Guest guest Posted January 1, 2001 Report Share Posted January 1, 2001 Hi Marilyn Welcome to the group, you will find a wealth of information of all kinds... but I'm sorry to hear you have RP to begin with...please let us know what kind of info you need and I'm sure someone has a file on it and will post it... if not we will try our best to find the info and post it to the group BTW, my name is Carmela, 42 yrs old and live in Montreal, Canada with my mom and sister.... I had my first RP attack in 1994 (nose only) and then again in Spring/Summer 2000 (temporal arteritis, nose)... I seem to be doing ok right now, we all kicked RP out the door at 12 midnight lol... so it's gone.... ) I hope you will find hope in this group just as I did... take care luv Carmela ************************** > >Reply-To: Rpolychondritis (AT) e >To: " Rpolychondritis (AT) e " Rpolychondritis (AT) e> >Subject: New member >Date: Mon, 01 Jan 2001 16:26:01 -0800 > >Hello, > >I am new to the list and would like to hear from others with RP. I was >diagnosed in May and things have really gone down hill, fast. I am 58, >live in WA, with my husband, son, and 2 fur children (cats, Rambo and >Sammy). My hobby is genealogy. >Happy New Year to all. Marilyn > _________________________________________________________________________ Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com. Quote Link to comment Share on other sites More sharing options...
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