cibess
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  • Boston, MA
  • United States
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At 12:47pm on July 26, 2013, Cordellia Amethyste Rose said…

No database.  In fact, if you go to the doctor, there's a big chance they won't have heard of it.  If you do see someone, make sure they're open-minded and willing to look at something new.  Take copies of the research done, which you can find on the links page.  You also might want to take copies of the articles written about it.  Be sure to mention that a real doctor with a PHD has studied this, and that it's being studied right now.  Mention that there are thousands of people online who say they have it.  There are many of us.  If they try to say it doesn't exist or misdiagnose you with the next closest thing they've heard of, walk out the door, and never go back.  Let us know how it goes.  

At 12:31pm on July 26, 2013, cibess said…
Thanks. Now what??? Can you help me? Do you have a database of practioners who help people like us?
At 9:05am on July 26, 2013, Cordellia Amethyste Rose said…

Welcome!  Thanks for joining!

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