The new setting for the VNS implant

On February tenth I had the implant turn up to 1.75 every two hours. the next day I had a dental appointment. The Dentist stayed in my mouth for one hour and ten minutes. I ended up crying and being sick for a day and a half. The next week, on the 18th he did only about 15 min of work and I skipped going on the 25th. It has been this stress that has kept me from going down further and faster from the drugs. Now the level is 60 cymbalta, 200 Provigil, 15 Paxil. When I am resting, or have relatively little stress my brain tingles. It is that feeling that I get when it know that I my brain is in a healthly zone. I can handle things better.
The teeth problems will continue for a while, so I will do the teeth appointments every other week.
(All this teeth work needed antibiotics, which caused more problems with depression because they further messed up my digestion by killing the flora in my intestines that provide for the digestion and immunity functions of the body-editor)

Back on paxil at 30mg

I am on 60 cymbalta and 200 provigil and now after this morning, thirty paxil. I have been noticing the symptoms of the disease returning. I am groggy throughout the day, I crave carbohydrates more and caffeine . I can't have the caffeine because of the fibrous nodes in my breasts. Somehow the more caffeine I have the more soreness in the breasts.
When the device is working the best I can eat very little, am more active, leave thoughts that disturb me, feel that I can get through anything. I just have a better quality of life all around.
The 1.50 at 2.5 hours worked for about 4 days as I went down on paxil. I was just taking the cymbalta and provigil. By the tenth day I was going into depression again. So I went back on 15 paxil and at times took 45mg a day this I did for about four days. Then for about a week I was fine just taking 15mg, then the down turn again getting more tired, more craving carbohydrates and so today I went back to 30mg.

Back on Paxil

I restarted the paxil on the 24th, just two days after the last post. I tried to mega dose it, going up to 45mg, 15mg in morning, 15 afternoon, and 15 mg in evening. I did this for three days and on the 28th I remained at 15 mg continuing each day. I seems that the mega dosing doesn't really help. I went off for the 9 days and it took 9 days to come back up. It has always been that way.
I went back on the simvastatin after one week off of it. I am getting the body soreness back, but not so bad.