Re: Neurological Lyme symptoms...

[Guest guest]

Jim,

Thank you for all of the information. My husband is currently using

the GB4000 with the SR4 amp. We moved recently and before that he

was using the GB4000 with the MOPA amp for free at a local health

food store and he seemed to get better herx reactions from the

MOPA. We just don't have the means to get the MOPA right now but

'it's on the list'..lol. I think I'm going to go with my gut and

have him skip the ID doc. I don't think he could handle things

getting worse at this point.

He hasn't used MMS yet but I want to start him on it soon. I have

been on this board for a while now but due to other family member's

health issues (my daughter has PANDAS and a degenerative

neuromuscular disease) I haven't had the time to really read up on

everything. Now that we have moved and I started a less stressful

job, I have more time to devote to getting my husband better. If

you could please provide more info on MMS, I would really appreciate

it.

He is taking magnesium oil. I just bought some at Whole Foods,

mixed it with water and he is spraying it on himself daily. I'm not

sure how to tell if he is getting enough though or if the brand from

Whole Foods is good or not. (I don't remember the name offhand).

He hasn't tried Essiac tea yet but I was going to order that soon

too. Any additional info you have on that as well would be

appreciated.

What would you recommend as a good binder. He is currently taking 2

charcoal capsules a day but because he is having so much brain fog,

I don't think that is enough. I was looking into Salt/C but he has

high blood pressure so I didn't feel comfortable trying that on him.

Do you know of anyone who has used MMS and the Essiac tea on kids?

My 11 year old son had 2 deer ticks in the spring of 2011 and since

then has become increasingly lethargic, achy, etc. We are using the

rife on him as well and he is having mild herx reactions but I want

to see about adding something else to help him along. He will need

a good detoxer because he is compound heterozygous for the MTHFR

gene which affects methylation and detox.

Thanks again for all of the info and for sending me more....

Recently we seem to be identifying with with the fish from the movie

Nemo..."just keep swimmin'. just keep swimmin'" haha!

Hi Barb,

Sorry to hear your husband is not doing to well..

Most of us have all the brain issues your husband does,

just the level of intensity of them

is what makes us all different..

Infectious disease doctors usually do not treat Lyme

properly, they are members

of the IDSA (Infectious Disease Society of America) and

in 2006, this organization

posted its faulty Lyme disease guidelines, basically

saying that Chronic Lyme

does not exist.. Within a week of this posting,

insurance companies stopped paying

for expensive antibiotic (abx) treatments for chronic

Lyme and many went with treatment

for Lyme as they could not afford the new CASH prices

doctors charged... AND most ID docs

stopped treating it altogether.. If you are going to

take your husband to this ID

doctor, I would try to find out if he's extensively

treated Lyme disease in the past

and with aggressive treatments... Even the best LLMDs

(Lyme Literate MD) who

have extensive experience in treating Lyme aggressively

still have many patients

not cured of Lyme... A good Lyme doctor understands

what abx to use and in what

order to prescribe it.. ......................