Guest guest Posted December 17, 2003 Report Share Posted December 17, 2003 I will send you the list from the European countries Tia, it's a bit closer then the US.....at least they will be doctors that yoru doctor can talk and correspond with, and hopefully from there, formulate a treatment approach for you! Jill Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2003 Report Share Posted December 17, 2003 > I will send you the list from the European countries Tia, it's a bit closer then the US. > Jill If you want any help in locating practitioners for alternative approaches, let me know. I just did a quick internet search in the " find a practitioner " section for the Upledger Institute and did find some listed for Cranial Sacral and Lymphatic Drainage as a start. According to my Jin Shin Do directory, there are a number of practitioners in Europe, none listed specifically for Greece but several in Italy and Germany. I also have some contacts who could do some checking for Polarity practitioners. Mike Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2003 Report Share Posted December 18, 2003 Hi, I was misdiagnosed with rheumatoid arthritis in England. We lived there for 5 years, until 2 years ago, in Lytham St.Annes. There is another web site/supprt group that is based in the uk, but it doesn't get much action. I did see Dr. Bird's and Dr Grahm's names there a lot. I think you may have to go to London. But, that's always a nice trip! Good Luck! help me find a doctor! Hi to all Hope you are all well and happy! My sort story: Years ago, when the problems started, and after I was misdiagnosed (rheumatoid arthritis)and treated with lots of meds, only one, out of the 6 best Doctors who exam me, knew and diagnosed this syndrome, I was his first case, but then he became very old. After I became a member of the UK's EDS support group they told me that one of the Best doctors in our field was Greek and that he could do a correct diagnose of the syndrome and so did he, bad the problem is that he only saw me ones and he lives very far away (USA). So here I was totally alone and with no Doctor...and then...my brother searched in the net (who is a computer maniac), and he finally presents to me " the groups in the net " ! I saw this list and joined it, " 425 people, ouaouuuuuuuuuu " I said, and realized that I might felt as I was the only one here in my country but I am definitely not alone in this beautiful world. So what's left for me now? A DOCTOR, if not here, at least somewhere nearer than USA! Who would know everything about EDS, become my doctor and finally answer me some questions, and lastly help me start a pregnancy. By the way, has anyone else; had a fall in his/her white blood cells? Mine, after I started the meds (11 years ago) fell from normal value to 2500(min)-3300(maximum). Now they are 2800. Nobody knows here, some docs say that this might be due to the meds I once took, some others simply don't know! Hugs to all, Tia Quote Link to comment Share on other sites More sharing options...
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