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I was curious if anyone else received a questionnaire from PIC in the mail

last week. Has anyone had any recent correspondence with this group. They

contacted me months ago stating they were starting a non-profit organization

and a newsletter. At the time they had a web page.

I tried e-mailing them several times but never received any reply until

recently when they sent a letter requesting a membership fee. I did not

reply. Now I have received a survey requesting lots of personal info. They

say it is to help get laws passed for the coverage of Neocate.

I am hoping this is a legitimate group. Anything I can do to help families

get coverage for Neocate is worthwhile. BUT, I am concerned because the only

recent correspondence I have received has given very little info while

requesting money and personal information.

Unfortunately, in today's society you can never be too careful. Has anyone

else heard from them. Have you responded. Has anyone been in touch with the

two women who started this group.

Jen

( (11/7/95) eosinophilic esophagitis, food allergies, asthma)

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