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Re: Dr. Visit.

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Lori,

Ive been on Tapazole for 2years before i came off of it,and been off

now for almost 1 month.

The only side effect i found was that you need to have your blood drawn

often,how often? every month.my levels went wacky there for awhile and by

having bloodwork done often it kept me from having terrible side effects and

keeping one step forward.Being on Tap for a long period of time will cause you

to become hypo, be careful, thats why i feel that anyone who's on Tap for a

period of time should have blood drawn often.

We all know it's no picnic going through all these symptoms that we experience

from thyroidism.

hope i helped u with your question.

sandy

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If you have no side effects to the Tapezole, I see no reason why you can't be

on it until you can get your thyroid under control by other means. I was on

it for about eight months--gradually beginning to taper off after three or

four months--w/no problems, and I have heard of people being on it for much

longer than that. Whatever, it it MUCH better than RAI, which should not even

be considered. Try ANYTHING ELSE--supplements, phytoestrogens, acupuncture,

herbs--just DON'T DESTROY YOUR THYROID (it is your friend).

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  • 9 years later...
Guest guest

Sounds like you have a good rheumatologist, .

I hope you'll be feeling much better very soon.

Not an MD

> [ ] Dr. Visit.

>

> Went to Rheumatologist today he told me the last blood test showed my

> RA was very aggressive and we needed to step up my treatment in order

> for me to function. He explained the risks and suggested that I start

> taking Embrel injections along with mtx. He also increased my mtx to

> six tablets a week. He said I may be in pain for a while longer but we

> would find a treatment plan that would work well for me. He also told

> me to start applying for SS. He also prescribed me Hydroco/APAP Tab 10-

> 325. I took them this evening and the medication helped me enough to

> walk around, that was good.

> I want to let everyone know I have not given up and read your emails

> daily. This disease sucks and people should understand how we feel

> daily. I have snapped at people before when I am in pain, it is good to

> have people who love you and understand what we are going through. Good

> luck to everyone and I will pray for everyone in here.

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I CAN USE ALL THE PRAYERS I CAN GET!! god bless,melyndagamez 3/29/08

10:22p.m.central time

[ ] Dr. Visit.

>

> Went to Rheumatologist today he told me the last blood test showed my

> RA was very aggressive and we needed to step up my treatment in order

> for me to function. He explained the risks and suggested that I start

> taking Embrel injections along with mtx. He also increased my mtx to

> six tablets a week. He said I may be in pain for a while longer but we

> would find a treatment plan that would work well for me. He also told

> me to start applying for SS. He also prescribed me Hydroco/APAP Tab 10-

> 325. I took them this evening and the medication helped me enough to

> walk around, that was good.

> I want to let everyone know I have not given up and read your emails

> daily. This disease sucks and people should understand how we feel

> daily. I have snapped at people before when I am in pain, it is good to

> have people who love you and understand what we are going through. Good

> luck to everyone and I will pray for everyone in here.

------------------------------------

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