike in T a month ago..before that I had a vertigo for nearly a month. When this resolved by itself I got very loud T in both (8 or even 9/10) - its really high pitched and also sounds like eletric wire buzzing.. if you know what I mean.
I went to ENT and neurologist which didn`t discover the reason for my condition or should I say didnt even try to
ENT even said that if I wanted my T to be gone they could cut both of my auditory nerves.. what an attitude!? Could believe it.. i started to cry.. he then prescribed Serc and Medrol and even sent me to some hearing tests which showed normal hearing.
I suspect that this major spike in my "little tiny cute" T was due to taking AD (remeron) 1,5 year now. I got it because of sleeping issues due to stress at work and not because of T. At that time it was so quiet, could barely hear it (1/10).
I dont know for sure if AD contributed to this spike, maybe it was a combination of my body being way too exhausted (demanding work, family, running 3-4 times per week for at least 10km..up to 20km at once, not eating enough and so on). I had my blood checked.. I am low in erythrocytes and leucocytes, holesterol, and also b12. I am taking the supplements B complex, B 12 for 3 weeks now but no improvement so far.
I am currently withdrawing from mirtazapine.. very slowly because of WD side-effects. I tried to wean myself of mirta but with no success. I am explaining to myself that this spike in T is a SIGN to stop hellish medicine that is messing with my brain
.
Because withdrawing from ad very slowly, I will be "clean" in like 2-3 month.. which is quite a long time. I only hope that this spike fades away once AD is out of my system.
Today I also started to take Medrol ( corticosteroid ) and I have quite a headache from it. Will I benefit from it..who knows.
I ve been not going to work for the 3rd week now (sick leave) as I cant sleep and function properly due to my loud T. I am really in a dark place right now, feeling so desperate, hopeless, crying.. i dunno if this nightmare will ever end? If only I knew this loud T is only temporary and will return to its baseline. Sigh
I have two little boys who need their mother, i have also few loans and cant afford to loose my job - but how will I be able to go to work again if my condition doesnt resolve? So many fears and questions arising. Huh.
I have to say that I am also lucky to have a great husband who is very supportive and is taking care of the kids and everything.
I also read success stories quite a lot lately..that gives me a little hope and comfort. So a big thanks to all of you posting your success stories and experiences..and also thanks for reading this
Best wishes,
Lana
let me introduce myself.. I`m 36 , come from Slovenia.
I have been having T for like 10 years now. I didnt really notice it as it didnt bother me at all. It was very quiet (1/10).At the beginning I thought that those sounds were normal, that everyboy have it
I think my T was noice induced ~ as a teen I was going to loud heavy metal 3-4 times per month without any ear protection..you know young and careless..sigh
I had a spike in T a month ago..before that I had a vertigo for nearly a month. When this resolved by itself I got very loud T in both (8 or even 9/10) - its really high pitched and also sounds like eletric wire buzzing.. if you know what I mean.
I went to ENT and neurologist which didn`t discover the reason for my condition or should I say didnt even try to
ENT even said that if I wanted my T to be gone they could cut both of my auditory nerves.. what an attitude!? Could believe it.. i started to cry.. he then prescribed Serc and Medrol and even sent me to some hearing tests which showed normal hearing.I suspect that this major spike in my "little tiny cute" T was due to taking AD (remeron) 1,5 year now. I got it because of sleeping issues due to stress at work and not because of T. At that time it was so quiet, could barely hear it (1/10).
I dont know for sure if AD contributed to this spike, maybe it was a combination of my body being way too exhausted (demanding work, family, running 3-4 times per week for at least 10km..up to 20km at once, not eating enough and so on). I had my blood checked.. I am low in erythrocytes and leucocytes, holesterol, and also b12. I am taking the supplements B complex, B 12 for 3 weeks now but no improvement so far.
I am currently withdrawing from mirtazapine.. very slowly because of WD side-effects. I tried to wean myself of mirta but with no success. I am explaining to myself that this spike in T is a SIGN to stop hellish medicine that is messing with my brain
.Because withdrawing from ad very slowly, I will be "clean" in like 2-3 month.. which is quite a long time. I only hope that this spike fades away once AD is out of my system.
Today I also started to take Medrol ( corticosteroid ) and I have quite a headache from it. Will I benefit from it..who knows.
I ve been not going to work for the 3rd week now (sick leave) as I cant sleep and function properly due to my loud T. I am really in a dark place right now, feeling so desperate, hopeless, crying.. i dunno if this nightmare will ever end? If only I knew this loud T is only temporary and will return to its baseline. Sigh
I have two little boys who need their mother, i have also few loans and cant afford to loose my job - but how will I be able to go to work again if my condition doesnt resolve? So many fears and questions arising. Huh.
I have to say that I am also lucky to have a great husband who is very supportive and is taking care of the kids and everything.
I also read success stories quite a lot lately..that gives me a little hope and comfort. So a big thanks to all of you posting your success stories and experiences..and also thanks for reading this
Best wishes,
Lana
Member
