Re: Re: Spouses (was Feeling Pretty Hopeless)

[Guest guest]

i'm certain my husband has ld.  he grew up spending summers at their cabin in the woods n. of spokane.  he remembers lots of ticks.  he has had a lot of anxiety his whole life, and some other mood symptoms.  also, he has degenerative arthritis in all his large joints and some smaller ones, quite advanced.  

then i know i got infected (my fibro since 1981 may have been ld dr. said) or reinfected, here in the early 2000s, not sure if he did.  maybe that is why he  doesn't show a lot of the same symptoms as i do.  but dr said bart is sexually transmittted, maybe babs too, be we don't think he has babs., but probably does bart.  i think his has gone to his joints, where as mine is more systemic.  

who knows?  he is having more problems since his knee replacement surgery so maybe with the immune system stressed????barbara

 

Barb, that's very interesting that your llmd said most spouses are also affected. I remember at one point early in my treatment becoming very anxious that my husband was infected. Dr. J tested him with kinesiology, and found he had both candida and LD. We actually stopped having sex at all for several months. But his symptoms are very minor compared to mine. Shortly after we met he began have bouts of pink-eye quite often. We also believe his prostate problems are at least partly caused by LD. He has taken quite a bit of olive leaf and we are now both on lauricidin. And occasionally he takes a month of tinadazole. May will be the strongest full moon of this year, so he'll do that then. But he has been functioning very well, I think.

They say that once you are under treatment, LD is no longer likely to be sexually transmitted. But I was not diagnosed until 9 years after we were married. At the time he was diagnosed, Dr.J thought he may have caught it sleeping outdoors in Oregon. Anything is possible!

Khaya

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> > Juli ,

> > please how much CS did you try every day ?

> > did you do the mms every hour and how many drops each hour ?

> > The fungu smakes sens and is a big and demending issue

> > can you go back to the rife machin where you had a herx on a regular basis

> > ?

> > if you psend 4 minute son a frequency with no herxing where do you coil

> > please exactly ?What freuqnecies did you use for each coinfection you were

> > scaneed for ?

> > I am progressing even thought I have big heavy metalissue to the point I

> > cannot touch it at all .

> > To me the symptoms you discribe are soem of my own herx or theone of my

> > husband I ma wondering if you do nto know yet how looks like your own herx

> > my husband

> > herx is getting yelow , brain fog then if too severe

> > headach.

> > mine are if i let it go further thanmy regular one (

> > neuro ) sweating pain fatigue always

> > did you try to take bicarbonat eof sodium for the acid reflux a tea spoon

> > in a glass of water ? woudl you be acidic may be ?

> > What detox do you uses ?

> > I pu tall theses question to allow everyone here to see if they had

> > similar experience .

> > Sometime a protocol or two just doe snto work for us or just it would owrk

> > but doing it differntly , do you have DMSO at home ?

> > I go to bed chto chat tomorow

> > kindly Marie

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> > *From:* Juli Mancini

> > *To:* " Lyme_and_Rife " <Lyme_and_Rife >

> > *Sent:* Tuesday, March 13, 2012 10:20 PM

> > *Subject:* Re: OT: Feeling Pretty Hopeless

> >

> >

> > Marie,

> >

> > Thank you for your encouragement...I don't often write although I have

> > been a member here for a while...but it's been a tough week. I have tried

> > salt C, almost every antibiotic treament, herbs, CS, MMS, Coil. But for me,

> > as soon as I beat something back another one comes up and the sypmtoms are

> > subltley different so I treat the new thing...so feels like I'm jumping

> > around a lot. When I tried salt C and MMS I stuck with both for 6 months,

> > the salt C really irritated my stomach and the MMS did not cause me to

> > herx...I was too affraid to go higher than the recommended dose. Rifing I

> > have done periodically but had no herxing, so I went to someone who has an

> > f-scan and a different rife and I responded twice to his with a herx but

> > that was it. I would take the printout from the f-scan and bring it home

> > and I would cover 15 frequencies a day at 4 to 5 minutes each trying to

> > find one that I reacted to. I respond mostly to antibotics but and fearful

> > of staying on any one longer than one month without breaks. I developed a

> > hernia, acid reflux and yeast issues which I try to clean up in between.

> > Lately, my skin feels like its cold or burning...and I have been sweating

> > at night both new symptoms in addition to the headaches, anxiety, craziness

> > and brain fog. I guess my problem is that I have so many things going on,

> > I'm so overwhelmed. I know I have heavy metal issues too.

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> > Warmest Regards,

> > Juli Mancini

> > Blume Design Creative Services

> > Designer.Photographer.Writer

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