Re: [Everything doTERRA] Re: Fibromyalgia and oils

Yes, Fibro is different in all of us. I have Fibromyalgia, and mine was affirmatively diagnosed through my Chronic Myofacial Pain Syndrome because although you can have Fibro w/o the CMPS, you can't have the CMPS w/o the Fibro. I already knew I had it due to having about 15 symptoms from the list, but the only pain I have is the CMPS pain that flares in my right shoulder from my neck to my deltoid. I treat that pain with Deep Blue, and it's the first thing I've ever tried that makes it go away. I had 12 hours of relief the first time I used it (and it's one of the things that sold me on our oils), and the next time I used it my attack ended...at a time when it was in the upswing, and hadn't even reached it's peak and hold level and time yet. 

Today another attack was starting and I put it on...we'll see how well it does, especially since I was also digging up a space, with my husband, for us to put in a new veggie garden. 

The rest of my Fibro, I treat with diet. No gluten, no sugar, no alcohol, lots of veggies, fish, poultry, very little pork or red meat (and only hormone-free and drug-free on the latter).

Enjoy your class. Would you mind sharing it afterward? That's a class I might consider holding as well, perhaps as an overall class about managing Fibromyalgia naturally.

~Diane Jarecki

Reiki Master Teacher

Spiritual Teacher

Wellness Coach

wingsoc@gmail.com

www.wingsochange.com

724-513-0055

"This is my simple religion. There is no need for temples; no need for complicated philosophy. Our own brain, our own heart is our temple; the philosophy is kindness." ~Dalai Lama

"I expect to pass through life but once. If therefore, there be any kindness I can show, or any good thing I can do to any fellow being, let me do it now, and not defer or neglect it, as I shall not pass this way again." ~William Penn

On Mon, Apr 11, 2011 at 2:04 PM, Jessi Harris <jessiharris5@yahoo.com> wrote:

On Apr 10, 8:24 pm, Ginny Eiseman <gi...@kpunet.net> wrote:
> I would also add that if one of your group tries and doesn't have the
> success rate you did to consider suggesting a Lyme disease test for
> them. Unfortunately, Lyme disease is commonly misdiagnosed as
> Fibromyalgia, especially if you live in a non-hot zone for ticks. I only
> mention it because I just spent the last 10 years being told that was
> what I had only to find out it was Lyme.
> gin
> Alaska
> On 4/10/2011 5:13 AM, Patricia Leavitt wrote:
>
>
>
> > The best thing you can tell your group is what helped you! There are many
> > who are building their own protocol depending on what oils works best for
> > them. Many of them swear by the LLV, Past Tense, Deep Blue,
> > Frankincense and
> > OnGuard.
> > Teach them to muscle test so they use the best oils for them'- Hide quoted text -
>
> - Show quoted text -


Thanks for all of your input. I have been tested for lyme disease and
the dr said i didnt. but i am now thinking that i might go and get
tested again! I would love to hear more of how you deal with your
lyme. I am very nervous to teach this class just becasue fibromyalgia
is so different in all people. I like the idea of muscle testing tho.
that was a great suggestion. If anyone else has anymore information i
would greatly appreciate it! Thanks to you all Jessi

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