Guest guest Posted August 26, 2002 Report Share Posted August 26, 2002 Welcome to , Dr. Wolkerstorfer, I am the group Moderator; you can email me personally at liliwigg@... - terribly sorry you have had to wait so long - the time change from your Austria to my California is considerable and I just turned on my computer for the day! You can also contact me through this address; List owner: -owner You are our first member from Austria! We have members throughout Europe, including Germany and Switzerland; perhaps they will speak up now! I would have responded to your German post, but for lack of practice, now all I can do is read your language, but unable to write back! Again, welcome to ! Yes, I believe there is a German CMT page - will look for it for you and post if I find it. There are several European language CMT pages. ~ Gretchen/the Moderator You are not alone with ! Recent Neurocast Statistics show 50% of us have CMT Type 1; 20-40% of us have CMT Type 2; 10-15% of us have CMT Type X; And 20% of us show NO family history. For more information on these and other statistics, visit http://www.neurocast.com and click on 'previous sessions'. Look for the title " Diagnosing Peripheral Neuropathies " . is Charcot Marie Tooth Universal Services - for you, your loved ones, the medical and scientific community, and anyone who wants to learn how CMT/HMSN affects each of us through experiential sharing. Quote Link to comment Share on other sites More sharing options...
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