Jump to content
RemedySpot.com

Newbie questions....

Rate this topic


Guest guest

Recommended Posts

Guest guest

Hi, I was diagnosed HyperT/Graves back in Nov 2001. I've been off and on

Methimazole & Atenolol since then, due to Dr. Stupid who thought a roller

coaster ride would be nice once my levels were " normal " instead of cutting down

on the meds to keep me at a normal level.

My question is, now that my levels are high, showing HypoT......is it possible

that I'll still go back to being HyperT? I'm back with my first Dr who

prescribed the meds for me (he was shocked that Dr Stupid did the cold turkey

thing) and he cut my meds down, instead of taking them away. He did promise me

that it wasn't going to happen again since I'm back with him now. My new Gyno

also looked at me rather funny when I told her what meds I was taking and what

had happened for the first year I was on the meds. She even said what Dr Stupid

did wasn't good to do. (Amen to that) But, I'm confused and wonder if anybody

can give me any insight into whether once I'm weaned off the meds, (I hear they

don't like you to be on them for longer than 18 months) if the HyperT symptoms

might still be there or what to expect?

Thanx

Sandy

Link to comment
Share on other sites

Guest guest

Hi Sandy,

Your info is pretty general, so the response will be too. If you want to

share the lab results it could help with specific answers to your questions.

But I can say, having had GD since '94, and having been on

methimazole/tapazole most of the time since then, that there's absolutely no

rational reason to cut you off after 18 months, except perhaps the

endo-agenda of moving you towards RAI. Long term use has no side effects!

Granny who posts here, has been on for at least 23 years.

Sounds like the slow-wean is working for you, what is your current dosage?

Terry

>

> Reply-To: graves_support

> Date: Fri, 2 May 2003 19:40:41 -0500

> To: <graves_support >

> Subject: Newbie questions....

>

> Hi, I was diagnosed HyperT/Graves back in Nov 2001. I've been off and on

> Methimazole & Atenolol since then, due to Dr. Stupid who thought a roller

> coaster ride would be nice once my levels were " normal " instead of cutting

> down on the meds to keep me at a normal level.

>

> My question is, now that my levels are high, showing HypoT......is it possible

> that I'll still go back to being HyperT? I'm back with my first Dr who

> prescribed the meds for me (he was shocked that Dr Stupid did the cold turkey

> thing) and he cut my meds down, instead of taking them away. He did promise

> me that it wasn't going to happen again since I'm back with him now. My new

> Gyno also looked at me rather funny when I told her what meds I was taking and

> what had happened for the first year I was on the meds. She even said what Dr

> Stupid did wasn't good to do. (Amen to that) But, I'm confused and wonder if

> anybody can give me any insight into whether once I'm weaned off the meds, (I

> hear they don't like you to be on them for longer than 18 months) if the

> HyperT symptoms might still be there or what to expect?

>

> Thanx

> Sandy

>

>

Link to comment
Share on other sites

Guest guest

My current dosage went from 30 mgs to 20 mgs in the morning. Atenolol is also

taken one 50 mg tablet each morning. I'm glad to hear that there isn't any

nasty side effects for long term use, cuz I'm just not having RAI. I don't care

what they say, it ain't happening. :-)

I'll find my test results and post them so you can see where I'm at now.

Thanx

Sandy

Re: Newbie questions....

Hi Sandy,

Your info is pretty general, so the response will be too. If you want to

share the lab results it could help with specific answers to your questions.

But I can say, having had GD since '94, and having been on

methimazole/tapazole most of the time since then, that there's absolutely no

rational reason to cut you off after 18 months, except perhaps the

endo-agenda of moving you towards RAI. Long term use has no side effects!

Granny who posts here, has been on for at least 23 years.

>

>

Link to comment
Share on other sites

Guest guest

Sandy,

One thing you may want to try is splitting your dose, taking it in (ideally)

3 equal parts spread throughout the day, or at the very least, taking 10 mg.

in the AM and 10 in the PM. The package insert does say to do this, by the

way, even though most endos don't bother telling their patients. I think

this is because they (in their wisdom) deem us too irresponsible to take the

divided dose consistently. They may be right for some people, I know I

resisted splitting dose for a long, long time. Funny thing is, since I've

done it, I've been moving steadily towards remission, after being stuck with

the same numbers and dose for a long time. I truly thing the body needs not

to see-saw at all, even subtly--so the divided dose, which means your body

won't at any point run out of medicine, keeps you on an even keel and lets

you heal. That's my theory, anyway.

Terry

>

> Reply-To: graves_support

> Date: Fri, 2 May 2003 22:38:47 -0500

> To: <graves_support >

> Subject: Re: Newbie questions....

>

> My current dosage went from 30 mgs to 20 mgs in the morning. Atenolol is also

> taken one 50 mg tablet each morning. I'm glad to hear that there isn't any

> nasty side effects for long term use, cuz I'm just not having RAI. I don't

> care what they say, it ain't happening. :-)

>

> I'll find my test results and post them so you can see where I'm at now.

>

> Thanx

> Sandy

> Re: Newbie questions....

>

>

> Hi Sandy,

>

> Your info is pretty general, so the response will be too. If you want to

> share the lab results it could help with specific answers to your questions.

> But I can say, having had GD since '94, and having been on

> methimazole/tapazole most of the time since then, that there's absolutely no

> rational reason to cut you off after 18 months, except perhaps the

> endo-agenda of moving you towards RAI. Long term use has no side effects!

> Granny who posts here, has been on for at least 23 years.

>>

>>

>

>

>

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...