Guest guest Posted May 7, 2002 Report Share Posted May 7, 2002 welcome nina.Ican't write too much about this goup because i'm french an my english is very poor.But it's such a nice and friendly group .you can find help of each sort here.bienvenue Marie-pia Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2002 Report Share Posted May 8, 2002 --- nina5808 wrote: > I'M NEW TO THIS .DIDN'T KNOW THERE WAS A SUPPORT > GROUP FOR RP. I WAS > FEELING ALL ALONE...I'M LOOKING AT HAVING MY NOSE > CARTLAGE REPLACED > SOON..HAS ANYONE BEEN DOWN THAT ROAD TO HELP LET ME > KNOW WHAT I'M IN > FOR...COULD USE SOME ONE TO TALK TO....NINA > > Welcome, Nina - you are not now alone!! There are around 200 in this group, although obviously we are not all active all the time. I have a hole in the cartilage in my nose, but I have never had any suggestion that it could be replaced, so I can't help on that one. My name is Liz, I have had rp I think at least 14 years, but it was only diagnosed about 5 years ago. However, I am much better since I have been taking meds (pred, methotrexate, plaquenil) for it! Tell us a little more about yourself. This group comprises a great bunch of people, and we give each other support, sympathy and laughter. It was a blessing to me when I found it - well, it still is!!! Look forward to hearing more, love Liz __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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