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09/14/2007 07:26
BethAnn
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Hey, everyone! Check out this website! stopfibro.com What do you think?

BethAnn

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09/14/2007 10:32
TeaLady73
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New Test for Fibromyalgia

Dr Whitcomb as developed the first orthopedic test for Fibromyalgia. This test can be administered in his office and not only gives an absolute diagnosis for Fibromyalgia, but gives a positive indicator about how the patient will respond to treatment.

For more information call 530-543-1800.

if this is true and so great then why arent other docs using it?? KWIM???

Karen T


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09/14/2007 10:47
TeaLady73
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other then my last post, it seems to be a good site with lots of info, have you chacked out, fibrohope.org ?? its done by the fms association

Karen


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09/14/2007 10:50
ALB1
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Hey BethAnn, I don't have the time to watch the video but I will make time this weekend. Thanks for the heads up.

Jen

Post edited by: AmericanLadybug, at: 09/14/2007 12:51

My disabling chronic illness is more real than your imaginary medical expertise.
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09/14/2007 13:53
CJ
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hmmmm. Well I watched the video and found it personally difficult to tie in anything that was being said to FM. It was a discussion about adrenaline and anger and I don't see how that equates to Fibromyalgia unless he's saying that it's a state of mind.

Well, I can tell you it's not a state of mind having Fibromyalgia and I didn't eat the wrong pizza slice at the wrong time to get Fibromyalgia and I'm not a big fan of if I only eat these certain things I'll be cured.

That being said, apparently there are some people who do believe that diet can greatly help someone with FM. And that for them apparently it has worked for them. Well I think that's awesome... for them.

I'm very skeptical of anything that says the cure for Fibromyalgia is ...

I tend to stay on the side of science and believe that a cure doesn't exist, yet. However, there have been a good number of people that say that when they have used Lyrica it changed their lives and I truly believe them. I've seen people go from suffering to being able to feel alive again once they've started taking this drug. So if certain people say with a particular diet that they also felt the same way, I can't deny that they feel the way they do and that the method for them didn't work. Apparently it did work and that's great.

Where I get the most angry is when someone keeps emailing me or calling me or Private Messaging me to ask me when I'm going to "LET THEM" help me with my Fibromyalgia when I have expressed little or no interest in that method whatsoever. I'm great with a heads up, but I gotta say that if I'm being hounded by someone about something then for me it's no different than getting telemarketing calls.

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09/14/2007 14:20
BethAnn
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Please go back to the website and study it more carefully. Look for what he says is the cause of fibro and the total description. I think you might see that it all makes perfect sense. Dr Paul Whitcomb had fibo and now he doesn't. He understands perfectly what we are going through. Also, watch some of the testimonial videos--amazing. I can't wait to be able to go to the treatment center myself! I finally have hope! Please email me if you would like. I have been researching the imfo. a lot.

BethAnn

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09/14/2007 14:25
CJ
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Hey Bethann.

Thank you, but with all do respect I did go through the web information offered and didn't personally find it helpful, however, I like to keep an open mind so I'll read some more and see if there are any links to what I believe to be helpful and if so I'll endorse it.

Sorry. But I respect that it works for you and that if you feel it's helping you then that's awesome. But I still hold to what I said in my previous post and hope you will respect that.

Thank you again.

Post edited by: CJ aka Siskoray, at: 09/14/2007 17:07

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09/14/2007 14:32
BethAnn
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Dr. Whitcomb is being carefull so that the method of treatment is taught carefully and completely. There is one Chiropractor that is already trained and working with him. They already have a list of Drs. who want to learn the technique. I'm sure Osteopaths could learn also. Once you are able to study the complete website, you understand it. You can also call and speak to someone or even ask for the telephone #s of one of the already treated. I hope I am making sense as I am majorly foggy brained right now!
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09/14/2007 14:38
bshapiro
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Personally, I keep meaning to read up on this aspect of FMS but the whole thing makes my head hurt for some reason. Especially because Starlanyl is my FMS my FMS Goddess and she says that Adrenal disfunction is partly to blame. Again, I'm pretty vague on this other than my agreement that there are plans involved.

Starlanyl says that FMS is a dysfunction of the HPA Axis and somewhere in her book

Fibromyalgia and Chronic Myofascial Pain: A Survival Manual actually defines FMS that way. For quick take: go to Amazon and search for the word "adrenal" you'll find numerous references in the above-mentioned book but here's what she says on page 111

"... the hypothalamus of the pituitary glands (plus the type of gray matter in the nervous system) These glands, with the adrenals, formed the HPA Axis, the functioning of which is disrupted in FMS.

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09/14/2007 14:50
BethAnn
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Yes. That is it. If the C1 vertebrae is pressing on the menenges and the menenges is pulling on all the nerve roots then the body goes into "flight or fight" mode and super adrenaline. I know that's why I can't sleep well at night. I am stuck in stage 3 (dream state) and can't get into stage 4 which is the healing and full relaxation state. Once the C1 is stable and doesn't slip out of place any more, the healing of the body can start.
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