Re: Re:Oh the theories of this -- Brain fog

[Guest guest]

Actually I had the brain fog long before any narcotic meds. Also, I still get

it when I DONT take my medication. The hydrocodone actually helps lift my brain

fog and works on my fatigue as well as pain.

hugs,

Debra V.

Kate Court wrote:

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 a bit out of date, but still some helpful info.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.

[Guest guest]

I was thinking of the anti depressants and epileptic meds.

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.

[Guest guest]

So do I, Marti

wrote: I have to disagree. I have brain

fog without meds. It is part of this dd fibro. My 2 cents.

Kate Court wrote: I was thinking of the anti

depressants and epileptic meds.

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.

[Guest guest]

I don't think the brain fog was caused by meds. I had it before I

went on any of the meds. I was told then that it was from the celiac

disease as I hadn't been diagnosed yet with fibro. celiac disease

doesn't require any meds - just good healthy gluten free food.

Margaret B

> So do I, Marti

>

> wrote: I have to disagree. I

> have brain fog without meds. It is part of this dd fibro. My 2 cents.

>

> Kate Court wrote: I was thinking of the

> anti depressants and epileptic meds.

>

> Re: Re:Oh the theories of this -- Brain fog

>

> Actually I had the brain fog long before any narcotic meds. Also, I

> still get it when I DONT take my medication. The hydrocodone

> actually helps lift my brain fog and works on my fatigue as well as

> pain.

> hugs,

> Debra V.

>