Sorry you need to be here but glad you found us and shared your unusual story about how Wegs attacked you and how your doctors finally discovered how to help you.
Sorry you need to be here but glad you found us and shared your unusual story about how Wegs attacked you and how your doctors finally discovered how to help you.
Knowledge is power! Wisdom is using it to make good decisions!
Welcome Sophie - sorry u have to join the gang !! But it's the best place to be for help support & advice
Good luck x love x and good voice x
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Welcome to the forum Sophie,
I am glad you finally have a diagnosis but sorry that like me you have WG. It took 2 years or more for doctors to figure out what was wrong with me. Glad that you are finally receiving treatment and that your voice has recovered.
Karen
Karen; dx'ed April 2014
Welcome Sophie! If I could travel anywhere, my first pick would be Switzerland. My husband and I did a tour decades ago. Had a wonderful time in France, Germany, Italy, Austria, Switzerland and Holland. e have always wanted to go back and spend more time in Switzerland after our three wonderful days in Lucerne. Welcome again. This a a terrific group!
Jacquie (aka Lifelong Booknut)
Updated status: "Honorary Weggie"
Welcome Sophie. My best friend is a patent attorney here in the states. It would be hard to have WG and maintain such a stressful job. I hope you have been able to find a good balance.
Sophie, Do you get cortisone shots often? My ENT said they were an option for me a while ago (maybe 4 years) but at that point I was frightened by the idea. Now I think they might be worth it. I'm going to talk with my doctors about it.
Diagnosed October 2012
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