Hi everyone I'm new to this site

[Guest guest]

Hi, well i was diagnosed with late & chronic stage lyme last August, when i

finally found my lyme Dr I wasnt able to walk or talk & the pain was so bad that

i welcomed death!!! I went thru the guantlet of Dr.'s & went misdiagnosed for @

least 10-15 yrs. It's in every organ in my body, including my central nervous

system & brain. I never thought i would be sitting here today writing about my

story but happy to say i can walk & talk, i still have problems with my memory &

sometimes stutter, my right foot & leg hurt me very bad cause i guess i have

neuropathy from nerve damage, i hope i'm saying that right. I still get

involentary muscle movements, its worse @ night. I still suffer from the

headaches. I have some really good days, which i wish i could have that the rest

of my life but maybe someday. I hate the herxing, it feels like someone sucked

all of my energy out of me so I'm in bed alot but sleep doesnt come. I want to

sleep so bad & its so agravating when you just watch the clock tick away. I was

a nurse for many years & i was constantly on the go, finally December 7th 2007 i

had to resign my position because i wasnt able to do my job @ 100% so i walked

away, it was very devastating but i have come to accept it. I'm glad i saw this

site posted on another site i was on, i'm trying to learn all i can about tx for

lyme, i take the high doses of atx & next month will be a year, so i would like

some feed back...thx

[Guest guest]

Hang in there. This is a tough disease, but progress can be made. I've had Lyme for 17 years and wasn't diagnosed until two years ago. I am making progress with a Doug Coil rife machine, but improvement doesn't happen overnight. I need to look back in six months to a year intervals to measure my progress. Because I have a high bacteria load, I am thinking the best I can hope for is remission. I can't imagine being able to get rid of every spirochete in my body, but I do think someday I'll be able to live a fairly normal life with continual maintenance Doug Coil treatments.Steve"Whether it be good or bad, I hope I will always take responsibility for my life."

Hi, well i was diagnosed with late & chronic stage lyme last August, when i finally found my lyme Dr I wasnt able to walk or talk & the pain was so bad that i welcomed death!!! I went thru the guantlet of Dr.'s & went misdiagnosed for @ least 10-15 yrs. It's in every organ in my body, including my central nervous system & brain. I never thought i would be sitting here today writing about my story but happy to say i can walk & talk, i still have problems with my memory & sometimes stutter, my right foot & leg hurt me very bad cause i guess i have neuropathy from nerve damage, i hope i'm saying that right. I still get involentary muscle movements, its worse @ night. I still suffer from the headaches. I have some really good days, which i wish i could have that the rest of my life but maybe someday. I hate the herxing, it feels like someone sucked all of my energy out of me so I'm in bed alot but sleep doesnt come. I want to sleep so bad & its so agravating when you just watch the clock tick away. I was a nurse for many years & i was constantly on the go, finally December 7th 2007 i had to resign my position because i wasnt able to do my job @ 100% so i walked away, it was very devastating but i have come to accept it. I'm glad i saw this site posted on another site i was on, i'm trying to learn all i can about tx for lyme, i take the high doses of atx & next month will be a year, so i would like some feed back...thx