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Hello!

I can't tell you how happy I am to find this list. The web sites are

so scary!

I am going to be 38 in two weeks and have just had my first intense

flare up and diagnosis of RP. I am anxious to hear about others'

experiences, as I don't see a rheumatologist until Christmas Eve

day. I have heard enough about the dangers and prognosis, but I want

to hear how people are LIVING with this rare condition.

Please offer any information, experiences, etc... I don't know if

it's proper to post my email, so I will wait until i hear about that,

but if it is, people can also email me directly.

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Hello!

I can't tell you how happy I am to find this list. The web sites are

so scary!

I am going to be 38 in two weeks and have just had my first intense

flare up and diagnosis of RP. I am anxious to hear about others'

experiences, as I don't see a rheumatologist until Christmas Eve

day. I have heard enough about the dangers and prognosis, but I want

to hear how people are LIVING with this rare condition.

Please offer any information, experiences, etc... I don't know if

it's proper to post my email, so I will wait until i hear about that,

but if it is, people can also email me directly.

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