University of Athens. Well I was in their hospital, but did not get the help I need. I might have contributed to their research though, with my rare illness.
In the newsletter you state you have multiple international branches. I need contact details in both Germany and Greece, if available, please.
Thanks. Yes I know this publication; just reading it again, and it is enough to make me dispaire, cause I went undiagnosed for 8 years with no treatment whasoever, huge damage has been done, possibly irreversible, and I am being denied the treatment now. !!!
Hi, I have MMN and yes, I deteriorate considerably in cold weather. In fact, any time I have deteriorated, was in the winter. My MMN also started in the winter, or at least that’s when I noticed something was wrong. Many people with MMN do report getting worse in cold weather. Well, my hands just get unusable, and it’s not even so cold where I am now (Greece), but it’s too cold for my condition. Maybe it is similar with CIDP. See how you can keep yourself warm. For myself, I will be maybe the only person around going out with hand gloves, starting from tomorrow. There is not much else I can advise, just keep yourself warm if possible. Unfortunately, I didn’t get better in the spring, but that may be because I didn’t receive any treatment, being undiagnosed until only 2 weeks ago for several years.
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