Guest guest Posted November 28, 2001 Report Share Posted November 28, 2001 Hello All, My Name is Bill and I live in Philly. I am 48 years old and was diagnosed With RP 2 years ago. I have been fine. I have had only 2 flair ups in the 2 years.. It effects my right ear.It gets big and red..and gives me the worst pain I have ever had in my life. But I Am fine now..The doctor says I may get more flair ups or never again..Who Knows..I am glad I found this group. It is nice to talk with people who relate...Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2001 Report Share Posted November 28, 2001 Hello All, My Name is Bill and I live in Philly. I am 48 years old and was diagnosed With RP 2 years ago. I have been fine. I have had only 2 flair ups in the 2 years.. It effects my right ear.It gets big and red..and gives me the worst pain I have ever had in my life. But I Am fine now..The doctor says I may get more flair ups or never again..Who Knows..I am glad I found this group. It is nice to talk with people who relate...Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2001 Report Share Posted November 29, 2001 Bonjour Bill, Hope you find a lot of support and informations in this group. Bienvenue Marie-pia de france Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2001 Report Share Posted November 29, 2001 Bonjour Bill, Hope you find a lot of support and informations in this group. Bienvenue Marie-pia de france Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2001 Report Share Posted November 29, 2001 Hi Bill My name is chuck, i was diagnosed last april with RP and like you, it's generally located in my ears. I don't get to this site as much as i did when i first was diagnosed because of my work and a business i am trying to launch but feel free to write if you want to chat or say hello. this group is great for information and input, this disease can get you down.....see you later...chuck..cistn@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2001 Report Share Posted November 29, 2001 Hi Bill My name is chuck, i was diagnosed last april with RP and like you, it's generally located in my ears. I don't get to this site as much as i did when i first was diagnosed because of my work and a business i am trying to launch but feel free to write if you want to chat or say hello. this group is great for information and input, this disease can get you down.....see you later...chuck..cistn@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 4, 2001 Report Share Posted December 4, 2001 Hi Bill, Do you take any medication for this illness? Welcome to the group, I'm always behind, sorry. I hate you have RP but your in the best place now. Lots of informative folks out here. Take care, Lu My Name is Bill and I live in Philly. I am 48 years old and was diagnosed With RP 2 years ago. I have been fine. I have had only 2 flair ups in the 2 years.. It effects my right ear.It gets big and red..and gives me the worst pain I have ever had in my life. But I Am fine now..The doctor says I may get more flair ups or never again..Who Knows..I am glad I found this group. It is nice to talk with people who relate...Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 4, 2001 Report Share Posted December 4, 2001 Hi Bill, Do you take any medication for this illness? Welcome to the group, I'm always behind, sorry. I hate you have RP but your in the best place now. Lots of informative folks out here. Take care, Lu My Name is Bill and I live in Philly. I am 48 years old and was diagnosed With RP 2 years ago. I have been fine. I have had only 2 flair ups in the 2 years.. It effects my right ear.It gets big and red..and gives me the worst pain I have ever had in my life. But I Am fine now..The doctor says I may get more flair ups or never again..Who Knows..I am glad I found this group. It is nice to talk with people who relate...Thanks Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.