Re: pain/ inflammation

[Guest guest]

if you have pain? and you are a thyroid patient?

the odds are super high that your cells are not getting enough T3* thryodi

hormone -and that your FREE T3 and Reverse T3 tests are not Optimal .. optimal

VS normal

i had fibroymyalgia and " Adrenal Fatiuge " (HIGH cortisol) for decaades cuz my

doctors forced me onto Sinthroid (T4 only RX)

and they never assessed my adrenals

aka " Adrenal Fatigue " is really abotu our entire stress system, including brain

and all the stress hormones and neuropeptides the brain makes in stress mode

=the adrenals and cortisol are the tail end of a very huge pink elephant that

" Modern Medicine' has been ignoring in Thryod patients and othres !

TO get better

- fully assess all thryoid and autoimmune tests and SIgns/Symtpoms!

- fully test ferritin and Iron panel (related to cellular metabolic pathways

that do the REAL work IN our cells

- learn about " Adrenal Fatiuge " signs/symtposm and LIfestyle Guidelines! as

consistently following these daily rules helps remove much stressors from your

BODY/BRAIN total stress load

the brain's and body's stress 'chemicals' are very catabolic and have a profound

affect at our Cellular level! where the pain and 'tightness' and damage occurs.

= Fibromyalgia

*Unoptimal Thyroid hormone levels (All 5 Hormones btw:) is a HUGE stressor to

the stress system

which is why many patients who are not on the best treatment or dosage -for

them- will suffer from Fibromyalgia -or other related diseases.

-Carol

PS

Pain RX Drugs are 2 hard on our Gut health AND our liver which is already slowed

from being HYPOT.

>

> What do your doctors give you ladies for pain management and inflammation.

>

> Mine just put me on diclofen for right now since I am in so much pain and

> inflamed.  I was just wondering what you all take.

>

>

>

[Guest guest]

I am on the Levothyroxine ( generic for synthroid). I have often wondered about fibroymyalgia Don't doctors diagnosis this off symptoms?

I have a friend who recently found out she has Lyme disease. the doctors had been treating her for 15 years for fibroymyalgia she moved and a new doctor asked is she had ever been tested for Lyme. Not one doctor had ever asked her or figured out to test her. She suffered all these years.

The cataflam they put me on for inflamation has helped, but I feel like I am adding for medications for symptoms and not really treating the source of the problem.

I fell a couple years ago and hurt my lower back, but I know much of my pain the the Hashimoto's. It is so hard not to get just plain weary from the pain and other symptoms.

To: Thyroiditis Sent: Fri, January 21, 2011 12:31:34 PMSubject: Re: pain/ inflammation

if you have pain? and you are a thyroid patient?the odds are super high that your cells are not getting enough T3* thryodi hormone -and that your FREE T3 and Reverse T3 tests are not Optimal .. optimal VS normali had fibroymyalgia and "Adrenal Fatiuge" (HIGH cortisol) for decaades cuz my doctors forced me onto Sinthroid (T4 only RX) and they never assessed my adrenals aka "Adrenal Fatigue" is really abotu our entire stress system, including brain and all the stress hormones and neuropeptides the brain makes in stress mode=the adrenals and cortisol are the tail end of a very huge pink elephant that "Modern Medicine' has been ignoring in Thryod patients and othres !TO get better- fully assess all thryoid and autoimmune tests and SIgns/Symtpoms!- fully test ferritin and Iron panel (related to cellular metabolic pathways that do the REAL work IN our cells - learn about "Adrenal Fatiuge"

signs/symtposm and LIfestyle Guidelines! as consistently following these daily rules helps remove much stressors from your BODY/BRAIN total stress load the brain's and body's stress 'chemicals' are very catabolic and have a profound affect at our Cellular level! where the pain and 'tightness' and damage occurs. = Fibromyalgia *Unoptimal Thyroid hormone levels (All 5 Hormones btw:) is a HUGE stressor to the stress systemwhich is why many patients who are not on the best treatment or dosage -for them- will suffer from Fibromyalgia -or other related diseases.-CarolPS Pain RX Drugs are 2 hard on our Gut health AND our liver which is already slowed from being HYPOT.>> What do your doctors

give you ladies for pain management and inflammation.> > Mine just put me on diclofen for right now since I am in so much pain and > inflamed. I was just wondering what you all take.> > >

[Guest guest]

That is probably quite true. I found doctors were quite quick to throw drug after drug at me without bothering to look into the root cause. I had multiple doctors want to put me on Lyrica. My general pain issues are connected to being hypo and an odd reaction I have to steroids. Stopped the steroids and much of the joint pain and brain fog went away. If I am on enough thyroid meds my all over pain is tolerable and my back pain can be kept under control with tramadol and anti inflammatory patches. The root cause for many of my problems all came back to my thyroid. The steroids were for out of control allergies and asthma, then they wanted me to take lyrica to solve the side effects of the steroids. The root cause of the out of control allergies and asthma was being hypo. Lyrica is some very heavy duty stuff with lots of side effects. Doctors should not be handing it out like candy.

These anti-inflammatory patches are wonderful. The actual arthritis damage in my spine is localized in a couple of vertebrae so I put the patch over that area rather than taking NSAIDS or Celebrex. I have lots of bad reactions to NSAIDS. My doctor thought this was a better solution since less gets in your system. They make a night and day difference. They are Flector patches.

(in SD)

 

I am on the Levothyroxine ( generic for synthroid).   I have often wondered about fibroymyalgia  Don't doctors diagnosis this off symptoms?   

 

I have a friend who recently found out she has Lyme disease.  the doctors had been treating her for 15 years for fibroymyalgia  she moved and a new doctor asked is she had ever been tested for Lyme. Not one doctor had ever asked her or figured out to test her.  She suffered all these years.

 

The cataflam they put me on for inflamation has helped, but I feel like I am adding for medications for symptoms and not really treating the source of the problem.

I fell a couple years ago and hurt my lower back, but I know much of my pain the the Hashimoto's.  It is so hard not to get just plain weary from the pain and other symptoms.