Good grief!!! I think I could spend about three hours just "correcting" and commenting on all the stuff posted above since yesterday... So I think I will just stick to a few of the more 'practical' aspects for now as have a ton of Conv. stuff pressing.
I have started Potiga. First 5 days at 50mg. Currently taking 100mg. Tapering up 50mg per week. It helps! I have quiet hours after taking the pill. Quiet lasts 2-3 hours. No side effects whatsoever.
@Lake Girl ...Congratulations as our first female tiralee (explorer, guinea pig, whatever...).
However, and to all trialees if mentioning a dose..can you please post more than just a dose number. Can you please always say whether that is total per day, or three times a day, or something. The standard shorthand way of saying "three times a day" is TID. For instance Lake Girl, I don't know if you are just taking 50 mg total per day or TID, and thus 150 mg total per day.
Example of 50 mg for instance from
@theekarwash above...
Day 5 of 50mg once a day! Head noise is reduced, T is at a 2/10right now, it will change back to my 4/10 in the morning but still, this feels nice.
Thanks in advance.
Questions on dosage...I can assure you, that
there is no standard dosage or even method, for our trialees!
Just look at what
@theekarwash just said above. That's a potential "effect" at a total of 50 mg. Then we have others getting "effect" at a total of 1200 mg per day. There are variations of every kind in-between those.
I am in touch privately or are reading here of those who are mixing and matching daily doses depending on weekends v. weekdays; who have taken one large single dose; who are taking it QID = four times a day; who are taking it as needed depending on T levels; who are ramping up
really fast to avoid possible "homeostasis"; or are ramping up at glacial speed and holding for a longer term v. immediate effect.....and so on.
Yes the 'supposed' effective goal dose is 300 mg, or 400 mg TID for a total of 900 mg or 1200 mg per day, but that is the epilepsy model and somewhat the "research papers" model (where dose/plasma saturation was king
in vitro = petri dishes).
Thus to me at least, there is no real "dose" and "method" guideline worth beans yet. N sample is too small and reporting is "diverse".
Keppra/Levetiracetam (LEV)...Like
@Viking ...I can find zero evidence of it increasing tinnitus or any 'hearing stuff' in the normal sources I use (and trust by now) for "ototoxicity". I also can't see much on the Kv3 aspect, but no doubt many days of research could go to this task as it looks like a
great find Viking! It was approved in 2002 so is much more "acceptable" than Retigabine presumably.
So Trobalt works on four potassium channels rather than just one so this is why there are the side effects.
The channel that is malfunctioning is the kv3 potassium channel which causes the neurons to over fire.
Amandine...this is seriously jumping to conclusions we, or at least I (and I have spent a lot of time on this) would not state with any assurance.
When I try Trobalt I will ROTATE it with other drugs that suppress my tinnitus.
This means I will not develop tolerance, will not need to keep increasing dosage
to maintain potency and will not need to taper off, avoiding negative withdrawal effects.
MONDAY Trobalt
TUESDAY Lyrica
WEDNESDAY Klonopin
THURSDAY Gap Day
FRIDAY Repeat cycle
A lot of experienced drug users employ ROTATION for good reason and to great effect.
This approach could be especially beneficial if Trobalt, and maybe even AUT63,
have to be taken long-term.
Are you serious????????????? Really, I mean this question. (Also, if so, see above re variations in Retigabine dosage and methodology!!!)
Best, Zimichael