> 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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