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Dear Helen

I have been reading the emails on the forum for some time now and although I
dont personally have PD I saw your message requesting information on Deep
Brain Stimulation and thought that I would let you know that we can offer
DBS at a facility in Europe at Ghent, Belgium at a lower cost than it is in
the US.   If you like I can put you in touch with one of our specialists who
I'm sure would be only to willing to answer any questions that you may have.


warmest regards


Chas Seadon
Chief Executive

European Medical Care
Bruxelles
Belgium

Tel:  +32 (0) 2772 5515
Fax: +32 (0) 2772 5515
Freephone: 00800 27725515
Mobile: +32 (0) 478 390001
Email: [log in to unmask]
Website: www.euro-meds.com



I am new to this forrum but not to Parkinson's. More than 14 years ago I was
diagnosed as having Parkinso'n's when I went to my docor to see what was
causing all of the stiffness, feeling tired and many falls I'd been
taking and he said I most likely had had early stage parkinson's for at
least 3 or 4 years pryor to that.
My doctor put me on Sinemet right away. Like most people, as time went on,
my little blue friends became less
effective and as soon as it was approved about 4 or 5 years ago he added
Mirapex, a miracle drug for me.
We had tried many other drugs but none nearly as effective.  All in all,
even though my life style may have changed, I have done most everything I
wanted to do and did before except drive. My husband who is my wonderful
caregiver and very supportive family and friends have never made me feel
like a burden. I have found that people in general are very kind and
considerate even when I freeze and get in their way. My biggest problem has
been walking. Freezing and feeling sleepy have been a bother and my biggest
complaints until more than a year or so ago dyskinesias set in in full force
and it is getting worse. I said all that to ask others what, short of
surgery, they may have done or taken for help in this area. After watching
60 minutes last night, I'm beginning to wonder if Deep Brain Stimulation is
what I need to consider. My former Neur. tried to get me interested in
having it done
several years ago but it was too soon. I'd be vey intested in hearing from
anyone who has had the procedure
and is willing to share how it is working for them.

Thanks
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