Re:Oh the theories of this disease..... what confusion

[Guest guest]

My doctors told me that fibro is " neurological " so I guess that comes under

" central nervous system " . I wish they could figure out exactly what causes it

so then maybe they could figure out more meds.

Ruthie

[Guest guest]

I kind of agree with you and your docs Ruthie. I truly believe it is the

central nervous system

because just about every symptom of this can be traced to the affects of a

whacked out nervous system. Now, it is possible though that their is some kind

of toxin messing with the CNS. Or a chemical imbalance, or deficiency. etc.

But I really think that is the newest and best theory of this damn thing.

Thanks so much for being here for me. I don't know what I would do without

all my cyber friends at this site.

love ya for real,

Debra V.

Ruthie Dyer wrote:

My doctors told me that fibro is " neurological " so I guess that comes

under " central nervous system " . I wish they could figure out exactly what causes

it so then maybe they could figure out more meds.

Ruthie

[Guest guest]

Part of the confusion comes from newer research. From my

understanding fibro was once considered autoimmunie and is now

considered central nervous in the latest research.

>

> I'm reading that book by Dr. Wallace that Angie recommended. He

writes

> about the Autonomic Nervous System, which if I understood correctly

is a

> subset of the CNS. The actual physiology and stuff kind of was

over my

> head, but he refers often to the ANS being the root cause of FM.

And in

> case someone needs the title of the book, is is " Fibromyalgia- An

Essential

> Guide for Patients and Their Families. " It was written in 2003, so

already

> a bit out of date, but still some helpful info. I haven't finished

the book

> yet. I also bought Fibromyalgia for Dummies to read after I finish

with Dr.

> Wallace's book.

> Jeanne in WI

>

>

> >I kind of agree with you and your docs Ruthie. I truly believe it

is the

> >central nervous system

> > because just about every symptom of this can be traced to the

affects of

> > a whacked out nervous system. Now, it is possible though that

their is

> > some kind of toxin messing with the CNS. Or a chemical

imbalance, or

> > deficiency. etc.

> > But I really think that is the newest and best theory of this

damn thing.

> > Thanks so much for being here for me. I don't know what I would

do

> > without all my cyber friends at this site.

> > love ya for real,

> > Debra V.

>

[Guest guest]

I strongly beleive a lot of this brain fog is meds affecting out bodies how many

of us are on meds where confusion/ brain fog is part of the side effect list.

Re:Oh the theories of this disease..... what confusion

Part of the confusion comes from newer research. From my

understanding fibro was once considered autoimmunie and is now

considered central nervous in the latest research.

>

> I'm reading that book by Dr. Wallace that Angie recommended. He

writes

> about the Autonomic Nervous System, which if I understood correctly

is a

> subset of the CNS. The actual physiology and stuff kind of was

over my

> head, but he refers often to the ANS being the root cause of FM.

And in

> case someone needs the title of the book, is is " Fibromyalgia- An

Essential

> Guide for Patients and Their Families. " It was written in 2003, so

already

> a bit out of date, but still some helpful info. I haven't finished

the book

> yet. I also bought Fibromyalgia for Dummies to read after I finish

with Dr.

> Wallace's book.

> Jeanne in WI

>

>

> >I kind of agree with you and your docs Ruthie. I truly believe it

is the

> >central nervous system

> > because just about every symptom of this can be traced to the

affects of

> > a whacked out nervous system. Now, it is possible though that

their is

> > some kind of toxin messing with the CNS. Or a chemical

imbalance, or

> > deficiency. etc.

> > But I really think that is the newest and best theory of this

damn thing.

> > Thanks so much for being here for me. I don't know what I would

do

> > without all my cyber friends at this site.

> > love ya for real,

> > Debra V.

>

1. While it is wonderful to share our experiences with everyone on the list as

to what treatments do and don't work for us, pls always check with your dr.

Some treatments are dangerous when given along with other meds as well as to

certain health conditions or just dangerous in general.

2. If you are in a difficult situation (doesn't matter what it is) pls don't be

afraid to ask for help. It is the first step to trying to make that situation

better.

3. To unsubscribe the e-mail is:

Fibromyalgia_Support_Group-unsubscribe

4.. Also, it is not uncommon for more than one member to be feeling bad at the

same time when it comes to flares and b/c of that potentially take something

another member says the wrong way. And that includes the things that one member

may find funny (even if it's laughing at fibro itself) even though we who deal

with illness whether one such as fibro or multiple illnesses try to keep a sense

of humor.

5. Pls let's be gentle with each other, and if you are having a bad day pls let

us know so that we can do our best to offer our support.

Have a nice day everyone.