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In a message dated 08/05/2002 7:17:42 PM Pacific Daylight Time,

laughingbear@... writes:

>

> Hi I am new to the list .I have really bad leg cramps and nothing seems to

> help them. They are there all day, but at night in bed is when they really

> come hard and quick. Does anyone know of things that help get rid of them.

> I take calcium and magnesium, walk four

> times a day, take soma at bed time. Nothing is making a dent in the cramps

> and pain.

>

> Age: 57

>

> Male/female: Female

>

> What are the symptoms? leg pain, can't stand in one place more then a

> couple of minutes. Have trouble walking very far and can't stay seated for

> very long and still walk. Pain in other parts of body. Points all painful.

>

> Has you illness been diagnosed? Yes

>

> How long did you suffer before you got help? About six years.

>

> Is there a time that you can remember when it started? Yes after a flue

> bug hit I was unable to walk very far at all. That was the first real alarm

> signal.

>

> Some of us have found lack of exercise we are overweight. Have you found

> this to be a problem also? Am overweight have been for all of adult life.

> Only been a physical problem with the onset of fibro.

>

> Are you on disability? Yes

>

> If you are any pointers for others trying to get on disability? Just keep

> appealing. If can get state aid to say yes you have fibro it helps.

>

> What have you found that helps ease the pain, warm baths, medications etc.?

> Rest, soma for cramps . Not really anything but learning your body and

> trying not to overdo anything.

>

> Do you have sleep problems? How do you deal with it? Yes. I don't deal

> with it I need help in this area.

>

> Do you have family that understands your illness? No both daughters don't

> want to acknowledge their mom is sick.

>

> Some have found certain foods causes problems with CFS or Fibro, have you?

> I have food allergies like wheat, night shade family that when don't go

> near I feel better. But I haven't found anything that triggers fibro flare.

>

> What type of Doctor have you found that has helped you the most? One who is

> willing to listen is my current Dr. but he has no real handle on fibro. I

> am still looking for a Dr. who really has a clue on fibro. It's frustrating

> and I feel so hopeless. I mean I have to

> do research and then I have to convince my Dr. to go with a certain

> treatment.

>

>

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In a message dated 08/05/2002 7:17:42 PM Pacific Daylight Time,

laughingbear@... writes:

>

> Hi I am new to the list .I have really bad leg cramps and nothing seems to

> help them. They are there all day, but at night in bed is when they really

> come hard and quick. Does anyone know of things that help get rid of them.

> I take calcium and magnesium, walk four

> times a day, take soma at bed time. Nothing is making a dent in the cramps

> and pain.

>

> Age: 57

>

> Male/female: Female

>

> What are the symptoms? leg pain, can't stand in one place more then a

> couple of minutes. Have trouble walking very far and can't stay seated for

> very long and still walk. Pain in other parts of body. Points all painful.

>

> Has you illness been diagnosed? Yes

>

> How long did you suffer before you got help? About six years.

>

> Is there a time that you can remember when it started? Yes after a flue

> bug hit I was unable to walk very far at all. That was the first real alarm

> signal.

>

> Some of us have found lack of exercise we are overweight. Have you found

> this to be a problem also? Am overweight have been for all of adult life.

> Only been a physical problem with the onset of fibro.

>

> Are you on disability? Yes

>

> If you are any pointers for others trying to get on disability? Just keep

> appealing. If can get state aid to say yes you have fibro it helps.

>

> What have you found that helps ease the pain, warm baths, medications etc.?

> Rest, soma for cramps . Not really anything but learning your body and

> trying not to overdo anything.

>

> Do you have sleep problems? How do you deal with it? Yes. I don't deal

> with it I need help in this area.

>

> Do you have family that understands your illness? No both daughters don't

> want to acknowledge their mom is sick.

>

> Some have found certain foods causes problems with CFS or Fibro, have you?

> I have food allergies like wheat, night shade family that when don't go

> near I feel better. But I haven't found anything that triggers fibro flare.

>

> What type of Doctor have you found that has helped you the most? One who is

> willing to listen is my current Dr. but he has no real handle on fibro. I

> am still looking for a Dr. who really has a clue on fibro. It's frustrating

> and I feel so hopeless. I mean I have to

> do research and then I have to convince my Dr. to go with a certain

> treatment.

>

>

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In a message dated 08/05/2002 7:17:42 PM Pacific Daylight Time,

laughingbear@... writes:

>

> Hi I am new to the list .I have really bad leg cramps and nothing seems to

> help them. They are there all day, but at night in bed is when they really

> come hard and quick. Does anyone know of things that help get rid of them.

> I take calcium and magnesium, walk four

> times a day, take soma at bed time. Nothing is making a dent in the cramps

> and pain.

>

> Age: 57

>

> Male/female: Female

>

> What are the symptoms? leg pain, can't stand in one place more then a

> couple of minutes. Have trouble walking very far and can't stay seated for

> very long and still walk. Pain in other parts of body. Points all painful.

>

> Has you illness been diagnosed? Yes

>

> How long did you suffer before you got help? About six years.

>

> Is there a time that you can remember when it started? Yes after a flue

> bug hit I was unable to walk very far at all. That was the first real alarm

> signal.

>

> Some of us have found lack of exercise we are overweight. Have you found

> this to be a problem also? Am overweight have been for all of adult life.

> Only been a physical problem with the onset of fibro.

>

> Are you on disability? Yes

>

> If you are any pointers for others trying to get on disability? Just keep

> appealing. If can get state aid to say yes you have fibro it helps.

>

> What have you found that helps ease the pain, warm baths, medications etc.?

> Rest, soma for cramps . Not really anything but learning your body and

> trying not to overdo anything.

>

> Do you have sleep problems? How do you deal with it? Yes. I don't deal

> with it I need help in this area.

>

> Do you have family that understands your illness? No both daughters don't

> want to acknowledge their mom is sick.

>

> Some have found certain foods causes problems with CFS or Fibro, have you?

> I have food allergies like wheat, night shade family that when don't go

> near I feel better. But I haven't found anything that triggers fibro flare.

>

> What type of Doctor have you found that has helped you the most? One who is

> willing to listen is my current Dr. but he has no real handle on fibro. I

> am still looking for a Dr. who really has a clue on fibro. It's frustrating

> and I feel so hopeless. I mean I have to

> do research and then I have to convince my Dr. to go with a certain

> treatment.

>

>

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  • 3 months later...

Hi Arlyn,

Pretty frustrating isn't it? I'm sure that there are others on the board

who can offer more constructive advice. My problem seems to be the exact

opposite of yours. Normal range labs and very hypo. Thanks to a bunch of

very kind people on this list, I think I'm finally figuring it out.

Please don't despair. If you were stubborn enough to find this list, you

are probably stubborn enough to find some answers to your dilemma.

Hang in there,

Laurel

Re: Newbie

> Hi,

> Well that was $300 down...

> Saw an endo today. Said while I had all the symptoms, since my TSH was

> 2.3, I couldn't possibly be hyper.

> Suggested I see a psychiatrist.

> Anyone have normal numbers and are still being treated by their doctor?

> Would appreciate any input.

>

> Thanks,

>

> Arlyn

>

>

>

>

> -------------------------------------

> The Graves' list is intended for informational purposes only and is not

intended to replace expert medical care.

> Please consult your doctor before changing or trying new treatments.

> ----------------------------------------

> DISCLAIMER

>

> Advertisments placed on this yahoo groups list do not have the endorsement

of

> the listowner. I have no input as to what ads are attached to emails.

> --------------------------------------------------------------------------

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

>

>

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Hi Arlyn,

Pretty frustrating isn't it? I'm sure that there are others on the board

who can offer more constructive advice. My problem seems to be the exact

opposite of yours. Normal range labs and very hypo. Thanks to a bunch of

very kind people on this list, I think I'm finally figuring it out.

Please don't despair. If you were stubborn enough to find this list, you

are probably stubborn enough to find some answers to your dilemma.

Hang in there,

Laurel

Re: Newbie

> Hi,

> Well that was $300 down...

> Saw an endo today. Said while I had all the symptoms, since my TSH was

> 2.3, I couldn't possibly be hyper.

> Suggested I see a psychiatrist.

> Anyone have normal numbers and are still being treated by their doctor?

> Would appreciate any input.

>

> Thanks,

>

> Arlyn

>

>

>

>

> -------------------------------------

> The Graves' list is intended for informational purposes only and is not

intended to replace expert medical care.

> Please consult your doctor before changing or trying new treatments.

> ----------------------------------------

> DISCLAIMER

>

> Advertisments placed on this yahoo groups list do not have the endorsement

of

> the listowner. I have no input as to what ads are attached to emails.

> --------------------------------------------------------------------------

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

>

>

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  • 2 weeks later...

Hi,

Studies show that TSI is effective at predicting remission. Since your TSH

fell so much with the change of dosage, I suspect you're not quite

approaching remission just yet. 2.5 mg daily is the smallest recommended

maintenance dose for Tapazole. When you are in remission, then it's best to

wean off slowly using the 2.5 mg every other day to adapt your immune system

to the change. Take care, elaine

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Hi Pam -

Excellent ideas! If Zhi is getting too much iodine in her diet, that

may just be the last item to resolve and she could be in remission.

Judging by the T4 range she listed (0.9 to 1.8) it looks like this IS

the Free T4. Hopefully it is anyway. You never know what the lab

ranges are these days - some really screwy ones, but usually the

Total T4 is something like 5 to 12. She should double check on this

though, so thanks for pointing it out. Yes, the Total T4 doesn't

really tell you much because of the outside influences.

We missed ya!

Love ya,

Chris

>

> Now... ummmmm ...

> It is only T4 they tested here. So we really do not know what other

things

> could have influenced this reading. Is there any way to figure out

what her

> true FT4 numbers could even be close to ?

>

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Hi Pam -

Excellent ideas! If Zhi is getting too much iodine in her diet, that

may just be the last item to resolve and she could be in remission.

Judging by the T4 range she listed (0.9 to 1.8) it looks like this IS

the Free T4. Hopefully it is anyway. You never know what the lab

ranges are these days - some really screwy ones, but usually the

Total T4 is something like 5 to 12. She should double check on this

though, so thanks for pointing it out. Yes, the Total T4 doesn't

really tell you much because of the outside influences.

We missed ya!

Love ya,

Chris

>

> Now... ummmmm ...

> It is only T4 they tested here. So we really do not know what other

things

> could have influenced this reading. Is there any way to figure out

what her

> true FT4 numbers could even be close to ?

>

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Hi Pam -

Excellent ideas! If Zhi is getting too much iodine in her diet, that

may just be the last item to resolve and she could be in remission.

Judging by the T4 range she listed (0.9 to 1.8) it looks like this IS

the Free T4. Hopefully it is anyway. You never know what the lab

ranges are these days - some really screwy ones, but usually the

Total T4 is something like 5 to 12. She should double check on this

though, so thanks for pointing it out. Yes, the Total T4 doesn't

really tell you much because of the outside influences.

We missed ya!

Love ya,

Chris

>

> Now... ummmmm ...

> It is only T4 they tested here. So we really do not know what other

things

> could have influenced this reading. Is there any way to figure out

what her

> true FT4 numbers could even be close to ?

>

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  • 3 months later...
Guest guest

I would like some information from

>

> the group as my doctor thinks I am hyperthyroid. Is this the same as

>

> Graves disease?

Hi Lisbeth.

No, they are not the same, but both may respond well to anti-thyroid

drugs. The idea behind ATDs is that they suppress the overproduction of

thyroid hormone. Whether or not one returns to normal thyroid levels, on

a long term or permanent basis, is not a sure thing. BUT, treatment with

ATDs is relatively benign, compared with the standard treatment of

radioactive iodine (RAI), which destroys the thyroid, and will allow you

time to keep getting information.

You know, alot of people do OK after RAI, and I hope that all the people

on this list who have had RAI will stay in or join those ranks. However,

RAI will necessitate lifelong thyroid hormone replacement and there are

other not too rare complications; with all the rest of the medical stuff

you have to deal with you don't need that also.

How has he ruled out Graves Disease? Also, please feel free to share any

bloodwork results with the group, just including your labs normal ranges.

He should be taking a TSH, Free T4 and possibly T3, as well as

antibodies. If I have time, gotta run now, I'll send you info on

antibodies. Before starting you on ATDs you should also have an LFT

(liver function) and CBC.

Take care, Fay

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  • 1 year later...
Guest guest

In a message dated 3/10/2005 12:00:01 PM Eastern Standard Time,

lyn.worth@... writes:

> just bumping this one up as I recommended this site to Mo, telling her she

> would get excellent advice but I haven't seen any replies yet.

>

i didn't feel like I knew enough about adrenal to comment...but I do agree

that it appears that adrenal function is not optimum...and that adrenal fatigue

is apparent.

I do not think the DHEA was Normal - it was LOW ...and low DHEA is an

indicator of low adrenal function.

I would recommend Peatfield's protocol to her for adrenals.

here's one article, but there is another one if someone has the link.

http://home.no.net/ngrondal/durrant-p.html

cindi

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In a message dated 3/10/2005 12:00:01 PM Eastern Standard Time,

lyn.worth@... writes:

> just bumping this one up as I recommended this site to Mo, telling her she

> would get excellent advice but I haven't seen any replies yet.

>

i didn't feel like I knew enough about adrenal to comment...but I do agree

that it appears that adrenal function is not optimum...and that adrenal fatigue

is apparent.

I do not think the DHEA was Normal - it was LOW ...and low DHEA is an

indicator of low adrenal function.

I would recommend Peatfield's protocol to her for adrenals.

here's one article, but there is another one if someone has the link.

http://home.no.net/ngrondal/durrant-p.html

cindi

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Guest guest

In a message dated 3/10/2005 12:00:01 PM Eastern Standard Time,

lyn.worth@... writes:

> just bumping this one up as I recommended this site to Mo, telling her she

> would get excellent advice but I haven't seen any replies yet.

>

i didn't feel like I knew enough about adrenal to comment...but I do agree

that it appears that adrenal function is not optimum...and that adrenal fatigue

is apparent.

I do not think the DHEA was Normal - it was LOW ...and low DHEA is an

indicator of low adrenal function.

I would recommend Peatfield's protocol to her for adrenals.

here's one article, but there is another one if someone has the link.

http://home.no.net/ngrondal/durrant-p.html

cindi

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Guest guest

In a message dated 3/10/2005 1:08:27 PM Eastern Standard Time, usns@...

writes:

> My adrenals are not low functioning,

> yet I have low DHEA. Go figure.

>

>

and DHEA also goes low with age..as in over 50. :o

Cindi

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Guest guest

In a message dated 3/10/2005 2:21:02 PM Eastern Standard Time, usns@...

writes:

>

> Tish, what was that salary amount you told me I had to pay to keep

> you here??

i'm printing that post now - and have already forwarded it to two folks.

cindi

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Guest guest

In a message dated 3/10/2005 2:21:02 PM Eastern Standard Time, usns@...

writes:

>

> Tish, what was that salary amount you told me I had to pay to keep

> you here??

i'm printing that post now - and have already forwarded it to two folks.

cindi

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Guest guest

In a message dated 3/10/2005 2:21:02 PM Eastern Standard Time, usns@...

writes:

>

> Tish, what was that salary amount you told me I had to pay to keep

> you here??

i'm printing that post now - and have already forwarded it to two folks.

cindi

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Guest guest

In a message dated 3/10/2005 3:31:08 PM Eastern Standard Time, usns@...

writes:

> And I have the body of Madonna, the intellect of Einstein, two

> corvettes in our garage, and several mountain homes in the Swiss

> Alps.........

>

you've overdosed on the chocolate again too, haven't you?

cindi

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Guest guest

just bumping this one up as I recommended this site to Mo, telling her she would

get excellent advice but I haven't seen any replies yet.

Lynda (in the UK)

----- Original Message -----

From: hepaction@...

Hello everyone

I am Mo and this list has been recommended to me today. I am at the very

beginning stages of looking into the possibility that I am hypoadrenalic (if

that's the right word!) and hypothyroid. I have been assessed as such on

clinical signs and the first test I have done has come back today, the adrenal

profile. The figures are below.

I am hoping this group will be able to give me some feedback on these

figures to enable me to understand and maybe some tips about supplementation.

Salivary cortisol

8.00 10.2 6.0 to 33.0

noon 11.2 4.0 to 28.0 (this one was actually taken

at 1.30 pm)

4.00 6.1 4.0 to 11.8

midnight 5.0 1.0 to 5.0

DHEA

8.00 8.2 4.0 to 29.0

noon 7.1 2.5 to 13.0

4 pm 4.6 2.0 to 6.0

midnight 3.4 1.0 to 4.0

Comments:

Salivary cortisol relatively flat profile with values tending towards the

lower end of reference range (particularly early morning)

DHEA: overall profile indicates normal hormone output.

Not at all sure what this means apart from that my DHEA seems to be OK.

Any insights would be welcome. Thanks.

Mo

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Guest guest

just bumping this one up as I recommended this site to Mo, telling her she would

get excellent advice but I haven't seen any replies yet.

Lynda (in the UK)

----- Original Message -----

From: hepaction@...

Hello everyone

I am Mo and this list has been recommended to me today. I am at the very

beginning stages of looking into the possibility that I am hypoadrenalic (if

that's the right word!) and hypothyroid. I have been assessed as such on

clinical signs and the first test I have done has come back today, the adrenal

profile. The figures are below.

I am hoping this group will be able to give me some feedback on these

figures to enable me to understand and maybe some tips about supplementation.

Salivary cortisol

8.00 10.2 6.0 to 33.0

noon 11.2 4.0 to 28.0 (this one was actually taken

at 1.30 pm)

4.00 6.1 4.0 to 11.8

midnight 5.0 1.0 to 5.0

DHEA

8.00 8.2 4.0 to 29.0

noon 7.1 2.5 to 13.0

4 pm 4.6 2.0 to 6.0

midnight 3.4 1.0 to 4.0

Comments:

Salivary cortisol relatively flat profile with values tending towards the

lower end of reference range (particularly early morning)

DHEA: overall profile indicates normal hormone output.

Not at all sure what this means apart from that my DHEA seems to be OK.

Any insights would be welcome. Thanks.

Mo

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Guest guest

just bumping this one up as I recommended this site to Mo, telling her she would

get excellent advice but I haven't seen any replies yet.

Lynda (in the UK)

----- Original Message -----

From: hepaction@...

Hello everyone

I am Mo and this list has been recommended to me today. I am at the very

beginning stages of looking into the possibility that I am hypoadrenalic (if

that's the right word!) and hypothyroid. I have been assessed as such on

clinical signs and the first test I have done has come back today, the adrenal

profile. The figures are below.

I am hoping this group will be able to give me some feedback on these

figures to enable me to understand and maybe some tips about supplementation.

Salivary cortisol

8.00 10.2 6.0 to 33.0

noon 11.2 4.0 to 28.0 (this one was actually taken

at 1.30 pm)

4.00 6.1 4.0 to 11.8

midnight 5.0 1.0 to 5.0

DHEA

8.00 8.2 4.0 to 29.0

noon 7.1 2.5 to 13.0

4 pm 4.6 2.0 to 6.0

midnight 3.4 1.0 to 4.0

Comments:

Salivary cortisol relatively flat profile with values tending towards the

lower end of reference range (particularly early morning)

DHEA: overall profile indicates normal hormone output.

Not at all sure what this means apart from that my DHEA seems to be OK.

Any insights would be welcome. Thanks.

Mo

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Guest guest

HI Mo. Actually I don't see any severe adrenal problems, though I do

note that you are on the lower side of the range except at midnight.

Are you having any symptoms which are profoundly adrenal related?

Have you tried the pupil test? What about thyroid tests? What you

need are the free T3 and free T4.

Janie

> I am Mo and this list has been recommended to me today. I am at

the very

> beginning stages of looking into the possibility that I am

hypoadrenalic (if

> that's the right word!) and hypothyroid. I have been assessed as

such on

> clinical signs and the first test I have done has come back today,

the adrenal

> profile. The figures are below.

> I am hoping this group will be able to give me some feedback on

these

> figures to enable me to understand and maybe some tips about

supplementation.

>

>

> Salivary cortisol

> 8.00 10.2 6.0 to 33.0

> noon 11.2 4.0 to 28.0 (this one was

actually taken

> at 1.30 pm)

> 4.00 6.1 4.0 to 11.8

> midnight 5.0 1.0 to 5.0

>

> DHEA

> 8.00 8.2 4.0 to 29.0

> noon 7.1 2.5 to 13.0

> 4 pm 4.6 2.0 to 6.0

> midnight 3.4 1.0 to 4.0

>

> Comments:

> Salivary cortisol relatively flat profile with values tending

towards the

> lower end of reference range (particularly early morning)

>

> DHEA: overall profile indicates normal hormone output.

>

> Not at all sure what this means apart from that my DHEA seems to

be OK.

>

> Any insights would be welcome. Thanks.

>

>

> Mo

>

>

>

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Guest guest

HI Mo. Actually I don't see any severe adrenal problems, though I do

note that you are on the lower side of the range except at midnight.

Are you having any symptoms which are profoundly adrenal related?

Have you tried the pupil test? What about thyroid tests? What you

need are the free T3 and free T4.

Janie

> I am Mo and this list has been recommended to me today. I am at

the very

> beginning stages of looking into the possibility that I am

hypoadrenalic (if

> that's the right word!) and hypothyroid. I have been assessed as

such on

> clinical signs and the first test I have done has come back today,

the adrenal

> profile. The figures are below.

> I am hoping this group will be able to give me some feedback on

these

> figures to enable me to understand and maybe some tips about

supplementation.

>

>

> Salivary cortisol

> 8.00 10.2 6.0 to 33.0

> noon 11.2 4.0 to 28.0 (this one was

actually taken

> at 1.30 pm)

> 4.00 6.1 4.0 to 11.8

> midnight 5.0 1.0 to 5.0

>

> DHEA

> 8.00 8.2 4.0 to 29.0

> noon 7.1 2.5 to 13.0

> 4 pm 4.6 2.0 to 6.0

> midnight 3.4 1.0 to 4.0

>

> Comments:

> Salivary cortisol relatively flat profile with values tending

towards the

> lower end of reference range (particularly early morning)

>

> DHEA: overall profile indicates normal hormone output.

>

> Not at all sure what this means apart from that my DHEA seems to

be OK.

>

> Any insights would be welcome. Thanks.

>

>

> Mo

>

>

>

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