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Re: help me find a doctor!

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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

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> 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

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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

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