Re: Welcome Sally

[Guest guest]

Sally, welcome to the best support group around. I'm sorry you need us, but

you will find almost anything you want here. From information, support, lots

of shoulders to cry on and most of all lots of laughter and hugs.

Please just jump right in and start asking all the questions you want.

There is never a silly question. We all learn by asking questions. Tell us

a little about yourself and where you live.

I live in Calif and have been diagnosed with RP for a little over 3 years.

Can't wait to get to know you better.

hugs

[Guest guest]

Hello Sally!

I'm sorry that you have RP, but I'm glad you found this group. I am

newly diagnosed, as of December, and have found so much support and

information through this group, that I don't know what I would have

done without it.

I am 38 yrs. old and live in Seattle. I have had minor symptoms of

RP for years, but had my first intensive flare (that is still active,

although much better now) in December.

I see Dr. Buckner here in Seattle, and you will see her name quite

often in the research about this condition.

I look forward to hearing from you!

Take care!

M

[Guest guest]

Sally,

Welcome to the group! So glad you found us. Please feel free to post all you like. We are here for you! No matter what the problem we like to hear about you the person.

I am 45, had RP for over 8 years and lead a fairly normal life. Okay as normal as possible for me!

Please tell us about yourself and where you live!

Lots of love

Glenda