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Hi Jen,<br>I'm sorry I don't know what that is

unless it means your antibodies are working overtime

fighting the disease. It sounds like your mind is working

over time on the stress factor. I know it's hard to

get your mind off of it. It drove me in to a 2 year

denial. The best consilation is it's a slow disease.

Catching it early is a big plus making chances of

arresting it a lot better. This new Peg combo is the third

drug out (even stronger) since the disease has been

recognized. I read on a post in another club that an even

newer drug has been discovered that is even more

promising to fight & arrest this thing. <br>Good

luck.<br>Reg

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Hi Jen,<br>I'm sorry I don't know what that is

unless it means your antibodies are working overtime

fighting the disease. It sounds like your mind is working

over time on the stress factor. I know it's hard to

get your mind off of it. It drove me in to a 2 year

denial. The best consilation is it's a slow disease.

Catching it early is a big plus making chances of

arresting it a lot better. This new Peg combo is the third

drug out (even stronger) since the disease has been

recognized. I read on a post in another club that an even

newer drug has been discovered that is even more

promising to fight & arrest this thing. <br>Good

luck.<br>Reg

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Thanks for your response Reg!<br><br>I posted

about a wk ago, but I can't remember what I wrote. My

mind is going too! LOL! He is my story in a nutshell.

I was pg and had a very rough pg after 2 m/c's.

Through the entire pg, i was Extremely fatigued. Almost

incapacitating. I thought it was because of the pregnancy. Now I

wonder. Anyway, at the end of the pg I had very bad right

upper quad pain. I told the OB about it, and he ran a

liver function test to see if my enzymes were elevated

because I had preeclampsia(high BP). They were fine, and

the end of March I delivered a healthy baby. My

symptoms got worse. I thought it was fatigue from a new

baby. The pain became more severe and persistant with

extreme nausea. I finally went to the MD in June, and he

suspected my gallbladder. Sent me for an u/s and blood

work. U/s came back ok, but enzymes were elevated. He

otld me to consider my blood infected, and ran Hep

A,B,andC antibody bloodtests. They all came back negative.

They ran some other tests, and never found anything.

My enzymes continued to slowly come down. My

symptoms however became worse. I itch, I am fatigued. The

pain in my ribs and back are horrible, and my joints

kill me! Sept 11th, they called to say my enzymes were

back to normal levels. 2 wks ago, they were elevated

once again. At that time my GI said he was sure I had

Hep C, and that I had a recent infection when they

tested back in June, and that is why it was negative. He

didn't want to test me again until Dec, and said even if

++ he wouldn't start any treatment on me. I have

since switched GI's. I see the new guy on Nov 5th,

where I will find out the results of my PCR test. I too

am in denial and can't believe I could have this!

Especially if it is a recent infection! I was told by the

pediatrician today that if I am +, that my 7 mth old son most

likely is too....I am heartsick.I want to crawl in a

whole and hide from the world. I know how many of you

feel about telling people what you have. My sweet

mother in law told me only prostitutes and drug addicts

get this disease. People can be sooo ignorant!

<br><br>Well, thanks for letting me vent!<br>Jen

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Thanks for your response Reg!<br><br>I posted

about a wk ago, but I can't remember what I wrote. My

mind is going too! LOL! He is my story in a nutshell.

I was pg and had a very rough pg after 2 m/c's.

Through the entire pg, i was Extremely fatigued. Almost

incapacitating. I thought it was because of the pregnancy. Now I

wonder. Anyway, at the end of the pg I had very bad right

upper quad pain. I told the OB about it, and he ran a

liver function test to see if my enzymes were elevated

because I had preeclampsia(high BP). They were fine, and

the end of March I delivered a healthy baby. My

symptoms got worse. I thought it was fatigue from a new

baby. The pain became more severe and persistant with

extreme nausea. I finally went to the MD in June, and he

suspected my gallbladder. Sent me for an u/s and blood

work. U/s came back ok, but enzymes were elevated. He

otld me to consider my blood infected, and ran Hep

A,B,andC antibody bloodtests. They all came back negative.

They ran some other tests, and never found anything.

My enzymes continued to slowly come down. My

symptoms however became worse. I itch, I am fatigued. The

pain in my ribs and back are horrible, and my joints

kill me! Sept 11th, they called to say my enzymes were

back to normal levels. 2 wks ago, they were elevated

once again. At that time my GI said he was sure I had

Hep C, and that I had a recent infection when they

tested back in June, and that is why it was negative. He

didn't want to test me again until Dec, and said even if

++ he wouldn't start any treatment on me. I have

since switched GI's. I see the new guy on Nov 5th,

where I will find out the results of my PCR test. I too

am in denial and can't believe I could have this!

Especially if it is a recent infection! I was told by the

pediatrician today that if I am +, that my 7 mth old son most

likely is too....I am heartsick.I want to crawl in a

whole and hide from the world. I know how many of you

feel about telling people what you have. My sweet

mother in law told me only prostitutes and drug addicts

get this disease. People can be sooo ignorant!

<br><br>Well, thanks for letting me vent!<br>Jen

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It can be hard when ignorance plays a part in our

lives,but love those people too,help them understand,remind

them who you are,and help them learn as we learn about

this diease we have.when afraid people feel threaten

and say hurtfull things,don't let them have a free

pass tho,educate yourself and them <br>My lifestyle

choices when younger is why I have to deal with this

now,my family already knows that,they've learned over

the past 9 years that I'm still me,just sick,not a

threat<br> " Love them anyways we're here for only a short time "

Smiles..jac

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It can be hard when ignorance plays a part in our

lives,but love those people too,help them understand,remind

them who you are,and help them learn as we learn about

this diease we have.when afraid people feel threaten

and say hurtfull things,don't let them have a free

pass tho,educate yourself and them <br>My lifestyle

choices when younger is why I have to deal with this

now,my family already knows that,they've learned over

the past 9 years that I'm still me,just sick,not a

threat<br> " Love them anyways we're here for only a short time "

Smiles..jac

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Jen,<br>I'm sorry to hear that. Has your son been

tested? If not, don't fall prey to insinuation. If you

think you contracted the virus during delivery there's

a good chance he could be virus free. I've read

that women who have the virus have perfectly normal

children. Remember this virus sometimes is fought off alone

by your own body. That's why some doc's wait a few

months before starting treatment. For all you know you

could have been carrying the virus for years & your

pregnancy weakened your system just enough to allow the

virus to surface. If, in fact, you do have it it could

subside again. I hope all turns out well. Keep in touch &

good luck.<br>Reg

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Jen,<br>I'm sorry to hear that. Has your son been

tested? If not, don't fall prey to insinuation. If you

think you contracted the virus during delivery there's

a good chance he could be virus free. I've read

that women who have the virus have perfectly normal

children. Remember this virus sometimes is fought off alone

by your own body. That's why some doc's wait a few

months before starting treatment. For all you know you

could have been carrying the virus for years & your

pregnancy weakened your system just enough to allow the

virus to surface. If, in fact, you do have it it could

subside again. I hope all turns out well. Keep in touch &

good luck.<br>Reg

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  • 4 months later...
Guest guest

Hello there

Just a quick question - I'm trying to find out about getting tests done

privately as I cannot get them done via my GP or via the endo. I think I

may have found somewhere which I shall tell you about for the information of

anyone from UK - if it works out.

Just need to check about the antibody test - is a thyroglobulin antibodies

(TgAb) test the same as the TSI that we talk about here????

Thanking you in advance,

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