well i guess it's time to post something again here...
it's been quite a while i wrote/asked something here.. now i have a lot of questions and hope to find an answer fore some or all of these.
First i want to remind you which symptoms are still bothering me..:
- brain fog (priority!!) - headaches.. very often frontal... sometimes in the back too.. sometimes on top of head - memory problems... - poor concentration.. etc. (the whole brainfog thing) - mental/psych issues.. - at bad days racing thoughts - slow bowel movement - farting (my poor girlfriend )
- vivid dreams EVERY night.. im talking about VIVID not VIOLENT dreams.. - sometimes a little bit sweating at night.. under pits - less appetite since got sick.. improved somewhat but still not like it was.. - muscle/weight loss - sometimes sore muscles - dark shadows under eyes (since got sick)
1.) I was diagnosed with the Bornavirus 2 weeks ago (besides my standardinfections since 3 years (borrelia, bartonella, mycoplasma, possible babesia, possible chlam. pneu.)). My doc put me on Amantadin recommented by a german professor who is doing some research in bornathings..
I started the Amantadine last week and am taking the full dose since thursday ... friday i got a flu (my girlfriend too.. so i knew it was a flu and no herx)... .. after I felt better on sunday.. my mind started to spin around extremly ... especially the racing thoughts were terrible today i feel sick with sore muscles.. more brainfog.. more shadows under my eyes.. feel weak.. and im asking myself:
Can you herx on an antiviral medicine???
2.)Like you see, i have done some protocols in the past... first i tried to target borrelia+bartonella... after that borrelia+babesia.. after that again borrelia+bartonella+candida (dont know if i have it?!).... the question is.. why am i feeling still bad (better then at the beginning but still not healthy enough...) after all these protocols.. did i forget something?!
which next step does make some sense?? i wanted to target the bornavirus first yet... after that i want to try a parasite cleanse + candida cleanse (with fluco) or some babesia treatment again... or all together?!
3.) how can i bind neurotoxins at the best?? i know about the standard detox like.. chlorella.. or activated charcoal.. but to be honest.. i dont feel like they do anything. I agree with my LLMD that your brainfog can be caused by neurotoxins.. but.. how can u get rid off them?? and HOW LONG do/did it take??! i tried a detox with chlorella.. felt nothing (4-6 chlorella tablets a day, too tiny dose?).. actually i take 5-10 activated charcoal tablets before i go to bed.. (abx in the morning)..
what detox/antioxidant stuff did work the best for your brain fog, plz tell me!?
Besides all the ABx I'm on probiotics and supplements too... next month i will buy some extra probiotics.. im taking alpha liponic acid too.. and from time to time vit. b complex.. magnesium.. stuff like that.
Im eating (almost) healthy... here and there i eat a burger or a pizza.. i dont mind.. sometimes after i ate a pizza i have a white coat on my tongue.. but not strong.. only slight.. when im not eating those (candida boosting) things i have no coat..
sry for this long text.. i hope you can help me a bit?!
greetz
edit: forgot to say.. my CD57 was at ~216 before treatment.. was retested after 1 year of treatment resolved in a score of ~392!!! (range 60-360)
[ 12-21-2011, 11:04 AM: Message edited by: daniel ]
Posts: 371 | From velocity of light | Registered: Sep 2009
| IP: Logged |
17hens
Frequent Contributor (1K+ posts)
Member # 23747
posted
Hi Daniel,
Nice to see you again, just wish it were under different circumstances.
I dont' have answers to all your questions but I do have something... the farting and white tongue and maybe even brain fog say yeast to me.
I have a friend who went thru treatment for lyme, bart, EBV and ended with doing this yeast diet. http://mccombsplan.com/
She swears by it. Says she never felt so good in her whole life.
-------------------- "My flesh and my heart may fail, but God is the strength of my heart and my portion forever." Psalms 73:26
bit 4/09, diagnosed 1/10 Posts: 3043 | From PA | Registered: Dec 2009
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/