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In a message dated 9/12/98 7:07:09 AM Eastern Daylight Time, MAILER-

DAEMON@... writes:

<<

, I have talked to you online a few times, and hve joined this group to

try to help myself with what I was told was hypothyroid, not hyperthyroidism.

So is this group something I should remain on, or will you be covering both

of

these problems? Thanks. Chris

>>

The original message was received at Sat, 12 Sep 1998 07:06:25 -0400 (EDT)

from root@localhost

----- The following addresses had permanent fatal errors -----

<Hyperthyroidism@...>

----- Transcript of session follows -----

.... while talking to relay102.jaring.my.:

>>> RCPT To:<Hyperthyroidism@...>

<<< 550 <Hyperthyroidism@...>... Relaying Denied

550 <Hyperthyroidism@...>... User unknown

Hypo-

Content-type: text/plain; charset=US-ASCII

Content-transfer-encoding: 7bit

X-Mailer: AOL 4.0 for Windows 95 sub 214

, I have talked to you online a few times, and hve joined this group to

try to help myself with what I was told was hypothyroid, not hyperthyroidism.

So is this group something I should remain on, or will you be covering both of

these problems? Thanks. Chris

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  • 2 months later...

, and everyone, the more people talk about their symptoms, the more I

realize how many are mine. the feelings of rage, which I experience at

times, not a violent rage, but just periods of feeling really irritated with

something or someone. these have surprised me, but I thought it had to do with

menopause... are we mistaking any and all symptoms we get to hypo or hyper?

How can we tell?

, I had increased my zinc to 100 mg a day 3 weeks ago, and wonder if I

should still be taking that much....I don't seem to feel better or worst,

maybe better , surely, not worst....how long can I take that amount? I'm

taking 4 mg of copper also?

Chris

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

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  • 1 year later...

In a message dated 2/7/00 9:22:12 PM Eastern Standard Time,

onelist writes:

<< Hypothetical question - If you had $1 million dollars to donate (doesn't

have to be non-profit necessarily):

Which political organization (to rally for CFIDS issues) would you support?

>>

This is a good question, Marty. My family and I have been giving every year

to

the CAA, but now they aren't directly funding research. I asked around a few

months ago and nobody knew of any other org that made research grants. Other

than the CAA, I would like to hear of other 501c3 options, especially money

that would go to research.

Mike

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In a message dated 2/7/00 10:49:25 PM Eastern Standard Time,

MCamp10139@... writes:

<< I would like to hear of other 501c3 options, especially money

that would go to research. >>

Mike, not only does all of our money (National CFIDS Foundation) go to

research from any excess, but a portion of everyone's dues go toward

research. Right now, we are the only national organization funding CFS

specifically and we are 501© 3.

Gail

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Mike,

The National CFIDS Foundation is run in it's entirety by volunteers. Money

from all membership dues are applied to research because they don't have a

highly paid executive director or overpaid lobbyist. They have financed

research done by Hemex and the HHV6 group in WI.

http://www.cfidsfoundation.org/

Jerry

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

From: <MCamp10139@...>

> This is a good question, Marty. My family and I have been giving every

year

> to

> the CAA, but now they aren't directly funding research. I asked around a

few

> months ago and nobody knew of any other org that made research grants.

Other

> than the CAA, I would like to hear of other 501c3 options, especially

money

> that would go to research.

>

> Mike

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In a message dated 2/8/00 1:24:52 AM Eastern Standard Time,

onelist writes:

<< Mike, not only does all of our money (National CFIDS Foundation) go to

research from any excess, but a portion of everyone's dues go toward

research. Right now, we are the only national organization funding CFS

specifically and we are 501© 3.

Gail >>

Thanks, Gail. Since I am not a big fan of HEmex, I would like to know where

the research money is going to go before I make the donation. Who decides

at the ncf?

Mike

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In a message dated 2/8/00 7:37:10 PM Eastern Standard Time,

MCamp10139@... writes:

<< Thanks, Gail. Since I am not a big fan of HEmex, I would like to know

where

the research money is going to go before I make the donation. Who decides

at the ncf?

>>

Actually, Hemex has already spent over $100,.000 out of their own pockets for

thier research. We funded only for the initial blind cultures to be given to

them (double-blinded) for about $4,000. Our grant to Drs. Knox and Carrigan

to find something that destroyed HHV-6A but be non-toxic to the patient is

still ongoing (with one success already). That was nearly triple. We've

also funded one pediatric study. Our plans for a future study will be one

that is to independently done to prove what one causative feature of CFIDS

leads to so that we can begin to fund methods to turn this around. Our

medical board makes not only the suggestions, but votes along with board

members. Board members are open to any member who can take on a part of our

group by themselves. The medical board is made up of medical progessionals

who are both patients and non-patients (about a 50-50 split). Treatment is a

priority.

Gail

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In a message dated 2/9/00 12:10:11 PM Eastern Standard Time,

moores@... writes:

<< If Hemex is willing to do studies for only 4000 buck then they are very

generous. I need to join your organization & I know you have given me the

address before but where do I send my check. >>

National CFIDS Foundation, Inc.

103 Aletha Rd.

Needham, MA 02492

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If Hemex is willing to do studies for only 4000 buck then they are very

generous. I need to join your organization & I know you have given me the

address before but where do I send my check.

steve

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In a message dated 2/9/00 2:30:04 PM Eastern Standard Time,

moores@... writes:

<< how much to join? >>

The annual dues is $25.00 with a portion of that going to research. (We have

no paid employees and practically no overhead.) We waive all members who

cannot afford that financially, though, and do not ask for reasons or proof

since we feel it's bad enough to not have the money.

Gail

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how much to join?

GAILRONDA@... wrote:

> From: GAILRONDA@...

>

> In a message dated 2/9/00 12:10:11 PM Eastern Standard Time,

> moores@... writes:

>

> << If Hemex is willing to do studies for only 4000 buck then they are very

> generous. I need to join your organization & I know you have given me the

> address before but where do I send my check. >>

>

> National CFIDS Foundation, Inc.

> 103 Aletha Rd.

> Needham, MA 02492

>

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

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  • 1 year later...
Guest guest

Dee,<br>Yes that is very intresting. I was wondering the same thing myself, the

connection between hypothroidism and ADHD.<br>Wonder if there is something to

it???<br>

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Guest guest

You know, I belong to a group like this for ADHD

children. I am going to ask them to see if any of the other

women in that club have Hypo Thyroid. Also, to see if

it happened after they had there first child. Boy,

we might have stumble onto something. Wish, we could

get paid for the study! LOL!!!<br><br>Wishing all is

well! Tonight or TOday is me and my Bo's 6 month

anniversary, and I am taking it easy, after my son is dropped

off with his father. I am not saying a word to my Ex,

and if he speaks to me, I am just going to tell him

to tell his lawyer to call mine. I am sooooooooooooo

stressed out this week with the new meds, and I still

looked like I was 9 months pregnant last night. This

morning, I woke up and felt like someone beat me up in my

stomach! I go next week for a check up. Still haven't lost

any weight. Very depressed. I got a spiral perm, and

my bangs are too kinky, I feel ugly, can't

concentrate, can't sleep well, my mind is all over the place.

I try to relax, but **POP** the stressors go right

into my head. I HATE THIS I HATE THIS I HATE

THIS!!!!!! I was wondering maybe I should go off of all the

benzo's and antidepressants, now they know I have a Hypo,

and see what happens? I will ask the doctor, but what

does everyone usually take?<br><br>Hope<br>Hoping for

piece of mind!

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  • 9 months later...

Is there a link between hypoglycemia and gallstones or gallbladder attack ?

I'm asking this question because I've got some pain at the upper right side all

day long.

The doctor comfirm that I have gallstones in the gallbladder but since I've got

hypoglycemia, I have to avoid all citrus fruit. So what can I do to resolve this

problem ?

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