Re: FMS and fibrin in blood

[Guest guest]

Hi everyone,

Just found out today that I have fibrin in my blood (from live blood analysis).

Then I find out that 75-95% of all FMS/CFS and other autoimmune diseases have a

hypercoagulation effect happening which may account for all the pain. I've gone

to over 25 doctors and not one of them knew this or checked for this. I can't

beleive it! What happens is that chemical exposure trippers this

hypercoagulation (which means thick blood) and because it covers the lining of

your arteries and veins the natural heparin (blood thinning part) can't get

activated. Then the fibrin starts getting dumped into your tissue also. (plus

it's not good for your heart). I have started to take Nattokase which is an

enzyme from Japan that specifically eats fibrin from your blood but I will also

take an anticoagulant drug for a while if neccisary. This has probably been

going on for years and years and nobody noticed??? Anyway we have to take it

into our own hands. I am going to the doctor on Monday and hopefully he will

give me the drug.. I just want to get it jump started to get this CRAP out of my

blood. Maybe this is the key for us with FMS to get better!!!!

Love to alol,

Judi

[Guest guest]

Judi, A warning. If you have candida do not let them give you heparin. It can trigger toxic shock. http://www.mercola.com/2003/aug/9/detoxification_biotoxins.htm I think this article might be the answer for many of us. It is basically what you are talking about and there is a treatment protocol to clear it up. If you are interested in finding a practitioner I can give you a number to call and find one in your area. Love, Anita Re: FMS and fibrin in blood Hi everyone,Just found out today that I have fibrin in my blood (from live blood analysis). Then I find out that 75-95% of all FMS/CFS and other autoimmune diseases have a hypercoagulation effect happening which may account for all the pain. I've gone to over 25 doctors and not one of them knew this or checked for this. I can't beleive it! What happens is that chemical exposure trippers this hypercoagulation (which means thick blood) and because it covers the lining of your arteries and veins the natural heparin (blood thinning part) can't get activated. Then the fibrin starts getting dumped into your tissue also. (plus it's not good for your heart). I have started to take Nattokase which is an enzyme from Japan that specifically eats fibrin from your blood but I will also take an anticoagulant drug for a while if neccisary. This has probably been going on for years and years and nobody noticed??? Anyway we have to take it into our own hands. I am going to the doctor on Monday and hopefully he will give me the drug.. I just want to get it jump started to get this CRAP out of my blood. Maybe this is the key for us with FMS to get better!!!!Love to alol,Judi

[Guest guest]

I have wondered about the thick blood theory too myself for awhile

and actually I do believe that it is def a possiblity for some of my

joint pain but when checked all the stuff has come out normal. I was

told a baby aspirin a day would help so that might be something to

think about. I tried regular aspirin and still had some little joint

pains in my fingers so I don't know, I may just be taking after my

dad and getting arthritis. I never had this kind of joint pain with

my implants or even the first year or two without them, so it seems

new. It goes away once I move around or take a hot shower. I had more

all over bruised type pain when I had implant illness. this is def

different.

I doubt I will ever know for sure what it is but I am ok, I feel

fantastic other than my little finger pain in the am's so I really

don't stress too much anymore

hugs

In , jaylow2100@a... wrote:

> Hi everyone,

>

> Just found out today that I have fibrin in my blood (from live

blood analysis). Then I find out that 75-95% of all FMS/CFS and other

autoimmune diseases have a hypercoagulation effect happening which

may account for all the pain. I've gone to over 25 doctors and not

one of them knew this or checked for this. I can't beleive it! What

happens is that chemical exposure trippers this hypercoagulation

(which means thick blood) and because it covers the lining of your

arteries and veins the natural heparin (blood thinning part) can't

get activated. Then the fibrin starts getting dumped into your tissue

also. (plus it's not good for your heart). I have started to take

Nattokase which is an enzyme from Japan that specifically eats fibrin

from your blood but I will also take an anticoagulant drug for a

while if neccisary. This has probably been going on for years and

years and nobody noticed??? Anyway we have to take it into our own

hands. I am going to the doctor on Monday and hopefully he will give

me the drug.. I just want to get it jump started to get this CRAP out

of my blood. Maybe this is the key for us with FMS to get better!!!!

> Love to alol,

> Judi