Guest guest Posted November 7, 2002 Report Share Posted November 7, 2002 Yola, welcome. Glad to have you part of the group. We have a lot of knowledge and a lot of fun here. I'm so sorry to hear that you have RP., I live in Calif, am 51 and have 3 daughters. My flares are mostly ears, nose and ribs. RP can affect the throat. If you continue to have problems i would definately have it checked out. Are you on any medications now? Just remember that we are all different and it can affect us all in so many differernt ways. We do have other members in Austrailia. might be your neighbors. LOL Go to our Foundation site at www.polychondritis.org and you will fine there Dr. Trenthams article and Dr. Karin Harps. I believe Dr. Harps is under links " e medicine" YOu might find out more about throat involement there. Also Dr. Buckners site is listed under research there. Please continue to ask questions or share what you have learned about RP with us. looking forward to getting to know you better. hugs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 7, 2002 Report Share Posted November 7, 2002 Yola Welcome to the group! I am glad you found us even if it was by mistake. You will find that this is the greatest group of people you will ever get to meet. They are a wealth of information that is for sure. Ask all the questions you like. If they don't have the answers they will help you find them. I live on the west coast of the United States in Oregon. I have had RP for over 8 years. Mine is under control except for a minor flare once in awhile. I am 45 am married to the same man for the last 28 years. We have raise two children and are attempting to raise our oldest grandchild. She is 7 and keeps us busy. I lead a fairly normal life....that is for me anyway. I work 40 plus hours a week and attempt to take care of my home and family. Lately have been working too much according to the group but it will end soon. Now for the answer to your question about the sore throat. This could be a prelude to a problem with RP there. You need to have it checked out that is for sure. Are you taking any meds for the RP? If so what kind? Predizone is the drug that most of us use to keep the damage down due to the RP. I think we all hate it but would rather deal with the pred. than the damage that the RP causes. Remember I am no dr. Go get it checked out and please keep posting we want to get to know you better. Lots of Love Glenda Quote Link to comment Share on other sites More sharing options...
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